CA2365099C - Transgenic plants that are resistant to a broad spectrum of pathogens - Google Patents

Abstract

Transgenic plants that express dermaseptin and/or temporin peptides are disclosed. In certain embodiments, these plants have enhanced, broad-spectrum pathogen resistance and are useful as agricultural or horticultural crops. In other embodiments, the plants are used to produce large quantities of the dermaseptin and/or temporin peptides.

Description

TRANSGENIC PLANTS THAT ARE RESISTANT TO A BROAD SPECTRUM
OF PATHOGENS

FIELD OF THE INVENTION
This invention relates to plants that are genetically engineered to express one or more peptides belonging to the temporin and/or dermaseptin families.
BACKGROUND OF THE INVENTION
Plants are hosts to thousands of infectious diseases caused by a vast array of phytopathogenic fungi, bacteria, viruses, and nematodes. These pathogens are responsible for significant crop losses worldwide, resulting from both infection of growing plants and destruction of harvested crops. The most widely practiced methods of reducing the damage caused by such pathogens involve the use of various chemical agents. Unfortunately, many pathogens develop resistance to such chemicals, and some pathogens (especially viruses) are not susceptible to control by chemical means. In addition, many of the chemical agents used are broad-spectrum toxins, and may cause serious environmental damage, as well as toxicity in humans.
Plant breeding and, more recently, genetic engineering techniques have also been employed to combat plant pathogens. In certain instances, breeders and molecular biologists have successfully engineered resistance to certain pathogens. In the last few years, a number of plant R (resistance) genes have been isolated from plants. When introduced into otherwise susceptible crops, these R genes produce enhanced resistance to certain pathogens. For example, U.S. patent No.
5,571,706 describes the isolation of the tobacco N gene, which confers enhanced resistance to Tobacco Mosaic Virus. However, while conventional breeding and genetic engineering approaches reported to date can successfully enhance pathogen resistance, they typically address problems caused by just one pathogen, or a small number of closely related pathogens. As a result, while crops produced using these approaches may have enhanced protection against one pathogen, conventional chemical agents must still be used to control others.

It would be of great agricultural benefit to be able to produce plants having enhanced resistance to a broad spectrum of pathogens, including bacterial and fungal pathogens. It is to such.plants that the present invention is directed.

SUMMARY OF THE INVENTION
The present inventors have discovered that the expression of certain peptides in transgenic plants confers broad spectrum pathogen resistance, including enhanced resistance to both fungal and bacterial pathogens. The peptides in question are small, positively charged (cationic) peptides belonging to the temporin and dermaseptin families, which occur naturally in the skin of certain species of frog.
Transgenic plants provided by the invention may be used in conventional agricultural applications, such as food crops. Alternatively, the plants may be harvested and processed to extract the expressed temporin and/or dermaseptin peptides, which may then be purified for use in medical and other applications.
The invention thus encompasses transgenic plants that express at least one dermaseptin or temporin peptide, and methods of making such plants. Parts of such plants, including seeds, fruit, stems, leaves and roots, may be utilized in conventional ways as food sources, or as a source of the dermaseptin or temporin peptides.
Because all plant types are susceptible to one or more plant pathogens, the present invention may be usefully applied to produce broad-spectrum resistance in any plant type. Thus, the invention may be applied to both monocotyledonous, dicotyledenous and gymnosperm plants, including, but not limited to maize, wheat, rice, barley, soybean, cotton, beans in general, rape/canola, alfalfa, flax, sunflower, safflower, brassica, cotton, flax, peanut, clover; vegetables such as lettuce, tomato, cucurbits, cassava, potato, carrot, radish, pea, lentils, cabbage, cauliflower, broccoli, Brussels sprouts, peppers; tree fruits such as citrus, apples, pears, peaches, apricots, walnuts; and flowers such as orchides, carnations and roses.

In its most basic form, the invention provides transgenic plants that express one or more dermaseptin and/or temporin peptides. Members of the dermaseptin and temporin peptide families are well known in the art. Examples of dermaseptins that may be used in the invention include, but are not limited to, the dermaseptins described by Mor. et al., Biochemistry, 30:8824-8830, 1991, Strahilevitz, Biochemistry, 33:10951-10960, 1994 and Wechselberger, Biochim. Biophys. Acta 1388: 279-283, 1998.
Examples of temporins that may be used include, but are not limited to, the temporins described by Simmaco et al., Eur. J. Biochem., 242:788-92, 1996. In their natural state (i.e., expressed in frog cells), both dermaseptin and temporin peptides are produced as precursor forms that are subsequently processed by proteolytic cleavage to form mature proteins. The mature forms of dermaseptins are typically about 27-34 amino acids in length, while the mature forms of temporins are typically about 10-13 amino acids in length. The invention contemplates the use of both the naturally occurring full-length (unprocessed) forms of these peptides, as well as the mature (processed) forms of the peptides and intermediate forms. In addition, synthetic forms of the peptides may also be employed. Synthetic forms of the peptides include any form that is not naturally occurring, and encompasses peptides that differ in amino acid sequence from the naturally occurring peptides, but which still retain dermaseptin or temporin biological activity. Such sequence variants will typically retain at least 40% amino acid sequence identity with at least one naturally occurring dermaseptin or temporin peptide.
Other synthetic forms of dermaseptins and temporins that may be employed include forms having N-terminal peptide extensions. Such peptide extensions may comprise portions of the precursor forms of dermaseptins or temporins that are usually removed during protein processing, or may be synthetic sequences. These N-terminal peptide extensions may serve to provide enhanced resistance to proteolytic cleavage, and may also enhance the antimicrobial activity of the peptides. Typically, these N-terminal extensions are of between 2 and 25 amino acids in length, although longer extensions may also be employed. Examples of N-terminal extension sequences that are utilized in certain embodiments include the peptide sequences MAMWK and MASRH. The AMWK sequence is a naturally-occurring peptide extension; it is part of the full-length dermaseptin-b peptide sequence that is normally cleaved during processing. The ASRH
is a synthetic extension sequence. In each case, the N-terminal methionine is added to the extension peptide to ensure proper expression of the peptide.
While the fundamental aspect of the invention is based on the expression of temporin and dermaseptin peptides in transgenic plants, other amino acid sequences may be joined to the peptides in order to produce fusion peptides. Expression of such fusion peptides in transgenic plants may provide even more effective broad-spectrum pathogen resistance than expression of temporin or dermaseptin peptides alone, or may enhance stability of the expressed dermaseptin/temporin molecule to provide higher expression levels, and thereby facilitate purification of the peptide from plant tissues.
Thus, in other embodiments, the invention provides transgenic plants that express a fusion peptide comprising:
(1) a first peptide sequence that is a dermaseptin or a temporin; and (2) a second peptide sequence operably linked to the first peptide sequence.
The second peptide sequence is typically, but not necessarily, linked to the amino (N-) terminus of the first peptide sequence.
In certain embodiments, the second peptide sequence comprises an anionic (negatively charged) "pro-region" peptide sequence. Such pro-region peptides serve to neutralize the cationic nature of the dermaseptin or temporin and may thus provide enhanced stability in the cellular environment. Thus, these pro-regions generally include a number of negatively charged amino acids, such as glutamate (Glu or E) and aspartate (Asp or D). Suitable pro-regions include those that are found in naturally occurring unprocessed (full-length) dermaseptin and temporin peptides, as well as anionic pro-regions from other peptides, including those of mammalian origin, such as the pro-region from sheep cathelin proteins. Fusion peptides that include such pro-regions may be represented as P-D or P-T, wherein P is the pro-region peptide, T is a temporin peptide and D is a dermaseptin peptide.
Although such pro-region peptides may be directly joined to the N-terminus of the dermaseptin or temporin peptide, it may be beneficial to join the two peptides using a spacer peptide. The use of spacer peptides to join two peptide domains is well known in the art; such spacer peptides are typically of between 2 and 25 amino acids in length, and provide a flexible hinge connecting the first peptide sequence to the second peptide.
Spacer sequences that have been used to provide flexible hinges connecting two peptide sequences include the glycine(4) serine spacer (GGGGS x3) described by Chaudhary et al., Nature 339: 394-397, 1989. Alternatively, an N-terminal peptide extension as described above may serve to provide the spacer peptide function. Fusion peptides that comprise a pro-region peptide, a spacer peptide and a dermaseptin or temporin peptide may be represented as P-S-D or P-S-T, wherein S represents the spacer peptide.

Spacer sequences may also include a cleavage site, such as a peptide sequence recognized and cleaved by a protease. Such sites facilitate removal of the pro-region from the dermaseptin or temporin peptide following purification from plant tissues.

These and other aspects of the invention are described in more detail in the 5 following sections.

In accordance with an aspect of the present invention, there is provided a method of making a transgenic plant expressing a dermaseptin or temporin cationic peptide which confers microbial resistance to the plant comprising:
introducing a nucleic acid molecule encoding a dermaseptin or temporin cationic peptide into a plant cell, thereby generating a transgenic plant cell; and growing the transgenic plant cell into a transgenic plant that expresses the dermaseptin or temporin cationic peptide, thereby conferring microbial resistance to the plant.

In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant comprising: expressing a recombinant nucleic acid molecule in a plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a fusion peptide having a formula selected from the group consisting of: (a) P-D; and (b) P-T, wherein D is a dermaseptin peptide, T is a temporin peptide and P is an anionic pro-region peptide.

In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising: expressing a recombinant nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a fusion peptide having a formula selected from the group consisting of (a) P-S-D; and (b) P-S-T, wherein D is a dermaseptin peptide, T is a temporin peptide, P is an anionic pro-region peptide and S is a spacer peptide.

In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising: expressing a nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a peptide comprising an amino acid sequence selected from the group consisting of: (a) SEQ IDs: 3-14 and fragments thereof; (b) amino acid sequences that differ from an amino acid sequence specified in (a) by one or more conservative amino acid substitutions; and (c) amino acid sequences that share at 5a least 40% sequence identity with an amino acid sequence specified in (a), wherein the peptide has dermaseptin biological activity.

In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising: expressing a nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a peptide comprising an amino acid sequence selected from the group consisting of (a) SEQ IDs: 17-26 and fragments thereof; (b) amino acid sequences that differ from an amino acid sequence specified in (a) by one or more conservative amino acid substitutions; and (c) amino acid sequences that share at least 50% sequence identity with an amino acid sequence specified in (a), wherein the peptide has temporin biological activity.

In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising: expressing in a plant a recombinant nucleic acid molecule encoding a peptide comprising an amino acid sequence selected from the group consisting of SEQ IDs: 28 and 34, wherein the peptide confers microbial resistance to the plant.
In accordance with an aspect of the present invention, there is provided a method of making a transgenic plant comprising:
expressing a recombinant nucleic acid molecule in a plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a fusion peptide having a formula selected from the group consisting of:
(a) P-D; and (b) P-T, wherein D is a dermaseptin peptide having dermaseptin biological activity, T
is a temporin peptide having temporin biological activity and P is an anionic pro-region peptide.

In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising:
expressing a recombinant nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a fusion peptide having a formula selected from the group consisting of:
(a) P-S-D; and 5b (b) P-S-T, wherein D is a dermaseptin peptide having dermaseptin biological activity, T
is a temporin peptide having temporin biological activity, P is an anionic pro-region peptide and S is a spacer peptide.
In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising:
expressing a nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a dermaseptin peptide comprising an amino acid sequence selected from the group consisting of:
(a) SEQ IDs: 3-14 and fragments thereof;
(b) amino acid sequences that differ from an amino acid sequence specified in (a) by one or more conservative amino acid substitutions; and (c) amino acid sequences that share at least 40% sequence identity with an amino acid sequence specified in (a), wherein the peptide has dermaseptin biological activity.
In accordance with another aspect of the present invention, there is provided a method of making a transgenic plant, comprising:

expressing a nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a temporin peptide comprising an amino acid sequence selected from the group consisting of.
(a) SEQ IDs: 17-26 and fragments thereof;
(b) amino acid sequences that differ from an amino acid sequence specified in (a) by one or more conservative amino acid substitutions; and (c) amino acid sequences that share at least 50% sequence identity with an amino acid sequence specified in (a), wherein the peptide has temporin biological activity.
SEQUENCE LISTING
The nucleic and amino acid sequences listed in the accompanying sequence listing are shown using standard letter abbreviations for nucleotide bases, and three letter code for amino acids. Only one strand of each nucleic acid sequence is shown, but the complementary strand is understood as included by any reference to the Sc displayed strand.

SEQ ID: 1 shows the dermaseptin b cDNA sequence.
SEQ ID: 2 shows the amino acid sequence of the precursor (unprocessed) dermaseptin b peptide.
SEQ ID: 3 shows the 27 amino acid sequence of the mature dermaseptin b peptide.
SEQ ID: 4 shows the 31 amino acid sequence of the mature dermaseptin B
peptide.
SEQ IDs: 5-14 show the amino acid sequences of various mature (processed) dermaseptin peptides.
SEQ ID: 15 shows a cDNA sequence encoding temporin G.
SEQ ID: 16 shows the amino acid sequence of the precursor (unprocessed) form of temporin G.
SEQ ID: 17 shows the 13 amino acid sequence of the mature temporin G peptide.
SEQ IDs: 18-26 show the amino acid sequences of various mature (processed) temporin peptides.
SEQ ID: 27 shows the nucleic acid sequence encoding MSRA2.
SEQ ID: 28 shows the amino acid sequence of MSRA2.
SEQ IDs: 29-32 show the oligos used to generate the nucleic acid sequence encoding MSRA2.
SEQ IDs: 33 shows the nucleic acid sequence encoding MSRA3.
SEQ ID: 34 shows the amino acid sequence of MSRA3.

16-03-2001 '22pm From-SIN MCCBURNEY 4165951163 T=215 P.11/12 CA 0000002E

SECS IDs: 33 shows the nucleic acid sequence encoding MSRA3.
SEQ ID: 34 snows the amino acid sequence of MSRA3.
SEQ IDs: 35-38 show the oligos used to generate the nucleic acid sequence encoding MSRA3.
s SEQ IDs: 39-41 show the amino acid sequences of various N -terminal extension sequences.
Brief Description of the Figures Figure 1 is a graph that shows the results from assays that tested the resistance of transgenic potato tubers to soft rot. Discs prepared from tubers of io Desiree control and transgenic plants expressing Demaseptin B (sample Nos.
Di, D2, D6, D10) or Temporin A (sample Nos. T1, T2, T3) were infected with E.
carotovora (black boxes) or left uninfected (white boxes). After 6 days at RT, rotted tissue was gently removed from the discs and the sensitivity/resistance to E. carotovora was expressed as the loss of weight of tuber tissue.
15 Figure 2 is a graph that shows the bactericidal effect of the peptides MSRA2 (Dermaseptin B) and MSRA3 (Temporin A) on E. coil. The cell cultures were incubated at room temperature in the presence of indicated concentration of Dermaseptin B (DSB; 7 g/ml, 30 g/ml, and 75 g/ml), Temporin A (TA; 75 pg/ml, 133 g/ml, 200 .g/ml) and a combination of Temporin A and 20 Dermaseptin B (133 g/ml Temporin A and 30 g/ml Dermaseptin B) for 4 hours, diluted and plated on LB plates. After overnight incubation at 37 C, the colonies were counted and the survival of bacteria was scored.
Figure 3 is a graph that shows the bactericidal effect of the peptides MSRA2 (Dermaseptin B) and MSRA3 (Temporin A) on E. carotovora. The cell 25 cultures were incubated at room temperature in the presence of indicated concentration of Dermaseptin S (DSB; 23 gg/ml, 45 pg/ml) or Temporin A (TA;
67 g/ml, 133 gg/ml) for 4 hours, diluted and plated on LB plates. After overnight incubation at 28 C, the colonies were counted and the survival of bacteria was scored.
30 I. Definitions Dermaseptin: As used herein, the term "dermaseptin" refers to any member of the family of naturally occurring cationic peptides termed dermaseptins, Empfangsteit 1645rt 22:21 AMENDED SHEET

these naturally occurring peptides that display dermaseptin biological activity as defined below.
Dermaseptins were first identified in skin extracts from the South American arboreal frog Phyllomedusa sauvagii (Mor et al., J. Biol. Chem., 269: 31635-31641, 1994). They are broad-spectrum microbiocidal peptides that inhibit growth of filamentous fungi as well as bacteria, yeast, and protozoa (Strahilevitz, Biochemistry, 33:10951-10960, 1994). Since the first dermaseptin, dermaseptin S, was identified, a number of other members of this peptide family have been characterized and cloned, including: dermaseptin-b, isolated from the skin of Phyllomedusa bicolor (Mor et al., J Biol. Chem., 269: 31635-31641, 1994). (SEQ ID: 2); two dermaseptins isolated from Pachymedusa dacnicolor, and encoded by clones PD-3-3 and PD-2-2, as described by Wechselberger, Biochim. Biophys. Acta 1388:279-283, 1998 (the peptide sequences of which are shown in SEQ IDs: 5-6, respectively); three dermaseptins isolated from Agalychnis annae and encoded by clones AA-3-6, AA-3-3, AA-3-1, as described by Wechselberger, Biochim. Biophys. Acta 1388:279-283, 1998 (the peptide sequences of which are shown in SEQ IDs: 7-9, respectively); and five dermaseptin peptides from Phyllomedusa sauvagii, termed dermaseptin 5, dermaseptin 4, dermaseptin 3, dermaseptin 2, and dermaseptin 1, as described by Mor and Nicolas, Journal Biochemical Chemistry, 269:1934-1939, 1994 (the peptide sequences of which are provided in SEQ IDs: 10-14, respectively). These sequences are readily available from public databases, including from GenBank.
Dermaseptin peptides are typically expressed as precursor forms of around 60-80 amino acids in length, and are subsequently processed to mature forms of around 27-34 amino acids in length. For example, the cDNA encoding dermaseptin-b (SEQ
ID:1; Amiche et al., J. Biol. Chem. 269:1747-1852, 1994; Chapentier et al., Biol.
Chem. 273:14690-14697, 1998; located in the GenBank nucleotide sequence database under accession number X72387) encodes a precursor peptide of 78 amino acids in length (SEQ ID: 2). This precursor form of dermaseptin-b is processed to produce two mature forms, termed dermaseptin b and dermaseptin B (Strahilevitz, Biochemistry, 33:10951-10960, 1994). Dermaseptin b (SEQ ID: 3) is 27 amino acids in length and comprises amino acid residues 49-75 of the precursor form.
Dermaseptin B is an alternative cleavage product of 31 amino acids in length, and includes an N terminal extension of 4 amino acids (AMWK) (SEQ ID: 4).
Dermaseptin B comprises amino acid residue 45-75 of the precursor form. With the exception of SEQ IDs: 1 and 2 which show the full-length precursor form of dermaseptin b, the dermaseptin peptides shown in the Sequence Listing represent the processed, mature forms of the peptides.
Given the availability of a wide range of dermaseptin peptide sequences, and the nucleic acid sequences that encode these peptides, one of ordinary skill in the art will readily be able to produce these peptides, and their corresponding nucleic acid sequences, using standard molecular biology techniques.
In addition to the use of the naturally occurring dermaseptin peptides described above, it will be apparent to one of skill in the art that the invention may be practiced using peptides that vary somewhat from the naturally occurring dermaseptin peptides, yet which nevertheless confer enhanced broad spectrum pathogen resistance when expressed in plants. For example, the N-terminal V-helical amphipathic segment of the mature dermaseptin peptides, particularly the first 18 amino acid residues, has been identified as important for antimicrobial activity (Mor et al., J
Biol. Chem., 269:31635-31641, 1994; Mor and Nicolas, Journal Biochemical Chemistry, 269:1934-39, 1994) and this fragment may be used in place of the full-length mature dermaseptin. Thus, the term "dermaseptin" also encompasses variant dermaseptin peptides, as well as fragments of the naturally occurring peptides, that share a specified level of sequence identity with a naturally occurring dermaseptin peptide, or that differ from a naturally occurring dermaseptin peptide by one or more conservative amino acid substitutions.
Such variant peptides and fragments retain dermaseptin biological activity, which may be assayed by the methods described below. A variant dermaseptin will typically share at least 40% amino acid sequence identity with a naturally occurring dermaseptin peptide (such as the one shown in SEQ ID: 3) as determined by the methods described below.
Dermaseptin biological activity: the ability of a dermaseptin peptide to inhibit bacterial growth and/or fungal growth. Dermaseptin biological activity can readily be ascertained by using the protocols given below.

The antibacterial activity of a given dermaseptin peptide is assessed by determining its ability to inhibit the growth of a pectinolytic bacterial strain such as Erwinia carotovora orEscherichia coli DHSS/. The activity of a given peptide is determined by serially diluting the peptide in LB and aliquoting 100 :1 to wells in a 96 well microtiter plate. A fresh bacterial culture (-0.3 A550) is then grown on Luria-Bertani medium (LB) (1% w/v tryptone and 0.5% w/v yeast extract) and diluted to 10-2 in LB to represent approximately 104 - 105 colony forming units (CFU) ml-1.

10 :1 of the bacterial culture is then inoculated into the wells containing the peptide and the samples are incubated at 37 C for 4 hours. The well contents are then diluted in LB, plated on LB agar and incubated overnight at 37 C. The colonies on plates corresponding to each dilution of dermaseptin (and a control to which no peptide was added) are then counted, and the antibacterial activity of the peptide under test is determined by comparison to the control plate.
The dermaseptin peptide is determined to have biological activity if, under the conditions of this assay, it is capable of inhibiting bacterial growth by at least 10% at a concentration of 7 :g per ml (i.e., at this concentration, the number of bacterial colonies is no more than 90% that of the control plate).
The antifungal activity of a given dermaseptin peptide is assessed by utilizing the fungal strains Phytophthora cactorum and/or Fusarium solani. The selected fungal strain is grown on Five Cereal Agar (FCA containing 20 gL-' five cereal baby food instant flakes, and 8 gL-' agar3 (Terras et al., The Plant Cell 7:573-588, 1995).
After 5 days growth at room temperature a mycelial plug is removed and placed upside down in the center of a fresh FCA plate. A sterile solution (10 :1) of the test peptide is then introduced into a well 3 cm from the edge of the plate and a control well containing sterile water is established on the same plate. Various concentrations of the test peptide may be tested on the same plate, or on other plates. The assay plates incubated for 5 days at room temperature, after which the zone of growth inhibition around each well is measured.
The dermaseptin peptide is determined to have biological activity if, under the conditions of this assay, it is capable of inhibiting fungal growth at a concentration of 5 :g per ml (i.e., there is a discernible zone of inhibition around a well containing this concentration of peptide).
Temporin: As used herein, the term "temporin" refers to any member of the family of naturally occurring cationic peptides termed temporins (Simmaco et al., 5 Eur. J. Biochem., 242:788-92. 1996) as well as fragments and variants of these naturally occurring peptides that display temporin biological activity as defined below.
Temporins are small cationic peptides with anti-microbial activity that were initially identified from a cDNA library prepared from the skin of the frog, Rana 10 temporaria. These peptides show some sequence similarity to hemolytic peptides isolated from Vespa venom, however, the temporin peptides are not hemolytic (Simmaco et al., Eur. J. Biochem., 242:788-92. 1996).
Ten members of the temporin family, temporins A, B, C, D, E, F, G, H, K, and L, have been described by Simmaco et al., Eur. J. Biochem., 242:788-92. 1996.
Like dermaseptins, temporins are typically expressed in a precursor form and subsequently processed to produce a mature form. For example, the cDNA molecule that encodes temporin G (shown in SEQ ID: 15, and located in the GenBank nucleotide database under accession number Y09395) encodes a 61 amino acid precursor form of temporin G (shown in SEQ ID: 16). Amino acids 1-22 comprise a signal sequence, amino acids 23-46 comprise a pro-region, and amino acids 47-59 comprise the processed, mature temporin G peptide (the mature form is shown in SEQ ID: 17).
In general, the predicted mature temporin peptides are between 10 and 13 amino acids long, and some have been found to be amidated at the C-terminus (Simmaco et al., Eur. J. Biochem., 242:788-92. 1996). The mature forms of temporins A, B, C, D, E, F, G, H, K, and L are shown in SEQ IDs: 18, 19, 20, 21, 22, 23, 17, 24, 25, and 26, respectively.
Given the availability of a wide range of temporin peptide sequences, and the nucleic acid sequences that encode these peptides, one of ordinary skill in the art will readily be able to produce these peptides, and their corresponding nucleic acid sequences, using standard molecular biology techniques.
In addition to the use of the naturally occurring temporin peptides described above, it will be apparent to one of skill in the art that the invention may be practiced using peptides that vary somewhat from the naturally occurring temporin peptides, yet which nevertheless confer enhanced broad spectrum pathogen resistance when expressed in plants. Thus, the term "temporin" also encompasses variant temporin peptides, as well as fragments of the naturally occurring peptides, that share a specified level of sequence identity with a naturally occurring temporin peptide, or that differ from a naturally occurring temporin peptide by one or more conservative amino acid substitutions.
Such variant peptides and fragments retain temporin biological activity, which may be assayed by the methods described below. A variant temporin will typically share at least 40% amino acid sequence identity with a naturally occurring temporin peptide (such as the one shown in SEQ ID: 17) as determined by the methods described below.
Temporin biological activity: the ability of a temporin peptide to inhibit bacterial growth.
The antibacterial activity of a given temporin peptide is assessed by determining its ability to inhibit the growth of a pectinolytic bacterial strain such as Erwinia carotovora orEscherichia coli DHSS/. The activity of a given peptide is determined by serially diluting the peptide in LB and aliquoting 100 :1 to wells in a 96 well microtiter plate. A fresh bacterial culture (-0.3 A550) is then grown on Luria-Bertani medium (LB) (1% w/v tryptone and 0.5% w/v yeast extract) and diluted to 10-2 in LB to represent approximately 104 - 105 colony forming units (CFU) ml"'.
10 :1 of the bacterial culture is then inoculated into the wells containing the peptide and the samples are incubated at 37 C for 4 hours. The well contents are then diluted in LB, plated on LB agar and incubated overnight at 37 C. The colonies on plates corresponding to each dilution of temporin (and a control to which no peptide was added) are then counted, and the antibacterial activity of the peptide under test is determined by comparison to the control plate.
The temporin peptide is determined to have biological activity if, under the conditions of this assay, it is capable of inhibiting bacterial growth by at least 10% at a concentration of 100 :g per ml (i.e., at this concentration, the number of bacterial colonies is no more than 90% that of the control plate).

The antifungal activity of a given temporin peptide is assessed by utilizing the fungal strains Phytophthora cactorum and/or Fusarium solani. The selected fungal strain is grown on Five Cereal Agar (FCA containing 20 gL-1 five cereal baby food instant flakes, and 8 gL"1 agar3 (Terras et al., The Plant Cell, 7:573-588, 1995). After 5 days growth at room temperature a mycelial plug is removed and placed upside down in the center of a fresh FCA plate. A sterile solution (10 :1) of the test peptide is then introduced into a well 3 cm from the edge of the plate and a control well containing sterile water is established on the same plate. Various concentrations of the test peptide may be tested on the same plate, or on other plates. The assay plates incubated for 5 days at room temperature, after which the zone of growth inhibition around each well is measured.
The temporin peptide is determined to have biological activity if, under the conditions of this assay, it is capable of inhibiting fungal growth at a concentration of 5 :g per ml (i.e., there is a discernible zone of inhibition around a well containing this concentration of peptide).
Transgenic plant: As used herein, this term refers to a plant that contains recombinant genetic material not normally found in a wild-type plant of this species.
Thus, a plant that is grown from a plant cell into which recombinant DNA is introduced by transformation is a transgenic plant, as are all offspring of that plant that contain the introduced transgene (whether produced sexually or asexually).
Sequence identity: The similarity between two nucleic acid sequences, or two amino acid sequences is expressed in terms of the level of sequence identity shared between the sequences. Sequence identity is typically expressed in terms of percentage identity; the higher the percentage, the more similar the two sequences are.
Methods of alignment of sequences for comparison are well known in the art.
Various programs and alignment algorithms are described in: Smith and Waterman, Adv. Appl. Math, 2:482, 1981; Needleman and Wunsch, J. Mol. Biol., 48:443, 1970;
Pearson and Lipman, Proc. Natl. Acad. Sci. USA, 85:2444, 1988; Higgins &
Sharp,Gene, 73:237-244, 1988; Higgins & Sharp, CABIOS, 5:151-153, 1989; Corpet et al., Nucleic Acids Research, 16:10881-10890, 1988; Huang, et al., Computer Applications in the Biosciences, 8:155-165, 1992; and Pearson et al., Methods in Molecular Biology, 24:307-331, 1994. Altschul et al., Nature Gene 6:119-129, presents a detailed consideration of sequence alignment methods and homology calculations.
The NCBI Basic Local Alignment Search Tool (BLAST) (Altschul et al., J.
Mol. Biol. 215:403-410, 1990) is available from several sources, including the National Center for Biotechnology Information (NCBI, Bethesda, MD) and on the Internet, for use in connection with the sequence analysis programs blastp, blastn, blastx, tblastn and tblastx. It can be accessed at http//www.ncbi.nlm.nih.gov/BLAST/. A description of how to determine sequence identity using this program is available at httpi//www.ncbi.nlm.nih.gov/BLAST/blast-help.html.
Variants of naturally occurring dermaseptin and temporin peptides useful in the present invention are typically characterized by possession of at least 40%
sequence identity counted over the full-length alignment with the amino acid sequence of a naturally occurring temporin or dermaseptin peptide when aligned using the NCBI Blast 2Ø1 (described in Altschul et al., Nucleic Acids Res.
25:3389-3402, 1997). For comparisons of amino acid sequences of greater than about 30 amino acids, the Blast 2 sequences function is employed using the default BLOSLTM62 matrix set to default parameters, (gap existence cost of 11, and a per residue gap cost of 1). When aligning short peptides (fewer than around 30 amino acids), the alignment should be performed using the Blast 2 sequences function, employing the PAM30 matrix set to default parameters (open gap 9, extension gap I
penalties). Proteins with even greater similarity to the reference sequences will show increasing percentage identities when assessed by this method, such as at least 45%, at least 50%, at least 70%, at least 80%, at least 85%, at least 90%, or at least 95%
sequence identity.
Recombinant: A recombinant nucleic acid is one that has a sequence that is not naturally occurring or has a sequence that is made by an artificial combination of two otherwise separated segments of sequence. This artificial combination is often accomplished by chemical synthesis or, more commonly, by the artificial manipulation of isolated segments of nucleic acids, e.g., by genetic engineering techniques.

Oligonucleotide (oligo): A linear polynucleotide sequence of up to about 100 nucleotide bases in length.
Probes and primers: Nucleic acid probes and primers may readily be prepared based on the amino acid sequence provided by this invention. A probe comprises an isolated nucleic acid attached to a detectable label or reporter molecule.
Typical labels include radioactive isotopes, ligands, chemiluminescent agents, and enzymes. Methods for labeling and guidance in the choice of labels appropriate for various purposes are discussed, e.g., in Sambrook et al., Molecular Cloning: A
Laboratory Manual, Cold Spring Harbor, 1989 and Ausubel et al., Current Protocals in Molecular Biology, Greene Publishing Associates and Wiley-Intersciences, 1987.
Primers are short nucleic acids, preferably DNA oligonucleotides 15 nucleotides or more in length. Primers may be annealed to a complementary target DNA strand by nucleic acid hybridization to form a hybrid between the primer and the target DNA strand, and then extended along the target DNA strand by a DNA
polymerase enzyme. Primer pairs can be used for amplification of a nucleic acid sequence, e.g., by the polymerase chain reaction (PCR) or other nucleic-acid amplification methods known in the art.
Methods for preparing and using probes and primers are described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor, 1989; Ausubel et al., Current Protocals in Molecular Biology, Greene Publishing Associates and Wiley-Intersciences, 1987; and Innis et al., PCR
Protocols, A Guide to Methods and Applications, 1990. PCR primer pairs can be derived from a known sequence, for example, by using computer programs intended for that purpose such as Primer (Version 0.5, (D 1991, Whitehead Institute for Biomedical Research, Cambridge, MA). One of skill in the art will appreciate that the specificity of a particular probe or primer increases with its length. Thus, for example, a primer comprising 20 consecutive nucleotides will anneal to a target with a higher specificity than a corresponding primer of only 15 nucleotides. Thus, in order to obtain greater specificity, probes and primers may be selected that comprise 20, 25, 30, 35, 40, 50 or more consecutive nucleotides.
Isolated: An "isolated" biological component (such as a nucleic acid or protein or organelle) has been substantially separated or purified away from other biological components in the cell of the organism in which the component naturally occurs, i.e., other chromosomal and extra-chromosomal DNA and RNA, proteins and organelles. Nucleic acids and proteins that have been "isolated" include nucleic acids and proteins purified by standard purification methods. The term also embraces 5 nucleic acids and proteins prepared by recombinant expression in a host cell as well as chemically synthesized nucleic acids.
Vector: A nucleic acid molecule as introduced into a host cell, thereby producing a transformed host cell. A vector may include nucleic acid sequences that permit it to replicate in a host cell, such as an origin of replication. A
vector may also 10 include one or more selectable marker genes and other genetic elements known in the art.
Operably linked: A first nucleic acid sequence is operably linked with a second nucleic acid sequence when the first nucleic acid sequence is placed in a functional relationship with the second nucleic acid sequence. For instance, a promoter 15 is operably linked to a coding sequence if the promoter affects the transcription or expression of the coding sequence. Generally, operably linked DNA sequences are contiguous and, where necessary to join two protein-coding regions, in the same reading frame. Two peptide sequences may be operably linked through a normal peptide bond, or by other covalent linkage.
II. Selection of Dermaseptin and Temporin Peptides a. Dermaseptin Peptides A listing of exemplary dermaseptin peptides is provided above. Nucleic acid molecules encoding these dermaseptin polypeptides may either be derived by simple application of the genetic code to the peptide sequence, or the naturally occurring cDNA or gene sequence may be employed. For example, a cDNA sequence encoding dermaseptin-b is provided in SEQ ID: 1 (and disclosed in Amiche et al., J.
Biol. Chem.
269:1747-852, 1994). Typically, the mature form of the dermaseptin peptide will be selected for expression. However, any fragment of a full-length dermaseptin peptide may be selected, contingent upon that fragment having dermaseptin biological activity if it is to be used to produce pathogen-resisting plants.

One of ordinary skill in the art will appreciate that the various dermaseptin peptides have varying degrees of anti-microbial activity, with some working more effectively against certain pathogens then others. Therefore, when selecting peptides for producing transgenic plants with enhanced pathogen resistance, the selection of a particular dermaseptin will be depend upon, among other factors, the type of plant in which the peptide is to be expressed, and the types of pathogens that commonly infect that plant type.
Having selected the desired dermaseptin peptide to be expressed, a nucleic acid molecule encoding the peptide may be produced by standard molecular biology techniques. Because the dermaseptin peptides are relatively short, the simplest way to synthesize the nucleic acid molecule will likely be via synthesis of overlapping oligonucleotides on a commercially available oligonucleotide synthesizer. The oligonucleotides can then be assembled into a full-length coding region in vitro. This approach also permits the selection of codons encoding particular amino acid residues that reflect the codon usage bias of the plant into which the nucleic acid molecule is to be introduced, thereby enhancing the expression efficiency. Detailed examples of the production of coding sequences using this approach are provided in the examples below.
b. Temporin Peptides A listing of exemplary temporin peptides is provided above. Nucleic acid molecules encoding these temporin peptides may either be derived by simple application of the genetic code to the peptide sequence, or the naturally occurring cDNA or gene sequence may be employed. For example, the cDNA sequence encoding temporin G is provided in SEQ ID: 15. Typically, the mature form of the temporin peptide will be selected for expression. However, any fragment of a full-length temporin peptide may be selected, contingent upon that fragment having dermaseptin biological activity if it is to be used to produce pathogen-resisting plants.
As with the selection of dermaseptin peptides, one of ordinary skill in the art will appreciate that the various temporin peptides have varying degrees of anti-microbial activity, with some working more effectively against certain pathogens then others. Therefore, when selecting peptides for producing transgenic plants with enhanced pathogen resistance, the selection of a particular temporin will be depend upon, among other factors, the type of plant in which the peptide is to be expressed, and the types of pathogens that cause losses in that plant type.
As described above for dermaseptins, the synthesis and assembly of overlapping oligonucleotides is a simple and convenient way to produce nucleic acid molecules that encode temporins.

c. Addition of Other Peptide Sequences The temporin and dermaseptin proteins may be also expressed in transgenic plants in the form of fusion proteins. Although any desired peptide may be fused to the selected dermaseptin or temporin protein for expression in plants, the expression of fusion proteins comprising an anionic pro-region peptide operably linked to the amino terminus of the dermaseptin or temporin is expected to be particularly beneficial. Any anionic pro-region peptide may be employed for this purpose, including the anionic pro-regions that are found in naturally occurring full-length (i.e., unprocessed) dermaseptin and temporin peptides. For example, the pro-region comprising amino acids 23-46 of temporin G (shown in SEQ ID: 16) may be used as a pro-region. Such pro-region peptides serve to neutralize the cationic nature of the dermaseptin or temporin and may thus provide enhanced stability in the cellular environment. Thus, these pro-regions generally include a number of negatively charged amino acids, such as glutamate (Glu or E) and aspartate (Asp or D).
Examples of other naturally occurring pro-region peptides that are known in the art include pro-region peptides of the following proteins: the human neutrophil defensin protein (Daher et al., Proc. Natl. Acad. Sci USA, 85:7327-7331, 1988); the bovine antimicrobial cathelicidin protein BMAP28 (Skerlavaj et al., J. Biol.
Chem.
271: 28375-381, 1996); the sheep antimicrobial cathelin family of proteins (Mahoney et al., FEBSLett. 377:519-522, 1995); bovine indolicidin (Del Sal et al., Biochem.
Biophys. Res. Commun. 187:467-472, 1992); the porcine antimicrobial peptides prophenin-2 and PR-39 (Zhao et al., FEBSLett. 367:130-134, 1995) and PMAP-37 (Tossi et al., Eur. J. Biochem, 15:941-946, 1995); the human antimicrobial lipopolysaccharide binding protein CAP 18 (Larrick et al., Infect. Immun.
63:1291-1297, 1995); and the murine protein E3 (Scott and Collins, Blood 88:2517-2530, 1996).

While the anionic pro-region peptide may be directly joined to the N-terminus of the cationic peptide, an alternative embodiment involves linking the pro-region peptide to the dermaseptin or temporin peptide using a spacer peptide sequence. The use of spacer peptides to join two peptide domains is well known in the art;
such spacer peptides are typically of between 2 and 25 amino acids in length, and provide a flexible hinge connecting the first peptide sequence to the second peptide. Spacer sequences that have been used to provide flexible hinges connecting two peptide sequences include the glycine(4)-serine spacer (GGGGS x3) described by Chaudhary et al., Nature 339:
394-397, 1989. Alternatively, an N-terminal peptide extension as described below may serve to provide the spacer peptide function. Spacer sequence peptides may also include a cleavage site, such as a peptide sequence recognized and cleaved by a protease, such as Factor Xa. Such sites facilitate removal of the pro-region from the dermaseptin or temporin peptide following purification from plant tissues. The use of anionic pro-region peptides and spacer peptides to express certain cationic peptides in microbial systems is known in the art and described in US Patent 5,593,866 to Hancock.
In certain embodiments, an N-terminal extension peptide sequence may be added to the dermaseptin or temporin peptide. Such peptide extensions may comprise portions of the precursor forms of dermaseptins or temporins that are usually removed during protein processing, or may be synthetic sequences. These N-terminal peptide extensions may serve to provide enhanced resistance to proteolytic cleavage, enhance transcription levels, or enhance the antimicrobial activity of the peptides.
Typically, these N-terminal extensions are of between 2 and 25 amino acids in length, although longer extensions may also be employed. Examples of N-terminal extension sequences that are utilized in certain embodiments include the peptide sequences AMWK, ASRH, and ALWK. The AMWK (SEQ ID: 39) sequence is a naturally-occurring peptide extension; it is part of the full-length dermaseptin-b peptide sequence that is normally cleaved during processing. The addition of this sequence to the N-terminus of dermaseptin b (to produce dermaseptin B) has been reported to enhance the in vitro antimicrobial activity of the peptide (Strahilevitz, Biochemistry, 33:10951-10960, 1995). The ASRH (SEG ID: 41), and ALWK (SEQ ID:41) peptides are synthetic extension sequence. In each case, an N-terminal methionine is added to ensure proper expression of the peptide. One of skill in the art will appreciate that the effect of adding any particular N-terminal extension peptide on the biological activity of the peptide being produced (dermaseptin or temporin) may readily be assessed using the biological activity assay described above.
d. Variant Dermaseptin and Temporin Peptides As described above, a number of naturally occurring temporin and dermaseptin peptides are known, exemplified by those shown in the Sequence Listing.
Variants on these naturally occurring peptides may be selected by introducing amino acid substitutions, additional amino acid residues, or by deleting amino acid residues.
These variant peptides may either be produced by chemical synthesis (for example, in order to confirm that the variant peptide retains functional activity), or may be produced in a biological expression system. In the latter instance, the nucleic acid sequence encoding the corresponding naturally occurring peptide can be manipulated so that it encodes the variant peptide. This can be done through a variety of methods, for example by using site-directed mutagenesis or the polymerase chain reaction.
Alternatively, because the peptides are relatively short molecules, the coding region for a variant peptide can simply be synthesized de novo and introduced into a suitable expression vector.
The simplest modifications of amino acid sequences involve the substitution of one or more amino acids for amino acids having similar biochemical properties.
These so-called conservative substitutions are likely to have minimal impact on the activity of the resultant protein. Thus, peptides that differ from naturally occurring temporin or dermaseptin peptides by one or more conservative amino acid substitutions may be used in the invention in place of the naturally occurring peptides.
Table 1 shows amino acids which may be substituted for an original amino acid in a protein and which are regarded as conservative substitutions.

Table 1 Original Residue Conservative Substitutions Ala ser Arg lys Asn gin; his Asp glu Gln asn Glu asp Gly pro His asn; gln Ile leu; val Leu ile; val Lys arg; gin; glu Met leu; ile Phe met; leu; tyr Ser thr Thr ser Trp tyr Tyr trp; phe Val ile; leu More substantial changes in functional or other features may be obtained by selecting substitutions that are less conservative than those in Table 1, i.e., selecting 5 residues that differ more significantly in their effect on maintaining (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a sheet or helical conformation, (b) the charge or hydrophobicity of the molecule at the target site, or (c) the bulk of the side chain. The substitutions which in general are expected to produce the greatest changes in protein properties will be those in which (a) a 10 hydrophilic residue, e.g., seryl or threonyl, is substituted for (or by) a hydrophobic residue, e.g., leucyl, isoleucyl, phenylalanyl, valyl or alanyl; (b) a cysteine or proline is substituted for (or by) any other residue; (c) a residue having an electropositive side chain, e.g., lysyl, arginyl, or histidyl, is substituted for (or by) an electronegative residue, e.g., glutamyl or aspartyl; or (d) a residue having a bulky side chain, e.g., 15 phenylalanine, is substituted for (or by) one not having a side chain, e.g., glycine.
Variant peptides having one or more of these more substantial changes may also be employed in the invention, provided that temporin or dermaseptin biological activity is retained.

More extensive amino acid changes may also be engineered into variant dermaseptin or temporin peptides. As noted above however, these variant peptides will typically be characterized by possession of at least 40% sequence identity counted over the full-length alignment with the amino acid sequence of their respective naturally occurring sequences using the alignment programs described above. In addition, these variant peptides will retain biological activity.
Confirmation that a dermaseptin or temporin peptide has biological activity may be achieved using the assay systems described above. Following confirmation that the peptide has the desired activity, a nucleic acid molecule encoding the peptide may be readily produced using standard molecular biology techniques. Where appropriate, the selection of the open reading frame will take into account codon usage bias of the plant species in which the peptide is to be expressed.

M. Introducing Dermaseptins and/or Temporins into Plants Once a nucleic acid sequence encoding a dermaseptin and/or a temporin peptide has been produced, standard techniques may be used to express the sequence in transgenic plants in order to confer pathogen resistance to the plant. The basic approach is to clone the nucleic acid into a transformation vector, such that it is operably linked to control sequences (e.g., a promoter) that direct expression of the nucleic acid in plant cells. The transformation vector is then introduced into plant cells by one of a number of techniques (e.g., electroporation), whole plants are regenerated from the cells, and progeny plants containing the introduced nucleic acid are selected. Preferably all or part of the transformation vector will stably integrate into the genome of the plant cell. That part of the transformation vector which integrates into the plant cell and which contains the introduced sequence and associated sequences for controlling expression (the introduced "transgene") may be referred to as the recombinant expression cassette.
Selection of progeny plants containing the introduced transgene may be made based upon the detection of an altered phenotype. Such a phenotype may result directly from the disease resistance conferred by the introduced sequence or may be manifested as enhanced resistance to a chemical agent (such as an antibiotic) as a result of the inclusion of a dominant selectable marker gene incorporated into the transformation vector.
Successful examples of the modification of plant characteristics by transformation with cloned nucleic acid sequences are replete in the technical and scientific literature. Selected examples, which serve to illustrate the knowledge in this field of technology include:
U.S. Patent No. 5,571,706 ("Plant Virus Resistance Gene and Methods") U.S. Patent No. 5,677,175 ("Plant Pathogen Induced Proteins") U. S. Patent No. 5,510,471 ("Chimeric Gene for the Transformation of Plants") U.S. Patent No. 5,750,386 ("Pathogen-Resistant Transgenic Plants") U.S. Patent No. 5,597,945 ("Plants Genetically Enhanced for Disease Resistance") U.S. Patent No. 5,589,615 ("Process for the Production of Transgenic Plants with Increased Nutritional Value Via the Expression of Modified 2S Storage Albumins") U.S. Patent No. 5,750,871 ("Transformation and Foreign Gene Expression in Brassica Species") U. S. Patent No. 5,268,526 ("Overexpression of Phytochrome in Transgenic Plants") U.S. Patent No. 5,780,708 ("Fertile Transgenic Corn Plants") U.S. Patent No. 5,538,880 ("Method For Preparing Fertile Transgenic Corn Plants") U.S. Patent No. 5,773,269 ("Fertile Transgenic Oat Plants") U.S. Patent No. 5,736,369 ("Method For Producing Transgenic Cereal Plants") U.S. Patent No. 5,610,042 ("Methods For Stable Transformation of Wheat").
These examples include descriptions of transformation vector selection, transformation techniques and the construction of constructs designed to over-express the introduced transgene.
a. Plant Types Diseases caused by many pathogens affect a wide variety of plant species.
These plants can be monocots, dicots or gymnosperms. Thus, for example, dermaseptins and/or temporin peptides may be introduced into plant species including, but not limited to, maize, wheat, rice, barley, soybean, cotton, beans in general, rape/canola, alfalfa, flax, sunflower, safflower, brassica, cotton, tobacco, flax, peanut, clover, cowpea, grapes; vegetables such as lettuce, tomato, cucurbits, cassava, potato, carrot, radish, pea, lentils, cabbage, cauliflower, broccoli, Brussels sprouts, peppers; tree fruits such as citrus, apples, pears, peaches, apricots, walnuts; fur trees such as Douglas fir and loblolly pine, and flowers such as carnations and roses.
b. Vector Construction and Choice of Promoters A number of recombinant vectors suitable for stable transfection of plant cells or for the establishment of transgenic plants have been described including those described in Pouwels et al., Cloning Vectors: A Laboratory Manual, 1985, supp., 1987; Weissbach and Weissbach, Methods for Plant Molecular Biology, Academic Press, 5:173-184, 1989; and Gelvin et al., Plant Molecular Biology Manual, Kluwer Academic Publishers, 1990. Typically, plant transformation vectors include one or more cloned sequences under the transcriptional control of 5' and 3' regulatory sequences and a dominant selectable marker. Such plant transformation vectors typically also contain a promoter regulatory region (e.g., a regulatory region controlling inducible or constitutive, environmentally-or developmentally-regulated, or cell- or tissue-specific expression), a transcription initiation start site, a ribosome binding site, an RNA processing signal, a transcription termination site, and/or a polyadenylation signal. Examples of constitutive plant promoters that may be useful for expressing a transgene include: the cauliflower mosaic virus (CaMV) 35S
promoter, which confers constitutive, high-level expression in most plant tissues (see e.g., Odel et al., Nature, 313:810, 1985; Dekeyser et al., Plant Cell, 2:591, 1990;
Terada and Shimamoto, Mol. Gen. Genet. 220:389, 1990; and Benfey and Chua, Science, 250:959-966, 1990) the nopaline synthase promoter (An et al., Plant Physiol.
88:547, 1988); the octopine synthase promoter (Fromm et al., Plant Cell, 1:977, 1989) and the 2x CaMV/35S promoter with a translational enhancer sequence (Kay et al., Science, 236:1299-1302, 1987).

A variety of plant gene promoters that are regulated in response to environmental, hormonal, chemical, and/or developmental signals, also can be used for expression of a transgene in plant cells, including promoters regulated by: (a) heat (Callis et al., Plant Physiol., 88:965, 1988; Ainley et al., PlantMol. Biol., 22:13-23, 1993; and Gilmartin et al., The Plant Cell, 4:839-949, 1992) (b) light (e.g., the pea rbcS-3A promoter, Kuhlemeier et al.. Plant Cell, 1:471, 1989, and the maize rbcS
promoter, Schaffner & Sheen, Plant Cell, 3:997, 1991); (c) hormones, such as abscisic acid (Marcotte et al., Plant Cell, 1: 471, 1989); (d) wounding (e.g., the potato Pinll promoter (Keil et al., Nucl. Acids. Res. 14: 5641-5650, 1986), the Agrobacterium mas promoter (Langridge et al.. Bio/Technology 10:305-308, 1989), and the grapevine vstl promoter (Weise et al.. Plant Mot Biol., 26:667-677, 1994);
and (e) chemicals such as methyl jasmonate or salicylic acid (see also Gatz et al..
Plant Mol. Biol. 48:89-108, 1997).
Alternatively, tissue specific (root, leaf, flower, and seed for example) promoters (Carpenter et al., The Plant Cell 4:557-571, 1992; Denis et al., Plant Physiol. 101:1295-1304, 1993; Opperman et al., Science 263:221-223, 1993;
Stockhause et al., The Plant Cell 9:479-489, 1997; Roshal et al., The EMBO J.
6:1155, 1987; Schernthaner et al., EMBO J. 7:1249, 1988; Yamamoto et al., Plant Cell 3:371-382, 1990; and Bustos et al., Plant Cell 1:839, 1989) can be fused to the coding sequence to obtain particular expression in respective organs.
Plant transformation vectors may also include RNA processing signals, for example, introns, which may be positioned upstream or downstream of the ORF
sequence in the transgene. In addition, the expression vectors may also include additional regulatory sequences from the 3'-untranslated region of plant genes, e.g., a 3' terminator region to increase mRNA stability of the mRNA, such as the PI-II
terminator region of potato or the octopine or nopaline synthase (NOS) 3' terminator regions.
Finally, as noted above, plant transformation vectors may also include dominant selectable marker genes to allow for the ready selection of transformants.
Such genes include those encoding antibiotic resistance genes (e.g., resistance to hygromycin, kanamycin, bleomycin, G418, streptomycin or spectinomycin) and herbicide resistance genes (e.g., phosphinothricin acetyltransferase).
c. Transformation and Regeneration Techniques Transformation and regeneration of both monocotyledonous and dicotyledonous plant cells is now routine, and the appropriate transformation technique will be determined by the practitioner. The choice of method will vary with the type of plant to be transformed; those skilled in the art will recognize the suitability of particular methods for given plant types. Suitable methods may include, but are not limited to: electroporation of plant protoplasts; liposome-mediated transformation; polyethylene glycol (PEG) mediated transformation;
transformation using viruses; micro-injection of plant cells; micro-projectile bombardment of plant cells; vacuum infiltration; and Agrobacterium tumefaciens (AT) mediated transformation. Typical procedures for transforming and regenerating plants are described in the patent documents listed at the beginning of this section.
5 d. Selection of Transformed Plants Following transformation and regeneration of plants with the transformation vector, transformed plants are usually selected using a dominant selectable marker incorporated into the transformation vector. Typically, such a marker will confer antibiotic resistance on the seedlings of transformed plants, and selection of 10 transformants can be accomplished by exposing the seedlings to appropriate concentrations of the antibiotic.
Selection can also be accomplished by exploiting the pathogen resistance that is conferred to the plant via the transgene. As described in the Examples below, such screening may be accomplished either after the transgenic plants have been 15 regenerated, or (depending on the transformation method used) may be performed on green transgenic callus prior to plant regeneration.

IV. Plants Containing Coding Regions for Multiple Cationic Peptides In some cases, the level of resistance that is conferred by a single copy of a 20 transgene encoding a dermaseptin or a temporin peptide may be enhanced by introducing multiple copies of a single cationic peptide gene, or several genes encoding different cationic peptides.
Through the use of genetic engineering it is possible to introduce coding regions for multiple cationic peptides into a single vector. Typically (though not 25 necessarily) such vectors comprise two or more dermaseptin and/or temporin open reading frames each operably linked to its own 5' and 3' regulatory sequences.
When introduced into plants, such vectors can result in the expression of multiple varieties of cationic peptides.
The creation of a plant containing multiple transgenes can also be accomplished through the use of standard breeding techniques. A transgene encoding a first cationic peptide can be introduced into a first plant and a second transgene encoding a second cationic peptide can be introduced into a second plant. The resulting transgenic plants can then be crossed to produce progeny that carry both transgenes.

V. Production and Isolation of Dermaseptins and Temporins The compositions and methods described above may be used not only to produce plants having enhanced, broad spectrum pathogen resistance, but may also be used for the large scale production of dermaseptins and temporins for a wide range of other applications. For example, temporins and dermaseptins produced in large quantities in plants may be purified and used in medical applications.
The production of biologically active peptides in plants is now widely practiced, and bulk expression and purification methods are well known.
Examples of constructs that facilitate the production of biologically active proteins in plants can be found in U.S. Patent 4,956,282 to Goodman et al. These constructs generally contain a promoter region and an additional nucleic acid sequence that encodes an amino acid sequence that is later utilized in the purification process. The amino acid sequence that is used to facilitate the isolation of the dermaseptin and/or temporin peptides can be subsequently cleaved and discarded.

EXAMPLES
1. Selection and Creation of Nucleic Acid Sequences Encoding the Dermaseptin and the Temporin Peptides a. Dermaseptin Coding Sequence A nucleic acid molecule was designed to encode the mature 27 amino acid form of dermaseptin b (SEQ ID: 3) with a 5 amino acid N-terminal extension sequence, MAMWK. This nucleic acid construct was designated MSRA2 and was synthesized using four overlapping oligonucleotides in a single PCR reaction.
The oligonucleotides used are shown in Table 2. The first two oligonucleotides (oligo #1 and oligo #2) contained the nucleic acid sequences encoding the N-terminal and the C-terminal portions of the peptide, respectively. These oligonucleotides were used in the PCR reaction at a 20 nM concentration. The second two oligonucleotides contained sequences recognized by various restriction enzymes. Specifically, oligo #3 contained restriction sites for Xbal, Kpnl and NcoI, and oligo #4 contained restriction site for SstI, Pstl and HindIll. These oligonucleotides were used at a concentration of 200 nM in the PCR reaction. Following amplification of the product, it was cloned using the built-in restriction sites into a conventional cloning vector.
The nucleic acid sequence of the coding region of MSRA2 is shown in SEQ ID:
27, and the encoded peptide is shown in SEQ ID: 28. Oligo #s 1-4 are shown in SEQ
IDs: 29-32.

Table 2 Oligo # 1: 5' - ATG GCC ATG TGG AAA GAC GTT CTG AAA AAG
(SEQ ID: 29) ATC GGT ACT GTC GCC CTC CAT GCA GGG - 3' Oligo # 2: 3' - TGA CAG CGG GAG GTA CGT CCC TTC CGG CGC
(SEQ ID: 30) GAA CCT CGT CAT CGG CTG TGG TAG AGC GTC ATT - 5' Oligo # 3: 5' - TCT AGA GGT ACC ATG GCC ATG TGG AAA GAC G -3' (SEQ ID: 31) Oligo # 4: 3' - GGC TGT GGT AGA GCG TCA TTC TCG AGA CGT CTT
(SEQ ID: 32) CGA AC - 5' The nucleotides in bold represent the regions of complementarity between oligo # 1 and oligo #2. The underlined portion of oligo #1 is identical to underlined portion of oligo #3, thus allowing oligo #3 to bind to the PCR product from the initial elongation of oligos #1 and #2.
Similarly, the underlined portions of oligo #4 are identical to the underlined portion of oligo #2. This allows oligo #4 to bind to the PCR product created by elongation of oligos #1 and #2.
b. Temporin Coding Sequence A nucleic acid molecule was designed to encode the mature 13 amino acid form of temporin A (SEQ ID:33) with a 6 amino acid N-terminal extension sequence, MASRHM. This nucleic acid construct was designated MSRA3 and was synthesized using four overlapping oligonucleotides in a single PCR reaction. The oligonucleotides used are shown in Table 3. The first two oligonucleotides (oligo #1 and oligo #2) contained the nucleic acid sequences encoding the prototype peptide.
However, unlike the oligonucleotides used to encode the prototype dermaseptin peptide, these oligonucleotides were fully complementary, thus eliminating the need for an initial elongation cycle prior to the binding of oligos #3 and #4.
Oligos #1 and #2 were used in the PCR reaction at a 20 nM concentration. The second two oligonucleotides contained sequences recognized by various restriction enzymes.
Specifically, oligo #3 contained restriction sites for Xbal, KpnI and Mel, and oligo #4 contained restriction site for SstI, and PstI. These oligonucleotides were used at a concentration of 200 nM in the PCR reaction.

Following amplification of the product, it was cloned using the built-in restriction sites into a conventional cloning vector. The nucleic acid sequence of the coding region of MSRA3 is shown in SEQ ID:33, and the encoded peptide is shown in SEQ ID: 34. Oligo #s 1-4 are shown in SEQ IDs: 35-38.
Table 3 Oligo # 1: 5' - ATG TTT CTG CCC CTA ATC GGG AGG GTT CTC TCG
(SEQ ID: 35) GGA ATC CTG TAA - 3' Oligo # 2: 3' - TAC AAA GAC GGG GAT TAG CCC TCC CAA GAG
(SEQ ID: 36) AGC CCT TAG GAC ATT - 5' Oligo # 3: 5' - GGT ACC TCT AGA CAT ATG TTT CTG CCC CTA - 3' (SEQ ID:37) Oligo # 4: 3' - GAG AGC CCT TAG GAC ATT CTC GAG ACG TC - 5' (SEQ ID: 38) The nucleotides in bold represent the regions of complementarity between oligo #1 and oligo #2. As depicted in the diagram these sequences are fully complementary. The underlined portions oligo #2 are complementary to the underlined portions of oligo #3 and the underlined portions of oligo #1 are complementary to the underlined portions of oligo #4.
The resulting double stranded DNA was then cloned into one or more of the vectors described below.

2. Vectors Containing Various Promoter Sequences The nucleic acid sequences encoding MRSA2 and MRSA3 were assembled into various plant transformation vectors, thereby placing them under the transcriptional control of a variety of different promoters.
Cloning MRSA2 and MRSA3 sequences into one such vector placed the respective sequences under the control of a promoter that contained two copies of the CaMV 35S promoter and an AMV RNA4 translation enhancing element (Kay et al., Science 236:1299-1302, 1987). The clones that resulted from ligation into this vector were given the prefix pD as a designation. Therefore, pDMSRA2 designates a vector which contains the MSRA2 construct under the control of the double CaMV 35S
promoter and the AMV RNA4 translational enhancer. Similarly, pDMSRA3 designates a vector that contains the MSRA3 construct under the control of the double CaMV 35S promoter with the AMV RNA4 translational enhancer.
Another vector was designed such that the MSRA2 construct was under the control of a rebuilt "super promoter". This promoter contained the mas (mannopine synthase) promoter/activator region (Langridge et al., Bio/Technology 10:305-308, 1989) preceded by a trimer of ocs (octopine synthase) upstream activating sequence (in inverted orientation). A more detailed description of this super promoter is provided in Ni et al., The Plant J., 7: 661-676, 1995. This particular construct also contained a coding region for a 6 x His tag, positioned upstream of and operably linked to the MSRA2 coding region. The 6 x His tag amino acid sequence is thus expressed as an N-terminal addition to the encoded dermaseptin/ MAMWK peptide.
The vector encoding this peptide was designated pRSHMSRA2.

3. Transformation of Potato and Tobacco Potato cultivars, Russert Burbank and Desiree, as well as tobacco were used as representative plant species for transformation. The transformation of the plants was performed according to DeBlock, Theoret. Appl. Genet. 76:767-774, 1988, with some modifications.
Briefly, transformations of tobacco and potato were carried out by isolating leaves (5 mm) and stems from 4-week-old shoots. These leaves and shoots were cut and further wounded by scratching with glass pipette tips. Wounded leaves and stems were then floated upside down on 15 ml of S2 medium in a petri dish. This medium contained the components listed in Murashige and Skoog, Physiol. Plant. 15:473-479, 1962, supplemented with 30 g/L sucrose 0.5 g/L MES, pH 5.5, and 20 g/L
mannitol.
60 l of LB medium containing Agrobacterium (transformed with the vector 5 of interest) in the late log phase of growth was added to each petri dish, and the dishes were then incubated at low light intensity (500 lux) for 3 days in the presence of the Agrobacterium. The plant tissue was then washed with S2 medium containing 1 g/L
carbenicillin, blotted dry on filter paper, and placed upside down on S4 medium. S4 medium contained the components listed in Murashige and Skoog, Physiol. Plant.
10 15:473-479, 1962 minus sucrose and supplemented with 200 mg/L glutamine, 0.5 g/L
MES, pH 5.7, 0.5 g/L PVP, 20 g/L mannitol, 20 g/L glucose, 40 mg/L adenine-S04, 0.5% agarose, 1 mg/L trans-zeatin, 0.1 mg/L NAA, 1 g/L carbenicillin and 50 g/ml kanamycin, 10 mg/L AgNO3). The plant tissue samples were placed at room temperature (RT) at 3000 lux to allow for callus formation. After two weeks, many 15 small calli formed at the wounded edges of the leaves and stems. The small calli were removed and transferred to fresh S6 medium (S4 without NAA). After 2-3 weeks, the calli were transferred to S8 medium (S6 supplemented with 0.1. mg/L GA3) to allow for shoot formation.
After two weeks on S8 medium, the first shoots (0.5 cm) were transferred to 20 Si medium. This medium contained the components described in Gamborg et al., Exp. Cell Res. 50:151-158, 1968, with the addition of 20 g/L sucrose, 150 mg/L
CaC12, 0.4% agarose, pH 5.8, 1 g/L carbenicillin and 50 g/ml kanamycin. The Si medium and the shoots were placed in Magenta jars to allow for root formation.
After one week the shoots had rooted. In order to avoid selecting identical shoots, transfer 25 of shoots from the same or closely linked calli was avoided.
The regenerated putative transgenic plants were transferred to MS medium containing 1 g/L carbenicillin and 50 g/ml kanamycin for further analysis.

4. Screening of Calli for Disease Resistance 30 A simplified early detection method for disease resistance assays was developed. Control and transgenic calli were grown on S4 medium (MS media without sucrose and supplemented with 200 mg/L glutamine, 0.5 g/L MES, pH 5.7, 0.5 g/L PVP, 20 g/L mannitol, 20 g/L glucose, 40 mg/L adenine-S04, 0.5%
agarose, 1 mg/L trans-zeatin, 0.1 mg/L NAA, 1 g/L carbenicillin and 50 g/ml kanamycin, mg/L AgNO3). The samples were then placed at RT at 3000 lux to allow for callus formation. After two weeks, many small calli formed at wounded edges of the leaves and stems. The small calli were removed and transferred to fresh S6 medium (S4 without NAA). After 2-3 weeks, the calli were transferred to fresh medium and grown in the presence of phytopathogens, Fusarium or Phytophthora. At the end of the experiments, calli that survived and stayed bright green were scored. No fungal resistant calli were found in the control samples, and calli that were resistant to the fungal pathogen were found to be transformed.

5. Molecular Characterization of Transgenic Plants DNA was isolated from the transgenic potato and tobacco plants using the methods described below. In some instances purification involved a more rigorous protocol and in others a simple crude extract procedure was performed.
The more rigorous extract procedure started by obtaining ten grams of fresh leaf tissue, and immediately freezing the sample in liquid nitrogen. The frozen tissue was then ground into a fine power and extracted with 20 ml extraction buffer (50 mM Tris-HC1 buffer, 5 mM EDTA, 0.35 M sorbitol, 0.1% BSA, 0.1% (3 mercaptoethanol, 10% PEG 4000). The homogenate was filtered through several layers of cheesecloth and one layer of miracloth. The final purification steps were then performed in accordance with Wagner et al., Proc. Natl. Acad. Sci. U.S.A.
84:2097-5100, 1987.
The crude extract procedure was used mainly when isolation was being done for the purposes of PCR analysis. For this procedure about 200 mg of fresh leaves were collected and ground in liquid nitrogen into a powder. 100 l of 0.5 N
NaOH was added to the powder and mixed (vortexed) for 30 seconds. The suspension was centrifuged for 5 minutes and 5 l of the supernatant was added into 45 l of 100 mM of Tris buffer (pH 8.0). This crude genomic DNA extract was used as the template for PCR amplification.

Detection of the presence or absence of the MSRA2 construct was achieved by performing a PCR reaction with the extracted genomic DNA and oligos # 3 and #

from Table 2 above. The expected size of the product from the reaction was 129 bp.
This method allowed for the identification of transgenic tobacco and potato plants transformed with the pDMSRA2 or pRSHMSRA2 constructs.
Detection of the MSRA3 construct was achieved by performing PCR reactions either with oligo #3 and oligo # 4 from Table 3 above or with a primer specific for the 2 x 35S CaMV promoter in combination oligo #4 from Table 3 above. Transgenic tobacco plants containing the pDMSRA3 construct were identified.
A control plant was also engineered to contain a GUS gene under the control of a super promoter containing the mas (mannopine synthase) promoter/activator region preceded by a trimer of the ocs (octopine synthase) upstream activating sequence (Ni et al., The Plant J. 7: 661-676. 1995). The insertion of this transgene into the tobacco plant genome was confirmed via PCR techniques.
In some cases, active expression of the transgene was confirmed by Northern blot analysis. The RNA substrate for these experiments was isolated and purified from the transgenic tobacco and potato plants. The protocol used for this isolation was performed in accordance with Verwoerd et al., Nucl. Acids Res. 17:2362, 1989.

6. Resistance to Bacterial Pathogens To examine the resistance of the transgenic potato and tobacco plants to the bacterial pathogen Erwinia carotovora, the bacteria were grown in LB media at RT
overnight (A600= 2.9). A 2 ml aliquote of Erwinia culture was diluted 5 times in dH2O and 1 ml of the diluted culture was added to 2 ml MS liquid media and used in the antibacterial assay. Freshly cut branches (-3.5 cm) from transgenic plants or control plants were inserted into the tubes containing the diluted Erwinia culture so that the bottom of the cut edge of the plant was immersed into the bacterial culture.
The test tubes were incubated at RT at 3000 lux and observed intermittently.
Transgenic potato plants containing pDMSRA2 and transgenic tobacco plants containing either pDMSRA2 or pRSHMSRA2 were tested as described and showed resistance to the pathogen: After one week of growth in the presence of the bacterial culture the transgenic plants were uninfected (as determined by visual inspection) and continued to grow. In sharp contrast, a control plant challenged with bacterial culture was severely infected after one week of incubation, growth was inhibited and the plant died after 2-3 weeks of exposure to fungal pathogens.
To examine the resistance of transgenic potato tubers to the bacterial pathogen Erwinia carotovora cv carotovora, a small well was made into tuber discs (2 cm diameter, 3 cm thick). Twenty microliters of 100x diluted overnight bacterial culture (approximately 2x107 CFU) was pipetted into the well and discs were incubated at room temperature for 6 days. Rotted tissue was then gently removed from the tuber discs and the loss of weight of the tissue determined. Results obtained from such assays showed that compared to the non-transgenic control the transgenic potato tissue is resistant to soft rot (Figure 1).
Bactericidal effects of antimicrobial peptides (SEQ ID NO: 34 (MRSA3) and SEQ ID NO: 28 (MRSA2)) were determined against Escherichia coil (Figure 2) and Erwinia carotovora (Figure 3) in microtiter plates in a final volume of 220 gl containing approximately 1x105 bacteria/ml and indicated concentration of antimicrobial peptides. The cell cultures were incubated at room temperature for 4 hours, diluted and plated on LB plates. After overnight incubation at 37 C (E.
coil) or 28 C (E. carotovora) the colonies were counted and the survival of bacteria was scored. Results from both assays showed that the peptides have significant antimicrobial activity.

7. Resistance to Fungi Mature plants were tested for their resistance to various fungi using the following protocol. One cm2 x 0.5 cm of Fusarium or Phytophthora sp. -containing media slices were cut and put in the center of fresh plates of V8 agar media (250 ml/L V8 juice, 7 grams/L agar) in a 9 cm petri dish and grown for about one month at room temperature, or until the fungal mycelia completely covered the petri dish.
Shoots of transgenic plants (-10 cm) were cut and transferred into MS medium for further growth. According to different treatments, plants were allowed to grow for 3 days or 2 weeks until the shoots rooted. Two 1 cm2 x 0.5 cm slices of the fungal agar were then applied to both sides of the plant shoots without wounding the plant.
The resulting degree of infection was then determined visually.

In a representative experiment, a transgenic potato plant transformed with pDMSRA2, tobacco plants transformed with either pRSHMRSA2 or pDMSRA2, and control potato and tobacco plants were exposed to Phytophthora cactorum. After days, Phytophthora cactorum had grown over the surface of MS medium, and penetrated into the roots and the stems of the control plants, causing impairment of vital plant functions. It was apparent that the roots in the control plants were severely damaged. The interaction between plants and fungi caused the secretion of yellow-brown pigments indicative of the decay process. Subsequently, the plants lost water and leaves became curly, the bottom of the stems softened, and the roots died.
However, the transgenic plants stayed healthy and had no disease symptoms even though the fungal mycelia completely covered the MS media.

The experiment described above was also used to test the transgenic plant's resistance to Phytophthora infestans. The results from these assays showed that the transgenic plants were also resistant to Phytophthora infestans.

Another experiment was performed challenging a pDMSRA2 transgenic potato plant with Fusarium solani. After 6 days, Fusarium grew all over the surface of MS
medium, the damage to the roots in the control plants was severe, and the base of stem was penetrated by Fusarium and the stems were softened and veins of infected leaves showed clear browning and necrosis. After several days, the control plant collapsed and died. However, the transgenic plant continued to grow even under the extreme fungal infestation by Fusarium solani.

Having illustrated and described the principles of the invention in multiple embodiments and examples, it should be apparent to those skilled in the art that the invention can be modified in arrangement and detail without departing from such principles. We claim all modifications coming within the spirit and scope of the following claims.

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SEQUENCE LISTING

<110> University of Victoria Innovation and Development Corporation <120> Transgenic Plants that are Resistant to a Broad Spectrum of Pathogens <130> 3055-27/PAR
<140>
<141>
<150> 60/125,072 <151> 1999-03-17 <160> 41 <170> Patentln Ver. 2.0 <210> 1 <211> 443 <212> DNA
<213> Phyllomedusa bicolor <220>
<221> CDS
<222> (58)..(294) <400> 1 ccacgcgtcc gattctgtcc tccagtactc aacacattct gaattgtaag aacaaac 57 atg gat atc ctg aag aaa tct ctt ttc ctt gta tta ttc ctt gga ttg 105 Met Asp Ile Leu Lys Lys Ser Leu Phe Leu Val Leu Phe Leu Gly Leu gtt tcc ctt tcc atc tgt gaa gaa gag aaa aga gaa aat gaa gat gag 153 Val Ser Leu Ser Ile Cys Glu Glu Glu Lys Arg Glu Asn Glu Asp Glu gag aaa caa gat gac gag caa agt gaa atg aag aga get atg tgg aaa 201 Glu Lys Gln Asp Asp Glu Gln Ser Glu Met Lys Arg Ala Met Trp Lys gat gtg tta aaa aaa ata gga aca gtg gcc tta cat gca gga aaa gcg 249 Asp Val Leu Lys Lys Ile Gly Thr Val Ala Leu His Ala Gly Lys Ala get tta ggt gca gtt get gat aca ata agt caa gga gag caa taa 294 Ala Leu Gly Ala Val Ala Asp Thr Ile Ser Gln Gly Glu Gln agtgaaaaaa atttaaaatt gaattactct aaatagaaca attagcaata attgtgtcaa 354 acctacatta aagcatactg aaccaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 414 aaaaaaaaaa aaaaaaaaaa aaaaaaaaa 443 <210> 2 <211> 78 <212> PRT
<213> Phyllomedusa bicolor <400> 2 Met Asp Ile Leu Lys Lys Ser Leu Phe Leu Val Leu Phe Leu Gly Leu Val Ser Leu Ser Ile Cys Glu Glu Glu Lys Arg Glu Asn Glu Asp Glu Glu Lys Gln Asp Asp Glu Gln Ser Glu Met Lys Arg Ala Met Trp Lys Asp Val Leu Lys Lys Ile Gly Thr Val Ala Leu His Ala Gly Lys Ala Ala Leu Gly Ala Val Ala Asp Thr Ile Ser Gln Gly Glu Gln <210> 3 <211> 27 <212> PRT
<213> Phyllomedusa bicolor <400> 3 Asp Val Leu Lys Lys Ile Gly Thr Val Ala Leu His Ala Gly Lys Ala Ala Leu Gly Ala Val Ala Asp Thr Ile Ser Gln <210> 4 <211> 31 <212> PRT
<213> Phyllomedusa bicolor <400> 4 Ala Met Trp Lys Asp Val Leu Lys Lys Ile Gly Thr Val Ala Leu His Ala Gly Lys Ala Ala Leu Gly Ala Val Ala Asp Thr Ile Ser Gln <210> 5 <211> 36 <212> PRT
<213> Pachymedusa dacnicolor <400> 5 Gly Met Trp Ser Lys Ile Lys Asn Ala Gly Lys Ala Ala Ala Lys Ala Ser Lys Lys Ala Ala Gly Lys Ala Ala Leu Gly Ala Val Ser Glu Ala Leu Gly Glu Gln <210> 6 <211> 31 <212> PRT
<213> Pachymedusa dacnicolor <400> 6 Ala Leu Trp Lys Thr Leu Leu Lys Lys Val Gly Lys Val Ala Gly Lys Ala Val Leu Asn Ala Val Thr Asn Met Ala Asn Gln Asn Glu Gln <210> 7 <211> 35 <212> PRT
<213> Agalychnis annae <400> 7 Gly Met Trp Ser Thr Ile Arg Asn Val Gly Lys Ser Ala Ala Lys Ala Ala Asn Leu Pro Ala Lys Ala Ala Leu Gly Ala Ile Ser Glu Ala Val Gly Glu Gln <210> 8 <211> 29 <212> PRT
<213> Agalychnis annae <400> 8 Gly Met Phe Thr Asn Met Leu Lys Gly Ile Gly Lys Leu Ala Gly Gln Ala Ala Leu Gly Ala Val Lys Thr Leu Ala Gly Glu Gln <210> 9 <211> 30 <212> PRT
<213> Agalychnis annae <400> 9 Ser Leu Trp Ser Lys Ile Lys Glu Met Ala Ala Thr Ala Gly Lys Ala Ala Leu Asn Ala Val Thr Gly Met Val Asn Gln Gly Glu Gln <210> 10 <211> 34 <212> PRT
<213> Phyllomedusa sauvagei <400> 10 Ala Leu Trp Lys Thr Met Leu Lys Lys Leu Gly Thr Met Ala Leu His Ala Gly Lys Ala Ala Leu Gly Ala Ala Ala Asp Thr Ile Ser Gln Gly Thr Gln <210> 11 <211> 34 <212> PRT
<213> Phyllomedusa sauvagei <400> 11 Ala Leu Trp Phe Thr Met Leu Lys Lys Leu Gly Thr Met Ala Leu His Ala Gly Lys Ala Ala Leu Gly Ala Ala Ala Asn Thr Ile Ser Gln Gly Thr Gln <210> 12 <211> 30 <212> PRT
<213> Phyllomedusa sauvagei <400> 12 Ala Leu Trp Lys Asn Met Leu Lys Gly Ile Gly Lys Leu Ala Gly Lys Ala Ala Leu Gly Ala Val Lys Lys Leu Val Gly Ala Glu Ser <210> 13 <211> 27 <212> PRT
<213> Phyllomedusa sauvagei <400> 13 Ala Leu Trp Met Thr Leu Leu Lys Lys Val Leu Lys Ala Ala Ala Lys Ala Leu Asn Ala Val Leu Val Gly Ala Asn Ala <210> 14 <211> 29 <212> PRT
<213> Phyllomedusa sauvagei <400> 14 Gly Leu Trp Ser Lys Ile Lys Thr Ala Gly Lys Ser Val Ala Lys Ala Ala Ala Lys Ala Ala Val Lys Ala Val Thr Asn Ala Val <210> 15 <211> 329 <212> DNA
<213> Rana temporaria <220>
<221> CDS
<222> (53)..(238) <400> 15 cccctccagc tgtctacatt ctcataacca actgaaccac ccgagcccaa ag atg ttc 58 Met Phe acc ttg aag aaa tcc ctc tta ctc ctt ttc ttc ctt ggg acc atc aac 106 Thr Leu Lys Lys Ser Leu Leu Leu Leu Phe Phe Leu Gly Thr Ile Asn tta tct ctc tgt gag gaa gag aga gat gcc gat gaa gaa aga aga gat 154 Leu Ser Leu Cys Glu Glu Glu Arg Asp Ala Asp Glu Glu Arg Arg Asp gat ctc gaa gaa agg gat gtt gaa gtg gaa aag cga ttt ttt cca gtg 202 Asp Leu Glu Glu Arg Asp Val Glu Val Glu Lys Arg Phe Phe Pro Val att gga agg ata ctc aat ggt att ttg gga aaa taa ccaaaaaaag 248 Ile Gly Arg Ile Leu Asn Gly Ile Leu Gly Lys ttaaaacttt ggaaatggaa ttggaaatca tctaatgtgg aatgtcattt agctaaatgc 308 acatcaaatg tcttataaaa a 329 <210> 16 <211> 61 <212> PRT
<213> Rana temporaria <400> 16 Met Phe Thr Leu Lys Lys Ser Leu Leu Leu Leu Phe Phe Leu Gly Thr Ile Asn Leu Ser Leu Cys Glu Glu Glu Arg Asp Ala Asp Glu Glu Arg Arg Asp Asp Leu Glu Glu Arg Asp Val Glu Val Glu Lys Arg Phe Phe Pro Val Ile Gly Arg Ile Leu Asn Gly Ile Leu Gly Lys <210> 17 <211> 13 <212> PRT
<213> Rana temporaria <400> 17 Phe Phe Pro Val Ile Gly Arg Ile Leu Asn Gly Ile Leu <210> 18 <211> 13 <212> PRT
<213> Rana temporaria <400> 18 Phe Leu Pro Leu Ile Gly Arg Val Leu Ser Gly Ile Leu <210> 19 <211> 13 <212> PRT
<213> Rana temporaria <400> 19 Leu Leu Pro Ile Val Gly Asn Leu Leu Lys Ser Leu Leu <210> 20 <211> 13 <212> PRT
<213> Rana temporaria <400> 20 Leu Leu Pro Ile Leu Gly Asn Leu Leu Asn Gly Leu Leu <210> 21 <211> 13 <212> PRT

<213> Rana temporaria <400> 21 Leu Leu Pro Ile Val Gly Asn Leu Leu Asn Ser Leu Leu <210> 22 <211> 13 <212> PRT
<213> Rana temporaria <400> 22 Val Leu Pro Ile Ile Gly Asn Leu Leu Asn Ser Leu Leu <210> 23 <211> 13 <212> PRT
<213> Rana temporaria <400> 23 Phe Leu Pro Leu Ile Gly Lys Val Leu Ser Gly Ile Leu <210> 24 <211> 12 <212> PRT
<213> Rana temporaria <400> 24 Leu Ser Pro Asn Leu Leu Lys Ser Leu Leu Gly Lys <210> 25 <211> 10 <212> PRT
<213> Rana temporaria <400> 25 Leu Leu Pro Asn Leu Leu Lys Ser Leu Leu <210> 26 <211> 13 <212> PRT
<213> Rana temporaria <400> 26 Phe Val Gln Trp Phe Ser Lys Phe Leu Gly Arg Ile Leu <210> 27 <211> 99 <212> DNA
<213> Phyllomedusa bicolor <220>
<221> CDS
<222> (1)..(99) <400> 27 atg gcc atg tgg aaa gac gtt ctg aaa aag atc ggt act gtc gcc ctc 48 Met Ala Met Trp Lys Asp Val Leu Lys Lys Ile Gly Thr Val Ala Leu cat gca ggg aag gcc gcg ctt gga gca gta gcc gac acc atc tcg cag 96 His Ala Gly Lys Ala Ala Leu Gly Ala Val Ala Asp Thr Ile Ser Gln taa 99 <210> 28 <211> 32 <212> PRT
<213> Phyllomedusa bicolor <400> 28 Met Ala Met Trp Lys Asp Val Leu Lys Lys Ile Gly Thr Val Ala Leu His Ala Gly Lys Ala Ala Leu Gly Ala Val Ala Asp Thr Ile Ser Gln <210> 29 <211> 57 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 29 atggccatgt ggaaagacgt tctgaaaaag atcggtactg tcgccctcca tgcaggg 57 <210> 30 <211> 63 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 30 ttactgcgag atggtgtcgg ctactgctcc aagcgcggcc ttccctgcat ggagggcgac 60 agt 63 <210> 31 <211> 31 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 31 tctagaggta ccatggccat gtggaaagac g 31 <210> 32 <211> 38 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 32 caagcttctg cagagctctt actgcgagat ggtgtcgg 38 <210> 33 <211> 60 <212> DNA
<213> Rana temporaria <220>
<221> CDS
<222> (1)..(57) <400> 33 atg gcc tct aga cat atg ttt ctg ccc cta atc ggg agg gtt ctc tcg 48 Met Ala Ser Arg His Met Phe Leu Pro Leu Ile Gly Arg Val Leu Ser gga atc ctg taa 60 Gly Ile Leu <210> 34 <211> 19 <212> PRT
<213> Rana temporaria <400> 34 Met Ala Ser Arg His Met Phe Leu Pro Leu Ile Gly Arg Val Leu Ser Gly Ile Leu <210> 35 <211> 45 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 35 atgtttctgc ccctaatcgg gagggttctc tcgggaatcc tgtaa 45 <210> 36 <211> 45 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 36 ttacaggatt cccgagagaa ccctcccgat taggggcaga aacat 45 <210> 37 <211> 30 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 37 ggtacctcta gacatatgtt tctgccccta 30 <210> 38 <211> 29 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:PCR primer <400> 38 ctgcagagct cttacaggat tcccgagag 29 <210> 39 <211> 4 <212> PRT
<213> Phyllomedusa bicolor <400> 39 Ala Met Trp Lys <210> 40 <211> 4 <212> PRT
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence:spacer sequence <400> 40 Ala Ser Arg His <210> 41 <211> 4 <212> PRT
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: spacer sequence <400> 41 Ala Leu Trp Lys

Claims (21)

Claims

1. A method of making a transgenic plant expressing a dermaseptin or temporin cationic peptide which confers microbial resistance to the plant comprising:
introducing a nucleic acid molecule encoding a dermaseptin or temporin cationic peptide into a plant cell, thereby generating a transgenic plant cell; and growing the transgenic plant cell into a transgenic plant that expresses the dermaseptin or temporin cationic peptide, thereby conferring microbial resistance to the plant.

2. The method of claim 1, wherein the nucleic acid molecule comprises a control sequence operably linked to the nucleic acid molecule encoding a dermaseptin or temporin cationic peptide.

3. The method of claim 1 wherein the dermaseptin peptide comprises an amino acid sequence selected from the group consisting of the amino acid sequences set forth in SEQ IDs: 3-14, and the temporin peptide comprises an amino acid sequence selected from the group consisting of the amino acid sequences set forth in SEQ IDs: 17, 18, 19, 23, and 26.

4. The method of claim 3 wherein the dermaseptin or temporin peptide further comprises an N terminal peptide extension of between 2 and 25 amino acids in length.

5. The method of claim 4 wherein the N terminal peptide extension is selected from the group consisting of AMWK, ASRH, and ALWK.

6. A method of making a transgenic plant comprising:
expressing a recombinant nucleic acid molecule in a plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a fusion peptide having a formula selected from the group consisting of:
(a) P-D; and (b) P-T, wherein D is a dermaseptin peptide having dermaseptin biological activity, T
is a temporin peptide having temporin biological activity and P is an anionic pro-region peptide.

7. A method of making a transgenic plant, comprising:
expressing a recombinant nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a fusion peptide having a formula selected from the group consisting of:
(a) P-S-D; and (b) P-S-T, wherein D is a dermaseptin peptide having dermaseptin biological activity, T
is a temporin peptide having temporin biological activity, P is an anionic pro-region peptide and S is a spacer peptide.

8. A method of making a transgenic plant, comprising:
expressing a nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a dermaseptin peptide comprising an amino acid sequence selected from the group consisting of:
(a) SEQ IDs: 3-14 and fragments thereof;
(b) amino acid sequences that differ from an amino acid sequence specified in (a) by one or more conservative amino acid substitutions; and (c) amino acid sequences that share at least 40% sequence identity with an amino acid sequence specified in (a), wherein the peptide has dermaseptin biological activity.

9. The method of claim 8, wherein the peptide further comprises an anionic pro-region peptide operably linked to the N-terminus of the peptide.

10. A method of making a transgenic plant, comprising:
expressing a nucleic acid molecule in the plant which confers microbial resistance to the plant, wherein the nucleic acid molecule encodes a temporin peptide comprising an amino acid sequence selected from the group consisting of:
(a) SEQ IDs: 17-26 and fragments thereof ;
(b) amino acid sequences that differ from an amino acid sequence specified in (a) by one or more conservative amino acid substitutions; and (c) amino acid sequences that share at least 50% sequence identity with an amino acid sequence specified in (a), wherein the peptide has temporin biological activity.

11. The method according to claim 8 wherein the peptide further comprises an anionic pro-region peptide operably linked to the N-terminus of the peptide.

12. A method of making a transgenic plant, comprising:
expressing in a plant a recombinant nucleic acid molecule encoding a peptide comprising an amino acid sequence selected from the group consisting of SEQ
IDs: 28 and 34, wherein the peptide confers microbial resistance to the plant.

13. A method of producing a biologically active dermaseptin or temporin cationic peptide comprising:

providing a transgenic plant made according to claim 1; and isolating the biologically active dermaseptin or temporin cationic peptide from the plant.

14. The method of claim 13, wherein the cationic peptide is selected from the group consisting of the dermaseptins set forth in SEQ ID NOs 3-14, and the temporins set forth in SEQ IS NOs 17, 18, 19, 23, and 26.

15. The method of claim 2, wherein the nucleic acid molecule comprises a vector.

16. The method of claim 1, wherein the temporin cationic peptide comprises temporin A, B, F, G, or L.

17. The method of claim 16, wherein the temporin cationic peptide comprises SEQ ID NO: 17, 18, 19, 23 or 26.

18. The method of claim 1, wherein the plant is a tobacco plant or a potato plant.

19. The method of claim 1, wherein the plant is resistant to bacteria or fungi.

20. The method of claim 19, wherein the bacteria is E. carotovora or E. coli.

21. The method of claim 19, wherein the fungi is Fusarium sp. or Phytophthora sp.