JPS6246159B2 - - Google Patents
Info
- Publication number
- JPS6246159B2 JPS6246159B2 JP53054242A JP5424278A JPS6246159B2 JP S6246159 B2 JPS6246159 B2 JP S6246159B2 JP 53054242 A JP53054242 A JP 53054242A JP 5424278 A JP5424278 A JP 5424278A JP S6246159 B2 JPS6246159 B2 JP S6246159B2
- Authority
- JP
- Japan
- Prior art keywords
- starch
- liquefaction
- concentration
- dextrin
- liquid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920002472 Starch Polymers 0.000 claims description 29
- 235000019698 starch Nutrition 0.000 claims description 29
- 239000008107 starch Substances 0.000 claims description 29
- 229920001353 Dextrin Polymers 0.000 claims description 15
- 239000004375 Dextrin Substances 0.000 claims description 15
- 235000019425 dextrin Nutrition 0.000 claims description 15
- 235000013336 milk Nutrition 0.000 claims description 12
- 239000008267 milk Substances 0.000 claims description 12
- 210000004080 milk Anatomy 0.000 claims description 12
- 108090000790 Enzymes Proteins 0.000 claims description 10
- 102000004190 Enzymes Human genes 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000007788 liquid Substances 0.000 description 12
- 229940088598 enzyme Drugs 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000004382 Amylase Substances 0.000 description 5
- 108010065511 Amylases Proteins 0.000 description 5
- 102000013142 Amylases Human genes 0.000 description 5
- 235000019418 amylase Nutrition 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000000855 fermentation Methods 0.000 description 3
- 230000004151 fermentation Effects 0.000 description 3
- 239000008103 glucose Substances 0.000 description 3
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 2
- 240000003183 Manihot esculenta Species 0.000 description 2
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 108090000637 alpha-Amylases Proteins 0.000 description 2
- 102000004139 alpha-Amylases Human genes 0.000 description 2
- 229940024171 alpha-amylase Drugs 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 241000228212 Aspergillus Species 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 description 1
- 102100022624 Glucoamylase Human genes 0.000 description 1
- 244000017020 Ipomoea batatas Species 0.000 description 1
- 235000002678 Ipomoea batatas Nutrition 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 108010019077 beta-Amylase Proteins 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229960004903 invert sugar Drugs 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K7/00—Maltose
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B30/00—Preparation of starch, degraded or non-chemically modified starch, amylose, or amylopectin
- C08B30/12—Degraded, destructured or non-chemically modified starch, e.g. mechanically, enzymatically or by irradiation; Bleaching of starch
- C08B30/18—Dextrin, e.g. yellow canari, white dextrin, amylodextrin or maltodextrin; Methods of depolymerisation, e.g. by irradiation or mechanically
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K1/00—Glucose; Glucose-containing syrups
- C13K1/06—Glucose; Glucose-containing syrups obtained by saccharification of starch or raw materials containing starch
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Emergency Medicine (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Jellies, Jams, And Syrups (AREA)
Description
【発明の詳細な説明】
本発明は澱粉に液化酵素を作用して液化しデキ
ストリン液を製造する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a dextrin solution by liquefying starch by acting on a liquefying enzyme.
グルコース、マルトース、転化糖等は澱粉を液
化して得られるデキストリン液に糖化アミラーゼ
β−アミラーゼ、等の酵素を作用させることによ
つて工業的に大量に生産されている。澱粉を液化
してデキストリンにするには通常澱粉に水を加え
30〜45%の濃度の澱粉乳とし、これに澱粉液化酵
素を高温で作用することによつて行われている
が、この際、澱粉乳の濃度が50%以上になると澱
粉乳の粘度は急激に上昇し、撹拌・輸送等の操作
が困難となり物理的問題が生ずるため50%以上に
することができない。従つて、澱粉乳を液化して
得られるデキストリン液及びデキストリン液の糖
化によつて得られる糖化液の濃度は通常35〜40%
が限度である。蒸発等の濃縮工程を行うことなく
高濃度糖化液が製造できれば、グルコース、マル
トースを製造する場合濃縮に要する費用が大巾に
削減できるので経済上のメリツトは大きいのであ
るが、高濃度糖化液を製造する場合高濃度デキス
トリン液を製造する技術が必要とされる。そこ
で、本発明者らは高濃度デキストリン液を製造す
る技術を開発すべく鋭意研究を重ねた結果、35〜
40%の澱粉乳を液化酵素で液化したデキストリン
液に新たに澱粉を加え50〜65%の澱粉乳とし、こ
れに液化酵素を補添し再び液化することによつて
50〜65%の高濃度デキストリン液を製造すること
ができた。本発明の方法について以下に説明す
る。 Glucose, maltose, invert sugar, etc. are industrially produced in large quantities by reacting enzymes such as saccharifying amylase β-amylase with a dextrin solution obtained by liquefying starch. To liquefy starch into dextrin, water is usually added to the starch.
This is done by making starch milk with a concentration of 30 to 45% and then treating it with starch liquefaction enzyme at high temperature, but at this time, when the concentration of starch milk exceeds 50%, the viscosity of starch milk suddenly decreases. It is not possible to increase the amount above 50% because this would make operations such as stirring and transportation difficult and cause physical problems. Therefore, the concentration of the dextrin solution obtained by liquefying starch milk and the saccharified solution obtained by saccharification of the dextrin solution is usually 35 to 40%.
is the limit. If high-concentration saccharified liquid could be produced without performing a concentration process such as evaporation, the cost required for concentration when producing glucose and maltose could be drastically reduced, which would have great economic merit. For production, a technology for producing a highly concentrated dextrin solution is required. Therefore, the present inventors conducted extensive research to develop a technology for producing high-concentration dextrin liquid, and as a result, 35-35~
40% starch milk is liquefied with a liquefying enzyme, then new starch is added to the dextrin solution to obtain 50-65% starch milk, which is then supplemented with a liquefying enzyme and liquefied again.
We were able to produce a high concentration dextrin solution of 50-65%. The method of the present invention will be explained below.
本発明で使用する澱粉液化酵素としては通常の
液化アミラーゼで良く、例えばバチルス属細菌又
はアスペルギルス属糸状菌等の微生物由来のα−
アミラーゼが使用され、液化酵素は特殊なもので
ある必要はなく市販品を用いて良好に実施され
る。 The starch liquefaction enzyme used in the present invention may be a normal liquefaction amylase, such as α-amylase derived from microorganisms such as Bacillus or Aspergillus.
Amylase is used; the liquefaction enzyme need not be specialized and commercially available products are readily available.
本発明の方法では、まず最初にタピオカ、甘藷
バレイシヨ澱粉に水を加え35〜40%の澱粉乳を作
る。澱粉乳はアルカリを用いてPHを6.5〜7.5に調
整する。この際要すればNaCl、Ca、Mg等酵素安
定化剤を添加し、上記液化アミラーゼを澱粉1g
当り20〜50単位添加し、80〜95℃で30〜60分間液
化する。液化後要すれば放冷しこれに新たに澱粉
を加え50〜65%の澱粉乳とする。このようにして
得られた澱粉乳の物性は最初の澱粉のそれと同様
であり、容易に撹拌・輸送でき物理的な問題はな
い。この高濃度澱粉乳を再び80〜95℃で30〜60分
間液化することにより高濃度デキストリン液が得
られる。本発明の方法はバツチ式のみならず連続
的に実施することもできる。連続的に行うには澱
粉乳化槽と液化槽を設け、液化したデキストリン
液の一部を乳化槽へ送つて循環せしめることによ
つて行われる。 In the method of the present invention, water is first added to tapioca, sweet potato and potato starch to make 35-40% starch milk. The pH of starch milk is adjusted to 6.5-7.5 using an alkali. At this time, if necessary, add enzyme stabilizers such as NaCl, Ca, Mg, etc., and add the above liquefied amylase to 1 g of starch.
Add 20-50 units per batch and liquefy at 80-95°C for 30-60 minutes. After liquefaction, if necessary, let it cool and add new starch to make 50-65% starch milk. The physical properties of the starch milk thus obtained are similar to those of the initial starch, and it can be easily stirred and transported without any physical problems. A high concentration dextrin solution is obtained by liquefying this high concentration starch milk again at 80 to 95°C for 30 to 60 minutes. The method of the invention can be carried out not only batchwise but also continuously. To carry out the process continuously, a starch emulsification tank and a liquefaction tank are provided, and a part of the liquefied dextrin liquid is sent to the emulsification tank and circulated.
このようにして得られた高濃度デキストリン液
は通常110〜120℃で10〜20分間加熱処理をした
後、通常の方法に従つてグルコアミラーゼ又はβ
−アミラーゼ等により酵素糖化され60〜65%の糖
化液となる。糖化液を精製し、濃縮晶析すること
によつてグルコース・マルドスが得られるが本発
明の方法の場合、通常の方法に比較して濃縮に要
する費用が大巾に削減できるため経済上極めて有
利である。 The high concentration dextrin solution obtained in this way is usually heated at 110 to 120°C for 10 to 20 minutes, and then treated with glucoamylase or β
-It is enzymatically saccharified by amylase etc. to become a 60-65% saccharified liquid. Glucose maldos can be obtained by purifying the saccharified liquid and concentrating and crystallizing it, but the method of the present invention is extremely economically advantageous because the cost required for concentration can be significantly reduced compared to conventional methods. It is.
酵素糖化液は種々の発酵の主原料として工業的
に大量に使用され、通常発酵槽へ連続的に供給
(フイード)される。この際フイード液の濃度は
高ければ高いほど発酵生産には有利であるので本
発明の方法で得られる糖化液は発酵原料として極
めて望ましいものである。 Enzymatic saccharification liquid is used industrially in large quantities as a main raw material for various fermentations, and is usually continuously fed to a fermenter. In this case, the higher the concentration of the feed liquid, the more advantageous it is to fermentation production, so the saccharified liquid obtained by the method of the present invention is extremely desirable as a raw material for fermentation.
以下実施例にて詳細に説明する。 This will be explained in detail in Examples below.
実施例 1
タピオカ澱粉2.1Kg(澱粉1.83Kgを含む)を水
2.2に懸濁し、1.3g/dlの苛性ソーダ液を用い
てPHを7.0に調整した。0.366gのクライスターゼ
(大和化成社の細菌α−アミラーゼ剤)を100mlの
水に溶かし、これを上記懸濁液に添加した。懸濁
液を撹拌しつつ液温を90℃に上げ90℃で30分間撹
拌しながら液化を行つた。液化後放冷し、液温60
℃とした後新たに1.8Kg(澱粉1.14Kg)を加え、
PHを7.0に調整した。Example 1 2.1Kg of tapioca starch (including 1.83Kg of starch) was added to water.
2.2, and the pH was adjusted to 7.0 using 1.3 g/dl caustic soda solution. 0.366 g of clystase (bacterial α-amylase agent manufactured by Daiwa Kasei Co., Ltd.) was dissolved in 100 ml of water, and this was added to the above suspension. While stirring the suspension, the liquid temperature was raised to 90°C, and liquefaction was performed while stirring at 90°C for 30 minutes. After liquefaction, let it cool down to a liquid temperature of 60
After cooling to ℃, add another 1.8Kg (1.14Kg of starch),
Adjusted pH to 7.0.
これに0.8gのクライスターゼを補添し再び90
℃で30分間液化を行つた。液化終了後小型オート
クレーブを用いて120℃、10分間加熱処理を行い
放冷して高濃度(61%)デキストリン液を得た
(DE.13.5)。 Add 0.8g of clystase to this and return to 90
Liquefaction was carried out for 30 minutes at °C. After completion of liquefaction, heat treatment was performed at 120°C for 10 minutes using a small autoclave, and the mixture was allowed to cool to obtain a high concentration (61%) dextrin liquid (DE.13.5).
この高濃度デキストリン液のPHを6N−硫酸で
4.8に調整し、これに2.26gのグルクザイム(天
野製薬社糖の糸状菌糖化アミラーゼ剤)を水100
mlに溶解して添加し、軽く撹拌しながら55℃で72
時間糖化を行つた。糖化液の分解率は98.5%直糖
濃度は60.53%であつた。 Adjust the pH of this highly concentrated dextrin solution with 6N-sulfuric acid.
4.8 and add 2.26g of gluczyme (Amano Pharmaceutical Co., Ltd. sugar filamentous saccharifying amylase agent) to 100% of water.
72 ml at 55°C with gentle stirring.
Time saccharification was performed. The decomposition rate of the saccharified liquid was 98.5%, and the direct sugar concentration was 60.53%.
Claims (1)
キストリン液を製造する方法に於て、澱粉液化液
に新たに澱粉を加え液化酵素を補添し液化するこ
とを特徴とする高濃度デキストリン液の製造法。1. A method for producing a dextrin solution by liquefying starch milk by applying a starch liquefaction enzyme, which is characterized in that starch is newly added to the starch liquefaction solution and a liquefaction enzyme is supplemented for liquefaction. Manufacturing method.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5424278A JPS5516A (en) | 1978-05-08 | 1978-05-08 | Production of high concentration dextrin solution |
GB7915645A GB2029846B (en) | 1978-05-08 | 1979-05-04 | Producing concentrated dextrin solutions |
MY8500372A MY8500372A (en) | 1978-05-08 | 1985-12-30 | Production of a concentrated dextrin solution |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5424278A JPS5516A (en) | 1978-05-08 | 1978-05-08 | Production of high concentration dextrin solution |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5516A JPS5516A (en) | 1980-01-05 |
JPS6246159B2 true JPS6246159B2 (en) | 1987-09-30 |
Family
ID=12965066
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5424278A Granted JPS5516A (en) | 1978-05-08 | 1978-05-08 | Production of high concentration dextrin solution |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPS5516A (en) |
GB (1) | GB2029846B (en) |
MY (1) | MY8500372A (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3814244A1 (en) * | 1987-07-23 | 1989-02-16 | Siemens Ag | CIRCUIT AND WINDING ARRANGEMENT FOR A MULTIPHASE ELECTRIC ROTATING MACHINE |
TW284788B (en) * | 1991-05-28 | 1996-09-01 | L Air Liquide Soliete And Nyme Dour L Expl Des Proce | |
JP3193494B2 (en) * | 1992-01-03 | 2001-07-30 | レール・リキード・ソシエテ・アノニム・プール・レテュード・エ・レクスプロワタシオン・デ・プロセデ・ジョルジュ・クロード | Method for producing high fructose corn syrup from glucose using noble gas |
AU4038793A (en) | 1992-04-03 | 1993-11-08 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | A method of controlling browning reactions using noble gases |
US5364777A (en) * | 1992-04-03 | 1994-11-15 | American Air Liquide | Method of improving lipase activity using noble gases |
US6342261B1 (en) | 1992-04-03 | 2002-01-29 | American Air Liquide | Method of preserving foods using noble gases |
US5382525A (en) * | 1992-11-27 | 1995-01-17 | American Air Liquide | Method of effecting increased performance of diagnostic enzyme reaction systems using noble gases |
CA2109458A1 (en) | 1992-11-27 | 1994-05-28 | Kevin C. Spencer | Method of improving processes using pectinase enzymes with noble gases |
US5328823A (en) * | 1992-11-27 | 1994-07-12 | American Air Liquide | Enzyme-based biosensors for detecting noble gases |
WO2006034708A1 (en) * | 2004-09-28 | 2006-04-06 | Danifo A/S | Process for the preparation of highly concentrated and stable carbohydrate |
CN104293863B (en) * | 2014-09-30 | 2017-07-14 | 江南大学 | A kind of preprocess method of promotion high concentration starch liquefacation |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS539333A (en) * | 1976-05-12 | 1978-01-27 | Cpc International Inc | Starch hydrolyzate having higher dryyweight |
-
1978
- 1978-05-08 JP JP5424278A patent/JPS5516A/en active Granted
-
1979
- 1979-05-04 GB GB7915645A patent/GB2029846B/en not_active Expired
-
1985
- 1985-12-30 MY MY8500372A patent/MY8500372A/en unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS539333A (en) * | 1976-05-12 | 1978-01-27 | Cpc International Inc | Starch hydrolyzate having higher dryyweight |
Also Published As
Publication number | Publication date |
---|---|
MY8500372A (en) | 1985-12-31 |
GB2029846B (en) | 1982-11-17 |
JPS5516A (en) | 1980-01-05 |
GB2029846A (en) | 1980-03-26 |
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