CS259045B1 - Method of d-glucose's and starch hydrolysis products' production - Google Patents
Method of d-glucose's and starch hydrolysis products' production Download PDFInfo
- Publication number
- CS259045B1 CS259045B1 CS254485A CS254485A CS259045B1 CS 259045 B1 CS259045 B1 CS 259045B1 CS 254485 A CS254485 A CS 254485A CS 254485 A CS254485 A CS 254485A CS 259045 B1 CS259045 B1 CS 259045B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- enzyme
- hydrolysis
- starch
- carried out
- reactors
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 15
- 230000007062 hydrolysis Effects 0.000 title claims 11
- 238000006460 hydrolysis reaction Methods 0.000 title claims 11
- 229920002472 Starch Polymers 0.000 title claims 6
- 239000008107 starch Substances 0.000 title claims 6
- 235000019698 starch Nutrition 0.000 title claims 6
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 title 1
- 229940088598 enzyme Drugs 0.000 claims 8
- 108090000790 Enzymes Proteins 0.000 claims 6
- 102000004190 Enzymes Human genes 0.000 claims 6
- 239000004382 Amylase Substances 0.000 claims 3
- 229920001542 oligosaccharide Polymers 0.000 claims 3
- 150000002482 oligosaccharides Chemical class 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 108010059892 Cellulase Proteins 0.000 claims 1
- 108010073178 Glucan 1,4-alpha-Glucosidase Proteins 0.000 claims 1
- 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 claims 1
- 239000004367 Lipase Substances 0.000 claims 1
- 102000004882 Lipase Human genes 0.000 claims 1
- 108090001060 Lipase Proteins 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 229940106157 cellulase Drugs 0.000 claims 1
- 230000006862 enzymatic digestion Effects 0.000 claims 1
- 230000002255 enzymatic effect Effects 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 235000019421 lipase Nutrition 0.000 claims 1
- 239000007791 liquid phase Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
- 239000007790 solid phase Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 101100066898 Mus musculus Flna gene Proteins 0.000 description 3
- 235000017399 Caesalpinia tinctoria Nutrition 0.000 description 2
- 241000388430 Tara Species 0.000 description 2
- 244000099147 Ananas comosus Species 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 244000089742 Citrus aurantifolia Species 0.000 description 1
- 241001459693 Dipterocarpus zeylanicus Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 240000006890 Erythroxylum coca Species 0.000 description 1
- 102100026933 Myelin-associated neurite-outgrowth inhibitor Human genes 0.000 description 1
- 235000008957 cocaer Nutrition 0.000 description 1
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 1
- 101150115538 nero gene Proteins 0.000 description 1
- 231100001143 noxa Toxicity 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
- C13K1/00—Glucose; Glucose-containing syrups
- C13K1/06—Glucose; Glucose-containing syrups obtained by saccharification of starch or raw materials containing starch
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/14—Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Emergency Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD26216184A DD238305A3 (de) | 1984-04-23 | 1984-04-23 | Verfahren zur herstellung von d-glucose und staerkehydrolysaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS259045B1 true CS259045B1 (en) | 1988-09-16 |
Family
ID=5556322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS254485A CS259045B1 (en) | 1984-04-23 | 1985-04-05 | Method of d-glucose's and starch hydrolysis products' production |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS6125494A (fr) |
| BE (1) | BE902257A (fr) |
| CS (1) | CS259045B1 (fr) |
| DD (1) | DD238305A3 (fr) |
| DE (1) | DE3512552A1 (fr) |
| FR (1) | FR2563234A1 (fr) |
| HU (1) | HUT37956A (fr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU659645B2 (en) | 1991-06-26 | 1995-05-25 | Inhale Therapeutic Systems | Storage of materials |
| US6509006B1 (en) | 1992-07-08 | 2003-01-21 | Inhale Therapeutic Systems, Inc. | Devices compositions and methods for the pulmonary delivery of aerosolized medicaments |
| US6582728B1 (en) | 1992-07-08 | 2003-06-24 | Inhale Therapeutic Systems, Inc. | Spray drying of macromolecules to produce inhaleable dry powders |
| ATE416755T1 (de) | 1994-03-07 | 2008-12-15 | Nektar Therapeutics | Verfahren und zusammensetzung für die pulmonale darreichung von insulin |
| US6290991B1 (en) | 1994-12-02 | 2001-09-18 | Quandrant Holdings Cambridge Limited | Solid dose delivery vehicle and methods of making same |
| US6565885B1 (en) | 1997-09-29 | 2003-05-20 | Inhale Therapeutic Systems, Inc. | Methods of spray drying pharmaceutical compositions |
| US6309623B1 (en) | 1997-09-29 | 2001-10-30 | Inhale Therapeutic Systems, Inc. | Stabilized preparations for use in metered dose inhalers |
| US7871598B1 (en) | 2000-05-10 | 2011-01-18 | Novartis Ag | Stable metal ion-lipid powdered pharmaceutical compositions for drug delivery and methods of use |
| PT1280520E (pt) | 2000-05-10 | 2014-12-16 | Novartis Ag | Pós à base de fosfolípidos para administração de fármacos |
| PT1458360E (pt) | 2001-12-19 | 2011-07-13 | Novartis Ag | Derivados de indole como agonistas do recetor s1p1 |
| DE102004060929B4 (de) * | 2004-12-17 | 2009-06-10 | Flottweg Gmbh & Co. Kgaa | Verfahren und Anlage zur Herstellung von Glukose aus einer Stärkelösung |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4011137A (en) * | 1974-08-26 | 1977-03-08 | Standard Brands Incorporated | Process for producing dextrose using mixed immobilized enzymes |
| US4287304A (en) * | 1980-01-14 | 1981-09-01 | National Distillers And Chemical Corp. | Fermentable sugar from the hydrolysis of starch derived from dry milled corn |
-
1984
- 1984-04-23 DD DD26216184A patent/DD238305A3/de not_active IP Right Cessation
-
1985
- 1985-04-05 CS CS254485A patent/CS259045B1/cs unknown
- 1985-04-06 DE DE19853512552 patent/DE3512552A1/de not_active Withdrawn
- 1985-04-19 FR FR8505970A patent/FR2563234A1/fr active Pending
- 1985-04-22 HU HU154285A patent/HUT37956A/hu unknown
- 1985-04-23 JP JP8559985A patent/JPS6125494A/ja active Pending
- 1985-04-23 BE BE0/214890A patent/BE902257A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| HUT37956A (en) | 1986-03-28 |
| DE3512552A1 (de) | 1985-10-24 |
| FR2563234A1 (fr) | 1985-10-25 |
| BE902257A (fr) | 1985-08-16 |
| DD238305A3 (de) | 1986-08-20 |
| JPS6125494A (ja) | 1986-02-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CS259045B1 (en) | Method of d-glucose's and starch hydrolysis products' production | |
| GB1328609A (en) | Thiophosphate analogues of nucleoside di-and triphosphates | |
| Das et al. | Selective oxidation of organic sulfides by mononuclear and dinuclear peroxotungsten (VI) complexes | |
| Ariela et al. | The role of carbonate in electro-catalytic water oxidation by using Ni (1, 4, 8, 11-tetraazacyclotetradecane) 2+ | |
| Sakano et al. | Preparation and enzymatic hydrolysis of maltosyl-α-cyclodextrin | |
| Odebunmi et al. | Kinetic and thermodynamic studies of glucose oxidase catalysed oxidation reaction of glucose | |
| Huang et al. | RNA enzymes with two small-molecule substrates | |
| CA2567507A1 (fr) | Production de dioxyde de chlore | |
| WO2005052124A3 (fr) | Modulation d'activite d'enzyme par changement de positions stereogeometriques reciproques de deux centres catalytiques dans une enzyme | |
| Percival et al. | Inhibition of phosphoglucomutase by vanadate | |
| Sierks et al. | Catalytic mechanism of glucoamylase probed by mutagenesis in conjunction with hydrolysis of α-D-glucopyranosyl fluoride and maltooligosaccharides | |
| Fierobe et al. | Enzymatic properties of the cysteinesulfinic acid derivative of the catalytic-base mutant Glu400→ Cys of glucoamylase from Aspergillus awamori | |
| Sigel et al. | Metal‐Ion‐Promoted Dephosphorylation of the 5′‐Triphosphates of Uridine and Thymidine, and a Comparison with the Reactivity in the Corresponding Cytidine and Adenosine Nucleotide Systems | |
| Hearon | The steady state kinetics of some biological systems: I | |
| Sumaoka et al. | Enormous acceleration by cerium (IV) for the hydrolysis of nucleoside 3′, 5′-cyclic monophosphates at pH 7 | |
| Booth | The xanthine oxidase-aldehyde system | |
| Takeda et al. | Cooperation of lanthanum ion and non-ianthanide metal ions for the hydrolysis of bis (4-nitrophenyl) phosphate | |
| Griffith | A nomograph for the hydrolytic degradation of pyro-and tripolyphosphates | |
| Liu et al. | Mutations to alter Aspergillus awamori glucoamylase selectivity. IV. Combinations of Asn20→ Cys/Ala27→ Cys, Ser30→ Pro, Gly137→ Ala, 311–314 Loop, Ser411→ Ala and Ser436→ Pro | |
| JP6321857B1 (ja) | 糖カルボン酸の製造方法 | |
| GB1482127A (en) | D-gluconic delta-lactam | |
| Matsuda et al. | Cascading Whiplash PCR with a nicking enzyme | |
| Voordouw et al. | Modification of the Thiol Residues of Pyridine Nucleotide Transhydrogenase from Azotobacter vinelandii: Activity Modulation by the Divalent Thiol Reagent p‐Aminophenylarsenoxide | |
| Baykov et al. | Fluoride inhibition of inorganic pyrophosphatase III. Dependence on the nature of substrate and metal ion cofactor | |
| Pütter et al. | The degradation of mefrusid the participation of a “lactonase” in drug metabolism |