Application ob hydrogen high pressure bioreactor using immobilized microorganisms
| Project/Area Number |
60850170
|
|---|
| Research Category |
Grant-in-Aid for Developmental Scientific Research
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
発酵工学
|
|---|
| Research Institution | Tokyo University of Agriculture and Technology |
|---|
Principal Investigator |
NISHIMURA Shigeo Tokyo University of Agriculture and Technology, Profeeor, 工学部, 教授 (90015008)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
橋本 葭人 千代田化工建設(株), バイオシステムプロジェクト部, 副主任
MATSUNAGA Tadashi Tokyo University of Agriculture and Technology, Associate Professor, 工学部, 助教授 (10134834)
HASHIMOTO Atsushi Chiyoda Chemical Engineering & Construction Co.,Ltd., Associate Chief
|
|---|
| Project Period (FY) |
1985 – 1987
|
| Project Status |
Completed (Fiscal Year 1987)
|
| Budget Amount *help |
¥7,600,000 (Direct Cost: ¥7,600,000)
Fiscal Year 1987: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1986: ¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1985: ¥5,200,000 (Direct Cost: ¥5,200,000)
|
|---|
| Keywords | Immobilized mictootganisms / Hydrogen high pressure bioreactor / L-Phenylalanine / Phenylalanine methy ester / Z-Aspartame / 脂肪酸 / L-フェニルアラニン / フェニルアラニンデヒドロゲナーゼ / バイオリアクター / ヒドロゲナーゼ |
|---|
| Research Abstract |
Immobilized microorganisms have been used for NADH regeneration under hydrogen high pressure. This NADH regeneration system has been applied to production of L-phenylalanine. We attempt to produce L-phenlalanine from phenylpyruvate by immobilized cells of Nocardis opaca. N.opace was cultivated in nutrient broth. The cultured cells were immobilized in 2% Ca-clginate. Continual production of phenylalanine was carried out in the medium containing phenylpyruvate, NH_4Cl and immobilized whole cells at 37゜C for 10h under 100atm hydrogen. Production rate of phenylalanine was 0.24 umol/min-cm^3 gel with a conversion of 82%. Immobilized cells retained 76% of phenylalanine production rate after 10h reactions were repeated 11 times with two intervening reactivation.
The immobilized N.opaca was applied to phenylalanine methyl ester production. NADH regeneration system was also cooperated in this system. production. of phenylalanine methyl ester was carrid out in water-organic solvent system containing phenlpyruvate methy ester, NH_4 Cl, NAD^+ and immobilized cells in the presence of hydrogen at 100atm. Immobilized cells of N. opara produced phenylalanine methy ester at the rate of 0.02 <micrn>mol/ min/cm^3 gel by 36h activated immobilized cells with a conversion of 80%. The phenylalanine methyl ester production was followed by synthesis of zaspartame from phenylpyruvate methyl ester, NH_4Cl, NAD^+, Z-aspartic acid by immobilized N.opara - thermolysin. production rate of Z-aspartame was 22.4 <micrn>mol/min/g thermolysin. The conversion was 86%.
Hydrogenation of fatty acid was carried out by metal catalysts and immobilized tumen bacteria. Linoleic acid was hydrogenated with high selectivity to oleic acid by palladium catalysts in the presence og added phenylacetaldehyde. Oleic acid was hydrogenated to steatic acid by immobilized Fusocillus sp. in water-ethyl acetate system.
|
Report
(3 results)
Research Products
(15 results)
