摘要:
β-D-galactosidase catalyzed reactions can be terminated by inhibiting β-D-galalctosidase in a method in which β-D-qalactosidase is brought in contact with a chelating agent at an alkaline pH range other than the optimal pH range for β-D-galactosidase.
摘要:
β-D-galactosidase catalyzed reactions can be terminated by inhibiting β-D-galalctosidase in a method in which β-D-qalactosidase is brought in contact with a chelating agent at an alkaline pH range other than the optimal pH range for β-D-galactosidase.
摘要:
A 2-substituted-thiazolldine-4-carboxylic acid is produced in a high yield by holding 2-amino-2-thiazoline-4-carboxylic acid and a carbonyl compound of the formula: wherein R, and R 2 are identical or different and each represents a hydrogen atom, a formyl group, a carboxyl group, a substituted or unsubstituted saturated or unsaturated alkyl group, or a substituted or unsubstituted aryl group, in aqueous solution in the presence of an effective amount of an enzyme of a microorganism, said enzyme being capable of converting 2-amino-thiazoline-4-carboxylic acid to L-cysteine, and said microorganism being capable of growing in a medium containing 2-amino-thiazoline-4-carboxylic acid as a nitrogen source and producing said enzyme.
摘要:
A 2-substituted-thiazolldine-4-carboxylic acid is produced in a high yield by holding 2-amino-2-thiazoline-4-carboxylic acid and a carbonyl compound of the formula: wherein R, and R 2 are identical or different and each represents a hydrogen atom, a formyl group, a carboxyl group, a substituted or unsubstituted saturated or unsaturated alkyl group, or a substituted or unsubstituted aryl group, in aqueous solution in the presence of an effective amount of an enzyme of a microorganism, said enzyme being capable of converting 2-amino-thiazoline-4-carboxylic acid to L-cysteine, and said microorganism being capable of growing in a medium containing 2-amino-thiazoline-4-carboxylic acid as a nitrogen source and producing said enzyme.
摘要:
Novel ethylamine derivatives of the formula (I) and salts thereof are useful as antihypertensive agents. wherein A is a linking group wherein the linkage is formed by a carbon or nitrogen atom; B is an aryl-containing group; C is hydrogen or optionally substituted alkyl, aralkyl or aryl, or C may be bonded to A to form an optionally substituted alkylene bridge; Q is an aryl- or heterocyclic aryl-containing group; X is a linking group wherein the linkage is formed by optionally substituted alkylene having from 2 to 20 carbon atoms and/or one or more hetero atoms selected from nitrogen and sulfur.