Applications of Hydrolytic and Decarboxylating Enzymes in Biotransformations
- 1 January 1994
- journal article
- Published by Taylor & Francis in Biocatalysis
- Vol. 9 (1-4) , 1-30
- https://doi.org/10.3109/10242429408992104
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Stereochemistry of the formation of lactaldehyde and acetoin produced by the pyruvate decarboxylases of yeast (Saccharomyces sp.) and Zymomonas mobilis: different Boltzmann distributions between bound forms of the electrophile, acetaldehyde, in the two enzymatic reactionsJournal of the Chemical Society, Perkin Transactions 1, 1993
- Enzymatic synthesis of glycosides using the β-galactosidase of Escherichia coli: regio- and stereo-chemical studiesJournal of the Chemical Society, Perkin Transactions 1, 1990
- Absolute configuration of the product of the acetolactate synthase reaction by a novel method of analysis using acetolactate decarboxylaseJournal of the Chemical Society, Perkin Transactions 1, 1990
- Synthesis of 2-Hydroxy-3-oxocarboxylic Esters From the Corresponding α,β-Unsaturated Esters by a Simple One-Step ProcedureSynthesis, 1989
- Biotransformations with acetolactate decarboxylase: unusual conversions of both substrate enantiomers into products of high optical purityJournal of the Chemical Society, Chemical Communications, 1988
- Catalysis by di-n-butyltin oxide of a tertiary ketol rearrangement: synthesis of intermediates and analogues of valine and isoleucine biosynthesisJournal of the Chemical Society, Chemical Communications, 1987
- Stereochemistry of the decarboxylation of α-acetolactate (2-hydroxy-2-methyl-3-oxobutanoate) by the acetolactate decarboxylase of Klebsiella aerogenesJournal of the Chemical Society, Perkin Transactions 1, 1984
- Kinetic Investigation of the a‐Chymotrypsin‐Catalyzed Hydrolysis of Peptide SubstratesEuropean Journal of Biochemistry, 1982
- Synthesis of the Enantiomeric Forms of 4-Hexanolide (γ-Caprolactone) from the Optically Active 5-Phenyl-4-pentene-2,3-diol Prepared from Cinnamaldehyde and Baker's YeastSynthesis, 1980
- The base-catalysed rearrangement of α-acetolactate (2-hydroxy-2-methyl-3-oxobutanoate) : a novel carboxylate ion migration in a tertiary ketol rearrangementJournal of the Chemical Society, Perkin Transactions 1, 1979