Molecular Basis for Enantioselectivity in the (R)- and (S)-Hydroxypropylthioethanesulfonate Dehydrogenases, a Unique Pair of Stereoselective Short-Chain Dehydrogenases/Reductases Involved in Aliphatic Epoxide Carboxylation
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Utah State University, Logan, Utah 84322
2. Department of Chemistry and Biochemistry, Montana State University, Bozeman, Montana 59717
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi100294m
Reference27 articles.
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2. Recent developments in asymmetric reduction of ketones with biocatalysts
3. Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part I: processes with isolated enzymes
4. A role for coenzyme M (2-mercaptoethanesulfonic acid) in a bacterial pathway of aliphatic epoxide carboxylation
5. Purification to Homogeneity and Reconstitution of the Individual Components of the Epoxide Carboxylase Multiprotein Enzyme Complex from Xanthobacter Strain Py2
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