Enantioselective reduction of prochiral ketones by engineered bifunctional fusion proteins.
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Whole-cell biotransformation systems for reduction of prochiral carbonyl compounds to chiral alcohol in Escherichia coliEnantioselective Synthesis of Vicinal (R,R)-Diols by Saccharomyces cerevisiae Butanediol Dehydrogenase.Spatial organization of multi-enzyme biocatalytic cascades.One-step synthesis of 12-ketoursodeoxycholic acid from dehydrocholic acid using a multienzymatic system.Multi-enzymatic one-pot reduction of dehydrocholic acid to 12-keto-ursodeoxycholic acid with whole-cell biocatalysts.Construction and evaluation of a novel bifunctional phenylalanine-formate dehydrogenase fusion protein for bienzyme system with cofactor regeneration.Assessing the stereoselectivity of carbonyl reductases toward the reduction of OPBE and docking analysis.Novel whole-cell biocatalysts with recombinant hydroxysteroid dehydrogenases for the asymmetric reduction of dehydrocholic acid.
P2860
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P2860
Enantioselective reduction of prochiral ketones by engineered bifunctional fusion proteins.
description
2010 nî lūn-bûn
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2010年の論文
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name
Enantioselective reduction of ...... bifunctional fusion proteins.
@en
Enantioselective reduction of ...... bifunctional fusion proteins.
@nl
type
label
Enantioselective reduction of ...... bifunctional fusion proteins.
@en
Enantioselective reduction of ...... bifunctional fusion proteins.
@nl
prefLabel
Enantioselective reduction of ...... bifunctional fusion proteins.
@en
Enantioselective reduction of ...... bifunctional fusion proteins.
@nl
P2860
P356
P1476
Enantioselective reduction of ...... bifunctional fusion proteins.
@en
P2093
Kathrin Hölsch
P2860
P304
P356
10.1042/BA20100143
P577
2010-08-02T00:00:00Z