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An Alkali-tolerant Carbonyl Reductase from Bacillus subtilis by Gene Mining: Identification and Application
Enantiopure alcohols have received much attention due to their widespread use as pharmaceutical intermediates. In the asymmetric biosynthesis of enantiopure alcohols, the excellent performance of carbonyl reductase makes it be the best choice as the biocatalysts. In this work, an alkali-tolerant car...
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Published in: | Catalysis letters 2019-11, Vol.149 (11), p.2973-2983 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Enantiopure alcohols have received much attention due to their widespread use as pharmaceutical intermediates. In the asymmetric biosynthesis of enantiopure alcohols, the excellent performance of carbonyl reductase makes it be the best choice as the biocatalysts. In this work, an alkali-tolerant carbonyl reductase (
Bs
CR, encoded by
yueD
) from
Bacillus subtilis
(strain 168) was obtained through gene mining, and successfully heterologously expressed in
Escherichia coli
with pET-32a.
Bs
CR showed excellent alkali resistance and even can keep more than 70% of its peak activity after incubation in Tris–HCl buffer at pH 9.0 for 40 h. The Michaelis constants and maximal velocity of the
Bs
CR to NADPH (A) and ethyl 4-chloroacetoacetate (B) are
K
m
A
= 5.390 × 10
−2
mmol/L,
K
m
B
= 1.855 mmol/L, and
V
max
= 147.3 μmol·min
−1
·mg
−1
, respectively. Applying the
E. coli
BL21(DE3)/pET-32a-yueD to catalyze asymmetric reduction of ethyl 4-chloroacetoacetate and acetophenone, the yield of
S
-CHBE reached 89.9% and
S
-1-phenyl ethanol reached 66.7%, and
e.e.
of both products reached more than 99%. This work provides a novel CR for asymmetric reduction.
Graphic Abstract
A carbonyl reductase (
Bs
CR) and its gene were identified through gene mining, and overexpressed in
Escherichia coli
BL21(DE3) for whole-cell biocatalytic asymmetric reduction |
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ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-019-02873-w |