Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii
Biotechnology and Bioengineering|Updated:2026-01-06
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Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii
Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii
中国化学工程学报(英文版)2020年28卷第8期 页码:2160-2166
Affiliations:
1. School of Biotechnology and Key Laboratory of Industrial Biotechnology of Ministry of Education, Jiangnan University,Wuxi,China,214122
2. China National Center for Food Safety Risk Assessment, NHC Key Laboratory of Food Safety Risk Assessment,Beijing,China,100022
3. State Key Laboratory of Food Science and Technology, Jiangnan University,Wuxi,China,214122
Han Zu, Hui Zhang, Anwen Fan, 等. Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii[J]. 中国化学工程学报(英文版), 2020,28(8):2160-2166. DOI: 10.1016/j.cjche.2019.12.015.
)-1,3-butanediol
Han Zu, Hui Zhang, Anwen Fan, 等. Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii[J]. 中国化学工程学报(英文版), 2020,28(8):2160-2166. DOI: 10.1016/j.cjche.2019.12.015.DOI:
Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii
摘要
Abstract
(
R
)-1
3-butanediol is an important pharmaceutical intermediate
and the synthesis of (
R
)-1
3-butanediol using green biological methods has recently been of interest for industrial application. Here
a novel strain QC-1 that efficiently transforms 4-hydroxy-2-butanone to (
R
)-1
3-butanediol was isolated from soil samples. Based on morphological
physiological
and biochemical tests and 5.8S-internal transcribed spacer sequencing
the strain was identified as
Pichia kudriavzevii
QC-1. The reaction conditions were optimized to 35 ℃
pH 8.0
rotation speed 200 rpm
and 6:5 mass ratio of glucose to 4-hydroxy-2-butanone. Evaluation of the effects of 4-hydroxy- 2-butanone concentrations on yield and cell survival rate showed that 85.60 g·L
-1
product accumulated
with an enantiomeric excess of more than 99%
when 30 g·L
-1
4-hydroxy-2-butanone was added at 0
10
and 30 h in a 3-L bioreactor. Thus
strain QC-1 showed excellent catalytic activity and stereoselectivity for the synthesis of (
R
)-1
3-butanediol from 4-hydroxy-2-butanone.
关键词
Keywords
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