Double substituted variant of Bacillus amyloliquefaciens esterase with enhanced enantioselectivity and high activity towards 1-(3′,4′-methylenedioxyphenyl)ethyl acetate
出版年份 2014 全文链接
标题
Double substituted variant of Bacillus amyloliquefaciens esterase with enhanced enantioselectivity and high activity towards 1-(3′,4′-methylenedioxyphenyl)ethyl acetate
作者
关键词
<em class=EmphasisTypeItalic >Bacillus amyloliquefaciens</em>, Esterase, Enantioselectivity, Iterative saturation mutagenesis, 1-(3′,4′-Methylenedioxyphenyl)ethanol
出版物
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 99, Issue 4, Pages 1701-1708
出版商
Springer Nature
发表日期
2014-08-08
DOI
10.1007/s00253-014-5992-0
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Stepwise and combinatorial optimization of enantioselectivity for the asymmetric hydrolysis of 1-(3’,4’-methylenedioxyphenyl)ethyl acetate under use of a cold-adapted Bacillus amyloliquefaciens esterase
- (2014) Jia-Yan Liu et al. BIOTECHNOLOGY AND BIOPROCESS ENGINEERING
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- (2012) Jingbo Ma et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- Multi-substrate fingerprinting of esterolytic enzymes with a group of acetylated alcohols and statistic analysis of substrate spectrum
- (2012) Jia-Yan Liu et al. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
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- (2012) Zhong Ni et al. JOURNAL OF MOLECULAR MODELING
- Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation Using Unsymmetrical Vicinal Diamine-Based Ligands: Dramatic Substituent Effect on Catalyst Efficiency
- (2011) Bo Zhang et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
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- (2011) Michael Kotik et al. JOURNAL OF BIOTECHNOLOGY
- Rational Protein Design of Paenibacillus barcinonensis Esterase EstA for Kinetic Resolution of Tertiary Alcohols
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- Rational creation of mutant enzyme showing remarkable enhancement of catalytic activity and enantioselectivity toward poor substrates
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- Bacillus subtilisEsterase (BS2) and its Double Mutant Have Different Selectivity in the Removal of Carboxyl Protecting Groups
- (2009) Efrosini Barbayianni et al. ADVANCED SYNTHESIS & CATALYSIS
- Improvement ofYarrowia lipolyticaLipase Enantioselectivity by Using Mutagenesis Targeted to the Substrate Binding Site
- (2009) F. Bordes et al. CHEMBIOCHEM
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- (2009) Anna SchlieÃmann et al. CHEMBIOCHEM
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- (2009) Min-Can Wang et al. TETRAHEDRON-ASYMMETRY
- Biochemical properties and potential applications of an organic solvent-tolerant lipase isolated from Serratia marcescens ECU1010
- (2008) Li-Li Zhao et al. PROCESS BIOCHEMISTRY
- Evaluation of EnantiopureN-(Ferrocenylmethyl)azetidin-2-yl(diphenyl)methanol for Catalytic Asymmetric Addition of Organozinc Reagents to Aldehydes
- (2007) Min-Can Wang et al. JOURNAL OF ORGANIC CHEMISTRY
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