119 related articles for article (PubMed ID: 23770562)
1. Development of a bioconversion system using Saccharomyces cerevisiae Reductase YOR120W and Bacillus subtilis glucose dehydrogenase for chiral alcohol synthesis.
Yoon SA; Kim HK
J Microbiol Biotechnol; 2013 Oct; 23(10):1395-402. PubMed ID: 23770562
[TBL] [Abstract][Full Text] [Related]
2. Asymmetric synthesis of (S)-ethyl-4-chloro-3-hydroxy butanoate using a Saccharomyces cerevisiae reductase: enantioselectivity and enzyme-substrate docking studies.
Jung J; Park HJ; Uhm KN; Kim D; Kim HK
Biochim Biophys Acta; 2010 Sep; 1804(9):1841-9. PubMed ID: 20601218
[TBL] [Abstract][Full Text] [Related]
3. Enantioselective bioconversion using Escherichia coli cells expressing Saccharomyces cerevisiae reductase and Bacillus subtilis glucose dehydrogenase.
Park HJ; Jung J; Choi H; Uhm KN; Kim HK
J Microbiol Biotechnol; 2010 Sep; 20(9):1300-6. PubMed ID: 20890095
[TBL] [Abstract][Full Text] [Related]
4. Production of (R)-Ethyl-4-Chloro-3-Hydroxybutanoate Using Saccharomyces cerevisiae YOL151W Reductase Immobilized onto Magnetic Microparticles.
Choo JW; Kim HK
J Microbiol Biotechnol; 2015 Nov; 25(11):1810-8. PubMed ID: 26239012
[TBL] [Abstract][Full Text] [Related]
5. Development of Saccharomyces cerevisiae reductase YOL151W mutants suitable for chiral alcohol synthesis using an NADH cofactor regeneration system.
Yoon SA; Jung J; Park S; Kim HK
J Microbiol Biotechnol; 2013 Feb; 23(2):218-24. PubMed ID: 23412065
[TBL] [Abstract][Full Text] [Related]
6. Development of a substrate-coupled biocatalytic process driven by an NADPH-dependent sorbose reductase from Candida albicans for the asymmetric reduction of ethyl 4-chloro-3-oxobutanoate.
Cai P; An M; Xu L; Xu S; Hao N; Li Y; Guo K; Yan M
Biotechnol Lett; 2012 Dec; 34(12):2223-7. PubMed ID: 22918792
[TBL] [Abstract][Full Text] [Related]
7. Characterization and site-directed mutation of a novel aldo-keto reductase from Lodderomyces elongisporus NRRL YB-4239 with high production rate of ethyl (R)-4-chloro-3-hydroxybutanoate.
Wang Q; Ye T; Ma Z; Chen R; Xie T; Yin X
J Ind Microbiol Biotechnol; 2014 Nov; 41(11):1609-16. PubMed ID: 25189809
[TBL] [Abstract][Full Text] [Related]
8. Asymmetric synthesis of (S)-3-chloro-1-phenyl-1-propanol using Saccharomyces cerevisiae reductase with high enantioselectivity.
Choi YH; Choi HJ; Kim D; Uhm KN; Kim HK
Appl Microbiol Biotechnol; 2010 Jun; 87(1):185-93. PubMed ID: 20111861
[TBL] [Abstract][Full Text] [Related]
9. A novel NADH-dependent carbonyl reductase from Kluyveromyces aestuarii and comparison of NADH-regeneration system for the synthesis of ethyl (S)-4-chloro-3-hydroxybutanoate.
Yamamoto H; Mitsuhashi K; Kimoto N; Matsuyama A; Esaki N; Kobayashi Y
Biosci Biotechnol Biochem; 2004 Mar; 68(3):638-49. PubMed ID: 15056898
[TBL] [Abstract][Full Text] [Related]
10. Asymmetric synthesis of (S)-4-chloro-3-hydroxybutanoate by sorbose reductase from Candida albicans with two co-existing recombinant Escherichia coli strains.
Cai P; An M; Xu S; Yan M; Hao N; Li Y; Xu L
Biosci Biotechnol Biochem; 2015; 79(7):1090-3. PubMed ID: 25765951
[TBL] [Abstract][Full Text] [Related]
11. Bioreduction with efficient recycling of NADPH by coupled permeabilized microorganisms.
Zhang W; O'Connor K; Wang DI; Li Z
Appl Environ Microbiol; 2009 Feb; 75(3):687-94. PubMed ID: 19047388
[TBL] [Abstract][Full Text] [Related]
12. Synthesis of optically pure ethyl (S)-4-chloro-3-hydroxybutanoate by Escherichia coli transformant cells coexpressing the carbonyl reductase and glucose dehydrogenase genes.
Kizaki N; Yasohara Y; Hasegawa J; Wada M; Kataoka M; Shimizu S
Appl Microbiol Biotechnol; 2001 May; 55(5):590-5. PubMed ID: 11414326
[TBL] [Abstract][Full Text] [Related]
13. A novel reductase from Candida albicans for the production of ethyl (S)-4-chloro-3-hydroxybutanoate.
An M; Cai P; Yan M; Hao N; Wang S; Liu H; Li Y; Xu L
Biosci Biotechnol Biochem; 2012; 76(6):1210-2. PubMed ID: 22790948
[TBL] [Abstract][Full Text] [Related]
14. Improved NADPH Regeneration for Fungal Cytochrome P450 Monooxygenase by Co-Expressing Bacterial Glucose Dehydrogenase in Resting-Cell Biotransformation of Recombinant Yeast.
Jeon H; Durairaj P; Lee D; Ahsan MM; Yun H
J Microbiol Biotechnol; 2016 Dec; 26(12):2076-2086. PubMed ID: 27666994
[TBL] [Abstract][Full Text] [Related]
15. Engineering cofactor preference of ketone reducing biocatalysts: A mutagenesis study on a γ-diketone reductase from the yeast Saccharomyces cerevisiae serving as an example.
Katzberg M; Skorupa-Parachin N; Gorwa-Grauslund MF; Bertau M
Int J Mol Sci; 2010 Apr; 11(4):1735-58. PubMed ID: 20480039
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of ethyl ( S)-4-chloro-3-hydroxybutanoate using fabG-homologues.
Yamamoto H; Matsuyama A; Kobayashi Y
Appl Microbiol Biotechnol; 2003 Apr; 61(2):133-9. PubMed ID: 12655455
[TBL] [Abstract][Full Text] [Related]
17. Bioconversion of ethyl 4-chloro-3-oxobutanoate by permeabilized fresh brewer's yeast cells in the presence of allyl bromide.
Yu MA; Wei YM; Zhao L; Jiang L; Zhu XB; Qi W
J Ind Microbiol Biotechnol; 2007 Feb; 34(2):151-6. PubMed ID: 17043805
[TBL] [Abstract][Full Text] [Related]
18. Purification and properties of a carbonyl reductase useful for production of ethyl (S)-4-chloro-3-hydroxybutanoate from Kluyveromyces lactis.
Yamamoto H; Kimoto N; Matsuyama A; Kobayashi Y
Biosci Biotechnol Biochem; 2002 Aug; 66(8):1775-8. PubMed ID: 12353647
[TBL] [Abstract][Full Text] [Related]
19. Cloning, overexpression, and mutagenesis of the Sporobolomyces salmonicolor AKU4429 gene encoding a new aldehyde reductase, which catalyzes the stereoselective reduction of ethyl 4-chloro-3-oxobutanoate to ethyl (S)-4-chloro-3-hydroxybutanoate.
Kita K; Fukura T; Nakase KI; Okamoto K; Yanase H; Kataoka M; Shimizu S
Appl Environ Microbiol; 1999 Dec; 65(12):5207-11. PubMed ID: 10583966
[TBL] [Abstract][Full Text] [Related]
20. Upscale production of ethyl (S)-4-chloro-3-hydroxybutanoate by using carbonyl reductase coupled with glucose dehydrogenase in aqueous-organic solvent system.
Liu ZQ; Ye JJ; Shen ZY; Hong HB; Yan JB; Lin Y; Chen ZX; Zheng YG; Shen YC
Appl Microbiol Biotechnol; 2015 Mar; 99(5):2119-29. PubMed ID: 25487888
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
