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PUBMED FOR HANDHELDS

Journal Abstract Search


190 related items for PubMed ID: 22113019

  • 1. Biochemical characterisation of a NADPH-dependent carbonyl reductase from Neurospora crassa reducing α- and β-keto esters.
    Richter N, Hummel W.
    Enzyme Microb Technol; 2011 May 06; 48(6-7):472-9. PubMed ID: 22113019
    [Abstract] [Full Text] [Related]

  • 2. Highly stereoselective reduction of prochiral ketones by a bacterial reductase coupled with cofactor regeneration.
    Ni Y, Li CX, Wang LJ, Zhang J, Xu JH.
    Org Biomol Chem; 2011 Aug 07; 9(15):5463-8. PubMed ID: 21670841
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  • 3. Biocatalytic properties of a recombinant aldo-keto reductase with broad substrate spectrum and excellent stereoselectivity.
    Ni Y, Li CX, Ma HM, Zhang J, Xu JH.
    Appl Microbiol Biotechnol; 2011 Feb 07; 89(4):1111-8. PubMed ID: 20981419
    [Abstract] [Full Text] [Related]

  • 4. A novel carbonyl reductase from Pichia stipitis for the production of ethyl (S)-4-chloro-3-hydroxybutanoate.
    Ye Q, Yan M, Xu L, Cao H, Li Z, Chen Y, Li S, Ying H.
    Biotechnol Lett; 2009 Apr 07; 31(4):537-42. PubMed ID: 19125224
    [Abstract] [Full Text] [Related]

  • 5. Purification and characterization of NADPH-dependent aldo-keto reductase specific for beta-keto esters from Penicillium citrinum, and production of methyl (S)-4-bromo-3-hydroxybutyrate.
    Itoh N, Asako H, Banno K, Makino Y, Shinohara M, Dairi T, Wakita R, Shimizu M.
    Appl Microbiol Biotechnol; 2004 Nov 07; 66(1):53-62. PubMed ID: 15338078
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  • 6. Molecular cloning and overexpression of the gene encoding an NADPH-dependent carbonyl reductase from Candida magnoliae, involved in stereoselective reduction of ethyl 4-chloro-3-oxobutanoate.
    Yasohara Y, Kizaki N, Hasegawa J, Wada M, Kataoka M, Shimizu S.
    Biosci Biotechnol Biochem; 2000 Jul 07; 64(7):1430-6. PubMed ID: 10945260
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  • 7. Systematic investigation of Saccharomyces cerevisiae enzymes catalyzing carbonyl reductions.
    Kaluzna IA, Matsuda T, Sewell AK, Stewart JD.
    J Am Chem Soc; 2004 Oct 13; 126(40):12827-32. PubMed ID: 15469278
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  • 8. Stereoselective ketone reduction by a carbonyl reductase from Sporobolomyces salmonicolor. Substrate specificity, enantioselectivity and enzyme-substrate docking studies.
    Zhu D, Yang Y, Buynak JD, Hua L.
    Org Biomol Chem; 2006 Jul 21; 4(14):2690-5. PubMed ID: 16826293
    [Abstract] [Full Text] [Related]

  • 9. Stereoselective, biocatalytic reductions of alpha-chloro-beta-keto esters.
    Kaluzna IA, Feske BD, Wittayanan W, Ghiviriga I, Stewart JD.
    J Org Chem; 2005 Jan 07; 70(1):342-5. PubMed ID: 15624945
    [Abstract] [Full Text] [Related]

  • 10. [Biochemical characterization and substrate profile of a highly enantioselective carbonyl reductase from Pichia pastoris].
    Tian L, Liu W, Chen X, Feng J, Yang H, Wu Q, Zhu D, Ma Y.
    Sheng Wu Gong Cheng Xue Bao; 2013 Feb 07; 29(2):169-79. PubMed ID: 23697162
    [Abstract] [Full Text] [Related]

  • 11. 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 Feb 07; 76(6):1210-2. PubMed ID: 22790948
    [Abstract] [Full Text] [Related]

  • 12. Purification and characterization of a novel NADH-dependent carbonyl reductase from Pichia stipitis involved in biosynthesis of optically pure ethyl (S)-4-chloro-3-hydroxybutanoate.
    Cao H, Mi L, Ye Q, Zang G, Yan M, Wang Y, Zhang Y, Li X, Xu L, Xiong J, Ouyang P, Ying H.
    Bioresour Technol; 2011 Jan 07; 102(2):1733-9. PubMed ID: 20933386
    [Abstract] [Full Text] [Related]

  • 13. Construction of a two-strain system for asymmetric reduction of ethyl 4-chloro-3-oxobutanoate to (S)-4-chloro-3-hydroxybutanoate ethyl ester.
    Xu Z, Liu Y, Fang L, Jiang X, Jing K, Cen P.
    Appl Microbiol Biotechnol; 2006 Mar 07; 70(1):40-6. PubMed ID: 16175366
    [Abstract] [Full Text] [Related]

  • 14. Rabbit 3-hydroxyhexobarbital dehydrogenase is a NADPH-preferring reductase with broad substrate specificity for ketosteroids, prostaglandin D₂, and other endogenous and xenobiotic carbonyl compounds.
    Endo S, Matsunaga T, Matsumoto A, Arai Y, Ohno S, El-Kabbani O, Tajima K, Bunai Y, Yamano S, Hara A, Kitade Y.
    Biochem Pharmacol; 2013 Nov 01; 86(9):1366-75. PubMed ID: 23994167
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