Literature DB >> 11849937

Microbial epoxide hydrolases for preparative biotransformations.

A Steinreiber1, K Faber.   

Abstract

Epoxide hydrolases from microbial sources are highly versatile biocatalysts for the asymmetric hydrolysis of epoxides on a preparative scale. Besides kinetic resolution, which furnishes the corresponding vicinal diol and remaining non-hydrolysed epoxide in nonracemic form, enantioconvergent processes are possible: these are highly attractive as they lead to the formation of a single enantiomeric diol from a racemic oxirane. The data accumulated over recent years reveal a common picture of the substrate structure selectivity pattern of microbial epoxide hydrolases and indicate that substrates of various structural types can be selectively hydrolysed with enzymes from certain microbial sources.

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Year:  2001        PMID: 11849937     DOI: 10.1016/s0958-1669(01)00262-2

Source DB:  PubMed          Journal:  Curr Opin Biotechnol        ISSN: 0958-1669            Impact factor:   9.740


  21 in total

1.  High yield recombinant expression, characterization and homology modeling of two types of cis-epoxysuccinic acid hydrolases.

Authors:  Gu-Zhen Cui; Shan Wang; Yifei Li; Yi-Jun Tian; Yingang Feng; Qiu Cui
Journal:  Protein J       Date:  2012-06       Impact factor: 2.371

2.  Nitropyrrolins A-E, cytotoxic farnesyl-α-nitropyrroles from a marine-derived bacterium within the actinomycete family Streptomycetaceae.

Authors:  Hak Cheol Kwon; Ana Paula D M Espindola; Jin-Soo Park; Alejandra Prieto-Davó; Mickea Rose; Paul R Jensen; William Fenical
Journal:  J Nat Prod       Date:  2010-11-23       Impact factor: 4.050

3.  Effect of ionic liquids on epoxide hydrolase-catalyzed synthesis of chiral 1,2-diols.

Authors:  Cinzia Chiappe; Elsa Leandri; Bruce D Hammock; Christophe Morisseau
Journal:  Green Chem       Date:  2007       Impact factor: 10.182

4.  Removal of distal protein-water hydrogen bonds in a plant epoxide hydrolase increases catalytic turnover but decreases thermostability.

Authors:  Ann Thomaeus; Agata Naworyta; Sherry L Mowbray; Mikael Widersten
Journal:  Protein Sci       Date:  2008-05-30       Impact factor: 6.725

5.  Visualizing the Mechanism of Epoxide Hydrolysis by the Bacterial Virulence Enzyme Cif.

Authors:  Christopher D Bahl; Kelli L Hvorecny; Christophe Morisseau; Scott A Gerber; Dean R Madden
Journal:  Biochemistry       Date:  2016-01-22       Impact factor: 3.162

6.  Protein engineering of epoxide hydrolase from Agrobacterium radiobacter AD1 for enhanced activity and enantioselective production of (R)-1-phenylethane-1,2-diol.

Authors:  Lingyun Rui; Li Cao; Wilfred Chen; Kenneth F Reardon; Thomas K Wood
Journal:  Appl Environ Microbiol       Date:  2005-07       Impact factor: 4.792

7.  A broadly applicable and practical oligomeric (salen) Co catalyst for enantioselective epoxide ring-opening reactions.

Authors:  David E White; Pamela M Tadross; Zhe Lu; Eric N Jacobsen
Journal:  Tetrahedron       Date:  2014-07-08       Impact factor: 2.457

8.  Production of epoxide hydrolases in batch fermentations of Botryosphaeria rhodina.

Authors:  Guido Melzer; Stefan Junne; Roland Wohlgemuth; Dietmar C Hempel; Peter Götz
Journal:  J Ind Microbiol Biotechnol       Date:  2008-01-22       Impact factor: 3.346

9.  Characterization of the SgcF epoxide hydrolase supporting an (R)-vicinal diol intermediate for enediyne antitumor antibiotic C-1027 biosynthesis.

Authors:  Shuangjun Lin; Geoffrey P Horsman; Yihua Chen; Wenli Li; Ben Shen
Journal:  J Am Chem Soc       Date:  2009-11-18       Impact factor: 15.419

10.  Farnesides A and B, sesquiterpenoid nucleoside ethers from a marine-derived Streptomyces sp., strain CNT-372 from Fiji.

Authors:  Ella Zafrir Ilan; Manuel R Torres; Jacques Prudhomme; Karine Le Roch; Paul R Jensen; William Fenical
Journal:  J Nat Prod       Date:  2013-08-29       Impact factor: 4.050

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