Literature DB >> 15811804

Advances in biocatalytic synthesis of pharmaceutical intermediates.

Sven Panke1, Marcel Wubbolts.   

Abstract

Biocatalytic synthesis of enantiomerically pure compounds for pharmaceutical intermediates is gaining momentum. This is the result of advances in genomics, screening and evolution technologies leading to the increased availability of new and robust biocatalysts suited for industrial-scale application, and is stimulated by an increased demand for catalysts that are able to address the increased complexity of active pharmaceutical ingredients. The vast majority of biotransformation reactions for the manufacturing of optically active pharmaceutical intermediates are still based on enantioselective ketone reductions and enantiospecific hydrolyses. This review aims to point at alternative reaction types and integrated multi-enzymatic steps that are emerging in large-scale applications.

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Year:  2005        PMID: 15811804     DOI: 10.1016/j.cbpa.2005.02.007

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  21 in total

Review 1.  Engineering the third wave of biocatalysis.

Authors:  U T Bornscheuer; G W Huisman; R J Kazlauskas; S Lutz; J C Moore; K Robins
Journal:  Nature       Date:  2012-05-09       Impact factor: 49.962

2.  Whole cell biotransformation for reductive amination reactions.

Authors:  Stephanie Klatte; Elisabeth Lorenz; Volker F Wendisch
Journal:  Bioengineered       Date:  2013-12-05       Impact factor: 3.269

3.  Metabolic Engineering of Raoultella ornithinolytica BF60 for Production of 2,5-Furandicarboxylic Acid from 5-Hydroxymethylfurfural.

Authors:  Gazi Sakir Hossain; Haibo Yuan; Jianghua Li; Hyun-Dong Shin; Miao Wang; Guocheng Du; Jian Chen; Long Liu
Journal:  Appl Environ Microbiol       Date:  2016-12-15       Impact factor: 4.792

4.  Didymosphaeria igniaria: a new microorganism useful for the enantioselective reduction of aryl-aliphatic ketones.

Authors:  Alina Świzdor; Tomasz Janeczko; Jadwiga Dmochowska-Gładysz
Journal:  J Ind Microbiol Biotechnol       Date:  2010-06-11       Impact factor: 3.346

5.  Engineering methylaspartate ammonia lyase for the asymmetric synthesis of unnatural amino acids.

Authors:  Hans Raj; Wiktor Szymański; Jandré de Villiers; Henriëtte J Rozeboom; Vinod Puthan Veetil; Carlos R Reis; Marianne de Villiers; Frank J Dekker; Stefaan de Wildeman; Wim J Quax; Andy-Mark W H Thunnissen; Ben L Feringa; Dick B Janssen; Gerrit J Poelarends
Journal:  Nat Chem       Date:  2012-04-29       Impact factor: 24.427

6.  How a single-point mutation in horseradish peroxidase markedly enhances enantioselectivity.

Authors:  Eugene Antipov; Art E Cho; Alexander M Klibanov
Journal:  J Am Chem Soc       Date:  2009-08-12       Impact factor: 15.419

7.  Protein engineering of toluene monooxygenases for synthesis of chiral sulfoxides.

Authors:  Roi Feingersch; Janna Shainsky; Thomas K Wood; Ayelet Fishman
Journal:  Appl Environ Microbiol       Date:  2008-01-11       Impact factor: 4.792

8.  Engineering yield and rate of reductive biotransformation in Escherichia coli by partial cyclization of the pentose phosphate pathway and PTS-independent glucose transport.

Authors:  Solvej Siedler; Stephanie Bringer; Lars M Blank; Michael Bott
Journal:  Appl Microbiol Biotechnol       Date:  2011-10-16       Impact factor: 4.813

9.  Reductive whole-cell biotransformation with Corynebacterium glutamicum: improvement of NADPH generation from glucose by a cyclized pentose phosphate pathway using pfkA and gapA deletion mutants.

Authors:  Solvej Siedler; Steffen N Lindner; Stephanie Bringer; Volker F Wendisch; Michael Bott
Journal:  Appl Microbiol Biotechnol       Date:  2012-08-01       Impact factor: 4.813

10.  A highly productive, whole-cell DERA chemoenzymatic process for production of key lactonized side-chain intermediates in statin synthesis.

Authors:  Matej Ošlaj; Jérôme Cluzeau; Damir Orkić; Gregor Kopitar; Peter Mrak; Zdenko Casar
Journal:  PLoS One       Date:  2013-05-07       Impact factor: 3.240

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