Literature DB >> 11282335

Biocatalytic modification of natural products.

S Riva1.   

Abstract

Natural products are ideal training compounds for enzymatic catalysis. New transformations have become possible on a preparative scale thanks to molecular biology, which has made many new enzymes available. Additionally, new synthetic pathways have been developed to regenerate expensive cofactors in situ and to improve enzyme selectivity.

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Year:  2001        PMID: 11282335     DOI: 10.1016/s1367-5931(00)00178-2

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


  5 in total

1.  An approach to the site-selective diversification of apoptolidin A with peptide-based catalysts.

Authors:  Chad A Lewis; Kate E Longcore; Scott J Miller; Paul A Wender
Journal:  J Nat Prod       Date:  2009-10       Impact factor: 4.050

2.  Specific 12 beta-hydroxylation of cinobufagin by filamentous fungi.

Authors:  Min Ye; Guiqin Qu; Hongzhu Guo; Dean Guo
Journal:  Appl Environ Microbiol       Date:  2004-06       Impact factor: 4.792

3.  Asymmetric catalysis at a distance: catalytic, site-selective phosphorylation of teicoplanin.

Authors:  Sunkyu Han; Scott J Miller
Journal:  J Am Chem Soc       Date:  2013-08-07       Impact factor: 15.419

Review 4.  The manzamines as an example of the unique structural classes available for the discovery and optimization of infectious disease controls based on marine natural products.

Authors:  Mark T Hamann
Journal:  Curr Pharm Des       Date:  2007       Impact factor: 3.116

5.  Influence of organic solvents on catalytic behaviors and cell morphology of whole-cell biocatalysts for synthesis of 5'-arabinocytosine laurate.

Authors:  Meiyan Yang; Hui Wu; Yan Lian; Xiaofeng Li; Furao Lai; Guanglei Zhao
Journal:  PLoS One       Date:  2014-08-19       Impact factor: 3.240

  5 in total

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