Literature DB >> 17518430

Revealing coupling patterns in isoprenoid alkylation biocatalysis.

Christopher T Walsh1.   

Abstract

Diversity of scaffold structure and function is a hallmark of the >50,000 isoprenoid natural products such as taxol. Whereas most members of this class are assembled by iterative head-to-tail enzymatic joining reactions between delta2- and delta3-isopentenyl diphosphate (IPP) monomers, dimerization of two delta2-IPP molecules has now been shown to account for three additional modes of "irregular" coupling patterns at the level of C10 monoterpene scaffolds.

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Year:  2007        PMID: 17518430     DOI: 10.1021/cb700094s

Source DB:  PubMed          Journal:  ACS Chem Biol        ISSN: 1554-8929            Impact factor:   5.100


  4 in total

1.  The biosynthetic origin of irregular monoterpenes in Lavandula: isolation and biochemical characterization of a novel cis-prenyl diphosphate synthase gene, lavandulyl diphosphate synthase.

Authors:  Zerihun A Demissie; Lauren A E Erland; Mark R Rheault; Soheil S Mahmoud
Journal:  J Biol Chem       Date:  2013-01-10       Impact factor: 5.157

2.  Molecular analysis of a 4-dimethylallyltryptophan synthase from Malbranchea aurantiaca.

Authors:  Yousong Ding; Robert M Williams; David H Sherman
Journal:  J Biol Chem       Date:  2008-04-04       Impact factor: 5.157

Review 3.  Microbial-based motor fuels: science and technology.

Authors:  Lawrence P Wackett
Journal:  Microb Biotechnol       Date:  2008-05       Impact factor: 5.813

4.  Synthetic Routes to Methylerythritol Phosphate Pathway Intermediates and Downstream Isoprenoids.

Authors:  Sarah K Jarchow-Choy; Andrew T Koppisch; David T Fox
Journal:  Curr Org Chem       Date:  2014-04       Impact factor: 2.180

  4 in total

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