Intragenomic enzyme complements

Research output: Contribution to journalLiterature reviewpeer-review

Abstract

Researchers in applied biocatalysis are now reaping the rewards of intensive effort and technological developments in the sequencing of the genomes of microbial and plant species The genomic resource contains the sequences of millions of new genes with potential application in industrial biotechnology and includes families of enzymes within discrete genomes that potentially catalyze equivalent chemical reactions One of the key emerging characteristics of these intragenomic complements of enzymes is the impressive breadth of catalytic diversity that is observed within them This diversity may have been acquired either in order to combat the spectrum of metabolic challenges with which the organism may be presented in its natural environment or as part of the biosynthetic machinery evolved to produce a spectrum of secondary metabolites that will prove to be advantageous in establishing a niche Attempts have been made to functionally characterize the intragenomic complements of enzyme families catalyzing diverse reactions including carbonyl reduction ester hydrolysis and Baeyer-Villiger oxidation in Gram-positive bacteria, yeasts, filamentous fungi and the plant Arabidopsis thaliana These studies are beginning to describe in detail for the first time the impressive range of catalytic potential within single organisms for attributes such as substrate range enantioselectivity or thermostabtlity each of which is of interest from an enzyme discovery perspective (c) 2010 Elsevier B V All rights reserved

Original languageEnglish
Pages (from-to)22-29
Number of pages8
JournalJournal of Molecular Catalysis B : Enzymatic
Volume68
Issue number1
DOIs
Publication statusPublished - Jan 2011

Keywords

  • Biocatalysis
  • Enzyme discovery
  • Genomics
  • High-throughput
  • Oxidoreductase
  • COMPLETE GENOME SEQUENCE
  • BAEYER-VILLIGER MONOOXYGENASE
  • BACTERIUM RHODOPSEUDOMONAS-PALUSTRIS
  • STREPTOMYCES-COELICOLOR A3(2)
  • MYCOBACTERIUM-TUBERCULOSIS
  • ARABIDOPSIS-THALIANA
  • CYTOCHROME-P450 COMPLEMENT
  • KETOREDUCTASE DOMAINS
  • ASPERGILLUS-NIDULANS
  • MICROBIAL ESTERASES

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