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. Author manuscript; available in PMC: 2010 Feb 10.
Published in final edited form as: Cell Mol Life Sci. 2009 Jan 21;66(9):1507–1517. doi: 10.1007/s00018-009-8704-7

Diversity in enoyl-acyl carrier protein reductases

R P Massengo-Tiassé 1, J E Cronan 1,2,
PMCID: PMC2819910  NIHMSID: NIHMS110635  PMID: 19151923

Abstract.

The enoyl-acyl carrier protein reductase (ENR) is the last enzyme in the fatty acid elongation cycle. Unlike most enzymes in this essential pathway, ENR displays an unusual diversity among organisms. The growing interest in ENRs is mainly due to the fact that a variety of both synthetic and natural antibacterial compounds are shown to specifically target their activity. The primary anti-tuberculosis drug, isoniazid, and the broadly used antibacterial compound, triclosan, both target this enzyme. In this review, we discuss the diversity of ENRs, and their inhibitors in the light of current research progress.

Keywords. Enoyl-acyl carrier protein reductase, fatty acid biosynthesis, Fatty acid synthesis II, triclosan, shortchain dehydrogenase reductase, medium-chain dehydrogenase reductase

Footnotes

Received 3 November 2008; received after revision 5 December 2008; accepted 8 December 2008


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