Literature DB >> 7737167

Specific inhibition of plant fatty acid elongation by a long-chain cerulenin analogue.

F Schneider1, C Cassagne.   

Abstract

Cerulenin analogues with 16 or 18 carbon atoms inhibit both ATP-dependent and acyl-CoA-dependent fatty acid elongations. Prior incubation of microsomes with inhibitors is necessary to obtain maximal inhibition. The analogues act on the first reaction of the elongation process catalysed by the 3-ketoacyl-CoA synthase. The 18-carbon analogue has no, or little, effect on the fatty acid synthesis, while cerulenin and its 16-carbon analogue totally inhibit this synthesis. The 18-carbon analogue appears to be a specific inhibitor of the synthesis of very long-chain fatty acids, with no effect on de novo fatty acid synthesis.

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Year:  1995        PMID: 7737167     DOI: 10.1111/j.1432-1033.1995.tb20313.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  2 in total

1.  A potent plant-derived antifungal acetylenic acid mediates its activity by interfering with fatty acid homeostasis.

Authors:  Tao Xu; Siddharth K Tripathi; Qin Feng; Michael C Lorenz; Marsha A Wright; Melissa R Jacob; Melanie M Mask; Scott R Baerson; Xing-Cong Li; Alice M Clark; Ameeta K Agarwal
Journal:  Antimicrob Agents Chemother       Date:  2012-03-19       Impact factor: 5.191

2.  Virus-induced silencing of Comt, pAmt and Kas genes results in a reduction of capsaicinoid accumulation in chili pepper fruits.

Authors:  Ma del Rosario Abraham-Juárez; Ma del Carmen Rocha-Granados; Mercedes G López; Rafael Francisco Rivera-Bustamante; Neftalí Ochoa-Alejo
Journal:  Planta       Date:  2007-11-13       Impact factor: 4.116

  2 in total

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