Schneider F, Cassagne C
Laboratoire de Biogenèse Membranaire, Centre National de la Recherche Scientifique, URA 1811, Université de Bordeaux 2, France.
Eur J Biochem. 1995 Mar 15;228(3):704-9. doi: 10.1111/j.1432-1033.1995.tb20313.x.
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.