Silvius J R, McElhaney R N
Can J Biochem. 1978 Jun;56(6):462-9. doi: 10.1139/o78-072.
A variety of potential inhibitors of de novo fatty acid biosynthesis have been tested for activity in Acholeplasma laidlawii B. Two compounds, avidin and N,N-dimethyl-4-oxo-2trans-dodecenamide (CM-55), an antimicrobial fatty amide, strongly inhibit de novo biosynthesis without nonspecific toxic effects at moderate dosages. Avidin is the more potent inhibitor, abolishing de novo fatty acid synthesis and greatly reducing the chain elongation of exogenous fatty acids at level of 25 U/l. CM-55 gives complete inhibition of de novo biosynthesis only at low temperatures and inhibits exogenous fatty acid elongation to a variable extent. However, CM-55 is still a more potent antilipogenic agent in this organism than is the fungal antibiotic cerulenin. Cells cultured with avidin grow only when one or more exogenous medium- or long-chain fatty acids are added to the growth medium. The extent of cell growth under these conditions depends primarily on the physical properties of the exogenous fatty acid(s). In general, fatty acids giving diacylglycerolipids of very high or very low fluidity are unsuitable growth substrates, while those whose diacylglycerol derivatives are of intermediate fluidity support fair to good cell growth.
多种潜在的从头脂肪酸生物合成抑制剂已在莱氏无胆甾原体B中测试其活性。两种化合物,抗生物素蛋白和N,N-二甲基-4-氧代-2-反式-十二碳烯酰胺(CM-55),一种抗菌脂肪酰胺,在中等剂量下能强烈抑制从头生物合成且无非特异性毒性作用。抗生物素蛋白是更有效的抑制剂,在25 U/l的水平下可消除从头脂肪酸合成并极大地降低外源脂肪酸的链延长。CM-55仅在低温下能完全抑制从头生物合成,并在不同程度上抑制外源脂肪酸延长。然而,在这种生物体中,CM-55仍是比真菌抗生素浅蓝菌素更有效的抗脂肪生成剂。用抗生物素蛋白培养的细胞仅在向生长培养基中添加一种或多种外源中链或长链脂肪酸时才能生长。在这些条件下细胞生长的程度主要取决于外源脂肪酸的物理性质。一般来说,产生流动性非常高或非常低的二酰基甘油脂质的脂肪酸是不合适的生长底物,而其二酰基甘油衍生物具有中等流动性的那些脂肪酸能支持良好到较好的细胞生长。