Bossie M A, Martin C E
Bureau of Biological Research, Nelson Laboratories, Rutgers University, Piscataway, New Jersey 08855-1059.
J Bacteriol. 1989 Dec;171(12):6409-13. doi: 10.1128/jb.171.12.6409-6413.1989.
The addition of unsaturated fatty acids to cultures of Saccharomyces cerevisiae significantly altered the microsomal lipid composition. Supplementation with either of the naturally occurring palmitoleic (16:1) or oleic (18:1) acids caused increased levels in membrane phospholipids and reduced levels of the complementary acid. Growth in the presence of equimolar quantities of 16:1 and 18:1 acids, however, produced a fatty acid composition similar to that found in unsupplemented cell membranes. Linoleic acid (18:2) was not found in S. cerevisiae grown under normal conditions. It was preferentially internalized and incorporated into microsomes, however, at levels exceeding 50% of the total fatty acid species. This resulted in an almost total loss of 16:1 and a reduction of 18:1 to 25% of its normal level. The delta-9 fatty acid desaturase, a microsomal enzyme that forms 16:1 and 18:1 from saturated acyl coenzyme A precursors, was affected by the presence of exogenous fatty acids. Enzyme activity toward the 16:0 coenzyme A substrate was elevated in microsomes from saturated-fatty-acid-supplemented cultures and sharply repressed following the addition of unsaturated fatty acids, including 18:2. Northern (RNA blot) and slot-blot analyses of mRNA encoded by the OLE1 gene, which appears to be the structural gene for the delta-9 desaturase, indicated that it was sharply reduced in unsaturated-fatty-acid-fed cells. These data suggest that a significant part of the regulation involves modulation of available transcripts.
向酿酒酵母培养物中添加不饱和脂肪酸会显著改变微粒体脂质组成。补充天然存在的棕榈油酸(16:1)或油酸(18:1)中的任何一种都会导致膜磷脂水平升高,而互补酸的水平降低。然而,在等摩尔量的16:1和18:1酸存在下生长,产生的脂肪酸组成与未补充脂肪酸的细胞膜中的脂肪酸组成相似。在正常条件下生长的酿酒酵母中未发现亚油酸(18:2)。然而,它被优先内化并整合到微粒体中,其水平超过总脂肪酸种类的50%。这导致16:1几乎完全丧失,18:1降至其正常水平的25%。δ-9脂肪酸去饱和酶是一种微粒体酶,可从饱和酰基辅酶A前体形成16:1和18:1,它受外源脂肪酸的存在影响。在补充饱和脂肪酸的培养物的微粒体中,针对16:0辅酶A底物的酶活性升高,在添加包括18:2在内的不饱和脂肪酸后急剧受到抑制。对似乎是δ-9去饱和酶结构基因的OLE1基因编码的mRNA进行的Northern(RNA印迹)和狭缝印迹分析表明,在不饱和脂肪酸喂养的细胞中它急剧减少。这些数据表明,调节的很大一部分涉及对可用转录本的调控。