Huang Y S, Chaudhary S, Thurmond J M, Bobik E G, Yuan L, Chan G M, Kirchner S J, Mukerji P, Knutzon D S
Ross Products Division, Abbott Laboratories, Columbus, Ohio 43215, USA.
Lipids. 1999 Jul;34(7):649-59. doi: 10.1007/s11745-999-0410-8.
Two cDNA clones with homology to known desaturase genes were isolated from the fungus Mortierella alpina. The open reading frame in one clone encoded 399 amino acids and exhibited delta12-desaturase activity when expressed in Saccharomyces cerevisiae in the presence of endogenous fatty acid substrate oleic acid. The insert in another clone contained an open reading frame encoding 457 amino acids and exhibited delta6-desaturase activity in S. cerevisiae in the presence of exogenous fatty acid substrate linoleic acid. Expression of the delta12-desaturase gene under appropriate media and temperature conditions led to the production of linoleic acid at levels up to 25% of the total fatty acids in yeast. When linoleic acid was provided as an exogenous substrate to the yeast cultures expressing the delta6-desaturase activity, the level of gamma-linolenic acid reached 10% of the total yeast fatty acids. Co-expression of both the delta6- and delta12-desaturase cDNA resulted in the endogenous production of gamma-linolenic acid. The yields of gamma-linolenic acid reached as high as 8% of total fatty acids in yeast.
从高山被孢霉中分离出两个与已知去饱和酶基因具有同源性的cDNA克隆。一个克隆中的开放阅读框编码399个氨基酸,当在酿酒酵母中表达且存在内源性脂肪酸底物油酸时,表现出Δ12-去饱和酶活性。另一个克隆中的插入片段包含一个编码457个氨基酸的开放阅读框,在酿酒酵母中存在外源性脂肪酸底物亚油酸时表现出Δ6-去饱和酶活性。在合适的培养基和温度条件下,Δ12-去饱和酶基因的表达导致酵母中亚油酸的产量高达总脂肪酸的25%。当向表达Δ6-去饱和酶活性的酵母培养物提供亚油酸作为外源性底物时,γ-亚麻酸的水平达到酵母总脂肪酸的10%。Δ6-和Δ12-去饱和酶cDNA的共表达导致酵母内源性产生γ-亚麻酸。γ-亚麻酸的产量高达酵母总脂肪酸的8%。