首页> 外文期刊>Applied Microbiology and Biotechnology >Toxicity of ricinoleic acid production in fission yeast Schizosaccharomyces pombe is suppressed by the overexpression of plg7, a phospholipase A2 of a platelet-activating factor (PAF) family homolog
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Toxicity of ricinoleic acid production in fission yeast Schizosaccharomyces pombe is suppressed by the overexpression of plg7, a phospholipase A2 of a platelet-activating factor (PAF) family homolog

机译:裂殖酵母粟酒裂殖酵母中蓖麻油酸生产的毒性被血小板活化因子(PAF)家族同源物plg7(磷脂酶A2)的过表达所抑制。

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摘要

In an effort to produce ricinoleic acid (RA), an important natural raw material with great values as a petrochemical replacement, in Schizosaccharomyces pombe, we introduced Claviceps purpurea oleate Δ12-hydroxylase gene (CpFAH12) to S. pombe, putting it under the control of an inducible nmt1 promoter. However, RA was toxic to S. pombe and the cells expressing CpFAH12 grew poorly at the normal growth temperature 30 C. To address its toxic mechanism in S. pombe, we screened for a S. pombe cDNA library and identified plg7, which encodes a phospholipase A2, as a suppressor that restored the growth defect without affecting the RA production. A lacZ fusion experiment showed that the expression of plg7 was inducible by RA. Thin layer chromatographic analysis confirmed a reduction in RA moiety in phospholipids and a concomitant increase in free RA in the plg7 overexpressed strain. Since RA is synthesized at the sn-2 position of phosphatidylcholine by Fah12p, and phospholipase A2 hydrolyzes the sn-2 acyl bond of phospholipids, we speculate that plg7 is a stress-responsive gene, and removal of RA moieties from phospholipids, major components of lipid bilayer membrane, by Plg7p would be its suppression mechanism.
机译:为了生产蓖麻油酸(RA)(石化替代品具有重要价值的重要天然原料),在粟酒裂殖酵母中,我们将粟酒裂殖酵母油酸酯Δ12-羟化酶基因(CpFAH12)引入了粟酒裂殖酵母,使其受到控制nmt1启动子的序列。但是,RA对粟酒裂殖酵母有毒性,表达CpFAH12的细胞在正常生长温度30℃下生长较差。为了解决其在粟酒裂殖酵母中的毒性机制,我们筛选了粟酒裂殖酵母cDNA文库并鉴定了plg7,该质粒编码磷脂酶A2,作为抑制生长缺陷而不抑制RA产生的抑制剂。 lacZ融合实验显示RA可诱导plg7的表达。薄层色谱分析证实,磷脂中RA部分的减少和plg7过表达菌株中游离RA的同时增加。由于RA通过Fah12p在磷脂酰胆碱的sn-2位置合成,并且磷脂酶A2水解磷脂的sn-2酰基键,因此我们推测plg7是应激反应基因,并且从磷脂的RA部分中去除了RA部分(磷脂的主要成分)脂质双层膜,被Plg7p抑制是其机制。

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