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磷脂:二酰基甘油酰基转移酶的双重作用:增强脂肪酸合成并将拟南芥叶片中的脂肪酸从膜脂转移至三酰甘油

Dual role for phospholipid:diacylglycerol acyltransferase: enhancing fatty acid synthesis and diverting fatty acids from membrane lipids to triacylglycerol in Arabidopsis leaves.

作者信息

Fan Jilian, Yan Chengshi, Zhang Xuebin, Xu Changcheng

机构信息

Biosciences Department, Brookhaven National Laboratory, Upton, New York 11973.

出版信息

Plant Cell. 2013 Sep;25(9):3506-18. doi: 10.1105/tpc.113.117358. Epub 2013 Sep 27.

Abstract

There is growing interest in engineering green biomass to expand the production of plant oils as feed and biofuels. Here, we show that phospholipid:diacylglycerol acyltransferase1 (PDAT1) is a critical enzyme involved in triacylglycerol (TAG) synthesis in leaves. Overexpression of PDAT1 increases leaf TAG accumulation, leading to oil droplet overexpansion through fusion. Ectopic expression of oleosin promotes the clustering of small oil droplets. Coexpression of PDAT1 with oleosin boosts leaf TAG content by up to 6.4% of the dry weight without affecting membrane lipid composition and plant growth. PDAT1 overexpression stimulates fatty acid synthesis (FAS) and increases fatty acid flux toward the prokaryotic glycerolipid pathway. In the trigalactosyldiacylglycerol1-1 mutant, which is defective in eukaryotic thylakoid lipid synthesis, the combined overexpression of PDAT1 with oleosin increases leaf TAG content to 8.6% of the dry weight and total leaf lipid by fourfold. In the plastidic glycerol-3-phosphate acyltransferase1 mutant, which is defective in the prokaryotic glycerolipid pathway, PDAT1 overexpression enhances TAG content at the expense of thylakoid membrane lipids, leading to defects in chloroplast division and thylakoid biogenesis. Collectively, these results reveal a dual role for PDAT1 in enhancing fatty acid and TAG synthesis in leaves and suggest that increasing FAS is the key to engineering high levels of TAG accumulation in green biomass.

摘要

通过工程改造绿色生物质以扩大作为饲料和生物燃料的植物油产量,这一领域正引发越来越多的关注。在此,我们表明磷脂:二酰基甘油酰基转移酶1(PDAT1)是叶片中三酰甘油(TAG)合成所涉及的一种关键酶。PDAT1的过表达增加了叶片TAG的积累,通过融合导致油滴过度膨胀。油质蛋白的异位表达促进了小油滴的聚集。PDAT1与油质蛋白共表达可使叶片TAG含量提高至干重的6.4%,且不影响膜脂组成和植物生长。PDAT1过表达刺激脂肪酸合成(FAS),并增加脂肪酸向原核甘油脂途径的通量。在真核类囊体脂质合成存在缺陷的三半乳糖二酰基甘油1-1突变体中,PDAT1与油质蛋白的联合过表达使叶片TAG含量提高至干重的8.6%,总叶片脂质增加了四倍。在原核甘油脂途径存在缺陷的质体甘油-3-磷酸酰基转移酶1突变体中,PDAT1过表达以类囊体膜脂为代价提高了TAG含量,导致叶绿体分裂和类囊体生物发生出现缺陷。总体而言,这些结果揭示了PDAT1在增强叶片脂肪酸和TAG合成中的双重作用,并表明增加FAS是在绿色生物质中工程化高水平TAG积累的关键。

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