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产油酵母弯假丝酵母D中的三酰甘油合成

Triacylglycerol synthesis in the oleaginous yeast Candida curvata D.

作者信息

Holdsworth J E, Ratledge C

机构信息

Department of Applied Biology, University of Hull, United Kingdom.

出版信息

Lipids. 1991 Feb;26(2):111-8. doi: 10.1007/BF02544004.

DOI:10.1007/BF02544004
PMID:2051892
Abstract

Low rates of triacylglycerol (TAG) biosynthesis were observed in cell-free extracts of Candida curvata, but rates were increased up to 10-fold by adding either alpha- or beta-cyclodextrins. Spheroplasts, whole or gently disrupted, had higher rates of incorporation of both [U-14C]glycerol 3-phosphate or [1-14C]oleate into triacylglycerol and the intermediates of its biosynthesis: lysophosphatic acid, phosphatidic acid and diacylglycerol. Fatty acyl-CoA synthetase was highest with palmitate, oleate and linoleate but was some 6- to 8-fold lower with stearate. Stearate and stearoyl-CoA were poorly incorporated into lipids. Subcellular fractionation of the spheroplasts into mitochondrial, microsomal, lipid bodies and supernatant fractions diminished the rates of 14C incorporation of oleate into triacylglycerol. By comparing the relative specific activities for each activity in each fraction, the fatty acyl-CoA synthetase activity appeared mainly in the lipid bodies, and that for phosphatidic acid formation was mainly in the mitochondrion; other activities were too weak and too dispersed for accurate assessment of their location. Recombining all the subcellular fractions restored triacylglycerol synthesizing activity. Omitting any single fraction from the mixture did not result in restoration of triacylglycerol synthesizing activity. Starvation of the yeast, which leads to utilization of the endogenous lipid reserves, stimulated fatty acyl-CoA synthetase activity, but diminished phosphatidic acid and triacylglycerol biosynthesis indicating probable induction of beta-oxidation in the peroxisomes and repression of lipid biosynthesis.

摘要

在弯孢念珠菌的无细胞提取物中观察到三酰甘油(TAG)生物合成速率较低,但通过添加α-或β-环糊精,速率可提高至10倍。完整或轻度破碎的原生质体将[U-14C]甘油3-磷酸或[1-14C]油酸酯掺入三酰甘油及其生物合成中间体(溶血磷脂酸、磷脂酸和二酰甘油)的速率更高。脂肪酸酰基辅酶A合成酶对棕榈酸、油酸和亚油酸的活性最高,但对硬脂酸的活性约低6至8倍。硬脂酸和硬脂酰辅酶A掺入脂质的能力较差。将原生质体亚细胞分级分离为线粒体、微粒体、脂质体和上清液部分,降低了油酸掺入三酰甘油的14C掺入速率。通过比较每个部分中每种活性的相对比活性,脂肪酸酰基辅酶A合成酶活性主要出现在脂质体中,而磷脂酸形成的活性主要出现在线粒体中;其他活性太弱且分布太分散,无法准确评估其位置。将所有亚细胞部分重新组合可恢复三酰甘油合成活性。从混合物中省略任何一个部分都不会导致三酰甘油合成活性的恢复。酵母饥饿会导致内源性脂质储备的利用,刺激脂肪酸酰基辅酶A合成酶活性,但会减少磷脂酸和三酰甘油的生物合成,这表明过氧化物酶体中可能诱导了β-氧化,脂质生物合成受到抑制。

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本文引用的文献

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Regulatory role of phosphatidate phosphatase in triacylglycerol synthesis of Saccharomyces cerevisiae.磷脂酸磷酸酶在酿酒酵母三酰甘油合成中的调控作用。
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Partial purification and properties of phosphatidate phosphatase in Saccharomyces cerevisiae.酿酒酵母中磷脂酸磷酸酶的部分纯化及性质
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