首页> 外文期刊>Journal of bacteriology >Phospholipid synthesis and lipid composition of subcellular membranes in the unicellular eukaryote Saccharomyces cerevisiae.
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Phospholipid synthesis and lipid composition of subcellular membranes in the unicellular eukaryote Saccharomyces cerevisiae.

机译:单细胞真核生物酿酒酵母中磷脂的合成和亚细胞膜的脂质组成。

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Subcellular membranes of Saccharomyces cerevisiae, including mitochondria, microsomes, plasma membranes, secretory vesicles, vacuoles, nuclear membranes, peroxisomes, and lipid particles, were isolated by improved procedures and analyzed for their lipid composition and their capacity to synthesize phospholipids and to catalyze sterol delta 24-methylation. The microsomal fraction is heterogeneous in terms of density and classical microsomal marker proteins and also with respect to the distribution of phospholipid-synthesizing enzymes. The specific activity of phosphatidylserine synthase was highest in a microsomal subfraction which was distinct from heavier microsomes harboring phosphatidylinositol synthase and the phospholipid N-methyltransferases. The exclusive location of phosphatidylserine decarboxylase in mitochondria was confirmed. CDO-diacylglycerol synthase activity was found both in mitochondria and in microsomal membranes. Highest specific activities of glycerol-3-phosphate acyltransferase and sterol delta 24-methyltransferase were observed in the lipid particle fraction. Nuclear and plasma membranes, vacuoles, and peroxisomes contain only marginal activities of the lipid-synthesizing enzymes analyzed. The plasma membrane and secretory vesicles are enriched in ergosterol and in phosphatidylserine. Lipid particles are characterized by their high content of ergosteryl esters. The rigidity of the plasma membrane and of secretory vesicles, determined by measuring fluorescence anisotropy by using trimethylammonium diphenylhexatriene as a probe, can be attributed to the high content of ergosterol.
机译:通过改进程序分离了酿酒酵母的亚细胞膜,包括线粒体,微粒体,质膜,分泌囊泡,液泡,核膜,过氧化物酶体和脂质颗粒,并分析了它们的脂质组成及其合成磷脂和催化固醇δ的能力。 24-甲基化。微粒体部分在密度和经典微粒体标记蛋白方面以及在磷脂合成酶的分布方面是异质的。磷脂酰丝氨酸合酶的比活性在微粒体亚组分中最高,这不同于携带磷脂酰肌醇合成酶和磷脂N-甲基转移酶的较重微粒体。证实了磷脂酰丝氨酸脱羧酶在线粒体中的唯一位置。在线粒体和微粒体膜中均发现了CDO-二酰基甘油合酶活性。在脂质颗粒部分中观察到了甘油3-磷酸酰基转移酶和甾醇δ24-甲基转移酶的最高比活。核膜和质膜,液泡和过氧化物酶体仅包含所分析的脂质合成酶的边缘活性。质膜和分泌囊泡富含麦角固醇和磷脂酰丝氨酸。脂质颗粒的特征在于其高含量的麦角甾醇酯。通过使用三甲基铵二苯基己三烯作为探针测量荧光各向异性来确定质膜和分泌囊的刚性,这归因于麦角固醇的含量高。

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