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含肌醇鞘脂类在酿酒酵母肌醇饥饿期间的作用。

Role of inositol-containing sphingolipids in Saccharomyces cerevisiae during inositol starvation.

作者信息

Hanson B A

出版信息

J Bacteriol. 1984 Sep;159(3):837-42. doi: 10.1128/jb.159.3.837-842.1984.

Abstract

The in vitro lipid requirements of UDP-N-acetylglucosamine-dolichol phosphate N-acetylglucosamine-1-phosphotransferase for the inositol-containing sphingolipids from Saccharomyces cerevisiae were characterized in terms of concentration and specificity. The effects of combinations of lipids, especially phosphatidylinositol and the inositol-containing sphingolipids, were also tested on the transferase. Phosphatidylinositol and phosphatidylglycerol stimulated the enzyme 3.3- and 2.8-fold, respectively. The inositol-containing sphingolipids, phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine did not stimulate the activity of the transferase. Phosphatidylcholine and phosphatidylethanolamine in combination with phosphatidylinositol had no effect on the transferase activity; however, the inositol-containing sphingolipids markedly inhibited the stimulation of the transferase by phosphatidylinositol. This inhibition by the sphingolipids was prevented if phosphatidylcholine, in addition to the other lipids, was present in the assay mixture. In addition, changes due to inositol starvation in the in vivo membrane lipid environment, i.e., phosphatidylinositol and the inositol-containing sphingolipids, were analyzed to determine whether they corresponded to the observed in vitro effects. Three hours after the beginning of inositol starvation, there were 9- and 14-fold reductions in the accumulation of phosphatidylinositol in membrane fractions IIA (vesicles) and IV (endoplasmic reticulum), respectively, although there was only a 6-fold reduction in membrane fraction I (plasma membrane). The accumulation of [14C]inositol into inositol-containing sphingolipids also reflected the differences in the cellular location of membranes.

摘要

从浓度和特异性方面对酿酒酵母含肌醇鞘脂UDP-N-乙酰葡糖胺-多萜醇磷酸N-乙酰葡糖胺-1-磷酸转移酶的体外脂质需求进行了表征。还测试了脂质组合,尤其是磷脂酰肌醇和含肌醇鞘脂对该转移酶的影响。磷脂酰肌醇和磷脂酰甘油分别使该酶活性提高了3.3倍和2.8倍。含肌醇鞘脂、磷脂酰胆碱、磷脂酰乙醇胺和磷脂酰丝氨酸均未刺激该转移酶的活性。磷脂酰胆碱和磷脂酰乙醇胺与磷脂酰肌醇联合使用对转移酶活性没有影响;然而,含肌醇鞘脂显著抑制了磷脂酰肌醇对转移酶的刺激作用。如果在测定混合物中除了其他脂质外还存在磷脂酰胆碱,则鞘脂的这种抑制作用可被阻止。此外,分析了体内膜脂质环境(即磷脂酰肌醇和含肌醇鞘脂)中由于肌醇饥饿引起的变化,以确定它们是否与体外观察到的效应相对应。在肌醇饥饿开始3小时后,膜组分IIA(囊泡)和IV(内质网)中磷脂酰肌醇的积累分别减少了9倍和14倍,尽管膜组分I(质膜)中仅减少了6倍。[14C]肌醇掺入含肌醇鞘脂的情况也反映了膜在细胞内位置的差异。

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