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膜磷脂平衡合成的调控。大肠杆菌中调控模型的实验测试。

Regulation of the balanced synthesis of membrane phospholipids. Experimental test of models for regulation in Escherichia coli.

作者信息

Jackson B J, Gennity J M, Kennedy E P

出版信息

J Biol Chem. 1986 Oct 15;261(29):13464-8.

PMID:3531205
Abstract

In Escherichia coli, highly effective regulation controls the balanced synthesis of membrane phospholipids, important for optimal growth. Regulation is such that normally about 70% of a common pool of cytosine liponucleotide precursor is utilized by phosphatidylserine synthase and eventually converted to phosphatidylethanolamine, while about 30% is utilized by the competing enzyme phosphatidylglycerophosphate synthase and converted to phosphatidylglycerol (25%) plus cardiolipin (5%). Although the ratio of phosphatidylglycerol to cardiolipin may vary with conditions of growth, the sum of these two lipids remains relatively constant at about 30% of the total. Alternative models, postulating coordinate regulation of the two competing enzymes, or independent feedback regulation are proposed. These models were tested in experiments in which phosphatidylglycerol was continuously removed from growing cells treated with arbutin (4-hydroxyphenyl-O-beta-D-glucoside), causing its conversion to arbutinphosphoglycerol (Bohin, J.-P., and Kennedy, E.P. (1984) J. Biol. Chem. 259, 8388-8393.) The synthesis of phosphatidylglycerol was increased by a factor of 7 in cells treated with arbutin, with only small changes in phospholipid composition and with no significant change in the level of phosphatidylglycerophosphate synthase. The synthesis of phosphatidylethanolamine was not significantly increased, decisively eliminating the model that requires coordinate regulation of phosphatidylserine synthase and phosphatidylglycerophosphate synthase, and supporting the model of independent feedback inhibition, sensitive to very small changes in composition of cellular phospholipids.

摘要

在大肠杆菌中,高效的调控机制控制着膜磷脂的平衡合成,这对最佳生长至关重要。调控方式如下:通常,胞嘧啶脂核苷酸前体的一个共同池中的约70%被磷脂酰丝氨酸合酶利用,并最终转化为磷脂酰乙醇胺,而约30%被竞争性酶磷脂酰甘油磷酸合酶利用,并转化为磷脂酰甘油(25%)加心磷脂(5%)。尽管磷脂酰甘油与心磷脂的比例可能随生长条件而变化,但这两种脂质的总和在总量的约30%处保持相对恒定。有人提出了替代模型,假定这两种竞争性酶存在协同调控,或存在独立的反馈调控。这些模型在实验中得到了验证,在实验中,用熊果苷(4-羟基苯基-O-β-D-葡萄糖苷)处理生长中的细胞,持续去除磷脂酰甘油,导致其转化为熊果苷磷酸甘油(博欣,J.-P.,和肯尼迪,E.P.(1984年)《生物化学杂志》259,8388 - 8393)。在用熊果苷处理的细胞中,磷脂酰甘油的合成增加了7倍,磷脂组成仅有微小变化,磷脂酰甘油磷酸合酶的水平没有显著变化。磷脂酰乙醇胺的合成没有显著增加,这决定性地排除了需要对磷脂酰丝氨酸合酶和磷脂酰甘油磷酸合酶进行协同调控的模型,并支持了对细胞磷脂组成的非常小变化敏感的独立反馈抑制模型。

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