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球形红假单胞菌中磷脂生物合成的体内代谢中间体。

In vivo metabolic intermediates of phospholipid biosynthesis in Rhodopseudomonas sphaeroides.

作者信息

Cain B D, Singer M, Donohue T J, Kaplan S

出版信息

J Bacteriol. 1983 Oct;156(1):375-85. doi: 10.1128/jb.156.1.375-385.1983.

Abstract

The in vivo metabolic pathways of phospholipid biosynthesis in Rhodopseudomonas sphaeroides have been investigated. Rapid pulse-chase-labeling studies indicated that phosphatidylethanolamine and phosphatidylglycerol were synthesized as in other eubacteria. The labeling pattern observed for N-acylphosphatidylserine (NAPS) was inconsistent with the synthesis of this phospholipid occurring by direct acylation of phosphatidylserine (PS). Rather, NAPS appeared to be kinetically derived from an earlier intermediate such as phosphatidic acid or more likely CDP-diglyceride. Tris-induced NAPS accumulation specifically reduced the synthesis of PS. Treatment of cells with a bacteriostatic concentration of hydroxylamine (10 mM) greatly reduced total cellular phospholipid synthesis, resulted in accumulation of PS, and stimulated the phosphatidylglycerol branch of phospholipid metabolism relative to the PS branch of the pathway. When the cells were treated with a lower hydroxylamine dosage (50 microM), total phospholipid synthesis lagged as PS accumulated, however, phospholipid synthesis resumed coincident with a reversal of PS accumulation. Hydroxylamine alone was not sufficient to promote NAPS accumulation but this compound allowed continued NAPS accumulation when cells were grown in medium containing Tris. The significance of these observations is discussed in terms of NAPS biosynthesis being representative of a previously undescribed branch of the phospholipid biosynthetic sequence.

摘要

已对球形红假单胞菌中磷脂生物合成的体内代谢途径进行了研究。快速脉冲追踪标记研究表明,磷脂酰乙醇胺和磷脂酰甘油的合成与其他真细菌相同。观察到的N-酰基磷脂酰丝氨酸(NAPS)的标记模式与通过磷脂酰丝氨酸(PS)直接酰化合成这种磷脂的情况不一致。相反,NAPS似乎是由动力学上更早的中间体如磷脂酸或更可能是CDP-二甘油酯衍生而来。Tris诱导的NAPS积累特异性地降低了PS的合成。用抑菌浓度的羟胺(10 mM)处理细胞大大降低了总细胞磷脂合成,导致PS积累,并相对于该途径的PS分支刺激了磷脂代谢的磷脂酰甘油分支。当用较低剂量的羟胺(50 microM)处理细胞时,随着PS积累,总磷脂合成滞后,然而,磷脂合成随着PS积累的逆转而恢复。单独的羟胺不足以促进NAPS积累,但当细胞在含有Tris的培养基中生长时,这种化合物允许NAPS持续积累。这些观察结果的意义在NAPS生物合成代表磷脂生物合成序列中一个以前未描述的分支的方面进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b10/215092/c244155186c7/jbacter00239-0387-a.jpg

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