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在酿酒酵母的多胺营养缺陷型中,多胺诱导胆碱转运及其在刺激胆碱掺入磷脂酰胆碱中的作用。

Induction of choline transport and its role in the stimulation of the incorporation of choline into phosphatidylcholine by polyamines in a polyamine auxotroph of Saccharomyces cerevisiae.

作者信息

Hosaka K, Yamashita S

出版信息

Eur J Biochem. 1981 May;116(1):1-6. doi: 10.1111/j.1432-1033.1981.tb05292.x.

Abstract
  1. A mutant of Saccharomyces cerevisiae, defective in ornithine decarboxylase, was isolated. A prolonged culture of the mutant in a polyamine-free medium resulted in a great decrease in the polyamine content and in cessation of growth. The addition of polyamines to the culture induced the growth after a lag period of 5--6.5 h. The growth rate in the presence of polyamine was comparable to that of the wild-type strain. The effectiveness of polyamines was as follows: spermidine greater than putrescine approximately equal to spermine. 2. Phosphatidylcholine-synthesizing activity during the lag phase of growth was determined by measuring the rate of incorporation of [14C]choline into phosphatidylcholine. The incorporation rate was markedly increased with time by polyamine prior to the initiation of cell division. Polyamines were effective in the following order: spermidine greater than putrescine approximately equal to spermine. Experiments with methylglyoxal bis(guanylhydrazone), an inhibitor of S-adenosylmethionine decarboxylase, showed that putrescine stimulates cell growth and choline incorporation into phosphatidylcholine after it has been converted into spermidine in the cell. 3. The induction of the choline transport system was shown to be responsible for the increase in the rate of incorporation of [14C]choline into phosphatidylcholine effected by polyamines. A low concentration of cycloheximide completely prevented the induction of choline transport by polyamines. The levels of the CDP-choline pathway enzymes such as choline kinase, cholinephosphate cytidyltransferase and cholinephosphotransferase were not significantly changed.
摘要
  1. 分离出了一株在鸟氨酸脱羧酶方面有缺陷的酿酒酵母突变体。该突变体在无多胺培养基中长时间培养导致多胺含量大幅降低且生长停止。向培养物中添加多胺会在5 - 6.5小时的延迟期后诱导生长。存在多胺时的生长速率与野生型菌株相当。多胺的有效性如下:亚精胺大于腐胺约等于精胺。2. 通过测量[14C]胆碱掺入磷脂酰胆碱的速率来测定生长延迟期的磷脂酰胆碱合成活性。在细胞分裂开始前,多胺随时间显著提高了掺入速率。多胺的有效性顺序如下:亚精胺大于腐胺约等于精胺。用S - 腺苷甲硫氨酸脱羧酶抑制剂甲基乙二醛双(脒腙)进行的实验表明,腐胺在细胞内转化为亚精胺后刺激细胞生长和胆碱掺入磷脂酰胆碱。3. 已表明胆碱转运系统的诱导是多胺导致[14C]胆碱掺入磷脂酰胆碱速率增加的原因。低浓度的环己酰亚胺完全阻止了多胺对胆碱转运的诱导。胆碱激酶、胆碱磷酸胞苷转移酶和胆碱磷酸转移酶等CDP - 胆碱途径酶水平没有显著变化。

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