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细菌信使核糖核酸的寿命

Lifetime of bacterial messenger ribonucleic acid.

作者信息

Moses V, Calvin M

出版信息

J Bacteriol. 1965 Nov;90(5):1205-17. doi: 10.1128/jb.90.5.1205-1217.1965.

Abstract

Moses, V. (University of California, Berkeley), and M. Calvin. Lifetime of bacterial messenger ribonucleic acid. J. Bacteriol. 90:1205-1217. 1965.-When cells from a stationary culture of Escherichia coli were placed in fresh medium containing inducer for beta-galactosidase, growth, as represented by increase in turbidity and by total protein synthesis, started within 30 sec. By contrast, beta-galactosidase synthesis was greatly delayed compared with induction during exponential growth. Two other inducible enzymes (d-serine deaminase and l-tryptophanase) and one repressible enzyme (alkaline phosphatase) showed similar lags. The lags were not due to catabolite repression. They could not be reduced by pretreatment of the culture with inducer, or by supplementing the fresh medium with amino acids or nucleotides. The lag was also demonstrated by an i(-) mutant constitutive for beta-galactosidase synthesis. An inhibitor of ribonucleic acid (RNA) synthesis, 6-azauracil, preferentially inhibited beta-galactosidase synthesis compared with growth in both inducible and constitutive strains. Puromycin, an inhibitor of protein synthesis, acted as an inhibitor at additional sites during the induction of beta-galactosidase synthesis. No inhibition of the reactions proceeding during the first 20 sec of induction was observed, but puromycin seemed to prevent the accumulation of messenger RNA during the period between 20 sec and the first appearance of enzyme activity after 3 min. It is suggested that these observations, together with many reports in the literature that inducible enzyme synthesis is more sensitive than total growth to some inhibitors and adverse growth conditions, can be explained by supposing that messenger RNA for normally inducible enzymes is biologically more labile than that for some normally constitutive proteins. The possible implications of this hypothesis for the achievement of cell differentiation by genetic regulation of enzyme synthesis are briefly discussed.

摘要

摩西,V.(加利福尼亚大学伯克利分校)和M. 卡尔文。细菌信使核糖核酸的寿命。《细菌学杂志》90:1205 - 1217。1965年。——当将来自大肠杆菌静止培养物的细胞置于含有β - 半乳糖苷酶诱导剂的新鲜培养基中时,以浊度增加和总蛋白质合成表示的生长在30秒内开始。相比之下,与指数生长期间的诱导相比,β - 半乳糖苷酶的合成被大大延迟。另外两种诱导酶(d - 丝氨酸脱氨酶和l - 色氨酸酶)和一种阻遏酶(碱性磷酸酶)表现出类似的延迟。这些延迟不是由于分解代谢物阻遏。用诱导剂预处理培养物,或在新鲜培养基中补充氨基酸或核苷酸,都不能减少这些延迟。β - 半乳糖苷酶合成组成型的i(-)突变体也表现出这种延迟。核糖核酸(RNA)合成抑制剂6 - 氮尿嘧啶,与诱导型和组成型菌株中的生长相比,优先抑制β - 半乳糖苷酶的合成。嘌呤霉素是一种蛋白质合成抑制剂,在β - 半乳糖苷酶合成诱导期间在其他位点起抑制剂作用。在诱导的前20秒内未观察到对反应的抑制,但嘌呤霉素似乎在20秒至3分钟后酶活性首次出现之间的时间段内阻止了信使RNA的积累。有人提出,这些观察结果,连同文献中许多报道,即诱导酶合成比总生长对某些抑制剂和不利生长条件更敏感,可以通过假设正常诱导酶的信使RNA在生物学上比某些正常组成型蛋白质的信使RNA更不稳定来解释。简要讨论了这一假设对通过酶合成的基因调控实现细胞分化的可能影响。

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Lifetime of bacterial messenger ribonucleic acid.细菌信使核糖核酸的寿命
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