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多胺对大肠杆菌多胺依赖性突变体核糖体合成及活性的刺激作用。

Polyamine stimulation of ribosomal synthesis and activity in a polyamine-dependent mutant of Escherichia coli.

作者信息

Kashiwagi K, Sakai Y, Igarashi K

机构信息

Faculty of Pharmaceutical Sciences, Chiba University, Japan.

出版信息

Arch Biochem Biophys. 1989 Jan;268(1):379-87. doi: 10.1016/0003-9861(89)90598-5.

Abstract

A polyamine-dependent mutant of Escherichia coli KK101 was isolated by treatment of E. coli MA261 with N-methyl-N'-nitro-N-nitrosoguanidine. In the absence of putrescine, doubling time of the mutant was 496 min. The mutation was accompanied by a change in the nature of the 30 S ribosomal subunits. Addition of putrescine to the mutant stimulated the synthesis of proteins and subsequently, this led to stimulation of RNA and DNA synthesis. Under these conditions, we determined which proteins were preferentially synthesized. Putrescine stimulated the synthesis of ribosomal protein S1 markedly, but stimulated ribosomal proteins S4, L20, and X1, and RNA polymerase slightly. The amounts of initiation factors 2 and 3 synthesized were not influenced significantly by putrescine. The preferential stimulation of the synthesis of ribosomal protein S1 occurred as early as 20 min after the addition of putrescine, while stimulation of the synthesis of the other ribosomal proteins and RNA polymerase appeared at 40 min. The stimulation of the synthesis of ribosomal RNA also occurred at 40 min after addition of putrescine. Our results indicate that putrescine can stimulate both the synthesis and the activity of ribosomes. The increase in the activity of ribosomes was achieved by the association of S1 protein to S1-depleted ribosomes. The early stimulation of ribosomal protein S1 synthesis after addition of putrescine may be important for stimulation of cell growth by polyamines.

摘要

用N-甲基-N'-硝基-N-亚硝基胍处理大肠杆菌MA261,分离得到一株大肠杆菌KK101的多胺依赖性突变体。在没有腐胺的情况下,该突变体的倍增时间为496分钟。该突变伴随着30S核糖体亚基性质的改变。向突变体中添加腐胺刺激了蛋白质的合成,随后,这又导致了RNA和DNA合成的刺激。在这些条件下,我们确定了哪些蛋白质是优先合成的。腐胺显著刺激核糖体蛋白S1的合成,但对核糖体蛋白S4、L20和X1以及RNA聚合酶的刺激较弱。腐胺对起始因子2和3的合成量没有显著影响。添加腐胺后最早在20分钟就出现了对核糖体蛋白S1合成的优先刺激,而对其他核糖体蛋白和RNA聚合酶合成的刺激则在40分钟出现。添加腐胺后40分钟也出现了对核糖体RNA合成的刺激。我们的结果表明,腐胺可以刺激核糖体的合成和活性。核糖体活性的增加是通过S1蛋白与去除S1的核糖体结合实现的。添加腐胺后对核糖体蛋白S1合成的早期刺激可能对多胺刺激细胞生长很重要。

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