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在体外刺激严谨因子介导的焦磷酸转移的大肠杆菌核糖体蛋白。

Ribosomal proteins of Escherichia coli that stimulate stringent-factor-mediated pyrophosphoryl transfer in vitro.

作者信息

Christiansen L, Neirhaus K H

出版信息

Proc Natl Acad Sci U S A. 1976 Jun;73(6):1839-43. doi: 10.1073/pnas.73.6.1839.

DOI:10.1073/pnas.73.6.1839
PMID:778846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC430402/
Abstract

Guanosine tetra- and pentaphosphate, (p)ppGpp, can be synthesized in vitro in a reaction containing only the enzyme (stringent factor), salts, and substrates (nonribosomal system). This reaction is greatly stimulated upon addition of methanol (methanol system) or by ribosomes, mRNA, and tRNA (ribosome system). Here we show that several ribosomal proteins alone stimulate the synthesis of (p)ppGpp in the presence of stringent factor (protein system). The optimal ionic conditions for the ribosome and protein systems are identical. The concentration of ribosomes or any stimulating ribosomal protein required for saturation of a given concentration of stringent factor is similar. Fifty of 54 ribosomal proteins were tested for stimulation in the protein system; 15 proteins showed high activity, seven of these from the 30S ribosomal subunit and eight from the 50S subunit. The physiological relevance of this finding is discussed.

摘要

四磷酸鸟苷和五磷酸鸟苷((p)ppGpp)可在仅含有该酶(严谨因子)、盐和底物的反应体系中体外合成(非核糖体系统)。加入甲醇(甲醇系统)或核糖体、信使核糖核酸(mRNA)及转运核糖核酸(tRNA)(核糖体系统)后,该反应会受到极大刺激。在此我们表明,仅几种核糖体蛋白在存在严谨因子的情况下就能刺激(p)ppGpp的合成(蛋白质系统)。核糖体系统和蛋白质系统的最佳离子条件相同。使给定浓度的严谨因子饱和所需的核糖体或任何具有刺激作用的核糖体蛋白的浓度相似。在蛋白质系统中对54种核糖体蛋白中的50种进行了刺激测试;15种蛋白表现出高活性,其中7种来自30S核糖体亚基,8种来自50S亚基。本文讨论了这一发现的生理相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/430402/6bc8757f065e/pnas00036-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/430402/6bc8757f065e/pnas00036-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/430402/6bc8757f065e/pnas00036-0076-a.jpg

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本文引用的文献

1
Codon specific, tRNA dependent in vitro synthesis of ppGpp and pppGpp.密码子特异性、依赖tRNA的体外合成ppGpp和pppGpp。
Nat New Biol. 1973 May 2;243(122):13-5.
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Transduction of linked genetic characters of the host by bacteriophage P1.噬菌体P1对宿主连锁遗传性状的转导
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The reliability of molecular weight determinations by dodecyl sulfate-polyacrylamide gel electrophoresis.通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定分子量的可靠性。
Mol Gen Genet. 1978 Nov 9;166(3):291-7. doi: 10.1007/BF00267621.
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Isolation and characterization of ribonuclease I mutants of Escherichia coli.大肠杆菌核糖核酸酶I突变体的分离与鉴定
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Ribosomal proteins. XIV. Isoelectric points of ribosomal proteins of E. coli as determined by two-dimensional polyacrylamide gel electrophoresis.核糖体蛋白质。十四。通过二维聚丙烯酰胺凝胶电泳测定的大肠杆菌核糖体蛋白质的等电点。
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Ribosomal proteins. Isolation of the proteins from 30S ribosomal subunits of Escherichia coli.核糖体蛋白。从大肠杆菌30S核糖体亚基中分离蛋白质。
Eur J Biochem. 1971 Nov 11;23(1):7-11. doi: 10.1111/j.1432-1033.1971.tb01584.x.
7
Ribosomal proteins. Isolation of proteins from 50S ribosomal subunits of Escherichia coli.核糖体蛋白。从大肠杆菌50S核糖体亚基中分离蛋白质。
Eur J Biochem. 1971 Nov 11;23(1):12-6. doi: 10.1111/j.1432-1033.1971.tb01585.x.
8
Ribosomal proteins. Protein compositions of biosynthetic precursors and artifical subparticles from ribosomal subunits in Escherichia coli K 12.核糖体蛋白。大肠杆菌K12核糖体亚基生物合成前体和人工亚颗粒的蛋白质组成。
Eur J Biochem. 1971 May 28;20(2):249-57. doi: 10.1111/j.1432-1033.1971.tb01388.x.
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Total reconstitution of functionally active 50S ribosomal subunits from Escherichia coli.来自大肠杆菌的功能活性50S核糖体亚基的完全重建。
Proc Natl Acad Sci U S A. 1974 Dec;71(12):4713-7. doi: 10.1073/pnas.71.12.4713.
10
Nonribosomal synthesis of guanosine 5',3'-polyphosphates by the ribosomal wash of stringent Escherichia coli.严谨型大肠杆菌核糖体洗脱液对鸟苷5',3'-多磷酸的非核糖体合成
Proc Natl Acad Sci U S A. 1973 Jul;70(7):2145-8. doi: 10.1073/pnas.70.7.2145.