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核糖体蛋白S1和延伸因子G在大肠杆菌生长周期中的水平。

Levels of ribosomal protein S1 and elongation factor G in the growth cycle of Escherichia coli.

作者信息

Lambert J M, Boileau G, Howe J G, Traut R R

出版信息

J Bacteriol. 1983 Jun;154(3):1323-8. doi: 10.1128/jb.154.3.1323-1328.1983.

DOI:10.1128/jb.154.3.1323-1328.1983
PMID:6343349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC217607/
Abstract

The relative levels of ribosomes, ribosomal protein S1, and elongation factor G in the growth cycle of Escherichia coli were examined with two-dimensional polyacrylamide gel electrophoresis. Nonequilibrium pH gradient polyacrylamide gel electrophoresis was used in the first dimension, and polyacrylamide gradient-sodium dodecyl sulfate gel electrophoresis was used in the second dimension. The identities of protein spots containing S1 and elongation factor G were confirmed by radioiodination of the proteins and peptide mapping of the radiolabeled peptides. The levels of ribosomes and ribosomal protein S1 were coordinately reduced during transition from exponential phase to stationary phase. There was no accumulation of S1 in the stationary phase. In marked contrast, the level of elongation factor G showed no significant change from exponential phase to stationary phase. The relative level of elongation factor G compared with ribosomes or S1 increased by about 2.5-fold during transition from exponential phase to stationary phase. The results show that there are differences between the regulation of the levels of elongation factor G and of ribosomal proteins, including S1, apparent during the transition from exponential to stationary phase.

摘要

利用二维聚丙烯酰胺凝胶电泳检测了大肠杆菌生长周期中核糖体、核糖体蛋白S1和延伸因子G的相对水平。第一维采用非平衡pH梯度聚丙烯酰胺凝胶电泳,第二维采用聚丙烯酰胺梯度 - 十二烷基硫酸钠凝胶电泳。通过蛋白质的放射性碘化和放射性标记肽段的肽图谱分析,确认了含有S1和延伸因子G的蛋白质斑点的身份。在从指数生长期向稳定期转变过程中,核糖体和核糖体蛋白S1的水平协同降低。在稳定期没有S1的积累。与之形成显著对比的是,延伸因子G的水平从指数生长期到稳定期没有显著变化。在从指数生长期向稳定期转变过程中,延伸因子G与核糖体或S1相比的相对水平增加了约2.5倍。结果表明,在从指数生长期到稳定期的转变过程中,延伸因子G和包括S1在内的核糖体蛋白水平的调节存在差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f350/217607/923d9b5e1f09/jbacter00247-0305-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f350/217607/a3e63982352d/jbacter00247-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f350/217607/923d9b5e1f09/jbacter00247-0305-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f350/217607/a3e63982352d/jbacter00247-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f350/217607/923d9b5e1f09/jbacter00247-0305-a.jpg

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本文引用的文献

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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
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Identification of proteins at the binding site for protein S1 in 70 S ribosomes and 30 S subunits by cross-linking with 2-iminothiolane.通过与2-亚氨基硫杂环戊烷交联鉴定70S核糖体和30S亚基中蛋白质S1结合位点的蛋白质
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In vivo stability, maturation and relative differential synthesis rates of individual ribosomal proteins in Escherichia coli B/r.大肠杆菌B/r中单个核糖体蛋白的体内稳定性、成熟过程及相对差异合成速率
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Stringent control of ribosomal protein gene expression in Escherichia coli.大肠杆菌中核糖体蛋白基因表达的严格控制。
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Polyuridylic acid binding and translating by Escherichia coli ribosomes: stimulation by protein I, inhibition by aurintricarboxylic acid.多聚尿苷酸与大肠杆菌核糖体的结合及翻译:受蛋白质I刺激,被金精三羧酸抑制
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Subunit I of G beta replicase and 30 S ribosomal protein S1 of Escherichia coli. Evidence for the identity of the two proteins.Gβ复制酶的亚基I与大肠杆菌的30S核糖体蛋白S1。两种蛋白质同一性的证据。
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