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从渗透调节表达系统中纯化活性大肠杆菌核糖体循环因子(RRF)。

Purification of active Escherichia coli ribosome recycling factor (RRF) from an osmo-regulated expression system.

作者信息

MacDougall J, Holst-Hansen P, Mortensen K K, Freistroffer D V, Pavlov M Y, Ehrenberg M, Buckingham R H

机构信息

CNRS-UPR 9073, Institut de Biologie Physico-chimique, Paris, France.

出版信息

Biochimie. 1997 May;79(5):243-6. doi: 10.1016/s0300-9084(97)83511-0.

DOI:10.1016/s0300-9084(97)83511-0
PMID:9258432
Abstract

Ribosome release factor (RRF) from Escherichia coli was overproduced from an osmo-expression vector. More than 40% of cell protein was RRF after 6 h of induction. A purification scheme is described that produced 50 mg of RRF from an initial culture of 2 L. The recycling time for ribosomes synthesising the tripeptide fMet-Phe-Leu in vitro in the absence of RF3 was reduced from 40 to 15 s by the addition of purified 1.5 microM RRF.

摘要

来自大肠杆菌的核糖体释放因子(RRF)通过渗透压表达载体过量表达。诱导6小时后,超过40%的细胞蛋白为RRF。描述了一种纯化方案,该方案从2升初始培养物中产生了50毫克RRF。在没有RF3的情况下,通过添加纯化的1.5微摩尔RRF,体外合成三肽fMet-Phe-Leu的核糖体的循环时间从40秒减少到15秒。

相似文献

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Purification of active Escherichia coli ribosome recycling factor (RRF) from an osmo-regulated expression system.从渗透调节表达系统中纯化活性大肠杆菌核糖体循环因子(RRF)。
Biochimie. 1997 May;79(5):243-6. doi: 10.1016/s0300-9084(97)83511-0.
2
Fast recycling of Escherichia coli ribosomes requires both ribosome recycling factor (RRF) and release factor RF3.大肠杆菌核糖体的快速循环需要核糖体循环因子(RRF)和释放因子RF3。
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Release factor RF3 abolishes competition between release factor RF1 and ribosome recycling factor (RRF) for a ribosome binding site.释放因子RF3消除了释放因子RF1与核糖体循环因子(RRF)之间对核糖体结合位点的竞争。
J Mol Biol. 1997 Oct 24;273(2):389-401. doi: 10.1006/jmbi.1997.1324.
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Expression in Escherichia coli, purification and characterization of Thermoanaerobacter tengcongensis ribosome recycling factor.嗜热栖热放线菌核糖体循环因子在大肠杆菌中的表达、纯化及特性研究
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Dual functions of ribosome recycling factor in protein biosynthesis: disassembling the termination complex and preventing translational errors.核糖体循环因子在蛋白质生物合成中的双重功能:拆解终止复合物并防止翻译错误。
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Specific interaction between the ribosome recycling factor and the elongation factor G from Mycobacterium tuberculosis mediates peptidyl-tRNA release and ribosome recycling in Escherichia coli.结核分枝杆菌核糖体循环因子与延伸因子G之间的特异性相互作用介导了大肠杆菌中肽基-tRNA的释放和核糖体循环。
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Ribosome recycling factor and release factor 3 action promotes TnaC-peptidyl-tRNA Dropoff and relieves ribosome stalling during tryptophan induction of tna operon expression in Escherichia coli.核糖体循环因子和释放因子3的作用促进TnaC-肽基-tRNA脱落,并在大肠杆菌色氨酸诱导tna操纵子表达过程中缓解核糖体停滞。
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Ribosome release factor RF4 and termination factor RF3 are involved in dissociation of peptidyl-tRNA from the ribosome.核糖体释放因子RF4和终止因子RF3参与肽基tRNA从核糖体上的解离。
EMBO J. 1998 Feb 2;17(3):808-16. doi: 10.1093/emboj/17.3.808.