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在优化的体外系统中天然信使核糖核酸的翻译速率

Rate of translation of natural mRNAs in an optimized in vitro system.

作者信息

Pavlov M Y, Ehrenberg M

机构信息

Department of Molecular Biology, BMC, Uppsala, Sweden.

出版信息

Arch Biochem Biophys. 1996 Apr 1;328(1):9-16. doi: 10.1006/abbi.1996.0136.

Abstract

We report results on in vitro translation of an mRNA coding for elongation factor TuB which was in vitro transcribed from the tufB gene from Escherichia coli. Translation occurs at a rate of about 10 codons per second, which is close to the in vivo rate. Protein elongation obeys Michaelis-Menten kinetics with respect to the concentrations of the elongation factors EF-Tu and EF-G in the translation system. The measured K(m) values for EF-Tu and EF-G are 10 and 0.25 microM, respectively. The obtained k(cat) and K(m) values were used to estimate the average k(cat)/K(m) of about 24 x 10(6) s-1 M-1 for the interaction of individual EF-TuGTPaa-tRNA complexes with ribosomes. The estimated k(cat)/K(m) value for EF-G is 36 x 10(6) s-1 M-1. We have also studied translation with a "hyperaccurate" ribosome variant that is pseudodependent on streptomycin (SmP). We have found that SmP ribosomes translate the TuB mRNA significantly slower than wild-type ribosomes do. This is mainly due to a threefold lower k(cat)/K(m) for the interaction of EF-TuGTPaa-tRNA complexes with SmP ribosomes.

摘要

我们报告了关于编码延伸因子TuB的mRNA体外翻译的结果,该mRNA是从大肠杆菌的tufB基因体外转录而来的。翻译以每秒约10个密码子的速度进行,这与体内速度相近。蛋白质延伸在翻译系统中遵循米氏动力学,与延伸因子EF-Tu和EF-G的浓度有关。测得的EF-Tu和EF-G的K(m)值分别为10和0.25微摩尔。所获得的k(cat)和K(m)值用于估计单个EF-TuGTPaa-tRNA复合物与核糖体相互作用的平均k(cat)/K(m)约为24×10(6) s-1 M-1。EF-G的估计k(cat)/K(m)值为36×10(6) s-1 M-1。我们还研究了用对链霉素假依赖性的“超精确”核糖体变体进行的翻译。我们发现,SmP核糖体翻译TuB mRNA的速度明显比野生型核糖体慢。这主要是由于EF-TuGTPaa-tRNA复合物与SmP核糖体相互作用的k(cat)/K(m)降低了三倍。

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