Pavlov M Y, Ehrenberg M
Department of Molecular Biology, BMC, Uppsala, Sweden.
Arch Biochem Biophys. 1996 Apr 1;328(1):9-16. doi: 10.1006/abbi.1996.0136.
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.
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。