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23S核糖体RNA中的突变会扰乱转运RNA的选择,并可能导致链霉素依赖性。

Mutations in 23 S ribosomal RNA perturb transfer RNA selection and can lead to streptomycin dependence.

作者信息

Bilgin N, Ehrenberg M

机构信息

Department of Molecular Biology, University of Uppsala, Sweden.

出版信息

J Mol Biol. 1994 Jan 21;235(3):813-24. doi: 10.1006/jmbi.1994.1041.

Abstract

Escherichia coli ribosomes with a G to C transversion at position 2661 in 23 S ribosomal RNA are more accurate in tRNA selection than wild-type ribosomes. This enhanced accuracy is due to improved initial selection of ternary complexes rather than proofreading of aminoacyl tRNAs. The 2661C mutation reduces the binding rate of cognate ternary complexes to the A-site. This binding rate deficiency becomes dramatic when ribosomes also harbour an S12 mutation with a streptomycin-resistant, hyperaccurate phenotype. In this case, severe loss of kinetic efficiency in EF-Tu function leads to cell death. Streptomycin restores viability by increasing the association rate of ternary complex to these doubly altered ribosomes. The binding rate of EF-G to 2661C ribosomes is also reduced while the translocation rate is unaffected.

摘要

在23S核糖体RNA的2661位发生G到C颠换的大肠杆菌核糖体,在tRNA选择上比野生型核糖体更精确。这种提高的精确性是由于三元复合物初始选择的改善,而非氨酰tRNA的校对。2661C突变降低了同源三元复合物与A位点的结合速率。当核糖体还带有具有链霉素抗性、超精确表型的S12突变时,这种结合速率缺陷变得显著。在这种情况下,EF-Tu功能的动力学效率严重丧失导致细胞死亡。链霉素通过增加三元复合物与这些双重改变的核糖体的结合速率来恢复活力。EF-G与2661C核糖体的结合速率也降低,而转位速率不受影响。

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