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合成生物学挑战了翻译、密码子偏爱和转录中长久以来的假说。

Synthetic biology challenges long-held hypotheses in translation, codon bias and transcription.

机构信息

Department of Cell and Molecular Biology, Uppsala University, Sweden.

出版信息

Biotechnol J. 2012 Jul;7(7):835-45. doi: 10.1002/biot.201200002. Epub 2012 Jun 14.

Abstract

Synthetic biology is a powerful experimental approach, not only for developing new biotechnology applications, but also for testing hypotheses in basic biological science. Here, examples from our research using the best model system, Escherichia coli, are reviewed. New evidence drawn from synthetic biology has overturned several long-standing hypotheses regarding the mechanisms of transcription and translation: (i) all native aminoacyl-tRNAs are not equally efficient in translation at equivalent concentrations; (ii) accommodation is not always rate limiting in translation, and may not be for any aminoacyl-tRNA; (iii) proline is the only N-alkyl-amino acid in the genetic code not because of special suitability for protein structure, but because of its comparatively high nucleophilicity; (iv) the usages of most sense codons in E. coli do not correlate with cognate tRNA abundances and (v) class II transcriptional pausing and termination by T7 RNA polymerase cannot be assumed to occur in vivo based on in vitro data. Implications of these conclusions for the biotechnology field are discussed.

摘要

合成生物学是一种强大的实验方法,不仅可用于开发新的生物技术应用,还可用于检验基础生物学中的假说。在这里,我们将通过使用最佳模型系统大肠杆菌的研究实例进行说明。来自合成生物学的新证据推翻了几个关于转录和翻译机制的长期假说:(i)并非所有天然的氨酰-tRNA 在等效浓度下在翻译中效率相同;(ii)在翻译中并非总是适应性起限速作用,而且可能对于任何氨酰-tRNA 都不是这样;(iii)脯氨酸是遗传密码中唯一的 N-烷基-氨基酸,不是因为特别适合蛋白质结构,而是因为其相对较高的亲核性;(iv)大肠杆菌中大多数有意义密码子的使用与相应 tRNA 的丰度无关;(v)基于体外数据,不能假设 T7 RNA 聚合酶的 II 类转录暂停和终止会在体内发生。讨论了这些结论对生物技术领域的影响。

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