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[核糖体上肽合成过程中GTP分解的化学计量。多聚尿苷酸上聚苯丙氨酸延伸过程中GTP水解的化学计量]

[Stoichiometry of GTP breakdown during peptide synthesis on the ribosome. Stoichiometry of GTP hydrolysis during elongation of polyphenylalanine on polyuridylic acid].

作者信息

Kakhniashvili D G, Smailov S K, Gogiia I N, Gavrilova L P

出版信息

Biokhimiia. 1983 Jun;48(6):959-69.

PMID:6349702
Abstract

The stoichiometry of GTP hydrolysis during poly(Phe) elongation by Phe on poly(U) covalently bound to Sepharose was determined. The concentrations of both EF-T and EF-G were saturating. The GTP/Phe stoichiometry was calculated without the usual correction for the uncoupled ribosomal EF-T and EF-G dependent GTP hydrolysis. At the Mg2+ optimum (6 mM) for the poly(Phe) elongation on poly(U) . Sepharose the stoichiometry ratio of GTP/Phe was 1.9/2.1. This indicates that two (or less) GTP molecules coupled with poly(Phe) elongation by Phe on poly(U) . Sepharose are hydrolyzed.

摘要

测定了在与琼脂糖共价结合的聚(U)上由苯丙氨酸进行聚(苯丙氨酸)延伸过程中GTP水解的化学计量关系。EF-T和EF-G的浓度均为饱和状态。计算GTP/苯丙氨酸的化学计量关系时,未对未偶联的核糖体EF-T和EF-G依赖性GTP水解进行常规校正。在聚(U)-琼脂糖上进行聚(苯丙氨酸)延伸的最佳Mg2+浓度(6 mM)下,GTP/苯丙氨酸的化学计量比为1.9/2.1。这表明在聚(U)-琼脂糖上由苯丙氨酸进行聚(苯丙氨酸)延伸过程中,有两个(或更少)GTP分子发生水解。

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