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Microbiology. 2006 Aug;152(Pt 8):2191-5.

Peptidyl-tRNA hydrolase and its critical role in protein biosynthesis.

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1
Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India.

Abstract

Peptidyl-tRNA hydrolase (Pth) releases tRNA from peptidyl-tRNA by cleaving the ester bond between the peptide and the tRNA. Genetic analyses using Escherichia coli harbouring temperature-sensitive Pth have identified a number of translation factors involved in peptidyl-tRNA release. Accumulation of peptidyl-tRNA in the cells leads to depletion of aminoacyl-tRNA pools and halts protein biosynthesis. Thus, it is vital for cells to maintain Pth activity to deal with the pollution of peptidyl-tRNAs generated during the initiation, elongation and termination steps of protein biosynthesis. Interestingly, while eubacteria possess a single class of peptidyl-tRNA hydrolase, eukaryotes possess several such activities, making Pth a potential drug target to control eubacterial infections. This review discusses the aspects of Pth that relate to its history and biochemistry and its physiological connections with various cellular factors.

PMID:
16849786
DOI:
10.1099/mic.0.29024-0
[Indexed for MEDLINE]
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