کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1953167 | 1057254 | 2009 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: On the role of an unusual tRNAGly isoacceptor in Staphylococcus aureus On the role of an unusual tRNAGly isoacceptor in Staphylococcus aureus](/preview/png/1953167.png)
In the available Staphylococcus aureus genomes, four different genes have been annotated to encode tRNAGly isoacceptors. Besides their prominent role in protein synthesis, some of them also participate in the formation of pentaglycine bridges during cell wall synthesis. However, until today, it is not known how many and which of them are actually involved in this essential procedure. In the present study we identified, apart from the four annotated tRNAGly genes, a putative pseudogene which encodes and expresses an unusual fifth tRNAGly isoacceptor in S. aureus (as detected via RT-PCR and subsequent direct sequencing analysis). All the in vitro transcribed tRNAGly molecules (including the “pseudogene-encoded” tRNAGly) can be efficiently aminoacylated by the recombinant S. aureus glycyl-tRNA synthetase. Furthermore, bioinformatic analysis suggests that the “pseudo”-tRNAGly(UCC) identified in the present study and two of the annotated isoacceptors bearing the same anticodon carry specific sequence elements that do not favour the strong interaction with EF-Tu that proteinogenic tRNAs would promote. This observation was verified by the differential capacity of Gly-tRNAGly molecules to form ternary complexes with activated S. aureus EF-Tu·GTP. These tRNAGly molecules display high sequence similarities with their S. epidermidis orthologs which also actively participate in cell wall synthesis. Both bioinformatic and biochemical data suggest that in S. aureus these three glycylated tRNAGly isoacceptors that are weak EF-Tu binders, possibly escape protein synthesis and serve as glycine donors for the formation of pentaglycine bridges that are essential for stabilization of the staphylococcal cell wall.
Journal: Biochimie - Volume 91, Issue 3, March 2009, Pages 344–351