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Functional characterisation of methyltransferase Sgm (CROSBI ID 522587)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa

Čubrilo, Sonja ; Maravić, Gordana Functional characterisation of methyltransferase Sgm // 1st MedILS Summer School, Structure and Evolution: from Bench to Terminal, Book of Abstracts. 2006. str. 25-26-x

Podaci o odgovornosti

Čubrilo, Sonja ; Maravić, Gordana

engleski

Functional characterisation of methyltransferase Sgm

Methylation is the most frequent posttranscriptional modification found in rRNA, exerted mostly by S-adenosyl-methionine dependent methylases. Furthermore, in addition to the essential set of enzymes, some antibiotic producing bacteria as well as ever growing number of antibiotic resistant strains contain different rRNA methylases, which protect their protein synthesis machinery from the destructive action of ribosomal antibiotics. The self-defense mechanism of natural producers of deoxystreptamine-containing aminoglycoside antibiotics is methylation of a specific guanine residue within the 16S rRNA. In addition, this is a relatively new mechanism of resistance found in members of clinically important Enterobacteriaceae family and in Pseudomonas aeruginosa and Serratia marcescens clinical strains. Methylation of 16S rRNA in aminoglycoside resistant bacteria is carried out by enzymes from the aminoglycoside resistance methylase (Agr) family, which are now found to be spreading among clinical strains by rapid horizontal transfer. Very little is known on the mechanism of action of Agr methylases, while the structural data virtually do not exist. We are therefore studying the molecular basis of this mechanism, in order to help to prevent it before it becomes omnipresent, especially among multiresistant pathogens. The aim of our study is to functionally characterise the methyltransferase Sgm. We cloned the sgm gene into vectors pUC19 and pET-25b(+) and developed the assays for functional tests in vivo. We are now optimising the conditions for the methylation test in vitro. By site-directed mutagenesis we will investigate the roles of evolutionary conserved amino acids and define the localisation of the active site and cofactor S-adenosyl-methione binding site. This will enable us to propose a reaction mechanism and to gain insight into possibilities of finding a specific inhibitor that would block aminoglycoside resistance based on ribosome methylation.

aminoglycosides; resistance; methyltransferase Sgm

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Podaci o prilogu

25-26-x.

2006.

objavljeno

Podaci o matičnoj publikaciji

1st MedILS Summer School, Structure and Evolution: from Bench to Terminal, Book of Abstracts

Podaci o skupu

1st MedILS Summer School Structure and Evolution: from Bench to Terminal

poster

18.07.2006-22.07.2006

Split, Hrvatska

Povezanost rada

Biologija