Literature DB >> 17092809

Origins of the aminoglycoside modifying enzymes.

P N Rather1.   

Abstract

The aminoglycosides represent an important class of antibiotics for the treatment of bacterial infections. Interaction of the aminoglycosides with the bacterial ribosome inhibits protein synthesis, which is their primary mode of action. However, in gram negative bacteria, the ability of aminoglycosides to perturb the cell envelope is also an important mode of action. A common mechanism for aminoglycoside resistance involves modifying enzymes which acetylate, phosphorylate or adenylylate the aminoglycoside. There exists a staggering number of aminoglycoside modifying enzymes in clinical isolates of bacteria. This diversity suggests multiple origins for the present day enzymes. In this review, the possible origins of these modifying enzymes will be presented. Previous proposals describing the origins of these enzymes will be reviewed and potential mechanisms for the development of new aminoglycoside modifying enzymes will be discussed.

Entities:  

Year:  1998        PMID: 17092809     DOI: 10.1016/s1368-7646(98)80044-7

Source DB:  PubMed          Journal:  Drug Resist Updat        ISSN: 1368-7646            Impact factor:   18.500


  5 in total

1.  Activation of the 2'-N-acetyltransferase gene [aac(2')-Ia] in Providencia stuartii by an interaction of AarP with the promoter region.

Authors:  D R Macinga; M R Paradise; M M Parojcic; P N Rather
Journal:  Antimicrob Agents Chemother       Date:  1999-07       Impact factor: 5.191

2.  Activation of the cryptic aac(6')-Iy aminoglycoside resistance gene of Salmonella by a chromosomal deletion generating a transcriptional fusion.

Authors:  S Magnet; P Courvalin; T Lambert
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

3.  Characterization of the chromosomal aac(6')-Iz gene of Stenotrophomonas maltophilia.

Authors:  T Lambert; M C Ploy; F Denis; P Courvalin
Journal:  Antimicrob Agents Chemother       Date:  1999-10       Impact factor: 5.191

4.  Aminoglycoside resistance in Mycobacterium kansasii, Mycobacterium avium-M. intracellulare, and Mycobacterium fortuitum: are aminoglycoside-modifying enzymes responsible?

Authors:  I I Ho; C Y Chan; A F Cheng
Journal:  Antimicrob Agents Chemother       Date:  2000-01       Impact factor: 5.191

Review 5.  Small-Molecule Acetylation by GCN5-Related N-Acetyltransferases in Bacteria.

Authors:  Rachel M Burckhardt; Jorge C Escalante-Semerena
Journal:  Microbiol Mol Biol Rev       Date:  2020-04-15       Impact factor: 11.056

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.