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PMID: 6269486 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

New plasmid-mediated aminoglycoside adenylyltransferase of broad substrate range that adenylylates amikacin.

Antimicrobial agents and chemotherapy ·Vol. 20 ·No. 1 ·1981-07-00 ·Pages 75-80

Coombe RG, George AM

Abstract

The same aminoglycoside 2"-adenylyltransferase was isolated from four gram-negative species which were among a random group of gentamicin-resistant isolates from the same hospital. The enzyme was partially purified from a crude extract which also contained a second modifying enzyme identified as APH(3')-I. The substrate range of the new aminoglycoside 2"-adenylyltransferase included the newer aminoglycosides sisomicin and amikacin, but showed much-reduced activity against gentamicins C2 and Cla. The pH optimum was 7.8 to 8.0 for every substrate, and the molecular weight of the enzyme molecule was estimated at approximately 29,000. Genetic experiments clearly established that both enzymes were expressed by a conjugative plasmid.

MeSH Terms
Amikacin/metabolism Aminoglycosides/metabolism Conjugation, Genetic Cross Infection/microbiology Gentamicins/genetics,metabolism Humans Hydrogen-Ion Concentration Kanamycin/analogs & derivatives Klebsiella pneumoniae/enzymology,genetics Molecular Weight Nucleotidyltransferases/genetics,metabolism Plasmids Substrate Specificity
Chemicals
Aminoglycosides Gentamicins Kanamycin Amikacin Nucleotidyltransferases gentamicin 2''-nucleotidyltransferase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Coombe R G
George A M
References (12)
12 references, click to expand
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1981-07-00
Pages
75-80
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC181636
Subset
IM
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