Journal article
Broad spectrum aminoglycoside phosphotransferase type III from Enterococcus: overexpression, purification, and substrate specificity.
Abstract
The aminoglycoside phosphotransferases (APHs) are responsible for the bacterial inactivation of many clinically useful aminoglycoside antibiotics. We report the characterization of an enterococcal enzyme, APH(3')-IIIa, which inactivates a broad spectrum of aminoglycosides by ATP-dependent O-phosphorylation. Overproduction of APH(3')-IIIa has permitted the isolation of 30-40 mg of pure protein/(L of cell culture). Purified APH(3')-IIIa is a …
Authors
McKay GA; Thompson PR; Wright GD
Journal
Biochemistry, Vol. 33, No. 22, pp. 6936–6944
Publisher
American Chemical Society (ACS)
Publication Date
June 7, 1994
DOI
10.1021/bi00188a024
ISSN
0006-2960
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AminoglycosidesAnti-Bacterial AgentsBase SequenceCarbohydrate SequenceDrug Resistance, MicrobialEnterococcusEscherichia coliGene Expression Regulation, BacterialGene Expression Regulation, EnzymologicKanamycin KinaseKineticsMolecular Sequence DataPhosphotransferases (Alcohol Group Acceptor)Recombinant ProteinsSubstrate Specificity