Affiliation:
1. Institute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan
Abstract
ABSTRACT
Together, the
fomA
and
fomB
genes in the fosfomycin biosynthetic gene cluster of
Streptomyces wedmorensis
confer high-level fosfomycin resistance on
Escherichia coli
. To elucidate their functions, the
fomA
and
fomB
genes were overexpressed in
E. coli
and the gene products were characterized. The recombinant FomA protein converted fosfomycin to fosfomycin monophosphate, which was inactive on
E. coli
, in the presence of a magnesium ion and ATP. On the other hand, the recombinant FomB protein did not inactivate fosfomycin. However, a reaction mixture containing FomA and FomB proteins converted fosfomycin to fosfomycin monophosphate and fosfomycin diphosphate in the presence of ATP and a magnesium ion, indicating that FomA and FomB catalyzed phosphorylations of fosfomycin and fosfomycin monophosphate, respectively. These results suggest that the self-resistance mechanism of the fosfomycin-producing organism
S. wedmorensis
is mono- and diphosphorylation of the phosphonate function of fosfomycin catalyzed by FomA and FomB.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
55 articles.
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