Affiliation:
1. Department of Biological Sciences, University of Alberta, Edmonton T6G 2E9, Canada
2. Glaxo SmithKline Pharmaceuticals, Worthing, West Sussex BN14 8QH, England
Abstract
ABSTRACT
An approximately 12.5-kbp region of DNA sequence from beyond the end of the previously described clavulanic acid gene cluster was analyzed and found to encode nine possible open reading frames (ORFs). Involvement of these ORFs in clavulanic acid biosynthesis was assessed by creating mutants with defects in each of the ORFs
. orf12
and
orf14
had been previously reported to be involved in clavulanic acid biosynthesis. Now five additional ORFs are shown to play a role, since their mutation results in a significant decrease or total absence of clavulanic acid production. Most of these newly described ORFs encode proteins with little similarity to others in the databases, and so their roles in clavulanic acid biosynthesis are unclear. Mutation of two of the ORFs,
orf15
and
orf16
, results in the accumulation of a new metabolite,
N
-acetylglycylclavaminic acid, in place of clavulanic acid.
orf18
and
orf19
encode apparent penicillin binding proteins, and while mutations in these genes have minimal effects on clavulanic acid production, their normal roles as cell wall biosynthetic enzymes and as targets for β-lactam antibiotics, together with their clustered location, suggest that they are part of the clavulanic acid gene cluster.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
42 articles.
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