Affiliation:
1. Department of Biochemistry, University of Toronto, Toronto, Canada
Abstract
ABSTRACT
We recently described 13-deoxytetrodecamycin, a new member of the tetrodecamycin family of antibiotics. A defining feature of these molecules is the presence of a five-membered lactone called a tetronate ring. By sequencing the genome of a producer strain,
Streptomyces
sp. strain WAC04657, and searching for a gene previously implicated in tetronate ring formation, we identified the biosynthetic genes responsible for producing 13-deoxytetrodecamycin (the
ted
genes). Using the
ted
cluster in WAC04657 as a reference, we found related clusters in three other organisms:
Streptomyces atroolivaceus
ATCC 19725,
Streptomyces globisporus
NRRL B-2293, and
Streptomyces
sp. strain LaPpAH-202. Comparing the four clusters allowed us to identify the cluster boundaries. Genetic manipulation of the cluster confirmed the involvement of the
ted
genes in 13-deoxytetrodecamycin biosynthesis and revealed several additional molecules produced through the
ted
biosynthetic pathway, including tetrodecamycin, dihydrotetrodecamycin, and another, W5.9, a novel molecule. Comparison of the bioactivities of these four molecules suggests that they may act through the covalent modification of their target(s).
IMPORTANCE
The tetrodecamycins are a distinct subgroup of the tetronate family of secondary metabolites. Little is known about their biosynthesis or mechanisms of action, making them an attractive subject for investigation. In this paper we present the biosynthetic gene cluster for 13-deoxytetrodecamycin in
Streptomyces
sp. strain WAC04657. We identify related clusters in several other organisms and show that they produce related molecules.
Funder
Cystic Fibrosis Canada
Government of Canada | Canadian Institutes of Health Research
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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