Affiliation:
1. Department of Molecular Microbiology, John Innes Centre, Norwich, United Kingdom
Abstract
ABSTRACT
The
bldC
locus, required for formation of aerial hyphae in
Streptomyces coelicolor
, was localized by map-based cloning to the overlap between cosmids D17 and D25 of a minimal ordered library. Subcloning and sequencing showed that
bldC
encodes a member of a previously unrecognized family of small (58- to 78-residue) DNA-binding proteins, related to the DNA-binding domains of the MerR family of transcriptional activators. BldC family members are found in a wide range of gram-positive and gram-negative bacteria. Constructed
ΔbldC
mutants were defective in differentiation and antibiotic production. They failed to form an aerial mycelium on minimal medium and showed severe delays in aerial mycelium formation on rich medium. In addition, they failed to produce the polyketide antibiotic actinorhodin, and
bldC
was shown to be required for normal and sustained transcription of the pathway-specific activator gene
actII-orf4
. Although
ΔbldC
mutants produced the tripyrrole antibiotic undecylprodigiosin, transcripts of the pathway-specific activator gene (
redD
) were reduced to almost undetectable levels after 48 h in the
bldC
mutant, in contrast to the
bldC
+
parent strain in which
redD
transcription continued during aerial mycelium formation and sporulation. This suggests that
bldC
may be required for maintenance of
redD
transcription during differentiation.
bldC
is expressed from a single promoter. S1 nuclease protection assays and immunoblotting showed that
bldC
is constitutively expressed and that transcription of
bldC
does not depend on any of the other known
bld
genes. The
bldC18
mutation that originally defined the locus causes a Y49C substitution that results in instability of the protein.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
37 articles.
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