Affiliation:
1. Department of Biotechnology, Faculty of Bioresource Sciences, Akita Prefectural University, Akita 010-0195
2. Department of Bioactive Molecules, National Institute of Infectious Diseases, Tokyo 162-8640
3. Bioresource Laboratories, MERCIAN Corporation, Fujisawa 251-0057, Japan
Abstract
ABSTRACT
The occurrence of pleiotropic mutants that are defective in both antibiotic production and aerial mycelium formation is peculiar to streptomycetes. Pleiotropic mutant KSB was isolated from wild-type
Streptomyces kasugaensis
A1R6, which produces kasugamycin, an antifungal aminoglycoside antibiotic. A 9.3-kb DNA fragment was cloned from the chromosomal DNA of strain A1R6 by complementary restoration of kasugamycin production and aerial hypha formation to mutant KSB. Complementation experiments with deletion plasmids and subsequent DNA analysis indicated that
orf5
, encoding 90 amino acids, was responsible for the restoration. A protein homology search revealed that
orf5
was a homolog of
rpoZ
, the gene that is known to encode RNA polymerase subunit omega (ω), thus leading to the conclusion that
orf5
was
rpoZ
in
S. kasugaensis
. The pleiotropy of mutant KSB was attributed to a 2-bp frameshift deletion in the
rpoZ
region of mutant KSB, which probably resulted in a truncated, incomplete ω of 47 amino acids. Furthermore,
rpoZ
-disrupted mutant R6D4 obtained from strain A1R6 by insertion of Tn
5 aphII
into the middle of the
rpoZ
-coding region produced neither kasugamycin nor aerial mycelia, similar to mutant KSB. When
rpoZ
of
S. kasugaensis
and
Streptomyces coelicolor
, whose deduced products differed in the sixth amino acid residue, were introduced into mutant R6D4 via a plasmid, both transformants produced kasugamycin and aerial hyphae without significant differences. This study established that
rpoZ
is required for kasugamycin production and aerial mycelium formation in
S. kasugaensis
and responsible for pleiotropy.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Reference42 articles.
1. Akagawa, H., K. Kawaguchi, and M. Ichihara. 1984. Plasmids of Streptomyces kasugaensis MB273: their pock formation, their dispensable endonuclease cleavage sites for pock formation, and transformation of S. kasugaensis MB273 by them. J. Antibiot.37:1016-1025.
2. Akagawa, H., Y. Takano, and K. Kawaguchi. 1987. Characterization of a natural cointegrate of the pock-forming plasmids pSK1∗ and pSK2∗ of Streptomyces kasugaensis MB273. J. Gen. Microbiol.133:1941-1949.
3. Bernan, V., D. Filpula, W. Herver, M. Bibb, and E. Katz. 1985. The nucleotide sequence of the tyrosinase gene from Streptomyces antibioticus and characterization of the gene product. Gene37:101-110.
4. Bibb, M. J., G. R. Janssen, and J. M. Ward. 1986. Cloning and analysis of the promoter region of the erythromycin-resistance gene (ermE) of Streptomyces erythraeus. Gene41:E357-E368.
5. The ppGpp synthetase gene (relA) of Streptomyces coelicolor A3(2) plays a conditional role in antibiotic production and morphological differentiation
Cited by
29 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献