Home LiteratureArticle Details
PMID: 2228956 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The level of a transcript required for production of a Streptomyces coelicolor antibiotic is conditionally dependent on a tRNA gene.

Journal of bacteriology ·Vol. 172 ·No. 11 ·1990-11-00 ·Pages 6189-93

Guthrie EP, Chater KF

Abstract

In Streptomyces coelicolor A3(2), bldA mutants are conditionally defective in aerial mycelium formation and fail to synthesize all four antibiotics produced by bldA+ strains. Previous studies showed that bldA specifies the tRNA for the rarely used leucine codon UUA. Here we describe experiments examining the abundance in a bldA mutant of a transcript involved in antibiotic production. With use of a bacteriophage-based integrative vector, a promotorless xylE reporter gene was inserted into a previously undescribed gene for an early step in biosynthesis of the red antibiotic undecylprodigiosin, located in the red gene cluster. With this transcriptional fusion present at unit copy number in the chromosome, xylE expression in a bldA+ strain was maximal late in growth in a liquid production medium and was virtually absent in a bldA mutant. On plates of a different medium, the bldA mutant was able to produce undecylprodigiosin and to express the red::xylE fusion, but both abilities were repressed by increasing the concentration of phosphate in the medium. These experiments showed that the undecylprodigiosin deficiency of bldA mutants cannot be accounted for by the presence of TTA codons in the red structural genes, but rather that bldA influences red gene mRNA abundance. In low-phosphate conditions, an alternative regulatory pathway can lead to red gene expression.

Related Genes
MeSH Terms
Anti-Bacterial Agents/biosynthesis Catechol 2,3-Dioxygenase Cloning, Molecular DNA, Bacterial/genetics,isolation & purification Dioxygenases Genes, Bacterial Genes, Regulator Genotype Oxygenases/genetics,metabolism Plasmids RNA, Transfer/genetics Streptomyces/enzymology,genetics Transcription, Genetic
Chemicals
Anti-Bacterial Agents DNA, Bacterial RNA, Transfer Oxygenases Dioxygenases Catechol 2,3-Dioxygenase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Guthrie E P
John Innes Institute, John Innes Centre for Plant Science Research, Norwich, United Kingdom.
Chater K F
References (19)
19 references, click to expand
  1. Characterization of temperate actinophage phi C31 isolated from Streptomyces coelicolor A3(2).
    J Virol. 1972 Feb;9(2):258-62 PMID: 5014931
  2. The improving prospects for yield increase by genetic engineering in antibiotic-producing Streptomycetes.
    Biotechnology (N Y). 1990 Feb;8(2):115-21 PMID: 1366556
  3. A morphological and genetic mapping study of bald colony mutants of Streptomyces coelicolor.
    J Gen Microbiol. 1976 Oct;96(2):299-315 PMID: 186556
  4. Isolation of DNA from agarose gels using DEAE-paper. Application to restriction site mapping of adenovirus type 16 DNA.
    Nucleic Acids Res. 1980 Jan 25;8(2):253-64 PMID: 6252542
  5. A pigmented mycelial antibiotic in Streptomyces coelicolor: control by a chromosomal gene cluster.
    J Gen Microbiol. 1980 Aug;119(2):333-40 PMID: 7229612
  6. New anthracyclines, feudomycins, produced by the mutant from Streptomyces coeruleorubidus ME130-A4.
    J Antibiot (Tokyo). 1981 Jul;34(7):783-90 PMID: 7287580
  7. Chromogenic identification of genetic regulatory signals in Bacillus subtilis based on expression of a cloned Pseudomonas gene.
    Proc Natl Acad Sci U S A. 1983 Feb;80(4):1101-5 PMID: 6405380
  8. Cloning of a Streptomyces gene for an O-methyltransferase involved in antibiotic biosynthesis.
    Mol Gen Genet. 1983;190(3):394-8 PMID: 6576223
  9. A new channel-forming antibiotic from Streptomyces coelicolor A3(2) which requires calcium for its activity.
    J Gen Microbiol. 1983 Dec;129(12):3565-73 PMID: 6321633
  10. Mutational cloning in Streptomyces and the isolation of antibiotic production genes.
    Gene. 1983 Dec;26(1):67-78 PMID: 6323253
  11. Molecular cloning of the whole biosynthetic pathway of a Streptomyces antibiotic and its expression in a heterologous host.
    Nature. 1984 May 31-Jun 6;309(5967):462-4 PMID: 6328317
  12. Resistance, regulatory and production genes for the antibiotic methylenomycin are clustered.
    EMBO J. 1985 Jul;4(7):1893-7 PMID: 2992952
  13. Phage-mediated cloning of bldA, a region involved in Streptomyces coelicolor morphological development, and its analysis by genetic complementation.
    J Bacteriol. 1985 Sep;163(3):965-72 PMID: 2993254
  14. Genetic and biochemical characterization of the red gene cluster of Streptomyces coelicolor A3(2).
    J Gen Microbiol. 1985 Sep;131(9):2431-41 PMID: 2999302
  15. Pleiotropic morphological and antibiotic deficiencies result from mutations in a gene encoding a tRNA-like product in Streptomyces coelicolor A3(2).
    Genes Dev. 1987 Dec;1(10):1305-10 PMID: 2448187
  16. New loci required for Streptomyces coelicolor morphological and physiological differentiation.
    J Bacteriol. 1988 Mar;170(3):1168-74 PMID: 3343216
  17. xylE functions as an efficient reporter gene in Streptomyces spp.: use for the study of galP1, a catabolite-controlled promoter.
    J Bacteriol. 1989 Dec;171(12):6617-24 PMID: 2592344
  18. Nucleotide sequence and transcriptional analysis of the redD locus of Streptomyces coelicolor A3(2).
    J Bacteriol. 1990 Jan;172(1):326-33 PMID: 2294088
  19. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
    Anal Biochem. 1976 May 7;72:248-54 PMID: 942051
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1990-11-00
Pages
6189-93
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC526799
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com