» Articles » PMID: 7096267

Plasmid Loss and Changes Within the Chromosomal DNA of Streptomyces Reticuli

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1982 Aug 1
PMID 7096267
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

The sporulating wild-type strain of Streptomyces reticuli, which produces a melanin pigment and the macrolide leucomycin, contains plasmid DNA of 48 to 49 megadaltons. Plasmidless variants had an altered secondary metabolism and a changed antibiotic resistance pattern. By using a new colony hybridization technique developed for streptomycetes, it could be shown that plasmidless variants could be transformed with the wild-type plasmid DNA, which, however, is quickly lost from regenerated mycelium. In contrast to the wild-type strain, the plasmidless variants contain amplified nucleotide sequences within the chromosomal DNA. The number and size of these sequences vary with the strain tested. Hybridization studies revealed that the reiterated sequences are neither amplified ribosomal nor plasmid genes, but are present in small concentrations within the wild-type chromosome. Some of them share extensive homologies with each other and are located at different positions within the chromosome. It is assumed that alterations in secondary metabolism are due to changes within both the chromosomal and the extrachromosomal DNAs of S. reticuli.

Citing Articles

Production and Screening of High Yield Avermectin B1b Mutant of Streptomyces avermitilis 41445 Through Mutagenesis.

Siddique S, Syed Q, Adnan A, Ashraf Qureshi F Jundishapur J Microbiol. 2014; 7(2):e8626.

PMID: 25147669 PMC: 4138686. DOI: 10.5812/jjm.8626.


Screening of mutant strain Streptomyces mediolani sp. AC37 for (-)-8-O-methyltetrangomycin production enhancement.

Jimenez J, Sturdikova M, Brezova V, Svajdlenka E, Novotova M J Microbiol. 2013; 50(6):1014-23.

PMID: 23274989 DOI: 10.1007/s12275-012-2025-5.


Conformational changes in the novel redox sensor protein HbpS studied by site-directed spin labeling and its turnover in dependence on the catalase-peroxidase CpeB.

Klare J, Ortiz de Orue Lucana D Antioxid Redox Signal. 2011; 16(7):639-48.

PMID: 21846213 PMC: 3277929. DOI: 10.1089/ars.2011.4080.


Extracellular and intracellular polyphenol oxidases cause opposite effects on sensitivity of Streptomyces to phenolics: a case of double-edged sword.

Yang H, Chen C PLoS One. 2009; 4(10):e7462.

PMID: 19826489 PMC: 2758597. DOI: 10.1371/journal.pone.0007462.


Chromosome mapping in Alcaligenes eutrophus CH34.

Sadouk A, Mergeay M Mol Gen Genet. 1993; 240(2):181-7.

PMID: 8355652 DOI: 10.1007/BF00277055.


References
1.
Lerch K, Ettinger L . Purification and characterization of a tyrosinase from Streptomyces glaucescens. Eur J Biochem. 1972; 31(3):427-37. DOI: 10.1111/j.1432-1033.1972.tb02549.x. View

2.
Okanishi M, Suzuki K, Umezawa H . Formation and reversion of Streptomycete protoplasts: cultural condition and morphological study. J Gen Microbiol. 1974; 80(2):389-400. DOI: 10.1099/00221287-80-2-389. View

3.
OCALLAGHAN C, Morris A, Kirby S, Shingler A . Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate. Antimicrob Agents Chemother. 1972; 1(4):283-8. PMC: 444209. DOI: 10.1128/AAC.1.4.283. View

4.
Helling R, Goodman H, Boyer H . Analysis of endonuclease R-EcoRI fragments of DNA from lambdoid bacteriophages and other viruses by agarose-gel electrophoresis. J Virol. 1974; 14(5):1235-44. PMC: 355640. DOI: 10.1128/JVI.14.5.1235-1244.1974. View

5.
Schrempf H, Bujard H, Hopwood D, Goebel W . Isolation of covalently closed circular deoxyribonucleic acid from Streptomyces coelicolor A3(2). J Bacteriol. 1975; 121(2):416-21. PMC: 245946. DOI: 10.1128/jb.121.2.416-421.1975. View