Amplification of a particular DNA sequence in Streptomyces ambofaciens RP181110 reversibly prevents spiramycin production

Research in Microbiology
1992.0

Abstract

Streptomyces ambofaciens RP181110 produces the macrolide antibiotic spiramycin. After treatment with ethidium bromide, 7 strains presenting an amplified sequence of DNA (ADS) were found in its progeny. These ADS were localized within the same amplifiable region of the RP181110 genome. It has been established that these amplified strains were non-producers (Spi-) and that the loss of one particular ADS was correlated with restoration of spiramycin production. Genome rearrangements such as deletions were detected on the same side of the amplifiable region in both amplified and deamplified strains.

Knowledge Graph

Similar Paper

Amplification of a particular DNA sequence in Streptomyces ambofaciens RP181110 reversibly prevents spiramycin production
Research in Microbiology 1992.0
An amplifiable and deletable locus of Streptomyces ambofaciens RP181110 contains a very large gene homologous to polyketide synthase genes
Microbiology 1996.0
Genetic and biochemical features of spiramycin biosynthesis in Streptomyces ambofaciens. Curing, protoplast regeneration and plasmid transfer.
The Journal of Antibiotics 1982.0
Modulation of Lipid Metabolism and Spiramycin Biosynthesis in <i>Streptomyces ambofaciens</i> Unstable Mutants
Applied and Environmental Microbiology 1999.0
Dispensable ribosomal resistance to spiramycin conferred by srmA in the spiramycin producer Streptomyces ambofaciens The EMBL/GenBank accession number for the nucleotide sequence described in this paper is AJ223970.
Microbiology 1999.0
Improvement of macrolide antibiotic-producing streptomycete strains by the regeneration of protoplasts.
The Journal of Antibiotics 1983.0
Resistance to spiramycin in Streptomyces ambofaciens, the producer organism, involves at least two different mechanisms
Journal of General Microbiology 1993.0
Resistance to macrolides, lincosamides and streptogramin type B antibiotics due to a mutation in an rRNA operon of Streptomyces ambofaciens.
The EMBO Journal 1988.0
Selection of Streptomyces ambofaciens mutants that produce large quantities of spiramycin and determination of optimal conditions for spiramycin production
Applied and Environmental Microbiology 1990.0
Cloning of spiramycin biosynthetic genes and their use in constructing Streptomyces ambofaciens mutants defective in spiramycin biosynthesis
Journal of Bacteriology 1990.0