ABSTRACT
A representative set of 19 mutants, with a known genealogy, of the virginiamycin producing strain Streptomyces virginiae 899 was investigated phenotypically and genotypically. Colour of the aerial and substrate mycelium were very variable both among spontaneous variants and those obtained after induced mutagenesis. At genotypic level, all mutants showed nearly identical BOX patterns, not reflecting the phenotypic heterogeneity observed. More than 40 years of forced mutational pressure did not cause huge chromosomal distortions but was most likely limited to base substitutions. The species S. virginiae, including besides producers of virginiamycin the type strain and non-type strains producing other bioactive compounds, is genomically heterogeneous on the basis of BOX-PCR fingerprinting and DNA-DNA hybridizations. The virginiamycin producing strain 899 does not belong to the species S. virginiae despite its phenotypic similarity to the latter.
Subject(s)
Genes, Bacterial , Point Mutation/physiology , Streptomyces/genetics , Streptomyces/physiology , Virginiamycin/biosynthesis , Base Composition , DNA Fingerprinting , DNA, Bacterial/analysis , DNA, Bacterial/genetics , Nucleic Acid Hybridization , Pigments, Biological , Point Mutation/genetics , Polymorphism, Genetic , Streptomyces/classificationABSTRACT
The actinomycete Kibdelosporangium aridum naturally produces ardacin, a new glycopeptide antibiotic, the biosynthetic pathway of which should involve the participation of a polyketide synthase (PKS). A K. aridum 2.9 kb BamHI genomic fragment homologous to actI (a locus of the PKS cluster catalyzing polyketide chain assembly for actinorhodin biosynthesis in Streptomyces coelicolor) was isolated by shotgun cloning. This DNA fragment, called ardI, was sequenced and the deduced protein products were compared with those of other polyketide synthase genes, revealing similarities ranging from 50 to 80%. ardI was further used to probe a cosmid library of the K. aridum genome. Three hybridizing cosmids were obtained which contain overlapping inserts, together covering a 50 kb region, and including, 15 kb away from ardI, a fragment homologous to actIII, which codes for the ketoreductase of the actinorhodin PKS of S. coelicolor. All these findings indicate that at least part of a polyketide biosynthetic gene cluster has been isolated from the genome of the ardacin producer K. aridum.
Subject(s)
Actinomycetales/genetics , Aminoglycosides , Anti-Bacterial Agents/biosynthesis , Bacterial Proteins/genetics , Genes, Bacterial , Multienzyme Complexes/genetics , Amino Acid Sequence , Anti-Bacterial Agents/chemistry , Base Sequence , Cloning, Molecular , DNA, Bacterial/genetics , Molecular Sequence Data , Open Reading Frames , Sequence Alignment , Sequence Homology, Amino Acid , Species Specificity , Streptomyces/geneticsABSTRACT
Using the RP4::mini-Mu in vivo cloning technique, van Gijsegem et al. (1985) isolated several pel and cel genes of Erwinia chrysanthemi (Ech) B374 strain. We have localized these genes on the Ech chromosome by co-transfer mapping of MudI1734 insertion mutants and refined the map by co-transposition analysis. This analysis has enabled us to identify another cel gene.