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Plasmids in different strains of Streptomyces ambofaciens: free and integrated form of plasmid pSAM2

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Summary

Five strains of Streptomyces ambofaciens were examined for their plasmid content. Among these strains, four belong to the same lineage (strains B) and the other was isolated independently (strain A). A large plasmid (ca. 80 kb), called pSAM1 in this paper and already described, was present in all B strains, and absent in strain A. A second plasmid, not described before, was found as covalently closed circular DNA in two of the four B strains. This plasmid with a size 11.1 kb was called pSAM2. A restriction map for 14 enzymes was established. Hybridization experiments showed that a unique sequence homologous to this plasmid is integrated in a larger replicon, which is not pSAM1 and is probably the chromosome, in all B strains and not in strain A. It seems probable that the integrated se1uence is the origin of the free plasmid found in two strains of the B family. It is noteworthy that the integrated form and the free plasmid may be found together. Transformation experiments proved that pSAM2 may be maintained autonomously in S. ambofaciens strain A and in S. lividans. pSAM2 is a self-transmissible plasmid, able to elicit the lethal zygosis reaction. pSAM2 was compared to the plasmids SLP1, pIJ110 and pIJ408, which all come from integrated sequences in three Streptomyces species and are found as autonomous plasmids after transfer to S. lividans. If pSAM2 resembles these plasmids in its origin, it does not appear to be related directly to them. Concerning their plasmid content, the two isolates of S. ambofaciens are very different. One of them contains neither pSAM1 not pSAM2. As this isolate produces spiramycin, these plasmids probably do not play an important role in spiramycin production. Apart from its intrinsic biological interest, pSAM2 may be useful in the construction of cloning vectors for S. ambofaciens. Very stable transformants might be obtained in certain strains of S. ambofaciens, because of the possibility of integration of the pSAM2 derivative vector.

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References

  • Bibb MJ, Freeman RF, Hopwood DA (1977) Physical and genetical characterization of a second sex factor, SCP2 for Streptomyces coelicolor A3 (2) Mol Gen Genet 154:155–166

    Google Scholar 

  • Bidd MJ, Ward JM, Hopwood DA (1978) Transformation of plasmid DNA into Streptomyces at high frequency. Nature 274:398–400

    Google Scholar 

  • Bibb MJ, Ward JM, Kieser T, Cohen SN, Hopwood DA (1981) Excision of chromosomal DNA sequences from Streptomyces coelicolor forms a novel family of plasmids detectable in Streptomyces lividans. Mol Gen Genet 184:230–240

    Google Scholar 

  • Daniels DL, Schroeder JL, Blattner FR, Szybalski W, Sanger F (1983) A molecular map of coliphage lambda. In: Hendrix RW, Roberts JW, Stahl FW, Weisberg RA (eds) Lambda II Appendix I. Cold Spring Harbor Laboratory, New York,p 469–517

    Google Scholar 

  • Hintermann G, Crameri R, Kieser T, Hütter R (1981) Restriction analysis of the Streptomyces glaucescens genome by agarose gel electrophoresis. Arch Microbiol 130:218–222

    Google Scholar 

  • Hopwood DA, Wright HM (1973) Transfer of a plasmid between Streptomyces species. J Gen Microbiol 77:187–195

    Google Scholar 

  • Hopwood DA, Wright HM (1976) Interactions of the plasmid SCP1 with the chromosome of Streptomyces coelicolor A32 (2). In McDonald KD (ed) Second International Symposium on the Genetics of Industrial Microoganisms. Academic Press, London, p 607–619

    Google Scholar 

  • Hopwood DA, Kieser T, Wright HM, Bibb MJ (1983) Plasmids, recombination and chromosome mapping in Streptomyces lividans 66. J Gen Microbiol 129:2257–2269

    Google Scholar 

  • Hopwood DA, Hintermann G, Kieser T, Wright HM (1984) Intergrated DNA sequences in three Streptomycetes form related autonomous plasmids after transfer to Streptomyces lividans. Plasmid 11:1–16

    Google Scholar 

  • Hütter R (1967) Systematik der Streptomyceten. Bibliotheka microbiologica fase 6, S Karger Verlag, Basel New York, p 274–275

    Google Scholar 

  • Ikeda H, Tanaka H, Omura S (1982a) Isolation and characterization of covalently closed circular DNA associated with chromosomal and membrane fraction from Streptomyces ambofaciens. J Antibiot 35:497–506

    Google Scholar 

  • Ikeda H, Tanaka H, Omura S (1982b) Genetic and biochemical features of spiramycin biosynthesis in Streptomyces ambofaciens. Curing, protoplast regeneration and plasmid transfer. J Antibiot 35:507–516

    Google Scholar 

  • Kieser T, Hopwood DA, Wright HM, Thompson CJ (1982) pIJ101, a multi-copy broad host-range Streptomyces plasmid: functional analysis and development of DNA cloning vectors. Mol Gen Genet 185:223–238

    Google Scholar 

  • Kirby R, Hopwood DA (1977) Genetic determination of methylenomycin synthesis by the SCP1 plasmid of Streptomyces coelicolor A3 (2). J Gen Microbiol 98:239–252

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular cloning. Cold Spring Harbor Laboratory, New York

    Google Scholar 

  • Ogata S, Koyama Y, Sakaki Y, Hayashida S (1983) Isolation of a linear DNA associated with pock formation in Streptomyces azureus. Agric Biol Chem 47:2127–2129

    Google Scholar 

  • Omura S, Ikeda H, Kitao C (1979) The detection of a plasmid in Streptomyces ambofaciens KA-1028 and its possible involvement in spiramycin production. J Antibiot 32:1058–1060

    Google Scholar 

  • Omura S, Ikeda H, Tanaka H (1981) Extraction and characterization of plasmids from macrolide antibiotic producing Streptomycetes. J Antibiot 34:478–482

    Google Scholar 

  • Ono H, Hintermann G, Crameri R, Wallis G, Hütter R (1982) Reiterated DNA sequences in a mutant strain of Streptomyces glaucescens and cloning of the sequence in Escherichia coli. Mol Gen Genet 186:106–110

    Google Scholar 

  • Pinnert-Sindico S, Ninet L, Preud'homme J, Cosar C (1955) A new antibiotic Spiramycin. Antibiotics annual 1954–1955 p 724–727

  • Pridham TG, Anderson P, Foley C, Lindenfelser LA, Hesseltine CW, Benetdict RC (1957) A selection of media for maintenance and taxnomic study of Streptomyces. Antibiotics annual 1956–1957, p 947–953

  • Rigby PWJ, Dieckmann M, Rhodes C, Berg P (1977) Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol 113:237–251

    Google Scholar 

  • Schrempf H, Bujard H, Hopwood DA, Goebel W (1975) Isolation of covalently closed circular deoxyribonucleic acid from Streptomyces coelicolor A3 (2). J Bacteriol 121:416–421

    Google Scholar 

  • Schrempf H (1982a) Role of plasmids in producers of macrolides. J Chem Tech Biotechnol 32:292–295

    Google Scholar 

  • Schrempf H (1982b) Plasmid loss and change within the chromosomal DNA of Streptomyces reticuli. J Bacteriol 151:701–707

    Google Scholar 

  • Schrempf H (1983) Deletion and amplification of DNA sequences in melanin-negative variants of Streptomyces reticuli. Mol Gen Genet 189:501–505

    Google Scholar 

  • Schroeder JL, Blattner FR (1978) Least-squares method for restriction mapping. Gene 4:167–174

    Google Scholar 

  • Thompson CJ, Ward JM, Hopwood DA (1980) DNA cloning in Streptomyces: Resistance genes from antibiotic-producing species. Nature 286:525–527

    Google Scholar 

  • Vivian A (1971) Genetic control of fertility in Streptomyces coelicolor A3 (2): plasmid involvement in the interconversion of UF and IF strains. J Gen Microbiol 69:353–364

    Google Scholar 

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Communicated by W. Gajewski

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Pernodet, JL., Simonet, JM. & Guérineau, M. Plasmids in different strains of Streptomyces ambofaciens: free and integrated form of plasmid pSAM2. Molec Gen Genet 198, 35–41 (1984). https://doi.org/10.1007/BF00328697

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  • DOI: https://doi.org/10.1007/BF00328697

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