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Excision of chromosomal DNA sequences from Streptomyces coelicolor forms a novel family of plasmids detectable in Streptomyces lividans

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Summary

When strains of Streptomyces coelicolor A3(2) lacking the previously identified autonomous plasmids SCP1 and SCP2 are crossed with Streptomyces lividans 66, some of the S. lividans progeny are able to elicit zones of growth inhibition (lethal zygosis), previously associated with the transfer of conjugative Streptomyces plasmids, when grown in contact with S. lividans 66. Some such progeny yield covalently closed circular (CCC) plasmid DNA, the size and restriction endonuclease cleavage pattern of which is constant for a particular isolate, but varies among isolates. These plasmid, which have been named SLP1.1, SLP1.2, ect., all confer resistance to lethal zygosis elicited by the others. Genetic and molecular characterization of the plasmids reveals that they are derived from the strA region of the chromosome of S. coelicolor. It is proposed that, before or during mating with S. lividans, the SLP1 sequences are excised from the chromosome, bringing varying regions of the surrounding chromosome with them, and can circularise to yield the SLP1 family of plasmids. Autonomous SLP1 plasmids can also be generated by cleaving total DNA of S. coelicolor with certain restriction enzymes, ligating it, and transforming the DNA into S. lividans.

The autonomous SLP1 plasmids exist within S. lividans in a few copies per chromosome, and act as fertility factors. They provide suitable vectors for DNA cloning since the segments of chromosomal DNA carried by the larger members of the family are dispensable.

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References

  • Bibb MJ (1981) Streptomyces plasmids: Their properties and use as cloning vehicles in antibiotic producing bacteria. In: Schlesinger D (ed) Microbiology 1981. American Society for Microbiology, Washington, DC, pp. 367–370

    Google Scholar 

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

    Google Scholar 

  • Bibb MJ, Hopwood DA (1981) Genetic studies of the fertility plasmid SCP2 and its SCP2* variants in Streptomyces coelicolor A3(2). J Gen Microbiol 126:427–442

    Google Scholar 

  • Bibb MJ, Schottel JL, Cohen SN (1980) A DNA cloning system for interspecies gene transfer in antibiotic-producing Streptomyces. Nature (Lond) 284:526–531

    Google Scholar 

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

    Google Scholar 

  • Bibb MJ, Ward JM, Hopwood DA (1980) Development of a cloning system for Streptomyces. Dev Ind Microbiol 21:55–64

    Google Scholar 

  • Carter JA, Chater KF, Bruton, CJ, Brown NL (1980) A comparions of DNA cleavage by the restriction enzymes SalPI and PstI. Nucleic Acids Res 8:4943–4954

    Google Scholar 

  • Chater KF, Hopwood DA (1982) Streptomyces genetics. In: Goodfellow M, Mordarski M, Williams ST (eds) Biology of the actinomycetes. Academic Press, London (in press)

    Google Scholar 

  • Gregory KF, Huang JCC (1964a) Tyrosinase inheritance in Streptomyces scabies. I. Genetic recombination. J Bacteriol 87:1281–1286

    Google Scholar 

  • Gregory KF, Huang JCC (1964b) Tyrosinase inheritance in Streptomyces scabies. II. Induction of tyrosinase deficiency by acridine dyes. J Bacteriol 87:1287–1294

    Google Scholar 

  • Gregory KF, Shyu WJ (1961) Apparent cytoplasmic inheritance of tyrosinase competence in Streptomyces scabies. Nature (Lond) 191:465–467

    Google Scholar 

  • Hayakawa T, Otake N, Yonehara H, Tanaka T, Sakaguchi K (1979) Isolation and characterization of plasmids from Streptomyces. J Antibiot 32:1348–1350

    Google Scholar 

  • Hopwood DA (1967) Genetic analysis and genome structure in Streptomyces coelicolor. Bact Rev 31:373–403

    Google Scholar 

  • Hopwood DA (1978) Extrachromosomally determined antibiotic production. Ann Rev Microbiol 32:373–392

    Google Scholar 

  • Hopwood DA (1979) Genetics of antibiotic production by actinomycetes. J Nat Products 42:596–602

    Google Scholar 

  • Hopwood DA, Bibb MJ, Ward JM, Westpheling J (1979) Plasmids in Streptomyces coelicolor and related species. In: Timmis KN, and Pühler A (eds) Plasmids of medical, environmental and commerical importance. Elsevier-North Holland, Amsterdam, pp 245–258

    Google Scholar 

  • Hopwood DA, Chater KF, Dowding JE, Vivian A (1973) Advances in Streptomyces coelicolor genetics Bacteriol Rev 37:371–405

    Google Scholar 

  • Hopwood DA, Thompson CJ, Ward JM, Kieser T, Wright HM (1981) Progress in the development of plasmid cloning vectors for Streptomyces. In: Schlesinger D (ed) Microbiology 1981, American Society for Microbiology, Washington DC, pp. 376–379

    Google Scholar 

  • Hopwood DA, Wright HM (1976) Interactions of the plasmid SCP1 with the chromosome of Streptomyces coelicolor A3(2). In: Macdonald KD (ed) Second International Symposium on the Genetics of Industrial Microorganisms. Academic Press, London, pp 607–619

    Google Scholar 

  • Hopwood DA, Wright HM, Bibb MJ, Cohen SN (1977) Genetic recombination through protoplast fusion in Streptomyces. Nature (Lond) 268:172–174

    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 

  • Kirby R, Wright LF, Hopwood DA (1975) Plasmid-determined antibiotic synthesis and resistance in Streptomyces coelicolor. Nature (Lond) 254:265–267

    Google Scholar 

  • Malik VS, Reusser F (1979) Restriction enzyme map for streptomycete plasmid pUC3. Plasmid 2:627–631

    Google Scholar 

  • Marmur J (1961) A procedure for the isolation of deoxyribonucleic acid from micro-organisms. J Mol Biol 3:208–218

    Google Scholar 

  • Nakano MM, Ozawa K, Ogawara H (1980) Isolation and characterization of a plasmid pSL1 from Streptomyces lavendulae. FEMS Microbiol Lett 9:111–113

    Google Scholar 

  • Okanishi M (1979) Plasmids and antibiotic synthesis in streptomycetes. In: Sebek OK and Laskin AI (eds) Genetics of industrial microorganisms. American Society for Microbiology, Washington, DC, pp 134–140

    Google Scholar 

  • Okanishi M, Manome T, Umezawa H (1980) Isolation and characteriaztion of plasmid DNA's in actinomycetes. J Antibiot 33:88–91

    Google Scholar 

  • Okanishi M, Ohta T, Umezawa H (1970) Possible control of formation of aerial mycelium and antibiotic production in Streptomyces by episomic factors. J Antibiot 23:45–47

    Google Scholar 

  • Schottel JL, Bibb MJ, Cohen SN (1981) Cloning and expression in Streptomyces lividans of antibiotic resistance genes derived from Escherichia coli. J Bacteriol, 146:360–368

    Google Scholar 

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

    Google Scholar 

  • Schrempf H, Goebel W (1977) Characterization of a plasmid from Streptomyces coelicolor A3(2). J Bacteriol 131:251–258

    Google Scholar 

  • Schrempf H, Goebel W (1979) Functions of plasmid genes in Streptomyces reticuli. In: Timmis KN and Pühler A (eds) Plasmids of medical, environmental and commerical importance. Elsevier-North Holland, Amsterdam, p 259–268

    Google Scholar 

  • Skurray RA, Reeves P (1973) Characterization of lethal zygosis associated with conjugation in Escherichia coli K12. J Bacteriol 113:58–70

    Google Scholar 

  • Sutcliffe JG (1978) pBR322 restriction map derived from the DNA sequence: accurate DNA size markers up to 4361 nucleotide pairs long. Nucleic Acids Res 5:2721–2728

    Google Scholar 

  • Thompson CJ, Ward JM, Hopwood DA (1980) DNA cloning in Streptomyces: resistance genes from antibiotic-producing species. Nature (Lond) 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 

  • Westpheling J (1980) Physical studies of Streptomyces plasmids. Ph. D. thesis, University of East Anglia, Norwich

    Google Scholar 

  • Wright LF, Hopwood DA (1976) Identification of the antibiotic determined by the SCP1 plasmid of Streptomyces coelicolor A3(2). J Gen Microbiol 95:96–106

    Google Scholar 

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Communicated by D. Sherratt

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Bibb, M.J., Ward, J.M., Kieser, T. et al. Excision of chromosomal DNA sequences from Streptomyces coelicolor forms a novel family of plasmids detectable in Streptomyces lividans . Molec. Gen. Genet. 184, 230–240 (1981). https://doi.org/10.1007/BF00272910

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