Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 May;177(10):2870–2877. doi: 10.1128/jb.177.10.2870-2877.1995

Integrative and free Spiroplasma citri oriC plasmids: expression of the Spiroplasma phoeniceum spiralin in Spiroplasma citri.

J Renaudin 1, A Marais 1, E Verdin 1, S Duret 1, X Foissac 1, F Laigret 1, J M Bové 1
PMCID: PMC176961  PMID: 7751299

Abstract

The replication region (oriC) of the Spiroplasma citri chromosome has been recently sequenced, and a 2-kbp DNA fragment was characterized as an autonomously replicating sequence (F. Ye, J. Renaudin, J. M. Bové, and F. Laigret, Curr. Microbiol. 29:23-29, 1994). In the present studies, we have combined this DNA fragment, containing the dnaA gene and the flanking dnaA boxes, with a ColE1-derived Escherichia coli replicon and the Tet M determinant, which confers resistance to tetracycline. The recombinant plasmid, named pBOT1, was introduced into S. citri cells, in which it replicated. Plasmid pBOT1 was shuttled from E. coli to S. citri and back to E. coli. In S. citri, replication of pBOT1 did not require the presence of a functional dnaA gene on the plasmid. However, the dnaA box region downstream of the dnaA gene was essential. Upon passaging of the S. citri transformants, the plasmid integrated into the spiroplasmal host chromosome by recombination at the replication origin. The integration process led to duplication of the oriC sequences. In contrast to the integrative pBOT1, plasmid pOT1, which does not contain the E. coli replicon, was stably maintained as a free extrachromosomal element. Plasmid pOT1 was used as a vector to introduce into S. citri the G fragment of the cytadhesin P1 gene of Mycoplasma pneumoniae and the spiralin gene of Spiroplasma phoeniceum. The recombinant plasmids, pOTPG with the G fragment and pOTPS with the spiralin gene, were stably maintained in spiroplasmal transformants. Expression of the heterologous S. phoeniceum spiralin in S. citri was demonstrated by Western immunoblotting.

Full Text

The Full Text of this article is available as a PDF (589.3 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bové J. M., Foissac X., Saillard C. Spiralins. Subcell Biochem. 1993;20:203–223. doi: 10.1007/978-1-4615-2924-8_7. [DOI] [PubMed] [Google Scholar]
  2. Bové J. M. Molecular features of mollicutes. Clin Infect Dis. 1993 Aug;17 (Suppl 1):S10–S31. doi: 10.1093/clinids/17.supplement_1.s10. [DOI] [PubMed] [Google Scholar]
  3. Chevalier C., Saillard C., Bové J. M. Organization and nucleotide sequences of the Spiroplasma citri genes for ribosomal protein S2, elongation factor Ts, spiralin, phosphofructokinase, pyruvate kinase, and an unidentified protein. J Bacteriol. 1990 May;172(5):2693–2703. doi: 10.1128/jb.172.5.2693-2703.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chirgwin J. M., Przybyla A. E., MacDonald R. J., Rutter W. J. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry. 1979 Nov 27;18(24):5294–5299. doi: 10.1021/bi00591a005. [DOI] [PubMed] [Google Scholar]
  5. Dybvig K. Mycoplasmal genetics. Annu Rev Microbiol. 1990;44:81–104. doi: 10.1146/annurev.mi.44.100190.000501. [DOI] [PubMed] [Google Scholar]
  6. Dybvig K. Transformation of Acholeplasma laidlawii with streptococcal plasmids pVA868 and pVA920. Plasmid. 1989 Mar;21(2):155–160. doi: 10.1016/0147-619x(89)90061-9. [DOI] [PubMed] [Google Scholar]
  7. Gasparich G. E., Hackett K. J., Stamburski C., Renaudin J., Bové J. M. Optimization of methods for transfecting Spiroplasma citri strain R8A2 HP with the spiroplasma virus SpV1 replicative form. Plasmid. 1993 May;29(3):193–205. doi: 10.1006/plas.1993.1022. [DOI] [PubMed] [Google Scholar]
  8. Godson G. N., Vapnek D. A simple method of preparing large amounts of phiX174 RF 1 supercoiled DNA. Biochim Biophys Acta. 1973 Apr 11;299(4):516–520. doi: 10.1016/0005-2787(73)90223-2. [DOI] [PubMed] [Google Scholar]
  9. Hanahan D. Studies on transformation of Escherichia coli with plasmids. J Mol Biol. 1983 Jun 5;166(4):557–580. doi: 10.1016/s0022-2836(83)80284-8. [DOI] [PubMed] [Google Scholar]
  10. King K. W., Dybvig K. Mycoplasmal cloning vectors derived from plasmid pKMK1. Plasmid. 1994 Jan;31(1):49–59. doi: 10.1006/plas.1994.1006. [DOI] [PubMed] [Google Scholar]
  11. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  12. Marais A., Bove J. M., Dallo S. F., Baseman J. B., Renaudin J. Expression in Spiroplasma citri of an epitope carried on the G fragment of the cytadhesin P1 gene from Mycoplasma pneumoniae. J Bacteriol. 1993 May;175(9):2783–2787. doi: 10.1128/jb.175.9.2783-2787.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Moriya S., Atlung T., Hansen F. G., Yoshikawa H., Ogasawara N. Cloning of an autonomously replicating sequence (ars) from the Bacillus subtilis chromosome. Mol Microbiol. 1992 Feb;6(3):309–315. doi: 10.1111/j.1365-2958.1992.tb01473.x. [DOI] [PubMed] [Google Scholar]
  14. Moriya S., Firshein W., Yoshikawa H., Ogasawara N. Replication of a Bacillus subtilis oriC plasmid in vitro. Mol Microbiol. 1994 May;12(3):469–478. doi: 10.1111/j.1365-2958.1994.tb01035.x. [DOI] [PubMed] [Google Scholar]
  15. Ogasawara N., Moriya S., Yoshikawa H. Initiation of chromosome replication: structure and function of oriC and DnaA protein in eubacteria. Res Microbiol. 1991 Sep-Oct;142(7-8):851–859. doi: 10.1016/0923-2508(91)90065-i. [DOI] [PubMed] [Google Scholar]
  16. Renaudin J., Bové J. M. SpV1 and SpV4, spiroplasma viruses with circular, single-stranded DNA genomes, and their contribution to the molecular biology of spiroplasmas. Adv Virus Res. 1994;44:429–463. doi: 10.1016/s0065-3527(08)60335-8. [DOI] [PubMed] [Google Scholar]
  17. Renbaum P., Abrahamove D., Fainsod A., Wilson G. G., Rottem S., Razin A. Cloning, characterization, and expression in Escherichia coli of the gene coding for the CpG DNA methylase from Spiroplasma sp. strain MQ1(M.SssI). Nucleic Acids Res. 1990 Mar 11;18(5):1145–1152. doi: 10.1093/nar/18.5.1145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Stamburski C., Renaudin J., Bove J. M. First step toward a virus-derived vector for gene cloning and expression in spiroplasmas, organisms which read UGA as a tryptophan codon: synthesis of chloramphenicol acetyltransferase in Spiroplasma citri. J Bacteriol. 1991 Apr;173(7):2225–2230. doi: 10.1128/jb.173.7.2225-2230.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Stamburski C., Renaudin J., Bové J. M. Mutagenesis of a tryptophan codon from TGG to TGA in the cat gene does not prevent its expression in the helical mollicute Spiroplasma citri. Gene. 1992 Jan 2;110(1):133–134. doi: 10.1016/0378-1119(92)90458-2. [DOI] [PubMed] [Google Scholar]
  20. Stephens M. A. Partial purification and cleavage specificity of a site-specific endonuclease, SciNI, isolated from Spiroplasma citri. J Bacteriol. 1982 Feb;149(2):508–514. doi: 10.1128/jb.149.2.508-514.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Su C. J., Chavoya A., Baseman J. B. Regions of Mycoplasma pneumoniae cytadhesin P1 structural gene exist as multiple copies. Infect Immun. 1988 Dec;56(12):3157–3161. doi: 10.1128/iai.56.12.3157-3161.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Weisburg W. G., Tully J. G., Rose D. L., Petzel J. P., Oyaizu H., Yang D., Mandelco L., Sechrest J., Lawrence T. G., Van Etten J. A phylogenetic analysis of the mycoplasmas: basis for their classification. J Bacteriol. 1989 Dec;171(12):6455–6467. doi: 10.1128/jb.171.12.6455-6467.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Williamson D. L., Renaudin J., Bové J. M. Nucleotide sequence of the Spiroplasma citri fibril protein gene. J Bacteriol. 1991 Jul;173(14):4353–4362. doi: 10.1128/jb.173.14.4353-4362.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Ye F., Laigret F., Whitley J. C., Citti C., Finch L. R., Carle P., Renaudin J., Bové J. M. A physical and genetic map of the Spiroplasma citri genome. Nucleic Acids Res. 1992 Apr 11;20(7):1559–1565. doi: 10.1093/nar/20.7.1559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Ye F., Renaudin J., Bové J. M., Laigret F. Cloning and sequencing of the replication origin (oriC) of the Spiroplasma citri chromosome and construction of autonomously replicating artificial plasmids. Curr Microbiol. 1994 Jul;29(1):23–29. doi: 10.1007/BF01570187. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES