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. 1989 Apr;2(Suppl):S146–S149. doi: 10.1128/cmr.2.suppl.s146

Introduction of cloned genes into Neisseria gonorrhoeae.

D C Stein 1
PMCID: PMC358092  PMID: 2497957

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S146

Selected References

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

  1. Biswas G. D., Graves J. F., Sox T. E., Tenover F. C., Sparling P. F. Marker rescue by a homologous recipient plasmid during transformation of gonococci by a hybrid Pcr plasmid. J Bacteriol. 1982 Jul;151(1):77–82. doi: 10.1128/jb.151.1.77-82.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Biswas G. D., Sox T., Blackman E., Sparling P. F. Factors affecting genetic transformation of Neisseria gonorrhoeae. J Bacteriol. 1977 Feb;129(2):983–992. doi: 10.1128/jb.129.2.983-992.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Biswas G. D., Sparling P. F. Entry of double-stranded deoxyribonucleic acid during transformation of Neisseria gonorrhoeae. J Bacteriol. 1981 Jan;145(1):638–640. doi: 10.1128/jb.145.1.638-640.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Campbell L. A., Yasbin R. E. Mutagenesis of Neisseria gonorrhoeae: absence of error-prone repair. J Bacteriol. 1984 Oct;160(1):288–293. doi: 10.1128/jb.160.1.288-293.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cannon J. G., Sparling P. F. The genetics of the gonococcus. Annu Rev Microbiol. 1984;38:111–133. doi: 10.1146/annurev.mi.38.100184.000551. [DOI] [PubMed] [Google Scholar]
  6. Flett F., Humphreys G. O., Saunders J. R. Intraspecific and intergeneric mobilization of non-conjugative resistance plasmids by a 24.5 megadalton conjugative plasmid of Neisseria gonorrhoeae. J Gen Microbiol. 1981 Jul;125(1):123–129. doi: 10.1099/00221287-125-1-123. [DOI] [PubMed] [Google Scholar]
  7. Genco C. A., Knapp J. S., Clark V. L. Conjugation of plasmids of Neisseria gonorrhoeae to other Neisseria species: potential reservoirs for the beta-lactamase plasmid. J Infect Dis. 1984 Sep;150(3):397–401. doi: 10.1093/infdis/150.3.397. [DOI] [PubMed] [Google Scholar]
  8. Gouby A., Bourg G., Ramuz M. Previously undescribed 6.6-kilobase R plasmid in penicillinase-producing Neisseria gonorrhoeae. Antimicrob Agents Chemother. 1986 Jun;29(6):1095–1097. doi: 10.1128/aac.29.6.1095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Graves J. F., Biswas G. D., Sparling P. F. Sequence-specific DNA uptake in transformation of Neisseria gonorrhoeae. J Bacteriol. 1982 Dec;152(3):1071–1077. doi: 10.1128/jb.152.3.1071-1077.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Guymon L. F., Esser M., Shafer W. M. Pyocin-resistant lipopolysaccharide mutans of Neisseria gonorrhoeae: alterations in sensitivity to normal human serum and polymyxin B. Infect Immun. 1982 May;36(2):541–547. doi: 10.1128/iai.36.2.541-547.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Johnson S. R., Anderson B. E., Biddle J. W., Perkins G. H., DeWitt W. E. Characterization of concatemeric plasmids of Neisseria gonorrhoeae. Infect Immun. 1983 May;40(2):843–846. doi: 10.1128/iai.40.2.843-846.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Koomey J. M., Falkow S. Cloning of the recA gene of Neisseria gonorrhoeae and construction of gonococcal recA mutants. J Bacteriol. 1987 Feb;169(2):790–795. doi: 10.1128/jb.169.2.790-795.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Koomey J. M., Gill R. E., Falkow S. Genetic and biochemical analysis of gonococcal IgA1 protease: cloning in Escherichia coli and construction of mutants of gonococci that fail to produce the activity. Proc Natl Acad Sci U S A. 1982 Dec;79(24):7881–7885. doi: 10.1073/pnas.79.24.7881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Morse S. A., Johnson S. R., Biddle J. W., Roberts M. C. High-level tetracycline resistance in Neisseria gonorrhoeae is result of acquisition of streptococcal tetM determinant. Antimicrob Agents Chemother. 1986 Nov;30(5):664–670. doi: 10.1128/aac.30.5.664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Phillips I. Beta-lactamase-producing, penicillin-resistant gonococcus. Lancet. 1976 Sep 25;2(7987):656–657. doi: 10.1016/s0140-6736(76)92466-1. [DOI] [PubMed] [Google Scholar]
  16. Piffaretti J. C., Arini A., Frey J. pUB307 mobilizes resistance plasmids from Escherichia coli into Neisseria gonorrhoeae. Mol Gen Genet. 1988 May;212(2):215–218. doi: 10.1007/BF00334687. [DOI] [PubMed] [Google Scholar]
  17. Roberts M., Falkow S. Conjugal transfer of R plasmids in Neisseria gonorrhoeae. Nature. 1977 Apr 14;266(5603):630–631. doi: 10.1038/266630a0. [DOI] [PubMed] [Google Scholar]
  18. Roberts M., Piot P., Falkow S. The ecology of gonococcal plasmids. J Gen Microbiol. 1979 Oct;114(2):491–494. doi: 10.1099/00221287-114-2-491. [DOI] [PubMed] [Google Scholar]
  19. Seifert H. S., So M. Genetic mechanisms of bacterial antigenic variation. Microbiol Rev. 1988 Sep;52(3):327–336. doi: 10.1128/mr.52.3.327-336.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Shafer W. M., Joiner K., Guymon L. F., Cohen M. S., Sparling P. F. Serum sensitivity of Neisseria gonorrhoeae: the role of lipopolysaccharide. J Infect Dis. 1984 Feb;149(2):175–183. doi: 10.1093/infdis/149.2.175. [DOI] [PubMed] [Google Scholar]
  21. Sox T. E., Mohammed W., Sparling P. F. Transformation-derived Neisseria gonorrhoeae plasmids with altered structure and function. J Bacteriol. 1979 May;138(2):510–518. doi: 10.1128/jb.138.2.510-518.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Sparling P. F. Genetic transformation of Neisseria gonorrhoeae to streptomycin resistance. J Bacteriol. 1966 Nov;92(5):1364–1371. doi: 10.1128/jb.92.5.1364-1371.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Stein D. C., Gregoire S., Piekarowicz A. Restriction of plasmid DNA during transformation but not conjugation in Neisseria gonorrhoeae. Infect Immun. 1988 Jan;56(1):112–116. doi: 10.1128/iai.56.1.112-116.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Stein D. C., Petricoin E. F., Griffiss J. M., Schneider H. Use of transformation to construct Neisseria gonorrhoeae strains with altered lipooligosaccharides. Infect Immun. 1988 Apr;56(4):762–765. doi: 10.1128/iai.56.4.762-765.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Stein D. C., Silver L. E., Clark V. L., Young F. E. Cloning genes for proline biosynthesis from Neisseria gonorrhoeae: identification by interspecific complementation of Escherichia coli mutants. J Bacteriol. 1984 May;158(2):696–700. doi: 10.1128/jb.158.2.696-700.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Stein D. C., Silver L. E., Clark V. L., Young F. E. Construction and characterization of a new shuttle vector, pLES2, capable of functioning in Escherichia coli and Neisseria gonorrhoeae. Gene. 1983 Nov;25(2-3):241–247. doi: 10.1016/0378-1119(83)90228-7. [DOI] [PubMed] [Google Scholar]
  27. Stein D. C., Young F. E., Tenover F. C., Clark V. L. Characterization of a chimeric beta-lactamase plasmid of Neisseria gonorrhoeae which can function in Escherichia coli. Mol Gen Genet. 1983;189(1):77–84. doi: 10.1007/BF00326058. [DOI] [PubMed] [Google Scholar]
  28. Tenover F. C., Stein D. C., Young F. E., Clark V. L. Construction and characterization of chimeric beta-lactamase plasmids of Neisseria gonorrhoeae with altered ability to be mobilized during conjugation. Sex Transm Dis. 1985 Apr-Jun;12(2):76–82. doi: 10.1097/00007435-198504000-00005. [DOI] [PubMed] [Google Scholar]
  29. Van Embden J. D., Dessens-Kroon M., Van Klingeren B. A new beta-lactamase plasmid in Neisseria gonorrhoeae. J Antimicrob Chemother. 1985 Feb;15(2):247–250. doi: 10.1093/jac/15.2.247. [DOI] [PubMed] [Google Scholar]
  30. West S. E., Clark V. L. Genetic loci and linkage associations in Neisseria gonorrhoeae and Neisseria meningitidis. Clin Microbiol Rev. 1989 Apr;2 (Suppl):S92–103. doi: 10.1128/cmr.2.suppl.s92. [DOI] [PMC free article] [PubMed] [Google Scholar]

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