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. 1995 May;63(5):1624–1630. doi: 10.1128/iai.63.5.1624-1630.1995

Cloning and characterization of the meningococcal polyphosphate kinase gene: production of polyphosphate synthesis mutants.

C R Tinsley 1, E C Gotschlich 1
PMCID: PMC173201  PMID: 7729865

Abstract

The pathogenic Neisseria species accumulate polyphosphate to levels between 10 and 20% of their total phosphate content. However, the significance of this compound for the growth and pathogenicity of these species is not understood. A previous report (C.R. Tinsley, B.N. Manjula, and E.C. Gotschlich, Infect. Immun. 61:3703-3710, 1993) describes the purification of polyphosphate kinase, the enzyme responsible for synthesis of polyphosphate, from Neisseria meningitidis BNCV. By use of probes based on the amino acid sequence of the purified enzyme, the structural gene ppk has been cloned and sequenced. The coding sequence is 2,055 bp long and codes for a protein of 77.2 kDa. The open reading frame of the cloned gene was interrupted by the insertion of a kanamycin resistance cassette, and ppk mutants were obtained in both Neisseria gonorrhoeae and N. meningitidis by transformation with the recombinant plasmid. Amounts of polyphosphate in the ppk mutants were reduced to between 2 and 10% of wild-type levels. The mutants grew less vigorously than wild-type organisms in vitro and showed a striking increase in sensitivity to killing by human serum.

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Selected References

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  1. Akiyama M., Crooke E., Kornberg A. The polyphosphate kinase gene of Escherichia coli. Isolation and sequence of the ppk gene and membrane location of the protein. J Biol Chem. 1992 Nov 5;267(31):22556–22561. [PubMed] [Google Scholar]
  2. Blake M. S., Gotschlich E. C. Purification and partial characterization of the major outer membrane protein of Neisseria gonorrhoeae. Infect Immun. 1982 Apr;36(1):277–283. doi: 10.1128/iai.36.1.277-283.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Church G. M., Gilbert W. Genomic sequencing. Proc Natl Acad Sci U S A. 1984 Apr;81(7):1991–1995. doi: 10.1073/pnas.81.7.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Crooke E., Akiyama M., Rao N. N., Kornberg A. Genetically altered levels of inorganic polyphosphate in Escherichia coli. J Biol Chem. 1994 Mar 4;269(9):6290–6295. [PubMed] [Google Scholar]
  5. Elkins C., Thomas C. E., Seifert H. S., Sparling P. F. Species-specific uptake of DNA by gonococci is mediated by a 10-base-pair sequence. J Bacteriol. 1991 Jun;173(12):3911–3913. doi: 10.1128/jb.173.12.3911-3913.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Frasch C. E., Chapman S. S. Classification of Neisseria meningitidis group B into distinct serotypes. I. Serological typing by a microbactericidal method. Infect Immun. 1972 Jan;5(1):98–102. doi: 10.1128/iai.5.1.98-102.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Frasch C. E., Gotschlich E. C. An outer membrane protein of Neisseria meningitidis group B responsible for serotype specificity. J Exp Med. 1974 Jul 1;140(1):87–104. doi: 10.1084/jem.140.1.87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Goodman S. D., Scocca J. J. Factors influencing the specific interaction of Neisseria gonorrhoeae with transforming DNA. J Bacteriol. 1991 Sep;173(18):5921–5923. doi: 10.1128/jb.173.18.5921-5923.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Goodman S. D., Scocca J. J. Identification and arrangement of the DNA sequence recognized in specific transformation of Neisseria gonorrhoeae. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6982–6986. doi: 10.1073/pnas.85.18.6982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gotschlich E. C. Genetic locus for the biosynthesis of the variable portion of Neisseria gonorrhoeae lipooligosaccharide. J Exp Med. 1994 Dec 1;180(6):2181–2190. doi: 10.1084/jem.180.6.2181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Harold F. M. Inorganic polyphosphates in biology: structure, metabolism, and function. Bacteriol Rev. 1966 Dec;30(4):772–794. doi: 10.1128/br.30.4.772-794.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hendley J. O., Powell K. R., Salomonsky N. L., Rodewald R. R. Electron microscopy of the gonococcal capsule. J Infect Dis. 1981 Jun;143(6):796–802. doi: 10.1093/infdis/143.6.796. [DOI] [PubMed] [Google Scholar]
  13. Hendley J. W., Powell K. R., Rodewald R., Holzgrefe H. H., Lyles R. Demonstration of a capsule on Neisseria gonorrhoeae. N Engl J Med. 1977 Mar 17;296(11):608–611. doi: 10.1056/NEJM197703172961105. [DOI] [PubMed] [Google Scholar]
  14. James J. F., Swanson J. The capsule of the gonococcus. J Exp Med. 1977 Apr 1;145(4):1082–1086. doi: 10.1084/jem.145.4.1082. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. KALTWASSER H. [The role of polyphosphate in phosphorus metabolism of an oxyhydrogen gas bacterium (Hydrogenomonas strain 20)]. Arch Mikrobiol. 1962;41:282–306. [PubMed] [Google Scholar]
  16. KELLOGG D. S., Jr, PEACOCK W. L., Jr, DEACON W. E., BROWN L., PIRKLE D. I. NEISSERIA GONORRHOEAE. I. VIRULENCE GENETICALLY LINKED TO CLONAL VARIATION. J Bacteriol. 1963 Jun;85:1274–1279. doi: 10.1128/jb.85.6.1274-1279.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kulaev I. S., Vagabov V. M. Polyphosphate metabolism in micro-organisms. Adv Microb Physiol. 1983;24:83–171. doi: 10.1016/s0065-2911(08)60385-9. [DOI] [PubMed] [Google Scholar]
  18. Martin P. R., Cooperider J. W., Mulks M. H. Sequence of the argF gene encoding ornithine transcarbamoylase from Neisseria gonorrhoeae. Gene. 1990 Sep 28;94(1):139–140. doi: 10.1016/0378-1119(90)90482-7. [DOI] [PubMed] [Google Scholar]
  19. Messing J. New M13 vectors for cloning. Methods Enzymol. 1983;101:20–78. doi: 10.1016/0076-6879(83)01005-8. [DOI] [PubMed] [Google Scholar]
  20. Mickelsen P. A., Sparling P. F. Ability of Neisseria gonorrhoeae, Neisseria meningitidis, and commensal Neisseria species to obtain iron from transferrin and iron compounds. Infect Immun. 1981 Aug;33(2):555–564. doi: 10.1128/iai.33.2.555-564.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Morse S. A. The biology of the gonococcus. CRC Crit Rev Microbiol. 1978;7(2):93–189. doi: 10.3109/10408417909083071. [DOI] [PubMed] [Google Scholar]
  22. Moxon E. R., Deich R. A., Connelly C. Cloning of chromosomal DNA from Haemophilus influenzae. Its use for studying the expression of type b capsule and virulence. J Clin Invest. 1984 Feb;73(2):298–306. doi: 10.1172/JCI111214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Murakami K., Gotschlich E. C., Seiff M. E. Cloning and characterization of the structural gene for the class 2 protein of Neisseria meningitidis. Infect Immun. 1989 Aug;57(8):2318–2323. doi: 10.1128/iai.57.8.2318-2323.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Noegel A., Gotschlich E. C. Isolation of a high molecular weight polyphosphate from Neisseria gonorrhoeae. J Exp Med. 1983 Jun 1;157(6):2049–2060. doi: 10.1084/jem.157.6.2049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Pepin C. A., Wood H. G. Polyphosphate glucokinase from Propionibacterium shermanii. Kinetics and demonstration that the mechanism involves both processive and nonprocessive type reactions. J Biol Chem. 1986 Apr 5;261(10):4476–4480. [PubMed] [Google Scholar]
  26. Reusch R. N., Sadoff H. L. Putative structure and functions of a poly-beta-hydroxybutyrate/calcium polyphosphate channel in bacterial plasma membranes. Proc Natl Acad Sci U S A. 1988 Jun;85(12):4176–4180. doi: 10.1073/pnas.85.12.4176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Russel M., Kidd S., Kelley M. R. An improved filamentous helper phage for generating single-stranded plasmid DNA. Gene. 1986;45(3):333–338. doi: 10.1016/0378-1119(86)90032-6. [DOI] [PubMed] [Google Scholar]
  28. Staden R. Automation of the computer handling of gel reading data produced by the shotgun method of DNA sequencing. Nucleic Acids Res. 1982 Aug 11;10(15):4731–4751. doi: 10.1093/nar/10.15.4731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Swanson J., Kraus S. J., Gotschlich E. C. Studies on gonococcus infection. I. Pili and zones of adhesion: their relation to gonococcal growth patterns. J Exp Med. 1971 Oct 1;134(4):886–906. doi: 10.1084/jem.134.4.886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Swanson J. Studies on gonococcus infection. XII. Colony color and opacity varienats of gonococci. Infect Immun. 1978 Jan;19(1):320–331. doi: 10.1128/iai.19.1.320-331.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Taha M. K., So M., Seifert H. S., Billyard E., Marchal C. Pilin expression in Neisseria gonorrhoeae is under both positive and negative transcriptional control. EMBO J. 1988 Dec 20;7(13):4367–4378. doi: 10.1002/j.1460-2075.1988.tb03335.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tinsley C. R., Manjula B. N., Gotschlich E. C. Purification and characterization of polyphosphate kinase from Neisseria meningitidis. Infect Immun. 1993 Sep;61(9):3703–3710. doi: 10.1128/iai.61.9.3703-3710.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wetzler L. M., Gotschlich E. C., Blake M. S., Koomey J. M. The construction and characterization of Neisseria gonorrhoeae lacking protein III in its outer membrane. J Exp Med. 1989 Jun 1;169(6):2199–2209. doi: 10.1084/jem.169.6.2199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Won J., Griffith R. W. Cloning and sequencing of the gene encoding a 31-kilodalton antigen of Haemophilus somnus. Infect Immun. 1993 Jul;61(7):2813–2821. doi: 10.1128/iai.61.7.2813-2821.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Wong T. P., Shockley R. K., Johnston K. H. WSJM, a simple chemically defined medium for growth of Neisseria gonorrhoeae. J Clin Microbiol. 1980 Apr;11(4):363–369. doi: 10.1128/jcm.11.4.363-369.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]

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