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. 1995 May;61(5):1770–1775. doi: 10.1128/aem.61.5.1770-1775.1995

Insertional Mutations in the Hydrogenase vhc and frc Operons Encoding Selenium-Free Hydrogenases in Methanococcus voltae

Y Berghofer, A Klein
PMCID: PMC1388437  PMID: 16535019

Abstract

Methanococcus voltae, which contains four different gene groups that encode [NiFe]-hydrogenases, was transformed with integration vectors to achieve polar inactivation of two of the four hydrogenase operons that encode the selenium-free enzymes Vhc and Frc. Transformants which were selected by their acquired puromycin resistance showed site-specific insertions in either the vhc or frc operon by single crossover events. Southern hybridization revealed tandem integrations of whole vectors in the vhc operon, whereas only one vector copy was found in the frc operon. Northern (RNA) hybridizations showed a pac transcript of defined size, indicating strong termination in front of the hydrogenase genes downstream. In spite of the apparent abolition of expression of selenium-free hydrogenases through these polar insertions, they were not lethal to cells upon growth in selenium-deprived minimal medium, which we had previously shown to strongly induce transcription of the respective operons in M. voltae. Instead, like wild-type control cultures, transformants responded to selenium deprivation only with a reduction in growth rate. We conclude that loss of the potential to express a selenium-free hydrogenase can nevertheless be balanced by very small amounts of selenium hydrogenases under laboratory conditions in which the hydrogen supply is not likely to be a limiting growth factor.

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Selected References

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  1. Berghöfer Y., Agha-Amiri K., Klein A. Selenium is involved in the negative regulation of the expression of selenium-free [NiFe] hydrogenases in Methanococcus voltae. Mol Gen Genet. 1994 Feb;242(4):369–373. doi: 10.1007/BF00281785. [DOI] [PubMed] [Google Scholar]
  2. Bertani G., Baresi L. Genetic transformation in the methanogen Methanococcus voltae PS. J Bacteriol. 1987 Jun;169(6):2730–2738. doi: 10.1128/jb.169.6.2730-2738.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  4. Cohen S. N., Chang A. C., Hsu L. Nonchromosomal antibiotic resistance in bacteria: genetic transformation of Escherichia coli by R-factor DNA. Proc Natl Acad Sci U S A. 1972 Aug;69(8):2110–2114. doi: 10.1073/pnas.69.8.2110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  6. Gernhardt P., Possot O., Foglino M., Sibold L., Klein A. Construction of an integration vector for use in the archaebacterium Methanococcus voltae and expression of a eubacterial resistance gene. Mol Gen Genet. 1990 Apr;221(2):273–279. doi: 10.1007/BF00261731. [DOI] [PubMed] [Google Scholar]
  7. Halboth S., Klein A. Methanococcus voltae harbors four gene clusters potentially encoding two [NiFe] and two [NiFeSe] hydrogenases, each of the cofactor F420-reducing or F420-non-reducing types. Mol Gen Genet. 1992 May;233(1-2):217–224. doi: 10.1007/BF00587582. [DOI] [PubMed] [Google Scholar]
  8. Jones J. B., Stadtman T. C. Selenium-dependent and selenium-independent formate dehydrogenases of Methanococcus vannielii. Separation of the two forms and characterization of the purified selenium-independent form. J Biol Chem. 1981 Jan 25;256(2):656–663. [PubMed] [Google Scholar]
  9. Klein A., Allmansberger R., Bokranz M., Knaub S., Müller B., Muth E. Comparative analysis of genes encoding methyl coenzyme M reductase in methanogenic bacteria. Mol Gen Genet. 1988 Aug;213(2-3):409–420. doi: 10.1007/BF00339610. [DOI] [PubMed] [Google Scholar]
  10. Lacalle R. A., Pulido D., Vara J., Zalacaín M., Jiménez A. Molecular analysis of the pac gene encoding a puromycin N-acetyl transferase from Streptomyces alboniger. Gene. 1989 Jul 15;79(2):375–380. doi: 10.1016/0378-1119(89)90220-5. [DOI] [PubMed] [Google Scholar]
  11. May H. D., Patel P. S., Ferry J. G. Effect of molybdenum and tungsten on synthesis and composition of formate dehydrogenase in Methanobacterium formicicum. J Bacteriol. 1988 Aug;170(8):3384–3389. doi: 10.1128/jb.170.8.3384-3389.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Micheletti P. A., Sment K. A., Konisky J. Isolation of a coenzyme M-auxotrophic mutant and transformation by electroporation in Methanococcus voltae. J Bacteriol. 1991 Jun;173(11):3414–3418. doi: 10.1128/jb.173.11.3414-3418.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Muth E., Mörschel E., Klein A. Purification and characterization of an 8-hydroxy-5-deazaflavin-reducing hydrogenase from the archaebacterium Methanococcus voltae. Eur J Biochem. 1987 Dec 15;169(3):571–577. doi: 10.1111/j.1432-1033.1987.tb13647.x. [DOI] [PubMed] [Google Scholar]
  14. Müller B., Allmansberger R., Klein A. Termination of a transcription unit comprising highly expressed genes in the archaebacterium Methanococcus voltae. Nucleic Acids Res. 1985 Sep 25;13(18):6439–6445. doi: 10.1093/nar/13.18.6439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Patel G. B., Choquet C. G., Nash J. H., Sprott G. D. Formation and Regeneration of Methanococcus voltae Protoplasts. Appl Environ Microbiol. 1993 Jan;59(1):27–33. doi: 10.1128/aem.59.1.27-33.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Patel G. B., Nash J. H., Agnew B. J., Sprott G. D. Natural and Electroporation-Mediated Transformation of Methanococcus voltae Protoplasts. Appl Environ Microbiol. 1994 Mar;60(3):903–907. doi: 10.1128/aem.60.3.903-907.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Sitzmann J., Klein A. Physical and genetic map of the Methanococcus voltae chromosome. Mol Microbiol. 1991 Feb;5(2):505–513. doi: 10.1111/j.1365-2958.1991.tb02134.x. [DOI] [PubMed] [Google Scholar]
  19. Sorgenfrei O., Klein A., Albracht S. P. Influence of illumination on the electronic interaction between 77Se and nickel in active F420-non-reducing hydrogenase from Methanococcus voltae. FEBS Lett. 1993 Oct 18;332(3):291–297. doi: 10.1016/0014-5793(93)80652-b. [DOI] [PubMed] [Google Scholar]
  20. Sorgenfrei O., Linder D., Karas M., Klein A. A novel very small subunit of a selenium containing [NiFe] hydrogenase of Methanococcus voltae is postranslationally processed by cleavage at a defined position. Eur J Biochem. 1993 May 1;213(3):1355–1358. doi: 10.1111/j.1432-1033.1993.tb17888.x. [DOI] [PubMed] [Google Scholar]
  21. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  22. Whitman W. B., Ankwanda E., Wolfe R. S. Nutrition and carbon metabolism of Methanococcus voltae. J Bacteriol. 1982 Mar;149(3):852–863. doi: 10.1128/jb.149.3.852-863.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]

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