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On the redox control of synthesis of anaerobically induced enzymes in enterobacteriaceae

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Abstract

Mutants of Escherichia coli were isolated in which transcription of the structural genes for hydrogenase (hyd) and for one of the components of formate dehydrogenase (fdh) (of the formate hydrogen-lyase complex) is coupled with that of the lacZ gene. They were — together with lac fusions of the nifH and nifL genes from Klebsiella — used to study regulation by redox control, of the expression of the respective structural genes. The following results were obtained: (i) β-galactosidase synthesis was fully repressed in the presence of O2 or nitrate (anaerobically), and induced in the absence of an external electron acceptor. Fumarate as terminal electron acceptor only marginally affected nif expression and partially repressed hyd and fdh expression. Redox control of the synthesis of hydrogenase and formate dehydrogenase, therefore, (as well as that of nif) acts at the level of transcription; the size of the redox potential seems to be correlated with the amount of repression; (ii) β-galactosidase synthesis in the hyd:: lac and fdh::lac fusion strains is induced by formate. At high concentrations formate reverses the repression by nitrate and fumarate but not that by oxygen.

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References

  • Bachmann BJ, Low KB (1980) Linkage map of Escherichia coli K12 Edition 6. Microbiol Rev 44:1–56

    PubMed  Google Scholar 

  • Balch WE, Wolfe RS (1976) New approach to the cultivation of methanogenic bacteria: 2-mercaptoethane sulfonic acid (HS-CoM)-dependent growth of Methanobacterium ruminantium in a pressurized atmosphere. Appl Env Microbiol 32:781–791

    Google Scholar 

  • Barrett EL, Jackson CE, Fukumoto HT, Chang GW (1979) Formate dehydrogenase mutants of Salmonella typhimurium: A new medium for their isolation and new mutant classes. Mol Gen Genet 177:95–101

    Article  PubMed  Google Scholar 

  • Begg YA, Whyte JN, Haddock BA (1977) The identification of mutants of Escherichia coli deficient in formate dehydrogenase and nitrate reductase activities using dye indicator plates. FEMS Microbiol Lett 2:47–50

    Article  Google Scholar 

  • Bukhari AI (1975) Reversal of mutator phage Mu integration. J Mol Biol 96:87–99

    PubMed  Google Scholar 

  • Casadaban MJ, Cohen SN (1979) Lactose genes fused to exogenous promoters in one step using a Mu-lac bacteriophage: in vivo probe for transcriptional control sequences. Proc Natl Acad Sci USA 76:4530–4533

    PubMed  Google Scholar 

  • Chippaux M, Guidici D, Abou-Jaoude A, Casse F, Pascal MC (1978) A mutation leading to total lack of nitrate reductase activity in Escherichia coli K12. Mol Gen Genet 160:225–229

    PubMed  Google Scholar 

  • Chippaux M, Bonnefoy-Orth V, Ratouchniak J, Pascal M (1981) Operon fusions in the nitrate reductase operon and study of the control of gene nirR in Escherichia coli. Mol Gen Genet 182:477–479

    PubMed  Google Scholar 

  • Cole JA, Wimpenny JWT (1966) The interrelationships of low redox potential cytochrome c552 and hydrogenase in facultative anaerobes. Biochim Biophys Acta 128:419–425

    Google Scholar 

  • Cox JC, Edwards ES, DeMoss JA (1981) Resolution of distinct seleniumcontaining formate dehydrogenase from Escherichia coli. J Bacteriol 145:1317–1324

    PubMed  Google Scholar 

  • Dixon R, Cannon FC, Kondorosi A (1976) Construction of a R plasmid carrying nitrogen fixation genes from Klebsiella pneumoniae. Nature 260:268–271

    PubMed  Google Scholar 

  • Dobrogosz WJ (1966) Altered endproduct patterns and catabolite repression in E. coli. J Bacteriol 91:2263–2269

    PubMed  Google Scholar 

  • Eady RR, Issack R, Kennedy C, Postgate JR, Ratcliffe HD (1978) Nitrogenase synthesis in Klebsiella pneumoniae: comparison of ammonium and oxygen regulation. J Gen Microbiol 104:277–285

    PubMed  Google Scholar 

  • Fraenkel DG, Neidhardt FC (1961) Use of chloramphenicol to study control of RNA synthesis in bacteria. Biochim Biophys Acta 53:96–100

    Article  PubMed  Google Scholar 

  • Giordano G, Medani C-L, Mandrand-Berthelot M-A, Boxer DH (1983) Formate dehydrogenase from Escherichia coli. FEMS Microbiol Lett 17:171–177

    Article  Google Scholar 

  • Glick BR, Zeisler J, Banaszuk AM, Friesen JD, Martin WG (1981) The identification and partial characterization of a plasmid containing the gene for the membrane-associated hydrogenase from E. coli. Gene 15:201–206

    Article  PubMed  Google Scholar 

  • Graham A, Boxer DH, Haddock BA, Mandrand-Berthelot M-A, Jones RW (1980a) Immunochemical analysis of the membrane-bound hydrogenase of E. coli. FEBS Lett 113:167–172

    Article  PubMed  Google Scholar 

  • Graham A, Jenkins HE, Smith NH, Mandrand-Berthelot M-A, Haddock BA, Boxer DH (1980b) The synthesis of formate dehydrogenase and nitrate reductase proteins in various fdh and chl mutants of Escherichia coli. FEMS Microbiol Lett 7:145–151

    Google Scholar 

  • Haddock BA, Jones CW (1977) Bacterial respiration. Bacteriol Rev 41:47–99

    PubMed  Google Scholar 

  • Hom SSM, Hennecke H, Shanmugam KT (1980) Regulation of nitrogenase synthesis in Klebsiella pneumoniae: effect of nitrate. J Gen Microbiol 117:169–179

    PubMed  Google Scholar 

  • Knappe J, Schmitt T (1976) A novel reaction of S-adenosyl-l-methionine correlated with the activation of pyruvate formate-lyase. Biochem Biophys Res Commun 71:1110–1117

    PubMed  Google Scholar 

  • Lambden PR, Guest JR (1976) Mutants of Escherichia coli K12 unable to use fumarate as an anaerobic electron acceptor. J Gen Microbiol 97:145–160

    PubMed  Google Scholar 

  • Lester RL, DeMoss JA (1971) Effects of molybdate and selenite on formate and nitrate metabolism in Escherichia coli. J Bacteriol 105:1006–1014

    PubMed  Google Scholar 

  • Lin ECC (1976) Glycerol dissimilation and its regulation in bacteria. Ann Rev Microbiol 30:535–578

    Article  Google Scholar 

  • Lorowitz W, Clark D (1982) Escherichia coli mutants with a temperaturesensitive alcohol dehydrogenase. J Bacteriol 152:935–938

    PubMed  Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall (1951) Protein determination with the Folin phenol reagent. J Biol Chem 193:265–275

    PubMed  Google Scholar 

  • Mandrand-Berthelot M-A, Wee MYK, Haddock B (1978) An improved method for identification and characterization of mutants of Escherichia coli deficient in formate dehydrogenase activity. FEMS Microbiol Lett 4:37–40

    Article  Google Scholar 

  • Merrick M, Hill S, Hennecke H, Hahn M, Dixon R, Kennedy C (1982) Repressor properties of the nifL gene product in Klebsiella pneumoniae. Mol Gen Genet 185:75–81

    Google Scholar 

  • Miller JH (1972) Experiments in molecular genetics. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York

    Google Scholar 

  • Pecher A, Blaschkowski HP, Knappe K, Böck A (1982) Expression of pyruvate formate lyase from the cloned structural gene. Arch Microbiol 132:365–371

    PubMed  Google Scholar 

  • Peck HD Jr, Gest H (1957) Formic dehydrogenase and the hydrogenlyase enzyme complex in the coli-aerogenes group. J Bacteriol 73:706–721

    PubMed  Google Scholar 

  • Shaw DJ, Guest JR (1981) Molecular cloning of the fnr gene of Escherichia coli K12. Mol Gen Genet 181:95–100

    PubMed  Google Scholar 

  • Shaw DJ, Guest JR (1982) Amplification and product identification of the fnr gene of Escherichia coli. J Gen Microbiol 128:2221–2228

    PubMed  Google Scholar 

  • St. John RT, Shah VK, Brill WJ (1974) Regulation of nitrogenase synthesis by oxygen in Klebsiella pneumoniae. J Bacteriol 119:266–269

    PubMed  Google Scholar 

  • Takagi M, Ishimoto M (1983) Escherichia coli mutants defective in trimethylamine-N-oxide reductase. FEMS Microbiol Lett 17:247–250

    Article  Google Scholar 

  • Wimpenny JWT, Cole JA (1967) The regulation of metabolism in facultative bacteria. III. The effect of nitrate. Biochim Biophys Acta 148:233–243

    PubMed  Google Scholar 

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Pecher, A., Zinoni, F., Jatisatienr, C. et al. On the redox control of synthesis of anaerobically induced enzymes in enterobacteriaceae. Arch. Microbiol. 136, 131–136 (1983). https://doi.org/10.1007/BF00404787

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  • DOI: https://doi.org/10.1007/BF00404787

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