Regulation of metabolic and electron transport pathways in the freshwater bacterium Beggiatoa leptomitiformis D-402

Microbiology

Volumn 74, Issue 4, 2005, Pages 388-394

  Muntyan, M S ^a   Grabovich, M Yu ^b   Patritskaya, V Yu ^c   Dubinina, G A ^c  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

^b VORONEZH STATE UNIVERSITY   (Russian Federation)

^c WINOGRADSKY INSTITUTE OF MICROBIOLOGY   (Russian Federation)

Author keywords

Cytochromes aa 3 and cbb 3; Freshwater Beggiatoa; Lithoautotrophy; Microaerophily; Mixotrophy; Sulfur metabolism

Indexed keywords

BEGGIATOA; BEGGIATOA LEPTOMITIFORMIS; PROTEOBACTERIA;

EID: 23944486474     PISSN: 00262617     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11021-005-0078-8     Document Type: Article

References (17)

1. Nelson, D.C., Wirsen, C.O., and Jannasch, H.W., Characterization of Large, Autotrophic Beggiatoa spp. Abundant at Hydrothermal Vents of the Guaymas Basin, Appl. Environ. Microbiol., 1989, vol. 55, no. 11, pp. 2909-2917.
2. Bernhard, J.M., Buck, K.R., Farmer, M.A., and Bowser, S.S., The Santa Barbara Basin Is a Symbiosis Oasis, Nature, 2000, vol. 403, pp. 77-80.
3. Strohl, W.R., Genus Beggiatoa, Bergey's Manual of Systematic Bacteriology, 2nd ed., 2002.
4. Grabovich, M.Yu., Dubinina, G.A., Lebedeva, V.Yu., and Churikova, V.V., Mixotrophic and Lithoheterotrophic Growth of the Freshwater Filamentous Sulfur Bacterium Beggiatoa leptomitiformis D-402, Mikrobiologiya, 1998, vol. 57, no. 4, pp. 383-388.
5. Grabovich, M.Y., Patritskaya, V.Y., Muntyan, M.S., and Dubinina, G.A., Lithoautotrophic Growth of the Freshwater Strain Beggiatoa D-402 and Energy Conservation in a Homogeneous Culture under Microoxic Conditions, FEMS Microbiol. Lett., 2001, vol. 204, no. 2, pp. 341-345.
6. Grabovich, M.Yu., Dubinina, G.A., Churikova, V.V., Glushkov, A.F., and Churikov, S.N., Peculiarities of the Carbon Metabolism of the Colorless Sulfur Bacterium Macromonas bipunctata, Mikrobiologiva, 1993, vol. 62, no. 3, pp. 421-429.
7. Petushkova, Yu.P. and Ivanovsky, R.N., Enzymes Involved in the Metabolism of Thiosulfate in Thiocapsa roseopersicina Grown under Various Conditions, Mikrobiologiya, 1976, vol. 45, no. 4, pp. 960-965.
8. Grabovich, M.Y., Muntyan, M.S., Lebedeva, V.Y., Ustiyan, V.S., and Dubinina, G.A., Lithoheterotrophic Growth and Electron Transfer Chain Components of the Filamentous Gliding Bacterium Leucothrix mucor DSM 2157 during Oxidation of Sulfur Compounds, FEMS Microbiol. Lett., 1999, vol. 178, pp. 155-161.
9. Marmur, J., A Procedure for the Isolation of DNA from Microorganisms, J. Mol. Biol., 1961, vol. 3, pp. 208-218.
10. Hagen, K.D. and Nelson, D.C., Use of Reduced Sulfur Compounds by Beggiatoa spp.: Enzymology and Physiology of Marine and Freshwater Strains in Homogeneous and Gradient Cultures, Appl. Environ. Microbiol., 1997, vol. 63, pp. 3957-3964.
11. Podkopaeva, D.A., Grabovich, M.Yu., and Dubinina, G.A., The Functional Role of Reduced Inorganic Sulfur Compounds in the Metabolism of the Microaerophilic Bacterium Spirillum winogradskii, Mikrobiologiya, 2005, vol. 74, no. 1, pp. 17-25.
12. Varghese, S., Tang, Y., and Imlay, J.A., Contrasting Sensitivities of Escherichia coli Aconitases A and B to Oxidation and Iron Depletion, J. Bacteriol., 2003, vol. 185, no. 1, pp. 221-230.
13. Muntyan, M.S., Dinarieva, T.Y., Baev, M.V., and Netrusov, A.I., Effect of Growth Conditions on the Synthesis of Terminal Oxidases in Methylobacillus flagellatus KT, Arch. Biochem. Biophys., 2002, vol. 398, no. 1, pp. 118-124.
14. 3-Type Cytochrome c Oxidase from Rhodobacter sphaeroides, a Proton-Pumping Heme-Copper Oxidase, Biochim. Biophys. Acta, 1998, vol. 1365, pp. 421-434.
15. Stackebrandt, E., Murray, R.G.E., and Trüper, H.G., Proteobacteria Classis Nov., a Name for the Phylogenetic Taxon That Includes the "Purple Bacteria and Their Relatives," Int. J. Syst. Bacteriol., 1988, vol. 38, pp. 321-325.
16. 3 Oxidase in Clinically Relevant Proteobacteria, Trends Microbiol., 2000, vol. 8, pp. 542-543.
17. 3 Oxidase Complex in Bacteria, Arch. Microbiol., 2004, vol. 181, pp. 89-96.