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A. Kot-Wasik, B. Zukowska, D. Dabrowska, J. Debska, J. Pacyna, J. Namiesnik (2003)
Physical, chemical, and biological changes in the Gulf of Gdansk ecosystem (southern Baltic Sea)Rev. Environ. Contam. Toxicol., 179
G. Muyzer, T. Brinkhoff, U. Nubel, C. Santegoeds, H. Schafer, C. Wawer (1997)
Molecular Microbial Ecology Manual
C. Vetriani, H.V. Tran, L.J. Kerkhof (2003)
Fingerprinting microbial assemblages from the oxic/anoxic chemocline of the Black SeaAppl. Environ. Microbiol., 69
J.W. Murray, H.W. Jannash, S. Honjo, R.F. Anderson, W.S. Reeburgh, Z. Top, G.E. Friederich, L.A. Codispoti, E. Izdar (1989)
Unexpected changes in the oxic/anoxic interface in the Black SeaNature, 338
L.N. Neretin, R.M. Abed, A. Schippers, C.J. Schubert, K. Kohls, M.M. Kuypers (2007)
Inorganic carbon fixation by sulfate-reducing bacteria in the Black Sea water columnEnviron. Microbiol., 9
N.V. Pimenov, I.I. Rusanov, S.K. Yusupov, J. Fridrich, A.Yu. Lein, B. Wehrli, M.V. Ivanov (2000)
Microbial processes at the aerobic-anaerobic interface in the deep-water zone of the Black SeaMicrobiology, 69
S. Lucker, D. Steger, K.U. Kjeldsen, B.J. MacGregor, M. Wagner, A. Loy (2007)
Improved 16S rRNA-targeted probe set for analysis of sulfate-reducing bacteria by fluorescence in situ hybridizationJ. Microbiol. Methods, 69
K.R. Hristova, M. Mau, D. Zheng, R.I. Aminov, R.I. Mackie, H.R. Gaskins, L. Raskin (2000)
Desulfotomacullum genusand subgenus-specific 16S rRNA hybridization probes for environmental studiesEnviron. Microbiol., 2
K. Daly, R.J. Sharp, A.J. McCarthy (2000)
Development of oligonucleotide probes and PCR primers for detecting phylogenetic subgroups of sulfate-reducing bacteriaMicrobiology-SGM, 146
F. Widdel, F. Back (1992)
The Prokaryotes
H.G. Truper, H.G. Schlegel (1964)
Sulfur metabolism in Thiorhodaceae. I. Quantitative measurements on growing cells of Chromatium okeniiAntonie van Leeuwenhoek, 30
R. Devereux, M.D. Kane, J. Winfrey, D.A. Stahl (1992)
Genusand group-specific hybridization probes for determinative and environmental studies of sulfatereducing bacteriaSyst. Appl. Microbiol., 15
U. Edwards, T. Rogall, H. Blocker, M. Emde, E.C. Bottger (1989)
Isolation and direct complete nucleotide determination of entire genes. Characterization of a gene coding for 16S ribosomal RNANucleic Acid Res., 17
R.I. Amann, B. Zarda, D.A. Stahl, K.H. Schleifer (1992)
Identification of individual prokaryotic cells by using enzyme-labeled, rRNA-targeted oligonucleotide probesAppl. Environ. Microbiol., 58
A. Brioukhanov, L. Pieulle, A. Dolla (2010)
Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology
J.R. Rezende, K.U. Kjeldsen, C.R. Hubert, K. Finster, A. Loy, B.B. Jorgensen (2013)
Dispersal of thermophilic Desulfotomaculum endospores into Baltic Sea sediments over thousands of yearsISME J., 7
J. Geets, B. Borremans, L. Diels, D. Springael, J. Vangronsveld, D. Lelie, K. Vanbroekhoven (2006)
DsrB gene-based DGGE for community and diversity surveys of sulfate-reducing bacteriaJ. Microbiol. Methods, 66
A.L. Bryukhanov, V.A. Korneeva, T.A. Kanapatskii, E.E. Zakharova, E.V. Men’ko, I.I. Rusanov, N.V. Pimenov (2011)
Investigation of the sulfate-reducing bacterial community in the aerobic water and chemocline zone of the Black Sea by the FISH techniqueMicrobiology, 80
Fluorescent in situ hybridization (FISH) and PCR were used for analysis of phylogenetic structure of anaerobic sulfate-reducing bacterial communities in oxygen-containing upper water layers of meromictic basins: the Black Sea and the Gdansk Deep of the Baltic Sea. In the Black Sea (continental slope at depths 30–70 m), cells of sulfate-reducing bacteria (SRB) hybridizing with 16S rRNA-specific FISH-probes for Desulfotomaculum, Desulfobacter, and Desulfovibrio genera were revealed, whereas Desulfomicrobium-related bacteria were prevalent in the chemocline zone at a 150-m depth. Besides Desulfotomaculum (SRB subgroup 1), Desulfobacter (SRB subgroup 4), and Desulfovibrio-Desulfomicrobium (SRB subgroup 6), nested PCR with the use of 16S rRNA gene-specific primers detected the presence of Desulfococcus–Desulfonema–Desulfosarcina (SRB subgroup 5) in the oxygen-containing water column of the Black and Baltic seas. Active enrichment SRB culture that contained bacterium Desulfosporosinus sp. as a major component was obtained from the Black Sea water sample collected at a 70-m depth.
Moscow University Biological Sciences Bulletin – Springer Journals
Published: Jan 6, 2016
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