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      Video-supported Analysis of Beggiatoa Filament Growth, Breakage, and Movement

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      1 , 2 , , 2 , 3 ,   1 , 2
      Microbial Ecology
      Springer-Verlag

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          Abstract

          A marine Beggiatoa sp. was cultured in semi-solid agar with opposing oxygen-sulfide gradients. Growth pattern, breakage of filaments for multiplication, and movement directions of Beggiatoa filaments in the transparent agar were investigated by time-lapse video recording. The initial doubling time of cells was 15.7 ± 1.3 h (mean ± SD) at room temperature. Filaments grew up to an average length of 1.7 ± 0.2 mm, but filaments of up to approximately 6 mm were also present. First breakages of filaments occurred approximately 19 h after inoculation, and time-lapse movies illustrated that a parent filament could break into several daughter filaments within a few hours. In >20% of the cases, filament breakage occurred at the tip of a former loop. As filament breakage is accomplished by the presence of sacrificial cells, loop formation and the presence of sacrificial cells must coincide. We hypothesize that sacrificial cells enhance the chance of loop formation by interrupting the communication between two parts of one filament. With communication interrupted, these two parts of one filament can randomly move toward each other forming the tip of a loop at the sacrificial cell.

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          The online version of this article (doi:10.1007/s00248-008-9367-x) contains supplementary material, which is available to authorized users.

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          Most cited references27

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          Massive natural occurrence of unusually large bacteria (Beggiatoa sp.) at a hydrothermal deep-sea vent site

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            Chemoautotrophic growth of a marine Beggiatoa in sulfide-gradient cultures

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              High Nitrate Concentrations in Vacuolate, Autotrophic Marine Beggiatoa spp.

              Massive accumulations of very large Beggiatoa spp. are found at a Monterey Canyon cold seep and at Guaymas Basin hydrothermal vents. Both environments are characterized by high sediment concentrations of soluble sulfide and low levels of dissolved oxygen in surrounding waters. These filamentous, sulfur-oxidizing bacteria accumulate nitrate intracellularly at concentrations of 130 to 160 mM, 3,000- to 4,000-fold higher than ambient levels. Average filament widths range from 24 to 122 (mu)m, and individual cells of all widths possess a central vacuole. These findings plus recent parallel discoveries for Thioploca spp. (H. Fossing, V. A. Gallardo, B. B. Jorgensen, M. Huttel, L. P. Nielsen, H. Schulz, D. E. Canfield, S. Forster, R. N. Glud, J. K. Gundersen, J. Kuver, N. B. Ramsing, A. Teske, B. Thamdrup, and O. Ulloa, Nature (London) 374:713-715, 1995) suggest that nitrate accumulation may be a universal property of vacuolate, filamentous sulfur bacteria. Ribulose bisphosphate carboxylase-oxygenase and 2-oxoglutarate dehydrogenase activities in the Beggiatoa sp. from Monterey Canyon suggest in situ autotrophic growth of these bacteria. Nitrate reductase activity is much higher in the Monterey Beggiatoa sp. than in narrow, laboratory-grown strains of Beggiatoa spp., and the activity is found primarily in the membrane fraction, suggesting that the vacuolate Beggiatoa sp. can reduce nitrate coupled to electron flow through an electron transport system. Nitrate-concentrating and respiration potentials of these chemolithoautotrophs suggest that the Beggiatoa spp. described here are an important link between the sulfur, nitrogen, and carbon cycles at the Monterey Canyon seeps and the Guaymas Basin hydrothermal vents where they are found.
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                Author and article information

                Contributors
                +49-421-2028804 , akamp@mpi-bremen.de
                Journal
                Microb Ecol
                Microbial Ecology
                Springer-Verlag (New York )
                0095-3628
                1432-184X
                12 March 2008
                October 2008
                : 56
                : 3
                : 484-491
                Affiliations
                [1 ]Institute for Microbiology, Leibniz University of Hannover, Hannover, Germany
                [2 ]Max Planck Institute for Marine Microbiology, Bremen, Germany
                [3 ]Center for Geomicrobiology, Department of Biological Sciences, University of Aarhus, Aarhus, Denmark
                Article
                9367
                10.1007/s00248-008-9367-x
                2755761
                18335158
                21c7905b-79ee-4362-bcb4-4e5278b6f5f2
                © Springer Science+Business Media, LLC 2008
                History
                : 22 April 2007
                : 6 December 2007
                : 27 January 2008
                Categories
                Original Article
                Custom metadata
                © Springer Science+Business Media, LLC 2008

                Microbiology & Virology
                Microbiology & Virology

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