Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide

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Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide. / Thar, Roland Matthias; Kühl, Michael.

In: Applied and Environmental Microbiology, Vol. 67, No. 12, 2001, p. 5410-5419.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Thar, RM & Kühl, M 2001, 'Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide', Applied and Environmental Microbiology, vol. 67, no. 12, pp. 5410-5419. https://doi.org/10.1128/AEM.67.12.5410-5419.2001

APA

Thar, R. M., & Kühl, M. (2001). Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide. Applied and Environmental Microbiology, 67(12), 5410-5419. https://doi.org/10.1128/AEM.67.12.5410-5419.2001

Vancouver

Thar RM, Kühl M. Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide. Applied and Environmental Microbiology. 2001;67(12):5410-5419. https://doi.org/10.1128/AEM.67.12.5410-5419.2001

Author

Thar, Roland Matthias ; Kühl, Michael. / Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide. In: Applied and Environmental Microbiology. 2001 ; Vol. 67, No. 12. pp. 5410-5419.

Bibtex

@article{89c11d1074c711dbbee902004c4f4f50,
title = "Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide",
abstract = "The motility of the purple sulfur bacterium Marichromatium gracile was investigated under different light regimes in a gradient capillary setup with opposing oxygen and sulfide gradients. The gradients were quantified with microsensors, while the behavior of swimming cells was studied by video microscopy in combination with a computerized cell tracking system. M. gracile exhibited photokinesis, photophobic responses, and phobic responses toward oxygen and sulfide. The observed migration patterns could be explained solely by the various phobic responses. In the dark, M. gracile formed an ~500-µm-thick band at the oxic-anoxic interface, with a sharp border toward the oxic zone always positioned at ~10 µM O2. Flux calculations yielded a molar conversion ratio Stot/O2 of 2.03:1 (Stot = [H2S] + [HS] + [S2]) for the sulfide oxidation within the band, indicating that in darkness the bacteria oxidized sulfide incompletely to sulfur stored in intracellular sulfur globules. In the light, M. gracile spread into the anoxic zone while still avoiding regions with >10 µM O2. The cells also preferred low sulfide concentrations if the oxygen was replaced by nitrogen. A light-dark transition experiment demonstrated a dynamic interaction between the chemical gradients and the cell's metabolism. In darkness and anoxia, M. gracile lost its motility after ca. 1 h. In contrast, at oxygen concentrations of >100 µM with no sulfide present the cells remained viable and motile for ca. 3 days both in light and darkness. Oxygen was respired also in the light, but respiration rates were lower than in the dark. Observed aggregation patterns are interpreted as effective protection strategies against high oxygen concentrations and might represent first stages of biofilm formation.",
author = "Thar, {Roland Matthias} and Michael K{\"u}hl",
year = "2001",
doi = "10.1128/AEM.67.12.5410-5419.2001",
language = "English",
volume = "67",
pages = "5410--5419",
journal = "Applied and Environmental Microbiology",
issn = "0099-2240",
publisher = "American Society for Microbiology",
number = "12",

}

RIS

TY - JOUR

T1 - Motility of Marichromatium gracile in Response to Light, Oxygen, and Sulfide

AU - Thar, Roland Matthias

AU - Kühl, Michael

PY - 2001

Y1 - 2001

N2 - The motility of the purple sulfur bacterium Marichromatium gracile was investigated under different light regimes in a gradient capillary setup with opposing oxygen and sulfide gradients. The gradients were quantified with microsensors, while the behavior of swimming cells was studied by video microscopy in combination with a computerized cell tracking system. M. gracile exhibited photokinesis, photophobic responses, and phobic responses toward oxygen and sulfide. The observed migration patterns could be explained solely by the various phobic responses. In the dark, M. gracile formed an ~500-µm-thick band at the oxic-anoxic interface, with a sharp border toward the oxic zone always positioned at ~10 µM O2. Flux calculations yielded a molar conversion ratio Stot/O2 of 2.03:1 (Stot = [H2S] + [HS] + [S2]) for the sulfide oxidation within the band, indicating that in darkness the bacteria oxidized sulfide incompletely to sulfur stored in intracellular sulfur globules. In the light, M. gracile spread into the anoxic zone while still avoiding regions with >10 µM O2. The cells also preferred low sulfide concentrations if the oxygen was replaced by nitrogen. A light-dark transition experiment demonstrated a dynamic interaction between the chemical gradients and the cell's metabolism. In darkness and anoxia, M. gracile lost its motility after ca. 1 h. In contrast, at oxygen concentrations of >100 µM with no sulfide present the cells remained viable and motile for ca. 3 days both in light and darkness. Oxygen was respired also in the light, but respiration rates were lower than in the dark. Observed aggregation patterns are interpreted as effective protection strategies against high oxygen concentrations and might represent first stages of biofilm formation.

AB - The motility of the purple sulfur bacterium Marichromatium gracile was investigated under different light regimes in a gradient capillary setup with opposing oxygen and sulfide gradients. The gradients were quantified with microsensors, while the behavior of swimming cells was studied by video microscopy in combination with a computerized cell tracking system. M. gracile exhibited photokinesis, photophobic responses, and phobic responses toward oxygen and sulfide. The observed migration patterns could be explained solely by the various phobic responses. In the dark, M. gracile formed an ~500-µm-thick band at the oxic-anoxic interface, with a sharp border toward the oxic zone always positioned at ~10 µM O2. Flux calculations yielded a molar conversion ratio Stot/O2 of 2.03:1 (Stot = [H2S] + [HS] + [S2]) for the sulfide oxidation within the band, indicating that in darkness the bacteria oxidized sulfide incompletely to sulfur stored in intracellular sulfur globules. In the light, M. gracile spread into the anoxic zone while still avoiding regions with >10 µM O2. The cells also preferred low sulfide concentrations if the oxygen was replaced by nitrogen. A light-dark transition experiment demonstrated a dynamic interaction between the chemical gradients and the cell's metabolism. In darkness and anoxia, M. gracile lost its motility after ca. 1 h. In contrast, at oxygen concentrations of >100 µM with no sulfide present the cells remained viable and motile for ca. 3 days both in light and darkness. Oxygen was respired also in the light, but respiration rates were lower than in the dark. Observed aggregation patterns are interpreted as effective protection strategies against high oxygen concentrations and might represent first stages of biofilm formation.

U2 - 10.1128/AEM.67.12.5410-5419.2001

DO - 10.1128/AEM.67.12.5410-5419.2001

M3 - Journal article

VL - 67

SP - 5410

EP - 5419

JO - Applied and Environmental Microbiology

JF - Applied and Environmental Microbiology

SN - 0099-2240

IS - 12

ER -

ID: 170551