Open AccessBook10.1007/978-1-4899-1582-5

Sulfate-reducing bacteria

- 01 Jan 1995

446

TL;DR: Characteristics and Activities of Sulfate-reducing Bacteria L.M. Tomei, and Molecular Biology of Redoxactive Metal Proteins from Desulfovibrio W.D. van Dongen.

Abstract: Characteristics and Activities of Sulfate-reducing Bacteria L.L. Barton, F.A. Tomei. Sulfate-reducing Archaea R.K. Thauer, J. Kunow. Taxonomic Relationships E. Stackebrandt, et al. Respiratory Sulfate Reduction J.M. Akagi. Characteristics of Electron Transfer Proteins L. Chen, et al. Solute Transport and Cell Energetics H. Cypionka. Molecular Biology of Redoxactive Metal Proteins from Desulfovibrio W.M.A.M. van Dongen. Ecology of Sulfate-reducing Bacteria G.D. Fauque. Biocorrosion W.A. Hamilton, W. Lee. Control in Industrial Settings T.R. Jack, D.W.S. Westlake. Metabolism of Environmental Contaminants by Mixed and Pure Cultures of Sulfate-reducing Bacteria B.D. Ensley, J.M. Suflita. Index.

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1. What contributions have the authors mentioned in the paper "Overcoming the anaerobic hurdle in phenotypic microarrays: generation and visualization of growth curve data for desulfovibrio vulgaris hildenborough" ?

The OmniLog unit this paper is designed to simultaneously measure phenotypic responses from a standardized inoculum to almost 2000 substrates, grouped into arrays.

Fig. 3. False color images (see text) representing growth curves from 96-well microplates: (a) under inoculated microplate, (b) over inoculated microplate, (c) properly inoculated microplate. Arrows show location of wells whose growth curves are plotted above each color image. The color legend for these plots is shown in Fig. 2.

Fig. 4. (a) Representative growth curves from standardized inoculum. Shown are averages of three biological replicates of D. vulgaris growth in OL at 30 °C in empty 96 well microtiter plates. Vertical lines represent one standard deviation. (b) Biological replicates of D. vulgaris growth in LS4D at 30 °C assays on the OmniLog™, in hungate tubes and measured at 600 nm, and literature reported growth curve (Mukhopadhyay et al., 2006).

Fig. 8. False color images (see text) used to detect problemmicroplates: (a) several rows of wells, indicated by left brace, are under inoculated, (b) high turbidity indicated by black arrows and orange lines are due to chemical reactions between the growth medium and well treatment, (c) spikes in signals indicated by red arrows and vertical banding are due to instrument malfunction. The color legend for these plots is shown in Fig. 2.

Table 2 Calculated accumulation rates (AR) of FeS precipitates from observed growth curves (see Fig. 4)

Fig. 5. Calibration of D. vulgaris with AODC (cell counts) and OD 600 nm. OD 600 nm values over 1.0 absorbance units were diluted prior to measurement.

Table 3 PM wells with unworkable abiotic reactions with D. vulgaris and LS4D media

Citations

Journal Article•10.1016/J.BIORTECH.2007.01.057

Inhibition of anaerobic digestion process: A review

Ye Chen, +2 more

- 01 Jul 2008

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TL;DR: This review provides a detailed summary of the research conducted on the inhibition of anaerobic processes and indicates that co-digestion with other waste, adaptation of microorganisms to inhibitory substances, and incorporation of methods to remove or counteract toxicants before an aerobic digestion can significantly improve the waste treatment efficiency.

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Sulfur Isotope Geochemistry of Sulfide Minerals

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- 01 Jan 2006

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Microbial diversity of soda lakes.

Brian E. Jones, +3 more

- 01 Aug 1998

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TL;DR: Although present-day soda lakes are geologically quite recent, they have probably existed since archaean times, permitting the evolution of independent communities of alkaliphiles since an early period in the Earth's history.

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References

Book Chapter•10.1007/978-1-4757-2191-1_21

Gram-Negative Mesophilic Sulfate-Reducing Bacteria

Friedrich Widdel, +1 more

- 01 Jan 1992

TL;DR: The utilization of polysaccharides or polypeptides, such as has been observed with the extremely thermophilic sulfate-reducing archaebacterium Archaeoglobus (Stetter, 1988; Stetter et al., 1987), has not been reported for mesophobic sulfate reducers.

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•Journal Article•10.1146/ANNUREV.BI.65.070196.002541

Electron Transfer In Proteins

Jay R. Winkler

- 18 May 1997

TL;DR: Analyses of electronic-coupling strengths suggest that the efficiency of long-range ET depends on the protein secondary structure: beta sheets appear to mediate coupling more efficiently than alpha-helical structures, and hydrogen bonds play a critical role in both.

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Microbiology and ecology of sulfate-and sulfur-reducing bacteria

Friedrich Widdel

- 01 Jan 1988

977

•Journal Article•10.1128/AEM.33.5.1162-1169.1977

Growth of desulfovibrio in lactate or ethanol media low in sulfate in association with H2-utilizing methanogenic bacteria.

Marvin P. Bryant, +3 more

- 01 May 1977

- Applied and Environmental Microbiology

TL;DR: The results with known mixtures of bacteria suggest that hydrogenase-forming, sulfate-reducing bacteria could be active in some methanogenic ecosystems that are low in sulfate, and it is suggested that lack of availability of H(2) for growth of methanogens is a major factor in suppression of meetinghanogenesis by sulfate in natural ecosystems.

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475

Sulphate-reducing bacteria

George T. Macfarlane, +1 more

- 01 Jan 1991

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Sulfate-reducing bacteria

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1. What contributions have the authors mentioned in the paper "Overcoming the anaerobic hurdle in phenotypic microarrays: generation and visualization of growth curve data for desulfovibrio vulgaris hildenborough" ?

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Citations

Inhibition of anaerobic digestion process: A review

Sulfur Isotope Geochemistry of Sulfide Minerals

Microbial Extracellular Polymeric Substances

Current and Past Strategies for Bacterial Culture in Clinical Microbiology

Microbial diversity of soda lakes.

References

Gram-Negative Mesophilic Sulfate-Reducing Bacteria

Electron Transfer In Proteins

Microbiology and ecology of sulfate-and sulfur-reducing bacteria

Growth of desulfovibrio in lactate or ethanol media low in sulfate in association with H2-utilizing methanogenic bacteria.

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