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Sulfate reduction organisms

The case of bacterial reduction of sulfate to sulfide described by Berner (1984) provides a useful example. The dependence of sulfate reduction on sulfate concentration is shown in Fig. 5-4. Here we see that for [SO ] < 5 mM the rate is a linear function of sulfate concentration but for [SO4 ] > 10 itiM the rate is reasonably independent of sulfate concentration. The sulfate concentration in the ocean is about 28 mM and thus in shallow marine sediments the reduction rate does not depend on sulfate concentration. (The rate does depend on the concentration of organisms and the concentration of other necessary reactants - organic carbon in this case.) In freshwaters the sulfate concentration is... [Pg.100]

The conditions under which these function and their regulation depend on the organism. For example, in Escherichia coli, oxygen represses the synthesis of the other reductases, and under anaerobic conditions the reductases for fumarate, DMSO, and TMAO are repressed by nitrate. This does not apply to Wolinella succinogenes in which sulfur represses the synthesis of the more positive electron acceptors nitrate and fumarate (Lorenzen et al. 1993). The DMSO reductase from Escherichia coli (Weiner et al. 1988) has a broad substrate versatility, and is able to reduce a range of sulfoxides and A-oxides. Anaerobic sulfate reduction is not discussed here in detail. [Pg.148]

Kuhn EP, GT Townsend, JM Suflita (1990) Effect of sulfate and organic carbon supplements on reductive dehalogenation of chloroanilines in anaerobic aquifer slurries. Appl Environ Microbiol 56 2630-2637. [Pg.492]

Belle Glade Carbonate Hot acid Organic plant wastes Neutralization Bacterial sulfate reduction Methane production... [Pg.837]

Hydrogen sulfide is a well known general metabolite produced on sulfate reduction by certain bacteria. Moreover, organic forms of sulfur can give rise to HS , hence H2S in certain bacteria. Thus, cysteine desulfhydrase (EC 4.4.1.1, cystathionine y-lyase) converts L-cysteine to H2S, pyruvate, and NH3. This enzyme shows a requirement for pyridoxal phosphate and the unstable ami-noacrylic acid is an intermediate (Equation 1) in the reaction ... [Pg.673]

Dissolved arsenic is correlated with ammonia (Fig. 4), consistent with a release mechanism associated with the oxidation of organic carbon. Other chemical data not shown here provide clear evidence of iron, manganese and sulfate reduction and abundant methane in some samples indicates that methanogenesis is also occurring. It is not clear however if arsenic is released primarily by a desorption process associated with reduction of sorbed arsenic or by release after the reductive dissolution of the iron oxide sorbent. Phreeqc analysis shows PC02 between 10"12 and 10"° bars and that high arsenic waters are supersaturated with both siderite and vivianite. [Pg.69]

The ground water from well 6 (site 1) yielded both the most depleted S13C and most enriched 834S. Isotopic compositions of this dual nature are consistent with methanogenesis and bacterial sulfate reduction, arising form interaction with organic-rich (bog) soils from below. [Pg.334]

Sulfate is needed as an electron acceptor for the sulfate reduction process, but normally, it is available in unlimited concentrations in wastewater. If this is not the case, iron sulfate may support the process. The anaerobic fermentation processes still proceed, and the odorous organic substances produced are generally not affected by the addition of iron salts. [Pg.156]

Sediment deposition on the seafloor traps interstitial water. After deposition, complex reactions take place in the sediment, most of them fueled by the decay of organic matter, such as sulfate reduction, denitrification,... Because of fast diffusion rates of most cations in seawater, the presence of interstitial water makes exchange between overlying sedimentary layers a much easier process than if sediment deposition was dry. The book by Berner (1980) is entirely dedicated to these processes and only a short example is given here. [Pg.461]

Let us consider sulfate reduction by bacterial activity at the expense of decaying solid organic matter. Berner suggests the simplified equation... [Pg.461]

The cycle of iron solubilization will continue as long as bacteria and/or plants produce organic ligands.The cycle will stop when sulfate reduction rates are high and organic ligand production is low. At this point soluble hydrogen sulfide reacts with Fe(II) to form sulfide minerals. The iron cycle shown in Fig. 10.15 for salt marsh sediments may also occur in other marine sedimentary systems. [Pg.363]

Bruchert V, Knoblauch C, Jorgensen BB (2001) Controls on stable sulfur isotope fractionation during bacterial sulfate reduction in Arctic sediments. Geochim Cosmochim Acta 65 763-776 Bryan BA, Shearer G, Skeeters JL, Kohl DH (1983) Variable expression of the nitrogen isotope effect associated with denitrification of nitrate. J Biol Chem 258 8613-8617 Canfield DE (2001) Biogeochemistry of sulfur isotopes. Rev Mineral Geochem 43 607-636 Chau YK, Riley JP (1965) The determination of selenium in sea water, silicates, and marine organisms. Anal Chim Acta 33 36-49... [Pg.314]

Habicht KS, Canfield DE (1997) Sulfur isotope fractionation during bacterial sulfate reduction in organic-rich sediments. Geochim CosmochimActa61(24) 5351-5361 Habicht KS, Gade M, Thamdrup B, Berg P, Canfield DE (2002) Calibration of sulfate levels in the Archean ocean. Science 298 2372-2374... [Pg.315]

In sediments that lie in coastal waters, organic carbon levels are high enough to support denitrification, iron respiration, sulfate reduction and methanogenesis. As shown in the idealized profile presented in Figure 12.3b, the depth of O2 penetration in organic-rich sediments is typically so shallow as to make the zones of aerobic respiration. [Pg.317]

A few examples of chemoautolithotrophic processes have been mentioned in this chapter, namely anaerobic methane oxidation coupled to sulfate reduction and the ones listed in Table 12.2 involving manganese, iron, and nitrogen. Another example are the microbial metabolisms that rely on sulfide oxidation. Since sulfide oxidation is a source of electrons, it is a likely source of energy that could be driving denitrification, and manganese and iron reduction where organic matter is scarce. [Pg.324]

In some cases the methods may be combined. Examples would include the biotechnological precipitation of chromium from Cr(VI)-containing wastes from electroplating factories by sulfate reduction to precipitate chromium sulfide. Sulfate reduction can use fatty acids as organic substrates with no accumulation of sulfide. In the absence of fatty acids but with straw as organic substrate, the direct reduction of chromium has been observed without sulfate reduction [43]. [Pg.158]

Kinetic isotope effects during microbial processes. Micro-organisms have long been known to fractionate isotopes during their sulfur metabolism, particularly during dissimilatory sulfate reduction, which produces the largest fractionations in the sulfur cycle... [Pg.73]


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See also in sourсe #XX -- [ Pg.49 ]




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Organic reduction

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Sulfate Reduction and Organic Carbon Mineralization

Sulfates reduction

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