Literature DB >> 8987358

Soil microorganisms as controllers of atmospheric trace gases (H2, CO, CH4, OCS, N2O, and NO).

R Conrad1.   

Abstract

Production and consumption processes in soils contribute to the global cycles of many trace gases (CH4, CO, OCS, H2, N2O, and NO) that are relevant for atmospheric chemistry and climate. Soil microbial processes contribute substantially to the budgets of atmospheric trace gases. The flux of trace gases between soil and atmosphere is usually the result of simultaneously operating production and consumption processes in soil: The relevant processes are not yet proven with absolute certainty, but the following are likely for trace gas consumption: H2 oxidation by abiontic soil enzymes; CO cooxidation by the ammonium monooxygenase of nitrifying bacteria; CH4 oxidation by unknown methanotrophic bacteria that utilize CH4 for growth; OCS hydrolysis by bacteria containing carbonic anhydrase; N2O reduction to N2 by denitrifying bacteria; NO consumption by either reduction to N2O in denitrifiers or oxidation to nitrate in heterotrophic bacteria. Wetland soils, in contrast to upland soils are generally anoxic and thus support the production of trace gases (H2, CO, CH4, N2O, and NO) by anaerobic bacteria such as fermenters, methanogens, acetogens, sulfate reducers, and denitrifiers. Methane is the dominant gaseous product of anaerobic degradation of organic matter and is released into the atmosphere, whereas the other trace gases are only intermediates, which are mostly cycled within the anoxic habitat. A significant percentage of the produced methane is oxidized by methanotrophic bacteria at anoxic-oxic interfaces such as the soil surface and the root surface of aquatic plants that serve as conduits for O2 transport into and CH4 transport out of the wetland soils. The dominant production processes in upland soils are different from those in wetland soils and include H2 production by biological N2 fixation, CO production by chemical decomposition of soil organic matter, and NO and N2O production by nitrification and denitrification. The processes responsible for CH4 production in upland soils are completely unclear, as are the OCS production processes in general. A problem for future research is the attribution of trace gas metabolic processes not only to functional groups of microorganisms but also to particular taxa. Thus, it is completely unclear how important microbial diversity is for the control of trace gas flux at the ecosystem level. However, different microbial communities may be part of the reason for differences in trace gas metabolism, e.g., effects of nitrogen fertilizers on CH4 uptake by soil; decrease of CH4 production with decreasing temperature; or different rates and modes of NO and N2O production in different soils and under different conditions.

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Year:  1996        PMID: 8987358      PMCID: PMC239458          DOI: 10.1128/mr.60.4.609-640.1996

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  142 in total

1.  Responses of methanotrophic activity in soils and cultures to water stress.

Authors:  S Schnell; G M King
Journal:  Appl Environ Microbiol       Date:  1996-09       Impact factor: 4.792

2.  Distribution and rate of methane oxidation in sediments of the Florida everglades.

Authors:  G M King; P Roslev; H Skovgaard
Journal:  Appl Environ Microbiol       Date:  1990-09       Impact factor: 4.792

3.  Evaluation of methyl fluoride and dimethyl ether as inhibitors of aerobic methane oxidation.

Authors:  R S Oremland; C W Culbertson
Journal:  Appl Environ Microbiol       Date:  1992-09       Impact factor: 4.792

4.  Streptomyces thermoautotrophicus sp. nov., a Thermophilic CO- and H(2)-Oxidizing Obligate Chemolithoautotroph.

Authors:  D Gadkari; K Schricker; G Acker; R M Kroppenstedt; O Meyer
Journal:  Appl Environ Microbiol       Date:  1990-12       Impact factor: 4.792

Review 5.  The biological role of nitric oxide in bacteria.

Authors:  W G Zumft
Journal:  Arch Microbiol       Date:  1993       Impact factor: 2.552

Review 6.  Intestinal microbiota of termites and other xylophagous insects.

Authors:  J A Breznak
Journal:  Annu Rev Microbiol       Date:  1982       Impact factor: 15.500

7.  The reaction of no with superoxide.

Authors:  R E Huie; S Padmaja
Journal:  Free Radic Res Commun       Date:  1993

8.  Nitric oxide and nitrous oxide production and cycling during dissimilatory nitrite reduction by Pseudomonas perfectomarina.

Authors:  O C Zafiriou; Q S Hanley; G Snyder
Journal:  J Biol Chem       Date:  1989-04-05       Impact factor: 5.157

9.  Carbonyl sulfide and carbon dioxide as new substrates, and carbon disulfide as a new inhibitor, of nitrogenase.

Authors:  L C Seefeldt; M E Rasche; S A Ensign
Journal:  Biochemistry       Date:  1995-04-25       Impact factor: 3.162

10.  [Diagnosis and surgical treatment of bilateral paralysis of the superior oblique muscle].

Authors:  G Klainguti; J Lang
Journal:  Klin Monbl Augenheilkd       Date:  1995-05       Impact factor: 0.700

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  222 in total

1.  Nitrite reductase genes (nirK and nirS) as functional markers to investigate diversity of denitrifying bacteria in pacific northwest marine sediment communities.

Authors:  G Braker; J Zhou; L Wu; A H Devol; J M Tiedje
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

2.  The periplasmic nitrate reductase in Pseudomonas sp. strain G-179 catalyzes the first step of denitrification.

Authors:  L Bedzyk; T Wang; R W Ye
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

3.  Enrichment of high-affinity CO oxidizers in Maine forest soil.

Authors:  K R Hardy; G M King
Journal:  Appl Environ Microbiol       Date:  2001-08       Impact factor: 4.792

4.  Family- and genus-level 16S rRNA-targeted oligonucleotide probes for ecological studies of methanotrophic bacteria.

Authors:  J Gulledge; A Ahmad; P A Steudler; W J Pomerantz; C M Cavanaugh
Journal:  Appl Environ Microbiol       Date:  2001-10       Impact factor: 4.792

5.  A new rate law describing microbial respiration.

Authors:  Qusheng Jin; Craig M Bethke
Journal:  Appl Environ Microbiol       Date:  2003-04       Impact factor: 4.792

6.  Actinobacterial nitrate reducers and proteobacterial denitrifiers are abundant in N2O-metabolizing palsa peat.

Authors:  Katharina Palmer; Marcus A Horn
Journal:  Appl Environ Microbiol       Date:  2012-06-01       Impact factor: 4.792

7.  Nitric oxide signaling and transcriptional control of denitrification genes in Pseudomonas stutzeri.

Authors:  K U Vollack; W G Zumft
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

8.  Molecular analyses of the methane-oxidizing microbial community in rice field soil by targeting the genes of the 16S rRNA, particulate methane monooxygenase, and methanol dehydrogenase

Authors: 
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

9.  Contribution of methanotrophic and nitrifying bacteria to CH4 and NH4+ oxidation in the rhizosphere of rice plants as determined by new methods of discrimination

Authors: 
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

10.  Rapid acyl-homoserine lactone quorum signal biodegradation in diverse soils.

Authors:  Ya-Juan Wang; Jared Renton Leadbetter
Journal:  Appl Environ Microbiol       Date:  2005-03       Impact factor: 4.792

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