Methanogenesis or biomethanation is the formation of methane by microbes known as methanogens. Organisms capable of producing methane have been identified only from the domain Archaea, a group phylogenetically distinct from both eukaryotes and bacteria, although many live in close association with anaerobic bacteria. The production of methane is an important and widespread form of microbial metabolism. In anoxic environments, it is the final step in the decomposition of biomass. Methanogenesis is responsible for significant amounts of natural gas accumulations, the remainder being thermogenic.
Methanogenesis in microbes is a form of anaerobic respiration. Methanogens do not use oxygen to respire; in fact, oxygen inhibits the growth of methanogens. The terminal electron acceptor in methanogenesis is not oxygen, but carbon. The carbon can occur in a small number of organic compounds, all with low molecular weights. The two best described pathways involve the use of acetic acid or inorganic carbon dioxide as terminal electron acceptors:
- CH3COOH → CH4 + CO2
During anaerobic respiration of carbohydrates, H2 and acetate are formed in a ratio of 2:1 or lower, so H2 contributes only ca. 33% to methanogenesis, with acetate contributing the greater proportion. In some circumstances, for instance in the rumen, where acetate is largely absorbed into the bloodstream of the host, the contribution of H2 to methanogenesis is greater.
However, depending on pH and temperature, methanogenesis has been shown to use carbon from other small organic compounds, such as formic acid (formate), methanol, methylamines, tetramethylammonium, dimethyl sulfide, and methanethiol. The catabolism of the methyl compounds is mediated by methyl transferases to give methyl coenzyme M.
The mechanism for the conversion of CH
3–S bond into methane involves a ternary complex of methyl coenzyme M and coenzyme B fit into a channel terminated by the axial site on nickel of the cofactor F430. One proposed mechanism invokes electron transfer from Ni(I) (to give Ni(II)), which initiates formation of CH
4. Coupling of the coenzyme M thiyl radical (RS.) with HS coenzyme B releases a proton and re-reduces Ni(II) by one-electron, regenerating Ni(I).
Some organisms can oxidize methane, functionally reversing the process of methanogenesis, also referred to as the anaerobic oxidation of methane (AOM). Organisms performing AOM have been found in multiple marine and freshwater environments including methane seeps, hydrothermal vents, coastal sediments and sulfate-methane transition zones. These organisms may accomplish reverse methanogenesis using a nickel-containing protein similar to methyl-coenzyme M reductase used by methanogenic archaea. Reverse methanogenesis occurs according to the reaction:
- SO42− + CH4 → HCO3− + HS− + H2O
Importance in carbon cycleEdit
Methanogenesis is the final step in the decay of organic matter. During the decay process, electron acceptors (such as oxygen, ferric iron, sulfate, and nitrate) become depleted, while hydrogen (H2) and carbon dioxide accumulate. Light organics produced by fermentation also accumulate. During advanced stages of organic decay, all electron acceptors become depleted except carbon dioxide. Carbon dioxide is a product of most catabolic processes, so it is not depleted like other potential electron acceptors.
Only methanogenesis and fermentation can occur in the absence of electron acceptors other than carbon. Fermentation only allows the breakdown of larger organic compounds, and produces small organic compounds. Methanogenesis effectively removes the semi-final products of decay: hydrogen, small organics, and carbon dioxide. Without methanogenesis, a great deal of carbon (in the form of fermentation products) would accumulate in anaerobic environments.
Enteric fermentation occurs in the gut of some animals, especially ruminants. In the rumen, anaerobic organisms, including methanogens, digest cellulose into forms nutritious to the animal. Without these microorganisms, animals such as cattle would not be able to consume grasses. The useful products of methanogenesis are absorbed by the gut, but methane is released from the animal mainly by belching (eructation). The average cow emits around 250 liters of methane per day. In this way, ruminants contribute about 25% of anthropogenic methane emissions. One method of methane production control in ruminants is by feeding them 3-nitrooxypropanol.
Some humans produce flatus that contains methane. In one study of the feces of nine adults, five of the samples contained archaea capable of producing methane. Similar results are found in samples of gas obtained from within the rectum.
Even among humans whose flatus does contain methane, the amount is in the range of 10% or less of the total amount of gas.
Many experiments have suggested that leaf tissues of living plants emit methane. Other research has indicated that the plants are not actually generating methane; they are just absorbing methane from the soil and then emitting it through their leaf tissues.
Methanogens are observed in anoxic soil environments, contributing to the degradation of organic matter. This organic matter may be placed by humans through landfill, buried as sediment on the bottom of lakes or oceans as sediments, and as residual organic matter from sediments that have formed into sedimentary rocks.
Role in global warmingEdit
Atmospheric methane is an important greenhouse gas with a global warming potential 25 times greater than carbon dioxide (averaged over 100 years), and methanogenesis in livestock and the decay of organic material is thus a considerable contributor to global warming. It may not be a net contributor in the sense that it works on organic material which used up atmospheric carbon dioxide when it was created, but its overall effect is to convert the carbon dioxide into methane which is a much more potent greenhouse gas.
Methanogenesis can also be beneficially exploited, to treat organic waste, to produce useful compounds, and the methane can be collected and used as biogas, a fuel. It is the primary pathway whereby most organic matter disposed of via landfill is broken down.
The presence of atmospheric methane has a role in the scientific search for extra-terrestrial life. The justification is that methane in the atmosphere will eventually dissipate, unless something is replenishing it. If methane is detected (by using a spectrometer for example) this may indicate that life is, or recently was, present. This was debated when methane was discovered in the Martian atmosphere by M.J. Mumma of NASA's Goddard Flight Center, and verified by the Mars Express Orbiter (2004) and in Titan's atmosphere by the Huygens probe (2005). This debate was furthered with the discovery of 'transient', 'spikes of methane' on Mars by the Curiosity Rover.
It is also argued that atmospheric methane can come from volcanoes or other fissures in the planet's crust and that without an isotopic signature, the origin or source may be difficult to identify.
On 13 April 2017, NASA confirmed that the dive of the Cassini orbiter spacecraft on 28 October 2015 discovered the Enceladus plume which has all the ingredients for methanogenesis-based life forms to feed from. Previous results, published in March 2015, suggested hot water is interacting with rock beneath the sea; the new findings support that conclusion and add that the rock appears to be reacting chemically. From these observations scientists have determined that nearly 98 percent of the gas in the plume is water, about 1 percent is hydrogen and the rest is a mixture of other molecules including carbon dioxide, methane and ammonia.
Permafrost degradation makes the largest future transfer of methane.
- Katz B. (2011). "Microbial processes and natural gas accumulations". The Open Geology Journal. 5: 75–83. doi:10.2174/1874262901105010075.
- Kietäväinen and Purkamo (2015). "The origin, source, and cycling of methane in deep crystalline rock biosphere". Front. Microbiol. 6: 725. doi:10.3389/fmicb.2015.00725. PMC 4505394. PMID 26236303.
- Cramer and Franke (2005). "Indications for an active petroleum system in the Laptev Sea, NE Siberia/publication/227744258_Indications_for_an_active_petroleum_system_in_the_Laptev_Sea_NE_Siberia". Journal of Petroleum Geology. 28 (4): 369–384. Bibcode:2005JPetG..28..369C. doi:10.1111/j.1747-5457.2005.tb00088.x.
- Thauer, R. K. (1998). "Biochemistry of Methanogenesis: a Tribute to Marjory Stephenson". Microbiology. 144: 2377–2406. doi:10.1099/00221287-144-9-2377.
- Conrad, Rolf (1999). "Contribution of hydrogen to methane production and control of hydrogen concentrations in methanogenic soils and sediments". FEMS Microbiology Ecology. 28 (3): 193–202. doi:10.1016/s0168-6496(98)00086-5.
- Finazzo C, Harmer J, Bauer C, et al. (April 2003). "Coenzyme B induced coordination of coenzyme M via its thiol group to Ni(I) of F430 in active methyl-coenzyme M reductase". J. Am. Chem. Soc. 125 (17): 4988–9. doi:10.1021/ja0344314. PMID 12708843.
- Ruff, S. Emil; Biddle, Jennifer F.; Teske, Andreas P.; Knittel, Katrin; Boetius, Antje; Ramette, Alban (31 March 2015). "Global dispersion and local diversification of the methane seep microbiome". Proceedings of the National Academy of Sciences of the United States of America. 112 (13): 4015–4020. Bibcode:2015PNAS..112.4015R. doi:10.1073/pnas.1421865112. ISSN 1091-6490. PMC 4386351. PMID 25775520.
- Scheller, Silvan; Goenrich, Meike; Boecher, Reinhard; Thauer, Rudolf K.; Jaun, Bernhard (3 June 2010). "The key nickel enzyme of methanogenesis catalyses the anaerobic oxidation of methane". Nature. 465 (7298): 606–608. Bibcode:2010Natur.465..606S. doi:10.1038/nature09015. ISSN 1476-4687. PMID 20520712.
- Krüger M, Meyerdierks A, Glöckner FO, et al. (December 2003). "A conspicuous nickel protein in microbial mats that oxidize methane anaerobically". Nature. 426 (6968): 878–81. Bibcode:2003Natur.426..878K. doi:10.1038/nature02207. PMID 14685246.
- Radio Australia: "Innovations – Methane In Agriculture." 15 August 2004. Retrieved 28 August 2007.
- Hristov, A. N., et al., "An inhibitor persistently decreased enteric methane emission from dairy cows with no negative effect on milk production", Proc. Natl. Acad. Sci. U. S. A. 2015, volume 112, 10663-10668. doi:10.1073/pnas.1504124112
- Miller TL; Wolin MJ; de Macario EC; Macario AJ (1982). "Isolation of Methanobrevibacter smithii from human feces". Appl Environ Microbiol. 43 (1): 227–32. PMC 241804. PMID 6798932.
- "Human Digestive System". Encyclopædia Britannica. Retrieved 22 August 2007.
- Kepler F, et al. (2006). "Methane emissions from terrestrial plants under aerobic conditions". Nature. 439 (7073): 187–191. Bibcode:2006Natur.439..187K. doi:10.1038/nature04420. PMID 16407949.
- Le Mer, J.; Roger, P. (2001). "Production, oxidation, Emission and Consumption of Methane by Soils: A Review". European Journal of Soil Biology. 37: 25–50. doi:10.1016/S1164-5563(01)01067-6.
- "Global Warming Potentials". Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change, 2007. 2007. Retrieved 24 May 2012.
- Nair, Athira (14 July 2015). "After Freedom Park, waste to light up Gandhinagar in Bengaluru". Economic Times.
- DoE Report CWM039A+B/92 Young, A. (1992)
- BBC article about methane as sign of life http://news.bbc.co.uk/2/hi/science/nature/4295475.stm
- European Space Agency, Methane in Martian Atmosphere http://www.esa.int/esaMI/Mars_Express/SEMZ0B57ESD_0.html
- Space.Com article about methane on Huygens http://www.space.com/scienceastronomy/ap_huygens_update_050127.html
- New Scientist article about atmospheric methane https://www.newscientist.com/article.ns?id=dn7059
- National Geographic Article about methane as sign of life http://news.nationalgeographic.com/news/2004/10/1007_041007_mars_methane.html
- Northon, Karen (13 April 2017). "NASA Missions Provide New Insights into 'Ocean Worlds'". NASA. Retrieved 13 April 2017.