Academic literature on the topic 'Methanogenesis Reaction'

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Journal articles on the topic "Methanogenesis Reaction"

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Shima, Seigo, Gangfeng Huang, Tristan Wagner, and Ulrich Ermler. "Structural Basis of Hydrogenotrophic Methanogenesis." Annual Review of Microbiology 74, no. 1 (2020): 713–33. http://dx.doi.org/10.1146/annurev-micro-011720-122807.

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Most methanogenic archaea use the rudimentary hydrogenotrophic pathway—from CO2 and H2 to methane—as the terminal step of microbial biomass degradation in anoxic habitats. The barely exergonic process that just conserves sufficient energy for a modest lifestyle involves chemically challenging reactions catalyzed by complex enzyme machineries with unique metal-containing cofactors. The basic strategy of the methanogenic energy metabolism is to covalently bind C1 species to the C1 carriers methanofuran, tetrahydromethanopterin, and coenzyme M at different oxidation states. The four reduction rea
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Lie, Thomas J., Kyle C. Costa, Boguslaw Lupa, Suresh Korpole, William B. Whitman, and John A. Leigh. "Essential anaplerotic role for the energy-converting hydrogenase Eha in hydrogenotrophic methanogenesis." Proceedings of the National Academy of Sciences 109, no. 38 (2012): 15473–78. http://dx.doi.org/10.1073/pnas.1208779109.

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Despite decades of study, electron flow and energy conservation in methanogenic Archaea are still not thoroughly understood. For methanogens without cytochromes, flavin-based electron bifurcation has been proposed as an essential energy-conserving mechanism that couples exergonic and endergonic reactions of methanogenesis. However, an alternative hypothesis posits that the energy-converting hydrogenase Eha provides a chemiosmosis-driven electron input to the endergonic reaction. In vivo evidence for both hypotheses is incomplete. By genetically eliminating all nonessential pathways of H2 metab
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Hao, L. P., L. Mazéas, F. Lü, J. Grossin-Debattista, P. J. He, and T. Bouchez. "Effect of ammonia on methane production pathways and reaction rates in acetate-fed biogas processes." Water Science and Technology 75, no. 8 (2017): 1839–48. http://dx.doi.org/10.2166/wst.2017.032.

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In order to understand the correlation between ammonia and methanogenesis metabolism, methane production pathways and their specific rates were studied at total ammonium nitrogen (TAN) concentrations of 0.14–9 g/L in three methanogenic sludges fed with acetate, at both mesophilic and thermophilic conditions. Results showed that high levels of TAN had significant inhibition on methanogenesis; this could, however, be recovered via syntrophic acetate oxidation (SAO) coupled with Hydrogenotrophic Methanogenesis (HM) performed by acetate oxidizing syntrophs or through Acetoclastic Methanogenesis (A
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Richards, Matthew A., Thomas J. Lie, Juan Zhang, Stephen W. Ragsdale, John A. Leigh, and Nathan D. Price. "Exploring Hydrogenotrophic Methanogenesis: a Genome Scale Metabolic Reconstruction of Methanococcus maripaludis." Journal of Bacteriology 198, no. 24 (2016): 3379–90. http://dx.doi.org/10.1128/jb.00571-16.

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ABSTRACTHydrogenotrophic methanogenesis occurs in multiple environments, ranging from the intestinal tracts of animals to anaerobic sediments and hot springs. Energy conservation in hydrogenotrophic methanogens was long a mystery; only within the last decade was it reported that net energy conservation for growth depends on electron bifurcation. In this work, we focus onMethanococcus maripaludis, a well-studied hydrogenotrophic marine methanogen. To better understand hydrogenotrophic methanogenesis and compare it with methylotrophic methanogenesis that utilizes oxidative phosphorylation rather
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Kim, In S., Henry H. Tabak, and James C. Young. "Modeling of the fate and effect of chlorinated phenols in anaerobic treatment processes." Water Science and Technology 36, no. 6-7 (1997): 287–94. http://dx.doi.org/10.2166/wst.1997.0602.

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Studies were conducted to assess the biotransformation kinetics and inhibitory effects of mono-, di-, and trichlorophenol on acetogenic and methanogenic reactions using a standardized anaerobic protocol (Young and Tabak, 1993). Intrinsic kinetic parameters were estimated for each reaction using the Monod model. Reductive dechlorination of the toxicants was investigated using acclimated mixed cultures under methanogenic conditions. The studies indicated that inhibition of acetogenesis and methanogenesis was best described using exponential rather than linear inhibition terms. A second significa
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Staley, Bryan F., Francis L. de los Reyes, and Morton A. Barlaz. "Effect of Spatial Differences in Microbial Activity, pH, and Substrate Levels on Methanogenesis Initiation in Refuse." Applied and Environmental Microbiology 77, no. 7 (2011): 2381–91. http://dx.doi.org/10.1128/aem.02349-10.

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ABSTRACTThe initiation of methanogenesis in refuse occurs under high volatile fatty acid (VFA) concentration and low pH (5.5 to 6.25), which generally are reported to inhibit methanogenicArchaea. One hypothesized mechanism for the initiation of methanogenesis in refuse decomposition is the presence of pH-neutral niches within the refuse that act as methanogenesis initiation centers. To provide experimental support for this mechanism, laboratory-scale landfill reactors were operated and destructively sampled when methanogenesis initiation was observed. The active bacterial and archaeal populati
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Nozhevnikova, Alla N., C. Holliger, A. Ammann, and A. J. B. Zehnder. "Methanogenesis in sediments from deep lakes at different temperatures (2–70°C)." Water Science and Technology 36, no. 6-7 (1997): 57–64. http://dx.doi.org/10.2166/wst.1997.0575.

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Methanogenic degradation of organic matter occurs in a wide temperature range from psychrophilic to extreme thermophilic conditions. Mesophilic and thermophilic methanogenesis is relatively well investigated, but little is known about low temperature methanogenesis and psychrophilic methanogenic communities. The aim of the present work was to study methanogenesis in a wide range of temperatures with samples from sediments of deep lakes. These sediments may be considered deposits of different types of microorganisms, which are constantly exposed to low temperatures. The main question was how ps
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Donoso-Bravo, A., C. Retamal, M. Carballa, G. Ruiz-Filippi, and R. Chamy. "Influence of temperature on the hydrolysis, acidogenesis and methanogenesis in mesophilic anaerobic digestion: parameter identification and modeling application." Water Science and Technology 60, no. 1 (2009): 9–17. http://dx.doi.org/10.2166/wst.2009.316.

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The effect of temperature on the kinetic parameters involved in the main reactions of the anaerobic digestion process was studied. Batch tests with starch, glucose and acetic acid as substrates for hydrolysis, acidogenesis and methanogenesis, respectively, were performed in a temperature range between 15 and 45°C. First order kinetics was assumed to determine the hydrolysis rate constant, while Monod and Haldane kinetics were considered for acidogenesis and methanogenesis, respectively. The results obtained showed that the anaerobic process is strongly influenced by temperature, with acidogene
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Jun, Wang, Xu Tingting, Yin Lichu, et al. "Nitrate addition inhibited methanogenesis in paddy soils under long-term managements." Plant, Soil and Environment 64, No. 8 (2018): 393–99. http://dx.doi.org/10.17221/231/2018-pse.

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Rice fields are a major source of atmospheric methane (CH<sub>4</sub>). Nitrate has been approved to inhibit CH<sub>4</sub> production from paddy soils, while fertilization as well as water management can also affect the methanogenesis. It is unknown whether nitrate addition might result in shifts in the methanogenesis and methanogens in paddy soils influenced by different practices. Six paddy soils of different fertilizer types and groundwater tables were collected from a long-term experiment site. CH<sub>4</sub> production rate and methanogenic archaeal ab
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Mogollón, J. M., A. W. Dale, H. Fossing, and P. Regnier. "Timescales for the development of methanogenesis and free gas layers in recently-deposited sediments of Arkona Basin (Baltic Sea)." Biogeosciences Discussions 8, no. 4 (2011): 7623–69. http://dx.doi.org/10.5194/bgd-8-7623-2011.

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Abstract. Arkona Basin (southwestern Baltic Sea) is a seasonally-hypoxic basin characterized by the presence of free methane gas in its youngest organic-rich muddy stratum. Through the use of reactive transport models, this study tracks the development of the methane geochemistry in Arkona Basin as this muddy sediment becomes deposited during the last 8 kyr. Four cores are modeled each pertaining to a unique geochemical scenario according to their respective contemporary geochemical profiles. Ultimately the thickness of the muddy sediment and the flux of particulate organic carbon are crucial
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Dissertations / Theses on the topic "Methanogenesis Reaction"

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Rashtchi, Ramina. "Assessing Aquitard Integrity: the Newmarket Till (Southern Ontario)." Thesis, Université d'Ottawa / University of Ottawa, 2020. http://hdl.handle.net/10393/40439.

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The Newmarket Till is a regional aquitard in southern Ontario that overlies the Illinoian to Middle Wisconsinan Lower Sediments and is overlain by the Oak Ridges Moraine (ORM). Geological investigations have mapped the distribution of the till and it is understood that erosional channels, subsequently infilled with fluvial material, breach the till and may create enhanced hydraulic connection between overlying and underlying aquifers. However, little is known about the protective capability of the Newmarket Till where it is intact. This study used natural tracers to assess the extent of transp
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Osborn, Stephen. "Elemental and Isotope Geochemistry of Appalachian Fluids: Constraints on Basin-Scale Brine Migration, Water-Rock Reactions, Microbial Processes, and Natural Gas Generation." Diss., The University of Arizona, 2010. http://hdl.handle.net/10150/194250.

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This study utilizes new geochemical analyses of fluids (formation water and gas) collected predominately from Devonian organic-rich shales and reservoir sandstones from the northern Appalachian Basin margin to investigate basin scale hydrologic processes, water-rock reactions, microbial activity, and natural gas generation. Elemental and isotopic composition of co-produced formation waters and natural gas show that the majority of methane in Devonian organic-rich shales and reservoir sandstones is thermogenic in origin with localized accumulations of microbial gas. Microbial methanogenesis app
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Hagemann, Birger. "Numerical and Analytical Modeling of Gas Mixing and Bio-Reactive Transport during Underground Hydrogen Storage." Thesis, Université de Lorraine, 2017. http://www.theses.fr/2017LORR0328/document.

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En rapport avec la transition énergétique, d’importantes capacités de stockage énergétique sont nécessaires pour intégrer la forte variation de la production énergétique au travers des centrales éoliennes et photovoltaïques. La transformation de l’énergie électrique en énergie chimique sous forme d’hydrogène est l’une des possibles techniques. La technologie de stockage de l’hydrogène souterrain, selon laquelle l’hydrogène est stocké dans les formations souterraines semblables au stockage du gaz naturel est actuellement un axe de recherche de plusieurs états européens. Par comparaison au stock
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Fernandes, Bruna Soares. "Influência da origem do inóculo e da adição de sulfato sobre a degradação de BTX em reator anaeróbio horizontal de leito fixo." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/18/18138/tde-15032016-134215/.

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O desenvolvimento industrial tem, como conseqüência, a maior geração de resíduos, muitos deles tóxicos aos seres vivos. Dentre esses, benzeno, tolueno e xilenos (BTX), derivados do petróleo, estão contaminando aqüíferos por acidentes no transporte e no armazenamento. Por esse motivo, diversas pesquisas têm sido realizadas buscando formas de biodegradar BTX. Esses trabalhos indicam que os principais fatores que podem influenciar a degradação biológica dos BTX são temperatura, pH, disponibilidade de nutrientes, concentração de tóxicos e diversidade de microrganismos. Visando contribuir com o est
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"Coupled Abiotic and Biotic Cycling of Nitrous Oxide." Doctoral diss., 2020. http://hdl.handle.net/2286/R.I.57072.

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abstract: Nitrous oxide (N2O) is an important greenhouse gas and an oxidant respired by a diverse range of anaerobic microbes, but its sources and sinks are poorly understood. The overarching goal of my dissertation is to explore abiotic N2O formation and microbial N2O consumption across reducing environments of the early and modern Earth. By combining experiments as well as diffusion and atmospheric modeling, I present evidence that N2O production can be catalyzed on iron mineral surfaces that may have been present in shallow waters of the Archean ocean. Using photochemical models, I showed
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Book chapters on the topic "Methanogenesis Reaction"

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Thauer, Rudolf K., Reiner Hedderich, and Reinhard Fischer. "Reactions and Enzymes Involved in Methanogenesis from CO2 and H2." In Methanogenesis. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2391-8_5.

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Frey, Perry A., and Adrian D. Hegeman. "Alkyltransferases." In Enzymatic Reaction Mechanisms. Oxford University Press, 2007. http://dx.doi.org/10.1093/oso/9780195122589.003.0019.

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A number of enzymes catalyze alkylation reactions, most of which are reactions of S-adenosyl-L-methionine (SAM) as a methylating agent in the biosynthesis of hormones, modification of DNA, and methyl esterification of proteins involved in signal transduction. Other examples of enzymatic alkylation include prenyl transfer reactions, adenosyltransfer from ATP to methionine in the biosynthesis of SAM, and adenosyltransfer from ATP to cob(I)alamin in the biosynthesis of adenosylcobalamin. Methyl group transfer is also the essential step in the reaction of methionine synthase, which uses 5-methyltetrahydrofolate as an alkylating agent. In an analogous reaction, an analog of 5-methyltetrahydrofolate is the methyl group donor in the methylation of coenzyme M to form methyl coenzyme M, the proximate precursor of methane in methanogenesis (see chap. 4). Glysosyl transfer is an alkylation reaction catalyzed by a large class of enzymes, the glycosyltransferases and glycosidases. The special nature of the glycosyl compounds and their potential for undergoing glycosyltransfer places them in their own class in biochemistry (see chap. 12). The reactivity of glycosyl compounds can be attributed to the contribution of the oxygen atom directly bonded to the glycosyl carbon, the locus of alkylation. In this chapter, we consider other enzymatic alkylations. Alkylation consists of the transfer of a carbon from a leaving group to a nucleophilic acceptor, as in eq.15-1, where R is H or an organic group. The rate is controlled by the reactivity of the nucleophile X:, the stability of the leaving group Y:, and the electrophilic reactivity of the central carbon atom. Alkylation may be regarded as one of the simplest organic chemical reactions because there are few complications in the mechanism. It is the reaction of a nucleophilic molecule with an electrophilic molecule to displace a leaving group. Enzymatic alkylations proceed by polar and not radical mechanisms. In organic chemistry, polar alkylation can occur either by an associative or one-step mechanism, as in fig. 15-1A, or by a dissociative or two-step mechanism through a carbocationic intermediate, as in fig. 15-1B. The chemical nature of the alkylating agent, the propensity of the leaving group to leave, and the polarity of the solvent determine the mechanism.
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Mullai, P., Eldon R. Rene, Hung Suck Park, and P. L. Sabarathinam. "Adaptive Network Based Fuzzy Interference System (ANFIS) Modeling of an Anaerobic Wastewater Treatment Process." In Handbook of Research on Industrial Informatics and Manufacturing Intelligence. IGI Global, 2012. http://dx.doi.org/10.4018/978-1-4666-0294-6.ch011.

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The successful operation of a high-rate anaerobic reactor, up flow anaerobic sludge blanket (UASB) reactor depends on the prevailing physico-chemical and biological conditions during its operation. The wastewater characteristics and composition, the hydrodynamics of the process, and microbial activity are critical for achieving long term, optimal reactor performance. Modeling UASBs can be beneficial for design, prediction, and control purposes. This chapter provides sufficient background information on the different biochemical stages of anaerobic treatment, viz., hydrolysis of biodegradable solids, acetogenesis and methanogenesis, the working of a UASB reactor, and some insight into mechanistic modeling of UASBs. The application of neural networks, and a conceptual neural fuzzy model, i.e., adaptive network based fuzzy inference system (ANFIS), to model the performance of UASB is systematically outlined in this chapter.
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Hassan, Siti Roshayu Binti, Mohamad Johari Abu, and Irvan Dahlan. "Industrial Wastewater Treatment." In Handbook of Research on Resource Management for Pollution and Waste Treatment. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-0369-0.ch014.

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The development of effective and simple methods for treating wastewater is a challenging task for environmental engineers. In this chapter, a novel modified anaerobic hybridized baffled (MAHB) bioreactor, which is a combination of regular suspended-growth and fixed biofilm systems together with the modification of baffled-reactor configurations, was proven to be a modest bioreactor for wastewater treatment rather than the commercial anaerobic baffled reactor (ABR). The significant advantages of this bioreactor were its ability to nearly realize the multi-stages anaerobic theory, allowing different bacterial groups to develop under more favourable conditions, reduced sludge bed expansion, no special gas or sludge separation required, and high stability to organic and toxic shock loads. The compartmentalization of this bioreactor results in a buffering zone between the primary acidification zone and active methanogenesis zone, and provided the strong ability to resist shock loads which broaden the usage of multi-phase anaerobic technology for industrial wastewater treatment.
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Reports on the topic "Methanogenesis Reaction"

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Krzycki, J. A. Transmethylation reactions during methanogenesis from acetate in Methanosarcina barkeri. [Annual report], August 1, 1991--April 1, 1993. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10165770.

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Krzycki, J. A. Transmethylation reactions during methanogenesis from acetate in Methanosarcina barkeri. Annual technical progress report, August 1993--July 1994. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10171609.

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