Complexity of temperature dependence in methanogenic microbial environments

古细菌 嗜热菌 有机质 微生物代谢 微生物 环境化学 微生物种群生物学 化学 微生物生态学 矿化(土壤科学) 微生物降解 生态学 细菌 生物 生物化学 遗传学 基因 土壤水分
作者
Ralf Conrad
出处
期刊:Frontiers in Microbiology [Frontiers Media SA]
卷期号:14: 1232946-1232946 被引量:51
标识
DOI:10.3389/fmicb.2023.1232946
摘要

There is virtually no environmental process that is not dependent on temperature. This includes the microbial processes that result in the production of CH 4 , an important greenhouse gas. Microbial CH 4 production is the result of a combination of many different microorganisms and microbial processes, which together achieve the mineralization of organic matter to CO 2 and CH 4 . Temperature dependence applies to each individual step and each individual microbe. This review will discuss the different aspects of temperature dependence including temperature affecting the kinetics and thermodynamics of the various microbial processes, affecting the pathways of organic matter degradation and CH 4 production, and affecting the composition of the microbial communities involved. For example, it was found that increasing temperature results in a change of the methanogenic pathway with increasing contribution from mainly acetate to mainly H 2 /CO 2 as immediate CH 4 precursor, and with replacement of aceticlastic methanogenic archaea by thermophilic syntrophic acetate-oxidizing bacteria plus thermophilic hydrogenotrophic methanogenic archaea. This shift is consistent with reaction energetics, but it is not obligatory, since high temperature environments exist in which acetate is consumed by thermophilic aceticlastic archaea. Many studies have shown that CH 4 production rates increase with temperature displaying a temperature optimum and a characteristic apparent activation energy ( E a ). Interestingly, CH 4 release from defined microbial cultures, from environmental samples and from wetland field sites all show similar E a values around 100 kJ mol −1 indicating that CH 4 production rates are limited by the methanogenic archaea rather than by hydrolysis of organic matter. Hence, the final rather than the initial step controls the methanogenic degradation of organic matter, which apparently is rarely in steady state.

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