Institute of Microbiology and Genetics, Georg-August-Universität Göttingen, Grisebachstraße 8, 37077 Göttingen, Germany.
Archaea. 2013;2013:920241. doi: 10.1155/2013/920241. Epub 2013 Feb 25.
Methyl-Coenzyme M reductase (MCR) as key enzyme for methanogenesis as well as for anaerobic oxidation of methane represents an important metabolic marker for both processes in microbial biofilms. Here, the potential of MCR-specific polyclonal antibodies as metabolic marker in various methanogenic Archaea is shown. For standard growth conditions in laboratory culture, the cytoplasmic localization of the enzyme in Methanothermobacter marburgensis, Methanothermobacter wolfei, Methanococcus maripaludis, Methanosarcina mazei, and in anaerobically methane-oxidizing biofilms is demonstrated. Under growth limiting conditions on nickel-depleted media, at low linear growth of cultures, a fraction of 50-70% of the enzyme was localized close to the cytoplasmic membrane, which implies "facultative" membrane association of the enzyme. This feature may be also useful for assessment of growth-limiting conditions in microbial biofilms.
甲基辅酶 M 还原酶(MCR)作为产甲烷菌和甲烷厌氧氧化的关键酶,是微生物生物膜中这两种过程的重要代谢标志物。本文展示了 MCR 特异性多克隆抗体作为各种产甲烷古菌代谢标志物的潜力。对于实验室培养的标准生长条件,证明了酶在 Methanothermobacter marburgensis、Methanothermobacter wolfei、Methanococcus maripaludis、Methanosarcina mazei 中的细胞质定位,以及在厌氧甲烷氧化生物膜中的定位。在镍耗尽培养基上的生长限制条件下,在培养物的低线性生长时,有 50-70%的酶部分定位于靠近细胞质膜,这意味着酶的“兼性”膜结合。这一特性对于评估微生物生物膜中的生长限制条件也可能是有用的。