Escalante-Semerena J C, Wolfe R S
J Bacteriol. 1985 Feb;161(2):696-701. doi: 10.1128/jb.161.2.696-701.1985.
Methanogenesis from the non-physiological C1 donors thioproline, thiazolidine, hexamethylenetetramine, formaldehyde (HCHO), and HOCH2-S-coenzyme M (CoM) was catalyzed by cell extracts of Methanobacterium thermoautotrophicum under a hydrogen atmosphere. Tetrahydromethanopterin (H4MPT) and HS-CoM were required in the reaction mixture. The non-physiological compounds were found to be in chemical equilibrium with HCHO, which has been shown to react spontaneously with H4MPT to form methylene-H4MPT, an intermediate of the methanogenic pathway at the formaldehyde level of oxidation. Highfield (360 MHZ) 1H and 13C nuclear magnetic resonance studies performed on the interaction between HCHO and HS-CoM showed that these compounds are in equilibrium with HOCH2-S-CoM and that the equilibrium is pH dependent. When methanogenesis from the non-physiological donors was followed under a nitrogen atmosphere, the C1 moiety from each compound underwent a disproportionation, forming methenyl-H4MPT+ and methane. The compounds tested served as substrates for the enzymatic synthesis of methenyl-H4MPT+.
在氢气氛围下,嗜热自养甲烷杆菌的细胞提取物催化了从非生理性C1供体硫代脯氨酸、噻唑烷、六亚甲基四胺、甲醛(HCHO)和羟甲基-S-辅酶M(CoM)生成甲烷的过程。反应混合物中需要四氢甲蝶呤(H4MPT)和HS-CoM。发现这些非生理性化合物与HCHO处于化学平衡状态,HCHO已被证明能与H4MPT自发反应形成亚甲基-H4MPT,这是甲烷生成途径在甲醛氧化水平的一种中间体。对HCHO与HS-CoM之间相互作用进行的高场(360 MHZ)1H和13C核磁共振研究表明,这些化合物与羟甲基-S-CoM处于平衡状态,且该平衡依赖于pH值。当在氮气氛围下追踪从非生理性供体生成甲烷的过程时,每种化合物的C1部分发生歧化反应,形成亚甲基-H4MPT+和甲烷。所测试的化合物可作为酶促合成亚甲基-H4MPT+的底物。