Somvanshi Tejas, Tran Mai Anh, Bao Jichen, Scheller Silvan
Department of Bioproducts and Biosystems, School of Chemical Engineering, Aalto University, 02150, Espoo, Finland.
Antonie Van Leeuwenhoek. 2025 Sep 20;118(10):154. doi: 10.1007/s10482-025-02165-x.
Corrinoid-dependent enzymes either catalyze methyltransfer reactions, or they generate substrate radicals using adenosylcobalamin for subsequent rearrangement reactions. The corrinoid-dependent methyltransferases are present in all domains of life and assumed to be exclusive for methyl-groups. In Methanosarcina, however, trace ethane production from ethanol has been shown in vivo, which led to the hypothesis that corrinoid-dependent methanol-specific methyltransferases are promiscuous towards also accepting ethyl-groups. Here, we show that the conversion of ethanol to trace amounts of ethane in Methanosarcina acetivorans involves homologous reactions of the known methanol-to-methane metabolism. The methanol methyltransferase (MtaB) activates ethanol and loads the ethyl-group onto the corrinoid-containing methyl-accepting protein (MtaC). Besides MtaCB, substrate promiscuity in corrinoid:coenzyme M methyltransferase (MtaA) and methyl-coenzyme M reductase (Mcr) are required to grant the microbe the capacity for ethane production. We show that the MtaCB subunits of M. acetivorans can activate ethanol, however, the ethane yields compared to methane are ca. 3 orders of magnitude lower. The ethyl-transfer capability was confirmed for each of the three MtaCB isozyme by quantifying the amount of ethane produced by mtaCB double deletion strains during growth in ethanol-supplemented media and in resting-cell suspensions. Ethane formation requires the cells to be grown on methanol to trigger the expression of the mtaCB genes, and detectable ethane formation starts only after all methanol has been consumed. Demonstrating that corrinoid-dependent methanol-specific methyltransferases process ethyl groups extends the pool of reactions to be considered in metabolic networks and suggests possible routes for biogenic ethane in nature.
钴胺素依赖性酶要么催化甲基转移反应,要么利用腺苷钴胺素产生底物自由基以进行后续的重排反应。钴胺素依赖性甲基转移酶存在于生命的所有领域,并且被认为对甲基具有专一性。然而,在甲烷八叠球菌中,已在体内证明从乙醇中产生微量乙烷,这导致了这样的假设,即钴胺素依赖性甲醇特异性甲基转移酶对乙基也具有通用性。在这里,我们表明,嗜乙酸甲烷八叠球菌中乙醇向微量乙烷的转化涉及已知的甲醇到甲烷代谢的同源反应。甲醇甲基转移酶(MtaB)激活乙醇并将乙基加载到含钴胺素的甲基接受蛋白(MtaC)上。除了MtaCB外,钴胺素:辅酶M甲基转移酶(MtaA)和甲基辅酶M还原酶(Mcr)中的底物通用性也是微生物产生乙烷所必需的。我们表明,嗜乙酸甲烷八叠球菌的MtaCB亚基可以激活乙醇,然而,与甲烷相比,乙烷产量约低3个数量级。通过定量mtaCB双缺失菌株在补充乙醇的培养基中生长以及在静止细胞悬浮液中生长期间产生的乙烷量,证实了三种MtaCB同工酶中的每一种都具有乙基转移能力。乙烷的形成要求细胞在甲醇上生长以触发mtaCB基因的表达,并且只有在所有甲醇都被消耗后才开始检测到乙烷的形成。证明钴胺素依赖性甲醇特异性甲基转移酶能够处理乙基,这扩展了代谢网络中需要考虑的反应库,并暗示了自然界中生物成因乙烷的可能途径。