H<sub>2</sub>‐forming <i>N</i><sup>5</sup>,<i>N</i><sup>10</sup>‐methylenetetrahydromethanopterin dehydrogenase from <i>Methanobacterium thermoautotrophicum</i>

Beatrix Schwörer, Vı́ctor M. Fernández, C. Zirngibl, Rudolf K. Thauer

European Journal of Biochemistry · 1993 · 58 citations · 19 references

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Abstract

H2-forming N5,N10-methylenetetrahydromethanopterin dehydrogenase is a novel hydrogenase found in most methanogenic archaea. It catalyzes the reversible conversion of N5,N10-methylenetetrahydromethanopterin (CH2 = H4MPT) to N5,N10-methenyltetrahydromethanopterin (CH identical to H4MPT+) and dihydrogen; CH2 = H4MPT + H+<-->CH identical to H4MPT(+) + H2; delta G degrees ' = + 5 kJ/mol. In the following investigation, the formation of H2, HD and D2 was studied in experiments in which either the methylene group of CH2 = H4MPT or water were deuterium labelled. In the case of CD2 = H4MPT and H2O, the dihydrogen formed immediately after the start of the reaction was composed of approximately 50% HD and 50% of H2 at all pH tested. In the case of CH2 = H4MPT and D2O, the dihydrogen generated was composed of approximately 50% HD and 50% D2 at pD 5.7 and of approximately 85% HD and 15% D2 at pD 7.0. Evidence is presented that the enzyme catalyzes a CH identical to H4MPT(+)-dependent isotopic exchange between HD and H2O and between HD and D2O, yielding H2 and D2, respectively. A catalytic mechanism aimed to explain these findings is discussed.

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