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Thermodynamics of methylenetetrahydrofolate reduction to methyltetrahydrofolate and its implications for the energy metabolism of homoacetogenic bacteria

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Abstract

The thermodynamics of the methylenetetrahydrofolate reduction to 5-methyltetrahydrofolate was studied with the methylenetetrahydrofolate reductase purified from the homoacetogenic bacterium Peptostreptococcus productus. The equilibrium constants were determined for the forward and backward reactions of methylenetetrahydrofolate reduction with NADH or acetylpyridine adenine dinucleotide (APADH), respectively, as the electron donors. From the equilibrium constants and the known standard redox potentials at pH 7 (E o′) of the couples NAD+/NADH or APAD+/APADH the E o′ of the couple methylene-/methyltetrahydrofolate was determined to be about-200mV. This value is different from values reported before for this couple. The implications for the mechanism of energy conservation of homoacetogens is discussed.

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Abbreviations

FH4 :

tetrahydrofolate

CH2=FH4 :

5,10-methylenetrahydrofolate

CH3-FH4 :

5-methyltetrahydrofolate

K eq :

equilibrium constant

ΔG o :

Gibb's free energy change under standard conditions (all concentrations of reactants = 1 M)

ΔG o′ :

ΔG o at pH 7 ([H+]=10-7 M)

E o :

standard redox potential

ΔG o :

standard redox potential difference of two reactants

ΔE o′ :

ΔE o at pH 7

R :

gas constant

F :

Faraday constant

APAD:

acetylpyridine adenine dinucleotide (NAD+-analogue)

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Wohlfarth, G., Diekert, G. Thermodynamics of methylenetetrahydrofolate reduction to methyltetrahydrofolate and its implications for the energy metabolism of homoacetogenic bacteria. Arch. Microbiol. 155, 378–381 (1991). https://doi.org/10.1007/BF00243458

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  • DOI: https://doi.org/10.1007/BF00243458

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