Nitrogen fixation redox energy

Some of the critical enzymes in our cells are metalloproteins, large organic molecules made up of folded polymerized chains of amino acids that also include at least one metal atom. These metalloproteins are intensely studied by biochemists, because they control life and protect against disease. They have also been used to trace evolutionary paths. The d-block metals catalyze redox reactions, form components of membrane, muscle, skin, and bone, catalyze acid-base reactions, control the flow of energy and oxygen, and carry out nitrogen fixation. 

Table 1 summarizes several redox transformations that can be accomplished in artificial photosynthetic assemblies including the photolysis of water, carbon dioxide reduction, and nitrogen fixation processes. The endoergicities of these transformations, and the number of electrons involved in the reduction processes, are also indicated in the table. It is evident that the energy per electron to drive the various transformations are met by visible light quanta. 

The role of ATP on a molecular level remains one of the great mysteries of the mechanism of nitrogen fixation. As discussed above, the overall thermodynamics of N2 reduction to NH3 by H2 or by its redox surrogate flavodoxin or ferredoxin is favorable. The requirement for ATP hydrolysis must therefore arise from a kinetic necessity. This requirement is fundamentally different from the need for ATP in other biosynthetic or active transport processes, wherein the free energy of hydrolysis of ATP is needed to overcome a thermodynamic limitation. 

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