The active site of the nitrogen‐fixing enzyme Mo‐nitrogenase is the M cluster ([MoFe 7 S 9 C ⋅ R‐homocitrate]), also known as the FeMo cofactor or FeMoco. The biosynthesis of this highly complex metallocluster involves a series of proteins. Among them, NifB, a radical‐SAM enzyme, is instrumental in the assembly of the L cluster ([Fe 8 S 9 C]), a precursor and all‐iron core of the M cluster. In the absence of sulfite, NifB assembles a precursor form of the L cluster called the L* cluster ([Fe 8 S 8 C]), which lacks the final ninth sulfur. EPR and MCD spectroscopies are used to probe the electronic structures of the paramagnetic, oxidized forms of both the L and L* clusters, labeled L Ox and [ L* ] Ox . This study shows that both L Ox and [ L* ] Ox have nearly identical EPR and MCD spectra, thus suggesting that the two clusters have identical structures upon oxidation; in other words, a sulfur migrates away from L Ox following oxidation, thereby rendering the cluster identical to [ L* ] Ox . It is proposed that a similar migration could occur to the M cluster upon oxidation, and that this is an instrumental part of both M cluster formation and nitrogenase substrate/inhibitor binding.
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Rupnik et al. (2019) studied this question.
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