Abstract

BackgroundThis study examines the structural features and phylogeny of the α subunits of 69 full-length NifD (MoFe subunit), VnfD (VFe subunit), and AnfD (FeFe subunit) sequences.Methodology/Principal FindingsThe analyses of this set of sequences included BLAST scores, multiple sequence alignment, examination of patterns of covariant residues, phylogenetic analysis and comparison of the sequences flanking the conserved Cys and His residues that attach the FeMo cofactor to NifD and that are also conserved in the alternative nitrogenases. The results show that NifD nitrogenases fall into two distinct groups. Group I includes NifD sequences from many genera within Bacteria, including all nitrogen-fixing aerobes examined, as well as strict anaerobes and some facultative anaerobes, but no archaeal sequences. In contrast, Group II NifD sequences were limited to a small number of archaeal and bacterial sequences from strict anaerobes. The VnfD and AnfD sequences fall into two separate groups, more closely related to Group II NifD than to Group I NifD. The pattern of perfectly conserved residues, distributed along the full length of the Group I and II NifD, VnfD, and AnfD, confirms unambiguously that these polypeptides are derived from a common ancestral sequence.Conclusions/SignificanceThere is no indication of a relationship between the patterns of covariant residues specific to each of the four groups discussed above that would give indications of an evolutionary pathway leading from one type of nitrogenase to another. Rather the totality of the data, along with the phylogenetic analysis, is consistent with a radiation of Group I and II NifDs, VnfD and AnfD from a common ancestral sequence. All the data presented here strongly support the suggestion made by some earlier investigators that the nitrogenase family had already evolved in the last common ancestor of the Archaea and Bacteria.

Highlights

  • The ability to perform biological nitrogen fixation is restricted to Bacteria and Archaea

  • We found that the four sets of sequences fell consistently into two groups based on BLAST scores, distinctive patterns of conserved covariant amino acid residues [4] and, in the case of NifD, different patterns of invariant residues in the sequences flanking the Cys-a275 and His-a442 (Azobacter vinelandii sequence numbering) residues that attach the FeMo cofactor to NifD [5]

  • Two Groups of NifD Sequences We reported earlier, based on the analysis of sequences from fourteen organisms of the proteins encoded by nifD, K, E, and N, that these sequences fall into two groups distinguished by distinctive characteristics of their amino acid sequences [3]

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Summary

Introduction

The ability to perform biological nitrogen fixation is restricted to Bacteria and Archaea. All N2-fixing organisms studied depend on a nitrogenase for the conversion of atmospheric nitrogen to ammonia and all have the genes encoding the subunits of molybdenum-containing nitrogenase. This enzyme is an a2b2 tetramer, where the two a subunits (the FeMo-protein) catalyze the ATP-dependent reduction of N2 to NH3, and b2 (referred to as the Fe-protein) mediates the coupling of ATP hydrolysis to electron transfer and is the only known electron donor that can support reduction by the MoFe protein [2]. NifD, and nifK, respectively, encode the a- and b-subunits of the MoFe-nitrogenase, whereas nifE and nifN are required for the synthesis of the MoFe cofactor. This study examines the structural features and phylogeny of the a subunits of 69 full-length NifD (MoFe subunit), VnfD (VFe subunit), and AnfD (FeFe subunit) sequences

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