NifEN: a versatile player in nitrogenase assembly, catalysis and evolution.

The Mo-nitrogenase catalyzes the reduction of N to NH at the cofactor of its catalytic NifDK component. NifEN shares considerable homology with NifDK in primary sequence, tertiary structure and associated metallocenters. Better known for its biosynthetic function to convert an all-iron precursor (L-cluster; [FeSC]) to a mature cofactor (M-cluster; [(R-homocitrate) MoFeSC]), NifEN also mimics NifDK in catalyzing substrate reduction at ambient conditions. The recently discovered ability of NifEN to reduce N to NH is particularly interesting, as it points to NifEN as a plausible, prototype ancient nitrogenase during evolution. Moreover, the dual function of NifEN in assembly and catalysis makes it a great template to reconstruct the functional variants or equivalents of NifDK, which could facilitate the mechanistic investigation and heterologous synthesis of nitrogenase. This perspective provides an overview of our recent studies of NifEN, with a focus on the implications of its functional versatility for nitrogenase assembly, catalysis and evolution.

© 2024. The Author(s), under exclusive licence to Society for Biological Inorganic Chemistry (SBIC).