| Literature DB >> 32022452 |
Joseph B Solomon1,2, Chi Chung Lee1, Andrew J Jasniewski1, Mahtab F Rasekh1,2, Markus W Ribbe1,2, Yilin Hu1.
Abstract
NifEN plays a crucial role in the biosynthesis of nitrogenase, catalyzing the final step of cofactor maturation prior to delivering the cofactor to NifDK, the catalytic component of nitrogenase. The difficulty in expressing NifEN, a complex, heteromultimeric metalloprotein sharing structural/functional homology with NifDK, is a major challenge in the heterologous expression of nitrogenase. Herein, we report the expression and engineering of Azotobacter vinelandii NifEN in Escherichia coli. Biochemical and spectroscopic analyses demonstrate the integrity of the heterologously expressed NifEN in composition and functionality and, additionally, the ability of an engineered NifEN variant to mimic NifDK in retaining the matured cofactor at an analogous cofactor-binding site. This is an important step toward piecing together a viable pathway for the heterologous expression of nitrogenase and identifying variants for the mechanistic investigation of this enzyme.Entities:
Keywords: bioinorganic chemistry; metalloenzymes; metalloproteins; nitrogenase; protein engineering
Year: 2020 PMID: 32022452 DOI: 10.1002/anie.201916598
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336