Department of Molecular Biology & Biochemistry, University of California, Irvine, Irvine, CA, 92697-3900, USA.
Department Chemistry, University of California, Irvine, Irvine, CA, 92697-2025, USA.
Angew Chem Int Ed Engl. 2020 Apr 20;59(17):6887-6893. doi: 10.1002/anie.201916598. Epub 2020 Mar 3.
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.
NifEN 在固氮酶的生物合成中起着至关重要的作用,它在将辅因子递送给固氮酶的催化组件 NifDK 之前,催化辅因子成熟的最后一步。NifEN 是一种复杂的、异源多聚体金属蛋白,与 NifDK 具有结构/功能同源性,其表达困难是固氮酶异源表达的主要挑战。本文报告了在大肠杆菌中表达和工程化的 Azotobacter vinelandii NifEN。生化和光谱分析表明,异源表达的 NifEN 在组成和功能上具有完整性,此外,一种经过工程改造的 NifEN 变体能够模拟 NifDK,在类似的辅因子结合位点上保留成熟的辅因子。这是为组装固氮酶异源表达的可行途径并鉴定该酶的机制研究变体迈出的重要一步。