Sickerman Nathaniel S, Hu Yilin, Ribbe Markus W
University of California, Irvine, Irvine, CA, United States.
University of California, Irvine, Irvine, CA, United States.
Methods Enzymol. 2017;595:261-302. doi: 10.1016/bs.mie.2017.07.006. Epub 2017 Aug 21.
Nitrogenase is a metalloenzyme system that plays a critical role in biological nitrogen fixation, and the study of how its metallocenters are assembled into functional entities to facilitate the catalytic reduction of dinitrogen to ammonia is an active area of interest. The diazotroph Azotobacter vinelandii is especially amenable to culturing and genetic manipulation, and this organism has provided the basis for many insights into the assembly of nitrogenase proteins and their respective metallocofactors. This chapter will cover the basic procedures necessary for growing A. vinelandii cultures and subsequent recombinant transformation and protein expression techniques. Furthermore, protocols for nitrogenase protein purification and substrate reduction activity assays are described. These methods provide a solid framework for the assessment of nitrogenase assembly and catalysis.
固氮酶是一种金属酶系统,在生物固氮过程中起着关键作用。研究其金属中心如何组装成功能实体以促进将氮气催化还原为氨是一个活跃的研究领域。固氮菌维涅兰德固氮菌特别适合培养和基因操作,该生物体为深入了解固氮酶蛋白及其各自的金属辅因子的组装提供了基础。本章将介绍培养维涅兰德固氮菌培养物以及后续重组转化和蛋白质表达技术所需的基本程序。此外,还描述了固氮酶蛋白纯化和底物还原活性测定的方案。这些方法为评估固氮酶的组装和催化作用提供了坚实的框架。