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来自需氧和厌氧来源的NifB蛋白的表达与纯化。

Expression and purification of NifB proteins from aerobic and anaerobic sources.

作者信息

Echavarri-Erasun Carlos, Arragain Simon, Scandurra Alessandro A, Rubio Luis M

机构信息

Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid, Campus de Montegancedo, Pozuelo de Alarcón, 28223, Madrid, Spain.

出版信息

Methods Mol Biol. 2014;1122:19-31. doi: 10.1007/978-1-62703-794-5_3.

Abstract

NifB is the key protein in the biosynthesis of nitrogenase iron-molybdenum cofactor. Due to its extreme sensitivity to O2 and inherent protein instability, NifB proteins must be purified under strict anaerobic conditions by using affinity chromatography methods. We describe here the methods for NifB purification from cells of the strict aerobic nitrogen-fixing bacterium Azotobacter vinelandii, the facultative anaerobic nitrogen-fixing bacterium Klebsiella pneumoniae, and the facultative anaerobic non-nitrogen fixing bacterium Escherichia coli recombinantly expressing a nifB gene of thermophilic origin.

摘要

NifB是固氮酶铁钼辅因子生物合成中的关键蛋白。由于其对氧气极度敏感且蛋白质本身不稳定,NifB蛋白必须通过亲和层析法在严格厌氧条件下进行纯化。我们在此描述了从严格好氧的固氮细菌维涅兰德固氮菌、兼性厌氧的固氮细菌肺炎克雷伯菌以及重组表达嗜热来源nifB基因的兼性厌氧非固氮细菌大肠杆菌的细胞中纯化NifB的方法。

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