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首页> 外文期刊>Journal of bacteriology >nifV-dependent, low-molecular-weight factor required for in vitro synthesis of iron-molybdenum cofactor of nitrogenase.
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nifV-dependent, low-molecular-weight factor required for in vitro synthesis of iron-molybdenum cofactor of nitrogenase.

机译:体外合成固氮酶的铁-钼辅因子所需的nifV依赖型,低分子量因子。

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The molybdate- and ATP-dependent in vitro synthesis of the iron-molybdenum cofactor of nitrogenase requires a low-molecular-weight factor. The factor is present in extracts of nitrogen fixation-derepressed cultures of Klebsiella pneumoniae and Azotobacter vinelandii, but not in extracts of repressed cultures of these bacteria. Analysis of K. pneumoniae Nif mutants has indicated that the nifV gene product is the only nif protein (besides nifA) necessary for the synthesis and accumulation of the factor. The factor is stable to oxygen, temperatures below 120 degrees C, and extremely acidic and basic conditions. The activity of the factor was completely destroyed by dry ashing or digestion with sulfuric acid. The factor has been partially purified by filtration through an Amicon PM-10 DIAFLO membrane and chromatography on DEAE-cellulose, hydroxylapatite, silica gel, and Sephadex G-25.
机译:依赖于钼酸盐和ATP的铁-钼辅助因子的体外合成固氮酶需要低分子量因子。该因子存在于固氮抑制的肺炎克雷伯菌和葡萄固氮菌的提取物中,但不存在于这些细菌的抑制培养物中。肺炎克雷伯菌Nif突变体的分析表明,nifV基因产物是该因子合成和积累所必需的唯一nif蛋白(nifA除外)。该因素对氧气,低于120摄氏度的温度以及极端酸性和碱性条件稳定。干灰化或用硫酸消化完全破坏了该因子的活性。该因子已通过Amicon PM-10 DIAFLO膜过滤并在DEAE-纤维素,羟磷灰石,硅胶和Sephadex G-25色谱上进行了部分纯化。

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