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微生物培养物中固氮酶活性的连续无损测定。

Continuous non-destructive determination of nitrogenase activity in microbiol cultures.

作者信息

LaRue T A, Kurz W G, Mallard C

出版信息

Can J Microbiol. 1975 Jul;21(7):980-3. doi: 10.1139/m75-144.

Abstract

The dinitrogen fixing enzyme nitrogenase (nitrogen:(acceptor) oxidoreductase)(EC 1.7.99.2) is monitored by its ability to reduce acetylene to ethylene. Low, non-inhibitory concentrations of acetylene (approximately 10(-7)mol/litre) are mixed with the gas flow aerating microbiol cultures, and acetylene and ethylene in the effluent gas are determined by gas chromatography. The procedure is safe, simple and carried out in situ without disturbing the growing culture. Transient changes in nitrogenase activity are easily detected. The technique may be automated.

摘要

通过将乙炔还原为乙烯的能力来监测双氮固定酶固氮酶(氮:(受体)氧化还原酶)(EC 1.7.99.2)。将低浓度、无抑制作用的乙炔(约10⁻⁷摩尔/升)与曝气微生物培养物的气流混合,通过气相色谱法测定废气中的乙炔和乙烯。该方法安全、简单,可在原位进行,不会干扰正在生长的培养物。固氮酶活性的瞬时变化很容易检测到。该技术可以实现自动化。

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