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Direct Measurements of Steady-State Kinetics of Cyanobacterial N2 Uptake by Membrane-Leak Mass Spectrometry and Comparisons Between Nitrogen Fixation and Acetylene Reduction

机译:膜泄漏质谱法直接测量蓝细菌氮吸收的稳态动力学以及固氮和乙炔还原的比较

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摘要

A mass spectrometer with a membrane-covered inlet was used to measure nitrogen fixation by following changes in the concentration of dissolved N2 in a stirred suspension of the cyanobacterium Anabaena variabilis in an open system. The results showed a good fit to Michaelis-Menten kinetics with a Km for N2 of 65 μM at 35°C, corresponding to 0.121 atmosphere of N2. Corresponding values for the Km for acetylene reduction were 385 μM (0.011 atmosphere at 35°C). Comparison of the values of Vmax for N2 uptake with those for the acetylene reduction assay under similar conditions gave an average value of 3.8 for the conversion factor between N2 and C2H2 reduction. Reduction of protons to hydrogen was completely inhibited at sufficiently high concentrations of C2H2, but even at saturating N2 concentrations, 1 mol of H2 was produced for every mole of N2 reduced. This explains the finding that the observed C2H2/N2 ratio is higher than the value of 3 expected from the requirement for two electrons for acetylene reduction and six for nitrogen reduction. The results correlate well with a mechanism for N2 reduction involving the equation: N2 + 8H+ + 8e → 2NH3 + H2 which gives a conversion factor between C2H2 and N2 of 4. It is proposed that, in general, 4 is a more appropriate value than 3 for the conversion factor.
机译:使用带有膜覆盖的入口的质谱仪通过跟踪开放系统中蓝细菌鱼腥藻搅拌悬浮液中溶解的N2浓度的变化来测量固氮。结果表明,与Michaelis-Menten动力学非常吻合,在35°C下N2的Km为65μM,相当于N2的气氛为0.121。乙炔还原的Km的对应值为385μM(35℃为0.011大气压)。在相似条件下比较N2吸收的Vmax值与乙炔还原分析的Vmax值,得出N2和C2H2还原之间的转换因子平均值为3.8。在足够高的C2H2浓度下,质子向氢的还原被完全抑制,但是即使在饱和的N2浓度下,每摩尔N2还原也会产生1 mol H2。这解释了以下发现:观察到的C2H 2 / N 2 比高于乙炔还原需要两个电子,氮还原需要六个电子所期望的3。结果与涉及以下方程的N 2 还原机制密切相关:N 2 + 8H + + 8e -→2NH 3 + H 2 ,给出C 2 H 2 和N 之间的转换因子提出了4的2 。通常,对于转换因子来说,4比3更合适。

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