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Gas Exchange in the Filamentous Cyanobacterium Nostoc punctiforme Strain ATCC 29133 and Its Hydrogenase-Deficient Mutant Strain NHM5

机译:丝状蓝藻点菌形菌株ATCC 29133及其缺乏氢化酶的突变株NHM5中的气体交换

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摘要

Nostoc punctiforme ATCC 29133 is a nitrogen-fixing, heterocystous cyanobacterium of symbiotic origin. During nitrogen fixation, it produces molecular hydrogen (H2), which is recaptured by an uptake hydrogenase. Gas exchange in cultures of N. punctiforme ATCC 29133 and its hydrogenase-free mutant strain NHM5 was studied. Exchange of O2, CO2, N2, and H2 was followed simultaneously with a mass spectrometer in cultures grown under nitrogen-fixing conditions. Isotopic tracing was used to separate evolution and uptake of CO2 and O2. The amount of H2 produced per molecule of N2 fixed was found to vary with light conditions, high light giving a greater increase in H2 production than N2 fixation. The ratio under low light and high light was approximately 1.4 and 6.1 molecules of H2 produced per molecule of N2 fixed, respectively. Incubation under high light for a longer time, until the culture was depleted of CO2, caused a decrease in the nitrogen fixation rate. At the same time, hydrogen production in the hydrogenase-deficient strain was increased from an initial rate of approximately 6 μmol (mg of chlorophyll a)−1 h−1 to 9 μmol (mg of chlorophyll a)−1 h−1 after about 50 min. A light-stimulated hydrogen-deuterium exchange activity stemming from the nitrogenase was observed in the two strains. The present findings are important for understanding this nitrogenase-based system, aiming at photobiological hydrogen production, as we have identified the conditions under which the energy flow through the nitrogenase can be directed towards hydrogen production rather than nitrogen fixation.
机译:点状诺氏菌ATCC 29133是共生起源的固氮异囊蓝藻。在固氮过程中,它会产生分子氢(H2),该氢会被摄取的氢化酶重新捕获。研究了点状猪笼草ATCC 29133及其不含加氢酶的突变菌株NHM5在培养物中的气体交换。在固氮条件下生长的培养物中,同时用质谱仪同时监测O2,CO2,N2和H2的交换。同位素示踪用于分离CO2和O2的释放和吸收。发现每个固定的N2分子产生的H2量随光照条件而变化,强光比N2固定产生更大的H2产量增加。在弱光和强光下,每固定的N2分子产生的H2比例分别约为1.4和6.1分子。在强光下孵育更长的时间,直到培养物中的CO2耗尽,导致固氮率降低。同时,缺氢酶缺陷菌株中的产氢量从大约6μmol(mg叶绿素a)-1 h-1的初始速率增加到大约9μmol(mg叶绿素a)-1 h-1的初始速率。 50分钟在两个菌株中观察到了源自固氮酶的光刺激的氢-氘交换活性。目前的发现对于理解基于氮酶的系统(针对光生物制氢)非常重要,因为我们已经确定了通过固氮酶的能量流可以直接用于制氢而不是固氮的条件。

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