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Metabolic Pathways for Photobiological Hydrogen Production by Nitrogenase- and Hydrogenase-containing Unicellular Cyanobacteria Cyanothece

机译:含氮和含氢酶的单细胞蓝细菌蓝藻产生光生物氢的代谢途径。

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摘要

Current biotechnological interest in nitrogen-fixing cyanobacteria stems from their robust respiration and capacity to produce hydrogen. Here we quantify both dark- and light-induced H2 effluxes by Cyanothece sp. Miami BG 043511 and establish their respective origins. Dark, anoxic H2 production occurs via hydrogenase utilizing reductant from glycolytic catabolism of carbohydrates (autofermentation). Photo-H2 is shown to occur via nitrogenase and requires illumination of PSI, whereas production of O2 by co-illumination of PSII is inhibitory to nitrogenase above a threshold pO2. Carbohydrate also serves as the major source of reductant for the PSI pathway mediated via nonphotochemical reduction of the plastoquinone pool by NADH dehydrogenases type-1 and type-2 (NDH-1 and NDH-2). Redirection of this reductant flux exclusively through the proton-coupled NDH-1 by inhibition of NDH-2 with flavone increases the photo-H2 production rate by 2-fold (at the expense of the dark-H2 rate), due to production of additional ATP (via the proton gradient). Comparison of photobiological hydrogen rates, yields, and energy conversion efficiencies reveals opportunities for improvement.
机译:目前对固氮蓝细菌的生物技术兴趣来自其强大的呼吸作用和产生氢的能力。在这里,我们量化了Cyanothece sp在黑暗和光诱导的H2外流。 Miami BG 043511并确立各自的来历。利用碳水化合物的糖酵解分解代谢(自动发酵)产生的还原剂,通过氢化酶产生黑暗,缺氧的H2。显示光H2是通过固氮酶发生的,需要照亮PSI,而通过共照射PSII产生的O2会抑制高于阈值pO2的固氮酶。碳水化合物还充当PSI途径的主要还原剂,该途径是通过NADH脱氢酶1型和2型(NDH-1和NDH-2)通过非光化学还原质体醌库而介导的。通过用黄酮抑制NDH-2来使还原剂通量仅通过质子偶联的NDH-1进行重定向,从而使光H2生成速率增加了2倍(以暗H2速率为代价)。 ATP(通过质子梯度)。光生物氢速率,产量和能量转换效率的比较显示出改进的机会。

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