Wiechmann Anja, Trifunović Dragan, Klein Sophie, Müller Volker
Molecular Microbiology and Bioenergetics, Institute of Molecular Biosciences, Goethe University Frankfurt, Max-von-Laue Str. 9, 60438, Frankfurt am Main, Germany.
Biotechnol Biofuels. 2020 Dec 21;13(1):208. doi: 10.1186/s13068-020-01851-4.
Capture and storage of the energy carrier hydrogen as well as of the greenhouse gas carbon dioxide are two major problems that mankind faces currently. Chemical catalysts have been developed, but only recently a group of anaerobic bacteria that convert hydrogen and carbon dioxide to acetate, formate, or biofuels such as ethanol has come into focus, the acetogenic bacteria. These biocatalysts produce the liquid organic hydrogen carrier formic acid from H + CO or even carbon monoxide with highest rates ever reported. The autotrophic, hydrogen-oxidizing, and CO-reducing acetogens have in common a specialized metabolism to catalyze CO reduction, the Wood-Ljungdahl pathway (WLP). The WLP does not yield net ATP, but is hooked up to a membrane-bound respiratory chain that enables ATP synthesis coupled to CO fixation. The nature of the respiratory enzyme has been an enigma since the discovery of these bacteria and has been unraveled in this study.
We have produced a His-tagged variant of the ferredoxin:NAD oxidoreductase (Rnf complex) from the model acetogen Acetobacterium woodii, solubilized the enzyme from the cytoplasmic membrane, and purified it by Ni-NTA affinity chromatography. The enzyme was incorporated into artificial liposomes and catalyzed Na transport coupled to ferredoxin-dependent NAD reduction. Our results using the purified enzyme do not only verify that the Rnf complex from A. woodii is Na-dependent, they also demonstrate for the first time that this membrane-embedded molecular engine creates a Na gradient across the membrane of A. woodii which can be used for ATP synthesis.
We present a protocol for homologous production and purification for an Rnf complex. The enzyme catalyzed electron-transfer driven Na export and, thus, our studies provided the long-awaited biochemical proof that the Rnf complex is a respiratory enzyme.
能量载体氢气以及温室气体二氧化碳的捕获与储存是人类目前面临的两大主要问题。化学催化剂已得到开发,但直到最近,一类能将氢气和二氧化碳转化为乙酸盐、甲酸盐或乙醇等生物燃料的厌氧细菌——产乙酸菌,才受到关注。这些生物催化剂能以有史以来最高的速率,从H + CO甚至一氧化碳中产生液态有机氢载体甲酸。自养型、氢氧化型和一氧化碳还原型产乙酸菌具有共同的特殊代谢方式来催化一氧化碳还原,即伍德-Ljungdahl途径(WLP)。WLP不会产生净ATP,但与一个膜结合呼吸链相连,该呼吸链能实现与二氧化碳固定相偶联的ATP合成。自这些细菌被发现以来,呼吸酶的本质一直是个谜,而本研究解开了这个谜团。
我们制备了来自模式产乙酸菌伍氏乙酸杆菌的铁氧化还原蛋白:NAD氧化还原酶(Rnf复合物)的His标签变体,将该酶从细胞质膜中溶解出来,并通过镍-亚氨基二乙酸亲和色谱法进行纯化。该酶被整合到人工脂质体中,并催化与铁氧化还原蛋白依赖性NAD还原相偶联的钠转运。我们使用纯化酶的研究结果不仅证实了伍氏乙酸杆菌的Rnf复合物是钠依赖性的,还首次证明了这个膜嵌入分子引擎能在伍氏乙酸杆菌的膜上产生一个可用于ATP合成的钠梯度。
我们提出了一种Rnf复合物的同源生产和纯化方案。该酶催化电子传递驱动的钠输出,因此,我们的研究提供了期待已久的生化证据,证明Rnf复合物是一种呼吸酶。