Rotte C, Stejskal F, Zhu G, Keithly J S, Martin W
Institut für Botanik III, Universität Düsseldorf, Düsseldorf, Germany.
Mol Biol Evol. 2001 May;18(5):710-20. doi: 10.1093/oxfordjournals.molbev.a003853.
Most eukaryotes perform the oxidative decarboxylation of pyruvate in mitochondria using pyruvate dehydrogenase (PDH). Eukaryotes that lack mitochondria also lack PDH, using instead the O(2)-sensitive enzyme pyruvate : ferredoxin oxidoreductase (PFO), which is localized either in the cytosol or in hydrogenosomes. The facultatively anaerobic mitochondria of the photosynthetic protist Euglena gracilis constitute a hitherto unique exception in that these mitochondria oxidize pyruvate with the O(2)-sensitive enzyme pyruvate : NADP oxidoreductase (PNO). Cloning and analysis of Euglena PNO revealed that the cDNA encodes a mitochondrial transit peptide followed by an N-terminal PFO domain that is fused to a C-terminal NADPH-cytochrome P450 reductase (CPR) domain. Two independent 5.8-kb full-size cDNAs for Euglena mitochondrial PNO were isolated; the gene was expressed in cultures supplied with 2% CO(2) in air and with 2% CO(2) in N(2). The apicomplexan Cryptosporidium parvum was also shown to encode and express the same PFO-CPR fusion, except that, unlike E. gracilis, no mitochondrial transit peptide for C. parvum PNO was found. Recombination-derived remnants of PNO are conserved in the genomes of Saccharomyces cerevisiae and Schizosaccharomyces pombe as proteins involved in sulfite reduction. Notably, Trypanosoma brucei was found to encode homologs of both PFO and all four PDH subunits. Gene organization and phylogeny revealed that eukaryotic nuclear genes for mitochondrial, hydrogenosomal, and cytosolic PFO trace to a single eubacterial acquisition. These findings suggest a common ancestry of PFO in amitochondriate protists with Euglena mitochondrial PNO and Cryptosporidium PNO. They are also consistent with the view that eukaryotic PFO domains are biochemical relics inherited from a facultatively anaerobic, eubacterial ancestor of mitochondria and hydrogenosomes.
大多数真核生物利用丙酮酸脱氢酶(PDH)在线粒体中进行丙酮酸的氧化脱羧反应。缺乏线粒体的真核生物也缺乏PDH,而是使用对氧气敏感的酶丙酮酸:铁氧化还原蛋白氧化还原酶(PFO),该酶定位于细胞质或氢化酶体中。光合原生生物纤细裸藻的兼性厌氧线粒体构成了一个迄今为止独特的例外,即这些线粒体利用对氧气敏感的酶丙酮酸:NADP氧化还原酶(PNO)氧化丙酮酸。对裸藻PNO的克隆和分析表明,cDNA编码一个线粒体转运肽,其后是一个N端PFO结构域,该结构域与一个C端NADPH-细胞色素P450还原酶(CPR)结构域融合。分离出了两个独立的5.8kb全长裸藻线粒体PNO cDNA;该基因在空气中含2%二氧化碳和氮气中含2%二氧化碳的培养物中表达。顶复门寄生虫微小隐孢子虫也被证明编码并表达相同的PFO-CPR融合蛋白,只是与纤细裸藻不同,未发现微小隐孢子虫PNO的线粒体转运肽。PNO的重组衍生残余物在酿酒酵母和粟酒裂殖酵母的基因组中作为参与亚硫酸盐还原的蛋白质而保守。值得注意的是,发现布氏锥虫编码PFO和所有四个PDH亚基的同源物。基因组织和系统发育表明,线粒体、氢化酶体和细胞质PFO的真核核基因可追溯到单一的真细菌获得事件。这些发现表明,无线粒体原生生物中的PFO与裸藻线粒体PNO和隐孢子虫PNO有共同的祖先。它们也与以下观点一致,即真核PFO结构域是从线粒体和氢化酶体的兼性厌氧真细菌祖先遗传而来的生化遗迹。