首页> 美国卫生研究院文献>Journal of Bacteriology >Molecular and phylogenetic characterization of pyruvate and 2-ketoisovalerate ferredoxin oxidoreductases from Pyrococcus furiosus and pyruvate ferredoxin oxidoreductase from Thermotoga maritima.
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Molecular and phylogenetic characterization of pyruvate and 2-ketoisovalerate ferredoxin oxidoreductases from Pyrococcus furiosus and pyruvate ferredoxin oxidoreductase from Thermotoga maritima.

机译:激烈热球菌丙酮酸和2-酮异戊酸铁氧还蛋白氧化还原酶的分子和系统发育特征以及海生热球菌的丙酮酸铁氧还蛋白氧化还原酶的分子和系统发育特征。

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摘要

Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains four distinct cytoplasmic 2-ketoacid oxidoreductases (ORs) which differ in their substrate specificities, while the hyperthermophilic bacterium Thermotoga maritima contains only one, pyruvate ferredoxin oxidoreductase (POR). These enzymes catalyze the synthesis of the acyl (or aryl) coenzyme A derivative in a thiamine PPi-dependent oxidative decarboxylation reaction with reduction of ferredoxin. We report here on the molecular analysis of the POR (por) and 2-ketoisovalerate ferredoxin oxidoreductase (vor) genes from P. furiosus and of the POR gene from T. maritima, all of which comprise four different subunits. The operon organization for P. furiosus POR and VOR was porG-vorDAB-porDAB, wherein the gamma subunit is shared by the two enzymes. The operon organization for T. maritima POR was porGDAB. The three enzymes were 46 to 53% identical at the amino acid level. Their delta subunits each contained two ferredoxin-type [4Fe-4S] cluster binding motifs (CXXCXXCXXXCP), while their beta subunits each contained four conserved cysteines in addition to a thiamine PPi-binding domain. Amino-terminal sequence comparisons show that POR, VOR, indolepyruvate OR, and 2-ketoglutarate OR of P. furiosus all belong to a phylogenetically homologous OR family. Moreover, the single-subunit pyruvate ORs from mesophilic and moderately thermophilic bacteria and from an amitochondriate eucaryote each contain four domains which are phylogenetically homologous to the four subunits of the hyperthermophilic ORs (27% sequence identity). Three of these subunits are also homologous to the dimeric POR from a mesophilic archaeon, Halobacterium halobium (21% identity). A model is proposed to account for the observed phenotypes based on genomic rearrangements of four ancestral OR subunits.
机译:先前的研究表明,嗜热古菌激烈热球菌含有四种不同的细胞质2-酮酸氧化还原酶(OR),它们的底物特异性不同,而嗜热细菌马氏嗜热菌仅包含一种丙酮酸铁氧还蛋白氧化还原酶(POR)。这些酶催化硫胺素PPi依赖性氧化脱羧反应中还原铁氧还蛋白的过程中酰基(或芳基)辅酶A衍生物的合成。我们在这里报告了对P. furiosus的POR(por)和2-酮异戊酸铁氧还蛋白氧化还原酶(vor)基因以及来自海生T. maritima的POR基因的分子分析,所有这些都包括四个不同的亚基。激烈疟原虫POR和VOR的操纵子组织是porG-vorDAB-porDAB,其中γ亚基被两种酶共享。滨海衣原体POR的操纵子组织是porGDAB。这三种酶的氨基酸水平相同,为46%至53%。它们的δ亚基各自包含两个铁氧还蛋白型[4Fe-4S]簇结合基序(CXXCXXCXXXCP),而它们的β亚基除硫胺素PPi结合域外还包含四个保守的半胱氨酸。氨基末端序列比较显示,P。furiosus的POR,VOR,吲哚丙酮酸OR和2-酮戊二酸OR都属于系统同源OR家族。此外,来自嗜温和中等嗜热细菌以及来自线粒体真核生物的丙酮酸单亚基OR各自包含四个域,这些域在系统上与超嗜热OR的四个亚基同源(27%序列同一性)。这些亚基中的三个也与嗜温古细菌Halobacterium halobium的二聚POR同源(同一性为21%)。提出了一个模型来解释基于四个祖先OR亚基的基因组重排的观察表型。

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