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Properties of R-Citramalyl-Coenzyme A Lyase and Its Role in the Autotrophic 3-Hydroxypropionate Cycle of Chloroflexus aurantiacus▿

机译:R-Citramalyl-辅酶A裂解酶的性质及其在桔小球藻自养3-羟基丙酸酯循环中的作用

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摘要

The autotrophic CO2 fixation pathway (3-hydroxypropionate cycle) in Chloroflexus aurantiacus results in the fixation of two molecules of bicarbonate into one molecule of glyoxylate. Glyoxylate conversion to the CO2 acceptor molecule acetyl-coenzyme A (CoA) requires condensation with propionyl-CoA (derived from one molecule of acetyl-CoA and one molecule of CO2) to β-methylmalyl-CoA, which is converted to citramalyl-CoA. Extracts of autotrophically grown cells contained both S- and R-citramalyl-CoA lyase activities, which formed acetyl-CoA and pyruvate. Pyruvate is taken out of the cycle and used for cellular carbon biosynthesis. Both the S- and R-citramalyl-CoA lyases were up-regulated severalfold during autotrophic growth. S-Citramalyl-CoA lyase activity was found to be due to l-malyl-CoA lyase/β-methylmalyl-CoA lyase. This promiscuous enzyme is involved in the CO2 fixation pathway, forms acetyl-CoA and glyoxylate from l-malyl-CoA, and condenses glyoxylate with propionyl-CoA to β-methylmalyl-CoA. R-Citramalyl-CoA lyase was further studied. Its putative gene was expressed and the recombinant protein was purified. This new enzyme belongs to the 3-hydroxy-3-methylglutaryl-CoA lyase family and is a homodimer with 34-kDa subunits that was 10-fold stimulated by adding Mg2 or Mn2+ ions and dithioerythritol. The up-regulation under autotrophic conditions suggests that the enzyme functions in the ultimate step of the acetyl-CoA regeneration route in C. aurantiacus. Genes similar to those involved in CO2 fixation in C. aurantiacus, including an R-citramalyl-CoA lyase gene, were found in Roseiflexus sp., suggesting the operation of the 3-hydroxypropionate cycle in this bacterium. Incomplete sets of genes were found in aerobic phototrophic bacteria and in the γ-proteobacterium Congregibacter litoralis. This may indicate that part of the reactions may be involved in a different metabolic process.
机译:绿屈挠菌中的自养CO2固定途径(3-羟基丙酸循环)导致将两分子碳酸氢盐固定为一分子乙醛酸酯。乙醛酸酯向CO2受体分子乙酰辅酶A(CoA)的转化需要与丙酰基-CoA(由一分子的乙酰基-CoA和一分子的CO2衍生)缩合为β-甲基苹果基-CoA,然后将其转化为对甲基苯甲酰-CoA。自养型细胞的提取物同时具有S-和R-瓜氨酸-CoA裂解酶活性,形成了乙酰-CoA和丙酮酸。丙酮酸从循环中移出并用于细胞碳生物合成。在自养生长期间,S-和R-柠檬醛-CoA裂解酶均上调了几倍。发现S-Citramalyl-CoA裂解酶活性归因于1-Malyl-CoA裂解酶/β-甲基苹果基-CoA裂解酶。该混杂酶参与CO 2固定途径,从1-甲基-CoA形成乙酰-CoA和乙醛酸酯,并将乙醛酸酯与丙酰-CoA缩合为β-甲基丙二酰-CoA。 R-Citramalyl-CoA裂解酶进行了进一步的研究。表达其推定基因并纯化重组蛋白。该新酶属于3-羟基-3-甲基戊二酰辅酶A裂解酶家族,是具有34 kDa亚基的同型二聚体,通过添加Mg2或Mn2 +离子和二硫赤藓糖醇可被10倍刺激。自养条件下的上调表明该酶在金黄色葡萄球菌的乙酰辅酶A再生途径的最终步骤中起作用。在Roseiflexus sp。中发现了与C. aurantiacus中固定CO2的基因相似的基因,包括R-柠氨酰-CoA裂解酶基因,表明该细菌存在3-羟基丙酸酯循环。在需氧光养细菌和γ-变形杆菌Congregibacter litoralis中发现了不完整的基因集。这可能表明部分反应可能涉及不同的代谢过程。

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