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Increased pyruvate orthophosphate dikinase activity results in an alternative gluconeogenic pathway in Rhizobium (Sinorhizobium) meliloti

机译:增加丙酮酸正磷酸二磷酸酯直立素酶活性导致Rhzobium(Sinorhizobium)Meliloti中的替代葡糖原途径

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The formation of phosphoenolpyruvate (PEP) is a major step in the gluconeogenic pathway in which tricarboxylic acid (TCA) cycle intermediates are converted to hexose sugars. In Rhizobium (now Sinorhizobium) meliloti this step is catalysed by the enzyme PEP carboxykinase (PCK) which converts oxaloacetate to PEP. R. meliloti Pck-mutants grow very poorly with TCA cycle intermediates as the sole source of carbon. Here, the isolation and mapping of suppressor mutations which allow Pck-mutants to grow on succinate and other TCA cycle intermediates is reported. Tn5 insertions which abolished the suppressor phenotype and mapped to the suppressor locus were located within the pod gene encoding pyruvate orthophosphate dikinase (PPDK). Strains carrying suppressor mutations had increased PPDK activity compared to the wild-type. The suppressor phenotype was dependent on the combined activities of malic enzyme and PPDK, which thus represent an alternative route for the formation of PEP in R. meliloti. PPDK activity was not required for symbiotic N2 fixation.
机译:磷酸丙酮酸(PEP)的形成是葡糖原途径的主要步骤,其中三羧酸(TCA)循环中间体转化为己糖糖。在Rhizobium(现在Sinorhizobium)Meliloti这一步骤由酶Pep羧基酶(PCK)催化,它将草酸乙酸盐转化为PEP。 R. Meliloti PCK-突变体与TCA循环中间体的唯一碳源生长非常差。这里,允许允许PCK突变体在琥珀酸盐和其他TCA循环中间体生长的抑制突变的分离和映射。废除抑制剂表型并映射到抑制器基因座的TN5插入位于编码丙酮酸正磷酸二磷酸氨基酶(PPDK)的POD基因内。与野生型相比,携带抑制突变的菌株增加了PPDK活性。抑制剂表型依赖于苹果胺酶和PPDK的组合活性,因此代表了eP在R.Meliloti中形成的替代途径。共生N2固定不需要PPDK活性。

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