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Evolution of enzymatic activities in the enolase superfamily: Characterization of the (D)-glucarate/galactarate catabolic pathway in Escherichia coli

机译:烯醇酶超家族中酶活性的演变:大肠杆菌中(D)-葡萄糖酸/半乳糖酸分解代谢途径的表征

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The genes encoding the enzymes in the (D)-glucarate/galactarate catabolic pathway have been identified in the Escherichia coli genome. These encode, in three transcriptional units, (D)-glucarate dehydratase (GlucD), galactarate dehydratase, 5-keto-4-deoxy-(D)-glucarate aldolase, tartronate semialdehyde reductase, a glycerate kinase that generates 2-phosphoglycerate as product, and two hexaric acid transporters. We also have identified a gene proximal to that encoding GlucD that encodes a protein that is 72% identical in primary sequence to GlucD (GlucD-related protein or GlucDRP). However, whereas GlucD catalyzes the efficient dehydration of both (D)-glucarate and (L)-idarate as well as their epimerization, GlucDRP is significantly impaired in both reactions. Perhaps GlucDRP is an example of gene duplication and evolution in progress in the E. coli chromosome. [References: 23]
机译:已经在大肠杆菌基因组中鉴定了编码(D)-葡萄糖酸盐/半乳糖酸盐分解代谢途径中的酶的基因。它们以三个转录单位编码(D)-葡萄糖酸脱水酶(GlucD),半乳糖酸脱水酶,5-酮-4-脱氧-(D)-葡萄糖醛缩酶,酒石酸半醛还原酶,产生2-磷酸甘油酸产物的甘油酸激酶。和两个己酸转运蛋白。我们还确定了与编码GlucD的基因最接近的基因,该基因编码的蛋白质与Gl​​ucD的一级序列(GlucD相关蛋白或GlucDRP)具有72%的同一性。然而,尽管GlucD催化(D)-葡萄糖酸盐和(L)-ida酸盐的有效脱水以及它们的差向异构化,但是在两个反应中GlucDRP均显着受损。也许GlucDRP是大肠杆菌染色体中正在进行的基因复制和进化的一个例子。 [参考:23]

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