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首页> 外文期刊>Journal of bacteriology >Cloning, characterization, and sequence analysis of the clcE gene encoding the maleylacetate reductase of Pseudomonas sp. strain B13.
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Cloning, characterization, and sequence analysis of the clcE gene encoding the maleylacetate reductase of Pseudomonas sp. strain B13.

机译:编码假单胞菌sp。马来酰乙酸还原酶的clcE基因的克隆,鉴定和序列分析。菌株B13。

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摘要

A 3,167-bp PstI fragment of genomic DNA from Pseudomonas sp. strain B13 was cloned and sequenced. The gene clcE consists of 1,059 nucleotides encoding a protein of 352 amino acids with a calculated mass of 37,769 Da which showed maleylacetate reductase activity. The protein had significant sequence similarities with the polypeptides encoded by tcbF of pP51 (59.4% identical positions), tfdF of pJP4 (55.1%), and tftE of Burkholderia cepacia AC1100 (53.1%). The function of TcbF as maleylacetate reductase was established by an enzyme assay.
机译:来自假单胞菌属物种的基因组DNA的3,167-bp PstI片段。克隆菌株B13并测序。 clcE基因由1,059个核苷酸组成,编码352个氨基酸的蛋白质,计算质量为37,769 Da,表现出马来酰乙酸还原酶活性。该蛋白质与pP51的tcbF(59.4%相同位置),pJP4的tfdF(55.1%)和洋葱伯克霍尔德菌AC1100的tftE(53.1%)编码的多肽具有明显的序列相似性。通过酶测定确定了TcbF作为马来酰乙酸还原酶的功能。

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