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Cloning expression and characterization of glucokinase gene involved in the glucose-6- phosphate formation in Staphylococcus aureus

机译:金黄色葡萄球菌葡萄糖6-磷酸形成过程中葡萄糖激酶基因的克隆表达及鉴定

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摘要

Glucose-6-phosphate (G-6-P) formation in Staphylococcus aureus is catalysed by glucokinase (glkA) gene under high glucose concentration leading to upregulation of various pathogenic factors; therefore the present study is aimed in the cloning and characterization of glk A gene from S. aureus ATCC12600. The glk A gene was cloned in the Sma I site of pQE 30, sequenced (Accession number: ) and expressed in E. coli DH5α. The recombinant glk A expressed from the resultant glk A 1 clone was purified using nickel metal chelate chromatography, the pure enzyme gave single band in SDS-PAGE with molecular weight of 33kDa. The rglk A showed very high affinity to glucose Km 5.1±0.06mM with Hill coefficient of 1.66±0.032mM. Analysis of glucokinase sequence of S. aureus showed presence of typical ATP binding site and ROK motif CNCGRSGCIE. Sequentially and phylogenetically S. aureus glk A exhibited low identity with other bacterial glk A and 21% homology with human glucokinase (GCK). Functionally, S. aureus glk A showed higher rate of G-6-P formation compared to human GCK which may have profound role in the pathogenesis.
机译:在高葡萄糖浓度下,葡糖激酶(glkA)基因催化金黄色葡萄球菌中的6-磷酸葡萄糖(G-6-P)形成,导致各种致病因子的上调。因此,本研究旨在克隆和鉴定金黄色葡萄球菌ATCC12600的glk A基因。将glk A基因克隆到pQE 30的Sma I位点,进行测序(登录号:)并在大肠杆菌DH5α中表达。使用镍金属螯合色谱法纯化由所得glk A 1克隆表达的重组glk A,该纯酶在SDS-PAGE中得到单条带,分子量为33kDa。 rglk A对葡萄糖Km 5.1±0.06mM具有很高的亲和力,希尔系数为1.66±0.032mM。金黄色葡萄球菌的葡萄糖激酶序列分析表明存在典型的ATP结合位点和ROK基序CNCGRSGCIE。在系统发育上,金黄色葡萄球菌glk A与其他细菌glk A的同源性较低,与人葡萄糖激酶(GCK)的同源性为21%。在功能上,与人GCK相比,金黄色葡萄球菌glk A显示出更高的G-6-P形成速率,而人GCK可能在发病机理中具有重要作用。

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