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Cloning and Expression of a Novel Phytase Gene (phyMS) from Mycobacterium smegmatis

机译:耻垢分枝杆菌新型植酸酶基因(phyMS)的克隆与表达

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Phytase, also known as phytate-degrading enzyme, catalyzes the hydrolysis of phytate (inositol hexakisphosphate) with sequential release of phosphate and lower inositol phosphate. We report here a new plasmid construct designated as pMSuia from pBAD-TOPO that harbors a 1.1 kb phytase gene (phyMS) from Mycobacterium smegmatis, and expression as well as characterization of the purified recombinant M. smegmatis phytase. DNA sequencing analysis and multiple alignment exercise indicated that the M. smegmatis phytase is different from both known acid and alkaline phytases. The active ~45 kDa recombinant enzyme was expressed and confirmed by enzyme assay and Western blot analyses. Ni-NTA affinity purified recombinant M. smegmatis phytase exhibited specific activity of 233.51 U/mg, optimal pH of 3 and 7 and optimal temperature of 60°C. The purified enzyme retains almost 30% of the initial activity after incubation at 90°C for 60 min. The enzyme showed broad substrate specificity with Km and Vmax of the recombinant enzyme for sodium phytate substrate of 0.105 ± 0.016 mM and 26.93 ± 1.21 mM min-1, respectively.
机译:植酸酶,又称肌醇六磷酸降解酶,催化肌醇六磷酸(肌醇六磷酸)的水解,依次释放出磷酸盐和低级肌醇磷酸。我们在这里报告了一个新的质粒构建体,命名为pBAD-TOPO中的pMSuia,其中包含来自耻垢分枝杆菌的1.1 kb植酸酶基因(phyMS),以及纯化的重组耻垢分枝杆菌植酸酶的表达和表征。 DNA测序分析和多重比对实验表明,耻垢分枝杆菌植酸酶不同于已知的酸性和碱性植酸酶。表达并通过酶测定和蛋白质印迹分析证实了〜45kDa的活性重组酶。 Ni-NTA亲和纯化的重组耻垢分枝杆菌植酸酶表现出比活性为233.51 U / mg,最适pH为3和7,最适温度为60°C。在90°C孵育60分钟后,纯化的酶几乎保留了初始活性的30%。该酶显示出广泛的底物特异性,重组酶对植酸钠底物的Km和Vmax分别为0.105±0.016 mM和26.93±1.21 mM min-1。

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