耻垢分枝杆菌植酸酶基因的克隆与表达

Tamrin Nuge, Y. Hashim, A. Farouk, H. Salleh
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引用次数: 10

摘要

植酸酶,又称植酸降解酶,催化水解植酸(六磷酸肌醇),并依次释放磷酸和低磷酸肌醇。本文报道了从pBAD-TOPO中提取的含有耻毛分枝杆菌植酸酶基因(phyMS) 1.1 kb的pMSuia质粒,以及纯化的重组耻毛分枝杆菌植酸酶的表达和特性。DNA测序分析和多重比对表明,耻垢分枝杆菌植酸酶不同于已知的酸性和碱性植酸酶。表达了活性~ 45kda的重组酶,并通过酶分析和Western blot分析证实了重组酶的活性。Ni-NTA亲和纯化的重组臭茅植酸酶比活性为233.51 U/mg,最适pH为3和7,最适温度为60℃。在90°C下孵育60分钟后,纯化酶保持了近30%的初始活性。该酶对植酸钠底物的Km和Vmax分别为0.105±0.016 mM和26.93±1.21 mM min-1,具有广泛的底物特异性。
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Cloning and Expression of a Novel Phytase Gene (phyMS) from Mycobacterium smegmatis
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.
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