为研究近暗散白蚁（Reticulitermes perilucifugus）β-葡萄糖苷酶RpBgl7，利用生物信息学分析β-葡萄糖苷酶RpBgl7的家族及结构特点，构建RpBgl7的重组表达载体pCold-TF-RpBgl7，在大肠杆菌中过量表达并纯化，分析其最适反应条件和酶动力学参数。结果表明，RpBgl7属于糖苷水解酶1家族，具有2个保守的谷氨酸催化残基Glu187和Glu394。RpBgl7在BL21(DE3)中过量表达，经过镍离子亲和层析1步纯化可得到高纯度RpBgl7重组蛋白。以4-硝基苯基-β-D-吡喃葡萄糖苷为底物，测得RpBgl7的最适pH值为6.0，最适温度为70 ℃；动力学参数K_m=0.13 mmol/L，k_cat=3.15 s^-1。RpBgl7可耐受Na⁺、K⁺、Mg²⁺、Cu²⁺和Ba²⁺，而Ca²⁺、Hg²⁺和Fe³⁺明显抑制RpBgl7的酶活力。

To characterize the β-glucosidase RpBgl7 from Reticulitermes perilucifugus,it was analyzed by bioinformatics methods to reveal its belonged family and structure.The recombinant vector pCold-TF-RpBgl7 was transferred into E.coli and overexpressed. RpBgl7 was purified to study its optimal conditions and kinetics.The results showed that,RpBgl7 belonged to glycoside hydrolase family 1,and contained 2 conserved catalytic residues Glu187 and Glu394.RpBgl7 overexpressed in BL21(DE3) was purified in one step using nickel chelating affinity chromatography with high purity.The optimal pH value of RpBgl7 was 6.0 and the optimum temperature was 70℃.The K_m and k_cat of RpBgl7 with p-nitrophenyl-β-D-glucopyranoside as substrate were 0.13 mmol/L and 3.15 s-1 ,respectively. RpBgl7 could be tolerant to Na⁺,K⁺,Mg²⁺,Cu²⁺and Ba²⁺,but it was strongly inhibited by Ca²⁺,Hg²⁺and Fe³⁺.