Expression and Characterization of Recombinant Endo-β-1,4-D-xylanases XynBTN63D from Soil Termite Abdomen in Escherichia coli BL21 (DE3)

A. A. I. Ratnadewi, Sabella Muyasyaroh, Fatih Harum, Wuryanti Handayani, Sudarko Sudarko
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Abstract

The xynBTN63D gene sub-cloned on the plasmid shuttle vector pESC and pYHM1 in the host Escherichia coli BL21 (DE3) was successfully expressed and characterized. The xynBTN63D gene in the soluble fraction of each plasmid is expressed at induction temperatures of 25, 30, 35, 37, and 40 °C with a molecular weight of ±30 kDa. The soluble fraction of the xynBTN63D gene in both plasmids was expressed at induction temperatures of 25, 30, 35, 37, and 40°C with a molecular weight of ±30 kDa. The recombinant XynBTN63D, purified using the fast protein liquid chromatography (FPLC) method also has a molecular weight of ±30 kDa, observed using the sodium dodecyl polyacrylamide sodium electrophoresis (SDS-PAGE) method. The recombinant XynBTN63D has a temperature of 40 °C and an optimum pH of 5.5. It shows stability from 4 to 40 °C after preincubation for 1 hour with relative activity on the pCES and pMH1 plasmid of more than 50%. Recombinant XynBT63D also showed pH stability after being preincubated for 24 hours by showing relative activity of 86-100% at pH 5.0 to 6.0 for each plasmid
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土壤白蚁腹部重组内切-β-1,4-D-木聚糖酶 XynBTN63D 在大肠杆菌 BL21 (DE3) 中的表达与表征
将 xynBTN63D 基因亚克隆到质粒穿梭载体 pESC 和 pYHM1 上,并在宿主大肠杆菌 BL21 (DE3) 中成功表达和鉴定。每个质粒可溶性部分中的 xynBTN63D 基因在 25、30、35、37 和 40 °C 的诱导温度下表达,分子量为 ±30 kDa。两个质粒中 xynBTN63D 基因的可溶性部分在 25、30、35、37 和 40 ℃ 的诱导温度下表达,分子量为 ±30 kDa。用快速蛋白质液相色谱法(FPLC)纯化的重组 XynBTN63D 的分子量也为±30 kDa,用十二烷基聚丙烯酰胺钠电泳法(SDS-PAGE)观察到的结果也是±30 kDa。重组 XynBTN63D 的温度为 40 °C,最适 pH 值为 5.5。在预孵育 1 小时后,它在 4 至 40 ℃ 范围内表现出稳定性,在 pCES 和 pMH1 质粒上的相对活性超过 50%。重组 XynBT63D 在预培养 24 小时后也显示出 pH 值稳定性,在 pH 值为 5.0 至 6.0 的条件下,每个质粒的相对活性为 86% 至 100%。
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