首页> 外文期刊>Brazilian Journal of Microbiology >Production and characterization of an enzyme complex from a new strain of Clostridium thermocellum with emphasis on its xylanase activity
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Production and characterization of an enzyme complex from a new strain of Clostridium thermocellum with emphasis on its xylanase activity

机译:从新的热纤梭菌菌株生产并鉴定酶复合物,重点是其木聚糖酶活性

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A new bacterial strain (ISO II) was isolated from manure cow and identified as phylogenetically close to the thermophilic cellulolytic bacterium Clostridium thermocellum. The new strain produced extracellular xylanase, pectinase, mannanase and cellulase activities when grown in liquid culture medium containing banana stem as carbon source. The enzyme production profile after growth on banana stem showed that xylanase and cellulase activities were detected in different incubation periods. An enzyme complex containing xylanase, cellulase and mannanase activities was isolated from culture supernatant samples of strainISO II. The complex was partially purified by ultrafiltration and gel filtration chromatography on Sephacryl S-300. Zymogram analysis after SDS-PAGE presented at least 05 subunits with xylanase activity. The enzyme showed single protein and xylanase activity bands after electrophoresis under non-denaturing conditions. The hydrolysis of xylan was optimal at temperature range of 55-75oC and pH 6.0. Xylanase activity was quite stable at 65oC, retaining 80% of its original activity after 12 h incubation. The apparent Km values, using insoluble and soluble arabinoxylans as substrates, were 1.54 and 11.53 mg/mL, respectively. Xylanase was activated by dithiothreitol, L-tryptophan and L-cysteine and strongly inhibited by N-bromosuccinimide and CoCl2. The characterization of mannanase showed Km and temperature optimum of 0.846 mg/mL and 65oC, respectively and pH 8.0. By contrast to xylanase, it was less stable at 65oC with half-life of 2.5 h and inhibited by dithiothreitol and Ca2+.
机译:从粪肥牛中分离出一种新的细菌菌株(ISO II),并在系统发育上接近嗜热纤维素分解细菌热纤梭菌(Clostridium thermocellum)。当新菌株在以香蕉干为碳源的液体培养基中生长时,产生了细胞外木聚糖酶,果胶酶,甘露聚糖酶和纤维素酶活性。在香蕉茎上生长后的酶生产概况表明,在不同的潜伏期中都检测到木聚糖酶和纤维素酶活性。从菌株ISO II的培养上清液样品中分离出一种含有木聚糖酶,纤维素酶和甘露聚糖酶活性的酶复合物。通过超滤和凝胶过滤层析在Sephacryl S-300上部分纯化该复合物。 SDS-PAGE后的谱线图分析显示了至少05个具有木聚糖酶活性的亚基。在非变性条件下电泳后,该酶显示单个蛋白质和木聚糖酶活性带。在温度范围55-75oC和pH 6.0时,木聚糖的水解效果最佳。木聚糖酶活性在65oC时非常稳定,孵育12小时后保留其原始活性的80%。使用不溶性和可溶性阿拉伯木聚糖作为底物的表观Km值分别为1.54和11.53 mg / mL。木聚糖酶被二硫苏糖醇,L-色氨酸和L-半胱氨酸激活,并被N-溴代琥珀酰亚胺和CoCl2强烈抑制。甘露聚糖酶的表征显示Km和最适温度分别为0.846 mg / mL和65°C,pH为8.0。与木聚糖酶相比,它在65oC时不稳定,半衰期为2.5小时,并被二硫苏糖醇和Ca2 +抑制。

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