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首页> 外文期刊>American Journal of Biochemistry and Biotechnology >Brevibacillus Thermoruber 9X-GLC, Bacteria Isolated from Hot Compost, Producer of a Beta-Glucosidase Resistant to Glucose Inhibition
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Brevibacillus Thermoruber 9X-GLC, Bacteria Isolated from Hot Compost, Producer of a Beta-Glucosidase Resistant to Glucose Inhibition

机译:Brevibacillus Thermoruber 9x-Glc,从热堆肥中分离的细菌,耐葡萄糖酶的生产商耐葡萄糖抑制

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The thermotolerant strain Brevibacillus thermoruber 9X-GLC produces large amounts of P-D-glucosidase and cellobiohydrolase when grown on cellobiose and avicel. 9X-GLC was isolated from hot compost of sugarcane bagasse and filter mud and selected for its high enzymatic activity from a Bacilli collection of 77 isolates from soils and compost. Culture supernatants and ultrafiltered concentrates from shaken flask cultures of 9X-GLC were tested for their P-D-glucosidase activity and stability under different conditions of temperature, pH and glucose concentration. The concentrated supernatant from 9X-GLC cultures on cellobiose as sole carbon source had its highest P-D-glucosidase activity at 55°C; pH= 6.0 and retained 60% of its activity at a glucose concentration of up to 200 mM. The effect of different carbon sources on growth and P-D-glucosidase activity of concentrated supernatants was tested in 48 h shaken flask cultures of 9X-GLC. Glucose, cellodextrin and cellobiose supported high cell densities(>2xl08 CFU/ml), whereas cellobiose and cellodextrin provided the best substrates for P-D-glucosidase production. The putative gene encoding P-D-glucosidase from 9X-GLC was obtained from PCR amplification and sequenced. The sequence of the putative structural gene of 2085 bp reveals 6 catalytic domains with high (>90%) homology to bacterialglycosidases.
机译:热电子菌株Brevibacillus Thermoruber 9X-Glc在纤维二糖和培养物上生长时产生大量的P-D-葡糖苷酶和纤维素水解酶。从甘蔗棒蔗渣和过滤器泥浆中分离出9x-glc,从土壤和堆肥中的77个分离物的杆菌收集中选择高酶活性。在不同的温度,pH和葡萄糖浓度下,测试培养上清液和9x-glc的摇瓶培养物的振荡瓶培养物的浓缩物,并在不同的温度,pH和葡萄糖浓度下进行稳定性。从9×glc培养物上浓缩的上清液作为唯一碳源的溶液源在55℃下具有最高的P-D-葡糖苷酶活性; pH = 6.0,并以高达200mm的葡萄糖浓度保留60%的活性。在9×glc的48小时摇瓶培养物中测试了不同碳源对浓浓缩上清液的生长和p-D-葡萄糖苷酶活性的影响。葡萄糖,纤维素,纤维二糖负载高细胞密度(> 2×10 8 CFU / mL),而纤维二糖和纤维素素提供了最佳的P-D-葡糖苷酶生产基材。编码来自9×glc的P-D-葡糖苷酶的推定基因从PCR扩增获得并测序。 2085bp的推定结构基因的序列揭示了具有高(> 90%)同源性的6个催化结构域与胆糖苷酶。

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