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Simultaneous production of high activities of thermostable endoglucanase and beta-glucosidase by the wild thermophilic fungus Thermoascus aurantiacus

机译:野生嗜热真菌嗜热曲霉同时生产高活性的热稳定内切葡聚糖酶和β-葡萄糖苷酶

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The culture-medium composition was optimised, on a shake-flask scale, for simultaneous production of high activities of endoglucanase and beta-glucosidase by Thermoascus aurantiacus using statistical factorial designs. The optimised medium containing 40.2 g l(-1) Solka Flee as the carbon source and 9 g l(-1) soymeal as the organic nitrogen source yielded 1130 nkat ml(-1) endoglucanase and 116 nkat ml(-1) beta-glucosidase activities after 264 h as shake cultures. In addition, good levels of beta-xylanase (3479 nkat ml(-1)) and low levels of filter-paper cellulase, beta-xylosidase, alpha-L-arabinofuranosidase, beta-mannanase, beta-mannosidase, alpha-galactosidase and beta-galactosidase were detected. Batch fermentation in a 5-1 laboratory fermenter using the optimised medium allowed the production of 940 nkat ml(-1) endoglucanase and 102 nkat ml(-1) beta-glucosidase in 192 h. Endoglucanase and beta-glucosidase showed optimum activity at pH 4.5 and pH 5, respectively, and they displayed optimum activity at 75 degrees C. Endoglucanase and beta-glucosidase showed good stability at pH values 4-8 and 4-7, respectively, after a prolonged incubation (48 h at 50 degrees C). Endoglucanase had half-lives of 98 h at 70 degrees C and 4.1 h at 75 degrees C, while beta-glucosidase had half-lives of 23.5 h at 70 degrees C and 1.7 h at 75 degrees C. Alkali-treated bagasse, steam-treated wheat straw, Solka flee and Sigmacell 50 were 66, 48.5, 33.5 and 14.4% hydrolysed by a crude enzyme complex of T. aurantiacus in 50 h. [References: 27]
机译:以摇瓶规模优化培养培养基的组成,以通过统计因子设计同时利用金黄色嗜热菌同时产生内切葡聚糖酶和β-葡萄糖苷酶的高活性。包含40.2 gl(-1)Solka Flee作为碳源和9 gl(-1)豆粕作为有机氮源的优化培养基产生1130 nkat ml(-1)内切葡聚糖酶和116 nkat ml(-1)β-葡糖苷酶活性264小时后摇动培养。此外,β-木聚糖酶(3479 nkat ml(-1))水平良好,滤纸纤维素酶,β-木糖苷酶,α-L-阿拉伯呋喃糖苷酶,β-甘露聚糖酶,β-甘露糖苷酶,α-半乳糖苷酶和β水平较低检测到β-半乳糖苷酶。使用优化的培养基在5-1实验室发酵罐中进行分批发酵,可在192小时内产生940 nkat ml(-1)内切葡聚糖酶和102 nkat ml(-1)β-葡萄糖苷酶。内切葡聚糖酶和β-葡萄糖苷酶分别在pH 4.5和pH 5时显示最佳活性,并且在75摄氏度时显示出最佳活性。内切葡聚糖酶和β-葡萄糖苷酶分别在pH值4-8和4-7后显示出良好的稳定性。延长孵育时间(在50摄氏度下48小时)。内切葡聚糖酶的半衰期在70摄氏度时为98小时,在75摄氏度时为4.1小时,而β-葡糖苷酶在70摄氏度时为23.5小时,而在75摄氏度时的半衰期为1.7小时。经处理的小麦秸秆,Solka羊毛和Sigmacell 50在60小时内被a曲霉​​的粗酶复合物水解了66%,48.5%,33.5%和14.4%。 [参考:27]

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