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首页> 外文期刊>British Biotechnology Journal >Optimization of Cultural and Nutritional Parameters for the Production of Laccase by Pleurotus ostreatus ARC280
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Optimization of Cultural and Nutritional Parameters for the Production of Laccase by Pleurotus ostreatus ARC280

机译:平菇ARC280生产漆酶的文化和营养参数的优化

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Aims: To optimize laccase production by submerged fermentation using an edible mushroom Pleurotus ostreatus ARC280. Study Design: Laccase activity was assayed by monitoring the product formation rate of enzymatic oxidation of syringaldazine spectrophotometrically at 525 nm. Place and Duration of Study: Department of Microbial Chemistry, Genetic Engineering and Biotechnology Division, National Research Centre, Dokki, Cairo, Egypt, between May 2009 and October 2010. Methodology: Pleurotus ostreatus ARC280 was maintained on potato dextrose agar medium. The liquid medium used for the laccase production by the fungal culture during its growth in submerged fermentation was selected from eight liquid media for inducing laccase production. Parameters such as incubation period, temperature, pH of the production medium, carbon and nitrogen sources and other nutritional parameters were studied using syringaldazine as a model substrate for laccase activity determination. Results: In the present work, Eight media with different components were screened. The enzyme formed by Pl. ostreatus ARC280 was localized mainly in the extra-cellular fraction. Laccase formation reaches its maximum value with specific activity of about 140 U/mg protein at the twenty-sixth day of incubation, pH 5.0 and 28oC. Among the various wastes used, corn stover induces the highest laccase production with specific activity of 75.48 U/mg protein. Soluble starch at 1.5% (w/v) and ammonium sulfate was found to be the best carbon and nitrogen sources for laccase formation, respectively. The optimal concentrations of Tween-80 and CuSO4. 5H2O, were found to be 0.1% (v/v) and 100μM and cause enzyme induction by about 44% and 19% than control, respectively. Conclusion: Laccase production by Pl. ostreatus ARC280 has been shown to depend markedly on the composition of the culture medium, carbon, nitrogen content and inducer compounds and governed by parameters such as pH of the production medium and other nutrition parameters.
机译:目的:通过食用平菇侧耳ARC280的深层发酵来优化漆酶生产。研究设计:漆酶活性通过分光光度法在525 nm处监测丁香嗪的酶促氧化反应的产物形成速率来测定。研究的地点和时间:2009年5月至2010年10月,埃及开罗Dokki国家研究中心微生物化学系,基因工程和生物技术部。方法:平菇ARC280保留在马铃薯葡萄糖琼脂培养基上。从用于诱导漆酶生产的八种液体培养基中选择用于真菌培养物在深层发酵过程中生长的漆酶生产所用的液体培养基。以丁香嗪为模板漆酶活性的测定底物,研究了潜伏期,温度,生产培养基的pH,碳氮源及其他营养参数。结果:在目前的工作中,筛选了八种具有不同成分的培养基。由P1形成的酶。平菇ARC280主要位于细胞外部分。在培养的第二十六天(pH 5.0和28oC)下,漆酶的形成达到了最大值,比活约为140 U / mg蛋白。在使用的各种废物中,玉米秸秆产生的漆酶产量最高,比活性为75.48 U / mg蛋白。发现1.5%(w / v)的可溶性淀粉和硫酸铵分别是形成漆酶的最佳碳源和氮源。 Tween-80和CuSO 4 的最佳浓度。发现5H 2 O的含量为0.1%(v / v)和100μM,分别比对照引起酶诱导约44%和19%。结论:Pl生产漆酶。已证明平菇ARC280明显取决于培养基的组成,碳,氮含量和诱导剂化合物,并受诸如生产培养基的pH和其他营养参数等参数支配。

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