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Characterization of Actinomycetes and Trichoderma spp. for cellulase production utilizing crude substrates by response surface methodology

机译:放线菌和木霉属的特征。反应面方法利用粗底物生产纤维素酶

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摘要

Laboratory bench scaling was done and an average of 1.85 fold increase by Response Surface Methodology (RSM) optimization was obtained. It was found that the predicted value (4.96 IU/ml) obtained by RSM is in close accordance with observed activity 5.14 IU/ml. Endoglucanases are mainly induced by CMC while Wheat bran (natural substrate) exoglucanase is more active when induced by avicel and cellulose. Addition of substrate beyond a level caused inhibition of cellulase production. The molecular weight of protein as determined by SDS-PAGE is very similar to molecular weight of cellulase of Trichoderma viride (T. viride) cellulase and Trichoderma reesei (T. reesei) endoglucanase. T. reesei β-glucosidase has high enzymatic activity on CMC substrate when compared with T. viride β-glucosidase. Secondary structure analysed by using Circular Dichroism confirmed that composition of celluase system is very similar to other analysed species. The cellulase was found to be active in pH range of 4.8-5.5; while temperature range varied from 50°C to 70°C. Although the enzymatic activity produced by mutants were lesser than the parent, but in one case mutants of Trichoderma reesei’s BGL has shown higher activity on cellulose.
机译:完成了实验室工作台缩放,并通过响应表面方法(RSM)优化获得了平均1.85倍的增长。发现通过RSM获得的预测值(4.96IU / ml)与观察到的活性5.14IU / ml非常接近。内切葡聚糖酶主要由CMC诱导,而麦麸(天然底物)外切葡聚糖酶在被avicel和纤维素诱导时活性更高。底物的添加超过一定水平会导致纤维素酶产生的抑制。通过SDS-PAGE测定的蛋白质的分子量与里氏木霉(里氏木霉)纤维素酶和里氏木霉(里氏木霉)内切葡聚糖酶的纤维素酶的分子量非常相似。与里氏木霉β-葡糖苷酶相比,里氏木霉β-葡糖苷酶对CMC底物具有高的酶促活性。使用圆二色性分析的二级结构证实纤维素酶系统的组成与其他分析物种非常相似。发现纤维素酶在4.8-5.5的pH范围内有活性。温度范围从50°C到70°C。尽管突变体产生的酶促活性低于亲本,但在一种情况下,里氏木霉的BGL突变体对纤维素具有更高的活性。

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