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Production and Characterization of Glucoamylase by Aspergillus niger

机译:黑曲霉生产葡糖淀粉酶的特性

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Background and Objective: Glucoamylase is a potent starch degrading enzyme whose cheap production has been an area of research. Its production by Aspergillus niger in solid-state fermentation was studied using dried garden pea peel as a substrate, which enormously reduced the production cost. The current study intended to produce glucoamylase by a cost-effective strategy and exhaustively characterize the enzyme. Material and Methods: Garden pea peel was used as a substrate in solid state fermentation by Aspergillus niger for the production of glucoamylase under process parameters. Response surface methodology, a statistical tool for optimization, was applied to setup the experimental design for glucoamylase production. Characterization studies of the enzyme were carried out with temperature, pH, metal salts and elemental composition analysis. Results and Conclusion: The process parameters were temperature, amount of substrate and time of fermentation. Glucoamylase production was highest in the pH range of 5.4- 6.2, was stable at pH 3.8, and maintained its maximum activity even at 70°C for 30 min. It showed higher catalytic efficiency when incubated with metal ions Fe2+, Cu2+, Mg2+, and Pb2+. Km and Vmax for glucoamylase were 0.387 mg of soluble starch ml-1 and 35.03 U μl-1 min-1, respectively. Glycogen was also used as a substrate, which gave an increased Km by 2.585, whose KI was found to be 0.631. Energy-dispersive X-ray spectroscopy was performed for obtaining composition of the pea peel. C, N, and O were found to be 12.53%, 29.9%, and 55.27% by atomic weights, respectively. Cost- and time-effective production of glucoamylase was achieved by utilizing dried garden pea peel (a vegetable residue) powder as the substrate for production. Its high stability ensures efficient utilization under industrial conditions. This work provides a very good platform for the enzyme immobilization studies and scale up production in future. Conflict of interest: The authors declare that there is no conflict of interest.
机译:背景与目的:葡糖淀粉酶是一种有效的淀粉降解酶,其廉价的生产一直是研究领域。以干豌豆皮为基质,研究了黑曲霉在固态发酵中的生产,极大地降低了生产成本。当前的研究旨在通过一种具有成本效益的策略来生产葡糖淀粉酶,并详尽地表征该酶。材料与方法:黑豌豆曲霉在固态发酵中使用豌豆皮作为底物,以在工艺参数下生产葡糖淀粉酶。使用响应面方法(一种用于优化的统计工具)来设置用于生产葡糖淀粉酶的实验设计。通过温度,pH,金属盐和元素组成分析对酶进行表征研究。结果与结论:工艺参数为温度,底物量和发酵时间。葡糖淀粉酶的产生在5.4-6.2的pH范围内最高,在pH 3.8时稳定,即使在70°C保持30分钟也能保持其最大活性。当与金属离子Fe2 +,Cu2 +,Mg2 +和Pb2 +一起孵育时,它显示出更高的催化效率。葡糖淀粉酶的Km和Vmax分别为0.387 mg可溶性淀粉ml-1和35.03 Uμl-1min-1。糖原也被用作底物,它使Km增加2.585,发现KI为0.631。进行能量分散X射线光谱法以获得豌豆皮的组成。发现C,N和O的原子量分别为12.53%,29.9%和55.27%。通过使用干豌豆皮(一种蔬菜残渣)粉末作为生产基质,可以实现成本高效且时间高效的葡糖淀粉酶生产。其高稳定性确保了在工业条件下的有效利用。这项工作为酶固定化研究和将来扩大生产提供了一个很好的平台。利益冲突:作者声明没有利益冲突。

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