Production and Optimization of Pectinase from Pectinolytic Fungi Cultivated on Mango peels and Pectin Subjected to Submerged Fermentation

Kelemu Mulluye, A. Kebede, N. Bussa
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引用次数: 1

Abstract

Pectinases are the group of enzymes that degrade pectin. This study was conducted with the aim of isolation of efficient pectinase producing pectinolytic fungi from the decomposing mango peels using extracted mango peels pectin as a growth substrate under submerged fermentation, determining optimum pectinase production conditions with regards to some physicochemical parameters. The organisms were screened for the production of pectinase using Pectin agar media, and the two active pectinolytic fungi (P1 and P2) were isolated. pectinase production media was later used for the Lab scale production of pectinase by inoculating p1 and p2 and incubating for 7 days. The enzyme was extracted after seven days of fermentation and every day tested for their pectinolytic activity. P2 showed relatively higher pectinolytic activity and was therefore used for further studies. P2 was inoculated into a broth containing mango pectin under submerged fermentation. Results indicate that a pectin yield of mango peel 17.75%. Different parameters optimization processes were investigated on submerged fermentation namely pH, incubation period, temperature and substrate concentration optima were found 6, 4 days, 35oC and 1.5% respectively. The result suggests that mango peels have high pectin content and can be used for the value-added synthesis of pectinase.
芒果果皮果胶分解真菌及果胶深层发酵生产果胶酶的研究
果胶酶是一组能降解果胶的酶。本研究以芒果果胶提取液为底物,在深层发酵条件下,从芒果果皮分解中分离出高效产果胶酶的果胶降解真菌,并根据理化参数确定最佳产果胶酶条件。利用果胶琼脂培养基筛选生产果胶酶的微生物,分离出两种具有活性的果胶分解真菌P1和P2。随后将果胶酶生产培养基接种p1和p2,孵育7天,用于实验室规模生产果胶酶。发酵7天后提取酶,每天检测其果胶溶酶活性。P2具有较高的果胶溶解活性,可用于进一步研究。将P2接种到含有芒果果胶的肉汤中,进行深层发酵。结果表明,芒果果皮的果胶收率为17.75%。通过对不同发酵条件下pH、孵育时间、温度和底物浓度的优化工艺进行了研究,得到的最佳发酵条件分别为6天、4天、35℃和1.5%。结果表明,芒果果皮具有较高的果胶含量,可用于果胶酶的增值合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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