以橘皮和玉米芯为底物固态发酵酿酒酵母生产果胶酶

M. S. Haske, M. Y. Iliyasu, A. Abdulrahman, S. M. Sani, T. Inusa, S. Isma’il, R. D. Umar, Z. M. Kabeer, H. Tahir, E. Agbo
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引用次数: 0

摘要

研究背景:废物特别是水果废物的降解很重要,因为这些废物会在环境中积累。由于果胶酶在工业上的广泛应用,果胶酶的生物合成成本较低。利用酿酒酵母菌降解这些废弃物产生果胶酶的能力。目的:对酿酒酵母菌进行分离鉴定,研究以玉米芯为原料在柑桔皮上生产果胶酶的最佳工艺条件,并研究所产酶在柑桔汁提取中的效果。研究地点和时间:该研究于2021年8月至9月在尼日利亚包奇州阿布巴卡尔塔法瓦巴莱瓦大学包奇微生物学实验室进行。方法:收集橙子售卖摊位的土壤样品,采用连续稀释法将溶液降低到更可用的浓度,并将样品在酵母蛋白胨葡萄糖琼脂(YPDA)上划线。28℃孵育3 ~ 9天。通过形态学和生化试验对分离酵母进行鉴定,并在不同的最佳条件下将分离菌接种于所制备的发酵培养基上。提取粗酶,用二硝基水杨酸试剂(DNS)法测定果胶酶活性。实验结果表明,所制备的果胶酶能有效地从橙泥中提取果汁。结果:在确定的最佳发酵条件下,以橘子皮和玉米芯为底物进行固态发酵,酿酒酵母菌具有较好的果胶酶水解能力。通过改变生产培养基的条件,对果胶酶的生产进行了优化。35℃孵育72小时,果胶酶活性为(2.81 + 2.31 ug/ml)。结论:在固态发酵条件下,可以成功地利用橘皮和玉米芯诱导酿酒酵母生产果胶酶。
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Pectinase Production from Saccharomyces Cerevisiae Using Orange Peels and Maize Cobs as Substrate for Solid-State Fermentation
Background of the Study: Degradation of wastes especially fruit waste is important because these wastes accumulate in the environment. The fruit wastes can be used to biosynthesize pectinase enzyme at a cheaper rate due its numerous industrial applications. The ability of Saccharomyces cerevisiae to degrade these wastes to produce pectinase enzyme was exploited. Aim: The aim of this study is to isolate and characterize Saccharomyces cerevisiae and study the optimal conditions needed for pectinase production on the orange peel with maize cobs and study the effectiveness of the enzymes produced in the extraction of orange juice. Place and Duration of Study: The study was conducted at the Microbiology Laboratory of Abubakar Tafawa Balewa University Bauchi, Bauchi State, Nigeria, between August to September 2021. Methodology: Soil samples from the orange seller stand was collected, serial dilution method was used to reduce the solution to a more usable concentration, and the samples were streaked on Yeast Peptone Dextrose Agar (YPDA). The plates were incubated for 3 to 9 days at 28+- oC. The isolated yeast was identified based on the morphological and biochemical test, the isolates were inoculated on the prepared fermentation media under different optimal conditions. The crude enzyme were extracted, and the extracts were tested for pectinase activity using the dinitrosalicylic reagent (DNS) method for the presence of reducing sugar. The resulting pectinase was determined to effectively extract juice from orange mash. Results: Saccharomyces cerevisiae showed relatively pectinase hydrolysis using orange peels and maize cobs as substrate by solid-state fermentation under predetermined optimum fermentation conditions. Optimization for the pectinase production was done by altering the conditions for the production medium. Pectinase activity of (2.81 + 2.31 ug/ml) was observed at 72hr of incubation at 35oC. Conclusion: The study demonstrates that orange peel and maize cob can be successfully used to induce the production of pectinase using Saccharomyces cerevisiae under solid-state fermentation.
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