Isolation of Pectinolytic Bacteria from Decayed Orange Peel (Citrus sinensis) in Clarification of Tea Extract

M. Sivasakthi, S. S. Sankar
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Abstract

Background: Production of microbial enzymes at the industrial scale and their commercialization has attained a lot of value and public focus. Usage of micro organisms as bio-reactors begins due to the evolution of enzymes produced by microorganisms. There are so many industrially significant enzymes are originated from microbes, that include pectinases, lipases, amylases, proteases, xylynases etc. Methods: The actual work involved the use of microbes isolated from the decaying orange peel and tomato pulp for the extraction of the pectinase enzyme. The organisms were isolated and screened from the samples and were cultured onto pectin agar plate. Morphological and microscopic identification revealed that the bacteria isolated was Bacillus sp. Pectinase production media was later used for the lab scale production of pectinase enzyme by inoculating the bacteria and incubating for 48 hours. The enzyme thus produced was purified by Various methods. The pectinase enzymes isolated from bacillus sp. were used for improvement of tea leaves quality and clarification. The enzymes were characterized and purified. Results: The outcome of both purified pectinase enzymes and crude enzyme preparation on the improvement of tea extracts were determined in terms of flavanoids (310mg/gm), DPPH (49mg/gm), caffeine content (0.56-0.95), moisture content (7.2-6.7%), ash (4.1-4.6%), total phenol content (285mg/gm), and pH(6) and the shelf life analysis of the tea produced. The results thus obtained can conclude that the use of Bacillus sp. in the industrial production of pectinase is highly beneficial. According to the findings obtained from the study the enzyme treated tea extract improves its various quality parameters than the tea extracts which is non enzyme treated. And the utilization of microbial pectinase produced from bio-waste were most cost effective and yield good results for industrial use.
陈皮中果胶溶解菌的分离纯化
背景:微生物酶的工业规模生产及其商业化已经获得了很大的价值和公众关注。微生物作为生物反应器的使用是由于微生物产生的酶的进化而开始的。有很多具有工业意义的酶来源于微生物,包括果胶酶、脂肪酶、淀粉酶、蛋白酶、木聚糖酶等。方法:实际工作涉及使用从腐烂的橘子皮和番茄果肉中分离的微生物提取果胶酶。从样品中分离和筛选生物体,并将其培养在果胶琼脂平板上。形态学和显微镜鉴定表明,分离的细菌是芽孢杆菌。果胶酶生产培养基后来用于实验室规模的果胶酶生产,方法是接种细菌并孵育48小时。通过各种方法纯化由此产生的酶。从芽孢杆菌中分离得到的果胶酶用于改善茶叶品质和澄清。对酶进行了表征和纯化。结果:从黄烷酸(310mg/gm)、DPPH(49mg/gm),咖啡因含量(0.56-0.95),水分含量(7.2-6.7%),灰分(4.1-4.6%),总酚含量(285mg/gm)和pH(6)等方面测定了纯化果胶酶和粗酶制剂对茶叶提取物的改善效果,并对所生产的茶叶进行了保质期分析。由此获得的结果可以得出结论,在果胶酶的工业生产中使用芽孢杆菌是非常有益的。根据研究结果,酶处理的茶提取物比未经酶处理的茶叶提取物改善了其各种质量参数。利用生物废弃物产生的微生物果胶酶是最具成本效益和工业应用效果的。
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