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Mannanase Enzyme from Bacillus subtilis P2-5 with Waste Management

机译:来自枯草芽孢杆菌P2-5的甘露酶酶,废物管理

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Nowadays, waste disposal has become a major of environment problem in Thailand because the volume of waste increase due to population growth and social behavior. It required optimal solutions in waste management. People should realize fundamental of 3R including reduce recycle and reuse in order to improve environment condition. This research interested in coffee grounds and tea waste because they were generated from household and industrial thus require to disposal or added value. The objective of this research was recycle coffee grounds and tea waste by utilize as a raw material for mannanase enzyme production. Mannanase enzyme can hydrolyze mannan structure, containing in plant such as konjac, ivory nut, locust bean gum, guar gum, palm kernel, coffee bean and copra meal. The methodology was a randomized complete block design to studied mannanase enzyme activity in different condition. There were two factors consist of inoculum percentage; Bacillus subtilis P2-5 had three levels (1, 3 and 5% (v/v) and three sources (locust bean gum, coffee grounds and tea waste) in producing medium (PM) for mannanase production. An analysis of variances (ANOVA) method was applied to determine the effect of inoculum percentage and regression analysis to predict mannanase enzyme activity. The test result found that inoculum percentage and three sources significantly affecting the mannanase enzyme activity. The prediction model had been formulated and prioritize source which produce the high mannanase enzyme activity as following tea waste, coffee grounds and locust bean gum, respectively. This research would be guidelines for waste management strategy to achieve sustainability approach.
机译:如今,废物处置已成为泰国环境问题的主要问题,因为由于人口增长和社会行为,废物量增加。它需要在废物管理中最佳解决方案。人们应该意识到3R的根本,包括减少回收和重用,以改善环境状况。这项研究对咖啡渣和茶垃圾感兴趣,因为它们是由家庭和工业产生的,因此需要处理或增加价值。本研究的目的是通过利用作为甘露糖酶产生的原料来回收咖啡渣和茶叶废物。甘露酶酶可以水解甘露甘露结构,含有Konjac,象牙色,蝗虫豆胶,瓜尔胶,棕榈仁,咖啡豆和椰子粉等植物。该方法是随机完全块设计,用于在不同条件下研究甘露酶酶活性。接种百分比有两个因素;枯草芽孢杆菌P2-5在生产培养基(PM)中有三种(1,3和5%(v / v)和三种来源(刺槐豆胶,咖啡和茶废物),用于甘露糖酶生产。差异分析(Anova应用方法以确定接种百分比和回归分析的效果,以预测甘露糖酶活性。发现结果发现,接种百分比和三种源显着影响甘露糖酶活性。预测模型已制定并优先考虑产生高的源甘油酶酶活性分别为茶叶废物,咖啡渣和蝗虫豆胶。本研究是达到可持续性方法的废物管理战略的指导方针。

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