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Development of Methodology for Concurrent Maximum Production of Alkaline Xylanase-Pectinase Enzymes in Short Submerged Fermentation Cycle

机译:在短浸没式发酵循环中的碱性木聚糖酶 - 果胶酶同时最大产量的方法的发展

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摘要

The aim of this study is to enhance the production of both enzymes concurrently in short fermentation cycle. In this study, effect of crude xylan and pectin substrates extracted from agro-residues, for the cost-effective, maximum concurrent production of xylanase-pectinase enzymes under submerged fermentation conditions was investigated. Crude xylan and crude pectin were extracted under alkaline and acidic conditions by using destarched, grinded wheat bran and citrus peel agro-wastes respectively. In order to make the production process more economical, different combinations with extracted substrates were tried for getting the maximum concurrent activity of both enzymes by reducing bacterial lag phase. Maximum alkaline xylanase activity of 296 ± 13 IU/ml and alkaline pectinase activity of 93 ± 7.0 IU/ml was achieved after 48 h of incubation, using production medium containing 2% wheat bran and 0.7% of crude pectin along with peptone, 0.5%; MgSO_4, 2.45%; pH 7.0 and 2% inoculum of 21 h old culture. This is the first report mentioning the utilization of agro-waste extracted pectin for enhanced production of pectinase in short incubation time, concurrently with xylanase.
机译:本研究的目的是在短发酵循环中同时增强两种酶的生产。在该研究中,研究了从农业残基中提取的粗氧化甘醇和果胶基材的效果,对于浸没式发酵条件下的木质酶 - 果胶酶的成本效率,最大的同时产生。通过使用Destached,研磨的小麦麸皮和柑橘果皮农业废物,在碱性和酸性条件下萃取粗Xylan和粗果胶。为了使生产过程更经济地,试图通过减少细菌滞后阶段来获得两种酶的最大同时活性的不同组合。在温育48小时后,使用含有2%小麦麸的生产培养基和蛋白胨0.5%的生产培养基,达到93±7.0IU / mL的最大碱性木聚糖酶活性为93±7.0 IU / mL和碱性果胶酶活性。 ; MgSO_4,2.45%; pH 7.0和2%的21小时旧文化的含量。这是提及农农渣中提取果胶的第一个报告,以加强与木聚糖酶同时孵育时间的果胶酶的产生。

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