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利用绿茶废弃物通过固态发酵优化多孔真菌KA038菌株高产内切葡聚糖酶的生产。

Optimization of high endoglucanase yields production from polypore fungus, strain KA038 under solid-state fermentation using green tea waste.

作者信息

Nguyen Kim Anh, Kumla Jaturong, Suwannarach Nakarin, Penkhrue Watsana, Lumyong Saisamorn

机构信息

Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.

Master's Degree Program in Applied Microbiology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Biol Open. 2019 Nov 29;8(11):bio047183. doi: 10.1242/bio.047183.

Abstract

Polypores are diverse macrofungi that have been extensively studied for their lignocellulolytic enzyme production capabilities. Currently, these enzymes are being used for many industrial purposes. However, the high cost associated with their production is the main barrier to their broader application. This work aimed to study the optimal medium and conditions for endoglucanase production using solid state fermentation. Seven polypore strains were used for endoglucanase activity screening. The fermentation experiments were carried out in 250 ml Erlenmeyer flasks with green tea waste as a substrate. Notably, strain KA038 showed the best level of activity (38.62 IU/gds). Various parameters such as moisture content, nitrogen source, initial pH value, inoculum size and incubation time were considered to determine the optimal conditions for endoglucanase production. The optimal medium consisted of green tea leaves as a carbon source, beef extract as an organic nitrogen source, NHHPO as an inorganic nitrogen source, pH 7.0 and an incubation temperature at 30°C for 4 days resulted in a high enzyme yield with strain KA038 (81.8 IU/gds).This article has an associated First Person interview with the first author of the paper.

摘要

多孔菌是多种多样的大型真菌,因其木质纤维素分解酶的生产能力而受到广泛研究。目前,这些酶正被用于许多工业用途。然而,与其生产相关的高成本是其更广泛应用的主要障碍。这项工作旨在研究使用固态发酵生产内切葡聚糖酶的最佳培养基和条件。使用七种多孔菌菌株进行内切葡聚糖酶活性筛选。发酵实验在250毫升锥形瓶中进行,以绿茶废料为底物。值得注意的是,KA038菌株表现出最佳的活性水平(38.62 IU/gds)。考虑了各种参数,如水分含量、氮源、初始pH值、接种量和培养时间,以确定内切葡聚糖酶生产的最佳条件。最佳培养基由绿茶叶作为碳源、牛肉膏作为有机氮源、磷酸二氢铵作为无机氮源组成,pH值为7.0,在30°C下培养4天,KA038菌株的酶产量很高(81.8 IU/gds)。本文对该论文的第一作者进行了相关的第一人称访谈。

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