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首页> 外文期刊>African Journal of Biotechnology >Improved keratinase production for feather degradation by Bacillus licheniformis ZJUEL31410 in submerged cultivation
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Improved keratinase production for feather degradation by Bacillus licheniformis ZJUEL31410 in submerged cultivation

机译:通过枯草芽孢杆菌31410在淹没的栽培中改善了角蛋白酶生产的羽毛降解

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摘要

Optimal medium was used to improve the production of keratinase by?Bacillus licheniformis?ZJUEL31410, which has a promising application in the transformation of feather into soluble protein. The results of single factor design revealed that the concentration of feather at 20 g/l and the initial pH at value 8 was the best for the production of keratinase and the degradation of feather. Ammonia salt and nitrate salt strongly restricted the production of keratinase and the degradation of feather. Result of Box-Behnken design (BBD) experiment which was used to optimize concentrations of glucose, corn steep flour and K2HPO4?for further improvement of keratinase productivity showed that the optimal medium was composed of glucose (20 g/l), corn steep flour (7.5 g/l), K2HPO4?(1 g/l) and feather (20 g/l). The result of submerged batch cultivation of?B. licheniformis?ZJUEL31410 in the 5 L fermentor indicated that the optimal medium had the highest keratinase and the degree of feather degradation (DFD) at 54.9 U/ml and 72.4%; both were 5 times more than the basal medium. The degradation of feather was verified by the analysis of scanning electron microscopy (SEM). This study provides a foundation for the production of keratinase and the conversion of feather to soluble protein through submerged fermentation process by?B. licheniformis?ZJUEL31410.
机译:最佳培养基用于改善角蛋白酶的产生β芽孢杆菌酶的产生βZjuel31410,其在羽毛转化为可溶性蛋白质中具有希望的应用。单因素设计的结果显示,20g / L的羽毛浓度和值8的初始pH是最适合在角蛋白酶的产生和羽毛的降解的最佳选择。氨盐和硝酸盐强烈地限制了角蛋白酶的产生和羽毛的降解。 Box-Behnken设计(BBD)实验的结果用于优化葡萄糖,玉米陡粉和K2HPO4浓度的实验?为了进一步提高角蛋白酶生产率,表明最佳培养基由葡萄糖(20g / L),玉米陡粒组成(7.5g / l),k2hpo4?(1 g / l)和羽毛(20 g / l)。淹没批量培养的结果?b。 Licheniformis?Zjuel31410在5L发酵罐中表明,最佳培养基具有最高角蛋白酶和羽毛降解程度(DFD),54.9u / ml和72.4%;两者比基础培养基多5倍。通过扫描电子显微镜(SEM)的分析验证了羽毛的劣化。本研究为通过浸没式发酵过程生产角蛋白酶和羽毛转化为可溶性蛋白质的基础。 licheniformis?zjuel31410。

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