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Production of amylases from Bacillus amyloliquefaciens under submerged fermentation using some agro-industrial by-products

机译:使用一些农业工业副产物在水下发酵条件下从解淀粉芽孢杆菌生产淀粉酶

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Thirty-one bacterial isolates out of 133 isolates, were obtained from rhizosphere of Egyptian clover plants, and had variant capability for starch degradation on starch agar medium. The isolate E109 was the most potent being 72.5 U ml-' and 2.5 for amylase activity and starch hydrolysis ratio (SHR), respectively, at 50 °C. The potent isolate El09 was identified based on phe-notypic characteristics, phylogenetic positions based on I6S rRNA gene analysis and base sequences (submitted to NCBI Gen Bank). 16S rRNA gene analysis confirmed that this isolate belonged to the genus Bacillus and it was most closely related to B. amyloliquefaciens (95% similarity). For the production of amylases, nine agro-industrial residues were added as carbon sources to the basal medium. The medium supplemented with potato starchy waste as the sole carbon source enhanced the enzyme activity more than soluble starch as control for a, P and y amylases activity, as it increased by B. amyloliquefaciens about 1.26 & 4 and 8-fold, respectively after 48 h at 50 °C using rotary shaker at 150 rpm. B. amyloliquefaciens gave the maximum values of
机译:从埃及三叶草植物的根际中获得了133个分离株中的31个细菌分离株,它们具有在淀粉琼脂培养基上降解淀粉的变异能力。分离株E109在50°C时的淀粉酶活性和淀粉水解率(SHR)最有效,分别为72.5 U ml-和2.5。根据phe-notypic特征,基于I6S rRNA基因分析的系统发育位置和碱基序列(提交给NCBI Gen Bank),鉴定出了有效的分离株El09。 16S rRNA基因分析证实该分离株属于芽孢杆菌属,与解淀粉芽孢杆菌最密切相关(95%相似性)。为了生产淀粉酶,向基础培养基中添加了九种农业工业残留物作为碳源。补充马铃薯淀粉废料作为唯一碳源的培养基比可溶淀粉作为a,P和y淀粉酶活性的对照的酶活性提高更多,因为淀粉淀粉芽孢杆菌在48后分别增加了1.26、4和8倍。使用旋转摇床以150 rpm在50°C下h。在50°C发酵30、30和36 h后,通过摇瓶技术分批培养,B。amyloliquefaciens在补充了2%马铃薯淀粉废物的培养基上给出了最大的

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