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Production and characterization of thermostable xylanase from Bacillus subtilis XP10 isolated from marine water

机译:从海水中分离出的枯草芽孢杆菌XP10产生热稳定的木聚糖酶并进行表征

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摘要

This study aims is to characterize an efficient bacterium, capable of producing thermostable xylanases. Different bacterial isolates were obtained on medium containing xylan as the sole carbon source from samples collected from Jeddah, Saudi Arabia. Out of 15 xylanase producing isolates, the best xylanase producer was XP10 which was selected for the enzyme production. It was identified based on morphological and some biochemical characters as a species belonging to the genusBacillus?and identified as?Bacillus subtilis?XP10. Identification was confirmed by 16S rDNA studies and restriction fragment length polymorphism. Factors affecting enzymes production were studied. Maximum xylanase production was 2.82 U/ml obtained at pH 8 for 4 days at 40°C and 120 rpm. The molecular weight of the purified enzyme was 23 kDa. Fivefold increasing in xylanase production was obtained by construction of recombinant?Escherichia coli?107 harboring recombinant vector pJET1.2/blunt/xynA.?The purified thermostable alkalotolerant xylanase can be used in the treatment of agricultural wastes as well as in the bioremediation of xylan-containing materials.
机译:这项研究的目的是表征一种能够产生热稳定木聚糖酶的有效细菌。在含有木聚糖作为唯一碳源的培养基上,从沙特阿拉伯吉达收集的样品中获得了不同的细菌分离株。在15种产生木聚糖酶的菌株中,最好的木聚糖酶生产者是XP10,它被选为酶的生产者。根据形态学和一些生化特征,将其鉴定为属于芽孢杆菌属的物种,并鉴定为枯草芽孢杆菌XP10。通过16S rDNA研究和限制性片段长度多态性证实了鉴定。研究了影响酶产生的因素。在40°C和120 rpm下,在pH 8下连续4天获得的最大木聚糖酶产量为2.82 U / ml。纯化的酶的分子量为23kDa。通过构建带有重组载体pJET1.2 /钝/ xynA的重组大肠杆菌107,木聚糖酶的产量增加了五倍。含材料。

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