首页> 外文期刊>Journal of applied microbiology >Biosynthesis of cyclodextrin glucosyltransferase by the free and immobilized cells of Bacillus cereus NRC7 in batch and continuous cultures.
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Biosynthesis of cyclodextrin glucosyltransferase by the free and immobilized cells of Bacillus cereus NRC7 in batch and continuous cultures.

机译:蜡状芽孢杆菌NRC7的游离和固定细胞分批和连续培养生物合成环糊精葡萄糖基转移酶。

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摘要

Aims: The objective of this study was to enhance the production of cyclodextrin glucanotransferase (CGTase) produced by a local isolate Bacillus cereus NRC7. Methods and Results: In batch culture, maximal CGTase activity (69 0 U ml--1) was reached after 24-h incubation period. In continuous production of CGTase by the free cells of B. cereus NRC7, maximal reactor productivity (11 76 KU l--1 h--1), with enzyme concentration of 49 0 U ml--1 and specific productivity of 904 6 U per g wet cells per h, was attained at dilution rate of 0 24 h--1, over a period of 640 h. Bacillus cereus NRC7 cells were immobilized on chitosan. The immobilization conditions with respect to matrix concentration and maximal cell loading were optimized for maximal CGTase production. In repeated batch operation, the activity of the immobilized cells was stable during ten cycles and the activity remained between 51 and 55 U ml--1. In packed-bed reactor, the immobilized cells showed maximal productivity (27 18 KU l--1 h--1) with enzyme concentration of 54 63 U ml--1 and specific productivity of 151 89 U per g wet cells per h at dilution rate of 0 5 h--1. The half-life of the immobilized cells was higher than 20 days. Conclusions: Continuous fermentation by the immobilized cells in packed-bed reactor is an appropriate potential technique for B. cereus NRC7 CGTase production that gave maximum productivity (27 18 KU l--1 h--1), which was 9 47-, 2 31-, 12 24- and 12 94-fold higher than the free cells in batch, free cells in continuous, immobilized cells in batch and repeated batch cultures, respectively. Significance and Impact of the Study: This is the first study that evaluates CGTase productivity, in different fermentation modes, in terms of specific productivity (U per gram cells per h). In continuous fermentation by immobilized cells, maximal levels of CGTase productivity are higher than the previously reported values
机译:目的:这项研究的目的是提高由局部分离的蜡样芽孢杆菌NRC7产生的环糊精葡聚糖转移酶(CGTase)的产量。方法和结果:在分批培养中,孵育24小时后达到最大CGTase活性(69 0 U ml -1 )。由B的游离细胞连续产生CGTase。 cereus NRC7,最大反应器生产率(11 76 KU l -1 h -1 ),酶浓度为49 0 U ml -在640 h的时间内,以0 24 h -1 的稀释率获得了-1 和比生产率/每小时904 6 U / g湿细胞。蜡状芽孢杆菌NRC7细胞固定在壳聚糖上。关于基质浓度和最大细胞载量的固定条件被优化以产生最大的CGTase。在重复的分批操作中,固定的细胞的活性在十个循环中是稳定的,并且活性保持在51和55 U ml -1 之间。在填充床反应器中,固定化细胞表现出最大的生产率(27 18 KU l -1 h -1 ),酶浓度为54 63 U ml -1 和比生产率为151 89 U / g湿细胞/ h,稀释率为0 5 h -1 。固定化细胞的半衰期高于20天。结论:固定床反应器中固定化细胞的连续发酵是B的一种合适的潜在技术。 cereus NRC7 CGTase产量最高(27 18 KU l -1 h -1 ),分别为9 47-,2 31-,分批培养的游离细胞比连续培养的游离细胞高12倍,分批培养的游离细胞比固定培养的游离细胞高12倍,而固定培养的重复细胞分别高12倍和12倍。研究的意义和影响:这是第一项根据比生产率(U /克细胞/小时)评估不同发酵模式下CGTase生产率的研究。在固定化细胞连续发酵中,CGTase生产力的最高水平高于先前报道的值

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