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首页> 外文期刊>Biotechnology Progress >Optimization of Cyclodextrin Glycosyltransferase Production from Klebsiella pneumoniae AS-22 in Batch,Fed-Batch and Continuous Cultures
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Optimization of Cyclodextrin Glycosyltransferase Production from Klebsiella pneumoniae AS-22 in Batch,Fed-Batch and Continuous Cultures

机译:分批,补料和连续培养从肺炎克雷伯菌AS-22生产环糊精糖基转移酶的优化

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摘要

Production of a novel cyclodextrin glycosyltransferase (CGTase)from Klebsiella pneumoniae AS-22 strain,which converts starch predominantly to alpha-CD at high convesion yields,in batch,fed-batch,and continuous cultures,is presented.In tach fermentations,optimization of different operating parameters such as temperature,pH,agitation speed,and carbon-source concentration resulted in more than 6-fold increase in CGTase activity.The enzyme production was further improved by two fed-batch approaches.First,usingglucose-based feed to increase cell density,followed by starch-based feed to induce enzyme production,resulted in high cell density of 76 g dry cell weight/L,although the CGTase production was low.Using the second approach of a single dextrin-based feed,20-fold higher CGTase was produced compared to that in batch fermentations with media containing tapioca starch.In continuous operation,more than 8-fold increase in volumetric CGTase productivity was obtained using dextrin-based media compared to that in batch culture using starch-based media.
机译:从肺炎克雷伯氏菌AS-22菌株生产新型环糊精糖基转移酶(CGTase),提出了以高常规收率,分批,分批分批补料和连续培养的主要将淀粉转化为α-CD的方法。温度,pH,搅拌速度和碳源浓度等不同操作参数导致CGTase活性增加了6倍以上。通过两种补料分批进料方法进一步提高了酶的产量。首先,使用葡萄糖基饲料增加细胞密度,随后是淀粉基饲料诱导酶的产生,尽管CGTase的产量很低,但细胞密度却高达76 g干细胞重/ L,尽管第二种方法是使用单一的糊精基饲料,但20倍与使用含木薯淀粉的培养基进行分批发酵相比,产生的CGTase更高。在连续操作中,使用糊精为基础的培养基可使CGTase的体积生产率提高8倍以上与使用淀粉基培养基的分批培养相比。

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