Park Juyi, Hong Soon-Kwang, Chang Yong Keun
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Republic of Korea.
J Microbiol Biotechnol. 2014 Dec 28;24(12):1622-8. doi: 10.4014/jmb.1405.05019.
DagA, a β-agarase, was produced by cultivating a recombinant Streptomyces lividans in a glucose medium or a mixed-sugar medium simulating microalgae hydrolysate. The optimum composition of the glucose medium was identified as 25 g/l glucose, 10 g/l yeast extract, and 5 g/l MgCl2·6H2O. With this, a DagA activity of 7.26 U/ml could be obtained. When a mixedsugar medium containing 25 g/l of sugars was used, a DagA activity of 4.81 U/ml was obtained with very low substrate utilization efficiency owing to the catabolic repression of glucose against the other sugars. When glucose and galactose were removed from the medium, an unexpectedly high DagA activity of about 8.7 U/ml was obtained, even though a smaller amount of sugars was used. It is recommended for better substrate utilization and process economics that glucose and galactose be eliminated from the medium, by being consumed by some other useful applications, before the production of DagA.
通过在葡萄糖培养基或模拟微藻水解物的混合糖培养基中培养重组淡紫链霉菌来生产β-琼脂酶DagA。葡萄糖培养基的最佳组成确定为25 g/l葡萄糖、10 g/l酵母提取物和5 g/l MgCl₂·6H₂O。据此,可获得7.26 U/ml的DagA活性。当使用含有25 g/l糖类的混合糖培养基时,由于葡萄糖对其他糖类的分解代谢阻遏作用,底物利用效率非常低,获得的DagA活性为4.81 U/ml。当从培养基中去除葡萄糖和半乳糖时,即使使用的糖量较少,也意外地获得了约8.7 U/ml的高DagA活性。建议在生产DagA之前,通过其他一些有用的应用消耗掉葡萄糖和半乳糖,从而从培养基中去除它们,以实现更好的底物利用和工艺经济性。