摘要
以玉米芯颗粒吸附桔青霉 (Penicilliumcitrinum)孢子 ,再用质量分数为 1.5%的海藻酸钠包埋吸附固定化细胞玉米芯颗粒 ,于摇瓶中进行分批培养 .实验结果表明 :在固定化细胞产酶的条件下 ,培养基中淀粉水解糖浓度为 9g/L ,蛋白胨浓度为 1g/L ,采用气升式反应器 ,产酶发酵周期为 50h ,发酵液中核酸P1 的活力高达 8.4 3mmol·s- 1 ·L- 1 .双载体固定化细胞经 30批次连续重复发酵产酶稳定在较高水平 。
Mycelia of Penicillium citrinum are absorbed by stone of maize and then wrapped up by 1.5% sodium alginate .The nuclease P 1 produced by the immobilized cells are studied in shaking flasks.The experiment shows that the glucose and peptone contents in medium are 9 g/L and 1 g/L respectively. In the three phase airlift reactor, the activity of nuclease P 1 reached 8.43 mmol·s -1 ·L -1 after 50 h culture. In the course of repeated batch culture , the immobilized cells keep high capacity and mechanical strength after 30 batches .
出处
《烟台大学学报(自然科学与工程版)》
CAS
2001年第1期37-41,共5页
Journal of Yantai University(Natural Science and Engineering Edition)
基金
国家教育部华东理工大学生物反应器工程国家重点实验室访问学者资助项目!(F2 0 0 -C - 0 9)
关键词
桔青霉
固定化细胞
核酸酶P1
玉米芯
藻酸钠
Penicillium citrinum
immobilized cell
nuclease P 1
stone of maize
sodium alginate