摘要
应用PCR技术从枯草杆菌168中分离出α-淀粉酶基因。将其引入分泌表达载体pBKE50后,用Tris-PEG法转入短短芽孢杆菌50中,发现α-淀粉酶以活性形式被分泌表达。酶测活分析表明α-淀粉酶活性约为出发菌枯草杆菌168的1.7倍。
Theα-amylase gene of Bacillus subtilis168was isolated by PCR and used to construct recombinant plasmid pBKE50/α-amy with vector pBKE50.Soluble and biologically activeα-amylase was secreted directly into the culture medium after pBKE50/α-amy had been introduced into Bacillus brevis50by the Tris-PEG method,and the amount of enzymes produced by Bacillus brevis50(pBKE50/α-amy)was1.7times larger than that produced by Bacillus subtilis168.
出处
《生物技术通讯》
CAS
2002年第3期167-169,共3页
Letters in Biotechnology