Song Jingyuan, Imanaka Hiroyuki, Imamura Koreyoshi, Minoda Masashi, Katase Toru, Hoshi Yukiko, Yamaguchi Shotaro, Nakanishi Kazuhiro
Graduate School of Natural Science and Technology, Okayama University, Kita-ku, Okayama, Japan.
Biosci Biotechnol Biochem. 2011;75(6):1194-7. doi: 10.1271/bbb.110014. Epub 2011 Jun 13.
A gene of β-galactosidase from Bacillus circulans ATCC 31382 was cloned and sequenced on the basis of N-terminal and internal peptide sequences isolated from a commercial enzyme preparation, Biolacta(®). Using the cloned gene, recombinant β-galactosidase and its deletion mutants were overexpressed as His-tagged proteins in Escherichia coli cells and the enzymes expressed were characterized.
基于从商业酶制剂Biolacta(®)中分离得到的N端和内部肽段序列,对环状芽孢杆菌ATCC 31382的β-半乳糖苷酶基因进行了克隆和测序。利用克隆得到的基因,重组β-半乳糖苷酶及其缺失突变体在大肠杆菌细胞中作为His标签蛋白进行了过量表达,并对表达的酶进行了表征。