报道了鸡肌腺苷酸激酶基因的克隆和在温控启动子PRPL调控下在大肠杆菌中的可溶性高效表达.SDS-PAGE分析表明,鸡肌腺苷酸激酶的含量可占大肠杆菌细胞总蛋白含量的38%.利用Johnson等的干冰/乙醇-冰水浴反复冻融法,可将此重组蛋白进行富集,纯度可达85%以上.鸡肌腺苷酸激酶可与抗兔肌腺苷酸激酶单克隆抗体产生强的交叉反应.
Chicken muscle adenylate kinase was overproduced in soluble form under the transcriptional control of the bacterial phage lambda PRPL promoters regulated by temperature sensitive repressors. SDS-PAGE analysis demon-strated that the enzyme was produced to the extent of as much as 38% of the total cellular protein. The soluble recombinant enzyme can be released from bacterial cells and enriched to purity of more than 85% by the Johnson's freeze/thaw method. Mouse anti-rabbit muscle adenylate kinase monoclonal antibody can strongly crossreact with the recombinant enzyme.
静恩烜,周波,罗杰,张洪杰.腺苷酸激酶基因在大肠杆菌中的可溶性高表达[J].生物化学与生物物理进展,1997,24(6):525-528
复制生物化学与生物物理进展 ® 2025 版权所有 ICP:京ICP备05023138号-1 京公网安备 11010502031771号