Okumura Shiro, Saitoh Hiroyuki, Ishikawa Tomoyuki, Wasano Naoya, Yamashita Satoko, Kusumoto Ken-Ichi, Akao Tetsuyuki, Mizuki Eiichi, Ohba Michio, Inouye Kuniyo
Fukuoka Industrial Technology Center, 1465-5 Aikawa, Kurume, Fukuoka 839-0861, Japan.
J Agric Food Chem. 2005 Aug 10;53(16):6313-8. doi: 10.1021/jf0506129.
Parasporal inclusion proteins produced by Bacillus thuringiensis strain A1470 exhibit strong cytotoxicity against human leukemic T cells when activated by protease treatment. One of the cytotoxic proteins was separated by anion exchange chromatography and gel filtration chromatography and designated Cry45Aa. Its gene was then expressed in recombinant Escherichia coli, in which the Cry45Aa precursor was accumulated in an inclusion body. It was solubilized in sodium carbonate buffer and processed with proteinase K, and cytotoxic activities of the protein against various mammalian cell lines were evaluated using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H tetrazolium bromide assay. The protein exhibited high cytotoxic activity against CACO-2, Sawano, MOLT-4, TCS, and HL60 cells and moderate activity against U-937 DE-4, PC12, and HepG2 cells. On the other hand, the EC50 values against Jurkat, K562, HeLa, A549, Vero, COS-7, NIH3T3, CHO, and four normal tissue cells (human primary hepatocyte cells, UtSMC, MRC-5, and normal T cells) were >2 microg/mL.
苏云金芽孢杆菌菌株A1470产生的伴孢晶体蛋白经蛋白酶处理激活后,对人白血病T细胞表现出强烈的细胞毒性。其中一种细胞毒性蛋白通过阴离子交换色谱和凝胶过滤色谱分离出来,命名为Cry45Aa。然后将其基因在重组大肠杆菌中表达,Cry45Aa前体在其中以包涵体形式积累。将其溶解于碳酸钠缓冲液中并用蛋白酶K处理,使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H溴化四唑法评估该蛋白对各种哺乳动物细胞系的细胞毒性活性。该蛋白对CACO-2、泽野、MOLT-4、TCS和HL60细胞表现出高细胞毒性活性,对U-937 DE-4、PC12和HepG-2细胞表现出中等活性。另一方面,对Jurkat、K562、HeLa、A549、Vero、COS-7、NIH3T3、CHO和四种正常组织细胞(人原代肝细胞、UtSMC、MRC-5和正常T细胞)的半数有效浓度值>2微克/毫升。