Sharma Manoj Kumar, Jani Dewal, Thungapathra M, Gautam J K, Meena L S, Singh Yogendra, Ghosh Amit, Tyagi Akhilesh Kumar, Sharma Arun Kumar
Department of Plant Molecular biology, University of Delhi South Campus, New Delhi 110021, India.
J Biotechnol. 2008 May 20;135(1):22-7. doi: 10.1016/j.jbiotec.2008.03.002. Epub 2008 Mar 20.
In earlier study from our group, cholera toxin B subunit had been expressed in tomato for developing a plant-based vaccine against cholera. In the present investigation, gene for accessory colonization factor (acf) subunit A, earlier reported to be essential for efficient colonization in the intestine, has been expressed in Escherichia coli as well as tomato plants. Gene encoding for a chimeric protein having a fusion of cholera toxin B subunit and accessory colonization factor A was also expressed in tomato to generate more potent combinatorial antigen. CaMV35S promoter with a duplicated enhancer sequence was used for expression of these genes in tomato. Integration of transgenes into tomato genome was confirmed by PCR and Southern hybridization. Expression of the genes was confirmed at transcript and protein levels. Accessory colonization factor A and cholera toxin B subunit fused to this protein accumulated up to 0.25% and 0.08% of total soluble protein, respectively, in the fruits of transgenic plants. Whereas protein purified from E. coli, in combination with cholera toxin B subunit can be used for development of conventional subunit vaccine, tomato fruits expressing these proteins can be used together with tomato plants expressing cholera toxin B subunit for development of oral vaccine against cholera.
在我们团队早期的研究中,霍乱毒素B亚基已在番茄中表达,用于开发一种抗霍乱的植物源疫苗。在本研究中,先前报道对在肠道中有效定殖至关重要的辅助定殖因子(acf)亚基A基因已在大肠杆菌和番茄植株中表达。编码霍乱毒素B亚基与辅助定殖因子A融合的嵌合蛋白的基因也在番茄中表达,以产生更强效的组合抗原。具有重复增强子序列的花椰菜花叶病毒35S启动子用于这些基因在番茄中的表达。通过PCR和Southern杂交确认转基因整合到番茄基因组中。在转录水平和蛋白质水平上确认了基因的表达。与该蛋白融合的辅助定殖因子A和霍乱毒素B亚基分别在转基因植物果实中积累至总可溶性蛋白的0.25%和0.08%。从大肠杆菌中纯化的蛋白与霍乱毒素B亚基结合可用于开发传统亚单位疫苗,而表达这些蛋白的番茄果实可与表达霍乱毒素B亚基的番茄植株一起用于开发抗霍乱口服疫苗。