Shahryari F, Safarnejad M R, Shams-Bakhsh M, Jouzani G R Salehi
Department of Microbial Biotechnology and Biosafety, Agricultural Biotechnology Research Institute of Iran (ABRII), Karaj, Iran.
Commun Agric Appl Biol Sci. 2010;75(4):789-95.
The witches' broom disease of lime (WBDL) caused by Candidatus Phytoplasma aurantifolia is the most devastating disease of acidian lime in southern part of Iran as it destroy thousands of trees yearly throughout these regions. Traditional methods such as eradication of infected trees and insect vector control have shown limited effect on this case. Therefore, alternative approaches such as plantibody-mediated resistance, have been considered. Throughout present study we prepared sufficient amount of antigen that is required for generation of specific monoclonal recombinant antibodies against Immunodominant membrane protein (IMP) which will be exploited for plantibody-mediated resistance approach. The gene encoding IMP protein was obtained by PCR amplification using specific primers and DNA extracted from the infected plants. Amplified fragment was then inserted into T/A cloning vector. Intact clones containing the right sequence was selected after digestion, PCR amplification and subsequent sequencing analysis. IMP encoding region having the right sequence was sub-cloned into pET28a bacterial expression vector. Large scale expression of His tagged recombinant protein was performed in the BL21-de3 strain of E. coli and purification under native conditions was carried out through immobilized metal ion affinity chromatography (IMAC) in a column containing Ni-NTA agarose beads. Successful expression and purification steps were confirmed by SDS-PAGE and western blotting analyses. The results obtained indicated the successful production of about 18 mg purified recombinant IMP protein with a low level of contamination in one liter cultured medium. Finally the purified protein was dialyzed in phosphate saline buffer and applied for immunization of mice.
由嗜酸橙原体(Candidatus Phytoplasma aurantifolia)引起的酸橙扫帚病(WBDL)是伊朗南部酸橙中最具毁灭性的病害,因为它每年在这些地区毁掉成千上万棵树。诸如砍伐受感染树木和控制昆虫媒介等传统方法在这种情况下效果有限。因此,人们考虑了诸如植物抗体介导抗性等替代方法。在本研究中,我们制备了足够量的抗原,用于产生针对免疫显性膜蛋白(IMP)的特异性单克隆重组抗体,该抗体将用于植物抗体介导的抗性方法。通过使用特异性引物进行PCR扩增,并从受感染植物中提取DNA,获得了编码IMP蛋白的基因。然后将扩增片段插入T/A克隆载体。经过消化、PCR扩增和后续测序分析后,选择含有正确序列的完整克隆。将具有正确序列的IMP编码区亚克隆到pET28a细菌表达载体中。在大肠杆菌的BL21-de3菌株中进行His标签重组蛋白的大规模表达,并通过固定化金属离子亲和色谱(IMAC)在含有Ni-NTA琼脂糖珠的柱中进行天然条件下的纯化。通过SDS-PAGE和蛋白质印迹分析确认了成功的表达和纯化步骤。所得结果表明,在一升培养基中成功产生了约18mg纯化的重组IMP蛋白,污染水平较低。最后,将纯化的蛋白在磷酸盐缓冲盐水中透析,并用于小鼠免疫。