In vitro elaboration Mutagenesis and cloning of the PA gene in Bacillus subtilis

Mohammad Abootaleb, Narjes Mohammadi Bandari
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引用次数: 2

Abstract

Background: The immune antigen of Bacillus anthracis is a protein that can attach to the surface receptor of all human cells. At the surface of cancer cells, there is a receptor that activates the uPA (Urokinase plasminogen) that do not exist in normal human cells. Objectives: The aim of this study was changing the location of the attachment of the PA gene by a directed mutation in order to attach only to the cancer cells.Methods: PA gene was extracted from the pMNA1 plasmid. The mutation on the PA gene was made by Overlap Extension PCR. The mutated segment was transferred to DH5α; the strain of Escherichia coli. With TA coning carrier. By restriction enzymes Hind III and BamH I the mutated PA gene was extracted and transferred to pWB980 and by electroporation method, it was transferred to the WB600 strain.Results: In this study, the mutation was occurred in sequences of PA gene by SOE PCR method resulting in a change in the genetic code of amino acid 194. The occurrence of mutation was confirmed by determining base sequences. Conclusion: Cancer is a severe disease that has a major impact on large groups of people which the problem of cancer is a leading cause of death across the world. One of the treatment methods of cancer is bacterial toxins if only cancer cells receive them. Therefore, these mutated PA proteins can be effective as novel therapeutic agents for the treatment of cancer.
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枯草芽孢杆菌PA基因的体外制备、诱变及克隆
背景:炭疽芽孢杆菌的免疫抗原是一种能附着于所有人体细胞表面受体的蛋白。在癌细胞的表面,有一种激活uPA(尿激酶纤溶酶原)的受体,这种受体在正常的人类细胞中不存在。目的:本研究的目的是通过定向突变改变PA基因的附着位置,以便仅附着在癌细胞上。方法:从pMNA1质粒中提取PA基因。利用重叠延伸PCR技术对PA基因进行了突变。将突变片段转移到DH5α;大肠杆菌菌株随着TA的到来。利用Hind III和BamH I酶提取突变的PA基因,并将其转移到pWB980上,再通过电穿孔法将其转移到WB600菌株上。结果:本研究通过SOE PCR方法在PA基因序列中发生突变,导致氨基酸194的遗传密码发生改变。通过测定碱基序列证实了突变的发生。结论:癌症是一种严重的疾病,对大量人群产生重大影响,癌症问题是世界各地死亡的主要原因。如果只有癌细胞接受细菌毒素,治疗癌症的方法之一就是细菌毒素。因此,这些突变的PA蛋白可以作为治疗癌症的新型治疗剂。
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