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Recombinant Protein for Biocontrol of Brown Rot Disease in Potato

机译:用于马铃薯褐腐病生物防治的重组蛋白

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In Egypt, potato has an important position among all vegetable crops. Potato crop is infected with the brown rot disease producing a major problem which caused by Ralstonia. Solanacearum. Soil samples were collected from Gharbia governorate, bacterial isolation was carried out using suitable media. Many bacterial isolates were obtained and used for bioagent against R. solanacearum. One isolate among all the examined isolate showed high antagonism activity against the R. solanacearum. This isolate was subjected to identification using the 16S rRNA gene and the sequence analysis revealed that the strain is Pantoea agglomerance. The bacterium was cultivated on PBG medium and the culture filtrate was fractionated, the entire fractions were used for the antagonism activity. One of these fractions showed high ability to control R. solanacearum (named Biocine). The Molecular weight of the purified Biocine was determined by SDS polyacrylamide gel electrophoresis revealing one band with a molecular weight of 29kDa. Differential display was used to study the Biocine regulating gene. Band in molecular weight 800bp were excised, cloned using TOPO TA cloning kit. The fragment was released using the EcoR1 restriction enzyme and subcloned into prokaryotic expression vector (Ptrac A). The recombinant bacteria were induced using the IPTG and the purified protein was obtained based on the His-tag technology. Bioassay was carried out for the purified recombinant protein compared with the wiled one, the same activity was shown. It could be concluded that production a high amount of biocine on semi-industrial scale available. To transfer the experiment from lab to the field are under study
机译:在埃及,马铃薯在所有蔬菜作物中都占有重要地位。马铃薯作物感染了褐腐病,这是由Ralstonia引起的主要问题。茄科。从加尔比亚省收集土壤样品,使用合适的培养基进行细菌分离。获得了许多细菌分离株,并将其用作抗青枯菌的生物制剂。在所有检查到的分离株中,有一个分离株对青枯菌具有高拮抗活性。使用16S rRNA基因对该分离株进行鉴定,序列分析表明该菌株为泛菌团。在PBG培养基上培养细菌,并分离培养滤液,将全部馏分用于拮抗活性。这些级分之一显示出高控制茄形青枯菌的能力(命名为Biocine)。通过SDS聚丙烯酰胺凝胶电泳确定纯化的Biocine的分子量,该分子量揭示出一条分子量为29kDa的条带。差异显示用于研究Biocine调节基因。切下分子量为800bp的条带,使用TOPO TA克隆试剂盒克隆。使用EcoR1限制酶释放该片段,并将其亚克隆到原核表达载体(Ptrac A)中。使用IPTG诱导重组细菌,并基于His-tag技术获得纯化的蛋白质。与纯化的重组蛋白相比,对它进行了生物测定,显示了相同的活性。可以得出结论,可以在半工业规模上生产大量生物素。将实验从实验室转移到野外的方法正在研究中

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