首页> 外文期刊>fresenius environmental bulletin >AGROINJECTION TECHNIQUE FORTRANSIENTGENE EXPRESSION AS RAPID AND HIGHLY EFFICIENT METHOD FOR POTATO AGROBACTERIUM-BASED TRANSFORMATION BY CRY1CA GENE
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AGROINJECTION TECHNIQUE FORTRANSIENTGENE EXPRESSION AS RAPID AND HIGHLY EFFICIENT METHOD FOR POTATO AGROBACTERIUM-BASED TRANSFORMATION BY CRY1CA GENE

机译:瞬时基因表达农业注射技术作为基于CRY1CA基因的马铃薯农杆菌转化的高效方法

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Potato is one of the major food crops and considered the fourth most important food crops worldwide.The insect and fungal infections are the significant constraints for potato production in the Arab countries,causing yield losses reaching more than 20.We have used and developed a rapid and low-cost transient transformation assay by using in-planta agroinfiltratoin in potato seeds slide,which transformation efficiency is higher than those of the conventional transient assays are.Polymerase chain reaction (PCR) was used to amplify a single copy of Bacillus thuringiensis Crystal Protein CrylCa (crylCa) gene from extracted DNA to screen for the presence or absence of this gene.Potato slices were agroinjected with plasmid pRI201-AN-GUS DNA for transient assay of P-glucuronidase gene (GUS).The transformation was performed using the disarmed A.tumefaciens strain LBA4404 harboring a binary vector pRI201-AN-GUS- CrylCa.Genetically modified potato plants were selected on kana-mycin-containing Murashige and Skoog medium (MS-media) and subcultured later to MS-media supplemented with 1.0 mg 1-1 6-Benzylaminopurine (BA) and 1.5 mg 1-1 -Naphthaleneacetic acid (NAA).A.tumefaciens strain LBA4404 carried out the plant binary vector pRI201-AN-GUS,and pRI201-AN-GUS-CrylCa were used for transient expression assay.The Synthetic CrylCa (crylCa) gene,under the control of a CaMV 35S and the caste,also contained P-glucuronidase (GUS) gene.Agroinjection is an efficient transient uidA expression assay for reporter gene and analysis of candidate genes in plants.The successful transformation of CrylCa gene potato plants will contribute to increasing yield and food security in the future.Finally we describe here a protocol for the genetic transformation of potato based on agroinjection using A.tumefaciens carrying a plasmid (pRI201-AN-GUS-CrylCa) expressing a reporter uidA gene in addition to describing transient expression evidence based on histological and molecular assays.Successful transformation of transgenic potato plants will contribute to increasing the yield and food security in Saudi Arabia in the near future.
机译:马铃薯是主要粮食作物之一,被认为是世界第四大粮食作物。虫害和真菌感染是阿拉伯国家马铃薯生产的重大制约因素,导致产量损失达到20%以上。我们采用并开发了一种快速、低成本的瞬时转化试验,在马铃薯种子玻片中使用植内农浸润曲素,其转化效率高于传统的瞬时试验。聚合酶链反应 (PCR) 用于从提取的 DNA 中扩增苏云金芽孢杆菌晶体蛋白 CrylCa (crylCa) 基因的单个拷贝,以筛选该基因的存在与否。马铃薯片农用注射质粒pRI201-AN-GUS DNA,用于P-葡萄糖醛酸酶基因(GUS)的瞬时测定。使用携带二元载体pRI201-AN-GUS-CrylCa的根癌不动杆菌菌株LBA4404进行转化,在含有假名霉素的Murashige和Skoog培养基(MS-培养基)上选择转基因马铃薯植株,然后传代培养到补充有1.0 mg 1-1 6-苄氨基嘌呤(BA)和1.5 mg 1-1-萘乙酸(NAA)的MS培养基中。根癌农株LBA4404采用植物二元载体pRI201-AN-GUS,采用pRI201-AN-GUS-CrylCa进行瞬时表达测定。合成CrylCa(crylCa)基因在CaMV 35S和种姓的控制下,还含有P-葡萄糖醛酸酶(GUS)基因。Agroinjection是一种高效的瞬时uidA表达测定方法,用于报告基因和植物候选基因的分析。CrylCa基因马铃薯植株的成功转化将有助于未来提高产量和粮食安全。最后,除了描述基于组织学和分子测定的瞬时表达证据外,我们还描述了一种基于农业注射的马铃薯遗传转化方案,该方案使用携带表达报告基因uidA基因的根癌杆菌(pRI201-AN-GUS-CrylCa)。转基因马铃薯植株的成功转化将有助于在不久的将来提高沙特阿拉伯的产量和粮食安全。

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