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首页> 外文期刊>Mycobiology >An Enzymolysis-Assisted Agrobacterium tumefaciens-Mediated Transformation Method for the Yeast-Like Cells of Tremella fuciformis
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An Enzymolysis-Assisted Agrobacterium tumefaciens-Mediated Transformation Method for the Yeast-Like Cells of Tremella fuciformis

机译:一种酶促农杆菌介导的转化方法,用于烟曲菌的酵母样细胞

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Agrobacterium tumefaciens -mediated transformation (ATMT), as a simple and versatile method, achieves successful transformation in the yeast-like cells (YLCs) of Tremella fuciformis with lower efficiency. Establishment of a more efficient transformation system of YLCs is important for functional genomics research and biotechnological application. In this study, an enzymolysis-assisted ATMT method was developed. The degradation degree of YLCs depends on the concentration and digestion time of Lywallzyme. Lower concentration (≤0.1%) of Lywallzyme was capable of formation of limited wounds on the surface of YLCs and has less influence on their growth. In addition, there is no significant difference of YLCs growth among groups treated with 0.1% Lywallzyme for different time. The binary vector pGEH under the control of T. fuciformis glyceraldehyde-3-phosphate dehydrogenase gene ( gpd ) promoter was utilized to transform the enzymolytic wounded YLCs with different concentrations and digestion time. The results of PCR, Southern blot, quantitative real-time PCR (qRT-PCR) and fluorescence microscopy revealed that the T-DNA was integrated into the YLCs genome, suggesting an efficient enzymolysis-assisted ATMT method of YLCs was established. The highest transformation frequency reached 1200 transformants per 10sup6/sup YLCs by 0.05% (w/v) Lywallzyme digestion for 15?min, and the transformants were genetically stable. Compared with the mechanical wounding methods, enzymolytic wounding is thought to be a tender, safer and more effective method.
机译:根癌农杆菌介导的转化(ATMT),作为一种简单而通用的方法,以较低的效率成功地在烟曲菌的酵母样细胞(YLC)中成功转化。建立更有效的YLC转化系统对于功能基因组学研究和生物技术应用至关重要。在这项研究中,开发了一种酶解辅助的ATMT方法。 YLCs的降解程度取决于Lywallzyme的浓度和消化时间。较低浓度(≤0.1%)的Lywallzyme能够在YLC表面形成有限的伤口,并且对其生长的影响较小。另外,在不同时间用0.1%Lywallzyme处理的组之间,YLCs的生长没有显着差异。利用烟曲霉甘油醛-3-磷酸脱氢酶基因(gpd)启动子控制下的二元载体pGEH转化了不同浓度和消化时间的酶解型YLCs。 PCR,Southern blot,定量实时荧光定量PCR(qRT-PCR)和荧光显微镜的结果表明,T-DNA已整合到YLCs基因组中,表明建立了一种有效的酶促水解YLCs ATMT方法。每10 6 个YLC的最高转化频率达到0.05%(w / v)的Lywallzyme消化15分钟,共1200个转化子,并且这些转化子具有遗传稳定性。与机械创伤方法相比,酶水解创伤被认为是一种温柔,安全,有效的方法。

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