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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:酶解辅助农杆菌催化术介导的Trowella Fucifordis的酵母状细胞的转化方法

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摘要

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 10(6) 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:土壤杆菌介导的转化(ATMT),作为一种简单而通用的方法,实现了效率较低的Imbella Fucifordis的酵母状细胞(YLC)的成功转化。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很重要。在该研究中,开发了一种酶解辅助的ATMT方法。 YLC的降解程度取决于Lywallzyme的浓度和消化时间。较低浓度(<= 0.1%)的溶液能够在YLC的表面上形成有限的伤口,对其生长的影响较小。此外,在不同时间对0.1%溶液治疗的基团中的YLC生长没有显着差异。用于控制T.Fucifordis甘油醛-3-磷酸脱氢酶基因(GPD)启动子的二元载体PGEH用于转化具有不同浓度和消化时间的酶解受伤的YLC。 PCR,Southern印迹,定量实时PCR(QRT-PCR)和荧光显微镜的结果表明,将T-DNA集成到YLC基因组中,建议建立了有效的酶解辅助ATMT方法。最高转化频率为每10(6)个YLC的1200个转化率为0.05%(w / v)溶液消化15分钟,转化体是遗传稳定的。与机械伤口方法相比,酶解伤口被认为是一种柔软,更安全和更有效的方法。

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