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A Comparison of the Phenotypic and Genetic Stability of Recombinant Trichoderma spp. Generated by Protoplast- and Agrobacterium-Mediated Transformation

机译:重组木霉属植物表型和遗传稳定性的比较。由原生质体和农杆菌介导的转化产生

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摘要

Four different Trichoderma strains, T. harzianum CECT 2413, T. asperellum T53, T. atroviride T11 and T. longibrachiatum T52, which represent three of the four sections contained in this genus, were transformed by two different techniques: a protocol based on the isolation of protoplasts and a protocol based on Agrobacterium-mediated transformation. Both methods were set up using hygromycin B or phleomycin resistance as the selection markers. Using these techniques, we obtained phenotypically stable transformants of these four different strains. The highest transformation efficiencies were obtained with the T. longibrachiatum T52 strain: 65-70 transformants/μg DNA when transformed with the plasmid pAN7-1 (hygromycin B resistance) and 280 transformants/107 spores when the Agrobacterium-mediated transformation was performed with the plasmid pUR5750 (hygromycin B resistance). Overall, the genetic analysis of the transformants showed that some of the strains integrated and maintained the transforming DNA in their genome throughout the entire transformation and selection process. In other cases, the integrated DNA was lost.
机译:四种不同的木霉菌株,哈茨木霉CECT 2413,曲霉木霉T53,阿特罗韦德T.T11和长曲霉T52,代表了该属四个部分中的三个,通过两种不同的技术进行了转化:基于原生质体的分离和基于农杆菌介导的转化的协议。两种方法均以潮霉素B或ph霉素抗性为选择标记。使用这些技术,我们获得了这四个不同菌株的表型稳定的转化体。用长毛拟杆菌T52菌株获得最高的转化效率:用质粒pAN7-1(潮霉素B抗性)转化时为65-70个转化子/μgDNA,当用农杆菌介导的转化时为280个转化子/ 107孢子。质粒pUR5750(潮霉素B抗性)。总体而言,对转化体的遗传分析表明,在整个转化和选择过程中,有些菌株在其基因组中整合并维持了转化DNA。在其他情况下,整合的DNA丢失了。

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