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首页> 外文期刊>BMC research notes >Generation of Trichoderma atroviride mutants with constitutively activated G protein signaling by using geneticin resistance as selection marker
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Generation of Trichoderma atroviride mutants with constitutively activated G protein signaling by using geneticin resistance as selection marker

机译:以遗传霉素抗性为选择标记的具有组成型激活的G蛋白信号转导的木霉属阿troviride突变体的产生

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Background Species of the fungal genus Trichoderma are important industrial producers of cellulases and hemicellulases, but also widely used as biocontrol agents (BCAs) in agriculture. In the latter function Trichoderma species stimulate plant growth, induce plant defense and directly antagonize plant pathogenic fungi through their mycoparasitic capabilities. The recent release of the genome sequences of four mycoparasitic Trichoderma species now forms the basis for large-scale genetic manipulations of these important BCAs. Thus far, only a limited number of dominant selection markers, including Hygromycin B resistance ( hph ) and the acetamidase-encoding amdS gene, have been available for transformation of Trichoderma spp. For more extensive functional genomics studies the utilization of additional dominant markers will be essential. Results We established the Escherichia coli neomycin phosphotransferase II-encoding nptII gene as a novel selectable marker for the transformation of Trichoderma atroviride conferring geneticin resistance. The nptII marker cassette was stably integrated into the fungal genome and transformants exhibited unaltered phenotypes compared to the wild-type. Co-transformation of T. atroviride with nptII and a constitutively activated version of the Gα subunit-encoding tga3 gene ( tga3 Q207L ) resulted in a high number of mitotically stable, geneticin-resistant transformants. Further analyses revealed a co-transformation frequency of 68% with 15 transformants having additionally integrated tga3 Q207L into their genome. Constitutive activation of the Tga3-mediated signaling pathway resulted in increased vegetative growth and an enhanced ability to antagonize plant pathogenic host fungi. Conclusion The neomycin phosphotransferase II-encoding nptII gene from Escherichia coli proved to be a valuable tool for conferring geneticin resistance to the filamentous fungus T. atroviride thereby contributing to an enhanced genetic tractability of these important BCAs.
机译:背景技术真菌木霉属的物种是纤维素酶和半纤维素酶的重要工业生产者,但也广泛用作农业的生物防治剂(BCA)。在后一种功能中,木霉菌种通过其真菌寄生能力刺激植物生长,诱导植物防御并直接拮抗植物病原真菌。四种真菌寄生木霉属物种的基因组序列的最新发布现在构成了对这些重要BCA进行大规模遗传操作的基础。迄今为止,只有有限数量的显性选择标记,包括潮霉素B抗性(hph)和编码乙酰胺酶的amdS基因,可用于木霉属菌种的转化。对于更广泛的功能基因组学研究,必须使用其他显性标记。结果我们建立了大肠杆菌新霉素磷酸转移酶II编码的nptII基因,作为转化赋予遗传霉素抗性的木霉阿troviride的新型选择标记。 nptII标记盒被稳定整合到真菌基因组中,与野生型相比,转化体表现出未改变的表型。阿特罗韦韦氏菌与nptII和编码Gα亚基的tga3基因(tga3 Q207L )的组成型激活形式的共转化导致大量有丝分裂稳定,抗遗传霉素的转化子。进一步的分析显示,与15个转化子的共转化频率为68%,这些转化子已将tga3 Q207L 进一步整合到了他们的基因组中。 Tga3介导的信号通路的组成性激活导致营养生长增加,并增强对抗植物病原宿主真菌的能力。结论来自大肠杆菌的编码新霉素磷酸转移酶II的nptII基因被证明是赋予对丝状真菌Atroviride遗传霉素抗性的有价值的工具,从而有助于增强这些重要BCA的遗传易处理性。

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