首页> 外文期刊>Journal of applied microbiology >Homologous expression of a mutated beta-tubulin gene does not confer benomyl resistance on Trichoderma virens
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Homologous expression of a mutated beta-tubulin gene does not confer benomyl resistance on Trichoderma virens

机译:突变的β-微管蛋白基因的同源表达不会赋予木霉菌苯菌灵抗性

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Aims: To clone the beta-tubulins and to induce resistance to benzimidazoles in the biocontrol fungus Trichoderma virens through site-directed mutagenesis. Methods and Results: Two beta-tubulin genes have been cloned using PCR amplification followed by the screening of a T. virens cDNA library. The full-length cDNA clones, coding for 445 and 446 amino acids, have been designated as T. virens tub1 and T. virens tub2. A sequence alignment of these two tubulins with tubulins from other filamentous fungi has shown the presence of some unique amino acid sequences not found in those positions in other beta-tubulins. Constitutive expression of the tub2 gene with a histidine to tyrosine substitution at position 6 (known to impart benomyl/methyl benzimadazol-2-yl carbamate resistance in other fungi), under the Pgpd promoter of Aspergillus nidulans, did not impart resistance to benomyl. Conclusions: The homologous expression of tub2 gene with a histidine to tyrosine mutation at position +6, which is known to impart benomyl tolerance in other fungi, does not impart resistance in T. virens. Significance and Impact of the Study: Unlike other Trichoderma spp., T. virens, has been difficult to mutate for benomyl tolerance. The present study, through site-directed mutagenesis, shows that a mutation known to impart benomyl tolerance in T. viride and other fungi does not impart resistance in this fungus. Understanding the mechanisms of this phenomenon will have a profound impact in plant-disease management, as many plant pathogenic fungi develop resistance to this group of fungicides forcing its withdrawal after a short period of use.
机译:目的:通过定点诱变来克隆生物控制真菌木霉中的β-微管蛋白并诱导对苯并咪唑的抗性。方法和结果:使用PCR扩增方法克隆了两个β-微管蛋白基因,然后筛选了T. virens cDNA文库。编码445和446个氨基酸的全长cDNA克隆被命名为T. virens tub1和T. virens tub2。这两种微管蛋白与来自其他丝状真菌的微管蛋白的序列比对表明,存在一些独特的氨基酸序列,这些氨基酸序列在其他β-微管蛋白的那些位置中找不到。在构巢曲霉的Pgpd启动子下,在第6位具有组氨酸对酪氨酸取代的组氨酸的组成型表达(已知在其他真菌中赋予苯菌灵/甲基苯并咪唑-2-基氨基甲酸酯抗性)不赋予对​​苯菌灵的抗性。结论:tub2基因在+6位具有组氨酸至酪氨酸突变的同源表达,已知在其他真菌中具有苯菌灵耐受性,而在T. virens中不具有抗性。研究的意义和影响:不同于其他木霉属物种,T。virens很难突变为苯菌灵耐受性。本研究通过定点诱变显示,已知在紫薇和其他真菌中赋予苯菌灵耐受性的突变不会在这种真菌中产生抗性。了解这种现象的机理将对植物疾病的管理产生深远的影响,因为许多植物病原真菌对这组杀菌剂产生抗药性,迫使其在短时间使用后被迫撤出。

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