首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Cotransformation of Trichoderma harzianum with β-Glucuronidase and Green Fluorescent Protein Genes Provides a Useful Tool for Monitoring Fungal Growth and Activity in Natural Soils
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Cotransformation of Trichoderma harzianum with β-Glucuronidase and Green Fluorescent Protein Genes Provides a Useful Tool for Monitoring Fungal Growth and Activity in Natural Soils

机译:哈茨木霉与β-葡萄糖醛酸苷酶和绿色荧光蛋白基因的共转化为监测天然土壤中真菌的生长和活性提供了有用的工具

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摘要

Trichoderma harzianum was cotransformed with genes encoding green fluorescent protein (GFP), β-glucuronidase (GUS), and hygromycin B (hygB) resistance, using polyethylene glycol-mediated transformation. One cotransformant (ThzID1-M3) was mitotically stable for 6 months despite successive subculturing without selection pressure. ThzID1-M3 morphology was similar to that of the wild type; however, the mycelial growth rate on agar was reduced. ThzID1-M3 was formed into calcium alginate pellets and placed onto buried glass slides in a nonsterile soil, and its ability to grow, sporulate, and colonize sclerotia of Sclerotinia sclerotiorum was compared with that of the wild-type strain. Wild-type and transformant strains both colonized sclerotia at levels above those of indigenous Trichoderma spp. in untreated controls. There were no significant differences in colonization levels between wild-type and cotransformant strains; however, the presence of the GFP and GUS marker genes permitted differentiation of introduced Trichoderma from indigenous strains. GFP activity was a useful tool for nondestructive monitoring of the hyphal growth of the transformant in a natural soil. The green color of cotransformant hyphae was clearly visible with a UV epifluorescence microscope, while indigenous fungi in the same samples were barely visible. Green-fluorescing conidiophores and conidia were observed within the first 3 days of incubation in soil, and this was followed by the formation of terminal and intercalary chlamydospores and subsequent disintegration of older hyphal segments. Addition of 5-bromo-4-chloro-3-indolyl-β-d-glucuronic acid (X-Gluc) substrate to recovered glass slides confirmed the activity of GUS as well as GFP in soil. Our results suggest that cotransformation with GFP and GUS can provide a valuable tool for the detection and monitoring of specific strains of T. harzianum released into the soil.
机译:使用聚乙二醇介导的转化,将哈茨木霉与编码绿色荧光蛋白(GFP),β-葡萄糖醛酸苷酶(GUS)和潮霉素B(hygB)抗性的基因共转化。尽管没有选择压力的连续传代培养,但一种共转化子(ThzID1-M3)在有丝分裂中稳定了6个月。 ThzID1-M3形态与野生型相似。但是,琼脂上的菌丝生长速率降低了。将ThzID1-M3制成藻酸钙小球,并置于非无菌土壤中的埋入玻璃载玻片上,并将其与核型菌核盘菌菌核的生长,发芽和定植能力与野生型菌核菌核的能力进行了比较。野生型和转化株均以高于本地木霉属菌种的水平定居菌核。在未经处理的对照中。野生型和共转化菌株之间的定殖水平没有显着差异。然而,GFP和GUS标记基因的存在使得引入的木霉与本地菌株的分化成为可能。 GFP活性是用于非破坏性监测天然土壤中转化体菌丝生长的有用工具。共转化菌丝的绿色在紫外线落射荧光显微镜下清晰可见,而在同一样品中的原生真菌几乎看不见。在土壤中孵育的前三天内观察到绿色荧光的分生孢子和分生孢子,随后形成末端和inter间的衣原体孢子,随后分解较旧的菌丝节段。将5-溴-4-氯-3-吲哚基-β-d-葡萄糖醛酸(X-Gluc)底物添加到回收的载玻片中,证实了土壤中GUS和GFP的活性。我们的结果表明,GFP和GUS的共转化可以为检测和监测释放到土壤中的哈茨木霉的特定菌株提供有价值的工具。

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