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首页> 外文期刊>BMC Microbiology >Development of a transformation system for Aspergillus sojae based on the Agrobacterium tumefaciens-mediated approach
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Development of a transformation system for Aspergillus sojae based on the Agrobacterium tumefaciens-mediated approach

机译:基于根癌土壤杆菌介导方法的大豆曲霉转化体系的开发

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Background Aspergillus sojae has been an important filamentous fungus in Biotechnology due to its use in diverse fermentative processes for the production of various food products. Furthermore, this fungus is a common expression system for the production of enzymes and other metabolites. The availability of molecular genetic tools to explore its biology is thus of big interest. In this study, an Agrobacterium tumefaciens-mediated transformation (ATMT) system for A. sojae was developed and its applicability evaluated. Results The donor plasmid named pRM-eGFP was constructed for ATMT of A. sojae. This plasmid contains the ble and egfp genes in its transfer DNA element (T-DNA) to confer phleomycin resistance and express the enhanced green fluorescent protein (EGFP) in A. sojae, respectively. Agrobacterium tumefaciens (LBA4404) harboring the donor plasmid and A. sojae (ATCC 20235) were co-cultured under diverse conditions to achieve ATMT. The maximum number of transformed fungi was obtained after three days of co-culturing at 28°C, and selection with 50?μg/ml phleomycin. Polymerase chain reaction (PCR), fluorescence microscopy and Western Blot analysis for EGFP expression confirmed successful genomic integration of the T-DNA element in A. sojae. The T-DNA was mitotically stable in approximately 40% of the fungal transformants after four generations of sub-culturing under phleomycin pressure. Conclusion We successfully established a new ATMT protocol for A. sojae. This transformation system should enable further protein expression studies on this filamentous fungus.
机译:背景技术大豆曲霉因其在用于生产各种食品的各种发酵过程中的使用而一直是生物技术中重要的丝状真菌。此外,这种真菌是用于产生酶和其他代谢产物的常见表达系统。因此,探索其生物学的分子遗传学工具备受关注。在这项研究中,大豆根癌农杆菌介导的转化(ATMT)系统被开发并评估了其适用性。结果构建了供体质粒pRM-eGFP。该质粒在其转移DNA元件(T-DNA)中包含ble和egfp基因,分别赋予抗磷脂酶并在大豆曲霉中表达增强的绿色荧光蛋白(EGFP)。将携带供体质粒的根癌农杆菌(LBA4404)和大豆曲霉(ATCC 20235)在不同条件下共培养以实现ATMT。在28°C共培养三天后,用50μg/ ml phleomycin进行筛选,获得了最大数量的转化真菌。聚合酶链反应(PCR),荧光显微镜和Western Blot分析用于EGFP表达证实了大豆曲霉中T-DNA元件的成功基因组整合。在phleomycin压力下进行四代传代培养后,T-DNA在约40%的真菌转化子中有丝分裂稳定。结论我们成功建立了针对大豆油曲霉的新ATMT协议。该转化系统应能够对该丝状真菌进行进一步的蛋白表达研究。

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