Zhong Yao Hua, Wang Xiao Li, Wang Tian Hong, Jiang Qiao
State Key Laboratory of Microbial Technology, Shandong University, Jinan, 250100, Shandong, People's Republic of China.
Appl Microbiol Biotechnol. 2007 Jan;73(6):1348-54. doi: 10.1007/s00253-006-0603-3. Epub 2006 Oct 5.
Filamentous fungus Trichoderma reesei QM9414 was successfully transformed with Agrobacterium tumefaciens AGL-1 for random integration of transforming DNA (T-DNA). Co-cultivation of T. reesei conidia or protoplasts with A. tumefaciens in the presence of acetosyringone resulted in the formation of hygromycin B-resistant fungal colonies with high transformation frequency. Nine randomly selected resistant clones were proved to be stable through mitotic cell division. The integration of the hph gene into T. reesei genome was determined by PCR and dot blot analysis. Transgenic T. reesei strains were analyzed using TAIL-PCR for their T-DNA contents. The results showed that T-DNA inserts occurred evidently by fusing DNA at T-DNA borders via random recombination, which suggests that Agrobacterium-mediated transformation is a potentially powerful tool towards tagged mutagenesis and gene transfer technology for T. reesei.
丝状真菌里氏木霉QM9414通过根癌农杆菌AGL-1成功转化,用于转化DNA(T-DNA)的随机整合。在乙酰丁香酮存在的情况下,里氏木霉分生孢子或原生质体与根癌农杆菌共培养,产生了具有高转化频率的潮霉素B抗性真菌菌落。通过有丝分裂细胞分裂证明,随机选择的9个抗性克隆是稳定的。通过PCR和斑点杂交分析确定了hph基因整合到里氏木霉基因组中。使用热不对称交错PCR(TAIL-PCR)分析转基因里氏木霉菌株的T-DNA含量。结果表明,T-DNA插入明显是通过随机重组在T-DNA边界处融合DNA发生的,这表明农杆菌介导的转化是一种用于里氏木霉标记诱变和基因转移技术的潜在强大工具。