An efficient genetic transformation system for Chinese medicine fungus Tolypocladium ophioglossoides

2020 ◽  
Vol 176 ◽  
pp. 106032
Author(s):  
Xin-ai Chen ◽  
Xian He ◽  
Min Zhang ◽  
Xu-ming Mao ◽  
Yong-quan Li
2019 ◽  
Author(s):  
Kai Zhang ◽  
Jianjie He ◽  
Lu Liu ◽  
Runda Xie ◽  
Lu Qiu ◽  
...  

Abstract Background Brassica napus is an important oilseed crop which offer a considerable amount for global vegetable oil production. The establishment of an efficient genetic transformation system with a convenient transgenic-positive screening method is of great importance for gene functional analysis and molecular breeding. However, to our knowledge, there are few such aforementioned systems available for efficient application in B. napus .Results Based on the well-established genetic transformation system in Brassica napus , five vectors companied with red fluorescence protein from Discosoma sp. ( DsRed ) were constructed and transformed via agrobacterium -mediated hypocotyl transformation. The average of 59.1% tissues were marked with red fluorescence by visual screening method in tissue culture medium, and 96.1% of which were amplified with the exogenous genes in eight different rapeseed varieties on average. In addition, the final transgenic-positive efficiency of the rooted plantlets was up to 90.7% from the red fluorescence marked tissues, which was much higher than that of the previous reports. Besides, DsRed also could be applicable to the seedlings, including of seed coats, roots, hypocotyls and cotyledons during seed germination. These results indicate that the high-efficiency genetic transformation system combining with the transgenic-positive visual screening method presented here will help us to efficiently and conveniently obtain transgenic-positive rapeseed plantlets.Conclusion A novel method was developed for rapidly, conveniently and high-efficiently obtaining the transgenic lines, which would help to obtain the higher proportion of transgenic positive regenerated plantlets, thereby avoiding the long period plant regeneration. This will benefit the gene functional study especially in high throughput molecular biology research.


2006 ◽  
Vol 52 (6) ◽  
pp. 469-472 ◽  
Author(s):  
Luiz Rodrigo I. Morioka ◽  
Márcia C. Furlaneto ◽  
Andréa C. Bogas ◽  
Patrícia Pompermayer ◽  
Rubens T. D. Duarte ◽  
...  

2013 ◽  
Vol 163 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Suo-Lian Guo ◽  
Xin-Qing Zhao ◽  
Ying Tang ◽  
Chun Wan ◽  
Md. Asraful Alam ◽  
...  

2021 ◽  
Vol 7 (2) ◽  
pp. 138
Author(s):  
Min Liang ◽  
Wei Li ◽  
Landa Qi ◽  
Guocan Chen ◽  
Lei Cai ◽  
...  

Fungi from unique environments exhibit special physiological characters and plenty of bioactive natural products. However, the recalcitrant genetics or poor transformation efficiencies prevent scientists from systematically studying molecular biological mechanisms and exploiting their metabolites. In this study, we targeted a guanophilic fungus Amphichorda guana LC5815 and developed a genetic transformation system. We firstly established an efficient protoplast preparing method by conditional optimization of sporulation and protoplast regeneration. The regeneration rate of the protoplast is up to about 34.6% with 0.8 M sucrose as the osmotic pressure stabilizer. To develop the genetic transformation, we used the polyethylene glycol-mediated protoplast transformation, and the testing gene AG04914 encoding a major facilitator superfamily transporter was deleted in strain LC5815, which proves the feasibility of this genetic manipulation system. Furthermore, a uridine/uracil auxotrophic strain was created by using a positive screening protocol with 5-fluoroorotic acid as a selective reagent. Finally, the genetic transformation system was successfully established in the guanophilic fungus strain LC5815, which lays the foundation for the molecular genetics research and will facilitate the exploitation of bioactive secondary metabolites in fungi.


2021 ◽  
Vol 289 ◽  
pp. 110429
Author(s):  
Xinhui Wang ◽  
Fengli Zhou ◽  
Jianlong Liu ◽  
Wenqian Liu ◽  
Shaoling Zhang ◽  
...  

2012 ◽  
Vol 78 (9) ◽  
pp. 3488-3491 ◽  
Author(s):  
Jinman Liu ◽  
Zhoujie Xie ◽  
Justin Merritt ◽  
Fengxia Qi

ABSTRACTWe have constructed the firstEscherichia coli-Veillonellashuttle vector based on an endogenous plasmid (pVJL1) isolated from a clinicalVeillonellastrain. A highly transformableVeillonellastrain was also identified. Both the shuttle vector and the transformable strain should be valuable tools for futureVeillonellagenetic studies.


2019 ◽  
Vol 10 ◽  
Author(s):  
Sudipta Shekhar Das Bhowmik ◽  
Alam Yen Cheng ◽  
Hao Long ◽  
Grace Zi Hao Tan ◽  
Thi My Linh Hoang ◽  
...  

1992 ◽  
Vol 56 (2) ◽  
pp. 228-232 ◽  
Author(s):  
Akihiro Hino ◽  
Chakamas Wongkhalaung ◽  
Shinya Kawai ◽  
Satoru Murao ◽  
Keiji Yano ◽  
...  

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