Biological Agents and Methods for Controlling Banana Fusarium Wilt
A technology for banana fusarium wilt and banana fusarium wilt, applied in botany equipment and methods, biocides, chemicals for biological control, etc., can solve the unclear development and regulation mechanism of banana fusarium wilt, and restrict the molecular resistance of banana fusarium wilt Problems such as the development of breeding work to achieve good results and the effect of inhibiting development
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Embodiment 1
[0040] So far, there is no effective method for the prevention and control of Fusarium wilt of banana. One important reason is that the pathogen has strong resistance. The early development of fungal spores is an important development process in its life history, and it is also the most critical link for its colonization on host plants. Most fungicides that have effective control effects on plant fungal diseases are aimed at the germination and early stages of fungal spores. of the developmental process. In view of this, the present invention identifies and verifies for the first time the key proteins and important metabolic pathways of the early development of Banana Fusarium wilt Tropical Race 4, and the research results can be used for the development of new fungicides and the induction of gene silencing in host plants to cultivate new disease-resistant species qualitative target sites.
[0041] 1. The present invention uses the latest quantitative proteomics method based ...
Embodiment 2
[0082] Application of embodiment 2 in cultivating resistant banana fusarium wilt transgenic banana new lines:
[0083] (1) Construction and genetic transformation of Foc TR4ERG6 and Foc TR4ERG11 double-stranded RNA overexpression vectors
[0084] The backbone of the overexpression vector is the pYL-RNAi vector (gifted by Liu Yaoguang, a researcher at the School of Life Sciences, South China Agricultural University), based on which the Foc TR4ERG6 and Foc TR4ERG11 double-stranded RNA overexpression vectors pYL-Ubi-ERG6 and pYL-Ubi-ERG11 were constructed.
[0085]The construction steps of the pYL-Ubi-ERG6 overexpression vector are as follows: select specific fragments from the two coding genes (SEQ ID NO.1 and 2) of the Foc TR4 ERG6 protein, and artificially synthesize the tandem fragments. The sequence of the tandem fragments is shown in SEQ ID NO As shown in .6, connect to the multiple cloning site 1 on the pYL-RNAi vector, then reversely connect the artificially synthesized t...
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