Biological agent and method for preventing and controlling banana wilt
A technology for banana fusarium wilt and banana fusarium wilt is applied in the directions of botanical equipment and methods, biocides, chemicals for biological control, etc. The development of breeding work, etc., to achieve good results and inhibit the effect of 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 "Shotgun"-based quantitative proteomi...
Embodiment 2
[0082] Application of embodiment 2 in cultivating resistant banana fusarium wilt transgenic banana new lines:
[0083] (1) Construction and genetic transformation of FocTR4ERG6 and FocTR4ERG11 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), and on this basis, the FocTR4ERG6 and FocTR4ERG11 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 FocTR4ERG6 protein, and artificially synthesize the tandem fragments. The sequence of the tandem fragments is shown in SEQ ID NO.6 , connected to the multiple cloning site 1 of the pYL-RNAi vector, and then the artificially synthesized tandem fragment was reverse...
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