Primers and method for detecting phytophthora capsici based on development of pectate lyase Pcpe l15 gene
A technology of Phytophthora capsici and primer pairs, which is applied in the field of primers for detection of Phytophthora capsici, can solve the problems of weak control effect, incapable of detection and early warning of pathogenic characteristics and occurrence trend of pathogenic bacteria, difficulty in controlling disease occurrence and prevalence, etc., to achieve The effect of blocking reproduction and spreading and reducing the cost of disease prevention and control
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Embodiment 1
[0028]Example 1. Acquisition of the primer pair pel15F-R for specific detection of Phytophthora capsici and its specificity and sensitivity
[0029] In this embodiment, Phytophthora capsici is used as the test material, and the Pcpel1-2 (GenBank number is respectively: FJ213434-5), Pcpel4 (GenBank number is: FJ213436), Pcpel9 ( GenBank number is: FJ213442), Pcpel11 (GenBank number is: FJ213444) and Pcpel15 (its nucleotide sequence is the sequence 3 in the sequence table) gene these 6 gene members in the difference of RNA transcript expression level in capsicum disease fruit, compare Related data information, Pcpel15 is defined as the target disease-causing gene, designs and synthesizes many pairs of specific primers of the Pcpel15 gene (sequence 3), tests the specificity of these primers to all the tested bacterial species and the sensitivity to the detection of Phytophthora capsici sex. A pair of primer pair pel15F-R with high specificity and sensitivity was selected from it...
Embodiment 2
[0111] Example 2, Pcpel15 gene-specific primer pair Pme6F-R detects different diseased tissues and diseased field soil DNA PCR
[0112] In this example, the detection effect of pel15F-R on the diseased field soil, diseased stems, diseased fruits and diseased leaves of Phytophthora capsici was tested. The specific method is as follows:
[0113] 1. DNA extraction
[0114] Transfer Phytophthora capsici SD33 to a V8 solid plate, and after culturing in the dark at 25°C for 2-3 days, take a colony piece (2 mm × 2 mm) from the edge of the colony by blowing air, and inoculate the wound on pepper (Zhongjiao No. 6) seedlings (7- 9 leaves) at the base of the stem, fruit, and micro-wounds of bacterial blocks of the same size were inoculated on pepper leaves, and then different diseased tissues were cut out, and diseased tissues were extracted with reference to the NaOH method of Wang et al. (Nucleic Acids Research, 1993, 21:4153-4154) DNA of DNA: Take a section of diseased stem, diseased...
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