Primer composition for LAMP (loop-mediated isothermal amplification) rapid detection of pomegranate fusarium sulphureum and application of primer composition
A technology of pomegranate dry rot pathogen and primer composition, which is applied in the direction of recombinant DNA technology, microbial measurement/inspection, biochemical equipment and methods, etc., to achieve the effects of shortening detection time, improving efficiency, and strong specificity
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Embodiment 1
[0051] The design of embodiment 1 LAMP primer
[0052] Download the elongation factor 1-alpha gene (accession number: JQ281778) gene sequence of Pomegranate dry rot from GenBank, according to the gene sequence, use PrimerExplorer V4 software to design a kind of LAMP detection primer, including 2 outer primers (F3 and B3) and 2 internal primers (FIP and BIP), the primer sequences are:
[0053] F3: 5'-GGTCACCGTGACTTCATCAA-3';
[0054] B3: 5'-CCTTCCACTCAGCAGTGTC-3';
[0055] FIP: 5'-CACCAGTACCGGAGGCAATGATCATGATCACTGGTACCTCGC-3'; BIP: 5'-GCTGGTATCTCCAAGGATGGCCACGATGAGCTGCTTGACAC-3'.
[0056] All primers were synthesized at 1OD with ddH 2 After O was dissolved, it was aliquoted, and the final concentration of F3 and B3 was 10 μM, and the final concentration of FIP and BIP was 40 μM, and stored at 4°C for future use.
Embodiment 2
[0057] The establishment of embodiment 2 LAMP amplification system,
[0058] Use two pairs of specific primers to carry out constant temperature LAMP amplification of the genomic DNA of the fungus to be identified. The total volume of the LAMP reaction is 20 μL. The reaction system is:
[0059]
[0060]
[0061] Supplement the total volume of the amplification system to 20 μL with sterile double distilled water.
[0062] The reaction condition of LAMP amplification is: 65°C for 60min.
[0063] The chromogenic agent is SYBR Green I.
Embodiment 3
[0064] Example 3 Detection of LAMP Reaction Specificity of Pomegranate Dry Rot Pathogen
[0065] In this experiment, the pomegranate dry rot fungus and 22 other common crop pathogens were used as test materials (see Table 1). The genomic DNA of the pathogenic bacteria of crops was used as a template, and the reaction system established in Example 2 was used to perform LAMP amplification respectively. When the template was pomegranate dry rot bacteria, the electrophoresis pattern formed ladder-like bands; when the template was other common pathogenic bacteria of crops, there was no bands, indicating that the LAMP reaction has good specificity (see figure 1 ).
[0066] Table 1 is used for screening the bacterial strain of primer specificity in the present embodiment
[0067]
[0068]
[0069] In the above table: + indicates that there are LAMP primer amplification bands and color changes; - indicates no amplification bands and color changes.
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