PCR (polymerase chain reaction) detection primers for fusarium verticillioide, kit containing primers and application
A technology for detecting primers and kits, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc., and can solve the problems that there are no reports of specific primers for the detection of Verticillium pseudomonas, and achieve specificity. Good performance, easy operation and high sensitivity
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Embodiment 1
[0024] Embodiment 1 is used for detecting the synthesis of the specific PCR primer of Fusarium pseudoverticillium
[0025] Download the translation elongation factor (TEF-1α) gene sequence (KC599245.1) of F.verticillioides from the FusariumCenter'sdatabase at PennState database, and use DNAMAN and other biological software to analyze the F.verticillioides and other Fusarium The TEF-1α gene sequences of spore species were compared and analyzed, and several highly specific sites were found that only existed in Verticillium spp., and a series of primers for detecting F. spp. were designed by using the software Primer5. , from which the most specific and sensitive primers Pr40 / Pf40 (Table 1) were screened out, and on this basis a PCR system for detecting Fusarium pseudoverticillium was established.
[0026] Table 1 Information of Pr40 / Pf40 primers for specific PCR detection of Verticillium pseudomonas
[0027]
[0028] The primers were synthesized by Shanghai Yingjun Biotechno...
Embodiment 2
[0031] Example 2 Utilize PCR primers Pr40 / Pf40 to detect the specificity and sensitivity analysis of Fusarium pseudoverticillium
[0032] 1.1 Sample source:
[0033] Fusarium used in this example includes Fusarium pseudoverticillium, Fusarium incognita, Fusarium asiatica, Fusarium oxysporum complex, Fusarium fujikura, Fusarium laminarum, Fusarium equisetum, Fusarium yellow and Solanum Fusarium, etc., provided by the Institute of Crop Science, Chinese Academy of Agricultural Sciences.
[0034] 1.2 Fusarium genomic DNA extraction:
[0035]The isolates of different Fusarium species isolated from single spores were transferred to different PDA medium respectively, cultured at 25°C for 7 days, the mycelia were scraped and dried and placed in 2.0mL centrifuge tubes. DNA was extracted with the Fungal Genomic DNA Rapid Extraction Kit (Shanghai Sangong). The content and purity were double detected by agarose gel electrophoresis and UV-VISspectrophotometer Q5000 ultraviolet-visible s...
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