Method for rapidly detecting bacterial canker of tomatoes and special primer for method
A technology for tomato canker and pathogens, applied in the field of rapid detection of tomato canker pathogens, can solve the problems that threaten tomato yield, quality fruit resistance, economic loss, etc.
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Embodiment 1
[0019] Embodiment 1, the acquisition of tomato canker bacterium template DNA
[0020] The tomato canker bacterium was cultivated in the modified 523 medium, shaken at 25°C for 3 days, collected the bacteria, added 100 μL of sterile water, heated at 95°C for 10 min, and centrifuged at 1000 r / min for 5 min to make a template.
Embodiment 2
[0021] Embodiment 2, tomato canker bacterium LAMP amplification and detection
[0022] The reaction system is: 2 μL template DNA in 25 μL total system, 0.4 mol / L Betaine betaine, MgSO 4 2.0 mmol / L, 4 U of Bst DNA polymerase, 1.0 mmol / L of dNTPs, 1.5 μL each of primer 1 and primer 2, 0.5 μL each of primer 3 and primer 4, 1×Isothermal Amplification Buffer.
[0023] The reaction program was as follows: incubation at 65°C for 40 min, inactivation at 80°C for 20 min.
[0024] The detection method is: take 5 μL LAMP amplification products and use 1.5% agarose gel electrophoresis to detect the amplification results (see figure 1 ).
[0025] Dilute SYBR Green I dye with 10×TBE, add it to the remaining amplification product at a ratio of 1 / 100, and observe the color change (see figure 2 ).
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[0026] figure 1 It is the result of 1.5% agarose gel electrophoresis detection of the LAMP amplification product of P. tomato canker.
[0027] figure 2 It is...
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