Application of cyclic dipeptide cyclo-(S)-pro-(S)-phe to prevention and control of bacterial wilt and/or rice blast
A cyclic dipeptide and bacterial wilt technology, which is applied in the field of plant disease prevention and control, can solve the problems of destroying ecological balance, polluting the environment, and pathogenic bacteria producing drug resistance, and achieves the effect of simple steps, simple operation, and obvious inhibitory effect
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Embodiment 1
[0034] 1. Strain and culture medium
[0035] Escherichia coli (Escherichia coli) GZ-34, whose preservation number is CCTCC NO:M 2016353, was preserved in the Chinese Type Culture Collection Center located in Wuhan University, Wuhan, China on June 27, 2016, and has applied for a patent in China CN 105969707 A discloses.
[0036] Ralstonia solanacearum GMI1000, purchased from ATCC.
[0037] LB solid medium: tryptone 10g, yeast extract 5g, NaCl 10g, agar 15g, H 2 Dilute to 1000ml with O, pH 7.0-7.2. Sterilize at 121°C for 20 minutes.
[0038] LB liquid medium: The only difference from LB solid medium is that it does not contain agar.
[0039] Preparation of TTC solid medium: tryptone 10g, acid hydrolyzed casein 1g, glucose 5g, agar 15g, H 2 Dilute O to 1000ml, pH 6.8-7.2; sterilize at 121°C for 20 minutes to obtain basic medium. TTC (2,3,5-triphenyltetrazolium chloride) was made into a 0.1% (w / v) solution with distilled water and sterilized by filtration with a bacterial fil...
Embodiment 2
[0061] Embodiment 2: the antibacterial activity assay of cyclic dipeptide
[0062] 1. Medium
[0063] TTC culture medium: same as embodiment 1.
[0064] TTC liquid culture medium: with embodiment 1.
[0065] Rice bran medium: rice bran 20g, yeast extract 2g, agar 11g, H 2 Dilute O to 1000ml, pH 6.8-7.2. Sterilize at 121°C for 20 minutes.
[0066] 2. Experimental steps
[0067] 2.1 Culture medium preparation
[0068] Same as example 1.
[0069] 2.2 Activation of strains
[0070] Same as example 1.
[0071] 2.3 Activity detection
[0072] Pick a single colony of R. solanacearum and inoculate it in 10mL of TTC liquid medium, and culture it with shaking at 220r / min at 28°C for one day, then add 0.1mL of R. solanacearum liquid to 10mL of melted TTC solid medium (cool to about 45°C ) into a flat plate, and after solidification, use a sterile puncher (8 mm in diameter) to punch holes in the center of the plate containing bacteria, one hole per plate, take out the bacterial b...
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