New burkholderia cenocepacia and application thereof
A technology of Burkholderia and onion, which is applied in the field of bacterial strains and antagonistic bacteria, can solve the problems of declining medicinal quality, weakened leaf photosynthesis, and inability to normally expand underground fibrous roots, and achieves good effects and strong cellulose. The effect of degradability
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Embodiment 1
[0022] Example 1 Screening and identification of antagonistic bacteria Burkholderia cepacia (Burkholderiacenocepacia) CJ-P8
[0023] 1. Screening of antagonistic bacteria Burkholderia cepacia (Burkholderiacenocepacia CJ-P8)
[0024] The antagonistic bacteria Burkholderia cepacia (Burkholderiacenocepacia CJ-P8) described in the present invention is screened from the rhizosphere soil of Pseudostellaria heterophylla.
[0025] 1.1LB medium preparation
[0026] Weigh 5g of LB dry powder (Haibo Biotechnology Co., Ltd., China) and 3g of agar powder (BIOSHARP, Japan), heat to dissolve with deionized water and dilute to 200mL. Autoclave at 115°C for 20 minutes, add natamycin (fungal antibiotic) when the temperature of the culture medium drops to about 55°C (touchable by hand) to prevent antibiotics from becoming ineffective due to high temperature, shake well and pour the plate quickly.
[0027] 1.2 Rhizosphere soil bacterial culture
[0028] Weigh 10g of heterophylla rhizosphere so...
Embodiment 2
[0037] Antibacterial effect detection of embodiment 2 antagonistic bacteria
[0038] Using PDA medium, inoculate activated Burkholderia cenocepacia CJ-P8 at a distance of 2.5 cm from the center of the circle, place it in a constant temperature incubator at 28°C for 48 hours in the dark, and inoculate each A variety of pathogenic fungi (Fusarium oxysporum specialized in heterophylla and Fusarium moniliforme, Fusarium oxysporum specialized in Rehmannia glutinosa) were cultured in a constant temperature incubator at 28°C in the dark for several days, and the formation of the inhibition zone was observed in real time . After culturing for 5 days, it was found that Burkholderia cepacia (Burkholderiacenocepacia CJ-P8) could effectively antagonize the mycelial growth of Pseudostellariae-specific Fusarium oxysporum, Moniliforme and Rehmannia-specific Fusarium oxysporum (such as image 3 shown).
Embodiment 3
[0039] Example 3 Optimization of the optimum medium for Burkholderia cepacia (Burkholderiacenocepacia CJ-P8)
[0040] Prepare the following medium to optimize the optimal growth medium of Burkholderia cenocepacia CJ-P8, the medium is as follows: 1) full LB solution; 2) 1 / 4LB solution; 3) 1 / 4LB+1 / 20MS; 4) 1 / 4LB+1 / 40MS; 5) 1 / 4LB+1 / 80MS; 6) 1 / 4LB+1 / 20MS+0.1wt.% brown sugar; 7) 1 / 4LB+1 / 40MS+0.1wt .% brown sugar; 8) 1 / 4LB+1 / 80MS+0.1wt.% brown sugar.
[0041] Among them, the formula of MS medium (no iron salts) is: 1) macroelements: 1900mg / LKNO 3 , 1650mg / LNH 4 NO 3 , 370mg / LMgSO 4 ·7H 2 O. 170mg / LKH 2 PO 4 , 440mg / LCaCl 2 2H 2 O; 2) Trace elements: 22.3mg / LMnSO 4 4H 2 O, 8.6mg / LZnSO 4 ·7H 2 O, 6.2mg / LH 3 BO 3 , 0.83mg / LKI, 0.25mg / LNa 2 MoO 4 ·7H 2 O, 0.025mg / LCuSO 4 ·5H 2 O, 0.025mg / LCoCl, 2.6mg / LH 2 O; 3) Organic matter: 2.0mg / L glycine, 0.5mg / L pyridoxine hydrochloride, 0.1mg / L ammonium sulfate hydrochloride, 0.5mg / L niacin, 100mg / L creatine; LB medium formu...
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