A strain of Burkholderia latta pn1 and its application
A technology of Holderia and cocci, which is applied in the direction of application, bacteria, and fungicides, can solve the problems of endophytic bacteria in moso bamboo that have not been reported for disease resistance and growth promotion, and that there are few endophytic bacteria in moso bamboo, so as to achieve excellent strain resources and strong The ability to secrete IAA and the effect of significant antibacterial activity
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Embodiment 1
[0025] Example 1: Isolation and identification of endophytic bacteria PN1 from Phyllostachys pubescens
[0026] The three- to four-year-old moso bamboos with good growth were selected from the moso bamboo plantations in Dagang Forest Farm, Guanshan Forest Farm and Jinggangshan Dajing Forest Farm in Yichun City, Jiangxi Province, respectively. The topsoil was removed, and the root system of Moso bamboo was dug out with a shovel to collect the fine roots of Moso bamboo. Rinse the root system of moso bamboo with distilled water for 3 times, and carry out surface disinfection according to the following steps: soak in 75% v / v alcohol for 1 min, soak in 3.25% v / v sodium hypochlorite for 3 min, soak in 75% v / v alcohol for 30 seconds, and then rinse with sterile water for 3 times . Grind the treated root tissue and collect the grinding liquid. Coat the NA plate with the sterile water after the last rinse (recipe of NA medium: beef extract 3g, peptone 10g, NaCl 5g, agar 16g, distilled...
Embodiment 2
[0033] Embodiment 2: Bacterial strain PN1 antagonizes the pathogenic bacteria of Phyllostachys pubescens blight
[0034] Use a puncher (diameter=5mm) to get the bacteria cake at the edge of the colony of the pathogenic bacteria C.phyllostachydis (C.phyllostachydis) of Phyllostachys pubescens for 5 days, connect it to the center of the PDA plate, and mark the bacterial strain to be tested activated with the NA slope The line was inoculated on both sides of the PDA plate, and only the pathogenic bacteria were inoculated as the control (CK), and each treatment was replicated three times. Incubate at 28°C for 4 days to observe the presence or absence of the inhibition zone, and measure the width of the inhibition zone.
[0035] Inoculate the Burkholderia latta PN1 with better bacteriostasis in the plate confrontation test on NB medium (the formula of NB medium: beef extract 3g, peptone 10g, NaCl 5g, distilled water 1000mL, pH 7.2, after mixing evenly ready to sterilize). 150mL sha...
Embodiment 3
[0039] Embodiment 3: Determination test of bacterial strain PN1 phosphorus-dissolving ability
[0040] Burkholderia latta PN1 was inoculated on NBRIP solid medium (glucose 10g, Ca 3 (PO 4 ) 2 5g, MgCl 2 5g, KCl 0.2g, MgSO 4 .7H 2 O 0.25g, (NH 4 ) 2 SO 4 0.1g, distilled water 1000mL, agar 15g, mix uniformly and sterilize to obtain), cultivate for 4 days and observe whether phosphorus-dissolving circles are produced. Quantitative determination of the phosphorus-solubilizing capacity of Burkholderia latta PN1 was performed using the method of Pikovskaya et al. After shaking and culturing Burkholderia latta PN1 in NB medium for 24 hours, inoculate it into a 100mL Erlenmeyer flask containing 50mL of NBRIP culture solution at an inoculation amount of 1% v / v, and connect the same volume of blank seed solution. NBRIP culture solution (without strains) was used as the control. Each inoculation treatment was repeated five times, 30°C, 180r / min shaking culture for 6 days, the...
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