Bacillus subtilis subsp. Deserticola strain and application thereof
A technology of Bacillus subtilis and Bacillus, applied in the direction of application, bacteria, fungicides, etc., can solve the problems of poor growth, death of the whole plant, economic loss, etc., to achieve large-scale production and popularization and application, short cultivation time, easy access to effects
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Embodiment 1
[0044] Bacillus subtilis subsp. desert ( Bacillus subtilis subsp. inaquosorum ) Acquisition, identification and preservation of CPBA-W01.
[0045] (1) Bacillus subtilis desert subspecies ( Bacillus subtilis subsp. inaquosorum ) Acquisition and identification of CPBA-W01.
[0046] Bacillus subtilis desert subspecies ( Bacillus subtilis subsp. inaquosorum ), which was isolated from the coral-like mycorrhiza of Panzhihua cycads. The samples were collected from the Cycad Nature Reserve in Panzhihua City, Sichuan Province, and stored at 4°C for later use.
[0047] Isolation of endophytic bacteria from coral mycorrhizal mycorrhizae of Cycas cycads by conventional tissue method: after washing the soil on the surface of coral mycorrhizae with distilled water, the coral root tissue was cut into 0.5 cm×0.5 cm tissue pieces, and sterilized with 75% alcohol for 1 min , and then sterilized with 0.1% mercury liter solution for 5 min, and finally rinsed with sterile water for 3 ...
Embodiment 2
[0056] Bacillus subtilis subsp. desert ( Bacillus subtilis subsp. inaquosorum ) Screening of CPBA-W01 strain.
[0057] (1) Screening of strains.
[0058] Preliminary screening of antagonistic bacteria was carried out by cross method. Concrete operation is as follows: with the root rot fungus of Molan ( Fusarium oxysporum ) as an indicator bacterium, inoculate a 6 mm agar block of pathogenic bacteria in the center of the improved PDA medium plate, and then inoculate a single colony of bacteria obtained by isolation and culture at an equidistant distance of 2.5 cm from the pathogenic bacteria, inoculate 4 strains per plate, and set 5 replicates After culturing at a constant temperature of 28°C for 3-5 days, observe the size of the inhibition zone and select the strain with the best antagonistic effect.
[0059] (2) Observation of results.
[0060] The isolated strains were screened by the criss-cross method, and the results showed that there were 3 strains with antagon...
Embodiment 3
[0062] Bacillus subtilis subsp. desert ( Bacillus subtilis subsp. inaquosorum ) Determination of the biocontrol effect of CPBA-W01 strain.
[0063] (1) Determination of biocontrol effect.
[0064] Perseverance culture method: with Molan root rot ( Fusarium oxysporum ) as the indicator bacteria, first use a 6 mm puncher to punch out the activated agar block of pathogenic bacteria, put it on the plate, and then inoculate the antagonistic bacteria by spot connection method, the distance between the two bacteria is 2.5 cm, the control group is only inoculated with the agar block of pathogenic bacteria, set 3 Repeatedly, cultured in a 28°C incubator for 3-5 days, observed the growth of pathogenic bacteria, measured the inhibition zone, calculated the inhibition rate, and finally screened out the antagonistic bacteria with the best antagonistic effect. The formula for calculating the bacteriostatic rate: bacteriostatic rate (%) = (control pathogen colony diameter - treatment p...
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