A strain of Alcaligenes faecalis bxo-4 and its application
A technology of Alcaligenes faecalis, bxo-4, applied in the application, bacteria, chemicals for biological control, etc., can solve the problems of too conservative and passive control methods, scarce biocontrol bacteria resources, etc., and achieve good development and application. Prospects, low requirements for cultivation conditions, and small impact on the ecological environment
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Embodiment 1
[0025] LB medium formula: tryptone 10 g, yeast extract powder 5 g, NaCl 10 g, agar powder 15 g, dilute to 1000 mL, pH 7.2. The above materials are LB liquid medium without agar powder.
[0026] The inventor collected paddy field soil from Zhongkai University of Agricultural Engineering on October 15, 2012, and separated strains by conventional dilution and separation methods. The specific steps were as follows: take 100 g of paddy field soil, fully dilute it with distilled water, and take 100 μl of soil droplets into the Sheng On a 10ml LB plate, pour 15ml of LB medium cooled to about 50°C, and shake the soil solution thoroughly, and then incubate at 26°C for 3 days, select a single colony, and perform three streaking dilutions and separation to obtain a single The colonies are stored at 4°C.
[0027] The strain was cultured on LB medium for 48 hours and observed, its single colony was round, white, with a smooth surface, opaque, slightly raised, and neat edges without wrinkles. ...
Embodiment 2
[0029] Example 2 Antibacterial spectrum of Alcaligenes facecalis Bio-4 culture medium
[0030] Taking the pathogens of several crop bacterial diseases as objects, the antibacterial spectrum of Alcaligenes facecalisBio-4 strain was determined by the inhibition zone method. Bacterial strains (antagonistic antibacterial Alcaligenes facecalis Bio-4 and pathogenic bacteria Xanthomonas oryzae pv. oryzae, X. oryzae pv. oryzicola, Ralstonia solanacearum) were inoculated into LB medium and cultured with shaking at 28 ℃, 200 r / min for 48 h. The three pathogenic bacteria strains were spread on the LB plate, and a sterile round paper sheet with a diameter of 6 mm was placed in the center of the plate, and 10 μL of the antagonistic bacteria Bio-4 was added to the round paper sheet. With the addition of LB liquid medium as a control, each treatment was repeated 3 times, cultured in a 28 ℃ constant temperature incubator for 4 days, and the inhibition radius was measured.
[0031] Table 1 Inhibit...
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