Pseudomonas brassicacearum Y1, culture method and application thereof, and soil conditioner
A technology of Pseudomonas rapeseed and Pseudomonas, which is applied in the field of agricultural microorganisms and can solve the problems of easy failure, pollution, and large amount of application
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Embodiment 1
[0048] Example 1 Screening to obtain Pseudomonas rape Y1
[0049] The screening process of Pseudomonas rapeseed Y1 is as follows:
[0050] (1) Retrieve soil samples from the wild walnut tree in Tekes County, Ili Kazak Autonomous Prefecture, Xinjiang, screen Pseudomonas rape Y1 according to the screening medium and conditions of Pseudomonas rape Y1, and isolate and purify, and finally obtain pure strains;
[0051] The screening medium is Ashby medium, the components are as follows: glucose 1%, KH 2 PO 4 0.02%, CaCO 3 0.5%, MgSO 4 ·7H 2 O 0.02%, NaCl 0.02%, CaSO 4 2H 2 O 0.01%, agar 2%, pH 7.0
[0052] Screening conditions: culture at 28°C for 7 days; observe through a microscope to determine whether it is a pure strain, and use the plate streak method to obtain pure strains;
[0053] (2) Prepare the suspension of Pseudomonas rape Y1 strain
[0054] Pick a single colony of the strain and insert it into a simple medium, the components of which are as follows: LB medium...
Embodiment 2
[0121] Example 2 Determination of Pseudomonas rape Y1 inhibiting pathogenic fungi
[0122] Two-point confrontation method: inoculate pathogenic fungi and isolated growth-promoting bacteria on two points 2 cm away from the center on the rye sucrose medium or PDA medium plate [inoculate Phytophthora infestans (Phytophthorainfestans) on rye medium] ; Inoculate Fusarium oxysporum (Fusarium oxysporum) and Sclerotinia (Sclerotinia sclerotiorum) respectively on the PDA medium]. Each treatment was repeated 3 times, and the plate inoculated with pathogenic fungi but not isolated growth-promoting bacteria was used as a control. Culture in dark at 18°C (Phytophthora infestans) or 25°C (Fusarium oxysporum, Sclerotinia sclerotiorum), observe the antibacterial effect after 7 days and calculate the antibacterial rate. Bacterial inhibition rate (%)=(control colony radius-treated colony radius) / control colony radius×100.
[0123] Result: if figure 1 Shown, in the inhibition test of potato...
Embodiment 3
[0128] The culture method of Pseudomonas brassicacearum Y1 (Pseudomonas brassicacearum Y1), comprises the steps:
[0129] (1) Pseudomonas rape Y1 was inoculated into a slant culture medium, activated and cultivated at a temperature of 25-30° C. for 10-16 hours to obtain an activated strain.
[0130] The composition of the slant medium is as follows: tryptone 1%, yeast extract 0.5%, NaCl 1%, agar 2%, pH 7.0.
[0131] (2) Inoculate the activated bacterial strain prepared in step (1) in a primary seed medium, and cultivate it for 10 to 16 hours at a temperature of 25 to 30° C. and a rotating speed of 160 to 240 r / min to obtain a seed solution;
[0132] Primary seed medium: starch starch 0.05%, glucose 0.05%, yeast extract 0.05%, peptone 0.05%, (NH 4 ) 2 SO 4 0.05%, K 2 HPO 4 0.03%, MgSO 4 ·7H 2 O 0.005%, pH 7.0.
[0133] (3) inoculate the seed solution prepared in step (2) in the secondary seed medium, the inoculum amount is 8-12% (volume percentage), and cultivate under ...
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