A special organophosphorus decomposing bacterium yp8 for tea trees and preparation method thereof
A technology of organophosphorus and decomposing bacteria, which is applied in the fields of biochemical equipment and methods, organic fertilizers, chemical instruments and methods, etc., and can solve the problems of low absorption of crops and accumulation of phosphorus elements.
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Embodiment 1
[0014] Embodiment 1, take the separation and identification of special organophosphate-decomposing bacteria for tea trees as an example
[0015] The inventors of the present invention collected soil samples from tea gardens in Shandong, placed them in sterile bags for low-temperature preservation, and brought them back to the laboratory for preservation at 4°C. Using organic phosphorus medium (glucose 10g, (NH 4 ) 2 SO 4 0.5g, NaCl 0.3g, KCl 0.3g, FeSO 4 ·7H 2 O0.03g, MgSO 4 ·7H 2 O 0.3g, MnSO 4 4H 2 O 0.03g, CaCO 3 5g, appropriate amount of lecithin, dilute to 1000mL, adjust the pH to 7.0-7.5) Screen the target strain from the soil. Combining traditional morphological, physiological and biochemical characteristics with PCR-based modern technology, the cultured strains were classified and identified, and finally an organophosphate-decomposing bacterium was screened out.
[0016] After morphological observation (such as figure 1 ), it was found that the colony of t...
Embodiment 2
[0020] Embodiment 2, prepare a kind of special organophosphorus decomposing bacteria bacterial agent of tea tree
[0021] (1) Preparation of solid composite carrier: mix wheat bran, peat, and diatomaceous earth in a mass percentage of 70%: 20%: 10%, then add distilled water (distilled water) of 1.5 times the total volume of wheat bran, peat, and diatomite pH=7), the solid composite carrier was obtained after high temperature sterilization at 120°C;
[0022] (2) Preparation of bacterial liquid seeds: first pick Pseudomonas putida YP8 and inoculate it into 100mL LB liquid medium (tryptone 10g, yeast extract 5g, sodium chloride 10g), and culture at 30°C with shaking, Cultivate until the OD value of the bacterial solution = 0.5. Then, the culture solution and the LB liquid medium that reached OD value = 0.5 were mixed according to the volume ratio of 1:25, and cultured with shaking at 30° C. for 24 hours to obtain the liquid seeds of the strain.
[0023] (3) inoculate the liquid...
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