Devosia sp and application thereof in degrading vomitoxin
A DeVosella technology is applied to a strain of DeVosella and its application field of degrading vomitoxin to achieve the effects of solving the problem of toxin pollution, degrading safety, and low production and use costs
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Embodiment 1
[0027] Example 1 Devosia sp. (Devosia sp.) DDB001 acquisition and identification
[0028]Soil samples were collected from a wheat field in Nanyang, Henan, and a 96-microwell plate was used as a culture carrier. First, a bacterial suspension capable of degrading vomitoxin was obtained through six consecutive toxin concentration gradient enrichment culture methods, and then the bacterial suspension was diluted by Coating method Spread on TY agar plate (yeast extract 4g / L, tryptone 8g / L, agar powder 15g / L, pH 7.2, sterilize at 121°C for 30min) with appropriate dilution, pick the degree of separation Colonies with good colony shape and different colors were detoxified in TY liquid medium (yeast extract 4g / L, tryptone 8g / L, pH7.2, sterilized at 121°C for 30min) with a DON concentration of 200μg / mL In the experiment, ethyl acetate extracted the residual toxin and carried out HPLC detection to verify the toxin degradation effect of each pure culture, and finally successfully obtained...
Embodiment 2
[0037] Example 2 Detoxification effect of Devosia sp. DDB001 in TY medium
[0038] The activated DDB001 was inoculated into 50 mL of TY liquid medium containing 200 μg / mL vomitoxin at an inoculation amount of 1%, and detoxified for two days under shaking conditions of 200 rpm, and extracted with ethyl acetate Residual deoxynivalenol, the residual content of deoxynivalenol in the final culture was detected by HPLC: the deoxynivalenol in TY was completely degraded, with a degradation rate of 100%, and toxin metabolites with a retention time of about 9 minutes (such as image 3 shown).
Embodiment 3
[0039] Example 3 Preparation of Devosia sp. DDB001 liquid bacterial agent
[0040] Solid medium components and proportions: yeast extract 0.8%, peptone 0.4%, NaCl 0.5%, agar powder 1.5%, pH7.2–7.4, high temperature steam sterilization at 121°C for 30min.
[0041] Components and proportions of seed medium: yeast extract 0.8%, peptone 0.4%, glucose 0.2%, sodium chloride 0.5%, pH7.2–7.4; fermentation medium components and proportions: yeast extract 0.8%, peptone 0.4 %, Glucose 0.2%, NaCl 0.5%, K 2 HPO 4 ·3H 2 O0.3%, KH 2 PO 4 0.075g / L, pH7.2–7.4.
[0042] (1) Strain activation: Inoculate De Vosella DDB001 with the preservation number CGMCC No.7185 on a solid medium, culture it at 30°C for 3 days, measure its toxin degradation performance, and then inoculate it on the inclined surface of the test tube on standby.
[0043] (2) Seed culture: Pick a single colony from the slant medium and insert it into the seed medium, and cultivate it to the logarithmic phase at 30°C to obta...
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