Film coating liquid containing aspergillus flavus antagonistic bacteria and preparation method and application thereof
A technology of antagonistic bacteria and coating liquid, which is applied in the field of coating liquid containing antagonistic bacteria of Aspergillus flavus, can solve the problems of reduced efficacy, short duration of effect, contamination of Aspergillus flavus, etc., and achieve the effect of improving prevention
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Embodiment 1
[0029] The preparation of embodiment 1 aspergillus flavus antagonistic bacteria spore
[0030] Aspergillus niger spores: Aspergillus niger AS3.3928 (purchased from Shanghai Beinuo Biotechnology Co., Ltd.) was inoculated on Czapek's agar medium, cultured at 28°C for 5 days, and then the spores on the medium were dipped with cotton swabs in a sterile In 0.1% Tween-80, use an oscillator to oscillate evenly, and then use a hemocytometer to count and adjust its concentration to 10 10 A / mL spare.
Embodiment 2
[0031] The preparation of embodiment 2 Aspergillus flavus antagonistic bacteria extract
[0032] Using Aspergillus flavus antagonistic bacteria Aspergillus niger AS3.3928, Bacillus subtilis, and Saccharomyces cerevisiae as strains, fermented liquid was obtained through seed culture, expanded culture and fermentation production, wherein the number of effective viable bacteria in the fermented liquid was greater than 10 9 cfu / mL;
[0033] Centrifuge the above 400mL fermentation broth, discard the supernatant, and collect the bacteria; wash several times with sterile water, and finally collect the bacteria by centrifugation; add 40mL sterile PBS solution to the bacteria, mix well; add PMSF to the bacteria (1:500 scale). Place in an ultrasonic breaker to crush the bacteria with a power of 70%, break for 3s, stop for 5s, and 7min; centrifuge the broken bacteria at 10,000r / min for 20min, dissolve them with methanol, filter them with suction, and evaporate them to dryness by rotary ...
Embodiment 3
[0034] The inhibitory action of embodiment 3 antagonistic bacteria extracts to Aspergillus flavus
[0035] Sterilize the peanut meal by high-pressure steam, after cooling, divide it into 6 groups, each group has 3 parallels, and each parallel is 50g; add sterilized water to it, and make its water content reach 50%; add Aspergillus flavus to it Spore (ATCC 28539, purchased from Beijing Bei Nachuanglian Biotechnology Research Institute), the addition amount is 10 7 each / 50g; antagonistic bacteria extracts were added to the above six groups, and the added amounts were 0%, 0.05%, 0.1%, 0.3%, 0.5% and 1.0%. After mixing evenly, ferment at 30°C for 72 hours, stirring and keeping moist during the test; after the test, the total amount of Aspergillus flavus is determined as follows: figure 1 shown.
[0036] Depend on figure 1 It can be seen that the number of Aspergillus flavus in peanut meal without adding antagonistic bacteria extract increased slightly, and the number of Aspergi...
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