Application of food-grade microorganism in degradation of zearalenone
A zearalenone and microorganism technology, applied in the field of microorganisms, can solve the problems of low degradation rate, time-consuming and laborious organic solvents, high cost, and achieve the effects of high degradation efficiency, short degradation period and product safety.
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Embodiment 1
[0027] (1) Bacillus subtilis 168 and Bacillus natto CICC24640 were selected as the experimental strains, and appropriate medium and culture conditions were selected for inoculation and activation.
[0028] (2) Take 4 mL of corn oil, soybean oil, beer and milk, and add ZEN to make liquid food with a final concentration of ZEN of 0.5 μg / mL as the degradation matrix.
[0029] (3) Take Bacillus subtilis 168 and Bacillus natto CICC246403g respectively, and inactivate them by high-pressure steam (121°C, 20min). The inactivated Bacillus subtilis 168 and Bacillus natto CICC24640 were inoculated in the aforementioned strain degradation matrix. The samples were incubated under anaerobic conditions at 30°C for 1 h. The obtained suspension was centrifuged at 10000rpm, 4°C for 10min. The supernatant was collected and ZEN was extracted with a mixture of chloroform-methanol (9:1 v / v) for detection. The adsorption rates of ZEN in different liquid food matrices adsorbed by two kinds of inac...
Embodiment 2
[0035] (1) Bacillus subtilis 168 and Bacillus natto CICC24640 were selected as the experimental strains, and appropriate medium and culture conditions were selected for inoculation and activation.
[0036] (2) Soybean, flour and corn flour were selected as solid substrates, and the moisture content and pH value of the samples were adjusted to 30% and 7, respectively. The solid substrate was stirred to form a paste, followed by autoclaving at 121° C. for 20 minutes.
[0037] (3) Add ZEN to the sample base to make the final concentration 1mg / kg, and then inoculate 1mL of the overnight cultured strain (10 8 cfu / mL), all samples were performed in duplicate. The samples were incubated in a 37°C incubator after mixing. After 0h, 6h, 12h, 18h, 24h, 30h, 36h, 42h, and 48h, take out a certain amount and add chloroform-methanol (9:1, v / v) mixture to extract zearalenone, and use UPLC-DAD The ZEN in the sample is determined. Table 3 shows the degradation rates of ZEN in different soli...
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