Application of mycotoxin biodegradation agent to promotion of healthy pig production
A technology of biodegradation agent and mycotoxins, applied in the biological field, can solve the problems of unbalanced flora and damage to animals caused by mycotoxins, and achieve the effect of increasing daily weight gain
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Embodiment 1
[0045] 1. Test materials and methods
[0046]1.1 Experimental animal grouping and feeding management: The experimental location is a farm in Xinxiang, Henan. According to the principles of the same breed, similar parity, and similar body weight, 150 weaned “Du × Chang × Da” three-way hybrid piglets with an average weight of 11.03 kg were selected. They were randomly divided into 5 groups, with 3 repetitions in each group, 10 heads / replication, half male and half female, and each repetition was reared in a single pen. The feeding experiment was carried out for 60 days.
[0047] 1.2 Preparation of mycotoxin biodegradants
[0048] In the examples of the present invention, Lactobacillus (CGMCC1.2884), Bacillus subtilis (CGMCC1.0504) and Candida utilis (CGMCC2.0615) Aspergillus oryzae strains (preservation number CGMCC3.4437) were all purchased from China Microorganisms Culture Collection Management Committee General Microbiology Center.
[0049] Preparation of compound probiot...
Embodiment 2
[0081] 1 Test materials and methods
[0082] 1.1 Test material: The test sample comes from the liver tissue of piglets fed for 60 days, three repetitions in the three groups of A group (control group), D (AFB1+ZEA group) and E (AFB1+ZEA+mycotoxin biodegradant group) In each repeated slaughtering of a piglet, the liver was taken from the same position, and the blood on the tissue was rinsed with pre-cooled PBS, then quickly stored in liquid nitrogen, and then transferred to -80°C for independent data collection (Data-independent Acquisition, DIA) proteomic analysis.
[0083] 1.2 Protein extraction: all 9 sample proteins were extracted by cold acetone method, the samples were ground into powder in liquid nitrogen, and then dissolved in 2 mL lysate (7M urea, 2% SDS, 0.1% PMSF (Roche Ltd.Basel, Switzerland) , 65mMDTT), followed by ultrasonic homogenization on ice, 3min / time, a total of 3 times. Centrifuge at 15,000 rpm for 15 min at 4°C, and transfer the supernatant to a new EP ...
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