Freshwater fish compound preservative as well as preparation method and application thereof
A technology for composite preservation of freshwater fish, applied in biochemical equipment and methods, bacteria used in food preparation, applications, etc., can solve the problem of high residual amount of chemical preservatives, achieve enhanced antiseptic effect, wide antibacterial spectrum, and extend shelf life period effect
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example 1
[0030] Example 1 is a blank reference, is a sample of sterile water treatment, example 2 is the treatment group of antibacterial lipopeptide crude extract, and example 3, 4 and 5 are antibacterial lipopeptide crude extract, bacteriocin crude extract and thymol Treatment group for a mixture of three preservatives.
Embodiment 1
[0031] Embodiment 1 (blank reference)
[0032] Treatment A: Knock the head of fresh and live crucian carp to death, remove the head, tail and viscera, rinse with sterile water for 15-20 seconds, and drain in an environment below 10°C;
[0033] Treatment B: Grass carp slices, cut into 20g / piece, length 9cm, width 4cm, thickness 0.5cm grass carp fillets, washed with sterile water for 15-20S, and drained in an environment below 10°C.
[0034] Place the above-mentioned pretreated freshwater fish body in sterile water, and immerse all the fish body in the sterile water for 15 minutes. Drain the soaked fish in an environment below 10°C, place them in sterile trays, and store them at 4°C.
Embodiment 2
[0035] Embodiment 2 (contrast)
[0036] Preparation of antimicrobial lipopeptide crude extract: Bacillus amyloliquefaciens ES-2-4 was inoculated on test tube slant PAD agar medium (potato (peeled) 200g, glucose 20g, agar 15-20g, distilled water 1000ml, natural pH), 37°C Cultivate the activated strains in the incubator for 24 hours, and then inoculate the activated strains in the BPY medium containing the seed medium (5g beef extract, 5g yeast extract, 5g sodium chloride, 10g fish powder peptone, 10g glucose, 1000mL water. In a Erlenmeyer flask sterilized at 115° C. for 20 minutes), culture at 37° C. and 180 rpm for 24 hours to make a seed solution. The seed liquid was inoculated in Landy fermentation medium (glucose 42.0g, sodium glutamate 14.0g, MgSO 4 ·7H 2 O0.5g, KCl 0.5g, KH 2 PO 4 1g, FeSO 4 ·7H 2 O 0.15mg, MnSO 4 ·7H 2 O 5mg, CuSO 4 ·5H 2O 0.16mg, water 1000mL. 115°C autoclave for 20min), ferment at 33°C and 180rpm for 36h, take out, centrifuge at 9000rpm for...
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