Lactobacillus rhamnosus with ochratoxin A removing effect
A technology of Lactobacillus rhamnosus and ochratoxin, applied in the field of microorganisms, can solve the problems of limited clearance, low effect, and rarely used food juice, etc., and achieve the effect of wide application prospects and good tolerance
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Embodiment 1
[0030] Example 1: Drawing of the removal efficiency map of ochratoxin A degraded by Lactobacillus rhamnosus CCTCC M 2022013 at different pH.
[0031] 100 μL of activated L. rhamnosus Bm01 strain was inoculated into 5 mL of fresh MRS liquid medium (pH 3, 4, 5, 6 and 7) containing 50 ng / mL ochratoxin A. A medium containing only 50 ng / mL ochratoxin A was used as a control. Each group of samples was cultured in a 37°C incubator for 72 hours before sampling. After the samples were filtered through a 0.22 μm filter membrane, the content of ochratoxin A was determined by high performance liquid chromatography. Three replicates were set for each treatment, and the experiment was repeated twice.
Embodiment 2
[0032] Example 2: Drawing of the removal efficiency diagram of ochratoxin A degraded by Lactobacillus rhamnosus CCTCC M 2022013 at different temperatures.
[0033] 100 μL of activated L. rhamnosus Bm01 strain was inoculated into 5 mL of fresh MRS liquid medium containing 50 nμg / mL ochratoxin A. A medium containing only 50 ng / mL ochratoxin A was used as a control. Each group was cultured in an incubator at 15°C, 25°C and 37°C, respectively, and samples were taken at 0h, 24h, 48h, and 72h. After the samples were filtered through a 0.22 μm filter membrane, the content of patulin was determined by high performance liquid chromatography. Three replicates were set for each treatment, and the experiment was repeated twice.
Embodiment 3
[0034] Example 3: The scavenging effect of Lactobacillus rhamnosus CCTCC M 2022013 on ochratoxin A at different times.
[0035] The activated L. rhamnosus Bm01 strain was inoculated into fresh medium with 2% inoculum amount, and ochratoxin A standard was added to a final concentration of 50 ng / mL, and cultured in a 37°C incubator. Samples were taken at 0 h, 24 h, 48 h, and 72 h. After the samples were filtered through a 0.22 μm filter membrane, the content of ochratoxin A was determined by high performance liquid chromatography. Three replicates were set for each treatment, and the experiment was repeated twice.
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