Method for identifying waste oil by using Caenorhabditis elegans dormancy as biological marker
A technology of Caenorhabditis elegans and biomarkers, applied in biochemical equipment and methods, microbe measurement/inspection, etc., can solve the problems of complex operation, poor accuracy, low sensitivity, etc., and achieve convenient experimental operation and low cost , the effect of low experimental conditions
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specific Embodiment approach 1
[0007] Embodiment 1: This embodiment is a method for using Caenorhabditis elegans dormancy as a biomarker to identify waste oil, specifically as follows:
[0008] 1. Prepare medium: use NaCl, agar powder, peptone, 0.8mol / L~1.2mol / L CaCl 2 Aqueous solution, 0.8mol / L~1.2mol / L MgSO 4 Aqueous solution, phosphate buffer solution and distilled water are mixed evenly to obtain a culture medium, sealed and placed in a high-pressure steam sterilizer, and sterilized at 120°C for 15min to 25min, then cooled to 50°C to 60°C, and sterilized Add the edible oil to be tested under the environment, then transfer it to a petri dish, and finally dry it in a sterile environment at a temperature of 20°C for 8h to 12h to obtain a culture medium; Into the concentration of 1 × 10 9 pcs / mL~2×10 9 pcs / mL Escherichia coli OP50 bacterial liquid, then cultured at 37°C for 8h-12h, and then cultured for 46h with the inoculated Caenorhabditis elegans larvae. After 24h of culture, the Caenorhabditis elegan...
specific Embodiment approach 2
[0013] Specific embodiment two: the difference between this embodiment and specific embodiment one is: the phosphate buffer described in step one is made of KH 2 PO 4 , KOH and distilled water, KH in phosphate buffer 2 PO 4 The concentration is 1.36×10 -3 g / mL, the concentration of KOH is 0.18×10 -3 g / mL, and the pH of the phosphate buffer is 6.0. Others are the same as in the first embodiment.
[0014] Adopt following test to verify effect of the present invention:
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