Method for quick screening and assessment of pesticide residues in tea
A technology for pesticide residues and tea, which is applied in the biosafety assessment and application field of carbamate pesticide residues in tea, and can solve the problems affecting the accuracy and precision, sensitivity and specificity of microorganisms, and the lack of screening for butyric acid bacteria Work strains and other problems, to achieve the detection method is simple and easy, high sensitivity, good specificity effect
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Embodiment 1
[0029] The screening of embodiment 1 sensitive strain
[0030] Isolation and identification of butyric acid bacteria WZ001, straight or curved bacillus, 0.6-1.2×3.0-7.0μm, round end, single, paired, short chain, and occasionally long filamentous bacteria. Movement with perinatal flagella, spores ovoid, eccentric to subterminal, without exine and appendage filaments. Gram-positive, becoming negative in older cultures; often amyloid-positive. The cell wall contains DH-diaminopimelic acid; glucose is the only cell wall sugar. Light microscopy findings were consistent with the morphology of Clostridium butyricum. According to the "Bergery Bacterial Identification Manual", it can be judged that the bacteria belong to Clostridium butyricum. Some sugars can be fermented to produce hydrogen and butyric acid. Visible colonies in the solid medium are milky white, round and slightly convex, with irregular edges, 1-3 mm in diameter, slightly shiny surface, and bubbles in the liquid me...
Embodiment 2
[0031] Example 2 Screening of Tea Methomyl Residues
[0032] (1) Screening medium preparation:
[0033] Peptone 10g, beef extract 10g, yeast extract 5g, glucose 20g, sodium acetate 5g, K 2 HPO 4 2g, MgSO 4 ·7H2 O0.5g, MnSO 4 4H 2 O 0.2g, fructooligosaccharide 3g, diammonium citrate 2g, Tween-80 1mL, agar 15g, distilled water 1L, heat and dissolve the above ingredients to correct pH 6.5, autoclave at 115°C for 15-20 minutes;
[0034] (2) Bacterial suspension preparation:
[0035] Butyric acid bacteria WZ001 was inoculated on the slant medium of nutrient agar, cultured anaerobically at 35±2°C for 24 hours, washed the bacterial lawn with sterilized physiological saline, made a suspension, and transmitted light at a wavelength of 580nm in a 721 spectrophotometer. The excess rate is controlled at 0.7, and stored in a refrigerator at 2-8°C;
[0036] (3) Bacteria culture medium preparation:
[0037] Take a plate with a diameter of about 90mm and a height of 16-17mm, inject 20...
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