Method for determining antibacterial mechanism of zeolite molecular sieve antibacterial agent by high performance liquid chromatography
A technology of zeolite molecular sieve and antibacterial agent, which is applied in the biological field, can solve the problems of slow analysis of antibacterial mechanism and high material consumption, and achieve the effects of high sensitivity, simple operation, and less sample consumption
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Embodiment 1
[0021] Embodiment 1: zeolite molecular sieve antimicrobial agent is to escherichia coli bacteriostasis mechanism
[0022] (1) Amplification of Escherichia coli strains: Prepare 200 mL of liquid medium, adjust the pH to 7.0-7.2, and sterilize with high-pressure steam. Then inoculate the bacteria according to the amount of inoculating one ring per 100mL and shake well. Transfer to a shaking incubator at 37°C for 24 hours.
[0023] (2) Prepare zeolite molecular sieve antibacterial agent and potassium diformate solution with a concentration of 0mg / mL, 6mg / mL, 12mg / mL, 24mg / mL, 48mg / mL, 96mg / mL containing potassium diformate, each 3 Group.
[0024] (3) Expanded culture and antibacterial experiment: According to (2), after adding 3 blank control groups, a total of 21 100mL ordinary liquid culture media need to be prepared and sterilized. Then inoculate (1) bacterial suspension at 2 mL per bottle, add 100 mg of cefoxitin, transfer to a shaking incubator at 37°C for a total of 12 h...
Embodiment 2
[0029] Embodiment 2: zeolite molecular sieve antibacterial agent is to Staphylococcus aureus bacteriostasis mechanism
[0030] (1) Prepare potassium diformate solutions with concentrations of 0 mg / mL, 6 mg / mL, 12 mg / mL, 24 mg / mL, 48 mg / mL and 96 mg / mL, 3 groups for each.
[0031] (2) According to the number of groups in (1), add 3 blank control groups, prepare 100 mL of ordinary liquid medium each, and sterilize. Then add 2 mL of Staphylococcus aureus suspension in the logarithmic growth phase, and then add (1) 5 mL of antibacterial agent, mark it and transfer to 37°C for shaking culture for 18-24 hours. Take the Staphylococcus aureus suspension cultured for 24 hours and dilute it 100 times with liquid medium, continue shaking culture at 37°C for 12-18 hours, grow until the OD600 is about 3.6, take it out and centrifuge at 5000r / min for 15 minutes. Add 0.05mol / L pH 7.0 potassium phosphate buffer solution to the precipitate, and then sonicate (120W 15min). Centrifuge the bact...
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