Preparation detection method of biofilm
A detection method, biofilm technology, applied in biochemical equipment and methods, microbial determination/inspection, sustainable biological treatment, etc., can solve problems such as no clear method
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Embodiment 1
[0017] (1) Cleaning and sterilization of ceramsite: rinse ceramsite with water to remove dust and impurities, then place it in ultrasonic cleaning for 10 minutes, and sterilize at 121°C for 20 minutes.
[0018] (2) Cultivate microorganisms: add 200mL of liquid culture medium to a 500mL Erlenmeyer flask, inoculate the strain P.aeruginosaE1 cultivated to the logarithmic phase into the culture medium, and vibrate in a constant temperature shaker at 30°C with a rotation speed of 180rpm. After about 16 hours, the strain enters the mid-logarithmic growth phase, and the flask is taken out.
[0019] (3) Ceramsite film-hanging: add 100g of ceramsite after cleaning and sterilization into the conical flask treated in (2) on the ultra-clean bench, and then put the conical flask back into the shaker. , let the bacteria grow on the ceramsite.
[0020] (4) Biofilm detection: After the ceramsite was cultured in the culture medium for 6 hours, 6 medium-sized ceramsites were taken from the Erl...
Embodiment 2
[0022] (1) Cleaning and sterilization of ceramsite: rinse ceramsite with water to remove dust and impurities, then place it in ultrasonic cleaning for 10 minutes, and sterilize at 121°C for 20 minutes.
[0023] (2) Cultivate microorganisms: Add 150-200mL of liquid culture medium to a 500mL Erlenmeyer flask, inoculate the sulfate-reducing bacteria K4 cultivated to the logarithmic phase into the culture medium, and place them in a constant temperature shaker at 32°C and a speed of 180rpm Shake the culture, and the strain enters the middle logarithmic growth phase in about 18 hours, and the Erlenmeyer shaker flask is taken out.
[0024] (3) Ceramsite film-hanging: add 100g of ceramsite after cleaning and sterilization to the triangular difference treated in (2) on the ultra-clean bench, and then put the triangular flask back into the shaker, the culture condition is 32°C, the rotation speed is 100rmp , let the bacteria grow on the ceramsite.
[0025] (4) Biofilm detection: After...
Embodiment 3
[0027] (1) Cleaning and sterilization of ceramsite: wash ceramsite with water three times to remove dust and impurities, then place it in ultrasonic cleaning for 10 minutes, and sterilize at 121°C for 20 minutes.
[0028] (2) Cultivate microorganisms: add 150-200mL of liquid culture medium to a 500mL Erlenmeyer flask, inoculate the strain P.aeruginosa D2 cultivated to the logarithmic phase into the culture medium, and inoculate it in a constant temperature shaker at 30°C and a speed of 180rpm Shake the culture, and the strain enters the middle logarithmic growth phase in about 16 hours, and the Erlenmeyer shaker flask is taken out.
[0029] (3) Ceramsite film: add 100g of ceramsite after cleaning and sterilization into the triangular flask treated in (2) on the ultra-clean bench, then put the triangular flask back into the shaker, the culture condition is 30°C, the rotation speed is 100rmp , let the bacteria grow on the ceramsite.
[0030] (4) Biofilm detection: After the cer...
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