A kind of bacterial quorum sensing inhibitor and application thereof
A quorum sensing and inhibitor technology, applied in antibacterial drugs, organic chemistry, active ingredients of heterocyclic compounds, etc., can solve problems such as drugs that have not yet been seen, and achieve the effect of preventing disease infection and reducing swarm movement.
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Embodiment 1
[0019] Example 1: Purification and structural identification of psoralen and bergamot lactone in Chinese medicine fig leaves
[0020] Preparation method of methanol crude extract: Weigh 1g of raw materials and add 50ml of methanol solution for extraction, ultrasonic for 30 minutes, and then place on a shaker for 48 hours to shake and extract. Filtrate and filter residue were obtained by filtration. The slag was extracted twice with 20 ml of methanol solvent according to the above method to obtain a total of 3 filtrates, which were combined and concentrated in vacuo to obtain a crude extract.
[0021] Separation and purification of the compound: After the above-mentioned crude extract was mixed with an appropriate amount of silica gel H, it was separated by a vacuum silica gel column chromatography, using different proportions of eluent petroleum ether, petroleum ether: dichloromethane (1:5), Petroleum ether: dichloromethane (1:1), dichloromethane, dichloromethane: methanol (1...
Embodiment 2
[0028] Example 2: Analysis of compounds psoralen and bergamotide inhibiting QS activity of Chromobacter violaceum
[0029] Violet bacteria screening model and its method: overnight cultured Chromobacter violaceum CV026 was diluted to OD with LB liquid medium 600nm = 0.1, 10ml per bottle; add 20μl of different concentrations of compounds psoralen and bergamotide, 50μl of signal molecules and 20μl of kanamycin, respectively, put them in a shaker at 28°C and 160rmp for 18h; DMSO solvent as a blank control. After the cultivation, centrifuge at 6000rmp for 10min, suck out the supernatant, redissolve it with 1ml DMSO, and centrifuge again (6000rmp, 10min), pour the supernatant into the marked centrifuge tubes, and take 200μl supernatant in turn Add it to a 96-well microplate and measure the absorbance A at 585nm with a microplate reader 585 , to characterize the production of purple pigment of Chromobacterium violaceum; for the precipitate obtained by the second centrifugation, ad...
Embodiment 3
[0031] Example 3: Analysis of compounds psoralen and bergamot lactone inhibiting Pseudomonas aeruginosa swarming activity
[0032] Screening method for swarming: Take 14.8ml of hot melted swarming soft agar medium (glucose 10g; agar powder 5g; peptone 5g; yeast extract powder 2g; dissolve in 1L deionized water, sterilize at 121°C for 20min), After cooling to about 30°C, 200 μl of psoralen and bergamot lactone compound were added thereto, with final concentrations of 40 μg / ml and 160 μg / ml, respectively. Pour it into a flat plate, and after solidification, punch holes with a puncher, and put 2 μl of overnight cultured Pseudomonas aeruginosa PA01 (OD 600nm =0.1) Bacterial solution was added to the wells, incubated at a constant temperature of 37°C for 24 hours, and the phenomenon was observed.
[0033] Experimental results: 40 μg / ml psoralen and 160 μg / ml bergamot lactone can significantly inhibit the cluster movement of Pseudomonas aeruginosa PA01 ( image 3 ), indicating tha...
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