Active strain for inhibiting drug-resistant food-borne pathogenic bacteria and application thereof
A technology of food-borne pathogenic bacteria and pathogenic bacteria, applied in the field of microbiology, can solve problems such as damage to human health, impact on food quality, food preservative effect and safety doubts, and achieve broad-spectrum antibacterial activity and strong antibacterial activity effect of effect
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Embodiment 1
[0036] Example 1, 16S rDNA sequence analysis and phylogenetic tree construction of Pseudomonas fluorescens S-541
[0037]In the present invention, an active bacterial strain is isolated from vegetable garden soil in Baiyun District, Guangzhou City, Guangdong Province as a strain to be tested, and DNA is extracted from the active bacterial strain.
[0038] Extraction of the total DNA of the strain: Scrape an appropriate amount of the strain to be tested from the NA slant medium preserved at low temperature (4°C) in the laboratory, inoculate it in 100ml liquid medium, cultivate it at 28°C for 72 hours, and then use bacterial genome DNA extraction reagent Kit (BIOMIGA Company, USA) was used to extract genomic DNA, and the operation steps were carried out according to the instructions of the kit. The obtained genome was electrophoresed with 0.8% agarose, and the extraction effect was detected on a gel imager and used for genome sequencing.
Embodiment 2
[0042] Embodiment 2, the antibacterial activity assay of Pseudomonas fluorescens (Pseudomonas fluorescens) S-541 fermentation supernatant
[0043] 1) Obtaining the fermentation supernatant of Pseudomonas fluorescens S-541:
[0044] Pseudomonas fluorescens S-541 preserved on NA agar slant was inoculated into NB liquid medium for activation, and cultured at 37° C. on a shaker at 160 r / min for 24 hours. An appropriate amount of activated Pseudomonas fluorescens (Pseudomonas fluorescens) S-541 was inoculated in 100 mL of MH liquid medium according to the inoculum size of 10%, cultured at 37° C. on a shaking table at 160 r / min for 72 h. The cultured strain fermentation liquid was centrifuged at 8000 r / min at 4° C. for 10 min to obtain the fermentation supernatant.
[0045] 2) Antibacterial activity test of Pseudomonas fluorescens (Pseudomonas fluorescens) S-541 fermentation supernatant:
[0046] Take food-borne pathogenic bacteria and corresponding drug-resistant strains as indic...
Embodiment 3
[0052] Example 3, Pseudomonas fluorescens (Pseudomonas fluorescens) active product extraction, isolation and identification of S-541
[0053] Cultivate Pseudomonas fluorescens S-541 with MH solid medium for 2-4 days, extract with methanol for 24 hours, and then use a rotary evaporator to concentrate under reduced pressure at 40°C to obtain a crude extract with antibacterial active substances . The crude extract was dissolved in 5ml of methanol, filtered through a 0.22 μm membrane, separated and purified by semi-preparative liquid chromatography, the chromatographic conditions were as follows, instrument: Shimadzu LC-20A, chromatographic column: Waters C18 column (20mm×250mm, 5 μm), with volume fraction 15% methanol and ultrapure water as the mobile phase, the flow rate is 3mL / min, to obtain two parts of components A and B, such as image 3 .
[0054] Adopt antibacterial activity tracking, show good antibacterial activity in component A, therefore, adopt the same method to fu...
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