Cronobacter standard strain containing specific molecular target and its detection and application
A Cronobacter, molecular target technology, applied in the field of detecting the molecular target of Cronobacter and its standard bacteria, can solve the problem that the transmission characteristics of the bacteria cannot be well reflected, the detection rate of Cronobacter is not low, and the detection rate of Cronobacter is not low. The problem of high misjudgment rate, to achieve the effect of beautiful appearance, good molding and good water solubility
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Embodiment 1
[0035] The isolation and cultivation of embodiment 1 Cronobacter standard bacterial strain
[0036] The collected food samples were shredded thoroughly under aseptic conditions, and 25 g of each sample was weighed and added to 225 mL of modified lauryl sulfate tryptose broth-vancomycin (modified lauryl sulfate tryptose broth-vancomycin edium, mLST- Vm) in a homogenizing bag, homogenize continuously for 1-2 minutes on a slap-type homogenizer, and make a uniform dilution of 1:10. Use a pipette to draw 1mL of the 1:10 dilution, add it into a test tube containing 9mL mLST-Vm, shake it well, and prepare a 1:100 dilution. In addition, prepare 10 incremental dilutions at a time according to the above operation, and use a 1mL sterilized pipette tip for each increment, inoculate three test tubes containing 9mL mLST-Vm for each dilution, inoculate 1mL in each tube, and place at 37°C In the incubator, cultivate for 8h-18h. In addition, the remaining mixture was placed in an incubator...
Embodiment 2
[0041] Physiological and biochemical characteristics and serotype analysis of the Cronobacter standard strain of embodiment 2
[0042] Staining microscopy: smear suspicious colonies, perform Gram staining, and observe under an oil lens or a phase-contrast microscope. Cronobacter is a Gram-negative non-spore-forming bacterium with perinatal flagella about 3 μm in length and 1 μm in diameter. ( figure 1 )
[0043] Biochemical identification: Pick a single suspicious colony of pure culture and perform an oxidase test, and the colony with a negative oxidase reaction is identified using the AIP20E identification system ( figure 2 ).
[0044] Molecular identification: Cronobacter carries the fusA gene, biochemically identified as a strain of Enterobacter sakazakii, and the fusA gene amplification test was performed with the following primers. For the method, see (https: / / pubmlst.org / cronobacter / ). The amplified products were sequenced, and the species were determined by blast...
Embodiment 3
[0046] The drug susceptibility characteristic of embodiment 3 Cronobacter standard strains
[0047] Drug susceptibility test: After the strain was activated on a TSA plate, it was diluted with normal saline to a final concentration of 1×10 7 Cfu / mL was spread on the MH plate, and after the bacterial solution was dry, the antibiotic paper was pasted on the surface of the medium, and cultured at 37°C for 24h. The size of the inhibition zone was measured with a vernier caliper, accurate to 0.01mm. The selected antibiotics were as follows: ampicillin (AMP, 10 μg), cefazolin (KZ, 30 μg), cephalothin (KF, 30 μg), gentamicin (CN, 10 μg), tobramycin (TOB10), amida Carcin (AK30), ampicillin-sulbactam (SAM10), cefepime (FEP30), ceftriaxone (CRO30), ciprofloxacin (CIP, 5μg), imipenem (IPM10), trimethoprim Pyridine-sulfamethoxazole (SXT, 25 μg), aztreonam (ATM30), chloramphenicol (C, 30 μg), tetracycline (TE30), amoxicillin-clavulanic acid (AMC30). Escherichia coli ATCC25922 and Cron...
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