Method and kit for screening/detecting lactobacillus
A Lactobacillus and kit technology, applied in the field of bacterial detection, can solve the problems of high cost, huge workload, strong primer specificity, etc., and achieve the effect of strong application value, cost saving and time saving.
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Embodiment 1
[0024] Example 1 Primer Design
[0025] As shown in Table 1, according to the genome sequences of 14 kinds of Lactobacillus in the Genome database of NCBI, the conserved sequence of Lactobacillus was found, and the conserved sequence and Lactobacillus belonged to Pediococcus (Pediococcus) of Lactobacillus family, and Lactobacillus belonged to Lactobacillus order Enterococcus (Enterococcus), Lactococcus (Lactococcus) and Leuconostoc (Leuconostoc), and the corresponding sequence alignment of Bacillus (Bacillus) and Staphylococcus (Staphylococcus), which belong to the class Bacillus with Lactobacillus, design Lactobacillus-specific primers .
[0026] Table 1 List of 14 kinds of Lactobacillus and 5 kinds of related strains that have been sequenced
[0027]
[0028] In order to achieve the purpose of quickly screening out all Lactobacilli from samples to be tested containing a large number of microorganisms, the present invention needs to design a pair of primers, and the prime...
Embodiment 2
[0032] Embodiment 2 primer specificity experiment
[0033] For Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus brevis, Lactobacillus casei, Lactobacillus helveticus, Lactobacillus delbrueckii, Leuconostoc, Lactococcus lactis, Bacillus subtilis and Staphylococcus epidermidis for PCR amplification detection according to the following steps :
[0034] 1. Primers
[0035] Primers prepared in Example 1 were used.
[0036] 2. Template preparation
[0037] Pick trace amounts from single colonies of Lactobacillus acidophilus, Lactobacillus plantarum, Lactobacillus brevis, Lactobacillus casei, Lactobacillus helveticus, Lactobacillus delbrueckii, Leuconostoc, Lactococcus lactis, Bacillus subtilis and Staphylococcus epidermidis Put the bacteria into the PCR tube, put the PCR tube into the microwave oven, heat it at 100% power for 3 minutes, and then add the PCR system.
[0038] 3. PCR amplification
[0039] Using the heat-treated thalli in step 2 as a template, the...
Embodiment 3
[0053] Embodiment 3 The composition of kit of the present invention and its using method
[0054] 1. The composition of the kit
[0055] 25μL system:
[0056] Primers provided in Example 1: 0.5 microliters each
[0057] 10× PCR buffer: 2.5 μl
[0058] Magnesium chloride: 2 µl
[0059] dNTPs: 2 µl
[0060] exTaq enzyme: 0.25 µl
[0061] wxya 2 O: 17.25 µl
[0062] 2. How to use the kit
[0063] 1) Isolation of single colony: isolate a single colony of the strain from the sample to be tested;
[0064] 2), gene amplification:
[0065] Using the bacterial genomic DNA obtained in step 1) as a template, the kit was used for gene amplification. The reaction program was: 94°C for 5 minutes; 95°C for 40s, 57°C for 30s, 72°C for 100s, 30 cycles; 72°C for 10 minutes.
[0066] 3), result detection:
[0067] 5 μL of the reaction solution was taken for agarose gel (0.7% W / V) electrophoresis to detect the PCR amplification result.
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