Primer and method for identifying leuconostoc mesenteroides subsp.mesenteroides and application of leuconostoc mesenteroides subsp.mesenteroides
A technology for identification of Leuconostoc enteritiformis and its identification method, which is applied in the field of primers for identifying Leuconostoc enteritidis subspecies, which can solve the time-consuming, cumbersome identification of Leuconostoc enteritidis subspecies, and the impossibility of subspecies identification. Level identification and other issues to achieve the effect of accelerated application and simple identification
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Embodiment 1
[0029] Primer design and validation for the identification of Leuconostoc enteritidis subspecies:
[0030] By comparing and analyzing the existing genome sequences of Leuconostoc enterococci (see attached table 1 for each strain and its genome sequence extraction code), a ubiquitous GH70 glycosyltransferase coding gene was identified and named gtf1. The gtf1 gene contains two highly conserved base sequences encoding the GH70 domain. Between these two highly conserved sequences, there is a highly variable sequence, which shows a high degree of polymorphism in different strains ( polymorphism).
[0031] Table 1 The complete genome information of Leuconostoc enterolis
[0032]
[0033] The schematic diagram of the gtf1 gene and its encoded product is attached figure 1 As shown, we designed primers in the highly conserved GH70 coding region to amplify the central highly variable region, and identified the strain by sequencing the amplified product.
[0034] According to the ...
Embodiment 2
[0039] A method for identifying Leuconostoc enteritidis isolated from traditional foods at the level of Enteromenis subspecies, the method comprising the following steps:
[0040] (1) Taking Leuconostoc enterococci BD1710 isolated from traditional food in our laboratory as the test bacteria, the genomic DNA of the test strains was extracted, and the obtained DNA was used as a template for PCR amplification.
[0041] (2) Using the genomic DNA to be tested extracted from the above strains as a template, the PCR amplification reaction system is as follows: 2 μl of 2ng / μl DNA template, 1 μl of 0.5 μmol / L primer, 2 μl of 0.2mmol / L dNTP, 1.5mmol / L MgSO4 Add 1 μl, 2 μl of 10×PCR reaction buffer, 0.5 μl of 5U / μl rTaq DNA polymerase to 20 μl.
[0042] (3) Reaction parameters of PCR amplification: pre-denaturation at 95°C for 10 min; denaturation at 95°C for 30 s, annealing at 48°C for 30 s, extension at 72°C for 2 min, and 35 cycles; extension at 72°C for 15 min, and storage at 4°C.
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