Specific molecular marker DNA sequence of lactobacillus plantarum and application of specific molecular marker DNA sequence
A technology of Lactobacillus plantarum and molecular markers, which is applied in the field of specific molecular marker DNA sequences of Lactobacillus plantarum, can solve the problems of inconvenient molecular detection of Lactobacillus plantarum, and achieve the effects of low cost, short experiment time and simple operation
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Embodiment 1
[0042] The screening of the specificity PCR band of embodiment 1 different lactobacillus plantarum strains
[0043] (1) Template preparation
[0044] Each strain was activated, isolated and cultivated, and a single colony was selected from the obtained colonies, inoculated in 1ml of MRS medium, cultured anaerobically at 37°C for 24 hours, and centrifuged to obtain bacterial cells. The bacterial genome was extracted using a kit: TaKaRaminibest bacterial genomic DNA extraction kit ver.2.0 (Takara Biotechnology (Dalian) Co., Ltd.).
[0045] (2) PCR amplification
[0046] The system composition of PCR amplification is: 1 μ mol / L semi-random primer (its sequence is shown in SEQ ID NO.1), 0.5mmol / L dNTP, the Mg of 1.5mmol / L 2+ , 0.05U / μL Taq DNA polymerase, and 500ng (please express in concentration) genomic DNA template, the total volume is 50μL.
[0047] The PCR amplification program is: ①95°C, 5min; ②95°C, 30s; ③50°C, 30s; ④72°C, 2min;
[0048] (3) Acquisition of specific ban...
Embodiment 2
[0051] The acquisition of the specificity PCR band of embodiment 2 different lactobacillus plantarum strains
[0052] (1) Template preparation
[0053] Each strain was activated, isolated and cultivated, and a single colony was selected from the obtained colonies, inoculated in 1ml of MRS medium, cultured anaerobically at 37°C for 24 hours, and centrifuged to obtain bacterial cells. The bacterial genome was extracted using a kit: TaKaRaminibest bacterial genomic DNA extraction kit ver.2.0 (Takara Biotechnology (Dalian) Co., Ltd.).
[0054] (2) PCR amplification
[0055] The system composition of PCR amplification is: 2 μmol / L semi-random primer (its sequence is shown in SEQ ID NO.1), 1mmol / L dNTP, the Mg of 2.5mmol / L 2+ , 0.10U / μL Taq DNA polymerase, and 2ng / μL genomic DNA template in a total volume of 50 μL.
[0056] The PCR amplification program is: ① 95°C, 4min; ② 95°C, 20s; ③ 50°C, 20s; ④ 72°C, 60s;
[0057] (3) Acquisition of specific bands
[0058] The PCR product w...
Embodiment 3
[0060] The acquisition of the specific PCR band of embodiment 3 Lactobacillus plantarum strains
[0061] (1) Template preparation
[0062] The strains were activated, isolated and cultivated, and a single colony was selected from the obtained colonies, inoculated in 1ml of MRS medium, cultured anaerobically at 37°C for 24 hours, and centrifuged to obtain bacterial cells. The bacterial genome was extracted using a kit: TaKaRaminibest bacterial genomic DNA extraction kit ver.2.0 (Takara Biotechnology (Dalian) Co., Ltd.).
[0063] (2) PCR amplification
[0064] The system composition of PCR amplification is: 0.5 μ mol / L semi-random primer (its sequence is shown in SEQ ID NO.1), 0.2 mmol / L dNTP, the Mg of 1.0 mmol / L 2+ , 0.02U / μL Taq DNA polymerase, and 0.5ng / μL genomic DNA template in a total volume of 50 μL.
[0065] The PCR amplification program is: ① 96°C, 4min; ② 93°C, 40s; ③ 45°C, 40s; ④ 70°C, 120s;
[0066] (3) Acquisition of specific bands
[0067] The PCR product was...
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