A new drug-resistant gene of Mycobacterium tuberculosis and its application
A technology of Mycobacterium tuberculosis and drug-resistant genes, applied in the fields of application, antibacterial drugs, genetic engineering, etc., can solve problems such as unexplainable drug resistance, and achieve the effect of convenient anti-tuberculosis performance
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Embodiment 1
[0030] 1. Materials and methods
[0031] 1. Axgen plasmid extraction kit, TakaRa’s PMD18-T vector kit, Beijing Tiangen’s DNA gel recovery kit, TakaRa’s high-fidelity enzyme,
[0032] 2. Method
[0033] 2.1 Isolation of Mycobacterium tuberculosis containing MFG71 / 74-9 gene and drug sensitivity detection of first-line anti-tuberculosis drugs
[0034] Add an equal volume of 4wt% NaOH solution to the sputum samples from tuberculosis patients in Shanghai Pulmonary Hospital, vortex for 15-20 minutes, then add 20-40mL of 0.067mol / L PBS and mix well. Centrifuge at 3000g for 30min, remove the supernatant, add 0.5mL PBS to the precipitate and mix well; take 0.1ml of the treated specimen, inoculate acidic Roche medium aseptically, culture at 37°C until the colony grows, and then follow the basic professional committee of the Chinese Antituberculosis Association The "Tuberculosis Diagnosis Laboratory Inspection Regulations" edited for strain identification and drug susceptibility testin...
Embodiment 2
[0052] Embodiment 2, bacterial plasmid transduction experiment and drug resistance detection
[0053] 1. Materials
[0054] E.coli DH5α; Mycobacterium smegmatis (ATCC19420); Axgen plasmid mini-prep kit; TakaRa company's PMD18-T vector kit; E.coli-mycobacterium shuttle plasmid PVV16; Beijing Tiangen company's DNA gel Recovery kit, TakaRa's endonuclease BamHI and HindIII TakaRa's T4DNA ligase and high-fidelity enzyme.
[0055] 2. Method
[0056] 2.1 After extracting the PMD18-T-MFG71 / 74-9 recombinant plasmid obtained in Example 1 with a plasmid extraction kit, perform double digestion with BamHI and HindIII with PVV16 at the same time, and use the DNA gel recovery reagent for the digested product The cassette was recovered, and then ligated by T4 DNA ligase to obtain the PVV16-MFG71 / 74-9 recombinant plasmid, which was transformed into E.coli DH5α, and positive clones were screened by culturing on a plate containing Kan resistance at 37°C. The recombinant plasmid PVV16-MFG71 / 7...
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