Protein polynucleotide with separated verticillium dahliae and application thereof
A polynucleotide and protein technology, applied in the field of proteins isolated from Verticillium dahliae, can solve the problems of less protein sequence and gene sequence, and achieve the effects of quick onset, improved resistance, and improved disease resistance.
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Embodiment 1
[0026] Embodiment 1 The cultivation of Verticillium dahliae and preparation of fermented liquid
[0027] Inoculate the streaked bacterial block of Verticillium dahliae strain on PDA [take 200 grams of peeled potatoes, cut into pieces, add 1000 ml of water and boil for 30 minutes, filter the potato pieces, make up the filtrate to 1000 ml, add Glucose 20 grams, agar 15 grams, after melting, sub-package, sterilized at 121 ° C for 30 minutes] plates, cultured at 25 ° C for 2 weeks, picked the edge of the colony and inoculated in 200 mL of Czapek-Dox plus 1% hydrolyzed tyrosine (Sigma ) [sodium nitrate 3.0g, anhydrous dipotassium hydrogen phosphate 1.0g, magnesium sulfate heptahydrate 0.5g, potassium chloride KCl 0.5g, ferrous sulfate heptahydrate 0.01g, sucrose 30.0g (Beijing Chemical Plant, analytically pure), pH 5.6, add deionized water to 1L] liquid medium in a 500ml Erlenmeyer flask, culture at 25°C and 150r / min for 14 days to obtain a fermentation broth of Verticillium dahlia...
Embodiment 2
[0028] Preparation and monitoring of the crude protein elicitor of embodiment 2
[0029] The fermentation broth obtained in Example 1 was centrifuged at 4°C and 5000rpm for 1h (or 13000rpm for 30min), and the supernatant was collected and filtered twice with a 0.45mm membrane filter (Whatman) until there were no bacteria. Ammonium sulfate powder was added so that the final concentration of ammonium sulfate in the supernatant was 80% to precipitate the target protein, dialyzed at 4°C for 48h, and finally the obtained extracellular total protein was dissolved in Tris-HCl buffer (20mM, pH 8.0), The final protein concentration was 100 μg / mL. Protein content with BCA TM Protein assay kit (Thermo Scientific) was determined at a wavelength of 590 nm by GF-M2000 microplate reader (Shandong Gaomi Caihong Analytical Instrument Co., Ltd.).
[0030] Monitoring of biological activity: Tobacco with 5-7 true leaves grown for 2 months was used as material, Tris-HCl buffer solution and BSA s...
Embodiment 3
[0032] Example 3 Separation and purification of protein elicitors and determination of biological activity
[0033] use The explore 10 (GE Healthcare) protein purification instrument further purified the obtained total protein, and the sample was first passed through the HP Q HiTrap TM Anion exchange column (GE Healthcare), linear elution with NaCl (0%-100%, 30min), obtained 6 protein elution peaks, the applied protein concentration was 50μg / mL, the results showed that the 3rd protein peak , can strongly cause an allergic reaction to tobacco; the protein peak is further purified by pheny HP hydrophobic chromatography column (GE Healthcare) and electroelution to obtain an active single protein. The monitoring of protein elicitor activity during the above purification process was carried out according to the method in Example 2. The single protein peak is detected as a single band by 15% denatured polyacrylamide gel electrophoresis, indicating that the protein is of high puri...
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