Method for breeding gibberellic acid high-producing strains by performing low-energy ion induced mutation on gibberella
A technology of high-yield strains and low-energy ions, applied in the field of microbial mutagenesis, to achieve the effects of large-scale industrial production, good mutagenesis effect, and stable high-yield traits
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Embodiment 1
[0025] Get Gibberella strain and make 10 with sterile water 8 protoplast suspension per mL; take 0.1mL of protoplast suspension and evenly spread it on a sterile flat petri dish, and dry it in a sterile state; use energy 10keV, dose 1.5×10 14 ions / cm 2 Nitrogen ion beam, pulse injected into the air-dried protoplast, add 1mol / L sorbitol solution 10 times ice bath, the sorbitol solution used contains 10mmol / L Tris-Cl, pH7.5; 50mmol / L CaCl 2 . After suspending, spread it on the PDAS regeneration medium plate and culture it at 28°C for 5 days. The PDAS regeneration medium used contains 20% potato juice, 2% glucose, 3.5%~4.1% NaCl, 1.5%~2% agar, pH6. 0~6.5; select the cultured single strain with white round shape, normal shape, vigorous growth and diameter of 2~4mm to inoculate in a 500mL shaker flask filled with 100mL liquid fermentation medium, and culture it in a shaker at 28°C and 220rpm for 180h. 40 mutagenic single strains were randomly selected as the object of investiga...
Embodiment 2
[0028] Get Gibberella strain and make 10 with sterile water 9 protoplast suspension per mL; take 0.3mL protoplast suspension and evenly spread it on a sterile flat petri dish, and dry it under aseptic condition; use energy 20keV, dose 1.5×10 15 ions / cm 2 Nitrogen ion beam, pulse injected into the air-dried protoplast, add 1mol / L sorbitol solution 10 times ice bath, the sorbitol solution used contains 10mmol / L Tris-Cl, pH7.5; 50mmol / L CaCl 2 . After suspending, spread it on the PDAS regeneration medium plate and culture it at 28°C for 5 days. The PDAS regeneration medium used contains 20% potato juice, 2% glucose, 3.5%~4.1% NaCl, 1.5%~2% agar, pH6. 0~6.5; Select a single strain with a white round shape, normal shape, vigorous growth, and a diameter of 2~4mm to inoculate in a 500mL shaker flask containing 100mL of liquid fermentation medium, and culture it in a shaker at 28°C and 220rpm for 180h. 40 mutagenic single strains were randomly selected as the object of investigati...
Embodiment 3
[0031] The gibberellic acid-yielding gibberellic acid-producing gibberellic acid mutant strain obtained by mutagenesis was continuously passaged on the PDA slant medium (ingredients: 200g potato, 20g glucose, 15g agar, 1000mL tap water) for 12 consecutive passages. times, after each passage in the fermentation medium (ingredients: liquefied starch 100g / L, peanut cake powder 15g / L, soybean meal powder 3g / L, magnesium sulfate 0.75g / L, potassium dihydrogen phosphate 1.0g / L, pH 5~6) Medium culture, determination of gibberellic acid content, shake flask fermentation results see figure 1 . The content of gibberellic acid produced by fermentation of the original strain was 100%, compared with other generations, the result was that the amount of gibberellic acid produced after 10 passages was still stable, maintaining above 93%, indicating that the genetic stability of the mutant strain was better, Can be used as a potential production strain.
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