Zymomonas mobilis mutant strains tolerant to high-concentration acetic acid and applications thereof
A Zymomonas, high-concentration technology, applied in the field of microorganisms to achieve rapid and efficient production and good growth performance
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Embodiment 1
[0029] This embodiment illustrates the method for obtaining Zymomonas mobilis AQ8-1 and AQ8-9 by mutagenesis screening ZM4 as the starting strain:
[0030] 1) Irradiation mutagenesis was carried out on Zymomonas mobilis cells by the normal temperature plasma mutagenesis breeding technology. First, the starting strain ZM4 was activated and cultured at 30°C for 16 hours, and then the overnight culture (10 7 to 10 8 cells), centrifuge at 4°C for 5 min at 3000 rpm, wash the bacteria with normal saline and resuspend in 1 mL of normal saline; take 10 μL of the resuspended cells and place them in an ARTP mutagenesis breeding instrument for 120 s;
[0031] 2) Resuspend the cells after irradiation mutagenesis for 16 hours, and then spread them on a solid medium containing 7 g / L acetic acid for culture;
[0032] 3) All the colonies were selected and screened on a medium containing 8 g / L acetic acid. After repeated screening three times, two stable mutant strains were finally obtained, ...
Embodiment 2
[0034] Method for producing ethanol by fermenting mutant strains
[0035] 1) The preparation of fermentation medium: 50g / L glucose, 2g / L potassium dihydrogen phosphate, 10g / L yeast extract and 7g / L acetic acid, the pH of the medium at this time=3.92 (this pH value is added 7g / L pH reached naturally by acetic acid)
[0036] 2) Inoculate the strains on the fermentation medium and carry out fermentation culture: inoculate the strains AQ8-1, AQ8-9 and the starting strain on the medium respectively, the inoculum amount is 10%, and ferment and cultivate for 40-48 hours.
[0037] 3) ethanol is separated, and the conversion rate is calculated.
[0038] After 48 hours of fermentation and cultivation, the two mutant strains can consume all the glucose, and the ethanol conversion rates of the strains AQ8-1 and AQ8-9 reached 94% and 98% of the theoretical conversion rate respectively, while the conversion rate of the starting strain was only 12% of theoretical conversion.
Embodiment 3
[0040] Method for producing ethanol by fermentation of mutant strain
[0041] 1) Preparation of fermentation medium: 50g / L glucose, 2g / L potassium dihydrogen phosphate, 10g / L yeast extract, 8g / L acetic acid, pH3.86 (this pH value is the pH naturally achieved by adding 8g / L acetic acid )
[0042] 2) Inoculate the strains on the fermentation medium and carry out fermentation culture: inoculate the strains AQ8-1, AQ8-9 and the starting strain on the medium respectively, the inoculum amount is 10%, and ferment and cultivate for 60 hours.
[0043] 3) ethanol is separated, and the conversion rate is calculated.
[0044] After 60 hours, the two mutant strains could consume all the glucose, and the ethanol conversion rates of the strains AQ8-1 and AQ8-9 both reached 96% of the theoretical conversion rate, and the starting strains could not grow normally at this time.
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