Nannochloropsis sp. mutant strain and applications thereof
A technology of Nannochloropsis and mutant strains, which is applied in the field of microorganisms, can solve the problems of decreased algal cell activity, algal cell death, and damage to algal strains, and achieves strong insecticide and high temperature tolerance, and strong environmental adaptability , the effect of high fat content
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specific Embodiment 1
[0034] Screening and acquisition of specific embodiment 1ENN11-5 algal strains
[0035] The sterile algae liquid of Nannochloropsis sp. was subjected to EMS mutagenesis treatment, and sodium hypochlorite insecticide and hydroxyproline were added for repeated pressure treatment, primary screening and secondary screening, and finally a mutant strain ENN11-5 with excellent performance was obtained. The mutant algae strain is preserved in the General Microorganism Center of the China Committee for the Collection of Microorganisms, and the preservation number is CGMCC No.9321.
specific Embodiment 2
[0036] Specific embodiment 2ENN11-5 conventional culture evaluation
[0037] 1) 3cm column reactor evaluation: ENN11-5 green swimming cells in the logarithmic growth phase were inoculated in the prepared seawater medium to make the cell density reach OD 750 between 0.8-1.2, with wild-type ENN11 as the control. During the cultivation process, the light intensity is controlled at 50-500umol / m 2 .s, L:D=16:8 light-dark cycle culture. During the culture period, the pH value of the culture medium is adjusted between 7-9 by feeding a mixed gas of 1.5-2% carbon dioxide and air into the culture solution. The reactor used for the cultivation was a column reactor with an inner diameter of 30 mm and a length of 600 mm. After culturing for 8 days, the growth curve of the algae strain was measured.
[0038] Such as figure 1 As shown, the growth of ENN11-5 cultured under conventional conditions was significantly better than that of the wild strain ENN11, and the growth rate was 31.6%...
specific Embodiment 3
[0041] Specific embodiment 3ENN11-5 insecticide pressure culture evaluation
[0042] Inoculate the ENN11-5 green swimming cells in the logarithmic growth phase in the prepared seawater medium to make the cell density reach OD 750 between 0.8-1.2, with wild-type ENN11 as the control. During the cultivation process, the light intensity is controlled at 50-500umol / m 2 .s, L:D=16:8 light-dark cycle culture. During the culture period, the pH value of the culture medium is adjusted between 7-9 by feeding a mixed gas of 1.5-2% carbon dioxide and air into the culture solution. The reactor used for the cultivation was a column reactor with an inner diameter of 30 mm and a length of 600 mm. Add 25ppm available chlorine pressure at the beginning of inoculation, keep away from light for 8 hours, then culture under light, cultivate for 8 days, and measure the growth curve of the algae strain.
[0043] Such as image 3 As shown, after the addition of available chlorine pressure, the ...
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