Heterotrophic culture method for microalgae by utilizing starch and immobilized microorganism co-culture
A technology of immobilized microorganisms and heterotrophic culture, applied in microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve problems such as increasing production costs, difficulty in directly utilizing starch, and difficulty in direct utilization of microorganisms, and achieves carbon reduction. effect of source cost
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Embodiment 1
[0021] (1) In a 2L airlift reactor, add the medium containing 80g / L wheat starch, sterilize and cool;
[0022] (2) Inoculate Chlorella ellipsoides cultivated to the logarithmic growth phase with an inoculum of 10% (v / v);
[0023] (3) After the membrane-coated yeast was cultured to the logarithmic phase, it was immobilized by calcium alginate embedding, and the immobilized microspheres were added to the culture medium with a yeast cell content of 5% of the dry weight of microalgae cells start cultivating in
[0024] (4) Cultivate under the conditions of 25°C, 2vvm ventilation and pH 7.0, and collect the algae liquid after the cultivation.
[0025] Processing effect test:
[0026] No leakage of yeast cells was found during the cultivation process, and the final concentration of microalgae reached 3.8g / L.
Embodiment 2
[0028] (1) In a 500mL Erlenmeyer flask, add a medium containing 100g / L cornstarch, sterilize and cool;
[0029] (2) Insert Nannochloropsis algae cultivated to logarithmic growth phase with an inoculum size of 20% (v / v);
[0030] (3) After Aspergillus niger is cultivated to the logarithmic phase, it is immobilized by carrageenan embedding, and the immobilized microspheres are added to the culture medium with a cell content of 20% of the dry weight of microalgae cells of Aspergillus niger to start culturing ;
[0031] (4) Cultivate under the conditions of 15°C, 15vvm ventilation and pH 9.5, and collect the algae liquid after the cultivation.
[0032] Processing effect test:
[0033] No leakage of Aspergillus niger cells was found during the cultivation process, and the final concentration of microalgae reached 42.2g / L.
Embodiment 3
[0035] (1) In a 1L bubble column reactor, add the medium containing 50g / L sweet potato starch, sterilize and cool;
[0036] (2) insert the Haematococcus pluvialis cultivated to the logarithmic growth phase with an inoculum of 5% (v / v);
[0037] (3) After the Escherichia coli engineering bacteria with starch hydrolysis activity were cultivated to the logarithmic phase, they were immobilized by glutaraldehyde crosslinking, and the immobilized microspheres were added with a bacterial content of 12% of the dry weight of microalgae cells Start culturing in the culture medium;
[0038] (4) Cultivate under the conditions of 30° C., 0.1 vvm ventilation and pH 6.5, and collect the algae liquid after the cultivation.
[0039] Processing effect test:
[0040] No leakage of bacterial cells was found during the cultivation process, and the final concentration of microalgae reached 24.1g / L.
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