Culture medium and culture method of high-concentration photosynthetic bacteria
A technology of photosynthetic bacteria and culture methods, applied in the direction of bacteria, etc., can solve the problems of lack of nutrients, difficulty in maintaining the growth of bacterial cells, and weakening the ability of light penetration
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Embodiment 1
[0020] A culture medium for high-concentration photosynthetic bacteria, comprising the following components:
[0021] Sodium acetate 5.0g / L, sodium propionate 1.0g / L, yeast extract 4.0g / L, sodium chloride 2.0g / L, dipotassium hydrogen phosphate 0.5g / L, potassium dihydrogen phosphate 0.5g / L, magnesium sulfate 0.5g / L, sodium bicarbonate 2.0g / L, ammonium sulfate 1.0g / L, auxiliary nutrient solution 2mL, water 998mL, pH7.0~7.5; among them, the auxiliary nutrient solution is: niacinamide 0.005g / L, biological Vitamin 0.001g / L, calcium pantothenate 0.003g / L, vitamin B10.007g / L, vitamin B60.007g / L.
Embodiment 2
[0023] A method for cultivating high-concentration photosynthetic bacteria, comprising the following steps:
[0024] Step 1, strain preparation: use Rhodopseudomonas capsulata as the culture strain;
[0025] Step 2, preparation of fermentation medium: preparing medium according to the above-mentioned components;
[0026] Step 3, primary seed culture: insert a single colony of Rhodopseudomonas capsulata into a sterilized 30mL test tube culture medium, and seal it with a rubber stopper; cultivate it in a light incubator at a constant temperature at a temperature of 30-35°C and light intensity 3000~5000Lx; cultured to dark brown red, the bacterial concentration is 10 9 ~10 10 individual / mL, the culture was terminated, and the first-grade seed solution was obtained;
[0027] Step 4, secondary seed culture: use the primary seed liquid as the seed liquid, insert the inoculation amount of 15%~20% by volume into the sterilized 1000mL triangular flask culture solution, and seal it w...
Embodiment 3
[0032] Sampling was carried out every six hours, and OD was performed on 10-fold dilutions of the fermentation broth by a spectrophotometer 600nm value determination, the result is as figure 1 shown. After the experiment, the OD of the fermentation broth diluted 10 times in the control group 600nm The value is 1.28. while the OD of the experimental group 600nm The value was 2.57, twice that of the control group. Ferment according to the cultivation method of the present invention, the photosynthetic bacteria concentration in the fermented liquid will reach 20 * 10 9 individual / mL.
[0033] In the present invention, at the 36th hour and the 60th hour during the culture process, the nutrient enhancer concentrate for the growth of Rhodopseudomonas capsulata is supplemented to prolong the logarithmic phase of the growth of Rhodopseudomonas capsulatum. During the four-stage fermentation of photosynthetic bacteria, increase the light intensity by 10% to 20% every 12 hours. Ad...
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