Breeding method of high-temperature-resistant chlorella for aquaculture
A technology for aquaculture and chlorella, applied in the direction of microorganism-based methods, biochemical equipment and methods, single-cell algae, etc., can solve the problems of increasing production costs, unfavorable for high density of chlorella, waste of energy, etc., to achieve Improve the success rate, protect the stability, promote the effect of growth separation
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Embodiment 1
[0030] Embodiment 1: Breeding high temperature resistant chlorella
[0031] 1. Collect microalgae liquid from outdoor aquaculture water, and separate relatively pure chlorella single algae colony (purity is more than 80%, calculated by counting method) through plate marking and coating method.
[0032] Plate medium configuration is as follows:
[0033] (1) Nutrient solution mother solution formula (1L)
[0034] Table 1
[0035] Material name molecular formula level Weight (g) sodium nitrate NaNO 3
AR 75 Potassium dihydrogen phosphate dihydrate NaH 2 PO 4 2H 2 o
AR 5 Dipotassium hydrogen phosphate anhydrous K 2 HPO 4
AR 4 sodium bicarbonate NaHCO 3
AR 1 ammonium chloride NH 4 Cl
AR 1 yeast extract BR 2 plant peptone BR 1
[0036] Vitamin Mother Liquid Formula (100mL):
[0037] Table 2
[0038] Material name molecular formula level Weight (mg) ...
Embodiment 2
[0057] Embodiment 2: the contrast of breeding method
[0058] Culture medium of the present invention: culture medium in embodiment 1;
[0059] Conventional microalgae medium: BG11 (sodium nitrate 1.5g, dipotassium hydrogen phosphate 0.04g, magnesium sulfate heptahydrate 0.075g, calcium chloride heptahydrate 0.036g, sodium carbonate 0.02g, citric acid 0.006g, ferric ammonium citrate 0.006 g, EDTA0.001g, sterile water 1L.)
[0060] On the basis of the method in Example 1, different culture media and whether to add cell protection solution were used for comparison;
[0061] Breeding method of the present invention: embodiment 1 method;
[0062] Comparative breeding method: on the basis of the method in Example 1, replace the culture medium of the present invention with conventional microalgae culture medium and do not add cell protection solution, cultivate under the conditions of light intensity 10000lux and culture temperature 45°C for breeding;
[0063] Each method adopts ...
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