Quick efficient nostoc sphaeroides breeding method
An efficient and fast technology, applied in the field of cyanobacteria cultivation, to achieve the effects of simplifying the breeding process, shortening the breeding cycle, and increasing the growth and development speed
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Embodiment 1
[0027] The induction of embodiment 1 Gexian rice algae multiplication segment
[0028] Wash the Gexianmi spheres (diameter ≥ 3mm) and place them in an open container, soak them in purified water (it is appropriate to just immerse them), and place the container in an environment of about 500-10000lux for cultivation. 15-33°C. After the spheres of Gexianmi are completely broken, use a sieve to filter out the residue in the liquid, and collect the filtrate, which is dispersed with a large number of Gexianmi algae. The induction rate of this algae breeding section induction process is 100%.
Embodiment 2
[0029] The cultivation method of embodiment 2 Ge Xianmi algae section
[0030] ⅰ) Preparation of culture medium for algae breeding stage
[0031] Using purified water as the water source, the concentrations of various nutrients added are as follows:
[0032] MgSO 4 ·7H 2 O: 75mg / L; K 2 HPO 4 ·3H 2 O: 40mg / L; EDTA·2Na: 1mg / L; CaCl 2 2H 2 O: 9mg / L; Citric acid: 6mg / L; Ferric ammonium citrate: 6mg / L; Na 2 CO 3 : 20mg / L; H 3 BO 3 : 2.86g / L; MnCl 2 4H 2 O: 1.81g / L; ZnSO4 ·7H 2 O: 222 mg / L; Na 2 MoO 4 2H 2 O: 39mg / L; CuSO 4 ·5H 2 O: 79mg / L; Co(NO 3 ) 2 ·6H 2 O, 49mg / L.
[0033] There is no need to carry out any disinfection treatment on the culture medium of the algae breeding section, such as high-pressure steam sterilization.
[0034] ii) Cultivation of algae growth stage
[0035] The algae liquid collected in Example 1, which is dispersed with a large amount of Gexianmi algae growth section, is mixed with the algae growth section culture solution prepared ...
Embodiment 3
[0043] The budding propagation of embodiment 3 Ge Xianmi spherule (diameter≤2mm)
[0044] The Ge Xianmi that forms microsphere among the embodiment 2 carries out expansion culture. The cultivation light is 500-10000 lux, and the cultivation temperature is 15-33°C.
[0045] The concentrations of the various nutrients are as follows:
[0046] MgSO 4 ·7H 2 O: 0-75mg / L; K 2 HPO 4 ·3H 2 O: 0-40mg / L; EDTA·2Na: 0-1mg / L; CaCl 2 2H 2 O: 0-9mg / L; Citric acid: 0-6mg / L; Ferric ammonium citrate: 0-6mg / L; Na 2 CO 3 : 0-20mg / L; H 3 BO 3 : 0-2.86g / L; MnCl 2 4H 2 O: 0-1.81g / L; ZnSO 4 7H2O: 0-222mg / L; Na 2 MoO 4 2H 2 O: 0-39mg / L; CuSO 4 ·5H 2 O: 0-79mg / L; Co(NO 3 ) 2 ·6H 2 O: 0-49mg / L.
[0047] The source of culture water is still purified water, and tap water or clean natural water bodies (such as groundwater, river water, lake water or reservoir water) that meet the national drinking standards can also be selected. When formulating nutrients with culture water sources ...
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