Culture medium and culture method for long-term and continuous culture of Boveria Stevens
A culture medium and long-term technology, applied in fish farming, application, animal husbandry, etc., can solve the problems of endangering the healthy and sustainable development of the sea cucumber industry, affecting the growth and development of sea cucumbers, and the death of sea cucumbers, so as to achieve batch preparation and Application, stable and reliable sources of raw materials, low cost of cultivation
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[0020] Example 1: Comparison of the survival of the posterior insects under different medium conditions
[0021] The specific steps are as follows: After filtering sea water, boil disinfection, cool to 8 ~ 10 ° C, add yeast fermentation liquid concentrate to the final concentration of 2.5 mg / L, and add a subharidacillus CSDN-6, photosynthetic bacteria, and Bacillus to final concentration 10 5 CFU / mL, wherein group 1 is a sub-cheese Lactobacillus CSDN-6 + yeast fermentation fluid concentrate, group 2 is a photosynthetic bacterial + yeast fermentation liquid concentrate, group 3 is a Bacillus + yeast fermentation fluid concentrate. The above liquid is three medium of the outer pure cultivation of rear oral insects, and the medium of the body cavity liquid and the breathing tree tissue fragmentation in sterilization seawater is compared to the control.
[0022] In November 20020, there was a resect disease in Dalian a farm, and the sick thorn was taken back to the laboratory, and...
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[0026] Example 2: Selection of Yeast Fermentation Liquid Concentrates
[0027] The specific steps are as follows: After filtering sea water, boil 5 to 10 min, then cool it to 8 ~ 10 ° C, add 0.1 mg / L, 1.0 mg / L, 2.5 mg / L, 5.0mg / L, 10.0mg / L, 25mg / L. The yeast fermentation fluid concentrate, adequately mixed, add a sub-cheese CSDN-6 to final concentration of 10 5 CFU / ml, the liquid is a medium having an outer pure culture of rear oral insects.
[0028] In December 2020, the stabbin sanctuary of the patients with aushagus was taken back to the laboratory to dissect the breathing tree to produce water dip, and the microscope observation has a large number of hillous worms in the breathing tree. The posterior worm separated from the sick stabbed breathing tree is removed under the microscope and other organisms and other organisms; that is, according to the result of the count under the microscope, according to the post-mouth density of 100 / ml After the rear sodus transf...
Example Embodiment
[0032] Example 3: Culture Salinity Control
[0033] The specific steps are as follows: By adding fresh water to the sea, the medium is adjusted to 0 ‰, 2.5 ‰, 5 ‰, 10 ‰, 15 ‰, 20 ‰, 25 ‰, 30 ‰, 35 ‰, 40 ‰, 45 ‰, add 2.5mg / L yeast fermentation fluid concentrate and 10 5 CFU / mL of the sub-cheese CSDN-6, which is a medium having an outer pure culture medium of rear oral.
[0034] In December 2020, the stabbin dry transport of the suffering of aushagus was taken back to the laboratory, and the breathing tree was used to make a water dip film. The microscope observation has a large number of post-hugs to breathe in the breathing tree. The posterior worm separated from the sick stabbed breathing tree is removed under the microscope and other organisms and other organisms; that is, according to the result of the count under the microscope, according to the post-mouth density of 100 / ml After the lathem is transferred to the medium, 40 ml of water body, pH 7.8 ~ 8.5, temperature 8 ~ ...
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