Solid-state culture medium for benefitting long-term storage of haematococcus pluvialis algae and preparation method thereof
A technology of Haematococcus pluvialis and solid medium, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., which can solve the problems of prolonging the storage time of Haematococcus pluvialis species, easily polluting bacteria, excessive, etc. problems, to achieve the effect of convenient and quick microalgae breeding and inhibiting the growth of bacteria
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Embodiment 1
[0014] A kind of preparation method that is beneficial to the solid-state culture medium of long-term storage Haematococcus pluvialis species, comprises the following steps:
[0015] Step 1: Measure 1 liter of ultrapure water;
[0016] Step 2: 1.4g of sodium nitrate; 0.13g of sodium carbonate; 0.25g of magnesium sulfate; 0.05g of dipotassium hydrogen phosphate; 0.019g of ferric ammonium citrate; Sodium 0.010g; Zinc sulfate 0.000222g; Boric acid 0.00586g Manganese chloride 0.0018g; Cobalt nitrate 0.000894g; Sodium molybdate 0.00039g; Copper sulfate 0.000150g; 5ml; Vitamin B12 5ml was added to ultrapure water, and each component was dissolved;
[0017] Step 3: Add the solution obtained in step 2 into an autoclave, sterilize at 120°C for 20 minutes, and then store it in a sterile environment at a storage temperature of 40°C.
Embodiment 2
[0019] A kind of preparation method that is beneficial to the solid-state culture medium of long-term storage Haematococcus pluvialis species, comprises the following steps:
[0020] Step 1: Measure 1 liter of ultrapure water;
[0021] Step 2: 1.35g of sodium nitrate; 0.14g of sodium carbonate; 0.2g of magnesium sulfate; 0.08g of dipotassium hydrogen phosphate; 0.014g of ferric ammonium citrate; Sodium 0.005g; Zinc sulfate 0.0007g; Boric acid 0.0045g Manganese chloride 0.0028g; Cobalt nitrate 0.0006g; Sodium molybdate 0.0006g; Copper sulfate 0.00012g; Sodium acetate 0.8g; Agar powder 16g; 4ml; vitamin B12 6ml was added to ultrapure water, and each component was dissolved;
[0022] Step 3: Add the solution obtained in step 2 into an autoclave, sterilize at 120°C for 20 minutes, and then store it in a sterile environment at a storage temperature of 40°C.
Embodiment 3
[0024] A kind of preparation method that is beneficial to the solid-state culture medium of long-term storage Haematococcus pluvialis species, comprises the following steps:
[0025] Step 1: Measure 1 liter of ultrapure water;
[0026] Step 2: 1.3g of sodium nitrate; 0.15g of sodium carbonate; 0.15g of magnesium sulfate; 0.10g of dipotassium hydrogen phosphate; 0.009g of ferric ammonium citrate; Sodium 0.001g; zinc sulfate 0.001000g; boric acid 0.00286g manganese chloride 0.0036g; cobalt nitrate 0.000494g; sodium molybdate 0.00089g; copper sulfate 0.000079g; sodium acetate 1.0g; agar powder 15g; 2ml; vitamin B12 10ml was added to ultrapure water, and each component was dissolved;
[0027] Step 3: Add the solution obtained in step 2 into an autoclave, sterilize at 120°C for 20 minutes, and then store it in a sterile environment at a storage temperature of 40°C.
[0028] Examples 1-3 provide sufficient nitrogen source, phosphorus source, and carbon source to provide sufficient...
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