Method for inducing high-yield astaxanthin of Haematococcus pluvialis by trichromatic light complex culture
A technology of Haematococcus pluvialis and trichromatic light, which is applied in the directions of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of partial astaxanthin yield, high production cost, and complicated process.
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Embodiment 1
[0037] This example provides a method for producing astaxanthin using Haematococcus pluvialis, the steps taken are the same as the above-mentioned cultivation method of Haematococcus pluvialls, the specific parameters and differences are: select MCM medium, in The culture was carried out under the condition of 20-25°C, the light intensity was 3000lx, the light source used was white light source, and the strong light source of 10000lx white light source was still used to stimulate the induction when entering the induction stage. After the experiment was over, 8 parallel samples were taken to measure the content of astaxanthin according to the above-mentioned determination method of astaxanthin. As a result, the average content of astaxanthin was 4.58mg / L.
Embodiment 2
[0039] This example provides a method for producing astaxanthin using Haematococcus pluvialis, the steps taken are the same as the above-mentioned cultivation method of Haematococcus pluvialls, the specific parameters and differences are: select MCM medium, in Cultivate under the condition of 20-25°C, and the light intensity is 3000lx. Before Haematococcus pluvialis reaches the logarithmic phase, it is irradiated with red light; after reaching the induction phase, it is induced with 10000lx blue light after entering the logarithmic phase. After the experiment was over, 8 parallel samples were taken to measure the content of astaxanthin according to the above-mentioned determination method of astaxanthin. As a result, the average content of astaxanthin was 65.63 mg / L.
Embodiment 3
[0041] This example provides a method for producing astaxanthin using Haematococcus pluvialis, the steps taken are the same as the above-mentioned cultivation method of Haematococcus pluvialls, the specific parameters and differences are: select MCM medium, in Cultivation was carried out at 20-25°C, with a light intensity of 3000lx. Before Haematococcus pluvialis reached the logarithmic phase, it was irradiated with blue light; after reaching the induction phase, it was induced with 10000lx red light after entering the logarithmic phase. After the experiment was over, 8 parallel samples were taken to measure the content of astaxanthin according to the above-mentioned determination method of astaxanthin. As a result, the average content of astaxanthin was 9.02 mg / L.
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