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Method for promoting growth of Haematococcus Pluvialis and accumylation of astaxanthin by using plant hormones

A technology of Haematococcus pluvialis and phytohormones, applied in the directions of adding compounds to stimulate growth, microorganism-based methods, biochemical equipment and methods, etc. Accumulation of cyanin, low production cost, and the effect of increasing economic benefits

Inactive Publication Date: 2017-11-10
山东鸣惠生物科技股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Liu Jianguo et al. (2009) used naphthaleneacetic acid and 3-indolebutyric acid to improve the growth of Haematococcus pluvialis cells; Shang Minmin et al. (2015) used fulvic acid to promote the growth of Haematococcus pluvialis and astaxanthin The accumulation of phytohormones such as fulvic acid and 3-indole butyric acid used above are relatively expensive, and are not suitable for large-scale production.

Method used

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  • Method for promoting growth of Haematococcus Pluvialis and accumylation of astaxanthin by using plant hormones
  • Method for promoting growth of Haematococcus Pluvialis and accumylation of astaxanthin by using plant hormones
  • Method for promoting growth of Haematococcus Pluvialis and accumylation of astaxanthin by using plant hormones

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Embodiment 1

[0025] A method for promoting the growth of Haematococcus pluvialis and the accumulation of astaxanthin by using plant hormones, comprising the following steps:

[0026] 1. Fully dissolve naphthaleneacetic acid with 95% ethanol, and dilute it into pure water to prepare a 1g / L mother liquor;

[0027] 2. Prepare the growth medium of Haematococcus pluvialis, and add the mother liquor of naphthaleneacetic acid to the medium, and the concentration of naphthaleneacetic acid is 0mg / L, 2mg / L;

[0028] 3. Take the algae liquid in the logarithmic phase and inoculate the culture medium at a ratio of 1:5;

[0029] 4. Place the above-mentioned algae liquid at 24°C under 1000-4000lx light for ventilation and culture, measure the biomass every two days, and cultivate continuously for 8 days;

[0030] 5. Through data analysis, it is obtained that in the medium added with 2mg / L naphthaleneacetic acid, the growth rate of the algae fluid is accelerated, and after 8 days, the biomass is increase...

Embodiment 2

[0032] A method utilizing plant hormones to promote the growth of Haematococcus pluvialis, comprising the following steps:

[0033] 1. Fully dissolve naphthaleneacetic acid with 95% ethanol, and dilute it into pure water to prepare a 1g / L mother liquor;

[0034] 2. Prepare the growth medium of Haematococcus pluvialis, and add the mother liquor of naphthaleneacetic acid to the medium, and the concentration of naphthaleneacetic acid is 0 mg / L, 2 mg / L;

[0035] 3. Take the algae liquid in the logarithmic phase and inoculate the culture medium at a ratio of 1:10;

[0036] 4. Place the above-mentioned algae liquid at 24°C under 1000-4000lx light for ventilation and culture, measure the biomass every two days, and cultivate continuously for 10 days;

[0037] 5. Through data analysis, it is obtained that in the medium added with 2mg / L naphthaleneacetic acid, the growth rate of the algae fluid is accelerated, and after 10 days, the biomass is increased by 10% compared with the algae ...

Embodiment 3

[0039] A method utilizing plant hormones to promote the growth of Haematococcus pluvialis, comprising the following steps:

[0040] 1. Fully dissolve naphthaleneacetic acid with 95% ethanol, and dilute it into pure water to prepare a 1g / L mother liquor;

[0041] 2. Prepare microalgae growth medium, and add naphthaleneacetic acid mother liquor to the medium, and the concentration of naphthaleneacetic acid is 0 mg / L, 1 mg / L, 2mg / L and 3mg / L;

[0042] 3. Take the algae liquid in the logarithmic phase and inoculate the culture medium at a ratio of 1:5;

[0043] 4. Place the above-mentioned algae liquid at 24°C under 1000-4000lx light for ventilation and culture, measure the biomass every two days, and cultivate continuously for 8 days;

[0044] 5. Through data analysis, it is obtained that in the medium added with naphthaleneacetic acid, the growth rate of the algae liquid is significantly accelerated, and the biomass of the algae liquid in the medium with 3mg / L naphthaleneacetic...

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Abstract

The invention discloses a method for promoting the growth of Haematococcus Pluvialis and the accumylation of astaxanthin by using plant hormones. The method comprises: preparing a plant hormone mother liquor; preparing a Haematococcus Pluvialis culture medium; inoculating; and continuously carrying out ventilation culture on a Haematococcus Pluvialis liquid for 8-10 days at a temperature of 24 DEG C under 1000-4000 lx illumination, and measuring the biomass every two days. According to the present invention, the method is simple and easy to perform, the cost is low, the accumylation of astaxanthin cultured through the method has characteristics of rapid growth, high biomass and short induction period, and the astaxanthin content is increased significantly.

Description

technical field [0001] The invention belongs to the biotechnology field of cultivation, research, development and application of Haematococcus pluvialls, and specifically relates to a method for promoting the growth of Haematococcus pluvialls and the accumulation of astaxanthin by using plant hormones. Background technique [0002] Astaxanthin (ASTA, also known as astaxanthin) is a carotenoid with great antioxidant activity, similar to β-carotene, and is a red color found in river shrimp shells, oysters, and salmon Carotenoids, chemical name 3,3 , -Dihydroxy-4,4 , - Diketo beta-carotene. [0003] The antioxidant capacity of astaxanthin is 6,000 times that of vitamin C, 1,000 times that of vitamin E, 800 times that of coenzyme Q10, 700 times that of anthocyanins, 110 times that of β-carotene, 1,100 times that of nucleic acids, and 1,100 times that of lycopene. 1,800 times that of tea polyphenols, 320 times that of tea polyphenols, and 800 times that of lutein. Natural asta...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/12C12N1/38C12P23/00C12R1/89
Inventor 林真真马建魏本军兰振华胥洪明
Owner 山东鸣惠生物科技股份有限公司