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Schizochytrium sp.TIO1101 strain with high-yield DHA (docosahexaenoic acid) and fermentation method thereof

A technology of Schizochytrium sp. and fermentation medium, which is applied to high-yield DHA Schizochytrium algae strains and its fermentation field, which can solve the problem of low yield and achieve the effect of high DHA content and simple ingredients

Inactive Publication Date: 2011-09-28
THIRD INST OF OCEANOGRAPHY STATE OCEANIC ADMINISTATION +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there have been many studies on the production of DHA by fermentation and cultivation of Schizochytrium algae at home and abroad, but most of them have the problem of low yield.

Method used

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  • Schizochytrium sp.TIO1101 strain with high-yield DHA (docosahexaenoic acid) and fermentation method thereof
  • Schizochytrium sp.TIO1101 strain with high-yield DHA (docosahexaenoic acid) and fermentation method thereof
  • Schizochytrium sp.TIO1101 strain with high-yield DHA (docosahexaenoic acid) and fermentation method thereof

Examples

Experimental program
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Effect test

preparation example Construction

[0023] Preparation method of trace element compound solution: Na 2 · EDTA 6.0g, FeCl 3 ·6H 2 O 0.29g, H 3 BO 3 6.84g, MnCl 2 4H 2 O 0.86g, ZnCl 2 0.06g, CoCl 2 6H2O 0.026g, NiSO 4 ·6H 2 O 0.052g, CuSO 4 ·5H 2 O0.002g, NaMoO 4 2H 2 O 0.005g, make up 1L with distilled water.

[0024] The preparation method of vitamin complex solution: vitamin B1 (thiamin) 100mg, vitamin H (biotin) 0.5mg, vitamin B12 (cyanocobalamin) 0.5mg, distilled water to supplement 1L.

[0025] The preparation method of the fermentation medium: 120g of glucose, 20g of yeast extract, 15g of peptone, 3g of potassium dihydrogen phosphate, 2g of magnesium sulfate, 10ml of trace element compound solution, 5ml of vitamin compound solution, and 0.5 × seawater (diluted with fresh water 1 times seawater) to 1L.

Embodiment 1

[0026] Example 1, the isolation and identification of Schizochytrium TIO1101

[0027] 1. Isolation of Schizochytrium TIO1101 (pine pollen fishing method)

[0028] Take the decayed fallen leaves from the mangrove forest in Yundang Lake, Xiamen, cut them into small discs with a diameter of about 1.5 cm, wash them with sterile seawater containing 1 g / L of streptomycin and penicillin, and inoculate them on solid separation plates. Add about 3mL of sterile seawater and a small amount of sterile pine pollen to the plate, culture 4-5d at 28°C, pick pine pollen, and observe the culture that adheres to and grows on the pine pollen. The pine pollen of the adherent culture was then transferred to a new plate for streak separation until a pure culture was obtained. The resulting algae was named TIO1101.

[0029] 2. Identification of Schizochytrium TIO1101

[0030] 1. Observation of algae colony and cell morphology

[0031]After the culture was cultured on the isolation and purificatio...

Embodiment 2

[0045] Embodiment 2, the high-density heterotrophic fermentation of Schizochytrium TIO1101

[0046] 1. Fermentation

[0047] Add 6L of fermentation medium in a 10L fermenter, and then add 0.6L of Schizochytrium TIO1101 bacterial liquid, so that the concentration of Schizochytrium TIO1101 in the medium is about 1.0×10 6 Individual / mL; fermentation culture conditions are: temperature 25°C, pH value 6.0, rotation speed 300rpm (200-400rpm is acceptable), dissolved oxygen 10%, culture for 96h; carry out 10L fermentor fed-batch culture: from the moment of fermentation 12h Start to add glucose solution (composed of glucose and water, the concentration of glucose is 50g / L) and yeast extract solution (made up of yeast extract and water, the concentration of yeast extract is 10g / L) until the moment of fermentation 50h, the glucose solution The flow rate is 50mL / h, and the flow rate of the yeast extract solution is 20mL / h.

[0048] 2. Detection of biomass, oil and DHA content

[0049]...

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Abstract

The invention discloses a Schizochytrium sp.TIO1101 strain with high-yield DHA (docosahexaenoic acid) and a fermentation method thereof. The Schizochytrium sp.TIO1101 strain provided by the invention has a preservation number of CGMCC (China General Microbiological Culture Collection Center) No.4603. After the Schizochytrium sp.TIO1101 is subjected to high-density heterotrophic fermentation for 72h, the biomass liveweight, the lipid content and the DHA are respectively 120g / L, 54.3% and 51.4% of the content of total lipid, therefore the Schizochytrium sp.TIO1101 has development and application values extremely. The Schizochytrium sp.TIO1101 disclosed by the invention has the advantages that: the Schizochytrium sp.TIO1101is obtained through separation; the high-density heterotrophic fermentation of the Schizochytrium sp.TIO1101 is realized; and the lipid extracted from the Schizochytrium sp.TIO1101 cells obtained under the fermentation condition has high DHA content and purer components.

Description

technical field [0001] The invention relates to a high-yield DHA-producing Schizochytrium strain and a fermentation method thereof. Background technique [0002] Docosahexaenoic acid (DHA) mainly exists in the gray matter of the human brain and the retina. It is an essential fatty acid component to maintain the normal physiological metabolism of the human body. It has a very important physiological role in the development of the brain and vision of infants and young children. Vascular disease, improve human immunity, etc. DHA has aroused great interest and been widely used because of its unique physiological regulation function. [0003] The traditional source of DHA is deep-sea fish oil, but polyunsaturated fatty acids (PUFAs) extracted from fish oil have problems such as unstable yield, low yield, high cost, and other ω-6PUFAs. Nervous, traditional DHA resources have been unable to meet the growing market demand. Therefore, the development of new resources of DHA has be...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/12C12P7/64C12R1/89
Inventor 林祥志荣辉林秋云林汝榕张林吴欣李科马涌王昭凯杨善军
Owner THIRD INST OF OCEANOGRAPHY STATE OCEANIC ADMINISTATION
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