Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Liquid deep layer fermenting process for producing extracellular polysaccharide using medicinal fungus long root mushroom

A technology of liquid submerged fermentation and extracellular polysaccharide, applied in the field of bioengineering, can solve the problems of late start of research, long cycle and low yield.

Inactive Publication Date: 2005-10-19
SOUTHWEST UNIV
View PDF0 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Long root mushroom is a new type of medicinal fungus introduced and cultivated in China in recent years. It is currently in the cultivation test and promotion stage. Due to the shortcomings of solid cultivation, such as long cycle, low yield, and climate impact, its large-scale development and use are limited, and liquid cultivation is used. Submerged fermentation culture technology is currently a new production method for in-depth development of active polysaccharide resources of medicinal fungi, and has successfully achieved large-scale production in rare medicinal fungi such as Ganoderma lucidum, Lentinus edodes, Grifola frondosa, and Agaricus blazei. The research on liquid submerged fermentation technology started relatively late, especially in the engineering research on the production of active polysaccharides by fermenting rhizome mushrooms on the reactor, and there are no relevant reports yet.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Embodiment 1 (adding palmitic acid, fermentation control time 110 hours)

[0023] Strains: Oudemansiella radicata No. 1, purchased from the Strain Experimental Center of Huazhong Agricultural University.

[0024] (1) Test tube slant culture: cultivate slant strains in test tubes

[0025] Culture medium: PDA medium adds the bran juice of 5% (percentage by weight)

[0026] Culture conditions: culture temperature 26°C, culture time 8 days, pH 6.7.

[0027] (3) Shake flask seed culture

[0028] Seed medium (g / L): corn flour 10, peptone 2, soybean cake powder 3, sucrose 20, KH 2 PO 4 2. MgSO 4 ·7H 2 O2, VB 1 0.1;

[0029] Culture conditions: Cut the activated slant strains into soybean-sized mycelium pieces, inoculate 2-3 pieces into the liquid seed medium, fill the liquid in a 500ml triangular bottle with 100ml, cultivate on a rotary shaker, the speed is 180rev / min, and the culture temperature 26°C, pH 6.5, culture time 7 days.

[0030] (4) 7L fermenter culture ...

Embodiment 2

[0033] Embodiment 2 (do not add palmitic acid technology, fermentation control time 110 hours)

[0034] Strains: Oudemansiella radicata No. 1, purchased from the Strain Experimental Center of Huazhong Agricultural University.

[0035] (1) Test tube slant culture: cultivate the slant strains in the test tube,

[0036] Culture medium: PDA medium adds the bran juice of 5% (percentage by weight)

[0037] Culture conditions: culture temperature 28°C, culture time 10 days, pH 6.7.

[0038] (2) Shake flask seed culture

[0039] Seed medium (g / L): corn flour 20, peptone 2, soybean cake powder 3, sucrose 20, KH 2 PO 4 2. MgSO 4 ·7H 2 O 1, VB 1 0.1.

[0040] Culture conditions: Cut the activated slant strains into soybean-sized mycelium pieces, inoculate 2-3 pieces into the liquid seed medium, fill the liquid in a 500ml triangular bottle with 100ml, cultivate on a rotary shaker, the speed is 200rev / min, and the culture temperature 26°C, pH 6.5, culture time 7 days.

[0041] (...

Embodiment 3

[0044] Embodiment 3 (adding palmitic acid, fermentation control time is 113 hours)

[0045] Strains: Oudemansiella radicata No. 1, purchased from the Strain Experimental Center of Huazhong Agricultural University.

[0046] (1) Test tube slant culture: cultivate slant strains in test tubes

[0047] Culture medium: PDA medium adds the bran juice of 5% (percentage by weight)

[0048] Culture conditions: culture temperature 26°C, culture time 8 days, pH 6.5.

[0049] (2) Shake flask seed culture seed medium (g / L): corn flour 10, peptone 2, soybean cake powder 3, sucrose 20, KH 2 PO 4 2. MgSO 4 ·7H 2 O1, VB 1 0.1;

[0050] Culture conditions: Cut the activated slant strains into soybean-sized mycelium pieces, inoculate 2-3 pieces into the liquid seed medium, fill the liquid in a 500ml triangular bottle with 100ml, cultivate on a rotary shaker, the speed is 160rev / min, and the culture temperature 26°C, pH 6.5, culture time 8 days.

[0051] (3) 7L fermenter culture

[005...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The deep fermentation process uses the spawn of Oudemansiella radicata from Central-China Agricultural Univ. and includes the following steps: slant spawn culture, shake flask seed culture, 7L fermenting tank culture, and polysaccharide extraction and determination. The present invention selects corn powder and soybean cake powder as main fermentation material and has low production cost. It is found that palmitic acid is key nutritious additive factor capable of raising the yield of extracellular polysaccharide of Oudemansiella radicata up to 30-40 %. The fermentation process is controlled through on-line control of variation in dissolved oxygen concentration. The present invention can realize large scale fermentation with simple technological operation, and is suitable for industrial production.

Description

Technical field: [0001] The invention belongs to the technical field of bioengineering, and is a technique for preparing known or new organisms or their metabolites by cultivating and fermenting organisms. In particular, it relates to a liquid submerged fermentation process for producing exopolysaccharides by using the medicinal fungus Rhizome pilosula. Background technique [0002] Long-rooted mushroom (Oudemansiella radicata), also known as Oudemansiella radicata, long-rooted small Oudemansiella, big hair grass fungus, long-rooted money fungus, etc. Belongs to Basidiomycotina, Phytomycetes, Agaricales, Oleumaceae, and Ouderia genus. Long root mushroom is the top grade edible, with tender inner quality, crisp and delicious handle, rich in protein, amino acid, fat, carbohydrates, vitamins and trace elements, with high edible value, and is a rare edible and medicinal fungus. In 1977, the Japanese scholar Shigebe Oto and others confirmed that the polysaccharides of rhizome m...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12P19/04
Inventor 邹祥胡昌华
Owner SOUTHWEST UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products