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Trichoderma viride and culture method thereof

A technology of green Trichoderma and its cultivation method, which is applied in the field of bioengineering, can solve the problems of high cost of Trichoderma, limit the wide use of Trichoderma, and harsh production conditions, so as to increase the utilization rate of equipment, have good environmental benefits, and benefit the industry effect

Inactive Publication Date: 2017-09-01
CHAMBROAD CHEM IND RES INST CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The current culture method of Trichoderma mainly adopts the method of solid fermentation, and most of them use shallow plate fermentation and culture under constant temperature, humidity and sterile conditions. The production conditions are harsh, resulting in high cost of Trichoderma, which limits the wide use of Trichoderma. , the present invention has developed a low-cost, easy-to-implement method for the above-mentioned deficiencies

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] A kind of culture method of Trichoderma viride, its concrete steps are:

[0038] (1) Activation of Trichoderma viride strain

[0039] Place the Trichoderma viride strain on a PDA medium plate, culture it at 26°C for 4 days, and activate it;

[0040] (2) Preparation of liquid strains;

[0041] The activated Trichoderma viride strain was transferred to PD medium, cultured at 180rpm, 26°C for 48h;

[0042] Then transfer to Trichoderma viride liquid culture medium, 180rpm, 28 ℃ culture 48h;

[0043] Described Trichoderma viride liquid culture medium is by weight (w / w): glucose 0.3%, corn flour 2%, yeast extract powder 0.5%, magnesium sulfate 0.05%, potassium dihydrogen phosphate 0.04%, add water to 1000mL; The Erlenmeyer flask containing the above medium was sterilized in an autoclave at 121°C for 30 minutes;

[0044] The specific transfer process is as follows: on the aseptic operating table, use 10mL sterile water to make the bacteria suspension in the test tube slant...

Embodiment 2

[0053] A kind of culture method of Trichoderma viride, its concrete steps are:

[0054] (1) Activation of Trichoderma viride strain

[0055] Place the Trichoderma viride strain on a PDA medium plate, culture it at 30°C for 4 days, and activate it;

[0056] (2) Preparation of liquid strains

[0057] The activated Trichoderma viride strain was transferred to PD medium, cultured at 180rpm, 28°C for 24h;

[0058]Then transfer to Trichoderma viride liquid culture medium, 180rpm, 28 ℃ culture 48h;

[0059] Described Trichoderma viride liquid culture medium is by weight (w / w): glucose 0.5%, corn flour 1%, yeast extract powder 0.5%, magnesium sulfate 0.05%, potassium dihydrogen phosphate 0.04%, add water to 1000mL; The Erlenmeyer flask containing the above medium was sterilized in an autoclave at 121°C for 30 minutes;

[0060] The specific transfer process is as follows: on the aseptic operating table, use 10mL sterile water to make the bacteria suspension in the test tube slant c...

Embodiment 3

[0069] A kind of culture method of Trichoderma viride, its concrete steps are:

[0070] (1) Activation of Trichoderma viride strain

[0071] Place the Trichoderma viride strain on a PDA medium plate, culture it at 26°C for 7 days, and activate it;

[0072] (2) Preparation of liquid strains;

[0073] The activated Trichoderma viride strain was transferred to PD medium, cultured at 180rpm, 27°C for 36h;

[0074] Then transfer to Trichoderma viride liquid culture medium, 180rpm, 28 ℃ culture 48h;

[0075] Described Trichoderma viride liquid culture medium is by weight (w / w): glucose 0.3%, corn flour 2%, yeast extract powder 0.5%, magnesium sulfate 0.05%, potassium dihydrogen phosphate 0.04%, add water to 1000mL; The Erlenmeyer flask containing the above medium was sterilized in an autoclave at 121°C for 30 minutes;

[0076] The specific transfer process is as follows: on the aseptic operating table, use 10mL sterile water to make the bacteria suspension in the test tube slant...

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Abstract

The invention belongs to the technical field of biological engineering and in particular relates to trichoderma viride and a culture method thereof. The trichoderma viride provided by the invention is preserved in China General Microbiological Culture Collection Center (CGMCC), with the preservation number of CGMCC No. 5612. The culture method of the trichoderma viride, provided by the invention, mainly comprises the steps of activating trichoderma viride strains, preparing liquid strains, carrying out solid fermentation and drying, wherein solid fermentation adopts an edible mushroom fungus bag fermentation manner; according to the method provided by the invention, trichoderma viride spore powder is produced by utilizing a traditional edible mushroom production technology, so that the method has a reasonable process and low cost, is easy to implement and has good economic benefits, environment benefits and social benefits.

Description

technical field [0001] The invention belongs to the technical field of bioengineering, and in particular relates to a viride trichoderma and a cultivation method thereof. Background technique [0002] Trichoderma (Trichoderma spp.) belongs to the subphylum Deuteromycotina, Hyphophyceae, Synchospora, Cyclosporaceae, Myxosporum, widely exists in soil and air, and can survive in tropical to tundra zones It is the most studied plant biocontrol fungus so far. A large number of studies suggest that Trichoderma has multiple antagonistic mechanisms against plant pathogens, such as competition, reparasitism, enzyme lysis, antibiotic production, and induction of plant resistance. Most Trichoderma, such as Trichoderma viride, Trichoderma harzianum, Trichoderma korningen, Glioma viridans and other Trichoderma have broad-spectrum antagonistic effects, and the pathogenic fungi that can be antagonized include Rhizoctonia solani, Pythium, Phytophthora, Fusarium, white silkworm, etc. have ...

Claims

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Application Information

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IPC IPC(8): C12N1/14C12R1/865
CPCC12N1/14
Inventor 杨传伦马韵升张心青刘圣鹏徐泽平车树刚马娜娜秦培广冉新新王建平王春
Owner CHAMBROAD CHEM IND RES INST CO LTD