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New fermentation method

A fermentation method and seed technology are applied in the new fermentation field of microorganisms, which can solve the problems of insufficient oxygen supply, large bacterial content, mixed carriers, etc., and achieve the effects of simple preservation and processing technology, reduction of environmental pollution, and simple operation.

Active Publication Date: 2014-06-04
GUANGZHOU BAIWO BIOTECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] 1. The sterilization and disinfection of materials is difficult to do thoroughly, and the cost is high, which can easily cause bacterial contamination and affect product quality
[0014] 2. It is limited to microorganisms that grow in low humidity conditions, so the possible processes and products are more likely to be restricted, and generally more suitable for fungi
[0015] 3. It is not easy to evenly distribute substances and energy by stirring, so during the fermentation period, the addition of substances cannot be uniform, and the fermentation effect is not uniform.
[0016] 4. Fermentation in a relatively dense environment often causes problems with heat dissipation, and the lower part of the material is often insufficiently ventilated. In the case of uneven stirring, the growth of oxygen-consuming bacteria is not good, especially in mass production, which often limits its size. Scale capacity
[0017] 5. It is not easy to extract pure bacteria, often mixed with the carrier
[0018] 6. The subsequent drying process usually uses hot air drying, which causes a large loss in the number of viable bacteria
[0019] 7. The order of magnitude of the bacteria content of the finished product generally does not exceed about 100 billion / g, and it is usually difficult to reach about 100 billion / g

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Embodiment 1: the fermentative production of denitrifying pseudomonas

[0039] 1. Preparation of culture medium

[0040] 1. Seed culture medium (according to 1000mL)

[0041] Glucose 10g, dipotassium hydrogen phosphate: 1g, potassium dihydrogen phosphate: 1g, sodium citrate: 10g, potassium nitrate: 5g, magnesium sulfate: 0.2g, yeast extract: 1g, add water to a total volume of 1000mL, and adjust the pH to 8 .

[0042] Divide into 500mL Erlenmeyer flasks, each with 400mL of liquid; sterilize for 40min.

[0043] 2. Solid plate of fermentation medium (according to 1000mL)

[0044] Glucose 5g, flour 2g, fish meal 15g, potassium nitrate 5g, dipotassium hydrogen phosphate 1g, potassium dihydrogen phosphate 1g, magnesium sulfate 0.5g, yeast extract 0.2g, agar 20g, add water to a total volume of 1000mL, and adjust the pH to 8.0.

[0045] Fishmeal treatment: Boil fishmeal with a certain amount of water for 20-30 minutes, and the amount of water needs to be calculated into the...

Embodiment 2

[0058] Embodiment 2: Bacillus subtilis plate fermentation production technology

[0059] 1. Preparation of culture medium

[0060] 1. Seed medium (according to 1000mL)

[0061] Beef extract 3g, peptone 10g, sodium chloride 5g, glucose 10g, add water to 1000mL, adjust pH8.

[0062] Divide into 500mL Erlenmeyer flasks, each with 250mL of liquid; sterilize for 30min.

[0063] 2. Fermentation medium (according to 1000mL)

[0064] Waste molasses 20mL, flour 2g, fish meal 15g, liquid protein 10mL, manganese sulfate 1g, dipotassium hydrogen phosphate 1g potassium dihydrogen phosphate 1g, magnesium sulfate 0.5g, yeast extract 0.2g, agar 20g, add water to 1000ml, adjust pH to 8 . The treatment of fish meal and the preparation of plate culture medium are as in Example 1.

[0065] 2. Fermentation production:

[0066] 1. Seed Preparation

[0067] Aseptic operation, after activating the strain, take 2 to 3 rings of bacterial sludge into a triangular flask of seed medium, and cultiva...

Embodiment 3

[0078] Embodiment 3: Lactobacillus acidophilus plate fermentation production process

[0079] 1. Preparation of culture medium

[0080] 1. Seed medium (according to 1000mL)

[0081] Beef extract 10g, peptone 10g, whey powder 10g, glucose 20g, dipotassium hydrogen phosphate: 2g, manganese sulfate: 0.3g, diammonium citrate: 10g, sodium acetate: 2g, magnesium sulfate: 0.6g, yeast extract: 5g , Tween 801mL, add water to 1000mL, adjust pH to 6.2-6.4.

[0082] Divide into 500mL Erlenmeyer flasks, each with 300mL of liquid; sterilize for 20min.

[0083] 2. Fermentation medium (according to 1000mL)

[0084] Fish meal 20g, glucose 20g, whey powder 10g, agar 30g, dipotassium hydrogen phosphate: 2g, manganese sulfate: 0.3g, sodium acetate: 2g, magnesium sulfate: 0.6g, yeast extract: 2g, Tween 801-2mL, add water to 1000mL and adjust the pH to 6.2-6.4.

[0085] The treatment of fish meal and the preparation of plate culture medium are as in Example 1.

[0086] 2. Fermentation product...

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PUM

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Abstract

The invention discloses a new fermentation method, which mainly comprises the following steps of: (1) preparing liquid seeds; (2) preparing a solid plate: adding 18 to 32g of agar into each 1,000 ml of corresponding liquid fermentation culture medium for strict anaerobes, sterilizing, pouring into a plate, cooling, and preparing a solid plate culture medium containing liquid culture medium components by utilizing the solidification capacity of the agar on liquid; and (3) performing amplified fermentation: spraying the corresponding liquid seeds obtained by the step (1) to the surface of the solid plate uniformly, putting the sprayed solid plate in a fermentation chamber at the constant temperature of between 35 and 37 DEG C for closed fermentation culture, culturing for 24 to 72 hours according to different bacterial strains, and collecting bacterial sludge. The method has the advantages of low cost, simple operation, easy subsequent processing and suitability for the production of most of microbial bacterial strains; and through the method, products which break through the upper limit of bacterial concentration in the conventional microbial preparation products greatly can be produced, and about 1,000 billion / g bacterial powder products can be obtained.

Description

technical field [0001] The invention belongs to the field of microorganism cultivation, and in particular relates to a novel fermentation method of microorganisms. Background technique [0002] At present, in industrial fermentation, the main fermentation processes can be classified into solid-state fermentation and liquid fermentation. [0003] Liquid fermentation is a culture in which bacteria are inoculated into a fermenter, the bacteria cells are suspended in a liquid fermentation medium, and the growth is carried out by controlling parameters such as temperature, stirring, air, pressure, and nutrient concentration. method. Submerged liquid culture generally requires air and stirring, which is a traditional microbial fermentation culture method. It mainly has the disadvantages of expensive equipment, complex operation, low concentration of bacterial cells produced per unit culture medium, and high cost of bacterial liquid separation. [0004] Solid fermentation includ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/20C12R1/38C12R1/125C12R1/23
Inventor 张子曦
Owner GUANGZHOU BAIWO BIOTECH CO LTD
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