Preparation method of quantitative microorganism freeze-dried product

A technology of microorganisms and dry products, applied in the fields of biochemical equipment and methods, microorganisms, microorganisms, etc., can solve the problems of death of quality control strains, time-consuming, reducing work efficiency, etc., and achieve the effect of convenient inoculation and other operations and convenient use.

Active Publication Date: 2011-08-03
GUANGDONG HUANKAI MICROBIAL SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] So far, domestic strains have been in the form of relatively simple freeze-dried tubes, and there has been no research and development of strains with a certain amount of bacteria
In the process of opening the freeze-drying tube for resuscitation, a little carelessness may burst the freeze-drying tube, which is not only easier to contaminate the target bacteria, but also easier to burn or cut yourself, and it is easier to form aerosols during the operation, which is harmful to people. threat to the health of
[0007] At present, domestic grass-roots units and most production enterprises generally do not have strain management specialists, the preservation facilities are not compl...

Method used

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  • Preparation method of quantitative microorganism freeze-dried product
  • Preparation method of quantitative microorganism freeze-dried product

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preparation example Construction

[0027] A method for preparing a quantitative microbial freeze-dried product, comprising the following steps:

[0028] 1) Dilute the microorganisms in the stable period to obtain a uniform dilution and make a bacterial suspension with a quantitative concentration;

[0029] 2) Mix the bacterial suspension with the protective agent to obtain a mixed solution;

[0030] 3) Bottle the quantitative mixed solution, pre-freeze below -20°C, then vacuum freeze-dry and vacuum seal to obtain quantitative microbial freeze-dried products;

[0031] Wherein, the protective agent contains 0.1-10 parts by mass of water-soluble sugar, 0.1-5 parts by mass of skimmed milk powder, 0.1-20 parts by mass of gelatin, and 0-10 parts by mass of activated carbon.

[0032] Preferably, the pre-freezing temperature is -80 to -20°C.

[0033] Preferably, the protective agent contains 3-5 parts by mass of water-soluble sugar, 0.5-3 parts by mass of skimmed milk powder, 5-13 parts by mass of gelatin, and 0.01-4...

Embodiment 1

[0039] A method for preparing a quantitative microbial freeze-dried product, comprising the following steps:

[0040] 1) Dilute the standard bacterial strain Staphylococcus aureus ATCC6538 in the stable phase with 0.85% sterilized physiological saline, shake with an oscillator to obtain a uniform dilution, and make a bacterial suspension of quantitative concentration;

[0041] 2) Take quantitative bacterial suspension and protective agent by 10 8 The ratio of cfu / per gram of protective agent is mixed to obtain a mixed solution;

[0042] 3) Bottle the quantitative mixed solution, pre-freeze at -30°C, then vacuum freeze-dry, and vacuum seal to obtain quantitative microbial freeze-dried products;

[0043] Wherein, the protective agent is composed of 0.1 parts by mass of glucose, 4 parts by mass of skimmed milk powder, and 20 parts by mass of gelatin.

Embodiment 2

[0047] A method for preparing a quantitative microbial freeze-dried product, comprising the following steps:

[0048] 1) Dilute Escherichia coli CMCC (B) 44102 in the stable phase with 0.85% sterilized saline, shake with an oscillator to obtain a uniform dilution, and make a bacterial suspension of quantitative concentration;

[0049] 2) Take quantitative bacterial suspension and protective agent by 10 6The ratio of cfu / per gram of protective agent is mixed to obtain a mixed solution;

[0050] 3) Bottle the quantitative mixed solution, pre-freeze at -40°C, then vacuum freeze-dry, and vacuum seal to obtain quantitative microbial freeze-dried products;

[0051] Wherein, the protective agent is composed of 3 parts by mass of glucose, 3 parts by mass of skimmed milk powder, 8 parts by mass of gelatin, and 0.01 parts by mass of activated carbon.

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Abstract

The invention discloses a preparation method of a quantitative microorganism freeze-dried product. The preparation method comprises the following steps of: diluting microorganisms at a stable period to obtain uniform diluent and preparing the diluent into bacterial suspension with quantitative concentration; mixing the bacterial suspension with a protecting agent to obtain mixed liquor; and bottling quantitative mixed liquor, pre-freezing at the temperature of -30 DEG C, freezing and drying in vacuum, and sealing in vacuum to obtain the quantitative microorganism freeze-dried product, wherein the protecting agent comprises the following components in parts by weight: 0.1-10 parts of water-soluble sugar, 0.1-5 parts of defatted milk powder, 0.1-5 parts of antioxidant, 0.1-20 parts of gelatin and 0-10 parts of active carbon. The microorganism freeze-dried product prepared by adopting the preparation method contains basically quantitative microorganisms, and is convenient to use; and the activity of the microorganisms can be ensured when the product is stored at the temperature of below 8 DEG C, and the biological and chemical properties of the microorganisms do not change basically within the retention period.

Description

technical field [0001] The invention relates to a method for preparing a freeze-dried product of microorganisms, in particular to a method for preparing a quantitative freeze-dried product of microorganisms. Background technique [0002] Strains are an important biological resource, and strain preservation is an important basic work of microorganisms. The international community has always paid more attention to the preservation, sharing and exchange of microbial strain resources. As early as the end of the 19th century, Europe began to have some well-managed culture preservation institutions; in the early 20th century, some famous culture preservation institutions were established one after another. In 1904, NRRL was established in the United States, and in 1925, ATCC was established. At present, ATCC has developed Become the world's largest culture preservation and supply center. [0003] The preservation of quality control strains has been studied abroad, and its princip...

Claims

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Application Information

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IPC IPC(8): C12N1/00
Inventor 苏丽春何天文陈佐威卢勉飞蔡芷荷吴清平
Owner GUANGDONG HUANKAI MICROBIAL SCI & TECH
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