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Preparation method of quantitative microorganism freeze-dried product

A technology of microbial strains and dry products, applied in the direction of biochemical equipment and methods, microorganisms, microorganisms, etc., can solve the problems of time-consuming, death of quality control strains, increase of enterprise costs, etc., and achieve the advantages of convenient use, convenient inoculation and other operations Effect

Active Publication Date: 2012-11-14
GUANGDONG HUANKAI MICROBIAL SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] At present, domestic grass-roots units and most production enterprises generally do not have strain management specialists, the preservation facilities are not complete, and the professional operation level of microbiological inspection personnel is not high, so it is relatively easy to cause death, Variation, contamination, etc.
Moreover, the preserved strains often need to go through cumbersome processes such as resuscitation, transfer, and dilution during use, which not only consumes time and a lot of manpower and material resources, but also may affect the accuracy and reliability of the test results, seriously reducing work. Efficiency, so that the quality of the product cannot be guaranteed. If the experiment fails due to the strain problem, re-sampling is required, which delays the sales of the product and increases the cost of the enterprise.

Method used

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

Examples

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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 6 The 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, whereinthe 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 theactivity 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 present invention involves a method of preparing a microbial frozen -drying product, which specializes in a preparation method for quantitative microbial frozen dried products. Background technique [0002] A variety of bacteria is an important biological resource. The storage of bacteria is an important microbial basic work. Internationally, it has always paid more attention to the preservation and sharing exchanges of microbial fungus resources.As early as the end of the 19th century, Europe began to have some standardized bacteria storage agencies; in the early 20th century, some famous bacteria storage agencies were established one after another. The NRRL in 1904 was established in the United States. In 1925Become the world's largest bacterial storage supply center. [0003] The preservation of the mass control strain has been studied abroad. The principle is the same as the preservation of general bacteria. The current preservation methods adopted ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
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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