Culture collection process

A kind of strain preservation and strain preservation technology, applied in the field of strain preservation, can solve the problems of people who have no relevant knowledge, such as illness, insolvability, and environmental pollution, and achieve the effects of prolonging the preservation time, improving production efficiency, and reducing damage

Inactive Publication Date: 2008-11-19
药大制药有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

This method is very wasteful, and the disposal of the waste after the use of the same strains must be very careful. If you are not careful, it will pollute the environment, and even cause people wit

Method used

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  • Culture collection process

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Example Embodiment

The dry powder medium was added with purified water to make a semi-solid medium. In terms of mass, the composition of the dry powder medium is as follows:

Peptone 10

Sodium chloride 5

Beef Dip Powder 3

Agar 4

Divide and sterilize. Each test tube is filled with 10-20ml of culture medium, placed vertically in the incubator and cultured for 2 to 3 days, observe and test, and proceed to the next step after confirming the sterility. This step is to ensure that the purity of the inoculated bacteria is not destroyed by the bacteria. Pick a small amount of the prepared strain with an inoculation needle, puncture and inoculate it into the semi-solid medium, and puncture and inoculate 3 points parallel to the circular plane to ensure that the strain is surely inoculated into the medium. Pour 1~2cm high sterile liquid paraffin, stopper the test tube firmly, seal the bottle with a sealing film, and store it vertically in a refrigerator at 6~8℃.

Table 1 shows the relative bacterial concen...

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Abstract

The invention provides a spawn preservation method adopting semisolid low-temperature air-tight culture. A spawn is inoculated in an aseptic semisolid culture medium which is vertically stored at an ambient temperature of between 6 and 8 DEG C after aseptic liquid paraffin is added into the culture medium. The spawn is staphylococcus aureus, escherichia coli, pseudomonas aeruginosa, bacillus subtilis, clostridium orogenes, aspergillus niger or candida albicans. The specific process is as follows: preparing the semisolid culture medium, carrying out sub-package and sterilization, and then culturing for 2 to 3 days, inoculating the spawn into the semisolid culture medium in a mode of stab inoculation after asepsis is ensured, with the number of stab inoculation points parallel with the plane of the culture medium being no less than 3; pouring the aseptic liquid paraffin with a height of 1 to 2 cm into the culture medium which is sealed by a sealing film and is stored in a refrigerator at a temperature of between 6 and 8 DEG C. The method can not only prolong the spawn preservation time but also keep a relatively stable spawn concentration, thereby saving much cost for production and test, reducing the treatment and discharge of rejected material after spawn use, and reducing environmental hazard.

Description

technical field The invention relates to a strain preservation method. Background technique According to the "Pharmacopoeia of the People's Republic of China", the use of bacterial strains in the microbial limit test and sterility test of drugs is a must for positive controls. Required in validation. Therefore, the use and preservation of strains has always been the focus of microbiology laboratories for a long time. There are 7 strains commonly used, namely: Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, Clostridium sporogenes, Aspergillus niger, and Streptococcus albicans. At present, domestic drug manufacturers have been using the strain preservation technology many years ago, because this method has been used for many years and is relatively stable and reliable. This method is as follows: the bacterial strains purchased from the drug inspection institute and stored on a low-temperature inclined plane are used normally. The purchas...

Claims

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Application Information

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IPC IPC(8): C12N1/04C12R1/445C12R1/19C12R1/385C12R1/125C12R1/01C12R1/685C12R1/725
Inventor 王卉刘明越蔡振利
Owner 药大制药有限公司
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