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Refrigeration
Pure cultures can be successfully stored at 0-4°C either in refrigerators or in cold-rooms. This method is applied for short duration (2-3 weeks for bacteria and 3-4 months for fungi) because the metabolic activities of the microorganisms are greatly slowed down but not stopped. Thus their growth continues slowly, nutrients are utilized and waste products released in medium. This results in, finally, the death of the microbes after sometime.
Pure cultures can be successfully stored at 0-4°C either in refrigerators or in cold-rooms. This method is applied for short duration (2-3 weeks for bacteria and 3-4 months for fungi) because the metabolic activities of the microorganisms are greatly slowed down but not stopped. Thus their growth continues slowly, nutrients are utilized and waste products released in medium. This results in, finally, the death of the microbes after sometime.
Paraffin Method/ preservation by overlaying cultures with mineral oil
This is a simple and most economical method of maintaining pure cultures of bacteria and fungi. In this method, sterile liquid paraffin in poured over the slant (slope) of culture and stored upright at room temperature. The layer of paraffin ensures anaerobic conditions and prevents dehydration of the medium. This condition helps microorganisms or pure culture to remain in a dormant state and, therefore, the culture can be preserved form months to years (varies with species). The advantage of this method is that we can remove some of the growth under the oil with a transfer needle, inoculate a fresh medium, and still preserve the original culture. The simplicity of the method makes it attractive, but changes in the characteristics of a strain can still occur.
This is a simple and most economical method of maintaining pure cultures of bacteria and fungi. In this method, sterile liquid paraffin in poured over the slant (slope) of culture and stored upright at room temperature. The layer of paraffin ensures anaerobic conditions and prevents dehydration of the medium. This condition helps microorganisms or pure culture to remain in a dormant state and, therefore, the culture can be preserved form months to years (varies with species). The advantage of this method is that we can remove some of the growth under the oil with a transfer needle, inoculate a fresh medium, and still preserve the original culture. The simplicity of the method makes it attractive, but changes in the characteristics of a strain can still occur.
Cryopreservation
Cryopreservation (i.e., freezing in liquid nitrogen at -196°C or in the gas phase above the liquid nitrogen at -150°C) helps survival of pure cultures for long storage times.
Cryopreservation (i.e., freezing in liquid nitrogen at -196°C or in the gas phase above the liquid nitrogen at -150°C) helps survival of pure cultures for long storage times.
In this method, the microorganisms of culture are rapidly frozen in
liquid nitrogen at -196°C in the presence of stabilizing agents such as
glycerol or Dimethyl Sulfoxide (DMSO) that prevent the cell damage due
to formation of ice crystals and promote cell survival. This liquid
nitrogen method has been successful with many species that cannot be
preserved by lyophilization and most species can remain viable under
these conditions for 10 to 30 years without undergoing change in their
characteristics, however this method is expensive.
Lyophilization (Freeze-Drying)
Freeze-drying is a process where water and other solvents are removed from a frozen product via sublimation. Sublimation occurs when a frozen liquid goes directly to a gaseous state without entering a liquid phase.It is recommend using slow rates of cooling as this will result in the formation of vertical ice crystal structures, thus allowing for more efficient water sublimation from the frozen product.
Freeze-dried products are hygroscopic and must be protected from moisture during storage.
Freeze-drying is a process where water and other solvents are removed from a frozen product via sublimation. Sublimation occurs when a frozen liquid goes directly to a gaseous state without entering a liquid phase.It is recommend using slow rates of cooling as this will result in the formation of vertical ice crystal structures, thus allowing for more efficient water sublimation from the frozen product.
Freeze-dried products are hygroscopic and must be protected from moisture during storage.
Under these conditions, the microbial cells are dehydrated and
their metabolic activities are stopped; as a result, the microbes go
into dormant state and retain viability for years. Lyophilized or
freeze-dried pure cultures and then sealed and stored in the dark at 4°C
in refrigerators. Freeze-drying method is the most frequently used
technique by culture collection centers. Many species of bacteria
preserved by this method have remained viable and unchanged in their
characteristics for more than 30 years.
Advantage of Lyophilization
*Only minimal storage space is required; hundreds of lyophilized cultures can be stored in a small area
* small vials can be sent conveniently through the mail to other microbiology laboratories when packaged in a special sealed mailing containers
* Lyophilized cultures can be revived by opening the vials, adding liquid medium, and transferring the rehydrated culture to a suitable growth medium.
*Only minimal storage space is required; hundreds of lyophilized cultures can be stored in a small area
* small vials can be sent conveniently through the mail to other microbiology laboratories when packaged in a special sealed mailing containers
* Lyophilized cultures can be revived by opening the vials, adding liquid medium, and transferring the rehydrated culture to a suitable growth medium.
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