Preservation of Industrially Important Micro Organisms
The
selected microorganism of industrial interest must be preserved in its original
form for any further use and research. There are different methods for
microbial preservation. Suitable methods are selected based on the:
a. Type
of micro-organism
b. Effect
of the preservation method on the viability of micro-organism
c. Frequency
at which the cultures are withdrawn
d. Size
of the microbial population to be preserve
e. Availability
of resources
f. Cost
of the preservation method. Followings are some of the methods of microbial
preservation:
This
involves removal of water from the culture. Desiccation is used to preserve
actinomycetes (a form of fungi-like bacteria) for very long period of time. The
microorganisms can be preserved by desiccating on sand, silica gel, or paper
strips.
Microorganisms are grown on agar slopes in test
tubes and stored at 5 to −20 °C for
six months. If the surface area for growth is covered with mineral oil the
micro-organisms can be stored for one year.
This is the most commonly used technique to store
micro -organisms for a long period. Storage takes place at temperatures of
less than -196 °C and even less in vapour phase. Microorganisms are made stationary
and suspended in a cryoprotective agent before storing in liquid nitrogen.
This method is especially used for sporulating
microorganisms (organisms that produce spores). They are sterilized,
inoculated, and incubated to allow microbial growth, then dried at room
temperature. The resultant dry soil is stored at 4° to 5 °C.
This process is also known as freeze-drying. The
microbial culture is first filled in ampoules (glass vessels) and frozen, then
dried under vacuum. This is a most convenient technique, since it is cheap to
store and easy to ship. The disadvantage is that it is difficult to open the
freeze dried ampoules; also, several subcultures have to be done to restore
the original characteristics of the microorganisms.
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