Isolation of Pure Culture

A pure culture is usually derived from a mixed culture by transferring a small sample into a new, sterile growth medium in such a manner as to disperse the individual cells across the medium surface or by thinning the sample several times before inoculating the new medium. Hence, pure culture is defined as a laboratory culture containing a single species of organism.

Importance of Pure Culture

  • Desired known species of microorganisms can grow once pure culture is isolated.
  • Pure culture can be correctly identified for accurate study and testing of microorganisms in a clinical environment.
  • Experimenting with pure culture ensures the same results after the repetition of the experiment many times.
  • In pure culture, the spontaneous mutation rate is low.

Hence, pure culture is required to isolate which is carried out by:

  1. Streak plate method
  2. Pour plate method
  3. Spread plate method
  4. Serial dilution method
  5. Special methods:
  • (a) Single Cell Isolation Methods
  • (b) Enrichment Culture Method.
Types of isolation of pure culture
Flowchart: Types of isolation of the pure culture

1. Streak Plate Method

The principle of this method is that, by streaking, a dilution gradient is established across the face of the Petri plate where bacterial cells are deposited on the agar surface. This method is used most commonly to isolate pure cultures of bacteria where a small amount of mixed culture is placed on the tip of an inoculation loop and is streaked across the surface of the agar medium by different fashions (Fig. 1) and the plates are incubated to allow the growth of colonies and each colony is the progeny of a single microbial cell thus representing a clone of pure culture. Finally, the micro-organisms are separated from each other. The isolated colonies are picked up separately using a sterile inoculating loop and re-streaked onto fresh media to ensure purity.

Different types of streak plates
Fig. 1: Different types of streak plates

2. Pour Plate Method

The main principle of this method is a dilution of the inoculum in successive tubes containing liquefied agar medium to permit a thorough distribution of bacterial cells within the medium.

In this method, the mixed culture of bacteria is diluted directly in the liquid agar medium tube (42-45°C) and mixed well. In this method, a fixed amount of inoculum (generally 1 ml) from a broth/sample is placed in the center of a sterile petri dish using a sterile pipette. The contents of each tube are poured into separate Petri plates and then allowed to solidify. These plates are incubated to develop bacterial colonies both within the agar medium (subsurface colonies) and on the medium (surface colonies). Finally, isolated the colonies and are picked up by inoculation loop and streaked onto another Petri plate to insure purity (Fig. 2). This method is also used for determining the number of viable bacterial cells present in a culture.

Pour plate method
Fig. 2: Pour plate method

3. Spread Plate Method

The principle of this method involves using a sterilized spreader with a smooth surface made of metal or glass to apply a small number of bacteria suspended in a solution over a plate that needs to be dry and at room temperature so that the agar can absorb the bacteria more readily. A successful spread plate will have a countable number of isolated bacterial colonies evenly distributed on the plate.

The technique is easier to quantify bacteria in a solution. A drop of diluted liquid from each tube is placed on the center of an agar plate and spread evenly over the surface using a sterilized bent-glass-rod. The medium is incubated for the colonies development on the agar medium plates. The isolated colonies are picked up and transferred onto a fresh medium to ensure purity (Fig. 3).

Spread plate technique (Pure Culture)
Fig. 3: Spread plate technique

Some useful differences between pour plate and spread plate methods

ParametersPour plate methodSpread plate method
ProcedureInoculum from a sample is placed in the center of a sterile petri dish using a sterile pipette. Molten cooled agar (approx. 15 ml) is then poured into the petri dish containing the inoculum.Inoculum from a sample is pipette out and spread evenly on sterile nutrient agar by spreader.
AmountInoculum is 1 ml.Inoculum is 0.1 ml
MediumColonies are grown in solid culture medium.Colonies are grown in solid culture medium.
Sample ApplicationMore surface area is covered as the sample is spread throughout the media.The sample is spread only to a limited area i.e. only on the surface of the agar.
UsesIt is used to determine CFU/ml or PFU/ml.It is used to isolate specific clonal colonies.
Advantages1. It allows the growth of microaerophiles. 2. It helps in the identification of various bacteria, like an aerobe, anaerobe, or facultative aerobe bacteria.1. Picking surface colonies will not interrupt other colonies by digging out of agar. 2. Get even distribution of colonies.
Disadvantages1. Picking subsurface colonies can interrupt other colonies by digging out of agar. 2. Do not get even distribution of colonies.1. It does not allow the growth of microaerophiles. 2. It does not allow the growth of obligate anaerobes.
BenefitIt is beneficial to isolate certain bacteria which are motile and do not grow as a colony.It is beneficial for the isolation of bacteria from soil or water.
ApplicationThis technique is used in Bacteriologic examination of milk, a bacterial number of urine to signify urinary tract infection.This technique is used in enrichment, selection, and screening experiment.

4. Serial Dilution Method

A microorganism that predominates in a mixed culture can be isolated in pure form by a series of dilutions. The inoculum is subjected to serial dilution in a sterile liquid medium, and a large number of tubes of the sterile liquid medium are inoculated with aliquots of each successive dilution.

This dilution aims to inoculate a series of tubes with a microbial suspension so dilute that there are some tubes showing growth of only one individual microbe. Example: A culture containing 10 ml of liquid medium, containing 1,000 microorganisms i.e., 100 microorganisms/ml of the liquid medium. 1 ml of this medium is taken out and mixed with 9 ml of fresh sterile liquid medium, then resulted in the medium having 100 microorganisms in 10 ml or 10 microorganisms/ml. Further 1 ml of this suspension is added to another 9 ml of fresh sterile liquid medium, each ml is now contained a single microorganism. If this tube showed any microbial growth, there is a very high probability that this growth has resulted from the introduction of a single microorganism in the medium and represents the pure culture of that microorganism (Fig. 4).

Serial dilution method (Pure Culture)
Fig. 4: Serial dilution method

5. Special Methods

(a) Single Cell Isolation methods

An individual cell is picked out by this method from the mixed culture and is allowed to grow to procure pure culture. There are two methods used for the isolation of a single cell:

(i) Capillary pipette method: Several small drops of a suitably diluted culture medium are placed on a sterile glass-coverslip by a sterile pipette. Examine then each drop under the microscope until find one microorganism in one drop. This drop is then removed with a sterile capillary pipette to fresh medium for multiplication to yield a pure culture (Fig. 5).

Capillary pipette method (Pure Culture)
Fig. 5: Capillary pipette method

(ii) Micromanipulator method: Micromanipulators permits one to pick out a single cell from a mixed culture. This instrument is used in conjunction with a microscope to pick a single cell (particularly bacterial cell) from a hanging drop preparation. The micromanipulator has micrometer adjustments with a micropipette that can move in all directions. A series of hanging drops of a diluted culture is placed on a special sterile coverslip by a micropipette. Hanging drop is searched for a single microorganism cell. This cell is drawn into the micropipette by gentle suction and then transferred to a large drop of the sterile medium on another sterile coverslip. When the number of cells increases in that drop, the drop is transferred to a culture tube having a suitable medium that yields a pure culture of the required microorganism.

Advantage: It can be reasonably sure that the cultures come from a single cell. It can obtain strains within the species.

Disadvantage: The equipment is expensive and requires a skilled operator.

(b) Enrichment Culture Method:

This method is used to isolate those microorganisms that are present in relatively small numbers or have slow growth rates in the mixed culture. The enrichment culture strategy provides a specially designed cultural environment by incorporating a specific nutrient in the medium and by modifying the physical conditions of the incubation. The medium of known composition and specific condition of incubation favors the growth of desired microorganisms. This method is unsuitable for the growth of other types of microorganisms.

Make sure you also check our other amazing Article on : Bacterial Growth Curve
Sharing Is Caring:

Leave a Comment