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Streaking is to produce single colonies. If we are digging to the agar while streaking the microbes, instead of growing on the agar surface grows in the subsurface as well. These colonies may be difficult to isolate.

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Why is it necessary to touch a sterile part of the agar with the loop before touching the bacterial growth?

It is a way to check that the loop isn't hot since you flamed it just before. I have seen some actually sizzle.


What does it mean to inoculate an agar plate?

Inoculating an agar plate refers to transferring microorganisms onto the surface of the agar using a sterile inoculating loop. This allows the microorganisms to grow and form visible colonies that can be studied or identified.


When bacteria from a throat swab are streaked on blood agar why is the agar stabbed several times with the loop?

first of all the method of stabbing the agar is no only for throat sample but can be for all specimen except for liquid samples such as urine. the second thing is by stabbing the loop, you can save your time to sterile the loop back. and the other thing is to make sure the loop are no hot anymore..


How is air contamination prevented when an inoculating loop is used to introduce or take a bacterial sample from an agar plate?

Air contamination is prevented by sterilizing the inoculating loop with a Bunsen burner flame before and after use. This kills any potential airborne bacteria that could contaminate the sample. It's also important to keep the agar plate closed as much as possible while transferring the sample to further reduce the risk of contamination.


What is the procedural difference between using broth and agar as a source of bacteria for preparing a smear?

If your colonies were grown in broth, you can simply use your loop to collect loopfuls of liquid medium and smear that onto a glass slide. If they were grown on an agar plate you would have to add a few drops of water to the surface of the glass slide.

Related Questions

How do you determine when a loop is cool?

Touch it to the sterile agar in a plate. If it melts the agar, it is still hot. If it doesn't melt the agar, then it is cool enough.


Why is it necessary to touch a sterile part of the agar with the loop before touching the bacterial growth?

It is a way to check that the loop isn't hot since you flamed it just before. I have seen some actually sizzle.


What does it mean to inoculate an agar plate?

Inoculating an agar plate refers to transferring microorganisms onto the surface of the agar using a sterile inoculating loop. This allows the microorganisms to grow and form visible colonies that can be studied or identified.


Why is it necessary to cool the hot inoculating loop before placing it on the nutrient plate?

Cooling the hot inoculating loop before placing it on the nutrient plate helps prevent damage to the agar and cells in the culture. Placing a hot loop directly onto the agar can cause the agar to melt, killing the organisms in the culture and disrupting the growth surface. Additionally, cooling the loop ensures that the inoculation is done with precision to prevent contamination and ensure accurate results.


When bacteria from a throat swab are streaked on blood agar why is the agar stabbed several times with the loop?

first of all the method of stabbing the agar is no only for throat sample but can be for all specimen except for liquid samples such as urine. the second thing is by stabbing the loop, you can save your time to sterile the loop back. and the other thing is to make sure the loop are no hot anymore..


How do you set up a culture of bacteria on an agar plate?

To set up a culture of bacteria on an agar plate, first, ensure that all materials are sterile to prevent contamination. Using a sterile inoculating loop or swab, obtain a sample of the bacteria you wish to culture. Gently streak the loop across the surface of the agar in a zigzag or quadrant pattern to spread the bacteria. Finally, incubate the plate at an appropriate temperature for the specific bacteria, typically inverted to prevent condensation from dripping onto the agar surface.


What is the name of the streak when you apply specimen to agar plate?

The process of applying a specimen to an agar plate to grow colonies is known as streaking. This technique involves using an inoculating loop to spread the specimen across the surface of the agar in a pattern that promotes the isolation of individual colonies for further study.


What are the steps in properly streaking a plate?

When we have to isolate a specific microbial species from their mix culture or to grow any microbe on solid surface for their further studies then they can be grow on a culture medium containing a gel like substance known as agar which produce disticnt microbial colonies when inoculate in a petri dish containing the growth medium. The way by which the inoculation of microbial sample done is called a streak plate method in which the microbial sample is streak with the help of inoculating loop on the agar plate firmly, in the way so that the cell can be isolated. There are two more method to incoulate the microbial sample that are: pour plate and spread plate techniques.


When getting inoculums from a slant why is it necessary to touch a sterile part of the agar with the loop before touching the bacterial growth?

It is a way to check that the loop isn't hot since you flamed it just before. I have seen some actually sizzle.


Agar agar grain found in Germany?

Agar, or agar-agar, is not a grain, but rather an extract of seaweed. Agar translates to German as Agar-Agar Try whole- or health-food stores


How is air contamination prevented when an inoculating loop is used to introduce or take a bacterial sample from an agar plate?

Air contamination is prevented by sterilizing the inoculating loop with a Bunsen burner flame before and after use. This kills any potential airborne bacteria that could contaminate the sample. It's also important to keep the agar plate closed as much as possible while transferring the sample to further reduce the risk of contamination.


What is the procedural difference between using broth and agar as a source of bacteria for preparing a smear?

If your colonies were grown in broth, you can simply use your loop to collect loopfuls of liquid medium and smear that onto a glass slide. If they were grown on an agar plate you would have to add a few drops of water to the surface of the glass slide.