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.
It is best to use an inoculating loop when making smears from liquid media because they allow you to pick up enough media to make a good smear. Needles do not pick up enough media.
Don't allow the loop to penetate into the agar as that will yield a clump of bacteria
Because the colonies will run together.
The function of a wire loop is to transfer small amount of bacterial culture into broth. It is also used to move an agar plate for its continued 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.
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..
The plate cover is raised and held diagonally to protect the plate surface from any contamination in the air.
A inoculating loop is used for transfers from culture plates to culture tubes instead of the inoculating needle because the needle could puncture the agar in tube. The loop is much easier as well to get liquid amount into the tube.
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.
The function of a wire loop is to transfer small amount of bacterial culture into broth. It is also used to move an agar plate for its continued 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.
"because otherwise you will kill the bacteria from the heat, and you may also melt the agar jelly that you are innoculating the bacterium onto."
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..
The ability of cells being allowed to swim into and out of the loop's water film rather than scraping the agar surface of growth and then emulsifying cells on the slide is due to its morphology. The path chosen is due to the cell's make up.
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.
The plate cover is raised and held diagonally to protect the plate surface from any contamination in the air.
It is a way to check that the loop isn't hot since you flamed it just before. I have seen some actually sizzle.
A inoculating loop is used for transfers from culture plates to culture tubes instead of the inoculating needle because the needle could puncture the agar in tube. The loop is much easier as well to get liquid amount into the tube.
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
* Wrong temperature in the incubator * Not enough time in the incubator * No culture was obtained on the inoculating loop * Wrong type of agar for optimum growth (nutrients,etc.)