Go to http://www.tsienlab.ucsd.edu/Images.htm
you will find bacterial colonies will and can express functional fluorescent proteins.
As for the plasmid pQE30, it looks to fit into the category of expression at this level.
I would describe the appearance of the plate and note the total number of colonies (305) present. It is important to record any distinct characteristics of the colonies, such as color, size, and shape, and make note of any patterns or distribution of the colonies on the plate.
A high plate count in microbiology typically refers to the presence of a large number of bacterial colonies on a culture plate. The specific threshold for what is considered "high" can depend on the type of sample being tested and the laboratory's protocols. In general, a plate with more than 300 colonies may be indicative of contamination or a high bacterial load.
Failure to obtain isolated colonies on a streak plate could be due to overcrowding on the plate, improper streaking technique, or contamination of the plate from the environment or the inoculation source. It is important to streak the plate in a way that allows for sufficient separation of individual colonies to form.
The surface colonies on a pour plate larger than those within the medium especially aerobic bacteria within the medium would be a restriction of growth. The restriction of growth would be due to the lack of oxygen.
If bacterial colonies are found only in the first section of a streak plate, it could be due to uneven streaking technique where the majority of the bacteria were deposited in the initial section. The subsequent sections may not have received enough bacterial cells to form visible colonies. It is important to ensure an even distribution of bacteria while streaking to obtain colonies throughout the plate.
No
How do colonies on the surface of a pour plate differ from those suspended in the agar?
You would expect to find it in the plate labeled LB-, because that specific plate is the control plate, meaning it has nothing added to it, like the amipicilin or pFlouroGreen plasmid.
I would describe the appearance of the plate and note the total number of colonies (305) present. It is important to record any distinct characteristics of the colonies, such as color, size, and shape, and make note of any patterns or distribution of the colonies on the plate.
The pour plate method often results in colonies developing both down throughout the agar and on the surface. This is because the pour plate involves mixing the bacteria with the agar before pouring it into the plate, allowing for colonies to form at different depths within the agar.
By pour plate and then counting the colonies.
To accurately count colonies on an agar plate, one should use a colony counter or a grid system to track and tally individual colonies. It is important to ensure the plate is properly labeled and incubated under the correct conditions to allow colonies to grow distinctively. Counting should be done systematically and consistently to avoid errors.
Microbe colonies develop in larger sizes on sparsely seeded plates due to the abundance of plate surface they have for growth. Heavily seeded plates produce smaller colonies as they are forced to compete with one another for basic survival.
A high plate count in microbiology typically refers to the presence of a large number of bacterial colonies on a culture plate. The specific threshold for what is considered "high" can depend on the type of sample being tested and the laboratory's protocols. In general, a plate with more than 300 colonies may be indicative of contamination or a high bacterial load.
Failure to obtain isolated colonies on a streak plate could be due to overcrowding on the plate, improper streaking technique, or contamination of the plate from the environment or the inoculation source. It is important to streak the plate in a way that allows for sufficient separation of individual colonies to form.
The surface colonies on a pour plate larger than those within the medium especially aerobic bacteria within the medium would be a restriction of growth. The restriction of growth would be due to the lack of oxygen.
If bacterial colonies are found only in the first section of a streak plate, it could be due to uneven streaking technique where the majority of the bacteria were deposited in the initial section. The subsequent sections may not have received enough bacterial cells to form visible colonies. It is important to ensure an even distribution of bacteria while streaking to obtain colonies throughout the plate.