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Rachel Adams, Eleutherios

Kallergis, Jennifer Perera


Gene Expression
Conclusions:
Background/ Introduction: The predictions of the plasmid pUC18 causing
Gene expression is the process by which a growth on the agar plate was proven correct. E. coli
gene gets turned on in a cell to make RNA and grows exponentially with the aid of the plasmid
proteins. Gene expression may be measured Replace this with a graph/image/figure to since it is resisting the effects of ampicillin. Possible
by looking at the RNA, or the protein made sources of error would be that we did not get
aid in presenting your results. Don’t forget enough pUC18 with the LB/Amp 18 agar plate due to
from the RNA, or what the protein does in a
cell. In this experiment, we see how plasmids to add figure labels and captions little colonial growth instead of more colonies, like
react with bacteria. The plasmid used in this expected. Some questions that remain are, would
experiment is pUC18; an ampicillin-resistant scientist ever be able to manipulate ampicillin so it
gene that enables E. coli to grow in the can resist the effects of pUC18?
presence of an antibiotic.
Fun Facts
Materials and Methods: • The most common way to get E. coli is
through contaminated food such as
Results:
Two agar plates with Luria Broth-agar and two
plates with Luria Broth-agar and ampicillin was
meat, milk and produce
used. Using a sterile micropipette, 25 ul of cells As shown above, the agar plates with LB 18 and LB NP created • E. coli is a type of bacteria that normally
from the Eppendorf tubes labeled NP was lawn growth while LB/Amp 18 showed colonial growth. The lives inside our intestines, where it helps
dispensed into the LB NP plate. Similarly, 25 ul from reason while there is colonial growth is that pUC18 is resisting the body break down and digest food.
the Eppendorf tube labeled NP was dispensed into the ampicillin causing growth to occur. On the agar plate labeled • More than 700 serotypes of E. coli have
the LB/AMP NP plate. For the third and fourth agar LB/Amp NP, there is no growth because it is just ampicillin, no been identified.
plates, we dispensed 27 ul onto the LB P and plasmid resisting the antibiotic.
LB/Amp P plate. Both using a sterile micropipette
to obtain the plasmids from the Eppendorf tubes. PRO T IP! On agar plate labeled LB/Amp NP you see the Work Cited:
The cells were spread using the cell spreader after agar plate is damaged, this is why it is important to wait https://www.mayoclinic.org/diseases-conditions/e-coli/symptoms-causes/syc-
20372058#:~:text=The%20most%20common%20way%20to,increasing%20the%20risk%20of%20cont
it was sterilized using the ethanol and a flame. until the spreader cools before touching agar plate. amination.
https://wickhammicro.co.uk/knowledge-and-education/escherichia-
coli#:~:text=Interesting%20Facts%3A&text=This%20bacteria%20is%20the%20best,Nobel%20prizes
%20associated%20with%20it.&text=More%20than%20700%20serotypes%20of,coli%20have%20bee
n%20identified.&text=It%20causes%20infection%20by%20producing,on%20the%20type%20of%20E
.

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