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 .