1.
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Obtain your team plates. Observe your set of “+pGLO” plates under room light and with UV light. Record numbers of colonies and color of colonies. Fill in the table below.
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2.
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What two new traits do your transformed bacteria have?
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The transformed bacteria glows green under the UV light and the bacteria is now resistant to the antibiotic ampicillin.
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3.
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Estimate how many bacteria were in the 100 uL of bacteria that you spread on each plate. Explain your logic.
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An E. Coli cell is about 2 micrometers cubed and 1 micrometer is equal to (1e+9), which is 1,000,000,000. Since we spread 100 microliters of bacteria onto each plate, there were 100 times 1,000,000,000 bacteria on the plate, equalling a total of 100,000,000,000 bacteria that we spread on each plate.
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4.
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What is the role of arabinose in the plates?
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The role of the arabinose was to help the bacteria glow and to actually activate the pGLO plasmid. As was stated in the vodcast, the protein GFP is supposed to make the bacteria glow, but in order for the GFP to be activated, the arabinose is used to trigger that protein, making the bacteria glow..
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5.
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List and briefly explain three current uses for GFP (green fluorescent protein) in research or applied science.
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6.
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Give an example of another application of genetic engineering.
Genetic engineering has many applications in the medical field. One of the earliest applications of genetic engineering in pharmaceuticals was gene splicing to mass produce insulin in the body.
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