In this case, we need to understand what means each part of the treatments and what the goal is. I assume that we are looking to determinate the difference between an resistance strain and a non resistant strain in contact with an antibiotic. “ampR” means the ampicillin resistance gene. Ampicillin is the antibiotic and the E.coli is the specie.
Plate 1: Control Awar with E.coli + ampR: In this plate, we will observe a normal growth rate of the bacteria.
Plate 2: Agar + ampicillin with E.Coli + ampR : In this case, the E.coli is resistant against penicillin, so we should observe similar results than in Plate 1. A normal growth.
Plate 3: Control Agar with E.coli – ampR : Here, we will observe a normal growth because the agar plate does not posses any antibiotic and the bacteria wont be affected
Plate 4: Agar + ampicillin with E.coli- ampR: Finally, we will observe a reduced growth in comparison with the rest of the plates because the bacteria is not resistant against ampicillin.
what is the prediction for each of these petri dishes Petri Dish #1: Control Agar with...
PART IV: We can model the equilibrium process using BB's to represent molecules and petri dishes to separate "reactant molecules" from "product molecules." 1) Consider the simple equilibrium A = B For this BI Кф [A] and we'll assign a value to Koq of 8. Keq = 8.0 Get 2 petri dishes and place 27 BB's in one of them. These represent 27 "A" molecules, while the empty dish shows that there are "B" molecules. no [B] value is 8...
Exercise 7 Experimental Variables EXERCISE 7: EXPERIMENTAL VARIABLES Determine the variables tested in the each of the following experiments. If applicable, determine and identify any positive or negative controls 1. A study is being done to test the effects of habitat space on the size of fish populations. Different sized aquariums are set up with six goldfish in each one. Over a period of six months, the fish are fed the same type and amount of food. The aquariums are...
3 poi 7. The number of cells in a petri dish grows exponential with time. The function h models the number of cells present after t hours. Based on the function, which statement is NOT true? h(t) = 50(2): There were 50 cells initially in the petri dish. O The predicted number of cells doubles every 15 minutes. O Approximately 400 cells will be in the petri dish after 12 hours The predicted number of cells doubles every 4 hours.
27. Two species of yeast persist indefinitely when each species is grown on agar in separate petri dishes in the lab. However, when the species are grown together on agar in the same petri dish, only a single species remains after a few days. What is the most likely explanation for the elimination of one of the species? a) Competition between the two yeast species resulted in a change in the way the two species used the limited resource (agar)....
GROUP (Report 1 Growth Curve 1) The following table shows the measurements of bacterial growth in a specific period by the color Spectrophotometer Time time 3 hour Growth measurement 7.56 7.56 30.25 32.25 6 hour 9 hour 12 hour 32.25 15 hour 2.69 A) Draw the growth curve for bacteria B) Write a discussion of the results (Abbreviator) 2) The plate was inoculation with a fungal disc 1 cm, and then incubated for 7 days and 25C * The following...
Cloning/Transformation Homework Please indicate what you would see on each media plate given the following conditions (blue colonies or white colonies) E. coli cell Nutrient agar plate, no ampicillin, no X- gal E. coli cell Nutrient agar plate with ampicillin added, no X-gal OM OM 01 01 E. coli cell with plasmid CO ОООО Nutrient agar plate with ampicillin & X- gal added E. coli cell with plasmid and correctly inserted Insulin gene in the multiple cloning site C LB...
1. Fill in the table above with what you observe on your
plates.
2. Bacterial transformation occurred on which agar plate (s)?
What evidence do you have that the bacteria were transformed
here?
3. Which plates have glowing growth? Explain what causes
bacteria to glow.
II. Transformation of E. coli with Plasmid DNA (PGLO) 1. Three LB (Luria Broth) agar plates are obtained. The plates contain: • Plate A: LB-Agar/Ampicillin/Arabinose • Plate B: LB-Agar/Ampicillin • Plate C: LB-Agar 2. Three...
Short answer. Write your answer in the space provided. (1 point each) 6. Order the steps for the preparation of growing bacterial cells on solid agar plate. . place the cells in the cold for short-term storage measure the ingredients and prepare the nutrient agar in a heat-resistant glassware pour the agar into a Petri dish and let it solidify autoclave at 121 °C for 15 psi the agar for 15 minutes transfer the bacterial cells to the agar in...
1. In a transformation experiment, E. coli uptake pRGLO plasmids that carry GFP gene. The transformed bacterial cells are grown on an ampicillin-treated agar plate. Which of the following is considered as a vector? GFP gene C E. coli cell c ampicillin-treated agar plate 0.5 points QUESTION 2 1. What is the function of bla gene? Break down the ampicillin Regulate the transcription of GFP gene Express the fluorescent trait in bacteria Control the uptake of DNA molecules in bacteria...
wa y LOUR at the petri dish at this station. Use the data in live answer questions 1 - 3. Assume same size (volume) Bean Picture Mass of 1 bean (g) white 0.14 Black 0.28 Green 0.14 yellow 0.22 Whicle bean as the highest mass density W elboan has the highest-numbur density 5 BeanCo 3. Imagine the beans are really molecules in a mixture. What is the mole percent of Bean C? There are a total of 24 beans in...