13. The following dilutions were performed to determine the concentration of bacteria in a culture. What was the concentration of bacteria in the stock? 2 mL 1 mL 5 mL 10 mL 0.2 mL stock 6 mL 8 mL 20 mL 10 mL 150 colonies
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- 3. You were instructed to add 2.75 mL out of 5.0 mL of an undiluted sample to 125.25 mL of sterile diluent. Instead, you add all 5.0 mL to the 125.25 mL, What was the intended dilution and what was the actual dilution? ited States) E Focus OCT 30 W MacBook P DII DD F7 F8 F9 F10 F4 F5 F6 F3 2$ 4 081 R F G H. K < COAt the station there is a 2 mL microcentrifuge tube containing sheep blood and 3 tubes containing the following solutions: 0 mM, 300 mM, 600 mM of sucrose. The tubes are randomly labelled A, B, C. 2 mL of each solution were transferred to a different microcentrifuge tube, 20 ul of blood were then added to each tube, and they were mixed well by inverting the tube for multiple times. They were observed and it was determined whether the solution in each tube was hypotonic (Yes or No) relative to the blood cells. In addition, the solutions were diluted with water to help you determine which solution is which sucrose concentration. What sucrose concentration corresponds with each tube? Tube Hypotonic (Yes/No) Hypotonic after 1:1 dilution with water (Yes/No) Most likely Sucrose concentration (mM) A No Yes B Yes Yes C No No1. You wish to determine viable counts on a culture of Bacillus subtilis. You begin by pipetting 1 ml of culture into 99 ml of sterile water. After mixing the dilution well you make a series of 4 further dilutions of 10-1 each. From the three most dilute samples, you prepare three pour plates using 1 ml in each. After incubation you find the plate counts of the plates are 16, 245 and 890 respectively. a) Show the dilution scheme. b) What is the estimated viable count (cells/ml) in the original culture? 2. Scientific Notation. Fill in the missing information. a) 4.5 x 109 = _______ b) 50 x 107 = _______ c) 2300 x 1010 = _______ d) 0.54 x 108 = _______
- 1mL Stock #1 1mL 9mL #2 9mL #3 1mL A 9mL #4 0.1mL 1mL O O B 9mL #5 1mL 1mL 9mL #6 O Using the picture serial dilution scheme and the following information (plate A has 276 colonies, plate B has 298, plate C has 2, and plate D has 30), calculate the average number of colony forming units per mL in the stock tube. Make sure to only use countable plates. Round your answer to the nearest one. Write only the number with any needed commas or decimals. Do not include units. 0.1mL 1mk D OWrite a detailed description of the following plate 1- blood Agar plate 2-PEa Agar PlateA culture is incubated for 10 hours. 1 hours after inoculation it reached the exponential growth phase. At this time point the cell density was 1x10^4 cells/ml. 5 hours after inoculation (still during the exponential growth phase) the cell density was 1x10^7 cells. Calculate K and g(t). The growth constant (k) is minute. (round to 3 decimal points) The generation time (gt) is minutes. (round to whole number)
- A laboratory technician performed a series of 10 fold serial dilutions shown below. he plated 0.1 mL from each dilution tube onto NA and got the follow numbers per plate dilution 1:10 1:10 1:100 1:1000 1:10000 1:100000 colony count >1000 >1000 808 303 38 3 calculate the concentration of bacteria in the undiluted stock (in CFU/mL)Indicate whether you think that the number of cfu/ ml calculated would be too high or too low if you make this mistake. 1.You intend to add 9ml of broth (water) to each tube and 1 ml of culture. Instead, you add 5 ml of broth to each tube and 5 ml of culture to the first tube. Then, you make a serial dilution of 1 ml into and from each tube as described. 2. You prepare 9 ml of broth (water) in each tube. You add 1ml of culture of every tube. 3.You add 9 ml of broth (water) to each tube. You add 1 ml of culture to the first tube and mix. You get distracted, and transfer 1ml of the dilutant (mixture of culture and broth) to the third tube instead of the second. You perform the rest of the series as described.Below is a diagram of the serial dilution of a culture with 1 x 10º cells. Fill out the missing information. 250 Culture Diluent 1 x 10° cells/mL 9 mL 9 mL 9.9 mL 9.9 mL 99.9 mL Volume to add to diluent Final Dilution level Theoretical count after plating 100 uL
- Calculate the concentration of bacteriophage in the original culture from the following data. Be sure to include units. Show dilution factors for each test tube. Show the final dilution factor for test tube number 4. Show all your math. 0.1 ml 0.01 ml 0.001 ml 0.1 ml 1.0 ml plated 9.9 ml 9.99 ml 9.999 mi 9.9 m plaques Original Culture Test Test Test Test Tube #1 Tube #2 Tube #3 Tube #4 Dilution Factor: Concentration of Phage:Human error is a factor in the Kirby-Bauer procedure that often contributes to variation in zone size. Circle the effect on the zone size if the following occurred: ● ● Overinoculating the agar with bacteria: Waiting too long to place disks after inoculation: Using a culture that is less than 0.5 MacFarland: False increase False increase False increase False decrease False decrease False decrease1. You have a culture of yeast that is at a density of 8x107 cells/mL 2. A lab technician took a fecal sample and carried out the following dilutions: 1. Transferred 0.1 mL from the fecal sample 0.1 ml I ml 0.01 ml to 9.9 mL saline in tube A 2. Transferred 1 mL from A to 9 mL saline in tube B 3. Transferred 0.01 mL from B to 9.99 mL 0.1 ml A C saline in tube C 4. Transferred 0.1 mL from tube C to an agar plate 5. Counted 65 colonies on plate D 9.9 ml 9 ml 9.99 ml saline saline saline D 5. What is the concentration of cells in tube C? 6. What is the concentration of cells in the fecal sample? 1