Diagram illustrating Miles & Misra technique for determining viable counts: 10ul 10-5 106 104 10-7 3. Set up controls of the donor and recipient cultures as follows: Spread plate 0.1 ml of the donor culture over the surface of each of the 3 different selective media (i.e. nutrient agar + Ap; nutrient agar + Sm; nutrient agar + Rif) Similarly spread plate 0.1 ml of the recipient culture over the surface of each of the 3 selective media • What is the purpose of this step?
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![Diagram illustrating Miles & Misra technique for determining viable counts:
10ul
10-5
106
104
10-7
3. Set up controls of the donor and recipient cultures as follows:
• Spread plate 0.1 ml of the donor culture over the surface of each of
the 3 different selective media (i.e. nutrient agar + Ap; nutrient agar
+ Sm; nutrient agar + Rif)
• Similarly spread plate 0.1 ml of the recipient culture over the
surface of each of the 3 selective media
• What is the purpose of this step?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F7224d9f1-e881-4a28-9f8f-4dfb826c78a8%2Fbfc37ee4-7f5e-4531-be8d-597b67df95ec%2F95d8o9bs_processed.jpeg&w=3840&q=75)
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- In a fed-batch culture operating with intermittent addition of lactose solution, values ofthe following parameters are given at time t = 2, when the system is at a quasi-steady state. 1.Determine the initial volume of the culture 2. Determine the concentration of growth-limiting substrate and the total amount ofbiomass in the vessel at a quasi-steady state. 3. At which scenario of bioprocessing, a fed-batch system is recommended to be applied?N. benthamiana will be infiltrated with a solution containing OD600=0.3 of each experimental Agro containing construct and OD600=0.1 of p19. Calculate the volume of cultures (V construct; V p19) needed according to the formulas: V construct = V final × 0.3/OD600; V p19 = V final × 0.1/OD600. One mL of infiltrate is often enough to complete a small experiment. How to plan your final volume accordingly?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 decrease
- Hello, i'm having a hard time organzing the calculations when it comes to rate mL/h. I already solved this problem but I need your help to confirm if my calculations were correct. I would appreciate if you can add step by steps in order for me to understand it better, thank you! Order: Pulmocare 480 mg daily via PEG over 6 hours, followed by 50 mL sterile water flush. 1. The Pulmocare label states 100 mg/100 mL. At what rate in mL/h will you set the feeding pump to administer the Pulmocare? 2. Calculate the total amount of enteral fluid the patient will receive in 24h 3. How many milliliters of IV fluids is the patient receiving in 24h?volume of the quasi-steady-state culture was V0= 500 L, and the nutrient solution containing glucose was added at a constant flow rate of F = 50 L/h.Data: X0 (at the beginning of feeding) = 20 g/L, S0 = 300 g/L, max = 0.2 h-1, KS = 0.5 g/L and Y x/s= 0.3 g/g a) Determine the volume of the culture at t = 10hb) Determine the concentration of glucose at t = 10 hc) determine the concentration and total mass of cells at t = 10 hd) If product is associated with growth with α = 1.5 and P0 = 0.1 g/L, determine the concentration of product at t = 10h. (answer:P = 67,55 g/L)Time point (min) Absorbance of culture at 660nm Approximate cell concentration Approximate # cells in 1mL extract 0 0.298 1.49 x 108 cells/mL 1.49 x 108 cells 10 0.316 1.58 x 108 cells/mL 1.58 x 108 cells 20 0.374 1.87 x 108 cells/mL 1.87 x 108 cells 30 0.429 2.145 x 108 cells/mL 2.145 x 108 cells 40 0.512 2.56 x 108 cells/mL 2.56 x 108 cells 50 0.544 2.72 x 108 cells/mL 2.72 x 108 cells 60 0.607 3.035 x 108 cells/mL 3.035 x 108 cells a. Using these data, prepare a growth curve of this strain ofEscherichia coli (E. coli).b. Estimate the doubling time for this strain of E. Coli. Clearly showhow you estimated this value from the empirical data presented.
- Observe the following Plate counts and then determine the correct number of CFU/ml Plate 1 = 564 colonies at 10^-5 dilution Plate 2 = 422 colonies at 10^-6 dilution Plate 3 = 317 colonies at 10^-7 dilution Plate 4 = 93 colonies at 10^-8 dilution 93 x 10^10 CFU/ml 9.3 x 10^-9 CFU/ml 93 x 10^9 CFU/ml 93x 10^8 CFÜ/ml 93x 10^-8 CFU/ml asap pleaseAfter performing a plate and liquid lysate, it was found that the plate lysate achieved the common titre range of 1010-1011 pfu/ml whereas the liquid lysate achieved a range of 108 PFU/mL; what is the reason for the lower titre in different methodologies? How can we troubleshoot this issue in the future?Look at the table below and answer the following questions: Culture 1/10 1/50 1/100 1/200 dilution OD Reading 1 2.0 0.36 0.18 0.11 OD Reading 2 1.9 0.35 0.18 0.08 OD Reading 3 1.8 0.33 0.16 0.09 1. Which 2 dilution levels of the culture are the best to use to compute for its optical density? 2. What is the average optical density of the culture? (use values from 2 dilution levels)
- ANSWER THE FOLLOWING QUESTIONS REGARDING GEL ELECTROPHORESIS 1.why is it not advisable to move/touch the agarose gel in the process of hardening 2.what is the use or function of the TAE buffer that is poured or found in the gel box 3.how can you tell if agel is running 4.outline the process use in the preparation of agarose gel of 1.5 concentration 5.outline the processes/steps used in gel electrophoresis 6.name twoexamples of the dye used in gel electrophoresis 7.how do we prepare x1(concentration) TAE BUFFER form 50x TAE bufferQ.6. You have a bacterial culture. From this culture suspension, six serial dilutions are made, and 1 ml is plated onto Plate Agar from the last dilution. After incubation, X colonies are counted on the plate. Calculate CFU/mL of the original Sample? (X=9)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.