The following details the results of a serial dilution of E. coli: Effective Dilution Factor on...
The following details the results of a serial dilution of E. coli:
| Effective Dilution Factor on Plate | CFUs |
| 105 | 1095 |
| 106 | 178 |
| 107 | 5 |
| 108 | None |
The "effective dilution factor on plate" already takes into account
the fact that you plated 0.1 ml of the dilution.
How many CFUs/ml were present in the original sample?
| a. | 1.78 x 10^8 |
| b. | 1.14 x 10^8 |
| c. | 1.125 x 10^8 |
| d. | 1.095 x 10^8 |
Homework Answers
CFU/ml in the original sample = (no. of colonies x di;ution factor) / volume of culture plate
= (1095 x 104) / 0.1
= 1.095 x 108 CFU/ ml
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The following details the results of a serial dilution of E.
coli:
Effective Dilution
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m e usually performed, e.g., 10°>10% 10% 10%, etc. Two-fold or other dilution schemes can be applied as well. For accurate quantitation, it is important to use the selected dilution scheme consistently. correction factor is 10 (0.1 ml X 10-10 ml). If you plated 0.5 ml, the correction factor is 2. 1.-CFU/Dr Initial concentration, (lc) equals colony forming units (cfu) divided by dilution factor (Df). Note that each step of the dilution procedure reduces the...
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Report your answer below as a decimal with one significant digit
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A culture of E. coli was grown on suitable culture media; aliquots of the culture were serially diluted and spread plated aseptically on agar plate media at the times indicated in the table below. Upon overnight incubation at 37°C, colonies appeared and viable counts were colleted and displayed below. Hours 0 Viable Counts (CFU/mL) 2 .00 x 107 2.10 x 107 2.30 x 107 3.25 x 107 6.60 x 107 1.40...
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Standard plate count. Include formulas and calculations. Scientific notation. Show your work. UNITSI 7. Suppose you have 2.0 ml of an undiluted E.coli broth and need to begin your serial dilution by making a 10. solution. How much diluent would you need if you wanted to use the entire 2 ml of E. coli broth? 110-ml 102 = 2mL ol os dition 10 8. If you transfer 0.1 ml of...
please help with whatever possible. thank you so much in advance. Name One use of serial...
please help with whatever possible. thank you so much in
advance.
Name One use of serial dilutions is to calculate the concentration of microorganisms. Since it would usually be challenging or even impossible to actually count the number of microorganisms in a sample, the sample is diluted and plated to get a reasonable number of colonies to count (usually between 25 to 250 colonies is the goal). Since each colony on an agar plate theoretically grew from a single microorganism,...
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m e usually performed, e.g., 10°>10% 10% 10%, etc. Two-fold or other dilution schemes can be applied as well. For accurate quantitation, it is important to use the selected dilution scheme consistently. correction factor is 10 (0.1 ml X 10-10 ml). If you plated 0.5 ml, the correction factor is 2. 1.-CFU/Dr Initial concentration, (lc) equals colony forming units (cfu) divided by dilution factor (Df). Note that each step of the dilution procedure reduces the...
What is the concentration of cells in the starting sample if 1
ml was plated per dilution and the starting sample was river
water?
Report your answer below as a decimal with one significant digit
after the decimal and report the exponent the separate box. See
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report it as "5.2"
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A culture of E. coli was grown on suitable culture media; aliquots of the culture were serially diluted and spread plated aseptically on agar plate media at the times indicated in the table below. Upon overnight incubation at 37°C, colonies appeared and viable counts were colleted and displayed below. Hours 0 Viable Counts (CFU/mL) 2 .00 x 107 2.10 x 107 2.30 x 107 3.25 x 107 6.60 x 107 1.40...
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please help with whatever possible. thank you so much in
advance.
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