Step 1: Recall the viable count formula.
Each colony on the plate grew from one viable cell present in the volume of diluted sample spread on it. The viable count of the ORIGINAL culture comes from
\[ \text{CFU mL}^{-1} = \frac{\text{number of colonies}}{\text{volume plated (mL)}} \times \text{dilution factor} \]
Step 2: List the known values.
Number of colonies counted = 20.
Volume of diluted sample plated = \(50\ \mu\text{L} = 0.05\ \text{mL}\).
Dilution factor = 100, since the sample was diluted 100-fold before plating.
Step 3: Find the count in the diluted sample.
\[ \text{CFU mL}^{-1}\ \text{(diluted sample)} = \frac{20}{0.05} = 400\ \text{CFU mL}^{-1} \]
Step 4: Scale back up to the original, undiluted culture.
Since the plated sample was 100 times more dilute than the original culture, the original culture has 100 times more viable cells per mL:
\[ \text{CFU mL}^{-1}\ \text{(original culture)} = 400 \times 100 = 40000\ \text{CFU mL}^{-1} \]
Final Answer:
The viable cell count of the culture is
\[ \boxed{40000\ \text{CFU mL}^{-1}} \]