E. coli overnight culture
Estimate a liquid culture from duplicate spread plates.
Spread 0.1 mL · 3 dilutions · duplicates
Turn plate counts from several dilutions into CFU/mL or CFU/g, log10 and log reduction.
2 plates used · 30–300
log₁₀ 9.30
Maximum likelihood, 95% CI: 2.0 × 10⁹ [1.8 × 10⁹, 2.2 × 10⁹]
Explore plate-count scenarios, then load one into the calculator.
Estimate a liquid culture from duplicate spread plates.
Spread 0.1 mL · 3 dilutions · duplicates
Calculate a food sample's aerobic plate count using the FDA BAM method.
Source: FDA BAM Chapter 3, Example 2.1a
Review counts when successive dilutions disagree.
Food sample · 3 dilutions · triplicates
Include TNTC plates in the maximum-likelihood estimate instead of ignoring them.
Pour 1 mL · 2 TNTC plates
Compare treatment plates with a control and report a detection limit.
3 samples · control vs 2 treatments
Plot viable counts across time for control and drug groups.
2 groups · 5 time points
Go from your plates to a result in four steps.
Choose a sample type, plating method and volume. Use Compare samples for log reduction.
Enter each row's dilution and each plate's count. Type TNTC for crowded plates, or count colonies on a photo.
Choose a countable range (such as 30–300), ISO 7218 or FDA BAM; plates used in the result are highlighted.
Check the CFU concentration and log₁₀, then download PNG or SVG or copy the result and methods text.
Choose the formula that matches the plates used in your calculation.
C = colonies, V = plated volume (mL), d = dilution relative to the original sample.
Cᵢ, Vᵢ and dᵢ are the colony count, plated volume (mL) and dilution for each plate.
ΣC = total colonies, V = equal plated volume (mL), n₁ and n₂ = plate counts at each dilution, d = the less-diluted fraction.
| Parameter | Value |
|---|---|
| Colonies | 212 + 189 = 401 |
| Plated volume × dilution | 2.0 × 10⁻⁷ mL |
| Weighted calculation | 401 / 2.0 × 10⁻⁷ |
| Report | 2.0 × 10⁹ CFU/mL |
A 1 + 9 suspension is a 10⁻¹ dilution; enter the total dilution relative to the original sample. For example, 156 and 171 colonies at 10⁻⁷ with 0.1 mL plated give 1.6 × 10¹⁰ CFU/g.
TNTC means too numerous to count; TFTC means too few to count. Select a range appropriate for your method. Plates outside it may require an estimated result or a detection limit.
| Counting rule | Countable range | Plates used | All plates low | No colonies | TNTC |
|---|---|---|---|---|---|
| Countable range | 30–300 / 25–250 / 15–300 | Plates in range | Estimated | Below detection limit | All plates are TNTC. Use a more dilute sample. |
| ISO 7218 | ≤ 300 | Up to two consecutive eligible dilutions | Estimated | Below detection limit | Up to two consecutive eligible dilutions |
| FDA BAM | 15–300 | All exact and TNTC plates | Estimated | Below detection limit | All exact and TNTC plates |
The ISO rule uses up to two consecutive eligible dilutions with at least one plate containing 10 or more colonies. FDA BAM uses a maximum-likelihood estimate and a likelihood-ratio confidence interval. Check your laboratory protocol before reporting.
| Colonies counted | Reporting |
|---|---|
| 0 | Below detection limit |
| 1–3 | Present below a limit |
| 4–9 | Estimated |
| ≥ 10 | Calculated result |
ISO worked example: 168/215 and 14/25 at 10⁻² and 10⁻³, plated at 1 mL, give 19,181.8 and report as 19,000.
BAM rounds to two significant figures using the third digit; for example 14,500 becomes 14,000.
Log reduction is the base-10 decrease in viable counts between control and treated samples.
N₀ = control count and N = treated count, in the same units.
If no colonies are detected, use the detection limit and report a minimum reduction (≥).
LR = log reduction.
| Log reduction | Percent reduction | Survivors per 10⁶ |
|---|---|---|
| 1 | 90% | 100,000 |
| 2 | 99% | 10,000 |
| 3 | 99.9% | 1,000 |
| 4 | 99.99% | 100 |
| 5 | 99.999% | 10 |
| 6 | 99.9999% | 1 |
Compare viable counts over time; open points indicate results below the detection limit.
≥3 log₁₀ reduction from the initial inoculum = bactericidal activity at the specified time. Source: CLSI M26-A
A CFU is a viable cell or group of cells capable of forming a visible colony.
Divide the total colonies on selected plates by their total original-sample volume, ΣC/Σ(V × d). To count transformants per µg of plasmid DNA, use the transformation efficiency calculator.
Successive dilutions should give similar concentration estimates. Check labels, mixing and pipetting, and repeat if needed.
Report a detection limit for all-zero plates. Low positive counts may be estimated or reported as present below a limit depending on the selected rule.
Take the base-10 logarithm of the concentration; 2.0 × 10⁹ CFU/mL is log₁₀ 9.30.
Include the initial suspension in each total dilution relative to the original sample.
Yes. Select Drop 10 µL and enter each drop in a separate plate column.
Yes. Open the photo counter beside a cell and click each colony. The photo stays in your browser.
Your data stays in your browser. Copy or export the result without signing in.
Calculate a weighted count from your plate data in your browser.
Calculate CFU from your plates