Calculate microbial loads per gram from dilution data. Compare replicates, log values, and dry-basis estimates. Built for cleaner lab reviews, exports, charts, and records.
Submit the calculator to show CFU per gram, log values, exports, and the chart here.
Use the grid below. It shows three columns on large screens, two on smaller screens, and one on mobile.
| Sample | Weight (g) | Suspension (mL) | Dilution | Plated Volume (mL) | Replicate Counts | Average | CFU/g |
|---|---|---|---|---|---|---|---|
| Food A | 10 | 90 | 10^-4 | 0.1 | 112, 108, 115, 110 | 111.25 | 1.0013E+08 |
| Soil B | 5 | 45 | 10^-5 | 0.1 | 74, 79, 81 | 78.00 | 7.0200E+08 |
| Feed C | 25 | 225 | 10^-3 | 1.0 | 41, 39, 43 | 41.00 | 3.6900E+05 |
CFU/g = (Average colony count × Dilution factor × Suspension volume) ÷ (Plated volume × Sample weight)
For a plate made from a 10^-d dilution, the dilution factor equals 10^d.
Average colony count comes from the entered replicate plates.
Suspension volume is the liquid holding the sample after homogenization.
Plated volume is the amount transferred onto the agar.
When moisture is known, a dry-basis value is also estimated.
Dry-basis CFU/g = Wet-basis CFU/g ÷ (1 − moisture fraction)
CFU per gram estimates viable microorganisms in one gram of sample. It reflects colonies able to grow under the chosen culture conditions, not total cells.
Microbiology plates are usually labeled as 10^-1, 10^-2, and so on. Entering the exponent makes the dilution factor easy to apply during the final CFU per gram calculation.
Replicates reveal plating consistency and reduce random error. Their average gives a steadier estimate than relying on a single plate.
Many methods prefer roughly 30 to 300 colonies per plate. Plates below that range may be less stable, while crowded plates may underestimate true counts.
Use dry-basis reporting when comparing samples with different moisture contents. It normalizes counts to dry material and improves cross-sample interpretation.
No. It is a reporting aid. Your laboratory method, dilution scheme, media choice, incubation conditions, and SOP remain the controlling factors.
Use a higher dilution on the next run. Overcrowded plates can merge colonies and reduce count accuracy.
Use a lower dilution or plate a larger volume, if your method allows it. Very low counts increase uncertainty.
Important Note: All the Calculators listed in this site are for educational purpose only and we do not guarentee the accuracy of results. Please do consult with other sources as well.