🌿 Microtox® test — Vibrio fischeri

Environmental PN-EN ISO 11348-3

Biological toxicity test for water and wastewater based on inhibition of bioluminescence of Vibrio fischeri (Aliivibrio fischeri) bacteria. Rapid toxicity screening (15–30 min).

Overview

The Microtox® test (or its equivalents) is the fastest and most commonly used bioassay for assessing toxicity of waters, wastewaters, and aqueous extracts from soils and wastes. The bacterium Vibrio fischeri (formerly Photobacterium phosphoreum) naturally emits light (bioluminescence) due to the enzyme luciferase. Toxic substances inhibit bacterial metabolism, causing a decrease in luminescence intensity.

The result is EC50 (concentration causing 50% luminescence decrease) after 15 and 30 minutes of exposure, or percent luminescence inhibition for environmental samples. The test is used in waste classification (toxicity H14), wastewater toxicity assessment, and water quality control.

Method principle

Freeze-dried Vibrio fischeri bacteria are reconstituted in salt solution (2% NaCl) and exposed to a series of sample dilutions. Luminescence is measured with a luminometer before sample addition (I₀) and after 5, 15, and 30 minutes of exposure (I_t). Percent inhibition = [1 − (I_t/I_control)] × 100. EC50 is calculated from dose-response curve. Test temperature: 15°C (optimal for V. fischeri).

Applications

Key parameters

ParameterValue
Test organismVibrio fischeri (Aliivibrio fischeri), NRRL B-11177
Exposure time15 and 30 min
EndpointEC50 or % luminescence inhibition
Test temperature15 ± 1°C
Test time30–45 min (including preparation)

Standard

Standard number
PN-EN ISO 11348-3:2008
Title (PL)
Jakość wody — Oznaczanie hamowania bioluminescencji Vibrio fischeri (test hamowania świecenia) — Część 3: Metoda z zastosowaniem bakterii liofilizowanych
Title (EN)
Water quality — Determination of the inhibitory effect of water samples on the light emission of Vibrio fischeri (Luminescent bacteria test) — Part 3: Method using freeze-dried bacteria

Step-by-step procedure

1. Sample preparation

Adjust sample pH to 6–8 (if necessary). Adjust salinity to 2% NaCl. Filter (0.45 µm) if containing suspension.

⏱ Time: 15 min

2. Bacteria reconstitution

Add 1 mL cooled reconstitution solution to lyophilized ampoule. Mix gently. Incubate 15 min at 4°C.

⏱ Time: 15 min • 🌡 Temperature: 4°C

3. Dilution preparation

Prepare sample dilution series: 100, 50, 25, 12.5, 6.25% in 2% NaCl. Control = 2% NaCl.

⏱ Time: 10 min

4. Luminescence measurement I₀

Transfer bacteria to measurement vials (100 µL/vial). Measure initial luminescence I₀ in luminometer.

⏱ Time: 5 min

5. Sample addition

Add 900 µL sample/dilution to vials with bacteria. Mix gently.

⏱ Time: 5 min

6. Measurement after 15 and 30 min

Measure luminescence I₁₅ and I₃₀. Calculate % inhibition and EC50.

⏱ Time: 30 min • 🌡 Temperature: 15°C

Required equipment and apparatus

EquipmentExampleIndicative price
Microtox® luminometerModern Water Microtox M500, LUMIStox 300 (Hach)60,000–120,000 PLN
15°C cooling blockBuilt into luminometer or externalbuilt-in
Automatic pipettesEppendorf Research Plus 10–1000 µL800–2,000 PLN
Cuvettes/vials for luminometerBorosilicate glass vials, pack of 500 pcs.500–1,000 PLN

Reagents, media and consumables

ReagentCASDetails
Freeze-dried V. fischeri bacteriaMicrotox Acute Reagent, ampoules (5 tests/ampoule), store at -20°C
Reconstitution solution2% NaCl, sterile, cooled to 4°C
Diluent solution2% NaCl, for sample dilution preparation
Reference substance7778-50-9Potassium dichromate K₂Cr₂O₇ or ZnSO₄, for bacterial sensitivity validation

Health and safety (OHS)

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