Dehydratase, carbonate

Ecotoxicological Summary

Hazard for aquatic organisms

Freshwater

Hazard assessment conclusion:

PNEC aqua (freshwater)

PNEC value:

8.8 µg/L

Assessment factor:

1 000

Extrapolation method:

assessment factor

PNEC freshwater (intermittent releases):

88 µg/L

Marine water

Hazard assessment conclusion:

PNEC aqua (marine water)

PNEC value:

0.88 µg/L

Assessment factor:

10 000

Extrapolation method:

assessment factor

STP

Hazard assessment conclusion:

PNEC STP

PNEC value:

65 000 µg/L

Assessment factor:

1

Extrapolation method:

assessment factor

Sediment (freshwater)

Hazard assessment conclusion:

no exposure of sediment expected

Sediment (marine water)

Hazard assessment conclusion:

no exposure of sediment expected

Hazard for air

Air

Hazard assessment conclusion:

no hazard identified

Hazard for terrestrial organisms

Soil

Hazard assessment conclusion:

PNEC soil

PNEC value:

2.033 µg/kg soil dw

Extrapolation method:

equilibrium partitioning method

Hazard for predators

Secondary poisoning

Hazard assessment conclusion:

no potential for bioaccumulation

Additional information

GLP Daphnia study as selected as read-across from Xanthan lyase. Non-GLP studies are available on Carbonic anhydrase as a supporting studies.

Exposure of Daphnia magna to Xanthan lyase, batch PPE55581 gave EC50 value of greater than 1761.4 mg enzyme concentrate dry matter/L (equivalent to 100 mg aep/L). The No Observed Effect Concentration (NOEC) was the highest concentration tested, 1761.4 mg enzyme concentrate dry matter/L (equivalent to 100 mg aep/L).

Exposure of Daphnia magna to Carbonic anhydrase, batch PPE93985 has been investigated based on nominal concentrations revealed no effect on immobilization. The 48-hour EC50 value was greater than the highest concentration tested 676.6 mg enzyme concentrate dry matter/L (equivalent to 100 mg active enzyme protein/L). The NOEC is 676.6 mg enzyme concentrate dry matter/L (equivalent to 100 mg active enzyme protein/L).

The exposure of R. subcapitata to Carbonic anhydrase, batch PPE93985 was toxic to algae based on its algaestatic, CO2 quenching mode of action. 250 mg sodium bicarbonate and constant shaking were introduced to the test system. 72-hr EC50 was 59.4 mg enzyme concentrate dry matter, equivalent to 8.8 mg active enzyme protein/L. The study is non-GLP and analytical measurements have not been undertaken.

The lowest EC50 for Carbonic anhydrase was 8.8 mg active enzyme protein/L and was used for PNEC derivation and the assessment factors 1000 and 10000 were applied for fresh and marine water, respectively.

Inhibition control carried out with non-proteolytic enzymes in the test of ready biodegradability showed no inhibition of the activated sludge inoculum at an enzyme concentration above the expected levels in inlet to sewage treatment plants (STPs). Monitoring of enzymes in the inlet to municipal STPs (in Denmark) resulted in concentrations of less than 2 µg active enzyme protein (aep)/L which are below the initial concentration used in tests for ready biodegradability, where no inhibitory effects were observed. It is concluded that a study on activated sludge respiration inhibition does not need to be conducted. Therefore, the test enzyme is not considered to be toxic to microorganisms.

The PNEC value for STP is based on actual measurements of enzyme concentration in STP connected to manufacturing site. Up to 65000 µg aep/L were detected in STP connected to manufacturing site and since there was no negative impact observed, this concentration is the estimated PNEC value for STP.

PNEC values for sediment exposure have not been derived because the enzyme is readily biodegradable, highly water soluble and has a very low potential for adsorption to sediments. Exposure of the sediment to toxicologically significant concentrations of the enzyme is thus not expected.

As no soil ecotoxicity data are available for the test enzyme, the PNEC for soil is based on the PNEC for surface water using the equilibrium partitioning method. PNEC soil was estimated to 1.05 µg active enzyme protein/kg soil ww.

The enzyme is not expected to cause any significant secondary poisoning as it is ready biodegradable and has no bioaccumulation potential. Furthermore, as the test enzyme is a protein it is expected to be degraded in the gastrointestinal tract. Thus, PNEC oral is not relevant.

Conclusion on classification

Based on the aquatic toxicity studies and the ready biodegradation of the enzyme, the enzyme is not classified.