Effects of sodium metabisulfite treatments on Penaeus vannamei post mortem melanosis formation, sulfite levels and polyphenoloxidase activities

Sodium metabisulfite (SMBS) is the most widely used reagent for effective prevention of melanosis in the shrimp industry. Sulfite levels in shrimp frequently exceed guideline levels due to variations in SMBS application, disadvantaging consumers and causing economic losses. This study evaluates multiple factors that influence post-mortem melanosis development, sulfite residue in shrimp and phenol oxidizing enzyme activities. Factors include SMBS dipping solution parameters (concentration (1.5–2-5%), incubation time (5–20 min), salinity (0 and 20 ppt), condition of shrimp (dead or alive, stressed or unstressed) and repeated SMBS treatment. Based on the results of this study optimal concentration of SMBS dipping solutions in 20 ppt water was 2% with an incubation time of 10 min. Salt water use avoided exceeding 100 ppm (legal limits in US) sulfite concentration in shrimp. No polyphenoloxidase (PPO) activity was detectable in the hemolymph of shrimp treated with SMBS. However, it was possible to induce PPO activity in individual shrimp. No differences were detected in any tested parameter when using dead or alive shrimp for SMBS treatment. Cold stressed shrimp showed significantly increased melanosis development in controls ( p < 0.05). Treatment with SMBS effectively suppressed melanosis formation in stressed and unstressed shrimp with no significant differences between treatments. Repeated application of SMBS did not increase melanosis prevention, nor sulfite levels. PPO activity and endogenous trypsin activities were detected in post-mortem shrimp two days after SMBS treatment. Subsequent SMBS treatment did not inhibit PPO activity. Presumably PPO zymogens are not entirely inhibited by SMBS and likely activated post-mortem through endogenous proteases, including trypsin. • Sodium metabisulfite treatment of shrimp is recommended at a 2% dipping solution for 10 min in salt water. • Direct, post-mortem or repeated application of sodium metabisulfite does not result in different melanosis formation in shrimp. • Sodium metabisulfite treatment effectively inhibits polyphenoloxidases in the hemolymph. • Polyphenoloxidase zymogens remain partly functional in the hemolymph after sodium metabisulfite treatment.

Authors

Institutions

Publication Details

Journal
Aquaculture
Published
2026-04-16
DOI
https://doi.org/10.1016/j.aquaculture.2026.744035
Primary Topic
Invertebrate Immune Response Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Effects of sodium metabisulfite treatments on Penaeus vannamei post mortem melanosis formation, sulfite levels and polyphenoloxidase activities

Matthew James Slater, Enno Fricke, Mirko Bögner, Monika Weiß et al.
Aquaculture
Invertebrate Immune Response Mechanisms
article

Effects of sodium metabisulfite treatments on Penaeus vannamei post mortem melanosis formation, sulfite levels and polyphenoloxidase activities

Matthew James Slater, Enno Fricke, Mirko Bögner, Monika Weiß, Sabine Frischhut, Kyra Böckmann
article en

Abstract

Sodium metabisulfite (SMBS) is the most widely used reagent for effective prevention of melanosis in the shrimp industry. Sulfite levels in shrimp frequently exceed guideline levels due to variations in SMBS application, disadvantaging consumers and causing economic losses. This study evaluates multiple factors that influence post-mortem melanosis development, sulfite residue in shrimp and phenol oxidizing enzyme activities. Factors include SMBS dipping solution parameters (concentration (1.5–2-5%), incubation time (5–20 min), salinity (0 and 20 ppt), condition of shrimp (dead or alive, stressed or unstressed) and repeated SMBS treatment. Based on the results of this study optimal concentration of SMBS dipping solutions in 20 ppt water was 2% with an incubation time of 10 min. Salt water use avoided exceeding 100 ppm (legal limits in US) sulfite concentration in shrimp. No polyphenoloxidase (PPO) activity was detectable in the hemolymph of shrimp treated with SMBS. However, it was possible to induce PPO activity in individual shrimp. No differences were detected in any tested parameter when using dead or alive shrimp for SMBS treatment. Cold stressed shrimp showed significantly increased melanosis development in controls ( p < 0.05). Treatment with SMBS effectively suppressed melanosis formation in stressed and unstressed shrimp with no significant differences between treatments. Repeated application of SMBS did not increase melanosis prevention, nor sulfite levels. PPO activity and endogenous trypsin activities were detected in post-mortem shrimp two days after SMBS treatment. Subsequent SMBS treatment did not inhibit PPO activity. Presumably PPO zymogens are not entirely inhibited by SMBS and likely activated post-mortem through endogenous proteases, including trypsin. • Sodium metabisulfite treatment of shrimp is recommended at a 2% dipping solution for 10 min in salt water. • Direct, post-mortem or repeated application of sodium metabisulfite does not result in different melanosis formation in shrimp. • Sodium metabisulfite treatment effectively inhibits polyphenoloxidases in the hemolymph. • Polyphenoloxidase zymogens remain partly functional in the hemolymph after sodium metabisulfite treatment.

AquacultureVol. 622
Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung (DE), BASF (Germany) (DE)
BASF
Openalex Percentile: Top 12%
Invertebrate Immune Response Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.