Abstract
The phenomenon of hyperpigmentation (melanosis) in shellfish has long been attributed to phenoloxidase enzymes. Over the last number of years, the oxygen carrier hemocyanin, has demonstrated several immune- and physiological functionalities, most notably, inducible phenoloxidase activity. In this study, hemocyanin purified from the hemolymph of Nephrops norvegicus displays diphenoloxidase activity in the presence of a number of elicitors and retains structural and functional integrity throughout the process of freeze-thawing (at -25 degrees C). Conversely, cellular phenoloxidase activity (present in cell-lysates), demonstrates >98% reduction in activity after freeze-thawing. We present evidence that hemocyanin may act as a causative agent of hyperpigmentation in N. norvegicus. The inhibition of hemocyanin-derived phenoloxidase activity is discussed, and for the first time, the biophysical interactions of shellfish hemocyanin with known phenoloxidase inhibitors are presented. (C) 2013 Elsevier Ltd. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 361-369 |
| Number of pages | 9 |
| Journal | Food Chemistry |
| Volume | 140 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 15 Sept 2013 |
Keywords
- Hemocyanin
- Phenoloxidase
- Hyperpigmentation
- Innate immunity
- Enzyme inhibition
- Invertebrates
- PRAWN PENAEUS-JAPONICUS
- TYROSINASE INHIBITORS
- MUSHROOM TYROSINASE
- LIMULUS-POLYPHEMUS
- OXIDASE ACTIVATION
- PROPHENOLOXIDASE
- CONVERSION
- POLYPHENOLOXIDASE
- CATECHOLOXIDASE
- PURIFICATION
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