1989
DOI: 10.1111/j.1365-2621.1989.tb03111.x
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Effect of Bisulfite on Lobster Shell Phenoloxidase

Abstract: The role of bisulfite inhibition on the phenoloxidase (PO) catalyzed melanosis reaction in lobster was investigated. Bisulfite appears to inhibit melanosis by hvo mechanisms: (1) by reacting with intermediate quinones in the melanosis reaction, forming sulfoquinones, and (2) by irreversibly reacting with PO causing complete inactivation. The first mechanism is important because intermediate quinones (dopachrome) are the chroma for spectrophotometric analysis of PO activity.

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Cited by 33 publications
(24 citation statements)
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“…ascorbic acid, sulfoxide,sodium pirosulfite as reductants, L‐cysteine and glutathione ascouplers of o ‐quinones, sodium chloride, EDTA, carbon monoxideand diethyldithiocarbamate as chelators of copper atoms existingin an active site of tyrosinase, cinnamic acid, p ‐coumaricacid, and pherulic acid as analogs of substrate, and kojic acid and4‐hexylresorcinol as inhibitors belonging to other categories of inhibition mechanism). Part of the compounds describedabove have been reported as inhibitors of shrimp melanosis through thefollowing mechanisms; reducing o ‐quinones to o ‐diphenolsor Cu 2+ to Cu + byascorbic acid and its derivatives; 19 interactingwith the formation of o ‐quinone products by cysteine andbisulfite; 20 or decreasingthe oxygen uptake in the reaction by kojic acid 10 . Asmentioned above, ascorbic acid, kojic acid and bisulfite were reportedto inhibit mushroom tyrosinase activity and also PPO activity ofshrimp.…”
Section: Discussionmentioning
confidence: 92%
“…ascorbic acid, sulfoxide,sodium pirosulfite as reductants, L‐cysteine and glutathione ascouplers of o ‐quinones, sodium chloride, EDTA, carbon monoxideand diethyldithiocarbamate as chelators of copper atoms existingin an active site of tyrosinase, cinnamic acid, p ‐coumaricacid, and pherulic acid as analogs of substrate, and kojic acid and4‐hexylresorcinol as inhibitors belonging to other categories of inhibition mechanism). Part of the compounds describedabove have been reported as inhibitors of shrimp melanosis through thefollowing mechanisms; reducing o ‐quinones to o ‐diphenolsor Cu 2+ to Cu + byascorbic acid and its derivatives; 19 interactingwith the formation of o ‐quinone products by cysteine andbisulfite; 20 or decreasingthe oxygen uptake in the reaction by kojic acid 10 . Asmentioned above, ascorbic acid, kojic acid and bisulfite were reportedto inhibit mushroom tyrosinase activity and also PPO activity ofshrimp.…”
Section: Discussionmentioning
confidence: 92%
“…Sulphites are known to inhibit both enzymatic and nonenzymatic browning reactions. Bisulphite was reported to inhibit melanosis by two mechanisms: by reacting with intermediate quinones in the melanosis reaction that forms sulfoquinones and by irreversibly reacting with PO, causing complete inactivation (Ferrer, Otwell, & Marshall, 1989). However, HR forms an inactive complex with PO that is incapable of catalysing melanosis formation (Guerrero-Beltran, Swanson, & Barbosa-Canovas, 2005).…”
Section: Discussionmentioning
confidence: 98%
“…Bisulfite has been known to inhibit melanosis by 2 mechanisms: by reacting with intermediate quinones in the melanosis reaction that forms sulfoquinones, and by irreversibly reacting with PPO, causing complete inactivation (Ferrer, Otwell, & Marshall, 1989). Meanwhile, HR forms an inactive complex with PPO that is incapable of catalyzing melanosis formation (Guererro-Beltran, Swanson, & Barbosa-Cánovas, 2005).…”
Section: Discussionmentioning
confidence: 99%