Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.11.1.18 extracted from

  • Arnoldsson, K.; Andersson, P.; Haglund, P.
    Formation of environmentally relevant brominated dioxins from 2,4,6,-tribromophenol via bromoperoxidase-catalyzed dimerization (2012), Environ. Sci. Technol., 46, 7239-7244.
    View publication on PubMed
Search for more literature for 1.11.1.18

Organism

Organism UniProt Comment Textmining
Corallina officinalis Q8LLW7
-
-

Source Tissue

Source Tissue Comment Organism Textmining
commercial preparation
-
 Corallina officinalis
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
Br- + H2O2 + 2,4,6-tribromophenol
-
 Corallina officinalis 1,3,6,8-tetrabromodibenzo-p-dioxin formation of ppb-level yields of 1,3,6,8-tetrabromodibenzo-p-dioxin through direct condensation. Additionally, 1,3,7,9-tetrabromodibenzo-p-dioxin, 1,2,4,7-tetrabromodibenzo-p-dioxin, and/or 1,2,4,8-tetrabromodibenzo-p-dioxin and 1,3,7-tribromodibenzo-p-dioxin and 1,3,8-tribromodibenzo-p-dioxin are frequently formed but at lower yields. Reaction probably proceeds via bromine shifts or Smiles rearrangements, whereas the tribromodibenzo-p-dioxins may result from subsequent debromination processes ?