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Literature summary for 5.5.1.7 extracted from

  • Schmidt, E.; Knackmuss, H.J.
    Chemical structure and biodegradability of halogenated aromatic compounds. Conversion of chlorinated muconic acids into maleoylacetic acid (1980), Biochem. J., 192, 339-347.
    View publication on PubMedView publication on EuropePMC
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KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
0.0134
-
 3-methyl-cis,cis-muconate
-
 Pseudomonas sp.
0.0309
-
 2-methyl-cis,cis-muconate
-
 Pseudomonas sp.
0.0601
-
 2-chloro-cis,cis-muconate
-
 Pseudomonas sp.
0.0928
-
 cis,cis-muconate
-
 Pseudomonas sp.
0.1286
-
 3-chloro-cis,cis-muconate
-
 Pseudomonas sp.

Organism

Organism UniProt Comment Textmining
Pseudomonas sp.
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
 Pseudomonas sp.

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-Chloro-cis,cis-muconate 65% of the activity relative to 2-methyl-cis,cis-muconate Pseudomonas sp. 4-Carboxymethyl-2-chloro-but-2-en-4-olide trans-4-carboxymethylenebut-2-en-4-olide is produced after dehalogenation ?
2-Methyl-cis,cis-muconate most effective substrate Pseudomonas sp. ?
-
 ?
3-Chloro-cis,cis-muconate 73% of the activity relative to 2-methyl-cis,cis-muconate Pseudomonas sp. cis-4-Carboxymethylenebut-2-en-4-olide
-
 ?
3-Methyl-cis,cis-muconate 84% of the activity relative to 2-methyl-cis,cis-muconate Pseudomonas sp. ?
-
 ?
cis,cis-Muconate 36% of the activity relative to 2-methyl-cis,cis-muconate Pseudomonas sp. ?
-
 ?