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

BRENDA support

Literature summary extracted from

  • Kido, T.; Soda, K.
    Oxidation of anionic nitroalkanes by flavoenzymes, and participation of superoxide anion in the catalysis (1984), Arch. Biochem. Biophys., 234, 468-475.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.13.12.16 4-hydroxy-2,2,6,6-tetramethyl-piperidinooxy radical
-
 Cyberlindnera mrakii
1.13.12.16 cytochrome c O2 scavenger Cyberlindnera mrakii
1.13.12.16 dithiothreitol
-
 Cyberlindnera mrakii
1.13.12.16 epinephrine
-
 Cyberlindnera mrakii
1.13.12.16 GSH
-
 Cyberlindnera mrakii
1.13.12.16 additional information not affected by hydroxyl radical scavengers such as mannitol Cyberlindnera mrakii
1.13.12.16 NaBH4
-
 Cyberlindnera mrakii
1.13.12.16 NADH O2 scavenger Cyberlindnera mrakii
1.13.12.16 Nitro blue tetrazolium
-
 Cyberlindnera mrakii
1.13.12.16 Superoxide dismutase Cu and Zn-superoxide dismutase of bovine blood, Mn-superoxide dismutases of bacilli, Fe-superoxide dismutase of Serratia marcescens Cyberlindnera mrakii
1.13.12.16 Tiron i.e. pyrocatechol-3,5-disulfonate disodium salt Cyberlindnera mrakii

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
1.13.12.16 1.61
-
 2-Nitropropane anionic form of substrate Cyberlindnera mrakii
1.13.12.16 1.61
-
 propyl-2-nitronate anionic Cyberlindnera mrakii

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
1.13.12.16 additional information addition of Cu2+ and Zn2+ shows no effect Cyberlindnera mrakii

Organism

EC Number Organism UniProt Comment Textmining
1.13.12.16 Cyberlindnera mrakii
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
1.13.12.16
-
 Cyberlindnera mrakii

Reaction

EC Number Reaction Comment Organism Reaction ID
1.13.12.16 ethylnitronate + O2 = acetaldehyde + nitrite + other products superoxide as reactive intermediate Cyberlindnera mrakii
a

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.13.12.16 1-hydroxybutyl-2-nitronate + O2 anionic, expression on the basis of the reactivity of propyl-2-nitronate with 2-nitropropane dioxygenase: 31.5 Cyberlindnera mrakii ? + HNO2
-
 ?
1.13.12.16 2-hydroxybutyl-3-nitronate + O2 anionic, expression on the basis of the reactivity of propyl-2-nitronate with 2-nitropropane dioxygenase: 26.7 Cyberlindnera mrakii ? + HNO2
-
 ?
1.13.12.16 2-hydroxypentyl-3-nitronate + O2 anionic, expression on the basis of the reactivity of propyl-2-nitronate with 2-nitropropane dioxygenase: 32.3 Cyberlindnera mrakii ? + HNO2
-
 ?
1.13.12.16 2-nitropropane + O2 superoxide as reactive intermediate Cyberlindnera mrakii acetone + HNO2
-
 ?
1.13.12.16 ethylnitronate + O2 anionic, expression on the basis of the reactivity of propyl-2-nitronate with 2-nitropropane dioxygenase: 32.5 Cyberlindnera mrakii acetaldehyde + HNO2
-
 ?
1.13.12.16 nitroethane + O2
-
 Cyberlindnera mrakii acetaldehyde + HNO2
-
 ?
1.13.12.16 propyl-2-nitronate + O2 anionic Cyberlindnera mrakii acetone + HNO2
-
 ?
1.13.12.16 propylnitronate + O2 anionic, expression on the basis of the reactivity of propyl-2-nitronate with 2-nitropropane dioxygenase: 57.9 Cyberlindnera mrakii ? + HNO2
-
 ?

Synonyms

EC Number Synonyms Comment Organism
1.13.12.16 2-nitropropane dioxygenase
-
 Cyberlindnera mrakii

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
1.13.12.16 6.5
-
 assay at Cyberlindnera mrakii

Cofactor

EC Number Cofactor Comment Organism Structure
1.13.12.16 FAD dependent Cyberlindnera mrakii