From Wikipedia, the free encyclopedia
Linalool dehydratase
Identifiers
EC no. 4.2.1.127
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Search
PMC articles
PubMed articles
NCBI proteins

Linalool dehydratase ( EC 4.2.1.127, linalool hydro-lyase (myrcene-forming)) is an enzyme with systematic name (3S)-linalool hydro-lyase (myrcene-forming). [1] [2] This enzyme catalyses the following chemical reaction

(3S)- linalool myrcene + H2O

In absence of oxygen this enzyme can also catalyse the isomerization of (3S)-linalool to geraniol.

References

  1. ^ Brodkorb D, Gottschall M, Marmulla R, Lüddeke F, Harder J (October 2010). "Linalool dehydratase-isomerase, a bifunctional enzyme in the anaerobic degradation of monoterpenes". The Journal of Biological Chemistry. 285 (40): 30436–42. doi: 10.1074/jbc.m109.084244. PMC  2945536. PMID  20663876.
  2. ^ Lüddeke F, Harder J (2011). "Enantiospecific (S)-(+)-linalool formation from beta-myrcene by linalool dehydratase-isomerase". Zeitschrift für Naturforschung C. 66 (7–8): 409–12. doi: 10.5560/znc.2011.66c0409. PMID  21950166.

External links

From Wikipedia, the free encyclopedia
Linalool dehydratase
Identifiers
EC no. 4.2.1.127
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Search
PMC articles
PubMed articles
NCBI proteins

Linalool dehydratase ( EC 4.2.1.127, linalool hydro-lyase (myrcene-forming)) is an enzyme with systematic name (3S)-linalool hydro-lyase (myrcene-forming). [1] [2] This enzyme catalyses the following chemical reaction

(3S)- linalool myrcene + H2O

In absence of oxygen this enzyme can also catalyse the isomerization of (3S)-linalool to geraniol.

References

  1. ^ Brodkorb D, Gottschall M, Marmulla R, Lüddeke F, Harder J (October 2010). "Linalool dehydratase-isomerase, a bifunctional enzyme in the anaerobic degradation of monoterpenes". The Journal of Biological Chemistry. 285 (40): 30436–42. doi: 10.1074/jbc.m109.084244. PMC  2945536. PMID  20663876.
  2. ^ Lüddeke F, Harder J (2011). "Enantiospecific (S)-(+)-linalool formation from beta-myrcene by linalool dehydratase-isomerase". Zeitschrift für Naturforschung C. 66 (7–8): 409–12. doi: 10.5560/znc.2011.66c0409. PMID  21950166.

External links


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