Asymmetric bioreduction of activated alkenes using cloned 12-oxophytodienoate reductase isoenzymes OPR-1 and OPR-3 from Lycopersicon esculentum (tomato): a striking change of stereoselectivity

Angew Chem Int Ed Engl. 2007;46(21):3934-7. doi: 10.1002/anie.200605168.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / chemical synthesis
  • Aldehydes / chemistry
  • Alkenes / chemistry*
  • Arabidopsis Proteins / chemistry*
  • Carboxylic Acids / chemical synthesis
  • Carboxylic Acids / chemistry
  • Imides / chemical synthesis
  • Imides / chemistry
  • Isoenzymes / chemistry
  • Ketones / chemical synthesis
  • Ketones / chemistry
  • Lactones / chemical synthesis
  • Lactones / chemistry
  • Molecular Structure
  • Oxidation-Reduction
  • Oxidoreductases / chemistry*
  • Oxidoreductases Acting on CH-CH Group Donors / chemistry*
  • Solanum lycopersicum / enzymology*
  • Stereoisomerism

Substances

  • Aldehydes
  • Alkenes
  • Arabidopsis Proteins
  • Carboxylic Acids
  • Imides
  • Isoenzymes
  • Ketones
  • Lactones
  • OPR3 protein, Arabidopsis
  • Oxidoreductases
  • Oxidoreductases Acting on CH-CH Group Donors
  • 12-oxophytodienoate reductase