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Conversion of anthranilate synthase into isochorismate synthase: implications for the evolution of chorismate-utilizing enzymes.
Plach, Maximilian G; Löffler, Patrick; Merkl, Rainer; Sterner, Reinhard.
Affiliation
  • Plach MG; Institut für Biophysik und physikalische Biochemie, Universität Regensburg, 93040 Regensburg (Germany).
  • Löffler P; Institut für Biophysik und physikalische Biochemie, Universität Regensburg, 93040 Regensburg (Germany).
  • Merkl R; Institut für Biophysik und physikalische Biochemie, Universität Regensburg, 93040 Regensburg (Germany).
  • Sterner R; Institut für Biophysik und physikalische Biochemie, Universität Regensburg, 93040 Regensburg (Germany). Reinhard.Sterner@ur.de.
Angew Chem Int Ed Engl ; 54(38): 11270-4, 2015 Sep 14.
Article in En | MEDLINE | ID: mdl-26352034
ABSTRACT
Chorismate-utilizing enzymes play a vital role in the biosynthesis of metabolites in plants as well as free-living and infectious microorganisms. Among these enzymes are the homologous primary metabolic anthranilate synthase (AS) and secondary metabolic isochorismate synthase (ICS). Both catalyze mechanistically related reactions by using ammonia and water as nucleophiles, respectively. We report that the nucleophile specificity of AS can be extended from ammonia to water by just two amino acid exchanges in a channel leading to the active site. The observed ICS/AS bifunctionality demonstrates that a secondary metabolic enzyme can readily evolve from a primary metabolic enzyme without requiring an initial gene duplication event. In a general sense, these findings add to our understanding how nature has used the structurally predetermined features of enzyme superfamilies to evolve new reactions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chorismic Acid / Intramolecular Transferases / Anthranilate Synthase Language: En Journal: Angew Chem Int Ed Engl Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chorismic Acid / Intramolecular Transferases / Anthranilate Synthase Language: En Journal: Angew Chem Int Ed Engl Year: 2015 Document type: Article