Olfactory Perception of Cysteine−S-Conjugates from Fruits and Vegetables

Christian Starkenmann*, Benedicte Le Calvé, Yvan Niclass, Isabelle Cayeux, Sabine Beccucci and Myriam Troccaz
Corporate R&D Division, Firmenich SA, P.O. Box 239, CH-1211 Geneva 8, Switzerland
J. Agric. Food Chem., 2008, 56 (20), pp 9575–9580
DOI: 10.1021/jf801873h
Publication Date (Web): September 24, 2008
Copyright © 2008 American Chemical Society
* Author to whom correspondence should be addressed (telephone +41 22 780 34 77; fax +41 22 780 33 34; e-mail christian.starkenmann@firmenich.com).

Abstract

Abstract Image

Volatile sulfur compounds have a low odor threshold, and their presence at microgram per kilogram levels in fruits and vegetables influences odor quality. Sensory analysis demonstrates that naturally occurring, odorless cysteine−S-conjugates such as S-(R/S)-3-(1-hexanol)-l-cysteine in wine, S-(1-propyl)-l-cysteine in onion, and S-((R/S)-2-heptyl)-l-cysteine in bell pepper are transformed into volatile thiols in the mouth by microflora. The time delay in smelling these volatile thiols was 20−30 s, and persistent perception of their odor occurred for 3 min. The cysteine−S-conjugates are transformed in free thiol by anaerobes. The mouth acts as a reactor, adding another dimension to odor perception, and saliva modulates flavors by trapping free thiols.

Keywords:

Mouth microflora; Fusobacterium nucleatum; saliva; cysteine−S-conjugates; sensory analysis

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History

  • Published In Issue October 22, 2008
  • Article ASAPSeptember 24, 2008
  • Received: June 18, 2008
    Accepted: August 24, 2008
    Revised: August 13, 2008

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