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Hydroperoxide-lyase activity in mint leaves. Volatile C6-aldehyde production from hydroperoxy-fatty acids.
J Biotechnol. 2004 Jul 01; 111(1):59-65.JB

Abstract

The extraction of 13-hydroperoxide-lyase activity from mint leaves as well as its use for C6-aldehyde production was studied in this work. The enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid. Two mint species were tested: Mentha veridis and Mentha pulegium. The headspace injection method coupled to gas chromatography was used for volatile compound analysis. The optimal conditions for temperature and pH were, respectively, 15 and 7 degrees C. We also studied the specific synthesis of hexanal and hexenals respectively from 13(S)-hydroperoxy-linoleic acid and 13(S)-hydroperoxy-linolenic acid. Considerable quantities of aldehyde (up to 2.58 micromol) were produced after 15 min of cleavage reaction in 2 ml stirred at 100 rpm, especially in presence of extract of M. veridis. The conversion yields decreased from 52.5% as maximum to 3.3% when using initial hydroperoxide concentrations between 0.2 and 15 mM. An unsaturated aldehyde, the 3(Z)-hexenal was produced from 13(S)-hydroperoxy-linolenic acid. The 3(Z)-isomer was unstable and isomerized in part to 2(E)-hexenal. In this work, we observed a very limited isomerization of 3(Z)-hexenal to 2(E)-hexenal, since the reaction and the volatile purge were carried out successively in the same flask without delay or any contact with the atmosphere. These aldehydes contribute to the fresh green odor in plants and are widely used in perfumes and in food technology. Their importance increases especially when the starting materials are of natural biological origin as used in this work. GC-MS analysis allowed the identification of the products.

Authors+Show Affiliations

National Institute of Applied Science and Technology (INSAT), Tunis, Tunisia. mohamed.gargouri@insat.rnu.tnNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

15196770

Citation

Gargouri, Mohamed, et al. "Hydroperoxide-lyase Activity in Mint Leaves. Volatile C6-aldehyde Production From Hydroperoxy-fatty Acids." Journal of Biotechnology, vol. 111, no. 1, 2004, pp. 59-65.
Gargouri M, Drouet P, Legoy MD. Hydroperoxide-lyase activity in mint leaves. Volatile C6-aldehyde production from hydroperoxy-fatty acids. J Biotechnol. 2004;111(1):59-65.
Gargouri, M., Drouet, P., & Legoy, M. D. (2004). Hydroperoxide-lyase activity in mint leaves. Volatile C6-aldehyde production from hydroperoxy-fatty acids. Journal of Biotechnology, 111(1), 59-65.
Gargouri M, Drouet P, Legoy MD. Hydroperoxide-lyase Activity in Mint Leaves. Volatile C6-aldehyde Production From Hydroperoxy-fatty Acids. J Biotechnol. 2004 Jul 1;111(1):59-65. PubMed PMID: 15196770.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Hydroperoxide-lyase activity in mint leaves. Volatile C6-aldehyde production from hydroperoxy-fatty acids. AU - Gargouri,Mohamed, AU - Drouet,Philippe, AU - Legoy,Marie-Dominique, PY - 2003/09/01/received PY - 2004/03/15/revised PY - 2004/03/19/accepted PY - 2004/6/16/pubmed PY - 2005/2/11/medline PY - 2004/6/16/entrez SP - 59 EP - 65 JF - Journal of biotechnology JO - J Biotechnol VL - 111 IS - 1 N2 - The extraction of 13-hydroperoxide-lyase activity from mint leaves as well as its use for C6-aldehyde production was studied in this work. The enzyme cleaves 13(S)-hydroperoxy-C18 fatty acids into C6-aldehyde and C12-oxo-acid. Two mint species were tested: Mentha veridis and Mentha pulegium. The headspace injection method coupled to gas chromatography was used for volatile compound analysis. The optimal conditions for temperature and pH were, respectively, 15 and 7 degrees C. We also studied the specific synthesis of hexanal and hexenals respectively from 13(S)-hydroperoxy-linoleic acid and 13(S)-hydroperoxy-linolenic acid. Considerable quantities of aldehyde (up to 2.58 micromol) were produced after 15 min of cleavage reaction in 2 ml stirred at 100 rpm, especially in presence of extract of M. veridis. The conversion yields decreased from 52.5% as maximum to 3.3% when using initial hydroperoxide concentrations between 0.2 and 15 mM. An unsaturated aldehyde, the 3(Z)-hexenal was produced from 13(S)-hydroperoxy-linolenic acid. The 3(Z)-isomer was unstable and isomerized in part to 2(E)-hexenal. In this work, we observed a very limited isomerization of 3(Z)-hexenal to 2(E)-hexenal, since the reaction and the volatile purge were carried out successively in the same flask without delay or any contact with the atmosphere. These aldehydes contribute to the fresh green odor in plants and are widely used in perfumes and in food technology. Their importance increases especially when the starting materials are of natural biological origin as used in this work. GC-MS analysis allowed the identification of the products. SN - 0168-1656 UR - https://www.unboundmedicine.com/medline/citation/15196770/Hydroperoxide_lyase_activity_in_mint_leaves__Volatile_C6_aldehyde_production_from_hydroperoxy_fatty_acids_ DB - PRIME DP - Unbound Medicine ER -