Enzymatic synthesis of green notes with hydroperoxide-lyase from olive leaves and alcohol-dehydrogenase from yeast in liquid/gas reactor

被引:21
作者
Akacha, Najla Ben [1 ]
Gargouri, Mohamed [1 ]
机构
[1] Natl Inst Appl Sci & Technol, Biocatalysis & Bioproc Unit, Tunis 1080, Tunisia
关键词
Alcohol-dehydrogenase; Biosynthesis; Green note; Hydroperoxide-lyase; Liquid/gas bioreactor; Volatile extraction; FATTY-ACID HYDROPEROXIDE; LIPOXYGENASE PATHWAY; PURIFICATION; SUNFLOWER; OIL;
D O I
10.1016/j.procbio.2009.06.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydroperoxide-lyase is a suitable enzyme for the biocatalytic production of six-carbon aldehydes which are responsible for the "green notes" in many fruits and vegetables. The hydroperoxide-lyase isolated from olive leaves is used in this work. The effects of pH, temperature, and substrate and enzyme concentrations on hexenals generation were optimized. The main objective of this paper consists on the elaboration of a biocatalytic procedure for the synthesis of flavors with green odor characteristics. For this purpose an enzymatic liquid/gas reactor, where the synthesis of C6-compounds was coupled to their extraction, has been proposed. Hexenals were produced in two steps: (1) 13 hydroperoxy-linolenic acid was produced from hydrolyzed linseed oil in presence of soybean lipoxygenase. (2) 3Z- and 2E-hexenals (up to 0.36 g kg(-1) of reaction medium) were produced from 13 hydroperoxy-linolenic acid in presence of olive hydroperoxide-lyase at 50% yield. The hexenals were successfully reduced into their corresponding alcohols by adding yeast cells Saccharomyces cerevisiae containing alcohol-dehydrogenase activity to the same reactor. Significant amounts of 3Z-hexenol (up to 3.54 g; kg(-1) of olive leaves) were produced and extracted at a yield of 47.7% and with high purity when permeabilized yeast cells were used. (C) 2009 Published by Elsevier Ltd.
引用
收藏
页码:1122 / 1127
页数:6
相关论文
共 27 条
[1]  
ADRIANARISON RH, 1989, PLANT PHYSIOL, V91, P1280
[2]   Production of hexenol in a two-enzyme system: kinetic study and modelling [J].
Akacha, NB ;
Boubaker, O ;
Gargouri, M .
BIOTECHNOLOGY LETTERS, 2005, 27 (23-24) :1875-1878
[3]   Improvement and modelling of hexenal transfer in liquid-gas reactor [J].
Ben Akacha, Najla ;
Guizani, Om Elkhir ;
Gargouri, Mohamed .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2007, 143 (03) :276-283
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]  
BRASH A, 2006, Patent No. 7037693
[6]  
Brunerie P., 1997, US Patent, Patent No. [US5620879, 5620879]
[7]  
BRUNERIE P, 1989, Patent No. 12901
[8]  
DELCARTE J, 2000, BIOTECHNOL AGRON SOC, V3, P157
[9]  
GALLIARD T, 1976, BIOCHIM BIOPHYS ACTA, P181
[10]  
GARDNER HW, 1995, HORTSCIENCE, V30, P197