Contribution of the fermenting yeast strain to ethyl carbamate generation in stone fruit spirits

被引:61
作者
Schehl, Beatus
Senn, Thomas
Lachenmeier, Dirk W.
Rodicio, Rosaura
Heinisch, Juergen J.
机构
[1] Univ Osnabruck, Fachbereich Biol Chem, AG Chem, D-79076 Osnabruck, Germany
[2] Univ Osnabruck, Fachbereich Biol Chem, Fachgebiet Genet Genet, D-79076 Osnabruck, Germany
[3] Univ Oviedo, Inst Biotecnol, Dept Bioquim & Biol Mol, E-33006 Oviedo, Spain
[4] CVUA Karlsruhe, D-76187 Karlsruhe, Germany
[5] Univ Hohenheim, Fachgebiet Garungstechnol, Inst Lebensmitteltechnol, D-70593 Stuttgart, Germany
关键词
fermentation; Saccharomyces; yeast; spirit; ethyl carbamate;
D O I
10.1007/s00253-006-0736-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Fermented fruit and beverages frequently contain ethyl carbamate (EC), a potentially carcinogenic compound that can be formed by the reaction of urea with ethanol. Both are produced by the yeast Saccharomyces cerevisiae with ethanol as the major end product of hexose fermentation and urea as a by-product in arginine catabolism. In spirit production, EC can also be derived from cyanide introduced by stone fruit. To determine the relative contribution of yeast metabolism to EC production, we genetically engineered a diploid laboratory strain to reduce the arginase activity, thus blocking the pathway to urea production. For this purpose, strains with either a heterozygous CAR1/car1 deletion or a homozygous defect (car1/car1) were constructed. These strains were compared to the parental wild type and to an industrial yeast strain in cherry mash fermentations and spirit production. The strain with the homozygous car1 deletion showed a significant reduction of EC in the final spirits in comparison to the non-engineered controls. Nevertheless, using this strain for fermentation of stoneless cherry mashes did not completely impede EC formation. This indicates another, as yet unidentified, source for this compound.
引用
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页码:843 / 850
页数:8
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