Flavor release in the presence of melanoidins prepared from L-(+)-ascorbic acid and amino acids.
Flavor release in the presence of melanoidins prepared from L-(+)-ascorbic acid and amino acids.
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DOI:
10.1021/jf0200366
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发表时间:
2002-07
影响因子:
6.1
通讯作者:
C. Obretenov;J. Demyttenaere;K. Tehrani;A. Adams;M. Keršienė;N. De Kimpe*
中科院分区:
文献类型:
--
作者:
C. Obretenov;J. Demyttenaere;K. Tehrani;A. Adams;M. Keršienė;N. De Kimpe*
High-molecular-weight (HMW) water-soluble melanoidins were prepared from model systems of L-(+)-ascorbic acid-glycine, L-(+)-ascorbic acid-lysine, L-(+)-ascorbic acid-glutamic acid, and glucose-glycine using a very recently approved standard protocol. The amount of HMW water-soluble melanoidins prepared from L-(+)-ascorbic acid was over 5-15 times higher than the amount obtained from glucose. The study of the release of a model flavor compound, namely isoamyl acetate, from melanoidins by solid-phase microextraction (SPME) showed that SPME is a suitable technique for the analysis of flavor release from melanoidin-containing solutions. From the studies on the retention capacity of the melanoidins toward isoamyl acetate, an increased release of the flavor compound was observed from the melanoidins prepared from the L-(+)-ascorbic acid-glycine model system, whereas the opposite effect was observed from the melanoidins prepared from the L-(+)-ascorbic acid-lysine/glutamic acid model systems. The melanoidins prepared from the glucose-glycine model system had the same effect as the melanoidins prepared from the L-(+)-ascorbic acid-glycine model system.