Some taste molecules and their solution properties

被引:87
作者
Parke, SA [1 ]
Birch, GG [1 ]
Dijk, R [1 ]
机构
[1] Univ Reading, Dept Food Sci & Technol, Reading RG6 6AP, Berks, England
关键词
D O I
10.1093/chemse/24.3.271
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The solution properties of a variety of different sapid substances from all four basic taste modalities, namely, sweet (n = 24), salty (n = 7), sour (n = 11) and bitter (n = 2), have been investigated. Some multisapophoric molecules, i.e. molecules exhibiting more than one taste, have also been included in the study in an attempt to define their properties in relation to the tastes they exhibit; eight sweet-bitter and three sally-bitter molecules were used. The density and sound velocity of their solutions in water have been measured and their apparent volumes, apparent compressibilities and compressibility hydration numbers calculated and compared. Apparent molar volumes (phi v) and apparent specific volumes (ASV) reflect the state of hydration of the molecules, and thus their extent of interaction with water structure. The range of ASVs reported are 0.13-0.49 cm(3)/g for salty molecules, 0.55-0.68 cm(3)/g for sweet molecules, 0.53-0.88 cm(3)/g for sweet-bitter molecules and a much wider range (0.16-0.85 cm(3)/g) for sour molecules. Isentropic apparent specific compressibilities range from -2.33 x 10(-5) to -8.06 x 10(-5) cm(3)/g.bar for salty molecules, -3.38 x 10(-7) to -2.34 x 10(-5) cm(3)/g.bar for sweet molecules, +6.35 x 10(-6) to -2.22 x 10(-5) cm(3)/g.bar for sweet-bitter molecules and +6.131 x 10(-6) to -2.99 x 10(-5) cm(3)/g.bar for sour molecules. Compressibility hydration numbers are also determinable from the measurements of isentropic compressibilities and these reflect the number of water molecules that are disturbed by the presence of the solutes in solution. This study also shows that it is possible to group isentropic apparent molar compressibility values by the taste quality exhibited by the molecules in the same order as for ASV.
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页码:271 / 279
页数:9
相关论文
共 36 条
[1]   SOLVENT EFFECTS IN ORGANIC CHEMISTRY .V. MOLECULES IONS AND TRANSITION STATES IN AQUEOUS ETHANOL [J].
ARNETT, EM ;
BENTRUDE, WG ;
BURKE, JJ ;
DUGGLEBY, PM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (07) :1541-+
[2]  
BARTOSHUK LM, 1977, SENSORY PROPERTIES F, P5
[3]  
Birch G. G., 1993, Sweet-taste chemoreception., P129
[4]  
Birch G. G., 1987, Sweetness, P3
[5]  
Birch G. G., 1994, Food Quality and Preference, V5, P87, DOI 10.1016/0950-3293(94)90012-4
[6]   EVIDENCE FOR PROXIMITY OF SWEET AND BITTER RECEPTOR-SITES [J].
BIRCH, GG ;
MYLVAGANAM, AR .
NATURE, 1976, 260 (5552) :632-634
[7]   APPARENT SPECIFIC VOLUMES AND TASTES OF AMINO-ACIDS [J].
BIRCH, GG ;
KEMP, SE .
CHEMICAL SENSES, 1989, 14 (02) :249-258
[8]   ROLE OF THE ANOMERIC CENTER IN SUGAR SWEETNESS [J].
BIRCH, GG ;
SHAMIL, S ;
SHEPHERD, Z .
EXPERIENTIA, 1986, 42 (11-12) :1232-1234
[9]   Specific volumes and sweet taste [J].
Birch, GG ;
Parke, S ;
Siertsema, R ;
Westwell, JM .
FOOD CHEMISTRY, 1996, 56 (03) :223-230
[10]   STRUCTURE-ACTIVITY-RELATIONSHIPS IN SWEETNESS [J].
BIRCH, GG ;
SHAMIL, S .
FOOD CHEMISTRY, 1986, 21 (04) :245-258