- Open Access
Texture, taste and aroma: multi-scale materials and the gastrophysics of food
© Vilgis; licensee BioMed Central Ltd. 2013
- Received: 9 November 2012
- Accepted: 9 November 2012
- Published: 9 January 2013
The common feature of the large variety of raw and cooked foods is that they are multi-component materials that consist at least of proteins, carbohydrates, fat and water. These basic classes of molecules define most of the structural and textural properties of the foods cooked and processed in the kitchen. Given the different solubility of these components in the basic solvents, water and fat, it becomes clear that many physical properties, such as structure and texture are determined by a large number of competing interactions between these different components.
- Aroma Compound
- Cultural Science
- Odour Activity
- Aroma Release
- Soft Condensed Matter
Ole Mouritsen and Jens Risbo
Cooking and eating are definitely pleasures. Cooking and eating are definitely materials research fields. Cooking and eating are definitely complicated forms of physical, chemical and biological processes with only one aim: pleasure, satisfaction, and satiation. Natural materials as grown in fields, on trees or in water change their state, structure, colour, taste, and smell. Consequently cooking involves simultaneous and non-separable physical, chemical and biological processes in a highly coupled manner, unlike in classical physics, chemistry and biology. Cooking and eating define a new class of multidisciplinary scientific problems on many length and time scales. However, cooking and eating remain culture.
The conformation and dynamics of water-soluble long carbohydrates and partially water-soluble native or denatured proteins define, together with the water content, the textural properties of foods. In addition, local short-range interactions of these macromolecules with comparatively small ions (salts), polar molecules (water, low molecular weight sugars) and amphiphilic molecules (emulsifiers) have a strong influence on macroscopic properties, for example, the mouthfeel as it is demonstrated with simple model systems such as tasty multi-component gels.
These pure ‘materials properties’ are typical in the field of soft condensed matter physics but all foods live from their sensory properties, taste complexity and specific aroma release. Here again, the water–oil/fat solubility of taste and aroma compounds plays a significant role. Water dissolves most of the taste-relevant hydrophilic units (ions, protons, sugars, glutamine acid), whereas oils and fats act as ‘good solvents’ for the lipophilic aroma compounds. Consequently, the interplay between aroma release and odour activity with structure and texture properties follows certain fundamental physical principles. Some of these ‘universal’ features define a relation between structure, processing, solubility and aroma release and close the circle from materials to cultural sciences via the ‘culinary triangle’ developed by the anthropologist Claude Lévy-Strauss. The large variety of texture, taste and aroma can already be viewed in the ‘raw, cooked and fermented’ state of corresponding foods.
From a purely physical point of view, foods need to be treated as multi-scale systems. This becomes obvious from the sensory qualities of the food felt while eating. By biting, chewing, and swallowing, foods are destroyed by the teeth, aroma gets released, taste becomes released, broken food pieces are wetted by the salvia and are transformed to a partially liquid bolus that can be swallowed with pleasure. By translating these elementary processes into naïve physical ideas the relations to materials sciences become visible. The texture of the food is defined via its physical structure including the swelling and lubrication agents, water and oil. The rupture and breakdown of the structure determine, together with the water content and oil concentration, the aroma and taste release. The temperature of the food yields the perception intensity of the culinary sensation. Finally, size, surface states, wettability, and composition of the damaged food in the mouth determine volume and viscosity of the bolus, as well as the satiation.
Both the water and fat content of the foods determine the solution properties of aroma and taste-relevant compounds and ions, exploit spreading on the tongue and stimulate taste buds and trigeminal channels. At the highest level and smallest scales in the scheme shown in Figure1, aroma release takes place. Characteristically shaped volatile aroma compounds are detected by its receptors in the olfactory bulb.
‘Eating with pleasure’ involves thus the entire length scales ranging from macroscopic dimensions down to molecular scales almost simultaneously. Consequently, gastrophysics similarly involves many time scales, which are not independent and cannot be clearly separated from each other, since at the perception level all length and times matter - unlike in food processing where time and lengths scales can be selected to design certain properties of foods.
The basic taste qualities, sweet, sour, salty, bitter and umami of the foods are governed a number of small molecular compounds, which are in most cases water soluble. All sugars and sweeteners are ions or dipolar molecules, salts dissociate in their ions. The acid taste is related to proton activity and umami to a number of water-soluble molecules, the most well-known glutamic acid. Moreover, the ions and the overall ionic strength (salt content) in foods have some implication for the structure and texture of the foods. Monovalent ions contribute to the screening of electrostatic interactions. Bivalent ions can, under certain circumstances, provoke liquid-to-solid phase transitions like calcium or magnesium ions in certain alginates[1, 9].
Aroma compounds are, in contrast, mostly weakly water soluble but dissolve strongly in a fatty environment. Indeed, their odour activity is more or less determined by the volatility (a thermodynamic property defined by the corresponding vapour pressure) and the odour threshold (a physiological-chemical property). Both quantities can be easily measured in defined solvents at a certain temperature. Nevertheless, odour impressions turn out to be more complicated in real foods; many proteins in food have special (hydrophobic) binding sites for aroma compounds that define a ‘local’ vapour pressure. Thus the same aroma compound will appear with different odour activity values in different foods.
The study of simplified model systems is one of the basic approaches in all areas of physics. Model systems contain, despite a high degree of simplifications, most of the general features of the original system. In many cases, model systems define a class of universality valid for many systems. In gastrophysics (as in biophysics) the basic concept of universality does not lead to the most appropriate answer, since local interactions and their origin in a detailed chemical structure matters for the final result - in the ‘laboratory mouth’.
Nevertheless, a number of model systems, in most cases gels with different types of hydrocolloids have been developed that show significant differences in crack behaviour during chewing and mouthfeel, properties that are defined by length and time scales defined by the size of the molecules, respectively the mesh sizes of the gels. Their water binding as well as taste and aroma release are, however, determined by local scales and the rupture of individual chains forming the network. By adding different sugars (monosaccharides, disaccharides, sugar alcohols, and so on) it can be demonstrated how local properties such as hydrate shells have indeed a strong influence on the gelling properties and mouthfeel. These are indeed important questions especially for sweets, desserts and confectionaries. The interplay between hydrocolloids with different persistence length (stiffness) and polar and ionization (for example, agarose as a polar gelling agent, and xanthan as a rather stiff polyelectrolyte) and their different interactions with low molecular weight cosolutes, show ways how the strong effect of sugars on the elastic properties can be minimized[11–13]. Model systems in gastrophysics do then indeed have practical implications ranging from gastronomy to the food industry.
There exist many more examples how simple model systems show basic physical correlations between different food constituents. In addition, some of the dishes created by Ferran Adrià and others of that kitchen style can be viewed as physical model systems, for example when the same food is presented by different drying methods. Drying at moderate temperatures brings different textures and taste compared to freeze-drying or microwave drying. The differences are clear signs of the energy of water binding, the state diagram of the food and the corresponding thermodynamic pathways to the glassy state. Even when the remaining water content of the freeze-dried and temperature-dried food is similar, taste and mouthfeel are different. Both methods define therefore different culinary functions. Here as well, different length scales play essential roles: local scales and interactions (polarity, charges) on molecular scales up to the resulting porosity due to the water dehydration.
Gastrophysics joins many length and time scales. Apart from ‘food physics’ and physical-oriented chemistry, it also needs to take into account physical aspects of aroma chemistry and structural thermodynamic aspects of aroma compounds. It also ranges deep into the understanding of biophysical processes in cell physiology via the dynamics of receptors and psychophysics of perception. Even from a pure physicist’s point of view, cooking-related problems are non-trivial: most of them are of highly non-equilibrium nature. The final states of cooked food depend strongly on the pathway, that is, the ‘processing’. In contrast to many (classical physical) material properties, the resulting structure depends on the processes themselves and apart from a structure–property relationship, gastrophysics needs a clear structure-process-property-flavour relationship.
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