Sucrose and its substitutes.Sucrose (α D glucopyranosyl 1,2 β D fructofuranoside), called table sugar, is the most common sugar produced and accumulated by plants. 1) Large quantities of the disaccharide accumulate in the edible parts of some plants. 2) Currently, sucrose is used in many agro alimentary products. Nevertheless, though this disaccharide is cheap and easily produced from sugar cane or sugar beets, it is highly caloric. It is well known that the quantity and the frequency of sucrose consumption may induce metabolic and pathologic effects. Indeed, sucrose is efficiently metabolized, thereby influencing the glycaemia of the body and promoting dental caries.3) In mammals, sucrose is rapidly absorbed into the bloodstream in the small intestine and is hydrolysed into glucose and fructose. The ingestion of sucrose raises blood glucose and can cause problems for people suffering from defects in glucose metabolism, such as persons with hypoglycaemia or diabetes. These effects have stimulated the interest in finding other naturally occurring and synthetic sweeteners. Two parameters are critical for defining efficient sucrose substitutes; they should have nutritional qualities and not be harmful to the general health of the individual. 4) Many non or low cariogenic synthetic sugar substitutes are currently available and are found as ingredients in a variety of candies, drinks and diet food, and still novel compounds emerge. 5,6) The main sugar substitutes used to date are aspartame, saccharine, sucralose, and acésulfalme K. No sweetener is a perfect replacement for sucrose, the main limitation being their taste profiles. Moreover, sweeteners are among the most actively discussed additives because of their side effects on health, including dermatological problems, headaches, mood variations, respiratory difficulties, seizures and cancer. 7,8) Five different structural isomers of sucrose composed of glucose and fructose exist with inter glucosidic linkages being α 1,1 (trehalulose), α 1,3 (turanose), α 1,4 (maltulose), α 1,5 (leucrose) and α 1,6 (isomaltulose) as depicted in Fig. 1. These analogues are found in honey, sugar cane and other natural products in very low concentrations. Among these, isomaltulose is the sucrose analogue that has been most extensively studied.9 19) Isomaltulose ( α D glucopyranosyl 1,6 D fructofuranose ) , also known as palatinose, and trehalulose (α D glucopyranosyl 1,1 D fructopyranose) are natural and structural isomers of sucrose that have a sweet taste and very similar physical and organoleptic properties to sucrose. 20 22) Therefore they have been suggested as non cariogenic alternatives to sucrose and are widely used in health products and the food industry as e.g., soft drinks, chewing gums, cakes, candies, chocolate and toothpaste for isomaltulose and food and cosmetic products for trehalulose.
23)Isomaltulose and trehalulose properties and production. Isomaltulose and trehalulose possess sweetening powers of 30% and 70%, respectively, when compared to that of sucrose. 2,10,...