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Miraculin is a , a extracted from the fruit of Synsepalum dulcificum. The berry, also known as the miracle fruit, was documented by explorer Chevalier des Marchais, who searched for many different fruits during a 1725 excursion to its native West Africa.

Miraculin itself does not taste . When are exposed to miraculin, the protein binds to the sweetness receptors. This causes normally sour-tasting acidic foods, such as , to be perceived as sweet. The effect can last for one or two hours.


History
The sweetening properties of Synsepalum dulcificum berries were first noted by des Marchais during expeditions to West Africa in the 18th century. The term miraculin derived from experiments to isolate and purify the active that gave the berries their sweetening effects, results that were published simultaneously by Japanese and Dutch scientists working independently in the 1960s (the Dutch team called the glycoprotein mieraculin). The word miraculin was in common use by the mid-1970s.


Glycoprotein structure
Miraculin was first sequenced in 1989 and was found to be a 24.6  glycoprotein consisting of 191 and 13.9% by weight of various sugars.

Amino acids sequence of glycoprotein miraculin unit adapted from biological database of protein sequences. database entry P13087

The sugars consist of a total of 3.4 kDa, composed of a molar ratio of (31%), (30%), (22%), (10%), and (7%).

The of miraculin is a consisting of two dimers, each held together by a bridge. Both tetramer miraculin and native dimer miraculin in its crude state have the taste-modifying activity of turning sour tastes into sweet tastes. Miraculin belongs to the Kunitz STI protease inhibitor family.


Sweetness properties
Miraculin, unlike (another taste-modifying agent), is not sweet by itself, but it can change the perception of sourness to sweetness, even for a long period after consumption. The duration and intensity of the sweetness-modifying effect depends on various factors, such as miraculin concentration, duration of contact of the miraculin with the tongue, and acid concentration. Miraculin reaches its maximum sweetness with a solution containing at least 4*10−7 mol/L miraculin, which is held in the mouth for about 3 minutes. Maximum is equivalent in sweetness to a 0.4 mol/L solution of .
(2025). 9783319270272
Miraculin degrades permanently via denaturation at high temperatures and at pH below 3 or above 12.

Although the detailed mechanism of the taste-inducing behavior is unknown, it appears the sweet receptors are activated by acids which are related to sourness, an effect remaining until the perceive a neutral pH. Sweeteners are perceived by the human sweet taste receptor, hT1R2-hT1R3, which belongs to G protein-coupled receptors, modified by the two residues (i.e. His30 and His60) which participate in the taste-modifying behavior. One site maintains the attachment of the protein to the membranes while the other (with attached or ) activates the sweet receptor membrane in acid solutions.


As a sweetener
As miraculin is a readily soluble protein and relatively heat stable, it is a potential in acidic food, such as . While attempts to express it in and have failed, researchers have succeeded in preparing genetically modified E. coli bacteria that express miraculin. and have also been used for mass production of miraculin.

The use of miraculin as a food additive was denied in 1974 by the United States Food and Drug Administration.

(2009). 9780385662680, .
However, it can still be sold in the form of whole berries or tablets (as "dietary supplements"). In 2011 the FDA banned a certain brand of miraculin tablets imported from Taiwan as it was thought to be "hard candy" with non-approved sweeteners. Miraculin has a status in the . It is approved in as a safe , according to the List of Existing Food Additives published by the Ministry of Health and Welfare (published by the Japan External Trade Organization).


See also

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