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Damaged starch can be produced, for example, during the wheat milling process, or when drying the starch cake in a starch plant. [5] There is an inverse correlation between gelatinization temperature and glycemic index. [4] High amylose starches require more energy to break up bonds to gelatinize into starch molecules.
The occurrence of starch degradation into sugar by the enzyme amylase was most commonly known to take place in the Chloroplast, but that has been proven wrong. One example is the spinach plant, in which the chloroplast contains both alpha and beta amylase (They are different versions of amylase involved in the breakdown of starch and they ...
A solution of triiodide (I 3 −) (formed by mixing iodine and potassium iodide) can be used to test for starch. The colorless solution turns dark blue in the presence of starch. [70] The strength of the resulting blue color depends on the amount of amylose present. Waxy starches with little or no amylose present will color red.
Modified starch, bonded with phosphate, allows the starch to absorb more water and keeps the ingredients together. [8] Modified starch acts as an emulsifier for French dressing by enveloping oil droplets and suspending them in the water. Acid-treated starch forms the shell of jelly beans. Oxidized starch increases the stickiness of batter.
Amylopectin is a key component in the crystallization of starch’s final configuration, [4] [5] [6] accounting for 70-80% of the final mass. [7] Composed of α-glucose, it is formed in plants as a primary measure of energy storage in tandem with this structural metric.
Retrogradation is a reaction that takes place when the amylose and amylopectin chains in cooked, gelatinized starch realign themselves as the cooked starch cools. [1]When native starch is heated and dissolved in water, the crystalline structure of amylose and amylopectin molecules is lost and they hydrate to form a viscous solution.
There are two reactions occurring simultaneously in the solution. In the first, slow reaction, iodine is produced: H 2 O 2 + 2 I − + 2 H + → I 2 + 2 H 2 O. In the second, fast reaction, iodine is reconverted to two iodide ions by the thiosulfate: 2 S 2 O 2− 3 + I 2 → S 4 O 2− 6 + 2 I −. After some time the solution changes color to ...
Amylose A is a parallel double-helix of linear chains of glucose. Amylose is made up of α(1→4) bound glucose molecules. The carbon atoms on glucose are numbered, starting at the aldehyde (C=O) carbon, so, in amylose, the 1-carbon on one glucose molecule is linked to the 4-carbon on the next glucose molecule (α(1→4) bonds). [3]