ft 100 lect

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    The study of Food

    Raw food

    sometimes called live or living foodhas not been cooked or exposed to

    temperatures over 118 F.

    Contain enzymes and nutrients

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    Cooking of Carbohydrate

    Produced acrylamide

    Cancer causing chemical used for plastics and dyes

    The higher the temperature, the higher acryl amide

    Fryingoils oxidize creating harmful free radicals

    increasing the risk of cancer, heart disease andpremature aging.

    destroys Vitamins A and E ( protection against

    free radicals)

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    diets high in fat are connected with certaincancers, especially breast and prostate cancer

    A study reported in 2005 found that a low-fatdiet reduced the risk of breast cancerrecurrence in women treated for early-stagebreast cancer

    People can lower their fat consumption byeating less red meat and fewer high-fat dairyproducts

    Limiting consumption of alcoholic beveragesto one drink a day can also lower the risk ofcertain cancers

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    Certain free radicals can cause cell damage,

    injuring the lining of cell membranes,

    destroying mitochondria(the cells energy-

    producing organelles), and triggering cell

    death

    Studies show that dopamine-producing cells

    are particularly vulnerable to free-radical

    destruction

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    Antioxidants

    vitamin C in strawberries, oranges, broccoli,and brussels sprouts

    Beta-carotene in orange-colored fruits and

    vegetables and dark green, leafy vegetables,sweet potatoes, spinach, and carrots

    vitamin E in wheat germ oil and sunflower

    seeds

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    Carbohydrates

    One mole of Carbon

    2 moles of Hydrogen

    One mole of Oxygen

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    Starches

    Sugars Cellulose

    Monosaccharides Disaccharides

    Oligosaccharides

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    Sugars

    white crystalline carbohydrates

    soluble in water

    generally have a sweet taste

    Monosaccharides are simple sugars.

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    No. ofCarbons

    CategoryName

    Examples

    4 Tetrose Erythrose, Threose

    5 PentoseArabinose, Ribose,Ribulose, Xylose, Xylulose,Lyxose

    6 Hexose Allose, Altrose, Fructose,Galactose, Glucose,

    Gulose, Idose, Mannose,Sorbose, Talose, Tagatose

    7 Heptose Sedoheptulose,Mannoheptulose

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    Notes

    Many saccharide structures differ only in the

    orientation of the hydroxyl groups (-OH).

    This slight structural difference makes a big

    difference in the biochemical properties,

    organoleptic properties (e.g., taste)

    and the physical properties such as melting

    point and Specific density

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    Rotation (how polarized light is distorted).

    A chain-form monosaccharide that has a

    carbonyl group (C=O) on an end carbon

    forming an aldehyde group (-CHO) is classified

    as an aldose

    when the carbonyl group is on an inner atom

    forming a ketone, it is classified as a ketose.

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    D-ribose D- arabinose D- xylose

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    Ribose and De-oxyribose

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    Disacchari

    de

    Description Component

    monosaccharides

    sucrose common table

    sugar

    glucose 12 fructose

    maltose product of starch

    hydrolysis

    glucose 14 glucose

    trehalose found in fungi glucose 11 glucose

    lactose main sugar inmilk

    galactose 14 glucose

    melibiose found in

    legumes

    galactose 16 glucose

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    Sucrose, lactose, maltose

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    Sucrose, a saccharose, is ordinary table sugarfrom sugar cane or sugar beets, main ingredient inturbinado sugar, evaporated or dried cane juice,brown sugar, and confectioner's sugar

    Lactose has a molecular structure consisting of

    galactose and glucose, associated with lactoseintolerance

    Maltoseconsists of two -D-glucose moleculeswith the alpha bond at carbon 1 of one moleculeattached to the oxygen at carbon 4 of the secondmolecule. This is called a 14 glycosidic linkage.

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    Starch the major form of stored carbohydrate in

    plants, composed of a mixture of two

    substances: amylose, an essentially linearpolysaccharide, and amylopectin, a highly

    branched polysaccharide.

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    Cellulosea polymer of-D-Glucose, which in contrast to

    starch, is oriented with -CH2OH groupsalternating above and below the plane of thecellulose molecule thus producing long,unbranched chains

    The absence of side chains allows cellulosemolecules to lie close together and form rigidstructures.

    major structural material of plants. Wood is largelycellulose, and cotton is almost pure cellulose.

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    can be hydrolyzed to its constituent glucose units bymicroorganisms that inhabit the digestive tract oftermites and ruminants

    may be modified in the laboratory by treating itwith nitric acid (HNO3) to replace all the hydroxyl

    groups with nitrate groups (-ONO2) to producecellulose nitrate (nitrocellulose or guncotton) whichis an explosive component of smokeless powder

    Partially nitrated cellulose, known as pyroxylin, isused in the manufacture of collodion, plastics,lacquers, and nail polish.

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    Glucose metabolism

    absorbed by the digestive tract

    Maintained in the blood at an approximatelyconstant level

    readily catabolized for energy

    breaks down into carbon compounds

    readily oxidized to carbon dioxide and water andthen excreted

    If not used immediately for energy, glucose isconverted to glycogen

    and stored in the liver and muscles When these reserves are filled, glucose is

    converted to fat and deposited in adipose tissue

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    Sugar Beet a member of the goosefoot family

    the source of nearly 40 percent of the worldssugar supply.

    the root of the sugar beet is cut and crushed toremove the juice, juice is then processed, refined,and bleached to produce sugar, while the crushedpulp is used as a livestock feed

    Sugarcane is grown in tropical areas, and sugar

    beets are generally grown in temperate areas.Leading sugar beet producing countries includeGermany, France, Poland, the northwesternUnited States, and the former Soviet Union.