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Definiation of lipids
- a family of biomolecules that have the common property of being soluble in organic solvents but not in water.
- typically the lipid content of a plant cell can be extracted using an organic solvent such as ether, chloroform, or acetone
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Composition of waxes
fatty acids+ long chain of alcohols
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Composition of fats and oils
fatty acids+ glycerol
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Physical properties of fats
- melting pt- determined by length of the chain & degree of unsaturation
- saturated- higher mp than unsaturated with same number of carbon atoms
- more double bonds- lower mp ignoring # of carbons
- solubility- low in water
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Simple lipids
glycerol+ fatty acid
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complex lipids
alcohol+ fatty acid+ a third component
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Hydrolyzable lipids
these undergo hydrolytic cleavage into two or more considerably smaller compounds in the presence of an acid, a base, or a digestive enzyme. All of these contain at least one ester group
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Nohydrolyzable lipids
these don't undergo hydrolytic cleavage b/c they don't contain an ester or amide, phosphate, or acetal group
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Lipid function
- cell membrane structure
- energy storage
- hormones and vitamins
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Fatty acid structure
- long chain monocarboxylic acid
- size range C12-C14always and even number of carbons
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saturated vs. unsaturated
- saturated- no double bonds
- unsaturated- one or more double bonds
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Bond designation in fatty acids
18:3
- 18 tells number of C atoms
- 3 tells number of double bonds
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Delta notation
the delta sign after the number of double bonds indicates the placement of the double bonds
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MUFA
monounsaturated fatty acids have 1 double bond in the carbon chain
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PUFA
polyunsaturated fatty acid have 2 or more double bonds
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amphipathic
one part of the molecule is hydrophobic and another part is hydrophilic
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Structure of fats and oils
- chemically fats and oils are both esters
- the alcohol portion is always derived from glycerol and the acid portion is furnished by the fatty acid
- B/c glycerol has 3 OH groups, a single molecule of glycerol can be bonded to 3 different acid molecules
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triglycerides
- fats and oils
- a compound formed by the esterfication of three fatty acids to glycerol
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Linoleic acid
- an omega- 6 fatty acid
- this means that the end most double bond is located 6 carbons from the methyl end of the chain
- CH3(CH2)4(CH=CHCH2)2(CH2)6COOH
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Linolenic acid
an omega- 3 fatty acid where the end most carbon atom having the double bond is 3 carbons from the methyl end
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Olestra
a synthetic polyester of sucrose and fatty acids passes through the digestive tract unabsorbed
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melting points of fatty acids
- fats- soild at room temp
- oils- liquid at room temp
- waxes are solid- ester of a saturated fatty acid and a long chain alcohol containing from 14-30 carbons- serves as a protective coating in feathers
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waxes
- esters of fatty acid and long chain alcohols
- water insoluble and not easily hydrolyzed
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Neutral glycerides
- ester of glycerol and a fatty acid.
- principal function is energy storage- fat
- diagram in note!
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esterification of fatty acids
RCOOH+ROH--> RC(=O)OR+H2O
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hydrolysis of fatty acids
- RC-C(=O)-OR+ H2O-->R-C-OH + ROH
- important for fat and oil digestion
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saponification of fatty acids
- RCOOH+NaOH-->RCOO-Na++H2O
- the commerical production of the salt of fatty acids (soap)
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reactions of unsaturated fatty acids
- they can undergo the same reactions
- will also undergo addition
- most common addition is hydrogenation
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partial hydrogenation
- not all of the double bonds are converted to single bonds
- convert the oil into a solid
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hydrogenation
- decreases the degree of unsaturation, used to make margarines from oils
- now a health concern about the hydrogenation of food products.
- the problem is that during hydrogenation some of the cis-bonds are converted to trans
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summary of reactions
hydrolysis
saponification
esterification
hydrogenation
- hydrolysis-->glycerol+ 3 fatty acids
- saponification: 3 fatty acids+glycerol--> 3 fatty acid salts + 3 water
- esterification--> triacylglyerol + 3 water
- hydrogenation--> reduces the degree of PUFAs
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oxidation
- the C-C double bonds present in the fatty acid residues of a triacygylcerol are subject to oxidation with oxygen from the air as teh oxidizing agent
- producing both aldehyde and carboxylic acid products
- comerically prepared foods containing fats and oils nearly always contain antioxidants- substances that are more easily oxidized than the food
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eicosanoids
- oxygenated C20 fatty acids that function as a messenger
- these are "hormone like" molecules rather than true hormones b/c they are not transported in the blood stream to their site of action
- unsaturated
- some are essentail fatty acids
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Physiological effect of eicosanoids
- 1.inflammatory response
- 2.production of paon and fever
- 3.regulation of blood pressure
- 4.induciton of blood clotting
- 5.control of reproduction functions
- 6.regulation of the sleep/ wake cycle
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Prostaglandins
- all are dervied from arachidoric acid a twenty carbon fatty acid derivation that contains a cyclopentane ring and oxygen containing functional group
- most of these are synthesized from arachidonic acid by a ring closer at C 8 & 12
- the enzyme catalyzing this is called cycloxygenase (COX)
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COX-1
catalyzes the normal physiological function
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COX-2
responsibly for the production of prostaglands
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Smooth muscle contraction
prostaglandins stimulate contractions in the reproductive system
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GI tract
- prostoglandins will:
- inhibit the secretion of hydrocholoric acid in the stomach
- increase secration of mucus layer
- protects mucose from acid invasion
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NSAID
block the oxidation of an achidonic acid to form the various classes of eicosanoids (block COX-2)
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Leukotrienes
produced by WBC's in lungs
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Thromboxane
- produced by platelets in blood
- stimulates constriction of blood vessels
- Aggreation of platelets
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Steroids
broad class of compounds that all have the same base structure. a nonsaponifiable lipid
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Cholesterol
- most abundant steroid in the human body
- principal membrane lipid for fluidity
- insoluble in the aqueous medium of the blood
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How does cholesterol become water soluble
in order for it to be transported from the liver where it is synthesized, to the tissues, cholesterol combines w/ phospholipids & proteins to form small water soluble spherical particles called lipoproteins
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What does cholesterol do to the body's arteries
- LDL supply more cholesterol than is needed, LDLs deposit cholesterol in the wall of arteries forming plaque
- results in:
- increased bp from: narrowing of arteries, reduced ability to stretch
- clot formation leading to: MI, stroke
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What is cholesterol used for?
need for healthy cell membranes and it serves as teh starting material for the synthesis of all other steroids and vit. D
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LDLs
low density lipoproteins transport chloesterol from the liver to the tissue
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HDLs
high density lipoproteins transport cholesterol from the tissue bakc to the liver
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Bile Salts
- emulsifying agents that make dietary lipids soluble in the aqueous environment of the digestive tract
- these salts are released ino the intestine from the gallbladder
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Source for bile salts
- bile, a fluid secreted by the liver, stored in hte gallbladder, and released into the small intestine during digestion
- bile salts are cholesterol oxidation products
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Sex hormones
control reproduction and secondary sex hormones
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estrogen
- synthesized in the ovaries and adrenal cortex- the female sex hormone
- responsible for secondary sex characteristics, onset of puberty, regulation of the menstrual cycle, stimulate the development of the mammary glands
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androgens
- synthesized in the testes
- responsible for the male scondary sex characteristics
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progestins
- synthesized in the ovaries and the placenta
- prepare the lining of the uterus for implantation of the fertilized ovum
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