17675583 Structure and Function of Lipids
-
Upload
manisanthosh-kumar -
Category
Documents
-
view
216 -
download
4
description
Transcript of 17675583 Structure and Function of Lipids
-
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
I. Overview of LipidsA. Major CharacteristicsB. FunctionsC. Classification of Lipids
1. Simple Lipids2. Compound (or Complex) Lipids3. Precursor and Derived Lipids4. Steroid Lipids5. Miscellaneous Lipids
II. Fatty Acid (FA)A. Characteristics and StructureB. FunctionsC. Classification of FA
1. According to Chain Length2. According to Bond Type3. According to Source
D. Nomenclature and Common NotationsE. Other Matters
III. Triacylglycerol (TAG)F. Characteristics, Functions and TypesA. Structure
IV. PhospholipidG. Characteristics and Functions A. Glycerophospholipid B. Sphingolipids
V. GlycolipidH. Characteristics, Structure, and FunctionsI. Major Glycolipids in the Body
VI. CholesterolA. Characteristics, Structure, and FunctionsB. Phase Transition Temperature
VII. SummaryVIII. Attachment
I. Overview of LIPIDS
One of the four major groups of biomolecules Unlike proteins, nucleic acids, lipids refer to a
group of heterogeneous (no common structural unit) molecules unified by common chemical features.
Similar to carbohydrates, lipids are non-informational molecules
A. General Characteristics All lipids are:
1. insoluble in water;2. soluble in nonpolar solvents like ether,
benzene, chloroform, etc.; and3. present in biological systems
B. Functions
1. storage of excess energy (e.g. FAs in TAGs)
2. major source of caloric energy (e.g. FAs in TAGs can be hydrolyzed and mobilized for catabolism)
3. thermal insulation (e.g. adipose tissues in subcutaneous tissues) and thermal insulation (e.g. nonpolar lipids act as electrical insulators, allowing rapid propagation of depolarization waves along myelinated nerves)
4. cell membrane components (e.g. phospholipids, glycolipids, cholesterol)
5. lipoproteins (e.g. fat transporters like high
density and low-density lipoproteins = HDL and LDL)
6. essential for normal growth and function (e.g. DHA, docosahexaenoic acid, for brain development)
7. precursors of hormones, coenzymes and chemical mediators like your lipid-soluble vitamins (A, D, E, K); the prostaglandins (mediators of inflammatory and anaphylactic reactions), the thromboxanes (mediators of vasoconstriction) and the prostacyclins (active in the resolution phase of inflammation.)
8. bioeffectors/bioregulators (e.g. phosphatidylinositol can act as a secondary messenger)
9. Others: In small quantities, lipids are present as enzyme cofactors in electron carriers, as light absorbing pigments, as fat soluble vitamins (terpenes), as intracellular messengers, as hydrophobic anchors, etc.
C. Classification of Lipids
1. Simple lipids: Esters of fatty acids with various alcohols.
a. Fats: Esters of fatty acids with glycerol = acyl glycerols or glycerides; depending on the no. of esterified FA: mono-/di-/triacylglycerols. Oils are fats in the liquid state.
b. Waxes: Esters of fatty acids with higher molecular weight monohydric alcohols.
2. Compound (or Complex) lipids: Esters of fatty acids containing groups in addition to an alcohol and a fatty acid.
a. Phospholipids: Lipids containing, in addition to fatty acids and an alcohol, a phosphoric acid residue. They frequently have nitrogen containing bases and other substituents,
eg, in glycerophospholipids the alcohol is glycerol and in sphingophospholipids the alcohol is sphingosine.
b. Glycolipids (glycosphingolipids): Lipids containing a fatty acid, sphingosine, and carbohydrate.
3. Derived lipids: These include by-products of metabolic processes like fatty acids, glycerol, mono- and diacylglycerols, lysophosphatides, fatty aldehydes, ketone bodies.
4. Steroid Lipids: cholesterol, cholesteryl esters, cholesterol derivatives: bile acids, steroid hormones, vitamin D, phytosterols
**Because they are uncharged, acylglycerols (= glycerides), cholesterol, and cholesteryl esters are termed neutral lipids.
July 20, 200920144Page 1 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
http://en.wikipedia.org/wiki/Prostaglandinhttp://en.wikipedia.org/wiki/Prostacyclinhttp://en.wikipedia.org/wiki/Vasoconstrictorhttp://en.wikipedia.org/wiki/Thromboxanehttp://en.wikipedia.org/wiki/Anaphylaxishttp://en.wikipedia.org/wiki/Inflammation -
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
5. Miscellaneous Lipids: aliphatic hydrocarbons, carotenoids, squalene, terpenes (composed of isoprene units), vitamin E and K, glycerol ether, glycosyl glycerols (in plants)
IN FOCUS: Principal classes of STORAGE (triacylglycerols or triglycerides) and MEMBRANE LIPIDS, phospholipids, glycolipids and cholesterol. (see attachment; Fig. 1)
II. Fatty AcidA. Characteristics and Structure
1. A carboxylic acid with long chain hydrocarbon side chain:
where R = aliphatic (acyclic) hydrocarbon
s
i
d
e
c
h
a
i
n
2. usually biosynthesized by the concatenation or linking of 2 carbon units (acetyl CoA )
3. rarely found free in nature but occur in esterified form as the major components of various lipids.
B. Functions1. fuel energy2. maintenance of membrane fluidity 3. component of food oils (coconut oil, etc.)4. growth and devt (essential fatty acids)5. precursor of long-chain polyunsaturated fatty
acids (PUFAs) like arachidonic acid
C. Classification1. According to chain length (no. of methylene
groups or no. of carbon atoms)a. Short chain 2-5 C atomsb. Medium chain 6-12 C atomsc. Long Chain up to 25 C atoms
2. According to bond type a. Saturated FAs
alkyl side chain contain only single bonds;
exists in different conformations due to the complete freedom of rotation of the C-C bond flexible conformation
extended conformation is most stable
b. Unsaturated FAs alkyl side chain contain single and
double bonds cis-trans isomerism exists; double bonds along the side chain
produce kinks w/c contribute to fluidity and permeability.
kinks prevent efficient packing (weakening hydrophobic interaction; thus, an unsatd FA has a lower melting temperature than its satd counterpart
is further classified to: Monounsaturated
(monoethenoid, monoenoic) acids, containing one double bond.
Polyunsaturated (polyethenoid, polyenoic) acids, containing two or more double bonds.
3. According to sourcea. Non-essential fatty acids
can be synthesized by the body (e.g. palmitic acid, and other saturated and monoenoic FAs)
b. Essential fatty acids must be obtained from exogenous
sources (a.k.a. diet); humans lack the anabolic enzymes (desaturases that add a double bond in the 3 and 6 positions) that can synthesize FA with a double bond beyond C-9 (>9)
include your polyunsaturated fatty acids (PUFAs): linoleic, linolenic and arachidonic acids.
D. Nomenclature and Common Notations
1. Common and Systematic Names: see attachment; Table 1
2. Delta () Notation: x:y(m,n,) x = no. C atoms; y = no. of double bonds;
the positions of any double bonds are specified by superscript (m,n,) numbers following (delta).
E.g. a 18-carbon FA w/ one double bond between C-9 and C-10 (C-1 being the carboxyl carbon, C in COOH) & another bet. C-12 and C-13 is designated
18:2(9,12).
3. Omega () Notation Recall: The carbon atoms adjacent to the
carboxyl carbon (Nos. 2, 3, and 4) are also known as the , , and carbons, respectively, and the terminal methyl carbon (farthest from COOH) is known as the or n-carbon.
E.g. 9 indicates a double bond on the ninth carbon counting from the -carbon.
July 20, 200920144Page 2 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
Fig. 2 Linoleic Acid
-
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
In animals, additional double bonds are introduced only between the existing double bond (e.g. 9, 6, or 3) and the carboxyl carbon, leading to three series of fatty acids known as the 9, 6, and 3 [omega] families, respectively.
For the essential fatty acids:Linoleic acid 18:2(9,12) 186
Linolenic acid 18:3(9,12,15) 183Arachidonic acid 20:4(5,8,11,14) 206Docosahexaenoic acid (DHA) 22:6(4,7,10,13,16,19) 226
E. Other Matters
1. Why are essential fatty acids important?EFAs are directly associated with many life-sustaining biological functions:
maintenance of healthy cell membranes growth requirement for healthy skin (prevents dermatitis, dry
flaky skin) (omega-6) precursor of long chain polyunsaturated
fatty acids, PUFAs (fr. omega fatty acids) for brain devt (omega-3) visual acuity/retinal devt (omega-3)
EFAs are precursors of eicosanoids, w/c are signaling molecules made by oxygenation of twenty-carbon essential fatty acids, (EFAs)
e.g. Prostaglandins & Thromboxanes regulate inflammatory response produce pain induce sleep reproduction regulate blood coagulation
Leukotrienes muscle contractant properties chemotactic properties important in allergic reactions
and inflammation
2. More about DHA (Docosahexaenoic acid) Dietary sources: marine animals and
planktons, moss, ferns, seed oils (rapeseed, soya, walnut)
accumulates in the 3rd trimester of pregnancy
plays an important role in brain devt and in visual acuity or retinal devt
supplemented in infant milk formulation DHA & EPA antiatheromatous effect:
lower LDL-cholesterol, triglycerides competes with AA as cyclooxygenase
substrate, lowers thromboxane production, dec. platelet aggregation
associated with lower incidence of atherosclerosis & CVD (cardiovascular disease)
3. Trans Unsaturated Fatty Acids: Good or Bad?
Present in: margarine, breads, chips, fries, breast milk, shortening
Produced by the partial hydrogenation of unsatd FAs. by the microorganisms in the GI tract of cattle
Hydrogenation is done commercially to increase the melting point of cis-unsatd lipids, w/c makes them attractive for baking and extends their shelf-life. However, the process frequently has a side effect that turns some cis-isomers into trans-unsaturated fats instead of hydrogenating them completely.
Adverse Health Effects: essential fatty acid balance and growth
in infants high maternal intake inhibits low-chain
PUFA production necessary for fetal growth and devt, visual and CNS devt
The human lipase enzyme is ineffective with the trans configuration, so trans fat remains in the blood stream for a much longer period of time and is more prone to arterial deposition and subsequent plaque formation.
Unlike other dietary fats, trans fats are not essential; raise levels of "bad" LDL cholesterol and lowering levels of "good" HDL cholesterol.
increases risk for CVD, cardiovascular diseases.
III. Triacylglycerol (also called Triglyceride)A. Characteristics, Types and Functions
1. nonpolar, hydrophobic & water-insoluble = lipid
2. energy reservoir in animals (stored in reduced and anhydrous form in the adipocytes); major storage lipid: 3 FAs can be esterified to the glycerol (= efficient packing).
3. energy source: FAs can be hydrolyzed, mobilized and catabolized if needed by the body.
4. Can be simple: composed only of one kind of fatty acid; or mixed: composed of more than one type of FA.
B. Structure
+ R1COOH + R2COOH+ R3COOH
Basic structure of triacylglycerol
(if R1=R2=R3 simple TAG)
July 20, 200920144Page 3 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
http://en.wikipedia.org/wiki/High-density_lipoproteinhttp://en.wikipedia.org/wiki/Low-density_lipoproteinhttp://en.wikipedia.org/wiki/Essential_fatty_acidhttp://en.wikipedia.org/wiki/Essential_fatty_acidhttp://en.wikipedia.org/wiki/Oxygenationhttp://en.wikipedia.org/wiki/Lipid_signaling -
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
1-Stearoyl, 2-linoleoyl, 3-palmitoyl glycerol, a mixed triacylglycerol
IV. PhospholipidA. Characteristics and Functions
Amphipathic lipids with nonpolar aliphatic tails and polar phosphoryl-X head.
Amphiphilic or amphipatic property governs lipid aggregation into higher order structure:
spontaneous self assembly and self sealing principle behind the formation of amphipathic
lipid aggregates in water: micelles (transport of bile acids), liposomes (transport of drugs) and bilayers (membranes)
Major types of phospholipids: glycerophospholipids and sphingolipids
Functions: major components of cell membranes and
found in most tissues (e.g. phosphatidylethanolamine = cephalin and phosphatidylserine)
bioeffectors (phosphatidylinositol, etc.)
Phosphatidylinositols in cellular regulation.Phosphatidylinositol 4,5-bisphosphate in the plasma membrane is hydrolyzed by a specific phospholipase C in response to hormonal signals. Both products of hydrolysis act as intracellular messengers.
lung surfactant, maintains normal lung function (e.g. Dipalmitoyl lecithin = dipalmitoyl phosphatidylcholine)
detergent properties help solubilize cholesterol
donors of arachidonic acid for the synthesis of prostaglandins, thromboxanes and leukotrienes
B. Glycerophospholipid
1. also called phosphoglycerides2. membrane lipids in which two FAs are
attached in ester linkage to the first and second carbons of glycerol, and a highly polar or charged group is attached through a phosphodiester linkage to the third carbon
structural backbone: phosphatidic acid
3. Phospholipids may be regarded as derivatives
of phosphatidic, in which the phosphate is esterified with the OH of a suitable alcohol.
Doodle Space:
July 20, 200920144Page 4 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
Micelle Bilayer
Liposome
Aqueous cavity
-
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
C. Sphingolipid (~Sphingomyelins)
Sphingomyelins are found in large quantities in brain and nerve tissue. On hydrolysis, the sphingomyelins yield a fatty acid, phosphoric acid, choline, and a complex amino alcohol, sphingosine. No glycerol is present.
The combination of sphingosine plus fatty acid is known as ceramide, a structure also found in the glycosphingolipids (also in glycolipids)
General Structure:
V. GlycolipidA. Characteristics, Structure and Functions
1. Glycolipids are widely distributed in every tissue of the body, particularly in nervous tissue such as brain. They occur particularly in the outer leaflet of the plasma membrane, where they contribute to cell surface carbohydrates:
cell adhesion and cell recognition; some are antigens (e.g. ABO blood group substances); some are receptors for bacterial toxins
2. Structure: Lipids containing a fatty acid (FA) +
sphingosine (= ceramide), and one or more carbohydrate.
Their backbone is either sphingosine or dihydrosphingosine, both are
complex amino alcohols Fatty acids attach to the amino group
instead of attaching to the OH group.
B. Major Glycolipids in the Body1. Cerebrosides
the simplest glycosphingolipid in the body contains ceramide (FA + sphingosine) and
a single sugar residue (the head group) contains either glucose
(glucosylcerebroside or GlcCer) or galactose (galactosylcerebroside or GalCer)
GalCer major lipid of myelin; GlcCer major glycosphingolipid of
extraneural tissues but also present in small amounts in the brain; and precursor of most of the more complex glycosphingolipids
2. Sulfatides (Sulfogalactosylceramides) C3 sulfated cerebroside (specifically, a
galactosylcerebroside) or a cerebroside 3-sulfate
It is present in high amounts in myelin Present in early stages of Alzheimers disease and
associated with Metachromic Leukodystrophy.
3. Globoside Cerebroside + 2 or more sugars N-acetylgalactosamine as its side chain If globosides accumulate, Sandhoff disease may
occur
4. Gangliosides complex glycosphingolipids derived from
glucosylceramide that contain in addition one or more molecules of sialic acid (ceramides + oligosaccharide + at least sialic acid)
most common and principal sialic acid found in human tissues is n-acetylneuraminic acid or NeuAc or NANA
at least 60 gangliosides are known (differ mainly in the position and number of NeuAc)
Main functions include the following:o complex CHO group; receptor for
certain pituitary glycoprotein hormones
o bacterial protein toxin receptoro cell to cell recognitiono associated with Tay-Sachs disease
Gangliosides with one NeuAc: GM3, GM2, GM1 (G represents ganglioside, M is a monosialo-containing species, and subscript is a number assigned on the basis of chromatographic migration)
GM3 = [5-acetyl-alpha-neuraminic acid] + [beta-D-galactopyranose] + [beta-D-
July 20, 200920144Page 5 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
-
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
glucopyranose] + ceramide GM2 = GM3 + [N-acetyl-beta-D-
galactopyranose] GM2 accumulation in nerve cells of brain
and other tissues is associate with Tay-Sachs disease and Sandhoff disease
GM1 = GM2 + [beta-D-galactopyranose] GM1 is an important receptor in human
intestine for cholera toxin; GM2 for C. botulinum toxin
VI. CholesterolA. Characteristics, Structure, and Functions
the major sterol in the body (sterol = compound has one or more hydroxyl or OH group and no carbonyl or carboxyl group)
hydrophobic but with OH group widely distributed in all cells of the body but
particularly in nervous tissue major constituent of plasma membrane and
of plasma lipoproteins precursors of bile acids, steroid hormones
(adrenocortical and sex hormones), & vit. D often found as cholesteryl ester (-OH group
on position 3 is esterified with a long-chain FA)
occurs in animals but not in plants or bacteria with a steroid (cyclic) nucleus (derivative of
cyclopentanoperhydrophenanthrene ring) that resembles a phenanthrene to which a cyclopentane ring is attached.
has a planar confirmation It acts as a stabilizer by modifying
membrane fluidity (i.e. phase transition temperature)
B. Phase transition temperature (Tm)(Some explanations are obtained from Harpers Illustrated Biochemistry, 27e actually, similar din ng explanation ni Dr. Leano)
it is the temperature at which the structure undergoes the transition from ordered to disordered (i.e. melting)
the longer and more saturated fatty acid chains interact more strongly with each other via their long hydrocarbon chains, the higher the value of Tm (i.e. higher temperatures are required to increase the fluidity of the bilayer)
on the other hand, unsaturated bonds that exist in the cis configuration tend to increase the fluidity of a bilayer by decreasing the compactness of the side chain packing without diminishing hydrophobicity.
below Tm: increased fluidity (cholesterol interferes with interaction of hydrocarbon tails of FAs)
above Tm: limited fluidity (cholesterol limits disorder); more rigid than the hydrocarbon tails of the FAs and cannot move in the membrane to the same extent
at high cholesterol: phospholipid ratios, transition temperatures are altogether indistinguishable
VII. Summary Lipids have the common property of being
relatively insoluble in water (hydrophobic) but soluble in nonpolar solvents. Amphipathic lipids also contain one or more polar groups, making them suitable as constituents of membranes at lipid:water interfaces. The lipids of major physiologic significance are fatty acids and their esters, together with cholesterol and other steroids.
Special Thanks to our References: Lehninger PRINCIPLES OF BIOCHEMISTRY, 4e
Harpers ILLUSTRATED BIOCHEMISTRY, 27e Campbells BIOCHEMISTRY
Prof. Leaos lecture transcribed by Bryan Mesina, Jean Mendoza, Mark Mauricio and Marvin Masalunga
Doc Nics Biochemistry Module
Greetings from the Transcribers:
Alphius: Hi Class 2014! :-) I am Ralph Julius Mendoza. I hope that the reader of this trans will find this
July 20, 200920144Page 6 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
-
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
historical piece useful and inspiring. Good luck to everybody and may we get to know each other more
Should you have any question regarding our trans, Id be glad to be of service. Lets all love biochem :-)
Para iba naman ang greeting comics time! ~Mau~AFTG! (All For The Girls?! hahaha)
Oy Bryan ang haba ng greeting mo! Andaming girls sa greeting mo ha. Sino ba talaga sa kanila?! Hahahaha.
Bryan: Howdy 2014!! Hope yall enjoy our trans on nothin but fats!! Get it? Fats?? *insert silence here* Id like tah give an effer-y shoutout tah mah iMed peepz!! I miss yall so effin much!! We should hang more oftenseriously. Hello tah mah fellow iMed cheerdancers! Sana hindi niyo pa nakakalimutan yung mga steps!! Wed perform our routine again someday!! Haha! Hi tah thuh 8 Ducklings!! Hi too tah mah fellow Alphamales!! Sa next birthday ng isa satin ah! Hi tah Block 13 and 14 at sa mga nagfee-feeling na Block 14!! :P Sa bio25 at bio30
groupmates ko, reunion tayo! Siyempre, I wouldnt foget, hi tah mah 122 new friends!! Ive talked or have at least greeted 120 of ye..2 nalang!! And swear, Ive memorized all yer faces and names!! :D So tah those 2 people, watch out! One of these days..Id greet ye!! O eto, personal greetings: Denden, di ko pa kayang baguhin language ko! AA, may love interest ka na pala ah! Roland, I still hafta skin ye alive!! Pero not before yer boards sa Saturday..good luck!! Karla, sana maintindihan mo to..although I doubt it..haha! Mommy Carla Boz..i miss yer hugs! Lee-Ann, class picture!! :P Jegar and his narcoleptic buddies, we support ye!! Sa Saturday futsal club, laro ulit tayo! Shayne, hun, I miss ye! RR, gah! Lau, Julie (aka Bo-bo) and Dana, secret lang yun ah and thanx sa net!! Sa mga katokayo ko sa class, hey! Jesha, ligawan mo na kasi si Dr. Papa P! Jay, may bayad siehemhaha! Dogfish!! Maetrix, di ko na aalamin..kasi sasabihin mo din naman eventually sakin!! Alex, ano nang nickname ni blood brain barrier?? Hahaha! Jhing, September 5 ah! Bea, ye really look like Toniand Reese toohahaha! Sa mga fellow LOs ko na nagpapakahirap, saya no? Marvie!! Makakalimutan ba naman kita? Kahit na 3 seconds lang ang memory mo fo me..haha! I miss ye!! Lastly, a shoutout tah mah bestfriend Pito! Oi baller ko!! 4-words and Peace&Bounce man! B-) Waw..haba na pala nitong greeting ko..haha! 1:26am na sa clock koEFFER!!!
P.S.: Mau, ano? I-highlight ko? Hahaha! :P
Jean: CONG-GRA-TU-LATIONS! NOW NA!Tulong tayo lahat sa Lady Med! Sept 4 na! Yay. Yay. Yay. Seryoso ako.
September 4!!!!!!!!LADY MED!!!!!
VIII. ATTACHMENT
Fig. 1. Lipids-in-focus. Note the Common Denominator: Fatty Acid
Fig. 1. Lipids-in-focus. Note the Common Denominator: Fatty Acid
Table. 1. Some Naturally Occurring Fatty Acids: Structure, Properties, and Nomenclature
July 20, 200920144Page 7 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
-
Monday
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
*All acids are shown in their nonionized form. At pH 7, all free fatty acids have an ionized carboxylate. Note that numbering of carbon atoms begins at the carboxyl carbon.The prefix n- indicates the normal unbranched structure. For instance, dodecanoic simply indicates 12 carbon atoms, which could be arranged in a variety of branched forms; n-dodecanoic specifies the linear, unbranched form. For unsaturated fatty acids, the configuration of each double bond is indicated; in biological fatty acids the configuration is almost always cis.
July 20, 200920144Page 8 of 7 Mau, Jean, Alphius, Bryan
Prof. Milagros Leao
Lecture # 3 Structures and Functions Structures and Functions Exam 1
OS 201: Correlative Human Cell BiologyOS 201: Correlative Human Cell Biology
A.Characteristics and StructureB.FunctionsC.Classification of FA1.According to Chain Length2.According to Bond Type3.According to SourceD.Nomenclature and Common NotationsE.Other MattersF. Characteristics, Functions and TypesG.Characteristics and Functions H.Characteristics, Structure, and FunctionsI.Major Glycolipids in the Body