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Post by Dr Sarhan on Sun Jan 06, 2008 1:43 pm

Saponifiable and Nonsaponifiable Lipids
Lipids can be considered to be biological molecules which are soluble in organic solvents, such as chloroform/methanol, and are sparingly soluble in aqueous solutions. There are two major classes, saponifiable and nonsaponifiable, based on their reactivity with strong bases. The nonsaponifiable classes include the "fat-soluble" vitamins (A, E) and cholesterol.
Figure: Examples saponifiable and nonsaponifiable lipids

Saponification is the process that produces soaps from the reaction of lipids and a strong base. The saponifiable lipids contain long chain carboxylic acids, or fatty acids, esterified to a “backbone” molecule, which is either glycerol or sphingosine.
Note on nomenclature: Lipids are often distinguished from another commonly used word, fats. Some define fats as lipids that contain fatty acid that are esterified to glycerol. I will use the lipid and fat synonymously.
The major saponifiable lipids are triacylglycerides, glycerophospholipids, and the sphingolipids. The first two use glycerol as the backbone. Triacylglycerides have three fatty acids esterified to the three OHs on glycerol. Glycerophospholipids have two fatty acids esterified at carbons 1 and 2, and a phospho-X groups esterifed at C3. Spingosine, the backbone for spingolipids, has a long alkyl group connected at C1 and a free amine at C2, as a backbone. In spingolipids, a fatty acid is attached through an amide link at C2, and a H or esterified phospho-X group is found at C3. A general diagrams showing the difference in these structures is shown below.
Figure: Classification of common phospholipids, glycolipids, and triacylglyerides

The actual chemical structures of these lipids are shown below.
Figure: Structures of common phospholipids

Figure: Comparison of lipids with glycerol and sphingosine as backbones

Properties of Lipids

The structure of these molecules determines their function. For example, the very insoluble triacylglycerides are used as the predominant storage form of chemical energy in the body. In contrast to polysaccharides such as glycogen (a polymer of glucose), the Cs in the acyl-chains of the triacylglyceride are in a highly reduced state. The main source of energy to drive not only our bodies but also our society is that obtained through oxidizing carbon-based molecules to carbon dioxide and water, in a reaction which is highly exergonic and exothermic. Sugars are already part way down the free energy spectrum since each carbon is partially oxidized. 9 kcal/mol can be derived from the complete oxidation of fats, in contrast to 4.5 kcal/mol from that of proteins or carbohydrates. In addition, glycogen is highly hydrated. For every 1 g of glycogen, 2 grams of water is H-bonded to it. Hence it would take 3 times more weight to store the equivalent amount of energy in carbohydrates as is stored in triacylglyceride, which are stored in anhydrous lipid "drops" within cells . The rest of this unit on lipids will focus not on triacylglycerides, whose main function is energy storage, but on fatty acids and phospholipids, and the structures they form in aqueous solution.
The structure of fatty acids and phospholipids show them to amphiphilic - i.e. they have both hydrophobic and hydrophilic domains. Fatty acids can be represented in "cartoon-form" as single chain amphiphiles with a circular polar head group and a single acyl non-polar tail extending from the head. Likewise, phospholipids can be shown as double chain amphiphiles. Even cholesterol can be represented this way, with its single OH group as the polar head, and the rigid 4 member rings as the hydrophobic “tail”. Even through there are a very large number of fatty acids which can be esterified to C1 and C2 of phospholipids and a variety of P-X groups at C3, making the phospholipids and fatty acids extremely heterogeneous groups of molecules, their role in biological structures can be understood quite simply by modeling them either as single or double chain amphiphiles. This reduces their apparent complexity dramatically. In addition, they, in contrast to carbohydrates, amino acids, and nucleotides, do not form covalent polymers. Hence we will start our studies of biological molecules with lipids (fatty acids and phospholipids) and then apply our understanding of this class of molecules to the more complex systems of biological polymers. We will see that phospholipids and sphingolipids are essential components of membrane structure. Cholesterol is also found in membranes and is a precursor of steroid hormones.
Fatty acid structure and conformation

Fatty acids can be saturated (contain no double bonds in the acyl chain), or unsaturated (with either one -monounsaturated - or multiple - polyunsaturated - double bond(s)) . The table below gives the names, in a variety of formats, of common fatty acids.
Dr Sarhan
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Post by Dr Sarhan on Sun Jan 06, 2008 1:47 pm

Fatty acids can be named in many ways.

  • symbolic name: given as x:y (D a,b,c) where x is the number of C’s in the chain, y is the number of double bonds, and a, b, and c are the positions of the start of the double bonds counting from C1 - the carboxyl C. Saturated fatty acids contain no C-C double bonds. Monounsaturated fatty acids contain 1 C=C while polyunsaturated fatty acids contain more than 1 C=C. Double bonds are usual cis.
  • systematic name using IUPAC nomenclature. The systematic name gives the number of Cs (e.g. hexadecanoic acid for 16:0). If the fatty acid is unsaturated, the base name reflects the number of double bonds (e.g. octadecenoic acid for 18:1 D 9 and octadecatrienoic acid for 18:3D 9,12,15).
  • common name: (e.g. oleic acid, which is found in high concentration in olive oil)

You should know the common name, systematic name, and symbolic representations for these saturated fatty:

  • lauric acid, dodecanoic acid, 12:0
  • palmitic acid, hexadecanoic acid, 16:0
  • stearic acid, octadecanic acid, 18:0.

Learn the following unsaturated fatty acids -

  • oleic acid, octadecenoic acid, 18:1 D 9
  • linoleic acid, octadecadienoic acid, 18:2 D 9,12
  • a-linolenic acid, octadecatrienoic acid, 18:3 D 9,12,15 (n-3)
  • arachidonic acid, eicosatetraenoic acid, 20:4 D 5,8,11,14 (n-6)
  • eicosapentenoic acid (EPA), 20:5 D 5,8,11,14,17 (n-3) Note: sometimes written as eicosapentaenoic
  • docosahexenoic acid (DHA) 22:6 D4,7,10,13,16,19 (n-3) Note: sometimes written as docosahexaenoic

There is an alternative to the symbolic representation of fatty acids, in which the Cs are numbered from the distal end (the n or w end) of the acyl chain (the opposite end from the carboxyl group). Hence 18:3 D 9,12,15 could be written as 18:3 (w -3) or 18:3 (n -3) where the terminal C is numbered one and the first double bond starts at C3. Arachidonic acid is an (w -6) fatty acid while docosahexaenoic acid is an (w -3) fatty acid.
Note that all naturally occurring double bonds are cis, with a methylene spacer between double bonds - i.e. the double bonds are not conjugated. For saturated fatty acids, the melting point increases with C chain length, owing to increased likelihood of van der Waals (London or induced dipole) interactions between the overlapping and packed chains. Within chains of the same number of Cs, melting point decreases with increasing number of double bonds, owing to the kinking of the acyl chains, followed by decreased packing and reduced intermolecular forces (IMFs). Fatty acid composition differs in different organisms:

  • animals have 5-7% of fatty acids with 20-22 carbons, while fish have 25-30%
  • animals have <1% of their fatty acids with 5-6 double bonds, while plants have 5-6% and fish 15-30%

Many studies support the claim the diets high in fish that contain abundant n-3 fatty acids, in particular EPA and DHA, reduce inflammation and cardiovascular disease. n-3 fatty acids are abundant in high oil fish (salmon, tuna, sardines), and lower in cod, flounder, snapper, shark, and tilapia.
The most common polyunsaturated fats (PUFAs) in our diet are the n-3 and n-6 classes. Most abundant in the n-6 class in plant food is linoleic acid (18:2n-6, or 18:2D9,12), while linolenic acid (18:3n-3 or 18:3D9,12,15) is the most abundant in the n-3 class. These fatty acids are essential in that they are biological precursors for other PUFAs. Specifically,

  • linoleic acid (18:2n-6, or 18:2D9,12) is a biosynthetic precursor of arachidonic acid (20:4n-6 or 20:4D5,8,11,14)
  • linolenic acid (18:3n-3, or 18:3D9,12,15) is a biosynthetic precursor of eicosapentaenoic acid (EPA, 20:5n-3 or 20:5D5,8,11,14,17) and to a much smaller extent, docosahexaenoic acid (DHA, 22:6n-3 or 22:6D4,7,10,13,16,19).

These essential precursor fatty acids are substrates for intracelluar enzymes such as elongases, desaturases, and beta-oxidation type enzymes in the endoplasmic reticulum and another organelle, the peroxisome (involved in oxidative metabolism of straight chain and branched fatty acids, peroxide metabolism, and cholesterol/bile salt synthesis). Animals fed diets high in plant 18:2(n-6) fats accumulate 20:4(n-6) fatty acids in their tissues while those fed diets high in plant 18:3(n-3) accumulate 22:6(n-3. Animals fed diets high in fish oils accumulate 20:5 (EPA) and 22:6 (DHA) at the expense of 20:4(n-6).
Recent work has suggested that contrary to images of early hominids as hunters and scavengers of meat, human brain development might have required the consumption of fish which is highly enriched in arachidonic and docosahexaenoic acids. A large percent of the brain consists of lipids, which are highly enriched in these two fatty acids. These acids are necessary for the proper development of the human brain and in adults, deficiencies in these might contribute to cognitive disorders like ADHD, dementia, and dyslexia. These fatty acids are essential in the diet, and probably could not have been derived in high enough amounts from the eating of brains of other animals. The mechanism for the protective effects of n-3 fatty acids in health will be explored later in the course when we discuss prostaglandins synthesis and signal transduction.

Saturated fatty acids chains can exist in many conformations resulting from free rotation around the C-C bonds of the acyl chains. A quick review of the conformations of n-butane shows that the energetically most favorable conformation is one in which the two CH3 groups attached to the 2 methylene C’s (C2 and C3) are trans to each other, which results in decreased steric strain. Looking at a Neuman projection of n-butane shows the dihedral or torsional angle of this trans conformation to be 180 degrees. When the dihedral angle is 0 degrees, the two terminal CH3 groups are syn to each other, which is the conformation of highest energy. When the angle is 60 (gauche+) or 300 (gauche-) degrees, a higher, local minimum is observed in the energy profile. At a given temperature and moment, a population of molecules of butane would consist of some in the g+ and g- state, with most in the t state. The same applies to fatty acids. To increase the number of chains with g+tg- conformations, for example, the temperature of the system can be increased.
Triacylglyeride/Glycerophospholipid Structure

A cartoon diagram showing the generic structures of triacylglyerides, glycerophospholipid and sphingolipids are show above. In addition, the most common glycerophospholipids are shown. Learn the structures of phosphatic acid (PI), phosphatidyethanolamine (PE), phosphatidylcholine (PC) which is often called lechitin, and phosphatidylserine (PS) which is often called cephalin.
If you are working at a PC in a public access area, you can use a internet browser plug-in (which is already installed in those areas) called Chime. It will allow you to view and manipulate molecular models interactively on your computer. Every time you see the helix icon, the link will take you to a Chime model for the molecule listed. You should be able to see and rotate your molecule by placing the mouse cursor in the black window and using the commands given below:

  • Hold down the left mouse button and move the mouse around to rotate the molecule
  • Hold down both the shift key and the left mouse button, then move the mouse up to zoom out or down to zoom in
  • Hold down both the control button and the right mouse button, then move the mouse to translate the molecule on the xy axes

In addition, you can change the rendering of the molecule by moving the mouse cursor within the area of the molecule. Click and hold the right mouse button, and a new menu will appear that will allow additional manipulation of the molecule. Experiment with these commands.
Dr Sarhan
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