Lipid breakdown and
biosynthesis
Chemistry 256
Lipids are tied to metabolism through the TCA
cycle
The dihydroxyacetone
phosphate (DHAP)
made by glycolysis or
made from
oxaloacetate by
glyceroneogenesis;
thus this system
responds to the same
hormones involved in
regulation of
carbohydrate
metabolism.
Lipids are degraded by digestion prior to
absorption
• Triacylglycerols are 90% of dietary lipids.
• Digestion of these occurs at the lipid-water
interface since lipids are insoluble in water
and digestive proteins are soluble.
• Bile acids (or bile salts) are cholesterol
derivatives that help emulsify the mixture in
the small intestine.
• Lipases are the class of proteins that digest
the triacylglycerols.
Lipid digestion by lipases occurs by a
variety of mechanisms
All lipases convert
triacylglycerols
into fatty acids,
monoacylglycerols
or diacylglycerols.
The specific
mechanisms vary;
phospholipase A2
has a hydrophobic
channel that
allows lipids to
enter active site.
Lipid droplets are broken up into micelles (or at least smaller
membranes) which are then broken up into fatty acids and
other smaller parts which are absorbed by the intestinal cells.
Further in the cell, the fatty acids end up in the ER and are
packaged into chylomicrons (a type of lipoprotein), which
are then extruded into the lymphatic system.
VLDLs, IDLs and LDLs are synthesized by the liver for lipid
transport to tissues; tissues synthesize HDLs for transport to
liver. HDLs are the smallest particles and the most rich in
triacylglycerols.
Apolipoproteins surround the lipoproteins to hold them
together. Apolipoprotein B-100 (apoB-100) is a big (4536residue) monomeric protein with distinct polar and
nonpolar moieties to interact with membranes and the
lipoprotein.
Note the presence of cholesteryl
ester in the lipoprotein; it is a source
of cholesterol for cells.
Chylomicrons are delipidated in
the capillaries
Comparison of breakdown and synthesis
Breakdown versus synthesis
• Major difference: Even though two-carbon
units are added to the growing fatty acid
chain, it is malonyl-CoA (3 carbons), not
acetyl-CoA (2 carbons) that is added.
• In addition, bicarbonate is a required
substrate.
• Of course, this being a reduction, a lot of
energy-bearing molecules will be oxidized.
• So: many different enzymes than β-oxidation!
The sites of these activities
• In much the same way that
hormones like glucagon and
insulin regulate the glycolytic
and glucogenolytic pathways,
these hormones regulate the
breakdown and buildup of
fatty acids.
• Hormone-sensitive
triacylglycerol lipase is turned
on and off via
phosphorylation and
dephosphorylation, which is
triggered by cAMP
concentration.
Fatty acid oxidation
Depending on the original number of carbons, the excretion
product of fatty acid oxidation varies. This experiment by
Franz Knoop in 1904 (University of Freiburg) used benzenederivatized fatty acids fed to dogs, and showed that the fatty
acids were degraded two carbons at a time.
Fatty acids are activated by their attachment to coenzyme A,
facilitated by acyl-CoA synthetases. These are located on the
ER or the outer mitochondrial membrane.
Mixed anhydride intermediate initiated by a nucleophilic attack on ATP αphosphorus.
Fatty acids are oxidized
in the mitochondrial
matrix, and thus must be
transported in. The acyl
portion of the fatty acid
is transported and
reattached to CoA inside
the matrix.
Fatty acid oxidation to
produce a single acetylCoA unit also produces
a FADH2,which is
oxidized by the standard
electron-transport chain,
for a further 1.5 ATP.
Note the formation of a
trans-fatty acid in the
first step.
The fourth step (the one that
produces the acetyl-CoA)
involves a thiolase, which
proceeds as a Claisen ester
cleavage (the reverse of a
Claisen condensation).
Much energy can thus be produced
from a single fatty acid; one palmitate
(C16) yields 106 ATP.
Unsaturated fatty
acids require an
additional set of
enzymes, because an
adjacent set of double
bonds cannot be
formed. Note the
usage of some energy
to achieve this.
Odd-numbered fatty
acids yields propionylCoA, which is
converted to succinylCoA to enter the TCA.
Dorothy Hodgkin in
1956 (Oxford; Nobel
Prize, 1964)
determined the
structure of the
enzyme involved in
producing succinylCoA, using X-ray
crystallography. It is
a rare cobaltcontaining enzyme;
note its position in a
heme-like ring.
Ketone bodies are produced by the liver mitochondria as an
alternate fuel source for tissues like the heart and other
muscles, or the brain during starvation.
Fatty acid biosynthesis begins with acetyl-CoA
The malonyl-CoA then reacts with an acyl-carrier
protein (ACP) through a thiol group to make malonylACP; an acetyl-CoA does the same reaction to
produce acetyl-ACP. The malonyl-ACP and acetylACP react to make acetoacetyl-ACP, with the loss of a
CO2 and an ACP.
Much energy is
required: To make
palmitic acid, in
addition to 8 acetylCoA, 14 NADPH and
7 ATP are required.
The enzyme complex
is fatty acid sythase,
which is (not
surprisingly) a multifunction enzyme.
Other enzymes are
required to form
unsaturations.
Citrate shuttle allows acetyl-CoA out of mitochondrion
The site of fatty acid (and other lipid) biosynthesis is in the cytosol (usually the
endoplasmic reticulum), but the acetyl-CoA precursor is found in the
mitochondria. The inner mitochondrial membrane, as might be expected, is
impermeable to acetyl-CoA, so the acetyl-CoA is converted to pyruvate and then
to citrate and transported out of the mitochondrion, and then reconverted to
acetyl-CoA (similar to the aspartate/malate shuttle for gluconeogenesis).
Acetyl-CoA carboxylase produces malonyl-CoA
ACC is a 230-kD polypeptide (shown below), first step in turning acetyl-CoA into
a fatty acid. Citrate is an activator; fatty acids are an inhibitor (feedback).
Serine 79 is a phosphorylation site; phosphorylation by AMP-dependent protein
kinase inactivates enzyme.
Glucagon and
epinephrine activate
protein kinase A,
which inhibits
dephosphorylation of
serine 79, and thus
inhibits ACC; insulin
promotes
dephosphorylation,
which activates ACC.
α-ACC in adipose
tissue; β-ACC in heart
tissue
Triacylglyceride synthesis
Independent of fatty acid synthesis, triacylglycerol synthesis begins
with a glycolysis intermediate, dihydroxyacetone phosphate (DHAP)
undergoing reduction by glycerol-3-P dehydrogenase to glycerol-3phosphate.
Interestingly, the loss of glycerol-3-phosphate by liver tumor cells is
part of the mechanism of cancer (Howard, Morris and Bailey, “Etherlipids, a-glycerol phosphate dehydrogenase, and growth rate in tumors
and cultured cells”, Cancer Res., 1972)
Triacylglyceride synthesis
The fatty acid comes in, now, as the R (acyl)
group added with the help of glycerol-3phosphate acyltransferase (first step here).
Triacylglyceride synthesis
The previous slide
mechanism is found in
the endoplasmic
reticulum and
mitochondrion; this
alternate pathway
exists in peroxisomes
and bacteria, in which
the acyl transfer takes
place without going
through glycerol-3phosphate (Schjuman
and de Mendoza,
“Solving an old puzzle
in phospholipid
biosynthesis”, Nature
Chemical Biology
2006)
In any case, both pathways end at the
same molecule: lysophosphatidic acid,
and then on to triacylglycerides as the
other two acyl groups are
transferred…however, even as the second
fatty acid group is transferred, other types
of molecules can be made.
The synthesis of glycerophospholipids
• Note in this mechanism,
the head group is
phosphorylated and then
the diacylglycerol is
transferred.
• In the second step,
cytidine triphosphate
(CTP – a nucleotide) is
used as an energy source
and a phosphate source.
The synthesis of sphingolipids
• Sphingolipids deviate from the
triacylglyceride synthesis path;
instead, these molecules start
from t palmitoyl-CoA and
another acyl-CoA, as well as the
amino acid serine.
• At this point, the head group is
modified to include
carbohydrate units (ceramides).
The initiation of eicosanoid lipids
• To activate the arachidonic acid, an
unusual peroxide structure is formed,
requiring prostaglandin H2 synthase
which has the cyclooxygenase and
peroxidase function.
• Aspirin’s mechanism involves
acetylating a serine residue of
prostaglandin H2 synthase which
prevents the formation of PGH2, a
precursor to the pain signal
prostaglandins (Vain, “Inhibition of
prostaglandin synthesis as a mechanism
of action for aspirin-like drugs”, Nature
New Biology, 1971).
Steroid synthesis - the first steps (the amino acid
residue numbers refer to a HMG-CoA synthase enzyme)
Steroid synthesis
• HMG-CoA ( = 3-hydroxy-3methylglutaryl-coenzyme A) is a
necessary precursor. Note the
HMG unit is modified into the
isoprenoid structure on this
molecule.
Steroid synthesis
• The C30 cholesterol
precursor squalene is built
from the condensation of six
isoprene units, though a
farensyl intermediate.
• The farensyl intermediate is
made through the head-totail condensation of three
isoprenoid units, then the
squalene is made through
the head-to-head
condensation of two farensyl
units.
Steroid synthesis
• Another unusual structure, an epoxide (catalyzed by
squalene epoxidase) leads to the placement of the
hydroxy group at C-3.
Steroid synthesis
• The cyclization that results in
the fused ring structure of
cholesterol begins as a
consequence of the
reduction of the epoxide at
C-3 by oxidosqualene
cyclase.
Cholesterol synthesis
• The modification of lanosterol to cholesterol is a 19step process and occurs in the ER membrane. In the
liver, the C-3 alcohol can be esterified to make a
cholesteryl ester.