sphingolipid metabolism starts with palmitoyl-coa and serine, which is reduced and undergoes a...
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Sphingolipid metabolism
• Starts with palmitoyl-CoA and serine, which is reduced and undergoes a transacylation and desaturation to yield ceramide (containing sphingosine; refer to figure 10-13)
• Uses UDP activated sugars, but not CTP activated head groups
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Ceramide is a precursor for numerous glycosphingolipids
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Role of sphingolipids
• Abundant component of myelin sheath (25% in humans)
• Also widely distributed in membranes of plants (use phytosphingosine), and lower eukaryotes (yeast)
• These lipids are in a continuous state of turnover, defects in this metabolism leads to various diseases
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However, little is known about their specific biochemical function
• Gangliosides are receptors for specific agents such as influenza virus
• Some gangliosides promote growth of neural tissue in cell cultyre
• Biological signaling agents, possibly apoptosis as we will see in near future
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Fatty acid lipid membrane
• After lipids are synthesized in the ER, polar lipids are delivered to the Golgi apparatus, which serves as a clearinghouse sending specific lipids to specific targets using membrane vesicles
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Steroid metabolism• Sterols (steroids) are class of lipids that are
derivatives of a tetracyclic hydrocarbon
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Simplicity to complexity
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Cholesterol is made from acetyl-CoA
• Mevalonate formation is
the first stage of cholesterol
synthesis
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Acetate Mevalonate
• Catalyzed by thiolase, -hydroxy--methylglutaryl-CoA (HMG-CoA) synthase and reductase
• The reductase is the first committed step in this pathway; regulatory point
• This last step is a four electron reduction
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Mevalonate is converted to isoprene-
containing molecules
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A momentary diversion:
• Isoprenoids are
precursors for several
important biomolecules
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Back to cholesterol biosynthesis:
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Head to tail condensations ultimately result in a 30 carbon intermediate,
squalene
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Squalene is cyclized to cholesterol
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Regulation of cholesterol biosynthesis
• HMG-CoA reductase is a major target for regulation.
• Hormonal regulation by insulin and glucagon
• Ingestion of cholesterol inhibits endogenous cholesterol synthesis (control exerted at both transcriptional and translational levels)
• Additional sophistication in vertebrates
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Lipids and proteins
• Proteins mediate lipid
transport between tissues
• Proteins are also modified
by lipids
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Proteins and lipids produce particles with distinct densities
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These particles facilitate transport
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Cholesterol is taken up by receptor-mediated endocytosis
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Cholesterol synthesis is balanced with uptake
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Acyl-CoA:cholesterol acyltransferase (ACAT) generates cholesteryl esters
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Fate of cholesterol• Cholesterol is used by cells to decrease fluidity of
cell membrane
• Used in steroid hormone and bile salt biosynthesis
• Cholesterol can also be exported from liver as bile acids, cholesteryl esters, or biliary cholesterol– Bile acids aid in digestion
– Cholesteryl esters are transported to other other tissues to use cholesterol
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Bile acids are steroid derivatives with detergent properties
• Emulsify dietary lipids
• Secreted from liver, stored in gall bladder, passed through bile duct into intestine
• Bile acids represent a major metabolic fate of cholesterol, accounting for more than half of the 800 mg/day of cholesterol metabolized (steroid hormones represent about 50 mg of cholesterol per day)
• Bile acids are recycled through small intestine
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Cholate and chenodeoxycholate acid are prominent bile salts
• Note cytochrome
P450
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Cholesterol is the biosynthetic source of all steroid hormones
• Five major classes of hormones
– Progestins (regulate events during pregnancy and are precursors to all other steroid hormones)
– Glucocorticoids (promote gluconeogenesis, and in certain doses suppress inflammation rxns)
– Mineralocorticoids (regulate ion balance in kidney)
– Androgens (male sexual characteristic development and maintenance)
– Estrogens (female sexual characteristics development and maintenance)
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What stands out about steroid hormone biosynthesis?
• Role of cytochrome P450 and side chain cleavage in mitochondria
• Multiple hydroxylations• Central role of pregnenolone• Mammalian cells lack capacity for complete
degradation of steroids. Although a number of catabolic reactions occur, most are conjugated through their hydroxyl groups to glucuronate or sulfate, increasing solubility and allowing elimination through urine
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Other isoprenoid compounds:
• Vitamin A, D, K, E
• Terpenes – generic term for all compounds biosynthesized from isoprene precursors; hence all the molecules we have discussed today are terpenes.
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