Lipid Properties Flashcards

1
Q

Lipids

A

Organic substances soluble in organic solvents, making them easily seperated from organic material.

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2
Q

Structurually, what are fatty acids?

A

Carboxylic acids with long hydrocarbon side chains

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3
Q

What form are fatty acids mostly in?

A

Esterfied form.

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4
Q

Esterfied

A

A compound produced by combination of alcohol and acid.

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5
Q

How many carbons do FA most commonly have?

A

Between C16 and C18 carbons.

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6
Q

What are the most common fatty acids?

A

Palmitic, Oleic, Linoleic and Stearic acids.

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7
Q

Why are most fatty acids an even number of carbons?

A

Their synthesis happens in C2 units.

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8
Q

Unsaturated fatty acids

A

FA with double bonds, being either mono or poly.

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9
Q

Where do UFA double bonds occur most?

A

Between C9 and C10, and typically every third carbon in polyunsaturated fats.

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10
Q

How are PU fats identified in nomenclature?

A

Omega 3 and Omega 6 FA, identifying the last double-bonded carbon atom as counted from the methyl terminated end of the chain.

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11
Q

An example of PU nomenclature

A

Linolenic acid has double bonds between C9-10 and C12-C13, whilst a-linolenic acid between C9-C10, C12-13 and C15-C16

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12
Q

Why are unsaturated fats useful in membrane fluidity?

A

They are almost always in cis configuration, allowing a 30 degree bend in the chain, packing less efficinetly together.

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13
Q

Why do Unsaturated FA melting points decrease with degree of unsaturation?

A

Due to reduced VDW forces.

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14
Q

Saturated Fatty Acids

A

FA fully saturated with H, being highly flexible, allowing wide range of conformations due to free range of each bond

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15
Q

Why are fatty acid linear forms more favourable?

A

Have the least amount of steric interference between methyl groups.

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16
Q

Triacylglycerols

A

Non-polar, water insoluble substances of FA bound to a glycerol backbone.

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17
Q

Function of triglycerides

A

Energy reservoirs in animals

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18
Q

How are triacylglycerols named?

A

According to the placement of their glycerol moiety.

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19
Q

An example of triglyceride nomenclature?

A

1-palmitoleoyl-2-linoleoyl-3-stearoylglycerol, where palmitoleoyl is found on C1 of glycerol, linoleoyl on C2 and stearoylglycerol on C3

20
Q

Why are fats more efficent as metabolic energy stores?

A

They are less oxidised than carbohydrates and proteins, yielding far more energy per unit mass on complete oxidation

21
Q

How, based on how they’re stored, are fats more efficent than glycogen?

A

Fats are stored in anhydrous form, whilst glycogen holds twice its weight in water.

22
Q

How are adipocytes specialised for synthesis/storage of TAG?

A

Adipocytes are almost entirely filled with fat globules.

23
Q

What is the importance of adipocyte fat storage?

A

Allow survival from starvation for up to 2 to 3 months, whilst supplying thermal insulation.

24
Q

What is the most abundant membrane lipid?

A

Glycerophospholipids

25
What is the structure of glycerophospholipids?
A glycerol-3-phosphate backone, linked to a polar group, with C1 and C2 positions esterfied with fatty acids.
26
What is the saturation properties of glycerophospholipids?
They contain a saturated C16/18 at C1 with C2 occupied by unsaturated C16-20 FA.
27
What catalyses glycerophospholipid hydrolysis?
Phospholipases.
28
What is an example of glycerophospholipid hydrolysis?
Phospholipase A2 hydrolytically excises C2 fatty acid residue producing lysophospholipids, with disrupt lysis.
29
Sphingolipids
A lipid class contaiing the sphingosine.
30
Sphingosine
An amino alchol with an 18-carbon unsaturated alkyl chain
31
Ceramides
N-acyl fatty acid derivatives of sphingosines, parent compounds of sphingolipids.
32
What is the most common ceramide?
Sphingomyelin, ceramides bearing a phosphocholine or phosphoethanolamine head group.
33
How much of plasma membrane lipids are sphingomyelins?
10 to 20%
34
Cerebrosides
Ceramides with head groups of a single sugar residue, lacking phosphate groups being non-ionic
35
Gangliosides
Fats with ceramides attaching to oligosaccharides, including at least one sialic acid residue.
36
Why are gangliosides important in medical and physiological areas?
Due to their carbohydrate head groups which extend beyond the surfaces of cell membranes, acting as receptors for pituitary hormones that regulate physiological functions.
37
Isoprenoids
Lipids used in pigmentation, fragrances and vitamins.
38
What is an example of an Isoprenoid?
Isoprenoid ubiquinone, (coenzyme Q), which is reversible reduced and oxidised in the mitochondrial membrane.
39
Vitamin A
A fat-soluble vitamin deriving from carotene
40
How does Vitamin A relate to eyesight?
Retinol is oxidised to aldehyde form retinal, functioning as the eyes photoreceptor at low light intesities, causing retinal isomerization, triggering signalling pathways in optic nerves.
41
Vitamin K
A lipod important in blood clotting and bone formation
42
How does Vitamin K relate to blood clotting?
In carboxylates glu residues in blood clotting proteins, so deficiency has reduced carboxylation, resulting in inactive clotting proteins and excess bleeding.
43
Vitamin E
A highly hydrophobic molecule, incorporating into cell membranes functioning as an antioxidant to prevent oxidative damage to membrane proteins and lipids.
44
Elicosanoids
A non-membranous lipid active in production of pain and fever and regulating blood pressure, coagulation and reproduction.
45
What is the major lung surfactant lipid?
Dipalmitoyl Phosphatidylcholine, coating alveoli, decreasing surface tension.
46
How does the structure of DPPC allow them to pack closely?
They are sturated, thus extend straight out without bending and orientation in a signle layer with non-polar tails toward air.
47
Function of DPPC in surfactant?
In expiration, volume/SA of alveoli decreasing with full colappse prevented by DPPC.