Basic Metabolism Flashcards

1
Q

What are the 3 energy sources

A

Carbohydrates;
Lipids;
Proteins;

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2
Q

Carbohydrate, proteins and lipids yield how much energy per gram?

A

Carb, protein - 4kcal (17kJ);

Lipid - 9kcal;

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3
Q

Recommended intake of the 3 energy sources

A

Carbohydrate - 55%;
Lipids - 30%;
Proteins - 15%;

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4
Q

What is ATP

A

Adenosine triphosphate;

Energy currency of the cell;

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5
Q

ATP hydrolysis to ADP and Pi is?

Phosphorylation of ADP to form ATP is?

A

Exergonic;

Endergonic;

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6
Q

Gamma-phosphate bond of ATP is?

A

High energy bond

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7
Q

Catabolism

A

Energy yielding nutrients (fats, carbs, proteins) converted to energy poor products (CO2, H2O, NH3);

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8
Q

Anabolism

A
Precursor molecules (amino acids, sugars, fatty acids, nitrogenous bases) converted to complex molecules (protein, polysaccharides, lipids, nuclei acids);
Needs ATP and NADH;
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9
Q

3 stages

A
  1. Hydrolysis of complex molecules to component building blocks;
  2. Conversion of building blocks to Acetyl CoA (or other simple intermediates);
  3. Oxidation of acetyl CoA (oxidative phosphorylation)
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10
Q

Carbohydrate

A

CH2On;
Contains C combined with hydroxyl, keto, aldehyde and hydrogen;
Simple carbohydrates (monosaccharides);
Complex polymers (polysaccharides);

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11
Q

Simplest carbohydrate has?

A

3C;
Aldehyde or ketone group;

Example: glyceraldehyde - asymmetric C2 - has D and L enantiomers;

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12
Q
Generic names for:
3C;
4C;
5C;
6C;
7C;
9C;
A
Trioses;
Tetroses;
Pentoses;
Hexoses;
Heptoses;
Nonoses;
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13
Q

Glucose

A
Most abundant carbohydrate;
C6,H12,O6;
Exists in D and L enantiomers;
Found in plasma, cellls;
Stored as insoluble glycogen;
Comes from diet or body stores;
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14
Q

In solution glucose forms a 6 membered ring called? 5 membered is are called?

A

Pyranose;

Furanose;

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15
Q

Polysaccharides

A

Assembled from monosaccharide units joined by glycosidic bonds;
Same/diff monosaccharides;
May be branched - glycogen;

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16
Q

Major transported carbohydrate in blood

A

Glucose

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17
Q

Blood concentration of glucose is tightly controlled by

A

Hormones

18
Q

Fasting conc of glucose;

Following a high carb meal;

A

4mM;

8mM;

19
Q

Glusose is required by?

A

Brain and RBCs

20
Q

Majority of carbohydrates in diet are

A

Polysaccharides

21
Q

Digestion of carbohydrates

A

Salivary amylase in mouth (to oligosaccharides);
Pancreatic amylase in small intestine;
Final digestion my mucosal cells (disaccharides to monosaccharides);
Glucose taken into cells with Na+ by active transport;

22
Q

Glucose uptake

A

Taken into cells from blood by facilitated diffusion mediated by hexose transporter proteins in PM (GLUTs);
Tissue specific expression of different gluts;
Insulin increases activity/expression of GLUT 4, regulated uptake by muscle, adipose, heart;
Glucose uptake by brain GLUT3;
Kidney, pancreas, liver - GLUT 2;
RBCs - GLUT 1 - Insulin independent

23
Q

Hyperglycaemia

Hypoglycaemia

A

High blood glucose conc;

Low blood glucose conc;

24
Q

Glycolysis location. Yields?

A

Cytosol of every cell in the body;

ATP and intermediates;

25
Q

Glycolysis converts 6C glucose into

A

2 molecules of 3C pyruvate -aerobic;

Lactate - anaerobic

26
Q

Glucose conversion to glucose 6 phosphate

A

Glucose taken up by cell;
Rapidly phosphorylated to glucose 6 phosphate;
Traps glucose in cell;
Energy investment reaction
Isoenzymes responsible are - hexokinase (all tissues) and glucokinase (liver and pancreatic B cells);

27
Q

Hexokinase

A

Low Km -high affinity for glucose - provides glucose to all cells but easily saturated;
Low Vm - at high blood glucose enzyme saturated so all cells do not trap high levels of glucose;
Inhibited by high G6P;

28
Q

Glucokinase

A

High Km (Low affinity) - only traps glucose when blood glucose high (post prandial);
High Vm - liver sequesters glucose at high blood glucose (prevents hyperglycaemia);
Not inhibited by G6P; stimulated by glucose via a regulatory protein;
High insulin increases glucokinase levels;

29
Q

Glucose 6 phosphate to fructose 6 phosphate

A

Isomerized;
Enzyme: phosphoglucose isomerase;
Readily reversible, not regulatory;

30
Q

Fructose 6 phosphate to fructose 1 6 biphosphate

A

First committed step in glycolysis;
Energy investment step;
Highly regulated enzyme - phosphofructokinase-1 (PFK-1);
Inhibited allosterically by high ATP and citrate;
Activated allosterically by ADP and AMP;
In liver - allosterically regulated by fructose 2 6 biphosphate;

31
Q

Fructose 1 6 biphosphate to glyceraldehyde 3 phosphate

A

F 1 6 biphosphate cleaved by aldolase;
Products are glyceraldehyde 3 phosphate (GAP) and dihydroxyacetone (DHAP);
DHAP converted to GAP by triose phosphate isomerase;

32
Q

GAP to 1, 3 bis phosphoglycerate

A

Oxidation and phosphorylation;
Transfer of H+ and 2 electrons from GAP to co-factor NAD+ which is reduced to NADH (catalysed by GAP dehydrogenase);

H+ is also lost from GAP and a phosphate is added from Pi;
The coupling of oxidation of GAP (exergonic) and the formation of the bond with phosphate (endergonic) yields a high energy phosphate bond;

33
Q

1, 3 bis phosphoglycerate to 3-phosphoglycerate

A

High energy phosphate is transferred from 1,3 bPG to ADP to yield 3PG and ATP;
Substrate level phosphorylation;
2 ATP generated for each glucose;

34
Q

3 -posphoglycerate to 2-phosphoglycerate to phosphophenylpyruvate

A

Phosphate moved from C3 to C2 to yield 2-phosphoglycerate;
2PG dehydrated to PEP;
This re-arrangement generates a new high energy bond in PEP;

35
Q

PEP to Pyruvate

A

Pyruvate kinase converts PEP to pyruvate and at the same time transfers phosphate from PEP to ADP to form ATP;
Substrate level phosphorylation;
PK activated allosterically by fructose 1, 6 biphosphate;
When glucose Low, insulin/glucagon Low, cAMP high, PK phosphorylated and inactive;
In aerobic conditions pyruvate converted to Acetyl CoA and enter TCA cycle;

36
Q

Anaerobic glycolysis

A

Eg. strenuous exercise;
Respiratory chain cannot oxidise NADH to regenerate NAD+ (requires O2);
Glycolysis will convert NAD+ to NADH but NAD+ required for glycolysis to continue (GAPDH) step;
Pyruvate reduced to lactate by lactate dehydrogenase (LDH) to regenerate NAD+;
Different LDH isozymes in different tissues;

37
Q

Lactate and the Cori cycle

A

Lactate produced by erythrocytes normally; used by heart;
Heart LDH Low Km for lactate;
Converted to Pyruvate - TCA cycle;

Skeletal muscle produces high levels of lactate during anaerobic exercise, released to blood;
Live LDH (high Km for lactate) converts to pyruvate;
Converts pyruvate back to glucose (gluconeogenesis) and releases it to blood;

38
Q

Lactate acidosis

A

High blood lactase produced by:
Strenuous physical exercise, severe lung disease, high altitude, severe anaemia, CO poisoning;
Alcohol intoxication - reduction of NAD+ to NADH;
Von gierke’s disease - excess glycolytic activity;

High levels of blood lactate (lactic acid) - reduce blood pH - Hyperlactatemia

39
Q

Creating phosphate

A

High energy intermediate in muscle;
Can transfer phosphate to ADP;
Replenishes ATP;
Lasts few seconds;

40
Q

Adenylate kinase

A

ATP can be regenerated by adenylate kinase;
ATP:ADP:AMP 50,5,1;
Small fall in ATP leads to large rise in AMP;
Large changes in AMP regulate PFK etc;

41
Q

Other fates of Glucose 6 phosphate

A

Glycogen synthesis;
Converted back to glucose (liver only);
Pentose phosphate pathway (PPP) -
Generates ribose for nucleotide synthesis;
Generates NADPH for fatty acid synthesis;
NADPH required to prevent oxidative damage to proteins;