Basic Metabolism Flashcards

(41 cards)

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

18
Q

Fasting conc of glucose;

Following a high carb meal;

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
Glycolysis converts 6C glucose into
2 molecules of 3C pyruvate -aerobic; | Lactate - anaerobic
26
Glucose conversion to glucose 6 phosphate
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
Hexokinase
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
Glucokinase
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
Glucose 6 phosphate to fructose 6 phosphate
Isomerized; Enzyme: phosphoglucose isomerase; Readily reversible, not regulatory;
30
Fructose 6 phosphate to fructose 1 6 biphosphate
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
Fructose 1 6 biphosphate to glyceraldehyde 3 phosphate
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
GAP to 1, 3 bis phosphoglycerate
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
1, 3 bis phosphoglycerate to 3-phosphoglycerate
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
3 -posphoglycerate to 2-phosphoglycerate to phosphophenylpyruvate
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
PEP to Pyruvate
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
Anaerobic glycolysis
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
Lactate and the Cori cycle
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
Lactate acidosis
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
Creating phosphate
High energy intermediate in muscle; Can transfer phosphate to ADP; Replenishes ATP; Lasts few seconds;
40
Adenylate kinase
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
Other fates of Glucose 6 phosphate
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;