Metabolism Flashcards

(57 cards)

1
Q

In Glycolysis: What are the Carriers.

A

ATP, NADH, Acetyl CoA

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2
Q

What is the NET ATP from Glycolysis?

A

2

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3
Q

What is the NET ATP from TCA?

A

2

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4
Q

What is the NET ATP from ETC?

A

28

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5
Q

Draw the Process of Pyruvate in Anaerobic Conditions

A
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6
Q

What Happens when theres too much Lactate?

A

body pH drops, too acidic

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7
Q

What other Sugars other than Glucose can be used?

A

galactose and fructose from adipose tissues or liver

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8
Q

Describe Lactose Intolerance.

A
  • lactose is too big to pass through digestive tract lining
  • must be broken into galactose and glucose by lactase
  • if lactase is underproduced
  • lactose remains in GI tract
  • becomes fermented by bacteria
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9
Q

Describe Symptoms of Lactose Intolerance

A

farting, diarrhoea, cramps, bloating, nausea

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10
Q

Describe Galactosemia

A

inherited autosomal recessive disorder

  • deficiency of galactose-1-phosphate uridyl transferase
  • in the eye..
  • aldose reduces galactose into galacitol
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11
Q

What are the Symptoms of Galactosemia

A

cataracts in the eye, enlargement of liver, CNS failure

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12
Q

HOW does Fluoride kill cariogenic bacteria?

A

inhibits Enolase

  • enzyme needed to convert 2-phosphopglycerate into PEP
  • think glycolysis
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13
Q

State and Describe 4 Mechanisms in which Metabolism can be Regulated.

A
  1. Allosteric Regulation
    - enzyme activity can be inhibited by binding an effector molecule at a site other than the enzyme’s active site
  2. Association with Regulatory Protein
  3. Covalent Modification
    - phosphorylation
  4. Sequestration
    - alters accessibility of reactions, products and substrates
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14
Q

What are the 4 Main Enzymes in Glycolysis?

A

Hexokinase
Phosphofructokinase
Pyruvate Kinase
Pyruvate Dehydrogenase

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15
Q

How is Hexokinase Regulated?

A

Allosteric Regulation

  • inhibit Glucose into G-6-P
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16
Q

2 Ways in Which the Activity of Phosphofructokinase is Reduced?

A
  1. Allosteric Regulation by ATP
    - ATP is overproduced
    - binds to allosteric site
    - lowers the PFK affinity
  2. Sensitivity to pH
    - high acidity reduces activity
    - prevents formation of lactic acid
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17
Q

How Can Phosphofructokinase be Activated

A

by Fructose-2,6-Bisphosphate

  • binds to allosteric site
  • increase enzyme affinity for F-6-P
  • reduces affinity for ATP
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18
Q

How is the Activity of Pyruvate Kinase Regulated?

A

allosteric regulation and covalent modification

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19
Q

How is Pyruvate Kinase Activated?

A

Fructose-1,6-Bisphosphate

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20
Q

How is Pyruvate Dehydrogenase Regulated?

A

allosteric regulation and covalent modification

has 2 limiting sited
E2 Transacetylase - limited by Acetyl CoA
E3 Dihydrolipolydehydrogenase - limited by NADH

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21
Q

What are the Main Enzymes in TCA?

A

citrate synthase
isocitrate dehydrogenase
a-ketoglutarate dehydrogenase

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22
Q

Draw out Glycolysis

A
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23
Q

Where does Glycolysis Occur?

A

in the cystol of the cell

24
Q

What are the 5 Main Stages in Glycolysis and where do they occur, using enzymes?

A

1) Irreversible Phosphorylation
- hexokinase

2) Isomerisation - Aldose to Ketone
- phosphoglucose isomerase

3) Irreversible Phosphorylation
- phosphofructose kinase

4) Cleavage
- Aldose

5) Isomerisation
- Triose Phosphate Isomerase
- DHAP into GAP

25
Draw out Link Reaction
26
Where does Link Reaction Occur?
matrix of the mitochondria
27
Draw out TCA Cycle
28
What are the 9 Steps of TCA Cycle?
1. Condensation 2. Condensation 3. Hydration 4. Oxidative Decarboxylation 5. Oxidation Decarboxylation 6. Substrate Level Phosphorylation 7. Dehydrogenation 8. Hydration 9. Dehydrogenation
29
What is the only sugar the brain will use?
glucose
30
Draw Glycolysis.
31
Draw Glycolysis in the liver and in the muscles.
32
What 2 Enzymes are needed at a branch point?
Transferase Enzyme - transfers 3 glucose units from one end to another Amylo-a-1,6-glucosidase - hydrolyses the single glucose unit left behind
33
How does Adrenaline and Glucagon work? Draw it out. (cAMP)
34
Draw Out Glycogenesis
35
What is Anderson's Disease?
deficiency of branching enzyme liver failure and death in first year of life
36
Insulin activates PK, what is this?
protein kinase
37
how does protein kinase work, draw it out.
38
How does Gluconeogenesis work?
the opposite of glycolysis, bypassing the irreversible steps
39
Draw out the Steps of Gluconeogenesis
40
Where does Gluconeogenesis Occur?
in the liver
41
What are the precursors for Gluconeogenesis?
lactate glycerol amino acids
42
Draw out the roles of lactate and glycerol.
lactate into pyruvate by lactate dehydrogenase glycerol + ATP into glycerol phosphate + ADP + H+ into DHAP by glycerol kinase and then glycerol phosphate dehydrogenase
43
State Steps of ETC.
1. NADH-Q reductase complex 2. succinate dehydrogenase 3. cytochrome c reductase complex 4. cytochrome c oxidase complex
44
What is the Proton Motive Force?
change in ph + change in charge gradient
45
Describe Structure of ATP Synthase
two functional domains = F0 and F1
46
Describe F0 from ATP Synthase
- imbedded in the inner mitochondrial mem - has a proton pore - has multiple subunits C subunits rotate - has aspartic acid in the middle - when in contact with membrane = neutral charger - when in contact with a unit = negative charge B subunit stuck on the outside - 2 half channels - hydrogen diffuses in Galway
47
How does F0 work?
- aspartic acid in contact with a complex = negative charge - c subunits cant move - due to chemical gradient, protons move in = positive charge - c subunit rotates clockwise - repeats
48
What is the F1 Complex, Explain Subunits?
contains the catalytic activity of the synthase 5 Subunits 3 a, 3 b, 1g - only gamma rotates and determines the state - open state = ATP release - tense state = ATP produced
49
Describe Muscle Shuttle
- e- from NADH transport into mitochondria via glycerol-3-phosphate shuttle
50
Draw Muscle Shuttle.
51
How does ATP synthase travel in the Heart and Liver
Malate-Aspartate Shuttle
52
Draw Malate-Aspartate Shuttle.
NADH donates e- to oxaloacetate to form malate - malate dehydrogenase malate goes across the mitochondrial membrane malate back into oxaloacetate - mitochondria malate glutamine + oxaloacetate = aspartate - aminotransferase
53
What is the Purpose of the Pentose Pathway?
to oxidise glucose to create NADPH
54
Draw out Pentose Pathway
55
What is a Toxic Bi-Product of Oxidative Phosphorylation, what percents is it found in?
ROS 1%
56
How do you get rid of ROS?
NADPH - reduced glutathione::: - hydrogen peroxide into water using *glutathione peroxidase* - oxidised glutathione::: - uses *glutathione reductase* and NADPH to become reduced = repeat process
57
What Happens if you have a Deficiency in G-6-P Dehydrogenase?
no ability to produce NADPH = no detoxification - problem when under oxidative stress BUT INHIBITS MALARIA PARASITE