Metabolism Ch 6 Flashcards

1
Q

Anabolism vs Catabolism

A

Anabolism-biosynthetic process/assembly of subunits of a macromolecule *use ATP to drive reactions
Catabolism-process that degrades compounds to release energy *captures to make ATP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Enzymes

A

Catalysts that speed up reaction without heat (slows down activation energy)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

ATP

A

composed of ribose, adenine, 3 phosphate groups (most common form of energy)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Exergonic

A

adds power to endogenic, reactants have more free energy (energy is released in reaction)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Endergonic

A

products have more free energy, (reaction requires input of energy)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

3 Processes to generate ATP

A

Substrate level phosphorylation, Oxidative phosphorylation, and Photophosphorylation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Substrate level phosphorylation

A

Exergonic reaction powers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Oxidative phosphorylation

A

proton motive force drives

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Photophosphorylation

A

sunlight used to create proton motive force to drive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Role of Chemical source and Terminal Electron Acceptor (TEA)

A

More energy is released when difference in electronegativity is greater, Electron donor:energy source
Acceptor: Terminal electron acceptor (TEA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

3 Difference central metabolic pathways (CATABOLISM)

A

Glycolysis, Pentose phosphate pathway, Tricarboxylic acid cycle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Glycolysis (catabolism)

A

splits glucose (6c) to 2 pyruvates (3c), generates modests atp, reducing power, precursors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Pentose phosphate pathway (Catabolism)

A

primary role is production precursor metabolites, NADPH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Tricarboxylic acid cycle (CATABOLISM

A

oxidizes pyruvates from glycolysis, generates reducing power, precursor metabolites, ATP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Respiration vs Fermentation

A

Resp-transfers electrons from glucose to electron transport chain (ETC), ETC makes proton motive force,
Ferm- uses pyruvates or derivative as terminal electron acceptor (TEA) to regenerate NAD+, if cells cannot respire, will run out of carriers available to accept electrons and glycolysis will stop

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Two types of Respiration Catabolism

A

Aerobic-02 is TEA

Anaerobic-anything other than O2 is TEA, also uses modified versions of TCA

17
Q

Aerobic ATP Generated

A

Substrate level phos-
2 in glycolysis (net), 2 in TCA cycle=4
Oxidative Phos- 34
total-38

TEA-02
Uses ETC-Yes

18
Q

Fermentation ATP Generated

A

Substrate Phos-2 in glycolysis=ONLY 2
Oxidative Phos-0
TOTAL=2
Uses ETC-No

TEA-organic molecules, pyruvate or derivative

19
Q

Anaerobic

A

Uses ETC-YES

TEA-Anything other than 02, (So

20
Q

Coenzymes(cofactors)

A

assist different enzymes, include magnesium, zinc, copper, help bind to substrates
*Are organic cofactors, include electron carriers FAD,NAD+,NADP+

21
Q

Allosteric Regulation

A

enzyme activity is controlled by binding to allosteric site, which distorts enzyme shape, prevents the binding of substrates, regulatory is end products

22
Q

Enzyme Inhibition

A

Site to which inhibitor binds determines type,
1.Competitive Inhibitor
Non-competitive inhibitor

23
Q

Competitive Inhibitor

A

binds to active site of enzyme, chemical structure is similar to substrate which blocks the substrate resulting in halt of production

24
Q

Non-Competitive Inhibitor

A

binds to different site, allosteric inhibitors are example, action is reversible, but some are not
Enzymes changes shape, becomes nonfunctional