Exam 3 Metabolism 11/7 Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What are the different nutritional types of organisms in terms of carbon, energy, and electron acquisition?

A

All organisms need nutrients to produce to live, grow, and divide.

The process of incorporating nutrients into cellular parts is called assimilation.

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

Acquisition of Energy

A

Phototrophs – acquire energy from light energy to create ATP.

Chemotrophs – acquire energy from organic or inorganic compounds from the environment.

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

Acquisition of Electrons

A

Organotrophs – acquire electrons from organic molecules.

Lithotrophs – remove electrons from inorganic molecules.

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

Acquisition of Carbon

A

Heterotrophs – Assimilate carbon from pre-existing organic molecules.

Autotrophs – assimilate carbon from inorganic sources like CO2.

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

What are the basic principles of catabolism and energy that control metabolism?

A

Catabolism: Breaking down larger molecules to obtain energy and smaller precursors

Anabolism: Use of smaller precursor molecules and energy from catabolism to build macromolecular cell components

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

Metabolism is mediated by enzymes.

A

Enzymes catalyze biochemical reactions.

An enzyme’s active site binds specific substrates and helps to convert them to products.

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

Energy

Products of a chemical reaction must have a lower free energy than the reactants.

A

Energy released is known as Gibbs free energy (G).

Change in free energy in a reaction = ΔG°’

An energy-yielding reaction is exergonic (with a negative ΔG°’).

An energy-absorbing reaction is endergonic (with a positive ΔG°’).

Endergonic reactions in cells are coupled with exergonic reactions to drive them to completion.

The rate at which the reaction will occur is determined by its activation energy (EA).

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

Enzymes and activation energy

A

Enzymes jump-start reactions by lowering their EA, placing substrates in a more optimal arrangement.

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

Structure and Classification of Enzymes

A

Enzymes-catalysts

some enzymes are composed solely of one or more polypeptides

some enzymes are composed of one or more polypeptides and non-protein components

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

Cofactors=

A

coenzymes/prosthetic groups

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

Important Coenzymes

A

NAD+
NADP+
FAD
Coenzyme A

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

Factors Influencing Enzyme Activity

A

Enzymes can be denatured by temperature and pH

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

Effect of [substrate]Michaelis-Menton Kinetics

A

rate increases as [substrate] increases

no further increase occurs after all enzyme molecules are saturated with substrate

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

Enzyme Inhibition

A

competitive inhibitor

noncompetitive inhibitor

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

competitive inhibitor

A

directly competes with binding of substrate to active site

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

noncompetitive inhibitor

A

binds enzyme at site other than active site

changes enzyme’s shape so that it becomes less active

17
Q

Metabolic Regulation
3 major mechanisms

A

1) metabolic channeling

2) regulation of the synthesis of a particular enzyme

3) direct stimulation or inhibition enzyme

18
Q

Metabolic Channeling

A

differential localization of enzymes and metabolites

compartmentation
- differential distribution of enzymes and metabolites among separate cell structures or organelles

  • can generate marked variations in metabolite concentrations
19
Q

Post-Translational Regulation of Enzyme Activity
2 important reversible control measures

A

allosteric regulation

covalent modification

20
Q

Allosteric Regulation

A

most regulatory enzymes

activity altered by small molecule

*allosteric effector

—-binds non-covalently at regulatory site
—-changes shape of enzyme and alters activity
of catalytic site
—-positive effector increases enzyme activity
—-negative effector inhibits the enzyme

21
Q

Covalent Modification of Enzymes

A

reversible on and off switch

addition or removal of a chemical group (phosphate, methyl, adenyl)

advantages of this method
—-respond to more stimuli in varied and sophisticated ways
—-regulation of enzymes that catalyze covalent modification adds second level

22
Q

Feedback Inhibition

A

also called end-product inhibition

inhibition of one or more critical enzymes in a pathway regulates entire pathway
–pacemaker enzyme
——catalyzes the slowest or rate-limiting
reaction in the pathway

23
Q

Feedback inhibition if Pathway Splits

A

each end product regulates its own branch of the pathway

each end product regulates the initial pacemaker enzyme

24
Q

ATP—Energy currency of the cell

A

The most widely used form of chemical energy in the cell is adenosine triphosphate (ATP).

ATP is obtained in catabolic reactions and spent in anabolic reactions.