Bioenergetics Flashcards

1
Q

entropy

A

(S)

The measure of microscopic disorder of a system.

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2
Q

enthalphy

A

(H)

the total energy of a thermodynamic system; ΔH is the heat generated at constant pressure

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3
Q

free energy

A

(G)

energy of a reaction that can be used to do work (negative ΔG) or the energy required to drive a reaction (positive ΔG)

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4
Q

high energy compounds

A

compounds with large negative free energies of hydrolysis (compounds that release a large amount of energy upon hydrolysis)

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5
Q

first law of thermodynamics

A

energy can neither be created nor destroyed, E of the universe is constant

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6
Q

second law of thermodynamics

A

spontaneous reactions occur in directions that will increase the overall disorder of the universe. So, the entropy of the universe is always INCREASING (ΔS>0)

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7
Q

What are the two main categories of energy?

A

kinetic energy and potential energy

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8
Q

What is kinetic energy?

A

energy in motion

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9
Q

What is potential energy?

A

stored energy

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10
Q

Examples of potential energy

A

chemical bonds
concentration gradients
electric gradients
redox pairs

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11
Q

What has greater reduction potential and thus more energy, lipids or carbs?

A

Lipids (6 bonding e to C)

[Carbs: 4 bonding e to C]

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12
Q

Equation for calculating the free energy at NON-STANDARD conditions

A

ΔG=ΔG° + RTln[products/reactants]
R=1.987cal/mol K
T=temp in K
ΔG° = free energy in standard state (298 K, 7pH, 1 atm, 1M reactants in H2O)

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13
Q

Equation for free energy at EQUILIBRIUM

A

ΔG°= -RTlnKeq=2.3RTlogKeq

When ΔG = 0 (free energy at equilibrium

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14
Q

When Keq is <1, ΔG° is _____

A

positive

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15
Q

When Keq is >1, ΔG° is _____

A

negative

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16
Q

When Keq = 1, ΔG° is _____

A

zero

17
Q

Calculate Keq (at equilibrium)

A

Keq=kf/kr= [C][D]/[A][B] (when A+B–>C+D)

18
Q

Calculate ΔG (equation)

A

ΔG= ΔH-TΔS
H: change in enthalpy
S: change in entropy
T: temp

19
Q

For ΔG, what is spontaneous, what is nonspontaneous?

A

ΔG is negative for spontaneous reactions
ΔG is positive for nonspontaneous reactions
{spont doesn’t tell you rate!}

20
Q

Equation for conversion b/t free energy and redox potential.

A
ΔG=-nFΔE
*remember negative sign
F=96,500 joules/volt mol
n= number of electrons transferred
ΔE=reduction potential in volts
STANDARD CONDITIONS
21
Q

What is ΔE? more positive? more negative?

A

Measure of atom/molec’s readiness to accept electrons.
more positive? more likely to accept electrons (high reduction potential, OXIDIZING agent)
more negative? less likely to accept electrons; low reduction potential (REDUCING agent)

22
Q

Electrons flow from ____ to _____ reduction potentials.

A

Low to high reduction potentials.
[Move from compounds with low E, to high E (oxidized reactants), and RELEASE energy]
E=reduction potential in volts

23
Q

Standard free energy changes for a reaction are______, so reactions with _____ and _____ free energy changes can be coupled.

A

additive
positive and negative
[Nonspontaneous reactions may be coupled with highly spont. rxn with a common intermediate to drive the nonspont. reaction FORWARD.]

24
Q

Ex. of coupling reaction

A

ATP is often coupled with unfavorable rxns.

25
Q

High energy compounds

A

Compounds whose bonds are hydrolyzed w/ the release of large amounts of energy (ΔG<t mean high bond energy, just means there are large differences in STABILITY of the products and reactants of hydrolysis of high energy compounds)

26
Q

Examples of high energy bonds:

A
phophoanhydride bonds in ATP (beta and gamma are higher energy than alpha)
Thioester bond (C-S-CO-C in acetyl CoA compound)
Phophoenolpyruvate bond (C-O-P)
Phosphocreatine bond (P-N)
27
Q

Way to harvest energy for ATP production?

A

oxidation of glucose