Quiz 2 Flashcards

(39 cards)

1
Q

What is the protein solubility at the isoelectric point?

A

lowest possible, bcs neutral charge

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2
Q

What does thermodynamics allow us to tell about bioenergetics? What is important to consider when doing calculations?

A
  1. reversible?
  2. favoured

final and initial values used for ∆G/H/S no focus on the pathways

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3
Q

∆S of the universe is assumed to be a certain level of energy, what is it?

A

∆S universe > 0

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4
Q

Knowing that ∆S(universe) > 0, we can presume that the ∆G is?

A

∆G < 0

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5
Q

Processes that decrease the amount of energy in a system do what to the ∆G?

A

∆G < 0, favoured

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6
Q

Processes that increase the amount of disorder in a system do what to the ∆G?

A

∆G < 0, favoured

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7
Q

In biochemistry entropy can and does decrease within favorable reactions, how does the system make up for it?

A

entropy can decrease as long as the enthalpy is large enough to account for it
- energy expelled is greater than the energy lost for organization

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8
Q

What is the equation that connects free energy, equilibrium, and concentration?

A

∆G = ∆Gº + RTlnQ
∆Gº is the standard value
R is gas constant
T is temp in Kelvin
Q is products/reactants

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9
Q

Homeostasis is not ______-

A

equilibrium

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10
Q

The relationship between K and Q indicates the energy and reaction direction
Q < K
Q = K
Q > K

A

Q < K = -∆G = forward reactions (products)
Q = K = 0 = equilibrium
Q > K = +∆G = reverse reaction (reactants)

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11
Q

Unfavourable reactions exit in biochemistry but are driven in the forward direction by 2 things

A

Q/K > 1 (consume as fast as produce, or have high concentration of reactants

coupling favourable reactions

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12
Q

What is the full name of RNA

A

B-D-ribose (B-beta)

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13
Q

What is the full name of DNA

A

B-D-2-deoxyribose (B-beta)

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14
Q

The sugar that makes of the structure of primary nucleic acids is made of what and what does it look like?

A

5-carbons
Beta isomer at anomeric C

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15
Q

Difference between nucleosides and nucleotides

A

nucleosides = sugar + base
nucleotides = sugar + base + phosphate

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16
Q

On a nucleic acid drawing indicate the glycosidic bond and phosphodiester bonds

17
Q

What are the two conformations for nucleic acids? Draw + indicate which is used by DNA and RNA, and indicate why.

A

C2’ endo = DNA, 7.0A between phosphates

C3’ endo = RNA, 5.9A between phosphates

18
Q

Steric constraints hinder rotation around the glycosidic bond, this allows for two conformations, which is more favourable?

A
  • syn
  • anti = more favourable for double helix interstrand bonding
19
Q

Draw out the tautomeric conformations and which is more favourable

A

keto* <=> enol
amine* <=> imine

20
Q

Draw a Fisher projection, what are the steps

A
  1. orient acid up (into the page
  2. orient side chain down (also into the page)
  3. determine which side the amino group is on (Left = L, right = D)
20
Q

How are polynucleotides formed?

A

coupled reactions
- break high energy phosphate bonds

20
Q

Go over the 20 amino acids
- non-polar, polar, acidic, basic
- name, 3 letter code, 1 letter code
- pKa of ionizable side chains

21
Q

Two amino acids have beta branches with stereochem. What are they? Draw out the line drawing and Fisher projection

A

isoleucine = Ile = I
(L-L)

threonine = Thr = T
(L-D)

22
Q

Which amino acid is the most hydrophobic?

A

phenylalanine = Phe = F

23
Two unique aspects of cysteine
Cysteine = Cys = C (R-CH2-SH) 1. pKa = 7.4, can be charged close to neutral 2. disulfide bond, important for stabilization of the higher ups
24
How much can the pKa of select amino acids change depending on the microenvironment of the residue?
+/- 3 pH units
25
Amino acids are linked ______ by dehydration of the a-_____- of one residue and the a-_____ of the subsequent residue, to result in an amide bond (or_____ bond).
covalently a-COO- a-NH3+ peptide
26
Draw out peptide VFGI
find ss
27
Special rule for carbohydrate fisher projections
last stereogenic carbon determines whether (L or D)
28
How to determine the amount of stereocentres from chiral centres?
2^# of chiral centres
29
What to look for when naming monosaccharides?
- # carbons (6 - pyranose, 5 - furanose) - orientation of OH farthest from CH2OH (trans - a, cis - b)
30
Conformational isomers vs configurational isomers
conform = a difference in bond angle, can interchange no break covalent bond config = a difference in bond orientation, needs covalent bond rearrangement for interchange
31
Monosaccharide derivatives, write structure + name - b-D-glucose = reduction = phosphorylation = animation = oxidation product = anomeric dehydration
find ss
32
To overcome the thermodynamically unfavourable reaction, sugar monomers are “activated” by what?
conjugation to uridine diphosphate (UDP) to form the UDP-sugar
33
How functional diversity of polysaccharides? What jobs can they do?
- many monomers - not made by a template = structural, storage, info-encoding
34
Antigenic vs nonantigenic
antigenic- antibodies can be produced to target non-antigenic - no antibodies can be used
35
Self-assembly of lipids is driven by what two things?
- hydrophobic effect - VDW between tails
36
What do the numbers for #:#c∆# for the abbreviation of fatty acids indicate?
total carbons : # of double bonds : where double bonds are
37
There are four categories of membrane lipids that can be characterized based on their varied head-group chemistry
- glycerophospholipid - sphingolipid - glycoclyecrolipid - glycosphingolipid