Biological Chemistry Exam 1

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Last updated 9:12 PM on 7/3/26
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140 Terms

1
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A nucleotide differs from a nucleoside by the presence of which of the following?

Phosphate group

2
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Which structural feature of RNA is primarily responsible for its decreased stability compared to DNA

Presence of 2’ hydroxyl group on ribose

3
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Which statement best explains why purines must pair with pyrimidines in DNA

To maintain uniform diameter of the double helix

4
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Which component of nucleotides carries the negative charge of DNA

Phosphate group

5
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A researcher analyzes a nucleic acid sample and finds ribose sugars and uracil bases. Which molecule is most likely present?

mRNA

6
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Which bond links nucleotides together in a nucleic acid strand?

Phosphodiester bond

7
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Which nitrogenous base is classified as a pyrimidine?

Cytosine

8
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In double-stranded DNA, which base pair forms three hydrogen bonds?

G-C

9
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Which RNA type is directly responsible for bringing amino acids to the ribosome during protein synthesis?

tRNA

10
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Which nitrogenous base is classified as a pyrimidine?

Cytosine

11
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What is a Nucelotide?

Basic Building block (monomer) of (DNA and RNA)

12
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3 components of a Nucleotide

Nitrogenous base, Pentose Sugar, Phosphate groups

13
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What is a nucleoside

Base + Sugar only

14
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What are Nitrogenous bases

Heterocyclic, aromatic molecules that contain N

15
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Purines

Adenine (A)

Guanine (G)

16
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Purines Structure

Fused 6-membered + 5-membered rings

17
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Pyrimidines

Cytosine

Thymine → DNA only

Uracil → RNA only

18
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Pyrimidines Structure

Single 6-membered rings

19
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Phosphodiester bonds

Connects 3’ OH of one sugar to 5’ phosphate of next nucleotide

Form the sugar-phosphate backdown

20
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Base pairings (Hydrogen Bonds)

A-T

G-C

21
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Which base pair bonding is stronger?

G-C

22
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Clinical Relevance

GC- rich regions are more stable

DNA replication, transcription, and repair depend on strand complementarity

23
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mRNA

Codes for proteins

24
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tRNA

Brings amino acids

25
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rRNA

Forms ribosomes

26
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Purine metabolism disorders

Gout (uric acid accumulation)

27
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Cancer drugs

Blocks nucleotide synthesis

28
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Antivirals

Nucleoside analogs interfere with viral replication

29
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Essential amino acids must be obtained from the diet. Which of the following is essential?

Leucine

30
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Which amino acid is aromatic, hydroxylated, and is important for enzyme regulation?

Tyrosine

31
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Which amino acid is the precursor of serotonin and melatonin?

Tryptophan

32
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Which of the following amino acids is positively charged at physiological pH?

Lysine

33
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Which amino acid is non-chiral

Glycine

34
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Which amino acid contains a sulfur atom that can form disulfide bonds?

Cytseine

35
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Which amino acid is hydroxylated post-translationally to stabilize collagen

Proline

36
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Which of the following is not a standard amino acid used in protein synthesis?

Ornithine

37
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<p>What kind of structure is this? Also what type? and which?</p>

What kind of structure is this? Also what type? and which?

AA, positively charged, histidine

38
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<p>What kind of structure is this? Also what type? and which?</p>

What kind of structure is this? Also what type? and which?

AA, Hydrophobic, Valine

39
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LDL is considered “bad” because:

It deposits cholesterol in tissues

40
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VLDL transports?

Lipids made in the liver

41
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What is the main enzyme for lipid digestion?

Pancreatic lipase

42
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Lipids include which of the following?

All of the above

43
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High trans fat intake is linked to

Increased Cardiovascular disease

44
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Which enzyme starts lipid digestion

Gastric lipase

45
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If membrane lipids are modified to contain more saturated fatty acids, what happens to the membrane?

Increased rigidity

46
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Saturated fatty acids

Have no double bonds

47
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Omega fatty acids are classified by:

Position of first double bond from omega end

48
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If a genetic mutation prevents proper formation of chylomicrons, which process is most impaired?

Transport of dietary lipids to tissues

49
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Saturated fats pack tightly and are solid

True

50
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What do we mainly eat

Lipids (like triglycerides)

51
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What is the primary consequence of a bile obstruction (gallstones)

Decreased lipid emulsification

52
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What is the role of bile?

Emulsify lipids

53
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Lipids are absorbed in

Intestinal cells (enterocytes)

54
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After absorption, lipids are packaged into:

Chylomicrons

55
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Which is TRUE regarding lipid transport?

All of the above

56
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Where are chylomicrons formed?

Intestinal cells

57
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Where are VLDL produced?

Liver

58
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What is VLDL

a type of "bad cholesterol" produced by your liver

59
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What is LDL

low-density lipoprotein, is famous for carrying cholesterol,

60
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What is VLDL’s job

transport triglycerides, which are fats your body uses for energy or stores as excess fat.

61
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What is VLDL made of

mostly of triglycerides (about 50-60% of the particle).

62
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What is HDL

good cholesterol, that acts like a cleanup crew, scooping up excess cholesterol from your bloodstream and taking it back to the liver to be broken down.

63
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What is the main function of lipids?

Energy storage and membranes

64
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What is a fatty acid?

A molecule with a carboxylic acid and hydrocarbon tail

65
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Unsaturated fatty acids

Have at least one double bond?

66
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Lipid digestion involves everything except?

DNA Polymerase

67
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Which sequence best describes lipid transport after a high-fat meal

Intestine -> chylomicrons -> lymph -> blood

68
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Where does lipid digestion begin?

Stomach

69
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Omega-6 vs Omega-3 difference:

Position of double bond

70
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What is the biochemical consequence of partial hydrogenation of vegetable oil?

Conversion to trans fats

71
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Where do chylomicrons go first?

Lymphatic system

72
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Omega-3 fatty acids:

Are associated with reduced heart disease

73
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Fatty acids are:

Building blocks of lipids

74
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75
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Functions of lipids consist of everything except:

DNA replication

76
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Elevated VLDL levels in metabolic syndrome are most likely caused by:

Increased liver synthesis of triglycerides

77
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Chylomicrons transport:

Lipids from intestine

78
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Which statement is correct?

Lipids are made of fatty acids

79
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What is the expected physiological effect of increased omega-3 intake?

Reduced cardiovascular risk

80
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Why is glycogen highly branched?

To allow faster synthesis and degradation

81
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In glycogen synthesis, which molecule provides the energy to activate glucose?

UTP

82
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What is the main role of glycogen breakdown in muscle cells?

To provide energy for muscle contractions

83
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Why can the liver release free glucose into the blood but muscle cannot?

Muscle lacks glucose-6-phosphate

84
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Epinephrine stimulates glycogen breakdown primarily during:

Stress or Exercise

85
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Which hormone stimulates glycogen breakdown mainly in the liver during fasting?

Glucagon

86
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What is the effect of insulin on glycogen metabolism?

Activates glycogen synthase

87
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Which hormone predominates during the fed state?

Insulin

88
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What unique function does glycogenin perform?

Self-glycosylates to start glycogen synthesis

89
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What protein acts as the primer for glycogen synthesis?

Glycogenin

90
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What is one advantage of glycogen branching?

Increases number of ends for metabolism

91
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What is the function of the branching enzyme?

Create α-1,6 branches

92
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What type of bonds are formed by glycogen synthase?

α-1,4

93
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UDP-glucose serves as what during glycogen synthesis?

Activated glucose donor

94
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Which enzyme activates glucose by forming UDP-glucose?

UDP-glucose pyrophosphorylase

95
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During glycogen synthesis, glucose is first converted to which molecule?

Glucose-6-phosphate

96
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Which activity of the debranching enzyme breaks the α-1,6 bond?

Isomerase

α-1,6 glucosidase

97
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Which activity of the debranching enzyme moves three glucose residues to another chain?

Transferase activity

98
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The glycogen debranching enzyme has how many enzymatic activities?

Two

99
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Glycogen phosphorylase stops breaking glycogen when it is how many residues away from a branch point?

4

100
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Which enzyme is the rate-limiting enzyme of glycogen synthesis?

Glycogen synthase