Lecture 4 - Organic Molecules - Learning Objectives: Chapter 2.5 Flashcards

1
Q

Describe the basic structure of an amino acid.

A
- Amino acids are the monomers of proteins
Each has:
- Amino group
- alpha carbon
- Carboxyl group
- R group (side chain)
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2
Q

Describe how amino acids link together via peptide bonds to form proteins

A

Carbon of the carboxyl group of one amino acid is linked to the nitrogen in the adjacent amino acid by a covalent peptide bond

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3
Q

Identify and Define the three components of a nucleic acid.

A
- Nucleotides are the monomers of nucleic acids
Each has:
- 5-carbon sugar
- Nitrogenous Base
One or more phosphate groups.
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4
Q

Describe the difference between a deoxyribonucleotide and a ribonucleotide.

A

In DNA the 5-carbon sugar is deoxyribose.

In RNA, it is ribose.

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5
Q

Identify the five nitrogen-containing bases of nucleic acids and differentiate between the two
classes (purines and pyrimidines).

A

Purine:

  • adenine
  • guanine

Pyrimidine:

  • Thymine
  • Cytosine
  • Uracil (replaces Thymine in RNA)
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6
Q

Describe the process of nucleotide joining.

A
  • Joined by phosphodiester bonds.
  • The 5’ phosphate group of one nucleotide binds the 3’ OH group on the sugar of another nucleotide.
  • results in loss of water.
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7
Q

Describe the structure of DNA.

A
  • Double helix (two strands).
  • Sugar-phosphate backbones wrap around outside.
  • Complementary base- pairing on the inside
    (A-T and G-C)
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8
Q

Define a carbohydrate and identify/describe the two main classes of sugars.

A

Simple carbohydrates are monosaccharides:

  • exist as linear or cyclical structures
  • composed of carbon, hydrogen, oxygen
  • contain 5 or 6 carbons

Two main sugars are:

  • aldose, contains aldehyde group (H-C- -O) at end of chain.
  • Ketose, contains ketone group (C- -O) within chain
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9
Q

Define Mono-, Di-, and Polysaccharides.

A

Monosaccharides: One sugar
v Disaccharides: Two sugars linked together
v Polysaccharides: Many sugars linked together

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10
Q

Describe the cyclization process of ketose and aldose sugars.

A

Aldose:
The carbon in the aldehyde (-COH) of an aldose forms a covalent bond with the oxygen of the -OH of another carbon in the same molecule.
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11
Q

Describe the process of glycosidic bond formation.

A

Covalent bond between 1’ Carbon of one simple sugar and soome other Carbon of the same molecule.

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12
Q

Identify the major difference between lipids and the other three classes of biomolecules.

A

Lipids are NOT defined by chemical structure, they are defined by their hydrophobic nature.

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13
Q

• Describe and compare the three types of lipids

A

I. Fatty Acids (Triacylglycerol): long carbon chains attached to a carboxyl group.

II. Steroids: carbon rings

III. Phospholipids: glycerol
backbone + 2 fatty acid chains
+ phosphate head group

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14
Q

Describe the formation of a triacylglycerol.

A
Structure: glycerol’s 3 hydroxyl (–OH) groups covalently bind to the
carboxyl group (-COOH) of three fatty acids.
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15
Q

Compare saturated vs unsaturated fats.

A

Saturated Fats:
made up of fatty acids that do not contain C=C bonds
- saturated with hydrogen atoms.

Unsaturated Fats:
made up of fatty acids that contain C = C bonds
- kinks caused by double bonds reduce tightness of packing and lower melting temp.

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16
Q

Define Van der Waals forces and describe their role in lipid structure.

A

Fatty acids are uncharged: hydrocarbon chains contain no polar covalent bonds
……however……
- The constant motion of electrons leads to regions of slight charges: attract/repel molecules.
Forces are weaker than hydrogen bonds: many act together to
stabilize molecules.

17
Q

Describe the structure and function of a phospholipid.

A

Function: major component of the cell membrane

Structure: glycerol attached to two fatty acids and a phosphate containing
head group.