Macromolecules Chapter 5 Macromolecules n Large complex molecules

  • Slides: 49
Download presentation
Macromolecules Chapter 5

Macromolecules Chapter 5

Macromolecules n Large complex molecules n Carbohydrates, proteins, lipids & nucleic acids

Macromolecules n Large complex molecules n Carbohydrates, proteins, lipids & nucleic acids

Macromolecules n Polymer n Large molecule n Carboydrates, proteins, nucleic acids n Monomers n

Macromolecules n Polymer n Large molecule n Carboydrates, proteins, nucleic acids n Monomers n Smaller repeating units n Build polymers

Macromolecules n Monomers are connected by a dehydration reaction n Condensation reaction

Macromolecules n Monomers are connected by a dehydration reaction n Condensation reaction

Fig. 5 -2 a HO 1 2 3 H Short polymer HO Unlinked monomer

Fig. 5 -2 a HO 1 2 3 H Short polymer HO Unlinked monomer Dehydration removes a water molecule, forming a new bond HO 1 2 H 3 H 2 O 4 H Longer polymer (a) Dehydration reaction in the synthesis of a polymer

Macromolecules n Polymers are broken apart into monomers by hydrolysis n Bonds are broken

Macromolecules n Polymers are broken apart into monomers by hydrolysis n Bonds are broken by adding water

Fig. 5 -2 b HO 1 2 3 4 Hydrolysis adds a water molecule,

Fig. 5 -2 b HO 1 2 3 4 Hydrolysis adds a water molecule, breaking a bond HO 1 2 3 (b) Hydrolysis of a polymer H H H 2 O HO H

Carbohydrates n Simple sugars to complex polymers n Stored energy n Structure

Carbohydrates n Simple sugars to complex polymers n Stored energy n Structure

Carbohydrates Monosaccharides n Single sugar n – Glucose, fructose, galactose n n n Molecules

Carbohydrates Monosaccharides n Single sugar n – Glucose, fructose, galactose n n n Molecules contain carbon, hydrogen & oxygen in a 1: 2: 1 ratio CH 2 O End in –ose Aldose: aldehyde sugar Ketose: ketone sugar

Fig. 5 -3 a Aldoses Trioses (C 3 H 6 O 3) Pentoses (C

Fig. 5 -3 a Aldoses Trioses (C 3 H 6 O 3) Pentoses (C 5 H 10 O 5) Hexoses (C 6 H 12 O 6) Glyceraldehyde Ribose Glucose Galactose

Fig. 5 -3 b Ketoses Trioses (C 3 H 6 O 3) Pentoses (C

Fig. 5 -3 b Ketoses Trioses (C 3 H 6 O 3) Pentoses (C 5 H 10 O 5) Hexoses (C 6 H 12 O 6) Dihydroxyacetone Ribulose Fructose

Carbohydrates n Dissaccharides n Two monosaccharides combined n Glycoside linkage: n Covalent bond between

Carbohydrates n Dissaccharides n Two monosaccharides combined n Glycoside linkage: n Covalent bond between two sugars n Sucrose (glucose & fructose) n Maltose (glucose & glucose) n Lactose (glucose & galactose)

Fig. 5 -5 1– 4 glycosidic linkage Glucose Maltose (a) Dehydration reaction in the

Fig. 5 -5 1– 4 glycosidic linkage Glucose Maltose (a) Dehydration reaction in the synthesis of maltose 1– 2 glycosidic linkage Glucose Fructose (b) Dehydration reaction in the synthesis of sucrose Sucrose

Carbohydrates n Polysaccharides n Many monosaccharides combined n Starch (plant), glycogen (animal), cellulose (plant),

Carbohydrates n Polysaccharides n Many monosaccharides combined n Starch (plant), glycogen (animal), cellulose (plant), chitin

Fig. 5 -7 (a) and glucose ring structures Glucose (b) Starch: 1– 4 linkage

Fig. 5 -7 (a) and glucose ring structures Glucose (b) Starch: 1– 4 linkage of glucose monomers Glucose (b) Cellulose: 1– 4 linkage of glucose monomers

Fig. 5 -10 (a) The structure of the chitin monomer. (b) Chitin forms the

Fig. 5 -10 (a) The structure of the chitin monomer. (b) Chitin forms the exoskeleton of arthropods. (c) Chitin is used to make a strong and flexible surgical thread.

Lipids n Insoluble in water – Hydrophobic n Store energy n Make membranes

Lipids n Insoluble in water – Hydrophobic n Store energy n Make membranes

Lipids n Fats – Unsaturated – Saturated n Phospholipids – Glycerol, phosphate, fatty acid

Lipids n Fats – Unsaturated – Saturated n Phospholipids – Glycerol, phosphate, fatty acid n Steroids

Fats n Glycerol and fatty acids n Triglyceride n 3 fatty acids attached to

Fats n Glycerol and fatty acids n Triglyceride n 3 fatty acids attached to a glycerol

Fatty acid (palmitic acid) Glycerol (a) Dehydration reaction in the synthesis of a fat

Fatty acid (palmitic acid) Glycerol (a) Dehydration reaction in the synthesis of a fat

Fig. 5 -11 b Ester linkage (b) Fat molecule (triacylglycerol)

Fig. 5 -11 b Ester linkage (b) Fat molecule (triacylglycerol)

Fig. 5 -12 Structural formula of a saturated fat molecule Stearic acid, a saturated

Fig. 5 -12 Structural formula of a saturated fat molecule Stearic acid, a saturated fatty acid (a) Saturated fat Structural formula of an unsaturated fat molecule Oleic acid, an unsaturated fatty acid (b) Unsaturated fat cis double bond causes bending

Phospholipids n Cell membrane n Tails are hydrophobic n Hydrophilic head

Phospholipids n Cell membrane n Tails are hydrophobic n Hydrophilic head

Fig. 5 -14 Hydrophilic head Hydrophobic tail WATER

Fig. 5 -14 Hydrophilic head Hydrophobic tail WATER

Steroids

Steroids

Steroids

Steroids

Proteins n Amino acids n Building blocks of proteins n 20 different amino acids

Proteins n Amino acids n Building blocks of proteins n 20 different amino acids n Peptide bond n Polypeptide

Fig. 5 -18 Peptide bond (a) Side chains Peptide bond Backbone (b) Amino end

Fig. 5 -18 Peptide bond (a) Side chains Peptide bond Backbone (b) Amino end (N-terminus) Carboxyl end (C-terminus)

Fig. 5 -17 Nonpolar Glycine (Gly or G) Valine (Val or V) Alanine (Ala

Fig. 5 -17 Nonpolar Glycine (Gly or G) Valine (Val or V) Alanine (Ala or A) Methionine (Met or M) Leucine (Leu or L) Trypotphan (Trp or W) Phenylalanine (Phe or F) Isoleucine (Ile or I) Proline (Pro or P) Polar Serine (Ser or S) Threonine (Thr or T) Cysteine (Cys or C) Tyrosine (Tyr or Y) Asparagine Glutamine (Asn or N) (Gln or Q) Electrically charged Acidic Aspartic acid Glutamic acid (Glu or E) (Asp or D) Basic Lysine (Lys or K) Arginine (Arg or R) Histidine (His or H)

Protein Function n Enzyme catalysis n Defense n Transport n Support n Motion n

Protein Function n Enzyme catalysis n Defense n Transport n Support n Motion n Regulation n Storage

Protein structure n Primary n Secondary n Tertiary n Quaternary

Protein structure n Primary n Secondary n Tertiary n Quaternary

Primary Structure n Sequence of amino acids

Primary Structure n Sequence of amino acids

Secondary Structure n Hydrogen bonds between amino acids n Pleats or helix

Secondary Structure n Hydrogen bonds between amino acids n Pleats or helix

Tertiary structure n Attraction between side chains n Hydrophobic interaction n Disulfide bridges n

Tertiary structure n Attraction between side chains n Hydrophobic interaction n Disulfide bridges n Ionic bonds n Hydrogen bonds

Quaternary structure n Two or more polypeptide chains aggregate

Quaternary structure n Two or more polypeptide chains aggregate

Sickle cell anemia

Sickle cell anemia

Fig. 5 -22 Normal hemoglobin Primary structure 1 2 3 4 5 6 7

Fig. 5 -22 Normal hemoglobin Primary structure 1 2 3 4 5 6 7 Secondary and tertiary structures subunit Function Normal hemoglobin (top view) Secondary and tertiary structures Val His Leu Thr Pro Val Glu 1 2 3 Normal red blood cells are full of individual hemoglobin moledules, each carrying oxygen. 6 7 subunit Sickle-cell hemoglobin Function Molecules interact with one another and crystallize into a fiber; capacity to carry oxygen is greatly reduced. 10 µm Red blood cell shape 5 Exposed hydrophobic region Molecules do not associate with one another; each carries oxygen. 4 Quaternary structure Sickle-cell hemoglobin Quaternary structure Primary structure Val His Leu Thr Pro Glu 10 µm Red blood cell shape Fibers of abnormal hemoglobin deform red blood cell into sickle shape.

Structure n Denaturation: n Alter, unravel shape of protein n Temperature, p. H, salt

Structure n Denaturation: n Alter, unravel shape of protein n Temperature, p. H, salt n Chaperonins: n Proteins that help with structure

Nucleic Acids n DNA and RNA n Transfer & store genetic information n Nucleotides

Nucleic Acids n DNA and RNA n Transfer & store genetic information n Nucleotides are the subunits n Nitrogenous base n 5 carbon sugar n Phosphate group

Nucleic Acids n Pyrimidines n Cytosine, thymine and uracil n Single carbon ring n

Nucleic Acids n Pyrimidines n Cytosine, thymine and uracil n Single carbon ring n Purines n Adenine, guanine n Double ring structure

Nitrogenous Bases

Nitrogenous Bases

Fig. 5 -27 c-1 Nitrogenous bases Pyrimidines Cytosine (C) Thymine (T, in DNA) Uracil

Fig. 5 -27 c-1 Nitrogenous bases Pyrimidines Cytosine (C) Thymine (T, in DNA) Uracil (U, in RNA) Purines Adenine (A) Guanine (G) (c) Nucleoside components: nitrogenous bases

Fig. 5 -27 c-2 Sugars Deoxyribose (in DNA) Ribose (in RNA) (c) Nucleoside components:

Fig. 5 -27 c-2 Sugars Deoxyribose (in DNA) Ribose (in RNA) (c) Nucleoside components: sugars

DNA n n n n Double helix Sugar-phosphate backbone is on the outside of

DNA n n n n Double helix Sugar-phosphate backbone is on the outside of helix Run in opposite direction Antiparallel Base pairs held together by hydrogen bonds Adenine-thymine (uracil) Cytosine-guanine

DNA

DNA

DNA

DNA

Fig. 5 -28 5' end 3' end Sugar-phosphate backbones Base pair (joined by hydrogen

Fig. 5 -28 5' end 3' end Sugar-phosphate backbones Base pair (joined by hydrogen bonding) Old strands Nucleotide about to be added to a new strand 3' end 5' end New strands 5' end 3' end