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Chapter 2
Chemical Composition of
the Body
Human
Physiology
Atoms
• Smallest units of matter that can
undergo chemical change.
• Nucleus (center) contains:
▫ Protons (+ charge)
▫ Neutrons (no charge)
• Atomic mass:
▫ Sum of protons and neutrons.
Atoms
• Atomic Number
▫ Number of protons in an atom
• Neutral atom
▫ Number of protons = number of electrons
• Isotopes
▫ Vary in number of neutrons
▫ Same in atomic number
▫ Vary in atomic mass
Atoms
• Chemical element
▫ Includes all of the isotopic forms of a given atom
▫ Eg: Element Hydrogen: 3 isotopes
 Most common: one proton
 Deuterium: one proton, one neutron
 Tritium: one proton, two neutrons
 Commonly used in research
▫ 106 chemical elements
Elements
• Four elements important to living organisms
▫ Carbon (C)
▫ Nitrogen (N)
▫ Oxygen (O)
▫ Hydrogen (H)
Atoms
• Electrons (outside the nucleus):
▫ - charged
▫ Occupy orbitals surrounding nucleus.
• Valence electrons:
▫ Electrons in the outer most orbital that
participate in chemical reactions (if orbit
incomplete).
▫ Form chemical bonds.
Orbitals
• Also called shells or energy levels
• Electrons usually found within a given orbital
• Levels (and max number of electrons)
▫ First shell: 2 electrons
▫ Second shell: 8 electrons
▫ Third shell: usually 8 electrons
Chemical Bonds, Molecules, and
Ionic Compounds
• Chemical bonds:
▫ Interaction of valence electrons
between 2 or more atoms.
• # bonds determined by # electrons
needed to complete outer orbital.
Covalent Bonds
• Atoms share their valence
electrons.
• Nonpolar bonds:
▫ Electrons are equally distributed
between the two identical atoms.
▫ Strongest bond.
▫ H2
Covalent Bonds
• Polar bonds:
▫ Electrons are shared between two
different atoms.
▫ Electrons may be pulled more toward
more atom.
▫ Oxygen, nitrogen, phosphate pull
electrons towards themselves.
Ionic Bonds
• One or more valence electrons from
an atom are completely transferred
to a second atom.
• First atom loses electrons, +
charged (cation).
• Second atom has more electrons,
- charged (anion).
Ionic Bonds
• Cation and anion attract, form ionic
compound.
• Weaker than polar bonds.
• Dissociate easily when dissolved in
H20.
• NaCl Na+
and Cl-
Table Salt, an Ionically Bonded Molecule
Slide number: 1
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
17p
18n
11p
12n
11p
12n
17p
18n+
(+)
(–)
Na Cl+ NaCl
Table Salt, an Ionically Bonded Molecule
Slide number: 2
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
17p
18n
11p
12n
Na Cl+
Table Salt, an Ionically Bonded Molecule
Slide number: 3
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
17p
18n
11p
12n
Na Cl+
Table Salt, an Ionically Bonded Molecule
Slide number: 4
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
17p
18n
11p
12n
Na Cl+
Table Salt, an Ionically Bonded Molecule
Slide number: 5
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
17p
18n
11p
12n
Na Cl+
Table Salt, an Ionically Bonded Molecule
Slide number: 6
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
17p
18n
11p
12n
Na Cl+
(+) (–)
Table Salt, an Ionically Bonded Molecule
Slide number: 7
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
NaCl
11p
12n
(+)
17p
18n
(–)
Interaction with water
• Hydrophilic:
▫ Formation of hydration spheres.
▫ Polar covalent bonds.
• Hydrophobic:
▫ Cannot form hydration spheres.
▫ Nonpolar covalent bonds.
Hydrogen Bond
• Hydrogen forms a
polar bond with
another atom,
hydrogen has a
slight + charge.
• Weak attraction
for for a second
electronegative
atom.
Acids, Bases, and the pH Scale
• Acid:
▫ Molecule that can release protons (H+
).
▫ Proton donor.
• Base:
▫ Negatively charged ion that can combine with
H+
.
▫ Proton acceptor.
pH
• pH = log _1__
[H+
]
• Normal pH blood = 7.35 - 7.45.
• Buffer:
▫ System of molecules and ions that act
to prevent changes in [H+
].
Organic Molecules
• Molecules that contain carbon and
hydrogen.
• Carbon has 4 electrons in outer
orbital.
• Carbon covalently bonds to fill its
outer orbital with 8 electrons.
Organic Molecules
• Organic Chemistry: deals with molecules that
contain carbon
• More than 5 million organic compounds have
been identified
• The carbon atom can form bonds with a
greater number of different elements than
any other type of atom
Functional Groups
• Inactive “backbone” to which more reactive
atoms are attached.
Classes According to Functional
Groups
• Ketone and
aldehyde:
carbonyl group
• Organic acid:
carboxyl group
• Alcohol: hydroxyl
group
Stereoisomers
• Exactly the same atoms arranged in same
sequence.
• Differ in spatial orientation of a functional
group.
▫ D-isomers: right-handed
▫ L-isomers: left-handed
• Enzymes of all cells can combine only with
the L-amino acids and
D-sugars.
Four main classes of Organic
molecules
• Lipids
• Carbohydrates
• Proteins
• Nucleic Acids
Lipids
• GR: Lipos=Fat
• Diverse group of molecules.
• Insoluble in polar solvents (H20).
• Hydrophobic (nonpolar)
• Consist primarily of hydrocarbon
chains and rings.
Lipids
• Hydrocarbons
• Fatty acids
• Triglycerides
• Ketone Bodies
• Phospholipids
• Steroids
• Prostaglandins
Hydrocarbons
• Includes oils and
gases
• Carbons can be
single bonds
(saturated)
• Carbons can be
double bonded
(unsaturated)
Fatty acids
• Nonpolar hydrocarbon chain
▫ Can be saturated (are stright)
▫ Can be unsaturated (bend at the double bond)
▫ Can be poly unsaturated (multiple bends)
• Carboxyl group on one end
• Large group
Triglycerides
• Formed by condensation of glycerol and 3
fatty acids.
▫ Ester bond
• Fatty acid consists of hydrocarbon chain
with carboxylic acid end.
▫ May be saturated or unsaturated
▫ Saturated fats:
 Mostly animal sources
 Mostly solid at room temperature
▫ Unsaturated fats
 Mostly plant sources
 Mostly liquid at room temperature
Nutritional considerations of
triglycerides
• Also called fat or neutral fat
• Stored in adipose cells
• Total fat intake should be about 30% of total
energy intake
▫ Saturated fat >10%
• Saturated fats are implicated in heart disease
and stroke
▫ Data suggests they promote high blood
cholesterol
Phospholipids
• A number of categories
• All contain a phosphate group
• Most common
▫ Glycerol (3 carbons)
▫ Fatty Acids on carbon 1 and 2
▫ Phosphate group attached to carbon (and other
polar groups eg.: choline)
Lecithin
Phospholipid
• Are amphipathic: contain both polar and
nonpolar domains
▫ Head:
 contains polar groups
 Hydrophilic
▫ Tail:
 Contains fatty acids (nonpolar)
 Hydrophobic
Phospholipids
• Major component of cell membranes
▫ Hydrophylic heads orient to water
▫ Hydrophobic tails orient to each other
• Kind of phospholipid varies based on cell or
organelle
Micelle formation
Ketone Bodies
• Results from the hydrolysis of triglycerides by
adipocytes
▫ Liberates free FA into blood
▫ FA function as an acid in blood
• Most FA used as energy source by some
tissues
• If not, converted by liver into Ketone bodies
Ketone Bodies
4-carbon chunks
Ketone Bodies
• Produced in the rapid breakdown of FA
▫ Low-carbohydrate diets
▫ Uncontrolled Diabetes mellitus
• Ketosis: Elevated level of FA in blood
• Ketoacidosis: ketosis is high enough to lower
blood ph
Steroids
• Nonpolar and insoluble in H20.
• All have cholesterol as precursor.
Prostaglandins
• Prostaglandins:
▫ Fatty acid with cyclic hydrocarbon
group.
▫ Derived from arachidonic acid.
Prostaglandins
Carbohydrates
• Organic molecules that contain
carbon, hydrogen and oxygen.
• CH20
• General formula:
▫ CnH2nOn
• -ose denotes a sugar molecule
Carbohydrates
• Supply energy
▫ Glucose
▫ Complex carbohydrates
• Provide structural support
▫ cellulose
• Part of plasma membrane
• Monomer: monosaccarides
Carbohydrates
• Monosaccharide: the “simple sugars”
▫ Pentoses (5-carbons):
 Ribose: in RNA
 Deoxyribose: in DNA
▫ Hexoses (6-carbons):structural isomers
 Glucose, fructose and galactose
 Characteristics
 Soluable
 Sweet
 Alcoholic fermentation
Glucose
• Also called :
▫ Dextrose
▫ Transportable in the blood
 Blood glucose
▫ C6H12O6
Fructose
• Fruit sugar
Galactose
▫ C6H12O6
Carbohydrates
• Disaccharide:
▫ 2 monosaccharides joined covalently.
 Sucrose
 Glucose and fructose
 Maltose
 Glucose and glucose
 Lactose
 Glucose and galactose
Disaccharides
• Characteristics
▫ Sweet
▫ Soluable
▫ Can be fermented
• Formation: called condensation
▫ Requires an enzyme
▫ Removal of molecule of water
▫ Also called dehydration synthesis
▫ Formation of a covalent bond
Formation of Disaccharides
Hydrolysis
• Reverse of dehydration synthesis.
• Digestion reaction.
• H20 molecule split.
Carbohydrates
• Polysaccharides:
▫ Many monosaccharides joined covalently.
▫ General formula: (C6H10O5)n
▫ Characteristics:
 Devoid of taste
 Do not form solutions
 Iodine test
 Iodine +starch+blue
Polysaccarides• Kinds:
▫ Starch
 Glucose subunits
 branched
▫ Dextrins
▫ Glycogen (animal starch)
 Glucose subunits
 Branched
▫ Cellulose
 Glucose subunits
 Long, unbranched chains
Proteins
• General Information:
▫ GR: proteios=first rank
▫ ~50% of the organic material of the
body
▫ Functions
 Structural:
 Cell structures, CTs
 Functional:
 Enzymes, hormones, Hb, etc!
Proteins• Protein Structure
▫ Large molecules (polymers) composed
of amino acid sub-units (monomers).
▫ Amino Acid structure
 amino group (NH2)
 carboxylic acid group (COOH)
 Radical group (R): functional group
 H
Proteins
• 20 different standard amino acids.
▫ Based on the properties of the
functional group
▫ E.g.:
Proteins
• Dehydration synthesis:
▫ Amino end of one amino acid
combines with hydroxyl group of
carboxylic end of another amino acid.
• Peptide bond:
▫ Bond between two adjacent amino
acids.
Peptide bond
Proteins• Dipeptide: 2 amino acids
• Tripeptide: 3 amino acids
• Polypeptide: many amino acids
▫ Number of amino acids varies
▫ Up to 100 aa
• Protein
▫ Over 100aa
▫ Great variety!
Protein structure
• Four structural levels
▫ Primary structure
 Based on amino acid sequence
 Amino acid sequence determined by DNA
▫ Secondary structure
 Based on hydrogen bonding between close aa
▫ Tertiery structure
 3-D shape
▫ Quaternary structure
 Only in proteins with 2 or more polypeptide
chains
Secondary structure (2o
)
• Based on the primary structure
• Weak hydrogen bonds form between
hydrogen and oxygen of a different amino
acid.
• Two main kinds of secondary structure:
▫ Alpha helix: Bond cause chain to twist in a helix.
▫ Beta pleated sheet: interactions between lengths of
the polypeptide chain
Secondary structures
Tertitary structure
• Polypeptide chains bend and fold.
▫ Based on interactions with aa in different parts of
the polypeptide chain
 disulfide bonds: covalent
 Hydrogen bonds: weak
• Produce 3 -dimensional shapes.
• Chemical interaction of each protein produces
own characteristic tertiary structure
• Denaturing protein
▫ Irreversible disruption of tertiary structure
Bonds responsible for 3o
structure
Tertiary structure
Quaternary Structure
• Number of
polypeptide
chains covalently
linked together.
• Insulin,
hemoglobin
Conjugated proteins
• Protein combined with another type of
molecule
• Glycoproteins: carbohydrate with protein
▫ Membranes, hormone
• Lipoproteins: Lipid and protein
▫ Membranes, blood plasma
• Hemoproteins: iron and protein
▫ Hemoglobin, cytochromes
Nucleic Acids
• Include the macromolecules:
▫ DNA: deoxyribonucleic acid
▫ RNA: ribonucleic acid
• Involved in heredity and genetic regulation
• Are polymers:
▫ Monomeric subunit:nucleotides
▫ Bonded together in a dehydration synthesis
reaction
Nucleic Acids
Nucleotides• Structure of a nucleotide: 3 subunits
▫ Pentose sugar
▫ Phosphate group
▫ Nitrogenous base
 Purines: two rings
 Guanine
 Adenine
 Pyrimidines: one ring
 Cytosine
 Thymine
 Uricil
Nucleotide Structure
Nitrogenous Bases
DNA
• Huge molecules with simple structure
• Big time data storage!
• Structure
▫ Nucleotides
 Pentose sugar: Deoxyribose
 Bases:
 Purines: G and A
 Pyrimidines: C and T
▫ Form double-stranded helix
DNA
• Nucleotide strands: 2
▫ Sugar-phosphate backbone
▫ Bases stick out
▫ Bases bond to each other
• Base pairing:
▫ A – T
▫ G – C
▫ Called law of complementary base pairing
Nitrogenous Bases
DNA
RNA
• Means by which DNA directs cellular
activities
• Structure
▫ Pentose sugar: ribose
▫ Bases: uracil (not thymine)
▫ Single stranded
• Three main types
▫ Messenger RNA (mRNA)
▫ Transfer RNA (tRNA)
▫ Ribosomal RNA (rRNA)
DNA vs RNA

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Chemical composition of the body

  • 1. Chapter 2 Chemical Composition of the Body Human Physiology
  • 2. Atoms • Smallest units of matter that can undergo chemical change. • Nucleus (center) contains: ▫ Protons (+ charge) ▫ Neutrons (no charge) • Atomic mass: ▫ Sum of protons and neutrons.
  • 3. Atoms • Atomic Number ▫ Number of protons in an atom • Neutral atom ▫ Number of protons = number of electrons • Isotopes ▫ Vary in number of neutrons ▫ Same in atomic number ▫ Vary in atomic mass
  • 4. Atoms • Chemical element ▫ Includes all of the isotopic forms of a given atom ▫ Eg: Element Hydrogen: 3 isotopes  Most common: one proton  Deuterium: one proton, one neutron  Tritium: one proton, two neutrons  Commonly used in research ▫ 106 chemical elements
  • 5. Elements • Four elements important to living organisms ▫ Carbon (C) ▫ Nitrogen (N) ▫ Oxygen (O) ▫ Hydrogen (H)
  • 6. Atoms • Electrons (outside the nucleus): ▫ - charged ▫ Occupy orbitals surrounding nucleus. • Valence electrons: ▫ Electrons in the outer most orbital that participate in chemical reactions (if orbit incomplete). ▫ Form chemical bonds.
  • 7. Orbitals • Also called shells or energy levels • Electrons usually found within a given orbital • Levels (and max number of electrons) ▫ First shell: 2 electrons ▫ Second shell: 8 electrons ▫ Third shell: usually 8 electrons
  • 8.
  • 9. Chemical Bonds, Molecules, and Ionic Compounds • Chemical bonds: ▫ Interaction of valence electrons between 2 or more atoms. • # bonds determined by # electrons needed to complete outer orbital.
  • 10. Covalent Bonds • Atoms share their valence electrons. • Nonpolar bonds: ▫ Electrons are equally distributed between the two identical atoms. ▫ Strongest bond. ▫ H2
  • 11.
  • 12.
  • 13. Covalent Bonds • Polar bonds: ▫ Electrons are shared between two different atoms. ▫ Electrons may be pulled more toward more atom. ▫ Oxygen, nitrogen, phosphate pull electrons towards themselves.
  • 14.
  • 15. Ionic Bonds • One or more valence electrons from an atom are completely transferred to a second atom. • First atom loses electrons, + charged (cation). • Second atom has more electrons, - charged (anion).
  • 16. Ionic Bonds • Cation and anion attract, form ionic compound. • Weaker than polar bonds. • Dissociate easily when dissolved in H20. • NaCl Na+ and Cl-
  • 17. Table Salt, an Ionically Bonded Molecule Slide number: 1 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 17p 18n 11p 12n 11p 12n 17p 18n+ (+) (–) Na Cl+ NaCl
  • 18. Table Salt, an Ionically Bonded Molecule Slide number: 2 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 17p 18n 11p 12n Na Cl+
  • 19. Table Salt, an Ionically Bonded Molecule Slide number: 3 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 17p 18n 11p 12n Na Cl+
  • 20. Table Salt, an Ionically Bonded Molecule Slide number: 4 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 17p 18n 11p 12n Na Cl+
  • 21. Table Salt, an Ionically Bonded Molecule Slide number: 5 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 17p 18n 11p 12n Na Cl+
  • 22. Table Salt, an Ionically Bonded Molecule Slide number: 6 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 17p 18n 11p 12n Na Cl+ (+) (–)
  • 23. Table Salt, an Ionically Bonded Molecule Slide number: 7 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. NaCl 11p 12n (+) 17p 18n (–)
  • 24.
  • 25. Interaction with water • Hydrophilic: ▫ Formation of hydration spheres. ▫ Polar covalent bonds. • Hydrophobic: ▫ Cannot form hydration spheres. ▫ Nonpolar covalent bonds.
  • 26. Hydrogen Bond • Hydrogen forms a polar bond with another atom, hydrogen has a slight + charge. • Weak attraction for for a second electronegative atom.
  • 27. Acids, Bases, and the pH Scale • Acid: ▫ Molecule that can release protons (H+ ). ▫ Proton donor. • Base: ▫ Negatively charged ion that can combine with H+ . ▫ Proton acceptor.
  • 28. pH • pH = log _1__ [H+ ] • Normal pH blood = 7.35 - 7.45. • Buffer: ▫ System of molecules and ions that act to prevent changes in [H+ ].
  • 29. Organic Molecules • Molecules that contain carbon and hydrogen. • Carbon has 4 electrons in outer orbital. • Carbon covalently bonds to fill its outer orbital with 8 electrons.
  • 30. Organic Molecules • Organic Chemistry: deals with molecules that contain carbon • More than 5 million organic compounds have been identified • The carbon atom can form bonds with a greater number of different elements than any other type of atom
  • 31.
  • 32. Functional Groups • Inactive “backbone” to which more reactive atoms are attached.
  • 33. Classes According to Functional Groups • Ketone and aldehyde: carbonyl group • Organic acid: carboxyl group • Alcohol: hydroxyl group
  • 34. Stereoisomers • Exactly the same atoms arranged in same sequence. • Differ in spatial orientation of a functional group. ▫ D-isomers: right-handed ▫ L-isomers: left-handed • Enzymes of all cells can combine only with the L-amino acids and D-sugars.
  • 35. Four main classes of Organic molecules • Lipids • Carbohydrates • Proteins • Nucleic Acids
  • 36. Lipids • GR: Lipos=Fat • Diverse group of molecules. • Insoluble in polar solvents (H20). • Hydrophobic (nonpolar) • Consist primarily of hydrocarbon chains and rings.
  • 37. Lipids • Hydrocarbons • Fatty acids • Triglycerides • Ketone Bodies • Phospholipids • Steroids • Prostaglandins
  • 38. Hydrocarbons • Includes oils and gases • Carbons can be single bonds (saturated) • Carbons can be double bonded (unsaturated)
  • 39. Fatty acids • Nonpolar hydrocarbon chain ▫ Can be saturated (are stright) ▫ Can be unsaturated (bend at the double bond) ▫ Can be poly unsaturated (multiple bends) • Carboxyl group on one end • Large group
  • 40.
  • 41. Triglycerides • Formed by condensation of glycerol and 3 fatty acids. ▫ Ester bond • Fatty acid consists of hydrocarbon chain with carboxylic acid end. ▫ May be saturated or unsaturated ▫ Saturated fats:  Mostly animal sources  Mostly solid at room temperature ▫ Unsaturated fats  Mostly plant sources  Mostly liquid at room temperature
  • 42.
  • 43. Nutritional considerations of triglycerides • Also called fat or neutral fat • Stored in adipose cells • Total fat intake should be about 30% of total energy intake ▫ Saturated fat >10% • Saturated fats are implicated in heart disease and stroke ▫ Data suggests they promote high blood cholesterol
  • 44. Phospholipids • A number of categories • All contain a phosphate group • Most common ▫ Glycerol (3 carbons) ▫ Fatty Acids on carbon 1 and 2 ▫ Phosphate group attached to carbon (and other polar groups eg.: choline)
  • 46. Phospholipid • Are amphipathic: contain both polar and nonpolar domains ▫ Head:  contains polar groups  Hydrophilic ▫ Tail:  Contains fatty acids (nonpolar)  Hydrophobic
  • 47. Phospholipids • Major component of cell membranes ▫ Hydrophylic heads orient to water ▫ Hydrophobic tails orient to each other • Kind of phospholipid varies based on cell or organelle
  • 49. Ketone Bodies • Results from the hydrolysis of triglycerides by adipocytes ▫ Liberates free FA into blood ▫ FA function as an acid in blood • Most FA used as energy source by some tissues • If not, converted by liver into Ketone bodies
  • 51. Ketone Bodies • Produced in the rapid breakdown of FA ▫ Low-carbohydrate diets ▫ Uncontrolled Diabetes mellitus • Ketosis: Elevated level of FA in blood • Ketoacidosis: ketosis is high enough to lower blood ph
  • 52. Steroids • Nonpolar and insoluble in H20. • All have cholesterol as precursor.
  • 53. Prostaglandins • Prostaglandins: ▫ Fatty acid with cyclic hydrocarbon group. ▫ Derived from arachidonic acid.
  • 55. Carbohydrates • Organic molecules that contain carbon, hydrogen and oxygen. • CH20 • General formula: ▫ CnH2nOn • -ose denotes a sugar molecule
  • 56. Carbohydrates • Supply energy ▫ Glucose ▫ Complex carbohydrates • Provide structural support ▫ cellulose • Part of plasma membrane • Monomer: monosaccarides
  • 57. Carbohydrates • Monosaccharide: the “simple sugars” ▫ Pentoses (5-carbons):  Ribose: in RNA  Deoxyribose: in DNA ▫ Hexoses (6-carbons):structural isomers  Glucose, fructose and galactose  Characteristics  Soluable  Sweet  Alcoholic fermentation
  • 58. Glucose • Also called : ▫ Dextrose ▫ Transportable in the blood  Blood glucose ▫ C6H12O6
  • 59.
  • 62. Carbohydrates • Disaccharide: ▫ 2 monosaccharides joined covalently.  Sucrose  Glucose and fructose  Maltose  Glucose and glucose  Lactose  Glucose and galactose
  • 63. Disaccharides • Characteristics ▫ Sweet ▫ Soluable ▫ Can be fermented • Formation: called condensation ▫ Requires an enzyme ▫ Removal of molecule of water ▫ Also called dehydration synthesis ▫ Formation of a covalent bond
  • 65. Hydrolysis • Reverse of dehydration synthesis. • Digestion reaction. • H20 molecule split.
  • 66. Carbohydrates • Polysaccharides: ▫ Many monosaccharides joined covalently. ▫ General formula: (C6H10O5)n ▫ Characteristics:  Devoid of taste  Do not form solutions  Iodine test  Iodine +starch+blue
  • 67. Polysaccarides• Kinds: ▫ Starch  Glucose subunits  branched ▫ Dextrins ▫ Glycogen (animal starch)  Glucose subunits  Branched ▫ Cellulose  Glucose subunits  Long, unbranched chains
  • 68. Proteins • General Information: ▫ GR: proteios=first rank ▫ ~50% of the organic material of the body ▫ Functions  Structural:  Cell structures, CTs  Functional:  Enzymes, hormones, Hb, etc!
  • 69. Proteins• Protein Structure ▫ Large molecules (polymers) composed of amino acid sub-units (monomers). ▫ Amino Acid structure  amino group (NH2)  carboxylic acid group (COOH)  Radical group (R): functional group  H
  • 70.
  • 71. Proteins • 20 different standard amino acids. ▫ Based on the properties of the functional group ▫ E.g.:
  • 72. Proteins • Dehydration synthesis: ▫ Amino end of one amino acid combines with hydroxyl group of carboxylic end of another amino acid. • Peptide bond: ▫ Bond between two adjacent amino acids.
  • 74. Proteins• Dipeptide: 2 amino acids • Tripeptide: 3 amino acids • Polypeptide: many amino acids ▫ Number of amino acids varies ▫ Up to 100 aa • Protein ▫ Over 100aa ▫ Great variety!
  • 75. Protein structure • Four structural levels ▫ Primary structure  Based on amino acid sequence  Amino acid sequence determined by DNA ▫ Secondary structure  Based on hydrogen bonding between close aa ▫ Tertiery structure  3-D shape ▫ Quaternary structure  Only in proteins with 2 or more polypeptide chains
  • 76.
  • 77. Secondary structure (2o ) • Based on the primary structure • Weak hydrogen bonds form between hydrogen and oxygen of a different amino acid. • Two main kinds of secondary structure: ▫ Alpha helix: Bond cause chain to twist in a helix. ▫ Beta pleated sheet: interactions between lengths of the polypeptide chain
  • 79. Tertitary structure • Polypeptide chains bend and fold. ▫ Based on interactions with aa in different parts of the polypeptide chain  disulfide bonds: covalent  Hydrogen bonds: weak • Produce 3 -dimensional shapes. • Chemical interaction of each protein produces own characteristic tertiary structure • Denaturing protein ▫ Irreversible disruption of tertiary structure
  • 80. Bonds responsible for 3o structure
  • 82. Quaternary Structure • Number of polypeptide chains covalently linked together. • Insulin, hemoglobin
  • 83. Conjugated proteins • Protein combined with another type of molecule • Glycoproteins: carbohydrate with protein ▫ Membranes, hormone • Lipoproteins: Lipid and protein ▫ Membranes, blood plasma • Hemoproteins: iron and protein ▫ Hemoglobin, cytochromes
  • 84. Nucleic Acids • Include the macromolecules: ▫ DNA: deoxyribonucleic acid ▫ RNA: ribonucleic acid • Involved in heredity and genetic regulation • Are polymers: ▫ Monomeric subunit:nucleotides ▫ Bonded together in a dehydration synthesis reaction
  • 86. Nucleotides• Structure of a nucleotide: 3 subunits ▫ Pentose sugar ▫ Phosphate group ▫ Nitrogenous base  Purines: two rings  Guanine  Adenine  Pyrimidines: one ring  Cytosine  Thymine  Uricil
  • 89. DNA • Huge molecules with simple structure • Big time data storage! • Structure ▫ Nucleotides  Pentose sugar: Deoxyribose  Bases:  Purines: G and A  Pyrimidines: C and T ▫ Form double-stranded helix
  • 90. DNA • Nucleotide strands: 2 ▫ Sugar-phosphate backbone ▫ Bases stick out ▫ Bases bond to each other • Base pairing: ▫ A – T ▫ G – C ▫ Called law of complementary base pairing
  • 92. DNA
  • 93. RNA • Means by which DNA directs cellular activities • Structure ▫ Pentose sugar: ribose ▫ Bases: uracil (not thymine) ▫ Single stranded • Three main types ▫ Messenger RNA (mRNA) ▫ Transfer RNA (tRNA) ▫ Ribosomal RNA (rRNA)