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Microbiology: A
nd
Systems Approach, 2
ed.
Chapter 2: The Chemistry of
Biology
2.1 Atoms, Bonds, and Molecules:
Fundamental Building Blocks
Matter: anything that occupies space and
has mass
 Can be liquid, solid, or gaseous state
 Building blocks of matter- atoms








Subatomic particles of atoms- protons (p+),
neutrons (n0), and electrons (e-)
Protons and neutrons make up the nucleus,
electrons surround the nucleus
Held together by the attraction of positive protons
to negative electrons
Figure 2.1
Different Types of Atoms: Elements
and Their Properties
 Different numbers of protons, neutrons,

and electrons in atoms create different
elements
 Each element has a characteristic atomic
structure and predictable chemical
behavior
 Each assigned a distinctive name with an
abbreviated shorthand symbol
The Major Elements of Life and Their
Primary Characteristics
 Isotopes- variant forms of the same

element that differ in the number of
neutrons
 Radioactive isotopes used in research and
medical applications and in dating fossils
and ancient materials
 Electron orbitals and shells
Electron Orbitals and Shells








An atom can be envisioned as a central nucleus
surrounded by a “cloud” of electrons
Electrons rotate about the nucleus in pathways
called orbitals- volumes of space in which an
electron is likely to be found
Electrons occupy energy shells, from lower-energy
to higher-energy as they move away from the
nucleus
Electrons fill the orbitals and shells in pairs starting
with the shell nearest the nucleus
Each element, then, has a unuiqe pattern of
orbitals and shells
Figure 2.2
Bonds and Molecules







Most elements do not exist naturally in pure form
Molecule- the smallest particle of matter that can have
independent existence; a distinct chemical substance
that results from one atom of a noble gas (Ne) or the
combination of two or more atoms (can be two atoms
of the same element, such as O2).
Compounds- are combinations of two or more
different elements joined by chemical bonds.
Chemical Bonds- When two or more atoms share,
donate, or accept electrons
Types of bonds formed and to which atoms and
element bonds are determined by the atom’s valence
Figure 2.3
Covalent Bonds and Polarity:
Molecules with Shared Electrons
 Covalent bonds- between atoms that

share electrons (such as H2).
 The majority of molecules associated with

living things are composed of single and
double covalent bonds between C, H, O,
N, S, and P.
Figure 2.4
Polar vs. Nonpolar Molecules
 Some covalent bonds result in a

polar
molecule- an unequal distribution of
charge (ex. H2O).


Polarity is a significant property of many large
molecules, influencing both reactivity and
structure.

 An electrically neutral molecule is

nonpolar
 Van der Waals forces- weak attractions
between molecules with low levels of
polarity
Figure 2.5
Ionic Bonds: Electron Transfer Among
Atoms
•







Electrons transferred completely from one atom
to another, without sharing, results in an ionic
bond (ex. NaCl)
Crystals with ionic bonds, when dissolved in a
solvent, can separate in to charged particles
called ions in a process called ionization
Cations- positively charged ions
Anions- negatively charged ions
These ionic molecules that dissolve to form ions
are called electrolytes
Figure 2.6
Figure 2.7
Hydrogen Bonding
• Weak bond between
a H covalently
bonded to one
molecule and an O or
N atom on the same
or different molecule
(such as between
water molecules)

Figure 2.8
Chemical Shorthand: Formulas,
Models, and Equations
 Molecular formula- gives atomic symbols

and the number of atoms of the elements
involved in subscript (H2o, C6H12O6).
 Molecular formulas might not be unique

(glucose, galactose, and fructose, for
example)
 Structural formulas illustrate the
relationships of the atoms and the number
and types of bonds
Figure 2.9
Chemical Equations
 Equations are used to illustrate chemical

reactions



Reactants- Molecules entering the reaction
Products- the substances left by a reaction
Types of Reactions


Synthesis: reactants bond together to form
an entirely new molecule






A + B  AB
S + O2  SO2
2H2 + O2  2H2O (note that equations must be
balanced)

Decomposition: bonds on a single reactant
molecule are permanently broken to release
two or more product molecules



AB  A + B
2H2O2  2H2O + O2
Types of Reactions:
 Exchange: The reactants trade places
between each other and release products
that are combinations of the two


AB + XY

AX + BY (reversible reaction)
CATALYSTS
 Catalysts- increase the rate of the

reaction
 Catalysts lower the energy required to get
reactions started
 Enzymes are biological catalysts
 Most enzymes are proteins, but other
substances, e.g. RNA can occasionally
serve as enzymes
Solutions: Homogeneous Mixtures of
Molecules
Solution- a mixture of one or more solutes
uniformly dispersed in a solvent
 The solute cannot be separated by filtration or
settling
 The rule of solubility- “like dissolves like”
 Water- the most common solvent in natural
systems because of its special characteristics







Hydrophilic molecules- attract water to their surface
(polar)
Hydrophobic molecules- repel water (nonpolar)
Amphipathic molecules- have both hydrophilic and
hydrophobic properties
Concentration of Solutions
 Concentration- the amount of solute

dissolved in a certain amount of solvent


In biological solutions, commonly expressed
as molar concentration or molarity (M)
• One mole dissolved in 1 L
• One mole is the molecular weight of the compound
in grams
Figure 2.11
Acidity, Alkalinity, and the pH
Scale
Acidic solutions- when a component
dissolved in water (acid) releases excess
hydrogen ions (H+)
 Basic solutions- when a component releases
excess hydroxide ions (OH-)
 pH scale- measures the acid and base
concentrations of solutions






Ranges from 0 (most acidic) to 14 (most basic); 7
is neutral
pH = -log[H+]
Figure 2.12
Chap 2 micro bio lecture
Neutralization Reactions
 Neutralization

reactions- occur in
aqueous solutions containing both acids
and bases
 Give rise to water and other neutral byproducts
 HCl + NaOH  H2O + NaCl
The Chemistry of Carbon and Organic
Compounds
 Inorganic chemicals- usually do not

contain both C and H (ex. NaCl, CaCO 3)
 Organic chemicals- Carbon compounds

with a basic framework of the element
carbon bonded to other atoms


Most of the chemical reactions and structures
of living things involve organic chemicals
Carbon- the Fundamental Element of
Life
 Valence makes it an ideal atomic building

block
 Forms stable chains containing thousands
of C atoms, with bonding sites available
 Can form linear, branched, or ringed
chains
 Can form single, double, or triple bonds
 Most often associates with H, O, N, S, and
P
Figure 2.13
Functional Groups of Organic
Compounds
Special molecular groups or accessory
molecules that bind to organic compoundsfunctional groups
 Help define the chemical class of certain
groups of organic compounds
 Give organic compounds unique reactive
properties




Reactions of an organic compound can be
predicted by knowing the kind of functional group
or groups it carries
Chap 2 micro bio lecture
2.2 Macromolecules: Superstructures
of Life
Biochemistry- study of the compounds of life
 Biochemicals- organic compounds produced
by (or components of) living things







Four main families- carbohydrates, lipids,
proteins, and nucleic acids
Often very large, called macromolecules
All macromolecules except for lipids are formed
by polymerization
• Repeating subunits (monomers) are bound in to
chains of various lengths (polymers)
Carbohydrates
 Carbohydrates:

Sugars and

Polysaccharides


Most can be represented by the general
formula (CH2O)n, where n = the number of
units of this combination of atoms
Figure 2.14
Carbohydrates


Exist in a variety of configurations








Sugar (saccharide)- a simple carbohydrate with a
sweet taste
Monosaccharide contains 3-7 carbons
Disaccharide contains two monosaccharides
Polysaccharide contains five or more
monosaccharides

Monosaccharides and disaccharides are specified
by combining a prefix that describes a
characteristic of the sugar with the suffix –ose




Hexoses- six carbons
Pentoses- five carbons
Fructose- for fruit
The Nature of Carbohydrate
Bonds

Figure 2.15
The Functions of
Polysacharides




Structural support and
protection
Serve as nutrient and
energy stores
Cell walls in plants
and many
microscopic algae
from cellulose
Figure 2.16a
Other Important
Polysaccharides


Include agar,
peptidoglycan,
chitin,
lipopolysaccharide,
glycocalyx, and
glycogen

Figure 2.16b
Lipids: Fats, Phospholipids, and
Waxes
 Lipids- a variety of substances that are

not soluble in polar substances
 Will dissolve in nonpolar solvents
 Main groups of lipids


Triglycerides-a single molecule of glycerol
bound to three fatty acids
• Includes fats and oils
Figure 2.17
Phospholipids


PhospholipidsContain two fatty
acids attached to the
glycerol with a
phosphate group on
the third glycerol
binding site


Important membrane
molecules

Figure 2.18
Miscellaneous Lipids
 Steroids- complex ringed compounds

commonly found in cell membranes and
animal hormones


Best known- cholesterol

• Waxes- esters formed between a longchain alcohol and a saturated fatty acid
Figure 2.19
Proteins: Shapers of Life
 Predominant organic molecules
 Building blocks




amino acids

20 different naturally occurring forms
Basic skeleton- a carbon (the α carbon) linked
to an amino group (NH2), a carboxyl group
(COOH), a hydrogen atom (H), and a variable
R group
Peptide bond forms between the amino
group on one amino acid and the carboxyl
group on another.
Chap 2 micro bio lecture
Figure 2.20
Protein Structure and Diversity
Primary (1°) structure- the type, number, and
order of amino acids in the chain
 Secondary (2°) structure- when various
functional groups exposed on the outer surface of
the molecule interact by forming hydrogen bonds





Coiled configuration- α helix
Accordion pattern- β-pleated sheet

Tertiary (3°) structure- created by additional
bonds between functional groups
 Quarternary (4°) structure- more than one
polypeptide forms a large, multiunit protein

Figure 2.21
Protein Shape
 Each different type of protein develops a

unique shape, so it can only react with
molecules that fit its particular surface
features





Ex. enzymes and antibodies
Native state- the functional three-dimensional
form of a protein
Denatured- when the protein’s native state
has been disrupted
The Nucleic Acids: A Cell Computer
and Its Programs
DNA- specially coded genetic program
 DNA transfers its program to RNA
 Both are polymers of repeating units called nucleotides






Nucleotides- composed of three smaller units: a nitrogen base,
a pentose sugar, and a phosphate.
The nitrogen base can be one of two forms- a purine (two rings)
or a pyrimidine (one ring)
•
•
•
•

Two types of purines: adenine (A) and guanine (G)
Three types of pyrimidines: thymine (T), cytosine (C), and uracil (U)
DNA contains all of the nitrogen bases except uracil
RNA contains all of the nitrogen bases except thymine

The nitrogen base is covalently bonded to ribose in RNA and
deoxyribose in DNA
 Phosphate (PO43-) covalently bonds the sugars in series

Figure 2.22
Figure 2.23
The Double Helix of DNA
 Formed by two long polynucleotide

strands
 Linked along their length by hydrogen
bonds between complimentary pairs of
nitrogen bases



Adenine pairs with thymine
Cytosine pairs with guanine
Figure 2.24
RNA: Organizers of Protein Synthesis
Also consists of a long chain of nucleotides
 It is single stranded and contains ribose instead of
deoxyribose anduracil instead of thymine
 Several functional types of RNA formed using the
DNA template








Messenger RNA (mRNA)- a copy of a gene that
provides the order and type of amino acids in a
protein
Transfer RNA (tRNA)- a carrier that delivers the
correct amino acids for protein assembly
Ribosomal RNA (rRNA)- a major component of
ribosomes
ATP: The Energy Molecule of
Cells








Adenosine triphosphate (ATP)- a nucleotide
containing adenine, ribose, and three phosphates
High-energy compound that gives off energy when
the bond is broken between the outermost
phosphates
Releases and stores energy for cellular chemical
reactions
When the terminal phosphate bond is broken to
release energy, adenosine diphosphate (ADP) is
formed
ADP can be converted back to ATP when the third
phosphate is restored.
Figure 2.25
2.3 Cells: Where Chemicals Come to
Life
 The fundamental unit of life-

cell
 Fundamental characteristics of cells







Tend to be spherical, polygonal, cubical, or
cylindrical
Their protoplasm is encased in a cell or
cytoplasmic membrane
Chromosomes containing DNA
Ribosomes for protein synthesis
Eukaryotic and Prokaryotic
Cells
 Eukaryotic cells



Found in animals, plants, fungi, and protists
Contain organelles that perform cell functions
(such as the nucleus, Golgi apparatus,
endoplasmic reticulum, vacuoles, and
mitochondria)

 Prokaryotic cells



Only found n bacteria and archae
No nucleus or other organelles

 Cell

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Chap 2 micro bio lecture

  • 1. Microbiology: A nd Systems Approach, 2 ed. Chapter 2: The Chemistry of Biology
  • 2. 2.1 Atoms, Bonds, and Molecules: Fundamental Building Blocks Matter: anything that occupies space and has mass  Can be liquid, solid, or gaseous state  Building blocks of matter- atoms     Subatomic particles of atoms- protons (p+), neutrons (n0), and electrons (e-) Protons and neutrons make up the nucleus, electrons surround the nucleus Held together by the attraction of positive protons to negative electrons
  • 4. Different Types of Atoms: Elements and Their Properties  Different numbers of protons, neutrons, and electrons in atoms create different elements  Each element has a characteristic atomic structure and predictable chemical behavior  Each assigned a distinctive name with an abbreviated shorthand symbol
  • 5. The Major Elements of Life and Their Primary Characteristics  Isotopes- variant forms of the same element that differ in the number of neutrons  Radioactive isotopes used in research and medical applications and in dating fossils and ancient materials  Electron orbitals and shells
  • 6. Electron Orbitals and Shells      An atom can be envisioned as a central nucleus surrounded by a “cloud” of electrons Electrons rotate about the nucleus in pathways called orbitals- volumes of space in which an electron is likely to be found Electrons occupy energy shells, from lower-energy to higher-energy as they move away from the nucleus Electrons fill the orbitals and shells in pairs starting with the shell nearest the nucleus Each element, then, has a unuiqe pattern of orbitals and shells
  • 8. Bonds and Molecules      Most elements do not exist naturally in pure form Molecule- the smallest particle of matter that can have independent existence; a distinct chemical substance that results from one atom of a noble gas (Ne) or the combination of two or more atoms (can be two atoms of the same element, such as O2). Compounds- are combinations of two or more different elements joined by chemical bonds. Chemical Bonds- When two or more atoms share, donate, or accept electrons Types of bonds formed and to which atoms and element bonds are determined by the atom’s valence
  • 10. Covalent Bonds and Polarity: Molecules with Shared Electrons  Covalent bonds- between atoms that share electrons (such as H2).  The majority of molecules associated with living things are composed of single and double covalent bonds between C, H, O, N, S, and P.
  • 12. Polar vs. Nonpolar Molecules  Some covalent bonds result in a polar molecule- an unequal distribution of charge (ex. H2O).  Polarity is a significant property of many large molecules, influencing both reactivity and structure.  An electrically neutral molecule is nonpolar  Van der Waals forces- weak attractions between molecules with low levels of polarity
  • 14. Ionic Bonds: Electron Transfer Among Atoms •     Electrons transferred completely from one atom to another, without sharing, results in an ionic bond (ex. NaCl) Crystals with ionic bonds, when dissolved in a solvent, can separate in to charged particles called ions in a process called ionization Cations- positively charged ions Anions- negatively charged ions These ionic molecules that dissolve to form ions are called electrolytes
  • 17. Hydrogen Bonding • Weak bond between a H covalently bonded to one molecule and an O or N atom on the same or different molecule (such as between water molecules) Figure 2.8
  • 18. Chemical Shorthand: Formulas, Models, and Equations  Molecular formula- gives atomic symbols and the number of atoms of the elements involved in subscript (H2o, C6H12O6).  Molecular formulas might not be unique (glucose, galactose, and fructose, for example)  Structural formulas illustrate the relationships of the atoms and the number and types of bonds
  • 20. Chemical Equations  Equations are used to illustrate chemical reactions   Reactants- Molecules entering the reaction Products- the substances left by a reaction
  • 21. Types of Reactions  Synthesis: reactants bond together to form an entirely new molecule     A + B  AB S + O2  SO2 2H2 + O2  2H2O (note that equations must be balanced) Decomposition: bonds on a single reactant molecule are permanently broken to release two or more product molecules   AB  A + B 2H2O2  2H2O + O2
  • 22. Types of Reactions:  Exchange: The reactants trade places between each other and release products that are combinations of the two  AB + XY AX + BY (reversible reaction)
  • 23. CATALYSTS  Catalysts- increase the rate of the reaction  Catalysts lower the energy required to get reactions started  Enzymes are biological catalysts  Most enzymes are proteins, but other substances, e.g. RNA can occasionally serve as enzymes
  • 24. Solutions: Homogeneous Mixtures of Molecules Solution- a mixture of one or more solutes uniformly dispersed in a solvent  The solute cannot be separated by filtration or settling  The rule of solubility- “like dissolves like”  Water- the most common solvent in natural systems because of its special characteristics     Hydrophilic molecules- attract water to their surface (polar) Hydrophobic molecules- repel water (nonpolar) Amphipathic molecules- have both hydrophilic and hydrophobic properties
  • 25. Concentration of Solutions  Concentration- the amount of solute dissolved in a certain amount of solvent  In biological solutions, commonly expressed as molar concentration or molarity (M) • One mole dissolved in 1 L • One mole is the molecular weight of the compound in grams
  • 27. Acidity, Alkalinity, and the pH Scale Acidic solutions- when a component dissolved in water (acid) releases excess hydrogen ions (H+)  Basic solutions- when a component releases excess hydroxide ions (OH-)  pH scale- measures the acid and base concentrations of solutions    Ranges from 0 (most acidic) to 14 (most basic); 7 is neutral pH = -log[H+]
  • 30. Neutralization Reactions  Neutralization reactions- occur in aqueous solutions containing both acids and bases  Give rise to water and other neutral byproducts  HCl + NaOH  H2O + NaCl
  • 31. The Chemistry of Carbon and Organic Compounds  Inorganic chemicals- usually do not contain both C and H (ex. NaCl, CaCO 3)  Organic chemicals- Carbon compounds with a basic framework of the element carbon bonded to other atoms  Most of the chemical reactions and structures of living things involve organic chemicals
  • 32. Carbon- the Fundamental Element of Life  Valence makes it an ideal atomic building block  Forms stable chains containing thousands of C atoms, with bonding sites available  Can form linear, branched, or ringed chains  Can form single, double, or triple bonds  Most often associates with H, O, N, S, and P
  • 34. Functional Groups of Organic Compounds Special molecular groups or accessory molecules that bind to organic compoundsfunctional groups  Help define the chemical class of certain groups of organic compounds  Give organic compounds unique reactive properties   Reactions of an organic compound can be predicted by knowing the kind of functional group or groups it carries
  • 36. 2.2 Macromolecules: Superstructures of Life Biochemistry- study of the compounds of life  Biochemicals- organic compounds produced by (or components of) living things     Four main families- carbohydrates, lipids, proteins, and nucleic acids Often very large, called macromolecules All macromolecules except for lipids are formed by polymerization • Repeating subunits (monomers) are bound in to chains of various lengths (polymers)
  • 37. Carbohydrates  Carbohydrates: Sugars and Polysaccharides  Most can be represented by the general formula (CH2O)n, where n = the number of units of this combination of atoms
  • 39. Carbohydrates  Exist in a variety of configurations      Sugar (saccharide)- a simple carbohydrate with a sweet taste Monosaccharide contains 3-7 carbons Disaccharide contains two monosaccharides Polysaccharide contains five or more monosaccharides Monosaccharides and disaccharides are specified by combining a prefix that describes a characteristic of the sugar with the suffix –ose    Hexoses- six carbons Pentoses- five carbons Fructose- for fruit
  • 40. The Nature of Carbohydrate Bonds Figure 2.15
  • 41. The Functions of Polysacharides    Structural support and protection Serve as nutrient and energy stores Cell walls in plants and many microscopic algae from cellulose Figure 2.16a
  • 43. Lipids: Fats, Phospholipids, and Waxes  Lipids- a variety of substances that are not soluble in polar substances  Will dissolve in nonpolar solvents  Main groups of lipids  Triglycerides-a single molecule of glycerol bound to three fatty acids • Includes fats and oils
  • 45. Phospholipids  PhospholipidsContain two fatty acids attached to the glycerol with a phosphate group on the third glycerol binding site  Important membrane molecules Figure 2.18
  • 46. Miscellaneous Lipids  Steroids- complex ringed compounds commonly found in cell membranes and animal hormones  Best known- cholesterol • Waxes- esters formed between a longchain alcohol and a saturated fatty acid
  • 48. Proteins: Shapers of Life  Predominant organic molecules  Building blocks   amino acids 20 different naturally occurring forms Basic skeleton- a carbon (the α carbon) linked to an amino group (NH2), a carboxyl group (COOH), a hydrogen atom (H), and a variable R group Peptide bond forms between the amino group on one amino acid and the carboxyl group on another.
  • 51. Protein Structure and Diversity Primary (1°) structure- the type, number, and order of amino acids in the chain  Secondary (2°) structure- when various functional groups exposed on the outer surface of the molecule interact by forming hydrogen bonds    Coiled configuration- α helix Accordion pattern- β-pleated sheet Tertiary (3°) structure- created by additional bonds between functional groups  Quarternary (4°) structure- more than one polypeptide forms a large, multiunit protein 
  • 53. Protein Shape  Each different type of protein develops a unique shape, so it can only react with molecules that fit its particular surface features    Ex. enzymes and antibodies Native state- the functional three-dimensional form of a protein Denatured- when the protein’s native state has been disrupted
  • 54. The Nucleic Acids: A Cell Computer and Its Programs DNA- specially coded genetic program  DNA transfers its program to RNA  Both are polymers of repeating units called nucleotides    Nucleotides- composed of three smaller units: a nitrogen base, a pentose sugar, and a phosphate. The nitrogen base can be one of two forms- a purine (two rings) or a pyrimidine (one ring) • • • • Two types of purines: adenine (A) and guanine (G) Three types of pyrimidines: thymine (T), cytosine (C), and uracil (U) DNA contains all of the nitrogen bases except uracil RNA contains all of the nitrogen bases except thymine The nitrogen base is covalently bonded to ribose in RNA and deoxyribose in DNA  Phosphate (PO43-) covalently bonds the sugars in series 
  • 57. The Double Helix of DNA  Formed by two long polynucleotide strands  Linked along their length by hydrogen bonds between complimentary pairs of nitrogen bases   Adenine pairs with thymine Cytosine pairs with guanine
  • 59. RNA: Organizers of Protein Synthesis Also consists of a long chain of nucleotides  It is single stranded and contains ribose instead of deoxyribose anduracil instead of thymine  Several functional types of RNA formed using the DNA template     Messenger RNA (mRNA)- a copy of a gene that provides the order and type of amino acids in a protein Transfer RNA (tRNA)- a carrier that delivers the correct amino acids for protein assembly Ribosomal RNA (rRNA)- a major component of ribosomes
  • 60. ATP: The Energy Molecule of Cells      Adenosine triphosphate (ATP)- a nucleotide containing adenine, ribose, and three phosphates High-energy compound that gives off energy when the bond is broken between the outermost phosphates Releases and stores energy for cellular chemical reactions When the terminal phosphate bond is broken to release energy, adenosine diphosphate (ADP) is formed ADP can be converted back to ATP when the third phosphate is restored.
  • 62. 2.3 Cells: Where Chemicals Come to Life  The fundamental unit of life- cell  Fundamental characteristics of cells     Tend to be spherical, polygonal, cubical, or cylindrical Their protoplasm is encased in a cell or cytoplasmic membrane Chromosomes containing DNA Ribosomes for protein synthesis
  • 63. Eukaryotic and Prokaryotic Cells  Eukaryotic cells   Found in animals, plants, fungi, and protists Contain organelles that perform cell functions (such as the nucleus, Golgi apparatus, endoplasmic reticulum, vacuoles, and mitochondria)  Prokaryotic cells   Only found n bacteria and archae No nucleus or other organelles  Cell