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HBC1011 Biochemistry I
Trimester I, 2018/2019
Lecture 4-5: Biochemistry of Water
Ng Chong Han, PhD
MNAR1010, 06-2523751
chng@mmu.edu.my
Overview
• Water, the Biological Solvent
• Hydrogen Bonding and Solubility
• Cellular Reactions of Water
• Buffer Systems
2
• Water covers about 70% of the Earth’s surface
and makes up 45-95% of living organisms
3
Water = molecule of life
One of NASA‘s guiding policies in the search for alien life is to “follow the
water”. Water is fairly common in the universe, but most of this water is in
the form of ice. Solid water can't act as a lubricant for the molecular
processes of life, so the search is for liquid water - a commodity that is far
more rare in the universe.
4
5
NASA Mars
Exploration
Programme
Curiosity and
Water on Mars
6
Water in our bodies
Approximately 55% of blood is plasma
Plasma is mainly composed of:
90% of WATER
10%: blood proteins,
inorganic
ions,
glucose,
lipids,
amino acids,
hormones,
metabolic end products….
Each of us has 5-6 liters of blood
7
Biological roles of water
Water is a biological solvent
eg. Biological fluids for delivery of nutrients and removal of
wastes
Water serves as an essential buffer
to regulate temperature (high specific heat capacity) and pH
(buffer solutions)
Water is a participant in many biochemical reactions
eg. the principal reactant in the photosynthesis process
Physical and chemical properties of
water
8
• Chemical formula H2O: one molecule of
water has two hydrogen atoms
covalently bonded to a single oxygen
atom.
• Water appears in nature in all three
common states of matter (solid, liquid,
and gas)
• Liquid at standard temperature and
pressure, tasteless and odorless.
• The intrinsic colour of water and ice is a
very slight blue hue, although both appear
colorless in small quantities.
• Polarity: a separation of electric charge leading to its chemical
groups having an electric dipole or multipole moment.
• Polar molecules interact through dipole–dipole intermolecular
forces and hydrogen bonds. Molecular polarity is dependent on
the difference in electronegativity (a pull on the electrons)
between atoms in a compound.
• Polarity affects physical properties eg. surface tension, solubility,
and melting and boiling-points.
9
Polar Molecules
The two charges are present with a negative
charge in the middle (red shade), and a
positive charge at the ends (blue shade).
• The polarity of chemical bonds: Non-polar bonds, Polar
bonds, Ionic bonds
• Bonds can fall between one of two extremes — being
completely nonpolar or completely polar.
– A completely nonpolar bond occurs when the
electronegativities are identical.
– A completely polar bond is more correctly called an ionic
bond.
• The terms "polar" and "nonpolar" are usually applied
to covalent bonds, that is, bonds where the polarity is
not complete.
• While the molecules can be described as "polar
covalent", "nonpolar covalent", or "ionic", this is often a
relative term.
10
Polar Molecules
11
Covalent Ionic
Nonpolar Polar
Sharing of
electrons
Equal Unequal Transferred
Dipole movement No Partial Positive or
negative
Electronegativity <0.5 0.5-1.7 >1.7
Interactions Two
identical
nonmetals
Two different
nonmetals
Metal +
nonmetal
Comparison between nonpolar covalent,
polar covalent and ionic bonds
Dipole moment describes the charge separation in a molecule. The larger the
difference in electronegativities of bonded atoms, the larger the dipole moment. For
example, NaCl has the highest dipole moment because it has an ionic bond
13
Covalent and Noncovalent bonds
• Covalent bond: a chemical bond that involves the sharing of electron
pairs between atoms.
• Noncovalent bond: it does not involve the sharing of electrons, but
rather involves more dispersed variations of electromagnetic
interactions between molecules or within a molecule, eg ionic bond.
Covalent bonds
14
• If the two atoms have about equal attraction for electrons, a
nonpolar covalent bond (equal sharing) forms
• If the two atoms have different electronegativities, a polar
covalent bond (unequal sharing) forms
In polar bonds, one atom is slightly negative (δ-), while the
other is slightly positive (δ+)
• Electronegativity is a chemical property that describes the
tendency of an atom or a functional group to attract electrons
towards itself.
15
Noncovalent bonds
• Noncovalent bonds are important for
determining the structure of biomolecules.
• Types of noncovalent bonds or interactions
include:
– Hydrogen bonds
– Ionic bonds
– van der Waals forces
– Hydrophobic interactions
Noncovalent bonds
16
• Hydrogen bonds occur when a hydrogen atom (δ+) is
attracted by a negatively charged atom (δ-)
• Hydrogen bonds are weak (10% as strong as covalent).
Noncovalent bonds
17
• Ionic bonds are attractions between oppositely charged
atoms:
+  - for example, Na+ Cl-
• Positively charged atoms
are called cations,
always move to the
cathode.
• Negatively charged
atoms are called anions,
always move to the
anode.
Noncovalent bonds
18
Noncovalent bonds
19
• Hydrophilic molecules are ones that interact with water. These
molecules are polar: charged (+, -) or partially charged (δ+,δ-)
• Hydrophobic molecules do not interact with water, like oils and
fats. These molecules are nonpolar. These often have C’s and
H’s, but few or no O’s and N’s.
20
Noncovalent bonds
• Hydrophobic molecules tend to avoid water, hence
tend to bond together. This is called hydrophobic
interactions
• Very weak interactions between nonpolar molecules
that are tightly packed together are called van der
Waals forces
• Although these noncovalent interactions are
individually weak relative to covalent bonds, the
cumulative effect of many such interactions can be very
significant.
21
22
Water: Polar Molecules
• Since the water molecule is not
linear and the oxygen atom has a
higher electronegativity than
hydrogen atoms, the oxygen atom
carries a slight negative charge,
whereas the hydrogen atoms are
slightly positive.
• As a result, water is a polar
molecule with an electrical dipole
moment.
23
Water: Polar Molecules
• Water also can form an
unusually large number of
intermolecular hydrogen
bonds (four) for a molecule of
its size.
• These factors lead to strong
attractive forces between
molecules of water, giving rise
to water's high surface
tension and capillary forces.
POLES help to initiate…
HYDROGEN BONDING between
molecules!
THIS IS THE CHEMICAL BASIS FOR MOST OF
WATER’S ACTION IN LIFE PROCESSES
24
25
Hydrogen bonds in water
n Partial charges on atoms in water allow bonds to form
between molecules
• Hydrogen bonding
• results when H from one molecule is attracted to O of
a different molecule
d-
d+
d+
d-
O
1
4
3
2
Each molecule forms hydrogen bonds with 4
other molecules.
.
The H atom of one molecule of water interacts
with a lone pair of electrons in an orbital
of the O atom of another water molecule
26
These four hydrogen bonds increase the space the water molecules
take up, so water expands as it freezes, and ice is less dense than
liquid water. For these reasons, ice floats in liquid water
27
As a result, ice floats.
28
29
Biological importance of hydrogen
bonds
a. Between an alcohol and
water or between alcohol
molecules.
b. Between a carbonyl group
and water
c. Between 2 peptide chains
d. Between 2 complementary
base pairs in DNA
Water and H-bonds
30
• Hydrogen bonding between water molecules gives
water its special properties
– Cohesion
– Adhesion
– Surface Tension
– Temperature Moderation
31
Water Properties - Cohesion
• High Cohesion
– Binding of like molecules by H bonds
– High in water
– H-bonds constantly breaking and reforming
– most water molecules are bonded to
neighboring molecules at any instant
– Contributes to water transport in plants
32
Water Properties - Adhesion
• High Adhesion
– Clinging of one substance to another
– also involves H-bonds
– also contributes to water transport in plants
– water adheres to molecules of the walls of the
xylem vessels in plant stems (trunks) helps counter
the effects of gravity
33
Water Properties - Surface Tension
• High Surface Tension
– Measure of how difficult
it is to stretch or break
the surface of a liquid
– Higher in water than
other liquids
34
Water – Temperature moderation
High specific heat
Specific Heat: is the amount of heat that must be absorbed or lost
for one gram of a substance to change its temperature by 1°C.
Lots of heat is needed to break H-bonds and raise H2O temperature.
Therefore, H2O is a good insulator.
DAY or SUMMER NIGHT or WINTER
HEAT
HEAT
35
Water: solvent for life
Molecules dissolve in water,
which allows them to move
around more and interact.
Water facilitates all chemical
reactions in the body.
Since water is polar, the positive
and negative ends of a water
molecule will be attracted to
charged ions or other polar
molecules
36
Water and molecules
• Hydrophilic: hydros (water) and philia
(friendship)
– Ionic compounds dissolve in water
– Polar molecules (generally) are water soluble
• Hydrophobic: hydros (water) and phobos
(fear)
– Nonpolar compounds
37
Hydrophobicity
Solvent
Solute
Solution
• Polar molecules tend to be
hydrophilic.
• Substances that are ionic or
polar often dissolve in water
due to hydrogen and ionic
bonds.
38
Ion–dipole and dipole–dipole
interactions
Ion–dipole and dipole–dipole interactions help ionic and
polar compounds dissolve in water.
Hydrophobicity
39
• Hydrophobic compounds
and H2O don’t mix.
• Amphiphilic molecules are
part hydrophobic and part
hydrophilic
Amphiphile: amphis (both)
and philia (love, friendship)
40
Amphipathicity
• When an amphipathic compound is mixed with water,
the polar, hydrophilic region interacts favorably with
the solvent and tends to dissolve, but the nonpolar,
hydrophobic region tends to avoid contact with the
water.
It forms a stable structure,
called micelle in the water.
42
Cellular reactions of water
• Occasionally, a hydrogen atom shared by two water molecules
shifts from one molecule to the other.
– The hydrogen atom leaves its electron behind and is transferred
as a single proton - a hydrogen ion (H+).
– The water molecule that lost a proton is now a hydroxide ion
(OH-).
– The water molecule with the extra proton is a hydronium ion
(H3O+).
43
H2O H+ + OH-
Hydrogen
ion
Hydroxide
ion
• Reversible reaction
• At equilibrium the concentration of water molecules greatly
exceeds that of H+ and OH-.
• At equilibrium, the concentration of H+ or OH- is 10-7M (25°C)
• Hydroxide ions can accept a proton and be converted back into
water molecule
Dissociation of water molecules
44
• The ionization of water can be analyzed quantitatively.
• The concentrations of the reactants and the products at equilibrium:
The ratio of these concentrations defines the equilibrium constant
(Keq).
In case of water ionization: Keq= [H+] [OH-]
[H2O]
The concentration of water at equilibrium:
the mass of 1 liter of water is 1000g
And the mass of one mole of water is 18g
the pure water has a concentration of: 1000g/l = 55.5 mole/l or
18g/mole
= 55.5 M
Dissociation of water molecules
45
Keq = [H+] [OH-]
[H2O]
Keq(55.5 M) = [H+] [OH-]
The Keq for the ionization of water has been determined under
standard conditions of pressure (1 atm) and temperature (25°C)
(1.8x10-16 M)(55.5 M) = [H+] [OH-]
1.0 x 10-14 M2 = [H+] [OH-]
Its value is: Keq= 1.8x10-16 M (the electrical conductivity
of pure water)
Dissociation of water molecules
46
Because according to the chemical equation for
dissociation H+ and OH- must have equal concentrations in
pure water, then
Kw(ion product of water)=
[H+][OH-]=[H+]2= [OH-]2 =1.0 x 10-14 M2
[H+]= 1.0 x 10−14 M2
[H+]= [OH-]= 10-7 M
Dissociation of water molecules
Hydrogen ion concentrations expressed in exponential form are
difficult to work with. A more useful terminology is pH, defined
as the negative logarithm of the [H+].
As the ion product of water is constant, whenever [H+] is
greater than 1 × 10–7 M, [OH–] must be less than 1 × 10–7 M,
and vice versa. When [H+] is very high, as in a solution of
hydrochloric acid, [OH–] must be very low. From the ion
product of water we can calculate [H+] if we know [OH–], and
vice versa.
When [H+] = [OH-]
The solution is said
Neutral
When [H+] > [OH-] Acidic
When [H+] < [OH-] Basic
48
• The pH of a solution will depend little on the hydrogen
ions generated by the self-dissociation of water, but
rather on the presence of other substances (acids or
bases) that increase or decreases the H+ concentration.
• Acids and bases are chemical substances that change
the ionic properties of solutions.
49
Acids, bases and pH scale
• Some substances dissolve in water and release
hydrogen ions (H+); these are called acids. Their release
is called ionization.
• Acids release H+ ions in solution.
• If the reaction is complete, it is a strong acid, such as
HCl.
Hydrochloric acid in water
HCl H+ + Cl-
50
Acids, bases and pH scale
• Other substances dissolve in water and release
hydroxide ions (OH–); these are called bases.
• Bases accept H+ in solution.
• NaOH ionizes completely to Na+ and OH–. The OH–
absorbs H+ to form water. It is a strong base.
Sodium Hydroxide in water
NaOH Na+ + OH-
Acids, bases and pH scale
51
• Ionization of strong acids is virtually irreversible.
• Ionization of weak acids and bases is somewhat reversible.
• Many large molecules in biological systems contain weak acid or base
groups.
n Water is really a weak acid and has a slight tendency to ionize
into H+ and OH–.
n This ionization is very important for living creatures and the
chemical reactions they must perform because the H+ ion is so
reactive.
• Range from 0 to 14
• Basic pH > 7
• neutral pH = 7
• acidic pH < 7
The small p in pH stand for “potential” or “power”
52
pH is a negative
logarithmic
expression of
[H+]
53
54
• In pure H2O, [H+] and [OH-] = 10-7 M
pH = - log [H+]
So the pH of pure water is 7 Neutral
Acids, bases and pH scale
• The value of 7 for the pH of a neutral solution is derived from the
absolute value of the ion product of water at 25 °C.
• The pH scale is logarithmic, not arithmetic. When 2 solutions
differ by 1 pH unit, it means that one solution has 10X the H+
concentration of the other, but it does not tell us the absolute
magnitude of the difference.
• Acids are compounds that donate protons, and bases are
compounds that accept protons.
• Strong acids, such as hydrochloric acid (HCl), dissociate
completely.
• Weak acids, such as acetic acid, dissociate only to a limited
extent:
where HA is the acid, and A- is its conjugate base.
• The dissociation constant for a weak acid is
55
Acids, bases and pH scale
56
Weak acids and the acid
dissociation constant (Ka)
• The stronger the acid, the lower the pKa ; the stronger the
base, the higher its pKa.
• The pKa can be determined experimentally; it is the pH at
the midpoint of the titration curve for the acid or base.
Ka = [H+][CH3COO-]
[CH3COOH]
pKa is a measure of acid strength
Some compound, such as acetic acid, is monoprotic; it can give up only one proton.
Others are diprotic (H2CO3 (carbonic acid) or triprotic (H3PO4 (phosphoric acid)). The
dissociation constant (Ka) and its negative logarithm, the pKa for each pair are shown
on a pH gradient.
Titration curve of weak acids
58
Titration is used to determine the
amount of an acid in a given solution.
A measured volume of the acid is titrated
with a solution of a strong base, usually
sodium hydroxide (NaOH), of known
concentration.
The NaOH is added in small increments
until the acid is consumed (neutralized),
as determined with a pH meter.
The concentration of the acid in the
original solution can be calculated from
the volume and concentration of NaOH
added.
Titration curve of weak acids
59
This value is plotted against the amount of
NaOH expressed as a fraction of the total
NaOH required to convert all the acetic acid
(CH3COOH) to its deprotonated form,
acetate (CH3COO−).
The points yield the titration curve. At the
midpoint of the titration, the concentrations
of the proton donor and proton acceptor
are equal, and the pH is numerically equal
to the pKa.
The shaded zone is the useful region of
buffering power, generally between 10%
and 90% titration of the weak acid.
pKa, acids and bases
• The stronger the acid, the
smaller its pKa; the stronger
the base, the larger its pKa.
The pKa can be determined
experimentally; it is the pH at
the midpoint of the titration
curve for the acid or base.
60
Buffers
• Almost every biological process is pH dependent; a small change in
pH produces a large change in the rate of the process. The
enzymes that catalyze cellular reactions, and many of the
molecules on which they act, contain ionizable groups with
characteristic pKa values.
• In cells and tissues, phosphate and bicarbonate buffer systems
maintain intra-cellular and extra-cellular fluids at their optimum
(physiological) pH, which is usually close to pH 7. Enzymes
generally work optimally at this pH.
61
Criteria used to select buffer for a biochemical reaction.
• The pKa of the buffer should be close to the desired pH
• the substance chosen should not interfere with the reaction
being studied.
Optimal pH of some enzymes
• Pepsin is a digestive enzyme
secreted into gastric juice; trypsin,
a digestive enzyme that acts in the
small intestine; alkaline
phosphatase of bone tissue, a
hydrolytic enzyme thought to aid
in bone mineralization.
62
Buffers
63
Water has a very small [H+] (10-7).
Adding just a little bit of acid or base can change the pH
drastically.
Add 0.001 M HCl: pH goes from 7 to 3!
For many applications this sensitivity is undesirable.
One of the best ways to prevent pH swings is buffering:
the use of a mixture of a weak acid and its conjugate
base (which will be a weak base).
Buffers
64
How can pH changes be minimized?
• Buffers
– Substances that minimize changes in [H+] in
solution
– Present in all biological fluids
• Human blood maintained at pH 7.4
How do buffers work?
• accept H+ ions from the solution when in excess
• donate H+ ions to the solution when depleted
Buffers
• Whenever H+ or OH- is added to
a buffer, the result is a small
change in the ratio of the
relative concentrations of the
weak acid and its anion and
thus a small change in pH.
• The decrease in concentration
of one component of the
system is balanced exactly by an
increase in the other.
• The sum of the buffer
components does not change,
only their ratio.
65
• The shape of the titration curve of any weak acid is described by
the Henderson-Hasselbalch equation.
• For the dissociation of a weak acid HA into H+ and A-, the
Henderson-Hasselbalch equation can be derived as follows:
66
A Simple Expression Relates pH, pKa,
and Buffer Concentration
pH calculation
67
pH calculation
68
Calculate the relative amount of acetic acid and acetate ion present
when 0.5 mol of acetic acid is titrated with 0.1 mol of NaOH. Calculate
the values of the pH, given that pKa of acetic acid is 4.76.
When 0.1 mol of NaOH is added, 0.1 mol of acetic acid react with it to
form 0.1 mol of acetate ion, leaving 0.4 mol of acetic acid. The relative
amount of acetic acid and acetate ion is 80%:20% .
pH = p𝐾 𝑎 + log
0.2
0.8
pH = 4.76 + (-0.6)
= 4.16
Buffer action
• The addition of the acid to 0.1 M sodium acetate solution results
in a much gradual change in pH until the pH drops below 3.5.
• When hydrogen ions are added to the solution, they react with
acetate ion to form acetic acid. This reaction consumes some of
the added hydrogen ion so that the pH does not drop. Hydrogen
ions continue reacting with acetate ions until essentially all of
the acetate ion is converted into acetic acid. After this point,
added protons remain free in solution and the pH begins to fall
sharply again.
69
Summary
1. Water, a nonlinear, polar molecule, serves at least three
functions in the cell: It is an effective solvent, it is a reactant
molecule, and it is a temperature buffer. As a solvent, water is
able to dissolve biomolecules that are ionic and polar.
2. The most important reaction of water is its reversible ionization
to generate proton (H+) and the hydroxide ion (OH-). The extent
of ionization is quantified by the pH scale (pH = -log [H+]).
3. The strength of an acid is defined its pKa, the negative log of its
dissociation constant.
4. Blood and other cellular fluids are maintained at a constant pH
by natural buffer systems.
70

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216765 lecture 4 5

  • 1. HBC1011 Biochemistry I Trimester I, 2018/2019 Lecture 4-5: Biochemistry of Water Ng Chong Han, PhD MNAR1010, 06-2523751 chng@mmu.edu.my
  • 2. Overview • Water, the Biological Solvent • Hydrogen Bonding and Solubility • Cellular Reactions of Water • Buffer Systems 2
  • 3. • Water covers about 70% of the Earth’s surface and makes up 45-95% of living organisms 3
  • 4. Water = molecule of life One of NASA‘s guiding policies in the search for alien life is to “follow the water”. Water is fairly common in the universe, but most of this water is in the form of ice. Solid water can't act as a lubricant for the molecular processes of life, so the search is for liquid water - a commodity that is far more rare in the universe. 4
  • 6. 6 Water in our bodies Approximately 55% of blood is plasma Plasma is mainly composed of: 90% of WATER 10%: blood proteins, inorganic ions, glucose, lipids, amino acids, hormones, metabolic end products…. Each of us has 5-6 liters of blood
  • 7. 7 Biological roles of water Water is a biological solvent eg. Biological fluids for delivery of nutrients and removal of wastes Water serves as an essential buffer to regulate temperature (high specific heat capacity) and pH (buffer solutions) Water is a participant in many biochemical reactions eg. the principal reactant in the photosynthesis process
  • 8. Physical and chemical properties of water 8 • Chemical formula H2O: one molecule of water has two hydrogen atoms covalently bonded to a single oxygen atom. • Water appears in nature in all three common states of matter (solid, liquid, and gas) • Liquid at standard temperature and pressure, tasteless and odorless. • The intrinsic colour of water and ice is a very slight blue hue, although both appear colorless in small quantities.
  • 9. • Polarity: a separation of electric charge leading to its chemical groups having an electric dipole or multipole moment. • Polar molecules interact through dipole–dipole intermolecular forces and hydrogen bonds. Molecular polarity is dependent on the difference in electronegativity (a pull on the electrons) between atoms in a compound. • Polarity affects physical properties eg. surface tension, solubility, and melting and boiling-points. 9 Polar Molecules The two charges are present with a negative charge in the middle (red shade), and a positive charge at the ends (blue shade).
  • 10. • The polarity of chemical bonds: Non-polar bonds, Polar bonds, Ionic bonds • Bonds can fall between one of two extremes — being completely nonpolar or completely polar. – A completely nonpolar bond occurs when the electronegativities are identical. – A completely polar bond is more correctly called an ionic bond. • The terms "polar" and "nonpolar" are usually applied to covalent bonds, that is, bonds where the polarity is not complete. • While the molecules can be described as "polar covalent", "nonpolar covalent", or "ionic", this is often a relative term. 10 Polar Molecules
  • 11. 11
  • 12. Covalent Ionic Nonpolar Polar Sharing of electrons Equal Unequal Transferred Dipole movement No Partial Positive or negative Electronegativity <0.5 0.5-1.7 >1.7 Interactions Two identical nonmetals Two different nonmetals Metal + nonmetal Comparison between nonpolar covalent, polar covalent and ionic bonds Dipole moment describes the charge separation in a molecule. The larger the difference in electronegativities of bonded atoms, the larger the dipole moment. For example, NaCl has the highest dipole moment because it has an ionic bond
  • 13. 13 Covalent and Noncovalent bonds • Covalent bond: a chemical bond that involves the sharing of electron pairs between atoms. • Noncovalent bond: it does not involve the sharing of electrons, but rather involves more dispersed variations of electromagnetic interactions between molecules or within a molecule, eg ionic bond.
  • 14. Covalent bonds 14 • If the two atoms have about equal attraction for electrons, a nonpolar covalent bond (equal sharing) forms • If the two atoms have different electronegativities, a polar covalent bond (unequal sharing) forms In polar bonds, one atom is slightly negative (δ-), while the other is slightly positive (δ+) • Electronegativity is a chemical property that describes the tendency of an atom or a functional group to attract electrons towards itself.
  • 15. 15 Noncovalent bonds • Noncovalent bonds are important for determining the structure of biomolecules. • Types of noncovalent bonds or interactions include: – Hydrogen bonds – Ionic bonds – van der Waals forces – Hydrophobic interactions
  • 16. Noncovalent bonds 16 • Hydrogen bonds occur when a hydrogen atom (δ+) is attracted by a negatively charged atom (δ-) • Hydrogen bonds are weak (10% as strong as covalent).
  • 17. Noncovalent bonds 17 • Ionic bonds are attractions between oppositely charged atoms: +  - for example, Na+ Cl- • Positively charged atoms are called cations, always move to the cathode. • Negatively charged atoms are called anions, always move to the anode.
  • 19. Noncovalent bonds 19 • Hydrophilic molecules are ones that interact with water. These molecules are polar: charged (+, -) or partially charged (δ+,δ-) • Hydrophobic molecules do not interact with water, like oils and fats. These molecules are nonpolar. These often have C’s and H’s, but few or no O’s and N’s.
  • 20. 20 Noncovalent bonds • Hydrophobic molecules tend to avoid water, hence tend to bond together. This is called hydrophobic interactions • Very weak interactions between nonpolar molecules that are tightly packed together are called van der Waals forces • Although these noncovalent interactions are individually weak relative to covalent bonds, the cumulative effect of many such interactions can be very significant.
  • 21. 21
  • 22. 22 Water: Polar Molecules • Since the water molecule is not linear and the oxygen atom has a higher electronegativity than hydrogen atoms, the oxygen atom carries a slight negative charge, whereas the hydrogen atoms are slightly positive. • As a result, water is a polar molecule with an electrical dipole moment.
  • 23. 23 Water: Polar Molecules • Water also can form an unusually large number of intermolecular hydrogen bonds (four) for a molecule of its size. • These factors lead to strong attractive forces between molecules of water, giving rise to water's high surface tension and capillary forces.
  • 24. POLES help to initiate… HYDROGEN BONDING between molecules! THIS IS THE CHEMICAL BASIS FOR MOST OF WATER’S ACTION IN LIFE PROCESSES 24
  • 25. 25 Hydrogen bonds in water n Partial charges on atoms in water allow bonds to form between molecules • Hydrogen bonding • results when H from one molecule is attracted to O of a different molecule d- d+ d+ d- O
  • 26. 1 4 3 2 Each molecule forms hydrogen bonds with 4 other molecules. . The H atom of one molecule of water interacts with a lone pair of electrons in an orbital of the O atom of another water molecule 26
  • 27. These four hydrogen bonds increase the space the water molecules take up, so water expands as it freezes, and ice is less dense than liquid water. For these reasons, ice floats in liquid water 27
  • 28. As a result, ice floats. 28
  • 29. 29 Biological importance of hydrogen bonds a. Between an alcohol and water or between alcohol molecules. b. Between a carbonyl group and water c. Between 2 peptide chains d. Between 2 complementary base pairs in DNA
  • 30. Water and H-bonds 30 • Hydrogen bonding between water molecules gives water its special properties – Cohesion – Adhesion – Surface Tension – Temperature Moderation
  • 31. 31 Water Properties - Cohesion • High Cohesion – Binding of like molecules by H bonds – High in water – H-bonds constantly breaking and reforming – most water molecules are bonded to neighboring molecules at any instant – Contributes to water transport in plants
  • 32. 32 Water Properties - Adhesion • High Adhesion – Clinging of one substance to another – also involves H-bonds – also contributes to water transport in plants – water adheres to molecules of the walls of the xylem vessels in plant stems (trunks) helps counter the effects of gravity
  • 33. 33 Water Properties - Surface Tension • High Surface Tension – Measure of how difficult it is to stretch or break the surface of a liquid – Higher in water than other liquids
  • 34. 34 Water – Temperature moderation High specific heat Specific Heat: is the amount of heat that must be absorbed or lost for one gram of a substance to change its temperature by 1°C. Lots of heat is needed to break H-bonds and raise H2O temperature. Therefore, H2O is a good insulator. DAY or SUMMER NIGHT or WINTER HEAT HEAT
  • 35. 35 Water: solvent for life Molecules dissolve in water, which allows them to move around more and interact. Water facilitates all chemical reactions in the body. Since water is polar, the positive and negative ends of a water molecule will be attracted to charged ions or other polar molecules
  • 36. 36 Water and molecules • Hydrophilic: hydros (water) and philia (friendship) – Ionic compounds dissolve in water – Polar molecules (generally) are water soluble • Hydrophobic: hydros (water) and phobos (fear) – Nonpolar compounds
  • 37. 37 Hydrophobicity Solvent Solute Solution • Polar molecules tend to be hydrophilic. • Substances that are ionic or polar often dissolve in water due to hydrogen and ionic bonds.
  • 38. 38 Ion–dipole and dipole–dipole interactions Ion–dipole and dipole–dipole interactions help ionic and polar compounds dissolve in water.
  • 39. Hydrophobicity 39 • Hydrophobic compounds and H2O don’t mix. • Amphiphilic molecules are part hydrophobic and part hydrophilic Amphiphile: amphis (both) and philia (love, friendship)
  • 40. 40 Amphipathicity • When an amphipathic compound is mixed with water, the polar, hydrophilic region interacts favorably with the solvent and tends to dissolve, but the nonpolar, hydrophobic region tends to avoid contact with the water. It forms a stable structure, called micelle in the water.
  • 41.
  • 42. 42 Cellular reactions of water • Occasionally, a hydrogen atom shared by two water molecules shifts from one molecule to the other. – The hydrogen atom leaves its electron behind and is transferred as a single proton - a hydrogen ion (H+). – The water molecule that lost a proton is now a hydroxide ion (OH-). – The water molecule with the extra proton is a hydronium ion (H3O+).
  • 43. 43 H2O H+ + OH- Hydrogen ion Hydroxide ion • Reversible reaction • At equilibrium the concentration of water molecules greatly exceeds that of H+ and OH-. • At equilibrium, the concentration of H+ or OH- is 10-7M (25°C) • Hydroxide ions can accept a proton and be converted back into water molecule Dissociation of water molecules
  • 44. 44 • The ionization of water can be analyzed quantitatively. • The concentrations of the reactants and the products at equilibrium: The ratio of these concentrations defines the equilibrium constant (Keq). In case of water ionization: Keq= [H+] [OH-] [H2O] The concentration of water at equilibrium: the mass of 1 liter of water is 1000g And the mass of one mole of water is 18g the pure water has a concentration of: 1000g/l = 55.5 mole/l or 18g/mole = 55.5 M Dissociation of water molecules
  • 45. 45 Keq = [H+] [OH-] [H2O] Keq(55.5 M) = [H+] [OH-] The Keq for the ionization of water has been determined under standard conditions of pressure (1 atm) and temperature (25°C) (1.8x10-16 M)(55.5 M) = [H+] [OH-] 1.0 x 10-14 M2 = [H+] [OH-] Its value is: Keq= 1.8x10-16 M (the electrical conductivity of pure water) Dissociation of water molecules
  • 46. 46 Because according to the chemical equation for dissociation H+ and OH- must have equal concentrations in pure water, then Kw(ion product of water)= [H+][OH-]=[H+]2= [OH-]2 =1.0 x 10-14 M2 [H+]= 1.0 x 10−14 M2 [H+]= [OH-]= 10-7 M Dissociation of water molecules Hydrogen ion concentrations expressed in exponential form are difficult to work with. A more useful terminology is pH, defined as the negative logarithm of the [H+].
  • 47. As the ion product of water is constant, whenever [H+] is greater than 1 × 10–7 M, [OH–] must be less than 1 × 10–7 M, and vice versa. When [H+] is very high, as in a solution of hydrochloric acid, [OH–] must be very low. From the ion product of water we can calculate [H+] if we know [OH–], and vice versa.
  • 48. When [H+] = [OH-] The solution is said Neutral When [H+] > [OH-] Acidic When [H+] < [OH-] Basic 48 • The pH of a solution will depend little on the hydrogen ions generated by the self-dissociation of water, but rather on the presence of other substances (acids or bases) that increase or decreases the H+ concentration. • Acids and bases are chemical substances that change the ionic properties of solutions.
  • 49. 49 Acids, bases and pH scale • Some substances dissolve in water and release hydrogen ions (H+); these are called acids. Their release is called ionization. • Acids release H+ ions in solution. • If the reaction is complete, it is a strong acid, such as HCl. Hydrochloric acid in water HCl H+ + Cl-
  • 50. 50 Acids, bases and pH scale • Other substances dissolve in water and release hydroxide ions (OH–); these are called bases. • Bases accept H+ in solution. • NaOH ionizes completely to Na+ and OH–. The OH– absorbs H+ to form water. It is a strong base. Sodium Hydroxide in water NaOH Na+ + OH-
  • 51. Acids, bases and pH scale 51 • Ionization of strong acids is virtually irreversible. • Ionization of weak acids and bases is somewhat reversible. • Many large molecules in biological systems contain weak acid or base groups. n Water is really a weak acid and has a slight tendency to ionize into H+ and OH–. n This ionization is very important for living creatures and the chemical reactions they must perform because the H+ ion is so reactive.
  • 52. • Range from 0 to 14 • Basic pH > 7 • neutral pH = 7 • acidic pH < 7 The small p in pH stand for “potential” or “power” 52
  • 53. pH is a negative logarithmic expression of [H+] 53
  • 54. 54 • In pure H2O, [H+] and [OH-] = 10-7 M pH = - log [H+] So the pH of pure water is 7 Neutral Acids, bases and pH scale • The value of 7 for the pH of a neutral solution is derived from the absolute value of the ion product of water at 25 °C. • The pH scale is logarithmic, not arithmetic. When 2 solutions differ by 1 pH unit, it means that one solution has 10X the H+ concentration of the other, but it does not tell us the absolute magnitude of the difference.
  • 55. • Acids are compounds that donate protons, and bases are compounds that accept protons. • Strong acids, such as hydrochloric acid (HCl), dissociate completely. • Weak acids, such as acetic acid, dissociate only to a limited extent: where HA is the acid, and A- is its conjugate base. • The dissociation constant for a weak acid is 55 Acids, bases and pH scale
  • 56. 56 Weak acids and the acid dissociation constant (Ka) • The stronger the acid, the lower the pKa ; the stronger the base, the higher its pKa. • The pKa can be determined experimentally; it is the pH at the midpoint of the titration curve for the acid or base. Ka = [H+][CH3COO-] [CH3COOH] pKa is a measure of acid strength
  • 57. Some compound, such as acetic acid, is monoprotic; it can give up only one proton. Others are diprotic (H2CO3 (carbonic acid) or triprotic (H3PO4 (phosphoric acid)). The dissociation constant (Ka) and its negative logarithm, the pKa for each pair are shown on a pH gradient.
  • 58. Titration curve of weak acids 58 Titration is used to determine the amount of an acid in a given solution. A measured volume of the acid is titrated with a solution of a strong base, usually sodium hydroxide (NaOH), of known concentration. The NaOH is added in small increments until the acid is consumed (neutralized), as determined with a pH meter. The concentration of the acid in the original solution can be calculated from the volume and concentration of NaOH added.
  • 59. Titration curve of weak acids 59 This value is plotted against the amount of NaOH expressed as a fraction of the total NaOH required to convert all the acetic acid (CH3COOH) to its deprotonated form, acetate (CH3COO−). The points yield the titration curve. At the midpoint of the titration, the concentrations of the proton donor and proton acceptor are equal, and the pH is numerically equal to the pKa. The shaded zone is the useful region of buffering power, generally between 10% and 90% titration of the weak acid.
  • 60. pKa, acids and bases • The stronger the acid, the smaller its pKa; the stronger the base, the larger its pKa. The pKa can be determined experimentally; it is the pH at the midpoint of the titration curve for the acid or base. 60
  • 61. Buffers • Almost every biological process is pH dependent; a small change in pH produces a large change in the rate of the process. The enzymes that catalyze cellular reactions, and many of the molecules on which they act, contain ionizable groups with characteristic pKa values. • In cells and tissues, phosphate and bicarbonate buffer systems maintain intra-cellular and extra-cellular fluids at their optimum (physiological) pH, which is usually close to pH 7. Enzymes generally work optimally at this pH. 61 Criteria used to select buffer for a biochemical reaction. • The pKa of the buffer should be close to the desired pH • the substance chosen should not interfere with the reaction being studied.
  • 62. Optimal pH of some enzymes • Pepsin is a digestive enzyme secreted into gastric juice; trypsin, a digestive enzyme that acts in the small intestine; alkaline phosphatase of bone tissue, a hydrolytic enzyme thought to aid in bone mineralization. 62
  • 63. Buffers 63 Water has a very small [H+] (10-7). Adding just a little bit of acid or base can change the pH drastically. Add 0.001 M HCl: pH goes from 7 to 3! For many applications this sensitivity is undesirable. One of the best ways to prevent pH swings is buffering: the use of a mixture of a weak acid and its conjugate base (which will be a weak base).
  • 64. Buffers 64 How can pH changes be minimized? • Buffers – Substances that minimize changes in [H+] in solution – Present in all biological fluids • Human blood maintained at pH 7.4 How do buffers work? • accept H+ ions from the solution when in excess • donate H+ ions to the solution when depleted
  • 65. Buffers • Whenever H+ or OH- is added to a buffer, the result is a small change in the ratio of the relative concentrations of the weak acid and its anion and thus a small change in pH. • The decrease in concentration of one component of the system is balanced exactly by an increase in the other. • The sum of the buffer components does not change, only their ratio. 65
  • 66. • The shape of the titration curve of any weak acid is described by the Henderson-Hasselbalch equation. • For the dissociation of a weak acid HA into H+ and A-, the Henderson-Hasselbalch equation can be derived as follows: 66 A Simple Expression Relates pH, pKa, and Buffer Concentration
  • 68. pH calculation 68 Calculate the relative amount of acetic acid and acetate ion present when 0.5 mol of acetic acid is titrated with 0.1 mol of NaOH. Calculate the values of the pH, given that pKa of acetic acid is 4.76. When 0.1 mol of NaOH is added, 0.1 mol of acetic acid react with it to form 0.1 mol of acetate ion, leaving 0.4 mol of acetic acid. The relative amount of acetic acid and acetate ion is 80%:20% . pH = p𝐾 𝑎 + log 0.2 0.8 pH = 4.76 + (-0.6) = 4.16
  • 69. Buffer action • The addition of the acid to 0.1 M sodium acetate solution results in a much gradual change in pH until the pH drops below 3.5. • When hydrogen ions are added to the solution, they react with acetate ion to form acetic acid. This reaction consumes some of the added hydrogen ion so that the pH does not drop. Hydrogen ions continue reacting with acetate ions until essentially all of the acetate ion is converted into acetic acid. After this point, added protons remain free in solution and the pH begins to fall sharply again. 69
  • 70. Summary 1. Water, a nonlinear, polar molecule, serves at least three functions in the cell: It is an effective solvent, it is a reactant molecule, and it is a temperature buffer. As a solvent, water is able to dissolve biomolecules that are ionic and polar. 2. The most important reaction of water is its reversible ionization to generate proton (H+) and the hydroxide ion (OH-). The extent of ionization is quantified by the pH scale (pH = -log [H+]). 3. The strength of an acid is defined its pKa, the negative log of its dissociation constant. 4. Blood and other cellular fluids are maintained at a constant pH by natural buffer systems. 70