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Lecture Human anatomy and physiology - Chapter 2: Chemistry comes alive (part b)

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Biochemistry is the study of the chemical composition and reactions of living matter. All chemicals in the body fall into one of two major classes: organic or inorganic compounds. Organic compounds contain carbon. All organic compounds are covalently bonded molecules, and many are large. All other chemicals in the body are considered inorganic compounds. These include water, salts, and many acids and bases. Organic and inorganic compounds are equally essential for life.

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Part B: Chemistry Comes Alive: 

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 Most important inorganic compound in living organisms because of its properties

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◦ Dissolves and dissociates ionic substances

◦ Forms hydration layers around large charged molecules,  e.g., proteins (colloid formation)

◦ Body’s major transport medium

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Copyright © 2010 Pearson Education, Inc. Figure 2.12

Water molecule

Ions in solution Salt crystal

+

+

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◦ A necessary part of hydrolysis and dehydration synthesis  reactions

 Cushioning

◦ Protects certain organs from physical trauma, e.g., 

cerebrospinal fluid

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 Ionic compounds that dissociate in water

 Contain cations other than H+ and anions other 

than OH–

 Ions (electrolytes) conduct electrical currents in solution

 Ions play specialized roles in body functions (e.g., sodium, potassium, calcium, and iron)

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◦ Acids are proton (hydrogen ion) donors (release H +  in  solution)

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 pH = the negative logarithm of [H+] in moles per liter

 Neutral solutions:

◦ Pure water is pH neutral (contains equal numbers of H +   and OH)

◦ pH of pure water = pH 7: [H + ] = 10  –7  M

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◦  [H + ],   pH 

◦ pH scale is logarithmic: a pH 5 solution has 10 times  more H +  than a pH 6 solution

 Alkaline solutions 

◦  [H + ],   pH

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Copyright © 2010 Pearson Education, Inc. Figure 2.13

Concentration (moles/liter) [OH – ]

Household ammonia (pH=10.5–11.5)

Neutral

Household bleach (pH=9.5)

Egg white (pH=8) Blood (pH=7.4)

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 Slight change in pH can be fatal

 pH is regulated by kidneys, lungs, and buffers

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 Mixture of compounds that resist pH changes 

 Convert strong (completely dissociated) acids or bases into weak (slightly dissociated) ones

◦ Carbonic acid­bicarbonate system

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Contain carbon (except CO2 and CO, which are inorganic)

 Unique to living systems

 Include carbohydrates, lipids, proteins, and  nucleic acids

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 Many are polymers—chains of similar units (monomers or building blocks)

◦ Synthesized by dehydration synthesis

◦ Broken down by hydrolysis reactions

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Copyright © 2010 Pearson Education, Inc. Figure 2.14

+

Glucose Fructose

Water is released

Monomers linked by covalent bond

Monomers linked by covalent bond

Water is consumed

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◦ Major source of cellular fuel (e.g., glucose)

◦ Structural molecules (e.g., ribose sugar in RNA)

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Simple sugars containing three to seven C atoms

 (CH20)n

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Copyright © 2010 Pearson Education, Inc. Figure 2.15a

Example

Hexose sugars (the hexoses shown

here are isomers)

Example

Pentose sugars

Glucose Fructose Galactose Deoxyribose Ribose

Monomers of carbohydrates

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Double sugars

 Too large to pass through cell membranes

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Copyright © 2010 Pearson Education, Inc. Figure 2.15b

Example

Sucrose, maltose, and lactose

(these disaccharides are isomers)

Glucose Fructose Glucose Glucose Glucose

Galactose

Consist of two linked monosaccharides

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Polymers of simple sugars, e.g., starch and 

glycogen

 Not very soluble

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Copyright © 2010 Pearson Education, Inc. Figure 2.15c

Example

This polysaccharide is a simplified representation of

glycogen, a polysaccharide formed from glucose units.

Long branching chains (polymers) of linked monosaccharides

Glycogen

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Contain C, H, O (less than in carbohydrates), and  sometimes P

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 Composed of three fatty acids bonded to a glycerol molecule

 Main functions

◦ Energy storage

◦ Insulation

◦ Protection 

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Copyright © 2010 Pearson Education, Inc. Figure 2.16a

(a) Triglyceride formation

Three fatty acid chains are bound to glycerol by

dehydration synthesis

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Copyright © 2010 Pearson Education, Inc. Figure 2.16b

containing group (polar

Phosphorus-“head”)

Example

Phosphatidylcholine

Glycerol backbone

2 fatty acid chains (nonpolar “tail”)

Two fatty acid chains and a phosphorus-containing group are

attached to the glycerol backbone.

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 Steroids—interlocking four­ring structure

 Cholesterol, vitamin D, steroid hormones, and bile salts

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Copyright © 2010 Pearson Education, Inc. Figure 2.16c

Example

Cholesterol (cholesterol is the basis for all steroids formed in the body)

(c) Simplified structure of a steroid

Four interlocking hydrocarbon rings form a steroid.

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 Other fat­soluble vitamins

◦ Vitamins A, E, and K

 Lipoproteins

◦ Transport fats in the blood

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◦ Joined by peptide bonds

 Contain C, H, O, N, and sometimes S and P

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Copyright © 2010 Pearson Education, Inc. Figure 2.17

(c) Aspartic acid

(an acidic amino acid) has an acid group (—COOH) in the

R group.

(d) Lysine

(a basic amino acid) has an amine group (–NH 2 ) in the R group

(e) Cysteine

(a basic amino acid) has a sulfhydryl (–SH) group in the R group, which suggests that this amino acid is likely

to participate in intramolecular bonding

Amine

group

Acid group

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Copyright © 2010 Pearson Education, Inc. Figure 2.18

Amino acid Amino acid Dipeptide

The acid group of one amino acid is bonded to the amine group of the next, with loss of a water molecule.

Hydrolysis: Peptide

bonds linking amino acids together are broken when water is added to the bond.

+

Peptide bond

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Copyright © 2010 Pearson Education, Inc. Figure 2.19a

(a) Primary structure:

The sequence of amino acids forms the polypeptide chain.

Amino acid Amino acid Amino acid Amino acid Amino acid

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Copyright © 2010 Pearson Education, Inc. Figure 2.19b

to form a spiral structure, which is stabilized by hydrogen bonds.

and forth forming a “pleated” sheet Adjacent strands are held together by hydrogen bonds.

(b) Secondary structure:

The primary chain forms spirals ( -helices) and sheets ( -sheets).

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Copyright © 2010 Pearson Education, Inc. Figure 2.19c

Tertiary structure of prealbumin (transthyretin), a protein that transports the thyroid hormone thyroxine in serum and cerebro- spinal fluid.

(c) Tertiary structure:

Superimposed on secondary structure -Helices and/or -sheets are

folded up to form a compact globular molecule held together by

intramolecular bonds.

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Copyright © 2010 Pearson Education, Inc. Figure 2.19d

a functional prealbumin molecule Two identical prealbumin subunits join head to tail to form the dimer

(d) Quaternary structure:

Two or more polypeptide chains, each with its own tertiary structure,

combine to form a functional protein.

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 Shape change and disruption of active sites due 

to environmental changes (e.g., decreased pH or increased temperature)

 Reversible in most cases, if normal conditions are restored

 Irreversible if extreme changes damage the 

structure beyond repair (e.g., cooking an egg)

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the speed of a reaction (millions of reactions per minute!)

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Copyright © 2010 Pearson Education, Inc. Figure 2.20

Activation

energy

required

Less activation energy required

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◦ Largest molecules in the body 

 Contain C, O, H, N, and P

 Building block = nucleotide, composed of N­containing base, a pentose sugar, and a 

phosphate group

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 Adenine­containing RNA nucleotide with two additional phosphate groups

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Copyright © 2010 Pearson Education, Inc. Figure 2.23

Adenosine triphosphate (ATP) Adenosine diphosphate (ADP)

Adenosine monophosphate (AMP)

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 Phosphorylation: 

◦ Terminal phosphates are enzymatically transferred to  and energize other molecules 

◦  Such “primed” molecules perform cellular work (life  processes) using the phosphate bond energy

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Copyright © 2010 Pearson Education, Inc. Figure 2.24

Membrane protein

Relaxed smooth muscle cell

Contracted smooth muscle cell

+

+

+

Transport work: ATP phosphorylates transport

proteins, activating them to transport solutes (ions, for example) across cell membranes.

Mechanical work: ATP phosphorylates

contractile proteins in muscle cells so the cells can shorten.

Chemical work: ATP phosphorylates key

reactants, providing energy to drive energy-absorbing chemical reactions.

(a)

(b)

(c)

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