Biochemistry Lecture 1 October 24 2011

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    BIOCHEMISTRYand

    MICROBIAL PHYSIOLOGY

    MQT 1173

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    BIOCHEMISTRY

    Biochemists discuss chemistry with

    biologists, and biology with

    chemists, thereby confusing bothgroups. Among themselves, they

    talk about baseball.

    Credit: Anonymous

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    Biochemistry is a hybrid science:

    Biology is the science of living organisms and chemistry is the

    science of atoms and molecules, so biochemistry is the

    science of the atoms and molecules in living organisms.

    Its domain encompass all the living world with the unifying

    interest in the chemical structures and reactions that occur in

    living systems.

    Where can you find biochemistry? All through science, medicine,

    and agriculture.

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    Biochemistry underlies ordinary life in unseen ways:

    For example, take a middle-aged man who:

    Takes a drug to lower his serum cholesterol. That drug was

    developed by a pharmaceutical company's biochemists to inhibit a

    key enzyme involved in cholesterol biosynthesis.

    Shaves with a cream containing compounds that soften his

    beard. These active agents were developed after studies of thephysical properties of keratin, the protein in hair.

    Eats a breakfast cereal fortified with vitamins identified

    through nutritional biochemistry.

    Wears a shirt made from pest-resistant cotton. The cotton

    plants were bioengineered by biochemists through the transfer ofgenes from a bacterium into plants.

    Drinks milk before bedtime. His sleep is helped by the amino

    acids in the milk, which are converted by his brain into molecular

    signals that lead to a resting state in other parts of his brain.

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    Biochemistry has three main branches

    Metabolism study of the conversion of biological molecules,

    especially small molecules, from one to another

    forexample, the conversion of sugar into carbon dioxide andwater, or the conversion of fats into cholesterol. Metabolicbiochemists are particularly interested in the individualenzyme-catalyzed steps of an overall sequence ofreactions (called a pathway) that leads from onesubstance to another.

    Structural Biochemistry study of how molecules in livingcells work chemically. For example, structural biochemiststry to determine how the three-dimensional structure of

    an enzyme contributes to its ability to catalyze a singlemetabolic reaction.

    Molecular Genetics is concerned with the expression ofgenetic information and the way in which this informationcontributes to the regulation of cellular functions.

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    Chemical elements and biomolecules

    Around two dozen of the 94 naturally-occuring chemical

    elements are essential to various kinds of biological life.Most rare elements on Earth are not needed by life (exceptions

    being selenium and iodine), while a few common ones(aluminum and titanium) are not used.

    Most organisms share element needs, but there are a fewdifferences between plants and animals.

    For example ocean algae use bromine but land plants andanimals seem to need none.

    All animals require sodium, but some plants do not.

    Plants need boron and silicon, but animals may not (or mayneed ultra-small amounts).

    Just six elementscarbon, hydrogen, nitrogen, oxygen,calcium, and phosphorusmake up almost 99% of the massof a human body and require smaller amounts of at least 16

    more.

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    The four main classes of molecules in biochemistryare carbohydrates, lipids (Fatty acids), amino

    acids (proteins), and nucleic acids.Many biological molecules are polymers: in thisterminology, monomers are relatively smallmicromolecules that are linked together tocreate large macromolecules, which are knownaspolymers.

    When monomers are linked together to synthesizea biological polymer, they undergo a processcalled dehydration synthesis.

    Most of these are optically active, that is, they arefound in only one of the possible stereoisomers.

    (Stereoisomers are compounds that have the same kinds andnumbers of atoms but have different molecular arrangements)

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    Amino acids

    Generally, amino acids found in nature are the L-stereoisomers.

    Amino acids are the building blocks of proteins, and have an

    important role in energy metabolism and in cellular signaling.

    They are also a small but important part ofcell membranes.

    are molecules containing an amine group, a carboxylic acid groupand a side-chain that varies between different amino acids.

    The key elements of an amino acid are carbon, hydrogen, oxygen,and nitrogen.

    They are particularly important in biochemistry, where the termusually refers to alpha-amino acids.

    http://en.wikipedia.org/wiki/Moleculehttp://en.wikipedia.org/wiki/Aminehttp://en.wikipedia.org/wiki/Carboxylic_acidhttp://en.wikipedia.org/wiki/Side_chainhttp://en.wikipedia.org/wiki/Carbonhttp://en.wikipedia.org/wiki/Hydrogenhttp://en.wikipedia.org/wiki/Oxygenhttp://en.wikipedia.org/wiki/Nitrogenhttp://upload.wikimedia.org/wikipedia/commons/c/ce/AminoAcidball.svghttp://en.wikipedia.org/wiki/Nitrogenhttp://en.wikipedia.org/wiki/Oxygenhttp://en.wikipedia.org/wiki/Hydrogenhttp://en.wikipedia.org/wiki/Carbonhttp://en.wikipedia.org/wiki/Side_chainhttp://en.wikipedia.org/wiki/Side_chainhttp://en.wikipedia.org/wiki/Side_chainhttp://en.wikipedia.org/wiki/Carboxylic_acidhttp://en.wikipedia.org/wiki/Aminehttp://en.wikipedia.org/wiki/Molecule
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    Carbohydrates

    are molecules of the empirical formula Cm

    (H2O)

    nwhere n usually

    ranges from 3

    7 (where m could be different from n).

    They are found in sugars and starches and make up parts ofnucleotides (the energy currency of a cell, and the building blocksfor genetic information).

    They are also present in some components of all cell membranes.

    They are the central components of energy-producing pathways inbiology.

    Carbohydrates are made from monomers called monosaccharides.

    Monosaccharides include glucose , fructose, and deoxyribose

    When two monosaccharides undergo dehydration synthesis,water is produced, as two hydrogen atoms and one oxygen atomare lost from the two monosaccharides' hydroxyl group.

    http://en.wikipedia.org/wiki/Monosaccharideshttp://en.wikipedia.org/wiki/Glucosehttp://en.wikipedia.org/wiki/Fructosehttp://en.wikipedia.org/wiki/Deoxyribosehttp://en.wikipedia.org/wiki/Hydrogenhttp://en.wikipedia.org/wiki/Oxygenhttp://en.wikipedia.org/wiki/Hydrogenhttp://en.wikipedia.org/wiki/Hydroxyl_grouphttp://en.wikipedia.org/wiki/Hydroxyl_grouphttp://en.wikipedia.org/wiki/Oxygenhttp://en.wikipedia.org/wiki/Hydroxyl_grouphttp://en.wikipedia.org/wiki/Hydroxyl_grouphttp://en.wikipedia.org/wiki/Hydroxyl_grouphttp://en.wikipedia.org/wiki/Hydroxyl_grouphttp://en.wikipedia.org/wiki/Oxygenhttp://en.wikipedia.org/wiki/Hydrogenhttp://en.wikipedia.org/wiki/Deoxyribosehttp://en.wikipedia.org/wiki/Fructosehttp://en.wikipedia.org/wiki/Glucosehttp://en.wikipedia.org/wiki/Monosaccharides
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    Properties of GlucoseMolecular formula C6H12O6

    Molar mass 180.16 g/mol

    Melting point -D-glucose: 46 C,

    -D-glucose: 150 C

    Solubility in water Very soluble

    Properties of FructoseMolecular formula C6H12O6

    Molar mass 180.16 g/mol

    Melting point 103 C

    Solubility in water Very soluble

    http://en.wikipedia.org/wiki/Molar_masshttp://en.wikipedia.org/wiki/Melting_pointhttp://en.wikipedia.org/wiki/Solubilityhttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Molar_masshttp://en.wikipedia.org/wiki/Melting_pointhttp://en.wikipedia.org/wiki/Solubilityhttp://en.wikipedia.org/wiki/Waterhttp://upload.wikimedia.org/wikipedia/commons/e/e5/D-Fructose.svghttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Solubilityhttp://en.wikipedia.org/wiki/Melting_pointhttp://en.wikipedia.org/wiki/Molar_masshttp://upload.wikimedia.org/wikipedia/commons/1/14/DGlucose_Fischer.svghttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Solubilityhttp://en.wikipedia.org/wiki/Melting_pointhttp://en.wikipedia.org/wiki/Molar_mass
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    Properties of Deoxyribose

    Molecular formula C5H10O4

    Molar mass 134.13 g mol1

    Melting point 91 C

    Solubility in water Very soluble

    A molecule of sucrose (glucose + fructose), a disaccharide

    http://en.wikipedia.org/wiki/Molar_masshttp://en.wikipedia.org/wiki/Melting_pointhttp://en.wikipedia.org/wiki/Solubilityhttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Sucrosehttp://en.wikipedia.org/wiki/Disaccharidehttp://en.wikipedia.org/wiki/Disaccharidehttp://en.wikipedia.org/wiki/Sucrosehttp://upload.wikimedia.org/wikipedia/commons/b/b3/Sucrose-inkscape.svghttp://en.wikipedia.org/wiki/Waterhttp://en.wikipedia.org/wiki/Solubilityhttp://en.wikipedia.org/wiki/Melting_pointhttp://en.wikipedia.org/wiki/Molar_mass
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    LipidsClosely related to hydrocarbons (compounds containing

    hydrogen and carbon atoms exclusively), although they usually haveother atoms beside C and H.

    Constitute a broad group of naturally occurring molecules

    which include fats, waxes, sterols, fat-soluble vitamins (such as

    vitamins A, D, E and K), monoglycerides, diglycerides, phospholipids,and others.

    Characterized by limited solubility in water, essential

    components of membranes, important energy stores in plants and

    animals and signaling molecules

    May be broadly defined as hydrophobic or amphiphilic small

    molecules; the amphiphilic nature of some lipids allows them to form

    structures such as vesicles, liposomes, or membranes in an aqueous

    environment.

    http://en.wikipedia.org/wiki/Vesicle_%28biology%29http://en.wikipedia.org/wiki/Liposomehttp://en.wikipedia.org/wiki/Liposomehttp://en.wikipedia.org/wiki/Vesicle_%28biology%29
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    Biological lipids originate entirely or in part from two

    distinct types of biochemical subunits or "building blocks":

    ketoacyl and isoprene groups.

    Using this approach, lipids may be divided into eight

    categories: fatty acyls, glycerolipids, glycerophospholipids,

    sphingolipids, saccharolipids and polyketides (derived from

    condensation of ketoacyl subunits); and sterol lipids and prenol

    lipids (derived from condensation of isoprene subunits)

    Palmitic acid (C16H32O2)

    http://en.wikipedia.org/wiki/Fatty_acylshttp://en.wikipedia.org/wiki/Glycerolipidhttp://en.wikipedia.org/wiki/Glycerophospholipidhttp://en.wikipedia.org/wiki/Sphingolipidhttp://en.wikipedia.org/wiki/Saccharolipidhttp://en.wikipedia.org/wiki/Polyketidehttp://en.wikipedia.org/wiki/Polyketidehttp://en.wikipedia.org/wiki/Saccharolipidhttp://en.wikipedia.org/wiki/Sphingolipidhttp://en.wikipedia.org/wiki/Glycerophospholipidhttp://en.wikipedia.org/wiki/Glycerolipidhttp://en.wikipedia.org/wiki/Fatty_acyls
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    A nucleic acid is a complex, high-molecular-weight biochemical

    macromolecule composed of nucleotide chains that convey geneticinformation.

    The most common nucleic acids are deoxyribonucleic acid (DNA) andribonucleic acid (RNA).

    Nucleic acids are found in all living cells and viruses.

    Aside from the genetic material of the cell, nucleic acids often play arole as second messengers, as well as forming the base molecule for

    adenosine triphosphate, the primary energy-carrier molecule foundin all living organisms.

    Nucleic acid, so called because of its prevalence in cellular nuclei, isthe generic name of the family ofbiopolymers.

    Nucleosides and nucleotides

    http://en.wikipedia.org/wiki/Second_messengerhttp://en.wikipedia.org/wiki/Adenosine_triphosphatehttp://en.wikipedia.org/wiki/Cell_nucleushttp://en.wikipedia.org/wiki/Biopolymerhttp://en.wikipedia.org/wiki/Biopolymerhttp://en.wikipedia.org/wiki/Cell_nucleushttp://en.wikipedia.org/wiki/Adenosine_triphosphatehttp://en.wikipedia.org/wiki/Second_messenger
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    The monomers are called nucleotides, and each consists of threecomponents: a nitrogenous heterocyclic base(either a purine or apyrimidine), a pentosesugar, and a phosphate group.

    Different nucleic acid types differ in the specific sugar found in their

    chain (e.g. DNA or deoxyribonucleic acid contains 2-deoxyriboses).

    Possibly nitrogenous bases are different in the two nucleic acids :adenine, cytosine, and guanine occur in both RNA and DNA,

    while thymine occurs only in DNA and uracil occurs in RNA.

    http://en.wikipedia.org/wiki/Nucleotidehttp://en.wikipedia.org/wiki/Base_%28chemistry%29http://en.wikipedia.org/wiki/Purinehttp://en.wikipedia.org/wiki/Pyrimidinehttp://en.wikipedia.org/wiki/Pentosehttp://en.wikipedia.org/wiki/Sugarhttp://en.wikipedia.org/wiki/Phosphatehttp://en.wikipedia.org/wiki/Deoxyribosehttp://en.wikipedia.org/wiki/Adeninehttp://en.wikipedia.org/wiki/Cytosinehttp://en.wikipedia.org/wiki/Guaninehttp://en.wikipedia.org/wiki/Guaninehttp://en.wikipedia.org/wiki/Cytosinehttp://en.wikipedia.org/wiki/Adeninehttp://en.wikipedia.org/wiki/Deoxyribosehttp://en.wikipedia.org/wiki/Phosphatehttp://en.wikipedia.org/wiki/Sugarhttp://en.wikipedia.org/wiki/Pentosehttp://en.wikipedia.org/wiki/Pyrimidinehttp://en.wikipedia.org/wiki/Purinehttp://en.wikipedia.org/wiki/Base_%28chemistry%29http://en.wikipedia.org/wiki/Nucleotide
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    Adenosine, a nucleoside

    http://upload.wikimedia.org/wikipedia/commons/e/e8/Adenosin.svghttp://upload.wikimedia.org/wikipedia/commons/e/e2/Nucleotides_1.svg
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    General formulas of organic compoundsR represents an alkyl group (CH3(CH2)n)

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    General formulas of functional groups

    R represents an alkyl group (CH3(CH2)n)

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    General formulas of linkages

    common in biochemistry

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    Representations of the structure of ribose.

    (a) In the Fischer projection, ribose is drawn as a linear molecule.

    (b) In its usual biochemical form, the ribose molecule is in a ring, shown

    here as a Fischer projection.

    (c) In a Haworth projection, the ring is depicted as lying perpendicular to

    the page (as indicated by the thick lines, which represent the bonds closest

    to the viewer).

    (d) The ring of ribose is not actually planar but can adopt 20 possible

    conformations in which certain ring atoms are out-of-plane. In the

    conformation shown, C-2 lies above the plane formed by the rest of the

    ring atoms.

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    Types of Biochemical Reactions

    Many possible biochemical reactions fall into only a few types to

    consider:

    Oxidation and reduction:For example, the interconversion of an alcohol and an aldehyde.

    Movement of functional groups within/between moleculesFor example, the transfer of phosphate groups from one oxygen

    to another.

    Addition and removal of water:For example, hydrolysis of an amide linkage to an amine and a

    carboxyl group.

    Bond-breaking reactions:

    For example, carbon-carbon bond breakage.

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    All Organisms are Related

    The classification and grouping of organisms, the science called

    taxonomy, regards organisms as similar based on their visible

    characteristics. Thus, plants and animals were regarded as the two

    main kingdoms of life.

    Later, cell biologists divided organisms into prokaryotes and

    eukaryotes, that is, organisms without and with a nucleus.

    Most recently, a new taxonomy has been developed, largely byCarl Woese and associates, based on the information in the

    ribosomal RNA sequences.

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    Remarkably, the most information-rich classifications of life shows

    three main divisions, sometimes called domains, which aremore fundamental than the distinction between plants and

    animals, or prokaryotes and eukaryotes. These domains are:

    Eukarya: Includes organisms with a nucleus.This division includesplants, animals, and a large number of what are sometimes called

    protists, or organisms that can be seen only under a microscope,

    such as yeasts or paramecia.

    Bacteria: The second domain includes microorganisms without anucleus, including many that are familiar, like Escherichia coli.

    Archaea: The third groupis as different from bacteria as they arefrom eukarya on the molecular/biochemical level. These

    remarkable microorganisms inhabit niches often thought of as

    inhospitable to life for example, locations with high

    temperature, low oxygen, or high salt. Their biochemistry is

    unique and largely unexplored.

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