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    TheChemistryofMicrobiology

    Matter&Atoms

    Matter anythingthattakesupspaceandhasmass

    Atoms the

    smallest

    chemical

    units

    of

    matterWps.prenhall.com

    Atoms&AtomicStructure

    Nucleus structurecontainingneutronsandprotons

    Neutrons unchargedparticles

    Protons positivelychargedparticles

    Electrons negativelychargedsubatomicparticles

    circlinganucleus

    Electronshells

    Nucleus Proton(pNeutron(n

    +0

    ))

    Electron(e)

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    Atomic Number and Atomic Mass

    Anelementsatomic

    numberis

    the

    number

    ofprotonsinitsnucleus

    Elementalsymbol Anelementsmass

    numberisthesumofprotonsplusneutronsinthenucleus

    Electronsanegligible Atomicmass,the

    atomstotalmass,canbeapproximated bythemassnumber

    96 3

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    AtomsElectronsConfigurations

    ElectronConfigurations

    Onlytheelectronsofatomsinteract,sotheydetermineatom'schemicalbehavior

    Electronsoccupyelectronshells

    Valenceelectrons electronsinoutermostshellthatinteractwithotheratoms

    Neon,

    with

    two

    filledShells(10electrons)

    Firstshell

    Secondshell

    ++x

    z

    y

    =

    SecondshellFirstshell

    Electron shells of neon: three-dimensional view

    + =

    Firstshell Secondshell

    Electron shells of neon: two-dimensional view

    Figure2.3 Electronconfigurations.

    Figure2.4 Bohrdiagramsofthefirst20elementsandtheirplaceswithinthechartknownastheperiodictableoftheelements.

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    ChemicalBonds

    Valence combiningcapacityofanatom

    Positive ifatomhaselectronstogiveup

    Negativeifatomhasspacestofill

    Stablewhenouterelectronshellscontaineightelectrons

    Chemicalbonds atomscombinebysharingortransferringvalence

    electrons

    Molecule twoormoreatomsheldtogetherbychemicalbonds

    Compound amoleculecomposedofmorethanoneelement

    ChemicalBonds

    Covalentbond sharingofapairofelectronsbytwoatoms

    Nonpolarcovalentbonds

    Polarcovalentbonds

    Electronegativity attractionofatomforelectrons

    Themore

    electronegative

    an

    atom,

    the

    greater

    the

    pull

    its

    nucleus

    exertsonelectronsFigure2.5ab Fourmoleculesformedbycovalentbonds.

    ChemicalBonds

    Nonpolarcovalentbonds

    Sharedelectronsspendequalamountsoftime

    aroundeachnucleus

    Atomswithsimilarelectronegativities

    Nopoles

    exist

    Carbonatomsformfournonpolarcovalentbonds

    withotheratoms

    Organiccompoundscontaincarbonandhydrogen

    atoms

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    Figure2.5cd Fourmoleculesformedbycovalentbonds.

    ChemicalBonds

    PolarCovalentBonds

    Unequal sharingofelectronsduetosignificantly

    differentelectronegativities

    Mostimportantpolarcovalentbondsinvolve

    hydrogen

    Allow

    for

    hydrogen

    bondingFigure2.7 Polarcovalentbondinginawatermolecule.

    Figure2.6 Electronegativityvaluesofselectedelements.

    Electronegativityvaluesofselectedelements.

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    ChemicalBonds

    IonicBonds

    Occurwhentwoatomswithvastlydifferent

    electronegativitiescometogether

    Atoms:eitherpositive(cation)ornegative(anion)charges

    Cations andanionsattracteachotherandformionic

    bonds(noelectrons shared)

    Typicallyformcrystallineioniccompoundsknownassalts

    Figure2.8 Theinteractionofsodiumandchlorinetoformanionicbond.

    Figure2.9 DissociationofNaCI inwater.

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    ChemicalBonds

    HydrogenBonds

    ElectricalattractionbetweenpartiallychargedH+

    andfullorpartialnegativechargeonsameor

    differentmolecule

    Weakerthancovalentbondsbutessentialforlife

    Helptostabilize3Dshapesoflargemolecules

    Figure2.10 Hydrogenbonds.

    Water(H2O)

    Ammonia(NH3)

    Hydrogenbond

    ++

    +++

    ChemicalReactions

    Chemicalreactionsarethemakingandbreaking

    ofchemicalbonds

    Thestartingmoleculesofachemicalreactionare

    calledreactants

    Thefinalmoleculesofachemicalreactionare

    calledproducts

    Reactants Reaction Products

    2H2 2H2OO2+

    Chemical

    SeeFigure2.11a Twotypesofchemicalreactionsinlivingthings.

    ChemicalReactions

    SynthesisReactions

    Involvethe

    formation

    of

    larger,

    more

    complex

    molecules

    Requireenergy(endothermic)

    Commontypeisdehydrationsynthesis

    Watermoleculeformed

    All thesynthesis reactionsinanorganismarecalled

    anabolism

    Figure2.11a Twotypesofchemicalreactionsinlivingthings.

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    ChemicalReactions

    DecompositionReactions

    Breakbondswithinlargermoleculestoformsmalleratoms,ions,andmolecules

    Releaseenergy(exothermic)

    Commontypeishydrolysis

    Ioniccomponentsofwaterareaddedtoproducts

    Allthedecompositionreactionsinanorganismarecalledcatabolism

    Figure2.11b Twotypesofchemicalreactionsinlivingthings.

    ChemicalReactions

    ExchangeReactions

    Involvebreakingandformingcovalentbonds

    Haveendothermicandexothermicsteps

    Involveatomsmovingfromonemoleculeto

    another

    Sumofallchemicalreactionsinanorganismis

    calledmetabolism

    Water,Acids,Bases,andSalts

    Water

    Mostabundant

    substance

    in

    organisms

    Specialcharacteristicsduetotwopolarcovalentbonds

    Cohesivemolecules surfacetension

    Excellentsolvent

    Remainsliquidacrosswiderangeoftemperatures

    Canabsorbsignificantamountsofenergywithoutchanging

    temperature

    Participatesinmanychemicalreactions

    Figure2.12 Thecohesivenessofliquidwater.

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    Water,Acids,Bases,andSalts

    AcidsandBases

    Dissociatedbywaterintocations andanions

    Acid dissociatesintooneormoreH+ andoneor

    moreanions

    Base bindswithH+ whendissolvedintowater;

    somedissociateintocations andOH

    Figure2.13 Acidsandbases.

    Figure2.14 ThepHscale.

    ConcentrationofH+ in

    solutionexpressed

    usingthepHscale

    Metabolismrequires

    relativelyconstant

    balanceofacidsand

    bases

    Buffersprevent

    drasticchangesin

    internalpH

    Water,Acids,Bases,andSalts

    Salts

    Compoundsthat

    dissociate

    in

    water

    into

    cationsand

    anionsotherthanH+ andOH

    Cations andanionsofsaltsareelectrolytes

    Createelectricaldifferences betweeninsideandoutsideof

    cell

    Transferelectronsfromonelocationtoanother

    Formimportantcomponentsofmanyenzymes

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    OrganicMacromolecules

    Containcarbonandhydrogenatoms

    Atomsoftenappearinarrangements calledfunctionalgroups

    Macromolecules largemoleculesusedbyallorganisms

    Lipids

    Carbohydrates

    Proteins

    Nucleicacids

    Monomers basicbuildingblocksofmacromolecules

    OrganicMacromolecules

    Lipids

    Notcomposedofregularsubunits

    Areallhydrophobic

    Fourgroups

    Fats

    Phospholipids

    Waxes

    Steroids

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    Figure2.15 Fats(triglycerides).

    3

    Dehydrationsynthesis

    3fattyacids+Glycerol Fat(triglyceride)

    Esterbond

    Saturatedfattyacid

    Monounsaturatedfattyacid

    Figure2.16 Phospholipids.

    Organicgroup

    Phosphategroup

    Glycerol

    Saturatedfattyacid

    Unsaturatedfattyacid

    Doublebond

    Hydrophilic(polar)head

    Hydrophobic(nonpolar)tails

    Symbol Phospholipid bilayer

    Unsaturatedfattyacid

    Cell

    Phospholipid

    OrganicMacromolecules

    Lipids

    Waxes

    Containonelongchainfattyacidcovalentlylinkedto

    longchainalcoholbyesterbond

    Lackhydrophilichead

    Completelyinsolubleinwater

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    Phospholipids

    Cholesterol

    Cellmembrane

    Figure2.17 Steroids.

    OrganicMacromolecules

    Carbohydrates

    Organicmoleculescomposedofcarbon,hydrogen,andoxygen(CH2O)n

    Functions

    Longtermstorageofchemicalenergy

    Readyenergysource

    Partofbackbonesofnucleicacids

    Convertedtoaminoacids

    Formcellwall

    Involvedinintracellularinteractionsbetweenanimalcells

    OrganicMacromolecules

    Carbohydrates

    Types

    Monosaccharides

    Disaccharides

    Polysaccharides

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    Figure2.18 Monosaccharides(simplesugars).

    Glucose

    configuration configuration

    N-acetylglucosamine

    Acetyl

    group

    Figure2.19 Disaccharides.

    1,6bond

    Hydrogen

    bondsHydrogen

    bond

    1,6bond

    Cellulose

    Amylose

    (unbranched)

    1,4bonds

    1,4bonds

    1,4bond

    1,4bond

    Glycogen

    Figure2.20 Polysaccharides.

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    OrganicMacromolecules

    Proteins

    Mostlycomposed

    of

    carbon,

    hydrogen,

    oxygen,

    nitrogen,andsulfur

    Functions

    Structure

    Enzymaticcatalysis

    Regulation

    Transportation

    Defenseandoffense

    OrganicMacromolecules

    Proteins

    Aminoacids

    Themonomersthatmakeupproteins

    Mostorganisms useonly21aminoacidsinprotein

    synthesis

    Sidegroupsaffecthowaminoacidsinteractwithone

    anotherandhowaproteininteracts withother

    molecules

    Acovalentpeptidebondisformedbetweenamino

    acids

    Figure2.21 Aminoacids.

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    Figure2.22 Stereoisomers,moleculesthataremirrorimagesofoneanother.

    Figure2.23 Thelinkageofaminoacidsbypeptidebondsviaadehydrationreaction.

    Carboxylgroup

    Aminogroup

    Dehydrationsynthesis

    Peptidebond

    DipeptideAminoacid2Aminoacid1

    Figure2.24 Levelsofproteinstructure.

    Peptide

    bond

    Primary structure

    Amino

    acid1

    Amino

    acid2

    Amino

    acid3

    Aminoacid4

    helix

    Secondary structure

    pleatedsheet

    Hydrogenbond

    pleatedsheets

    helix

    T er ti ar y st ru ct ur e Q ua te rn ar y st ru ct ur e

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    OrganicMacromolecules

    NucleicAcids

    DNAandRNAarethegeneticmaterialof

    organismsandviruses

    RNAalsoactsasenzyme,bindsaminoacids,and

    helpsformpolypeptides

    OrganicMacromolecules

    Nucleic Acids

    Nucleotidesandnucleosides

    Nucleotides

    Monomersthatmakeupnucleicacids

    Composedofthreeparts

    Phosphate

    Pentosesugar deoxyriboseorribose

    Oneoffivecyclicnitrogenousbases

    Nucleosidesarenucleotideslackingphosphate

    Phosphategroup

    Purineorpyrimidinenitrogenousbase

    Pentosesugar

    Deoxyribose Ribose

    Purines Pyrimidines

    Adenine(A)(UsedinDNAandRNA)

    Thymine(T)(UsedinDNA)

    Guanine(G)(UsedinDNAandRNA)

    Cytosine (C)(UsedinDNAandRNA)

    Uracil(U)(UsedinRNA)

    Figure2.25 Nucleotides.

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    OrganicMacromolecules

    NucleicAcids

    Nucleicacidstructure

    ThreeHbondsformbetweenCandG

    TwoHbondsformbetweenTandA(DNA)orUandA

    (RNA)

    DNAisdoublestrandedinmostcellsandviruses

    The twostrandsarecomplementary

    The twostrandsareantiparallel

    Figure2.26 Generalnucleicacidstructure.

    5'end

    Deoxyribose

    Phosphate

    Adeninebase

    Guaninebase

    Thymine base

    Cytosinebase

    Twohydrogenbonds

    Threehydrogenbonds

    Sugarphosphatebackbones

    5' C

    4'

    3' 2'

    1'

    O

    3'end

    5' 3'

    5' 3'

    A

    G

    T

    C

    C

    A

    G

    G

    A

    C

    T

    OrganicMacromolecules

    NucleicAcids

    Nucleicacidfunction

    DNAisgeneticmaterialofallorganismsandofmany

    viruses

    Carriesinstructions forsynthesisofRNAandproteins

    Controlssynthesisofallmoleculesinanorganism

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    Figure2.27 ATP.