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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.