an overview of biochemistry for biochem480 - about · pdf filewhat is the meaning of life? ......

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An overview of biochemistry for bioCHEM480 These are some of the most important topics in covered in an introduction to macromolecular biochemistry in this course: Acid-Base chemistry, the concept of pK A , conjugate acid/base pairs, and the use of Henderson-Hasselbalch equation V2 (i.e. Voet, Voet and Pratt Chapter2) Principles of bio-energetics; the laws of thermodynamics, equilibria, kinetics, Enthalpy & entropy V1,V12 Non covalent interactions (NCIs) and specific intermolecular recognition (SIR) V2 Functional groups in organic compounds & their major reactions including redox reactions Amino acids; classification by types of “R” groups V4 The peptide bond and protein structures (primary, secondary and tertiary) V4 & 5 Collagen and elastin; structure/activity/biological function relationship of fibrous proteins V6 Myoglobin & Hemoglobin; structure/activity/biological function relationship of globular proteins V7 The structure-activity-biological function relationship of saccharides V8 Plasma membranes; structure/activity/biological function relationship of lipidsV9 Lipid digestion and transport by lipoproteins and atherosclerosis V20 Membrane transport V10 Enzymes: activity, efficiency, specifity active/binding/catalytic sites, V10 Enzyme kinetics; Michaelis-Menten, Lineweaver-Burk plots, and regulation V12 The structure-activity-biological function relationship of nucleic acids V3 DNA sequencing and DNA engineering V3 For future reference The bioCHEM 481 course (‘Intermediary Metabolism’) will concentrate on biochemistry as it relates to: Biochemical signaling V 13 Overview of metabolism V 14 Chemical energy production and consumption; oxidative phosphorylation V14 & 18 Metabolism of carbohydrates: glycolysis, TCA cycle, gluconeogenesis, PPP, glycogenolyssis and glyconeogenesis V15, 16 & 17 Metabolism of triacylglycerols: degradation and synthesis of fatty acids V20 Metabolism of amino acids. V21 The bioCHEM 482 course will concentrate on biochemistry as it relates to: The integration of metabolism by different organs and hormones to maintain a dynamic equilibrium in mammals. The molecular processes of nucleotide metabolism in eukaryotic cells, particularly, mammalian tissues. The molecular processes in photosynthesis in plant and bacterial cells. The relationship between biochemical events at the molecular level to physiological processes in whole animals. The correlations of abnormal biochemical processes with human diseases and syndromes. The relationship between biochemical events at the molecular level to physiological processes in whole animals. The correlations of abnormal biochemical processes with human diseases and syndromes.

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Page 1: An overview of biochemistry for bioCHEM480 - About · PDF fileWhat is the meaning of life? ... , there exists a biochemical unity of diverse living organisms in ... dynamic process

AnoverviewofbiochemistryforbioCHEM480 Thesearesomeofthemostimportanttopicsincoveredinanintroductiontomacromolecularbiochemistryinthiscourse:

• Acid-Basechemistry,theconceptofpKA,conjugateacid/basepairs,andtheuseof Henderson-HasselbalchequationV2(i.e.Voet,VoetandPrattChapter2)

• Principlesofbio-energetics;thelawsofthermodynamics,equilibria,kinetics, Enthalpy&entropyV1,V12

• Noncovalentinteractions(NCIs)andspecificintermolecularrecognition(SIR)V2• Functionalgroupsinorganiccompounds&theirmajorreactionsincludingredoxreactions• Aminoacids;classificationbytypesof“R”groupsV4 • Thepeptidebondandproteinstructures(primary,secondaryandtertiary)V4&5 • Collagenandelastin;structure/activity/biologicalfunctionrelationshipoffibrousproteinsV6 • Myoglobin&Hemoglobin;structure/activity/biologicalfunctionrelationshipofglobular

proteinsV7• Thestructure-activity-biologicalfunctionrelationshipofsaccharidesV8• Plasmamembranes;structure/activity/biologicalfunctionrelationshipoflipidsV9 • LipiddigestionandtransportbylipoproteinsandatherosclerosisV20• MembranetransportV10• Enzymes:activity,efficiency,specifityactive/binding/catalyticsites,V10 • Enzymekinetics;Michaelis-Menten,Lineweaver-Burkplots,andregulationV12 • Thestructure-activity-biologicalfunctionrelationshipofnucleicacidsV3• DNAsequencingandDNAengineeringV3

ForfuturereferenceThebioCHEM481course(‘IntermediaryMetabolism’)willconcentrateonbiochemistryasitrelatesto:

• BiochemicalsignalingV13• OverviewofmetabolismV14• Chemicalenergyproductionandconsumption;oxidativephosphorylationV14&18 • Metabolismofcarbohydrates:glycolysis,TCAcycle,gluconeogenesis,PPP,glycogenolyssisand

glyconeogenesisV15,16&17 • Metabolismoftriacylglycerols:degradationandsynthesisoffattyacidsV20 • Metabolismofaminoacids.V21

ThebioCHEM482coursewillconcentrateonbiochemistryasitrelatesto:

• Theintegrationofmetabolismbydifferentorgansandhormonestomaintainadynamicequilibriuminmammals.

• Themolecularprocessesofnucleotidemetabolismineukaryoticcells,particularly,mammaliantissues.

• Themolecularprocessesinphotosynthesisinplantandbacterialcells.

Preamble

PREAMBLE:TheVitalQuestions:

ForfuturereferenceThebioCHEM481course(‘IntermediaryMetabolism’)willconcentrateonbiochemistryasitrelatesto:

• BiochemicalsignalingV13• OverviewofmetabolismV14• Chemicalenergyproductionandconsumption;oxidativephosphorylationV14&18 • Metabolismofcarbohydrates:glycolysis,TCAcycle,gluconeogenesis,PPP,glycogenolyssisand

glyconeogenesisV15,16&17 • Metabolismoftriacylglycerols:degradationandsynthesisoffattyacidsV20 • Metabolismofaminoacids.V21

ThebioCHEM482coursewillconcentrateonbiochemistryasitrelatesto: • Theintegrationofmetabolismbydifferentorgansandhormonestomaintainadynamic

equilibriuminmammals. • Themolecularprocessesofnucleotidemetabolismineukaryoticcells,particularly,mammalian

tissues. • Themolecularprocessesinphotosynthesisinplantandbacterialcells. • Therelationshipbetweenbiochemicaleventsatthemolecularleveltophysiologicalprocessesin

wholeanimals. • Thecorrelationsofabnormalbiochemicalprocesseswithhumandiseasesandsyndromes. • Therelationshipbetweenbiochemicaleventsatthemolecularleveltophysiologicalprocessesin

wholeanimals.

• Thecorrelationsofabnormalbiochemicalprocesseswithhumandiseasesandsyndromes.

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Whyislifethewayitis?Whatisthemeaningoflife?WhatisanswertotheUltimateQuestionofLife,TheUniverse,andEverything?[42?]Itstartshere……..

5majortenetsofbiology/biochemistryCelltheory:Hooke,vanLeeuwenhoek,SchleidenandSchwannEvolution:Naturalselection:Darwin&WallaceDNAandinformationflow:TheCentralDogma:WatsonandCrick&(now)EpigeneticsEnergy:Transductionfromlightandchemicalstousefulenergy(ATP)MitchellRegulation…homeostasisandadaptingtochangesatthemolecular/cellularlevelsLivingorganismsareremarkablysimilaratthemolecularlevel**despitetheobservedbiologicaldiversity.Innature,thereexistsabiochemicalunityofdiverselivingorganismsinthatthereisawiderangeofadaptationsaroundacommonchemicalframework(Canyounamesomecommoncompoundsfoundinalllivingspecies?).Thisembodiesjusttheuseofafewelementsi.e.mainlyNCHOPSthatexploitstheabilityofC(andNtoalesserextent)toformstrong(singleanddouble)covalentbondstobothtoitselfandtheseotherelements,especiallyHNOS(withlinear,cyclicandbranchedskeletons)togetherwithalimitednumberofmetalcations(Na,K,Ca,Mg,Mn,Fe,Co,Zn,etc.)toformneutral,cationicandanionicchemicalspecies.Theuniquefeatureofalllivingcellsisthewayinwhichsomanyreactionsthattakeplaceintheorganellesofcells(andcellsintissuesandtissuesinorgansandorgansinorganismsandorganismsinecosystems,etc)areorganizedtoserveasinglepurpose,"life"!**However,theresomesignificantdifferencesbetween'biologicaldomains',i.e.(1)theabilityofsomearcheatosurviveinzerooxygenandseeminglyhostileconditions,i.e.>80oC,highpressures,highsalt,etc),(2)theinventionofphotosynthesisbybacteria(andpassedontoplants),(3)thepossessionofcytoskeletonsbyeukaryaallowingforlargeandcomplexcellstructures.Theunderlyingcommonalityofbiochemicalprocessesarebrieflyreviewedinthefollowing12concepts. Beforeyouembarkasastudentinthisbiochemistrycourseyoushouldreadtheseconceptsforunderstanding.

1. Cells:theirroleandtheircontents. Thecellisthefundamentalunitoflife.Cells,whethertheybeunicellularormulti-cellularorganisms,mustoperateas"open"thermodynamicsystemsbyestablishingadynamicequilibriumwiththelocalmicroenvironment.Livingorganismscreateandmaintainacomplexsystemusingenergy(solarorchemical)extractedfromtheenvironmentandtheyhavetheabilitytodischargewastes.

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Thereisnosuchitemasan‘averagecell’.Whatmakesthendifferent?

Allcellsarecomposedofamixtureof(a)smallchemicalspecies(organicandinorganic),(b)intermediate-sizedorganiccompounds,(c)macro-moleculesand(d)organellesinaclearhierarchy(seefigureonfollowingpage).

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Intheintestines, digestiveenzymescatalysetheconversion(viahydrolysisreactions)ofproteinstoaminoacidsV21,complexcarbohydratesto(mainly)glucoseV15,fats/oilstofattyacidcarboxylates(RCO2

-)andglycerolV20asinthereverseofthearrowsinthediagramaboveforproteinspolysaccharidesandtriglycerides. Thebacterialcellsharboredwithinthehumangastrointestinaltract(GIT)outnumberthehost’scellsbyafactorof10andthegenesencodedbythebacteriaresidentwithintheGIToutnumbertheirhost’sgenesbymorethan100times.Thesehumandigestivetractassociatedmicrobesarereferredtoasthegutmicrobiome.

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Thegutmicrobiotainhumansevolvethroughoutlifeandappeartoplayapivotalroleinbothhealthanddisease.Inahealthystate,thegutmicrobiotahavemyriadpositivefunctions,includingenergyrecoveryfrommetabolismofnondigestiblecomponentsoffoods,protectionofahostfrompathogenicinvasion,andmodulationoftheimmunesystem.Further,lackofthemisanecdotallyassociatedwithanumberofdiseases,syndromesand‘functionalaberrations’.

FuelMetabolism:

Asuccessfulorganismhastobeabletosynthesizecompoundsnotsuppliedbythedietinordertosurvive.Thisincludescompoundsofhighchemicalpotentialenergy(i.e.ATP)forbothgrowth,developmentandforprotectionofitsinternalenvironmentfromvariableexternalconditions(i.e.fromthewell-fedtostarvationstates,temperature,O2availability,xenobiotics,etc).

Fiveprocessesarerequired:

(1)conversionofnutrientsinthedietintouseablecompounds,

(2)oxidationofenergy-richmetabolites(seesection6page8)toATP

(3)storageandsubsequentmobilizationofnewenergy-richcompounds,

(4)biosynthesisofcrucialmetabolitesandnon-fuelmacromolecules(proteins,poly-nucleotides,somepolysaccharides,etc)

(5)detoxificationprocessesinwastedisposalpathways.

2.Macromolecules. Macromoleculesareubiquitousinalllivingspeciesandhavecomplexbutsomewhatflexiblestructures. Theystoreandexpressgeneticinformation,providefor

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compartmentation,regulatemanyfunctions,andimportantly,allowforbiologicalspecificitybyspecificinter/intra-molecularrecognition(SIR).Macromoleculesfoldintocomplex3-Dstructures(‘conformations’)insuchawayastoenhancetheirstabilitybymaximizingintra-(i.e.internallywithinthemacromolecule)andinter-(betweenthemacromoleculeandthesolvent-usuallywaterexceptinmembranesandmicelles)molecularnon-covalentinteractions(‘NCI’).V2. Macromoleculesspontaneouslyfoldtoachievetheconformationofhighestthermodynamicstabilitythatisorisveryclosetotheconformationofthehighestbiologicalactivity.Itshouldbenotedthatthisfoldingisadynamicprocessandthesemacro-moleculescantakeupmorethanoneconformation,andthereisaconstantswitchingbetweentheconformations(inequilibria)dominatedbythedrivetothermodynamicstabilityunderpossiblyconstantlychangingmicro-environments(i.e.temperature,pH).

Thedrivingforcesfortheformationofthese3Dstructuresisconsideredtobepredominatelyentropicallydriven.Recallthatforanyspontaneousprocess(ΔGo=ΔHo-TΔSoV1),ΔGomustbe<0.[ChangeisconventionallyabbreviatedΔ]Considerthefoldingofaproteinfromtherandomorunfoldedconformationjustformedontheribosometoformingitsnativeorfoldedconformation.TheNCINETenthalpychangesis~0,butthespontaneityinvivorequiresNETΔSo>0.

Initially,watermoleculeshavetoform'cages'thatsurroundthenonpolarorhydrophobic‘R’groupsoftheaminoacidresiduesintherandomconformation.Asthemacromoleculefoldsthesenon-polar groupsonthepolypeptidechainformanon-polarcorethatstabilisesthemacromoleculebythe'expulsionorfreeingup'(tobulksolution)ofthesewatermolecules.TheeffectofthisistocauseextensivedisorderofthewatermoleculesandthusΔSoisNETpositiveandthusdrivestheNETspontaneousfolding(withΔGo<0).V2

Someproteins(especiallymultisub-unitand/ormulti-domainproteins)areknowntouseotherproteins(disulfideisomerases)V4andchaperoninsV5)tocatalysetheseproteinfoldingprocesses.

Manyoftheseindividualmacro-moleculeswithspecificbiochemicalrolesthenspontaneouslyselfassembleinto"supra-molecularassemblies"(suchaschromosomes,ribosomes,multi-enzymecomplexes,membranes,seehierarchydiagramabove).

Thechemicalstructureandthemicroenvironmentofamacromoleculedeterminesitschemical(re)activitywhichinturndeterminesitsbiologicalfunction.Thisisknownasthe'structure/activity/biologicalfunction'(SAF)relationship[St->Act->Biol.Funct.]

Thusanychangesinstructure(chemicalorconformational:temporaryorpermanent)willcausechangesinactivityandfunction[ΔSt->ΔAct->ΔBF]Anexampleisaproteinbecoming'denatured'bychangesinpH;ΔpH->Δ[ConjugateBaseorCB]/[conjugateacidorCA]foreveryionisablegroup->ΔNCI->ΔStructure/conformation->ΔActivity->ΔBiolFunct).

Sicklecellanaemiarepresentsanotherexample:(V7)ThisdiseaseiscausedbyagenemutationthatleadstoachangeinaminoacidresidueonthesurfaceoftheβsubunitfromHbA(theβ6isaGlu)toHbS(β6isaVal).Thus,comparingHbAandHbS,therewillbeanalterationofthetypeofNCIsthatinwhichthese‘R’groupswillbeinvolved. ThisHbAGluwillbesolvatedbywaterwhereasinHbS,theValhasanon-polarhydrophobic‘R’group.To‘avoid’thisexposureoftheisopropylgroupinValtowater,HbSundercertainconditions,changesitsstructureandaggregatesintoinsolublefibrils. ThusachangeinstructurecauseschangesinNCIsthatcauseschangesinstructuresthatinturncausesachangeinbiologicalfunction(i.e.decreasedabilitytotransportoftransportofO2)

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Otherexamplesinclude(1)cysticfibrosis(CF)usuallycausedbya3base/1aminoacidresiduedeletionintheCFTRproteinthatresultsinmisfoldingthanleadstoachangeinmembranepermeability,(V9)and(2)phenylketonuria(PKU)causedbymutationsinthePAHgeneandthusdiminishedenzymeactivitycauseabuildupofPhe(andsomeofitscatabolites)thathasadeleteriousphysiologicaleffect. (V21)

Mostmacromoleculesarechemicallyalteredorprocessedfromtheirinitialformationtothemature,activeconformation. Examplesinclude(i)modificationofaminoacidresiduesincollagenV5,(ii)additionofthehemeunittohemoglobin,myoglobin,andcytochromes,(iii)covalentmodificationbyphosphorylationinregulatoryenzymes,(iv)formationofglycoproteins,proteoglycansandglycolipidsV8(v)conversionoftheprimarytranscript(hnRNA)tothematuremRNAineukaryotesand,(vi)themethylationandacetylationofthebasesofDNAandthehistonesinthechromosomes(in‘epigenetics’).Mostprocessingrequiresspecificenzymesandrepresentsaformofregulationinvivo.

3.BiochemicalReactions. Thebiochemicalreactionsthattakeplacewithinthecellareasubsetofordinaryorganicreactions. Thesamerulesofelectronflow[relatedto(a)relativebondstrengths(b)bondbreaking&formation,(c)orbitalinteractionsofnucleophilicandelectrophilicatoms/sitesandthermodynamicstabilityofreactionintermediatesapplyinvivoasinvitroasdothelawsofthermodynamics!Biochemistry,asmostgeneralisedtextscurrentlypresentit,isacontinuationoforganicchemistrybutinaspecialmedium(water,pH7.4,ionicstrength~0.2M,37oC,etc).Thetypicalundergraduatebiochemistrycourseisinessenceanadvancedorganicchemistrycoursethatfeaturesthemoleculesandchemicalprocessesof'life'(seeearlier).Asyoustudyit,youwilldrawheavilyonwhatyoulearnedinorganicchemistry,aswellasgeneralchemistryI.e.bioenergetics).Examinationofapathway,i.e.glycolysis(V15),TCAcycle(V17),andFAcatabolism(V20)oftheproteins,fats/oilsandcarbohydrates,etcwillrevealtypesofreactionscoveredonorganicchemistry;i.e.dehydrationofalcohols,formationandhydrolysisofesters,amideandacetals,aldol/Claisen/mixedaldol-Claisencondensations,oxidationofalcoholsandaldehydes,etc.Onemajoromissionintheundergraduatecurriculumistheubiquitous(invivo)nucleophilicsubstitutionatP=OthatisusuallynotcoveredbutisanalogoustothesametypeofreactionatC=O(viaapentahedralratherthantetrahedralintermediate)requiringincomingnucleophilesandleavinggroupsusuallyphosphatesorthioethers).4. Metabolic Pathways. Biochemical reactions are organised in specific 'metabolic' pathways(glycolysis, gluconeogenesis, FA catabolism and synthesis, PPP (V15) amino acid and nucleosidecatabolism and synthesisV23, etc.Many intermediarymetabolites [‘IM’] (i.e. glucose-6’P, pyruvate,acetyl-CoA, succinate, asp(D), glu(E) etc.) servemore than one function, i.e. catabolised for energy(leadingtoATPformation)orusedas'building'blocksforthesynthesisoflargercompounds(requiringATP).FormoreclickontheselinksOverviewofCatabolismandATP/NADProles.

InordertoachievetheoptimaluseoftheATPsynthetisedbyanorganism,itiscrucialthatthefluxofchemicalsthroughthesepathwaysberegulatedtoprevent‘futilecycling’.Suchregulationisachievedbycontroloftheactivitiesofspecificenzymesbyallostericeffectors,covalentmodification,hormones,etc.(See#9belowformore.)Thediagrambelowillustratesbothsomeofthepathwaysand,importantly,theessentialinter-connectivityofthesepathways.

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AmajorityofthecompoundsinlivingorganismscontainonlyC,HandO.ThenextmostcommoncombinationisCHOandN(aminoacids,proteins,nucleotides,etc).Onaverybasiclevel,‘CHO’endsupasCO2andwaterbutwithnitrogencontainingcompounds,organismsrequirespecialisedpathwaystoeliminateexcessnitrogenouscompounds.Inhumans,thisisaccomplishedmainlybytheformationandexcretionoftheverywater-solubleureaintheurineV21.Thisissynthetisedintheliverandeliminationviathekidneys.Anyammoniatransientlyformedbythedeaminationofaminoacidsetc istransportedfrommosttissuestotheliverwheretheNisincorporatedintoureabytheureacyclerequiringATP.TheureaandTCAcyclesarechemicallyinterconnected.

TransportofwaterinsolubleIMs:Therearealimitednumberofcompoundsoflowsolubilitiesinwater(i.eO2,cholesterols,TAG,FFA)sotheseneedspecifictransportpathwaystoensuretheappropriateconcentrationsofsuchcompoundsattheirspecificsitesofaction.5.Enzymes. Most,butnotall,reactionsinvivowouldeffectivelyNOTtakeplace(especiallyunderthespecialconditionsofmostcells)withoutthepresenceofspecificenzymes(V11). All(almost!)biochemicalreactionstakeplaceinactivesitesofenzymes:substratesbindcustomisedbindingsitesandthechemistry(bondbreakingandformation)ofthereactionsarecontrolledbythecatalyticsiteoftheenzyme.Thereiselectronic(byNCIs)andsteric(byspacerequirements)complementaritybetweenthesubstratesandthebindingsites.Thesubstrates"dock"ontothebindingsitesinspecificorientations(thiscontrolstheregiospecificityofreactions)insuchawaythattheflowofelectrons(see#3above)allowedinthe"catalyticsite"isinonlyonespecificdirection(thiscontrolsthestereospecificityofreactions).Thepresenceofenzymesisthekeytowhatreactionsactuallytakeplace(andatwhatrate)ataspecificbiologicalsitegiventhatthereusuallymanyhundredsofcompoundsavailableatanysuchsite.Specificinter-andintra-molecularrecognition[SIR]isoneofthecharacteristicsofbiochemistryandisespeciallyimportantinenzymespecificity.. Theratesofbiochemicalreactions(andthustherateofaccumulationofproducts)arecontrolledbytheconcentrationofenzymesintheir'active'conformation[Enz]active.[Enzyme]iscontrolled(ata'coarse'level)byboththerateofformationofthehnRNAfromthegeneandrateofprocessingofthe

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hnRNAtomRNA(..andthislatterprocessishighlyregulatedbysmallRNAmolecules).Othertypesofenzymeactivity'fine'regulationareallosterismandhormone-controlledcovalentmodificationbyphosphorylation(requiring‘kinases’)anddephosphorylation(requiringphosphatases’).SeeVp617foranexampleTheseenzymescanberegulatedinwellorganisedin‘enzymecascades’(SeeVp424&535foranexample Fluxinbiochemicalpathwaysisregulatedbychangesintheactivitiesofspecificenzymes. Enzymaticactivityisregulatedbymultiplemechanismincluding(1)bindingviaNCIsofspecificintermediarymetabolites(allostericregulators),e.g.ATP,ADP,NAD+,NADH,NADP+,NADPHetc.usingnegativefeedbackandforwardactivation,(2)reversiblecovalentmodificationoftenbyphosphorylation/dephosphorylationofAAresiduessuchasTyr(Y)andSer(S)ontheproteininreactionsthatrequirespecificenzymesand(3)byhormonaldirectedactivation/deactivationofproteins)V12. Generally,entirebiochemicalpathwaysarecontrolledbytheregulationofoneortwospecificenzymes,PFK-1inglycolysis,ACCinfattyacidmetabolismandHMGCoAreductaseincholesterolsynthesis. Clicktheselinksforexamplesofregulationinthesespecificpathways:TCA&Glycolysis.

Manyenzymes,especiallytransferases(V11),requirenon-protein‘co-factors’forfullbiologicalactivity. Theseco-factorscanbemetalions,coenzymes(derivedfromwatersolublevitamins(V14)heme,etc.Someareboundtotheenzymebynon-covalentinteractions(NCIs)andotherbycovalentbonds.6.RedoxReactions:DerivingEnergy. Thebasisofvirtuallyallenergytransductionprocessesinlivingcellsisthroughredoxreactions(i.e.electronflow)Oxidationreactions(involvingreleaseofelectrons)arenearlyalwaysexothermic/exogonicwhereasreductionreactions(involvingacceptanceofelectrons)arenearlyalwaysendothermic/endogonic.Thusfood(carbohydrates,fats/oilsandproteins)isdigestedintheintestinesbyhydrolysisreactionstoproducts(glucose,fattyacids,glycerolandaminoacids)thatcancrosstheepithelialcellsintothebloodstreamandaresubsequently(incatabolicprocesses)oxidisedbyconvertinghighenergyC-HbondsintoC=Oinatwopartprocessinvolving(1)hydrideiontransferfrom'intermediarymetabolites'toNAD+andFAD(nature'stwooxidisingagents)and(2)recycling/oxidizingtheresultantNADH&FADH2backtoNAD+&FADbythereducingagentoxygen(usually)withtheconcomitantformationofATPfromADP&Piinthemitochondria.V14BiosynthesisisNETreductionandsorequiresareducingagent(NADPH)andanenergysource(ATP)

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Linkedimagestoillustratethisredoxconcept:Glycolysis TCA Gly/TCA FAcatabolism FAmeta Lipid Fuelmeta ETS/NADH ETS/ATP ETS/detail7.SyntheticReactions:UsingEnergy. Manybiochemicalsyntheticreactionsrequireenergy:thisisusuallycarriedoutbychemicallyactivating(1)onesubstratebyreactionwithATP(oritsequivalent,UTP,GTP,CTP,etc)toformphosphateestersormixedcarboxylic/phosphoricanhydridesor(2)activatinganenzymebyphosphorylatingspecificfunctionalgroups(i.e.OHinaminoacidresidues).Thusistheexogonicityofonereaction(ATPtoADPorAMP)isusedto'drive'theendogonicityofanotherreactionsothattheNETΔGomustbe<0 Examples:ATPCoupledreactionsActivationofaminoacidfortransfertotRNA 8.Compartmentalization. Biochemicalreactionsarelocalisedintimeandspaceinacell.Compartmentationisakeytoacell'sorganisation.Thisseparationismaintainedbywaterinsolublelipidmembranes.However,theseorganisationalprocessesdecreaseentropyandthusrequireenergyforthesynthesisandsubsequentassemblyofthemembranesbuttheNETresultisΔGo<0solifeproceeds!

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9.Signaltransduction. Communicationbetweendifferenttissuesisrequiredinmulti-cellorganisms.Thisrequireshormones(thatcanbeproteins,peptides,steroidsandamines)tobereleasedbyonetissuetocauseoneormorebiochemicalchangesinanothertissue.Membrane-boundreceptorsinitiallybind(byspecificNCIs)thesechemicalmessengers(V13)andchangethe'biochemistry'(thepathways)insidethecell.

10.GenometoProteomeandback!. ConventionalversionCurrentversion

GeneticinformationisstoredasDNA(usingmainlyonlyfourdifferentbases(A,G,C&T) andisusedtodirectthesynthesisofproteinsviaRNAintermediates(usingmainlyfourdifferentbases(A,G,C&U)invirtuallyallorganisms(exceptretroviruses).SeeCentralDogmasabove TheseconddiagramreflectsthecurrentideasdeducedfromrecentepigeneticstudiesthatsomesmallRNAsandproteinhistonesareinvolvedinthecontrolofgeneexpression.Thischangeseverything! Clearlyareal“paradigmshift”Eachgenus/speciesisdefinedbyadistinctsetofmacromoleculescodedfromthegenome.Thelastpartofthiscoursetherewillbecoverageofproteinsandnucleicacids.Itisassumedthatyouarefamiliarwiththefundamentalbuildingblocksofproteins,theaminoacids,andofDNA&RNA,thenucleotidebases(seebelow)alongwithageneralunderstandingofthestructureofDNAandRNA,andhowtheyareproducedand,inthecaseofDNA,replicated,andofthegeneticcode.

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TheGeneticCodeV27, insidefrontorbackVVPcoverandnextpage

ThegeneticcodereferstothetripletsequenceofbasesinRNAthatrecognizethespecifictRNAcarryingaminoacidstobeincorporatedintoprotein.EachtripletonribonucleotidesiscalledacodonandspecifiesatRNAcorrespondingtooneofthe20aminoacids,oritencodesastopsignal.Athreebasecodeproduces64possibletripletcodons(43or4x4x4=64),andeachisusedforanaminoacidorastopcodon,sothegeneticcodeisdegenerate(thatis,someaminoacidsareencodedbymorethanonecodon).ThecodonsaretranslatedsequentiallyfromastartsiteonthemRNA,aninitiationcodon,whichisalmostalwaysAUG,whichencodesmethionine.ThestopcodonsareUGA,UAA,andUAG.Thegeneticcodeisnearlyuniversal,mitochondriaexcepted,butdifferentorganismsdouseparticularcodonspreferentiallytoinsertthesameaminoacid.

TheAminoAcidsV4&21

BycoverageofV4,youwillneedtobefamiliarwiththestructures(androlesinproteinsofAAresidues)ofalltheaminoacidsandtheirabbreviations(boththreeletterandoneletter).ThemostimportantaspectisknowingthefunctionalgroupsofeachAAandhowtheAAareclassifiedintousefulgroups NEUTRAL(polar/aliphaticnonpolar/aromaticnon-polar),IONIC(charged+/-),andwhethertheFGsarehydrophobicorhydrophilicorboth!).

ManipulationoftheHenderson-Hasselbalchequationisamustforthiscourse!

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11. Biochemical Interconnectedness. Organelles, cellsandorganismsarechemicallydependentoneachother(‘synergy’).Ecologyfortheday!Tosurviveyouhavetobeahunter-gathererinthewilds,your garden or at the supermarket for nutrients. All terrestrial species rely on the physical andchemicaldecompositioninsoilofthewastes/deadofsomeorganismssothatthedecayproductsarethefuelforothers(Ncycleimage).Natureistheultimaterecycler! Manyenvironmentalproblemshavebeencausedbytheinductionand(over-)useofnon-biodegradablecompoundssuchasbiocidesincludingDDT-e.g.RachaelCarlson'sSilentSpring-,CFCs(stratosphericozonethinning),PCBs,syntheticpolymers-plastics,fibers,foams,paints,etc)inthelast150years.12.EvolutionaryInterconnectedness. Allsuccessfulorganismsmustbecapableofself-assembly,self-replication,catalysis,andallowforsomemutations. Thisisthebasisoftheevolutionarydevelopmentoflife. Biochemicalsystemshavebeenevolvingatleast~3.8billionyearsandalllivingsystemsarerelatedthroughacommonevolutionarypathway.Livingorganismsareremarkablysimilaratthemolecularleveldespitetheobservedbiologicaldiversity.Thus,innature,thereexistsabiochemicalunityofdiverselivingorganismsinthatthereisawiderangeofadaptationsaroundacommonchemicalframework.