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16. Biogenetic Pathways

Ametabolic pathway is a seriesof chemical reactions
occurring within a cell, catalyzed by enzymes, resulting
ineithertheformationofametabolicproducttobeused orstoredbythecell,ortheinitiationofanothermetabolic
pathway. Mainly metabolic pathways are concerned with:
Degradingmaterialstakeninasfood
They are required to synthesize specialized molecules
fromthebasiccompounds.
Theseprocesses demonstrate the fundamental unity ofall living matter, and are collectively described as
primary metabolism,with the compounds involved in
the pathways being termed primary metabolites. Primary metabolic pathways, which synthesize, degrade, and
generallyinterconvertcompoundscommonlyencountered inallorganisms.Theyareneededforgeneralgrowthand physiologicaldevelopmentofplantiswidelydistributed innatureandarealsoutilizedasfoodbyman.Typically, primarymetabolites are foundacross all species within
broad phylogenetic groupings, and are produced using the same pathway (or nearly the same pathway) in all these species.
The secondary metabolites such as alkaloids, glycosides,
avonoids,volatileoils,etc.arebiosyntheticallyderived fromprimary metabolites. Secondary metabolites, by
contrast,are often species-specic (or foundin only a smallsetofspeciesinanarrowphylogeneticgroup),and withoutthesecompoundstheorganismsuffersfromonly amild impairment, lowered survivability/fecundity, aestheticdifferences, or else nochange in phenotype at all.Theyareproducedforeasilyappreciatedreasons,e.g. astoxicmaterialsprovidingdefenceagainstpredators,as volatileattractantstowardsthesameorotherspecies,or
as colouring agents to attract or warn other species, but it
islogicaltoassumethatalldoplaysomevitalroleforthe well-beingoftheproducer.
Important features of secondary metabolites
They are unnecessarily restricted to a taxonomic group.
Theyprovide most of the pharmacologically active
natural products. Though secondary metabolites present in lesser quantities, they are main constituents
responsiblefor medicinal utility, hence areexpensive
to produce.
Theyareproductsduetoanyenvironmentalstressesor anyabnormalcondition,orserveasdefensive,protective oroffensivechemicalsagainstmicroorganisms,insects andhigherherbivorouspredators.
Theyalso act as waste or secretory productsof plant metabolismandareofpharmaceuticalimportance.
List of important secondary metabolites
Plant drug Secondary metabolite Activity
Cinnamomum zeylanicum Quinine alkaloids Antimalarial Catharanthus roseus Vincristin and vinblastin Anticancer Taxus species Taxol Anticancer Papaver somniferum Morphine Analgesic Digitalis purpurea Digitalis glycosides Cardiotonics
List of major metabolic pathways
Cellular respiration Glycolysis
Anaerobic respiration Kreb’s cycle/Citric acid cycle Oxidative phosphorylation
Creation of energetic compounds from non-living matter Photosynthesis (plants, algae, cyanobacteria)
Chemosynthesis (some bacteria)
Other pathways occurring in living organisms Fatty acid oxidation (β-oxidation)
Gluconeogenesis HMG-CoA reductase pathway (isoprene prenylation) Pentose phosphate pathway (hexose monophosphate) Porphyrin synthesis (or haeme synthesis) pathway Urea cycle
Basic metabolic pathways
Glycolysis(EMI:Embden-MeyerhofPathway):Glycolysis
represents an anabolic pathway common in both aerobic and anaerobic organisms. Glycolysis is the metabolic
pathwaythat converts glucose, C
,into pyruvate.
6H12O6
Thefreeenergyreleasedinthisprocessisusedtoformthe
high energy compounds, ATP (adenosine triphosphate)
andNADH(reducednicotinamideadeninedinucleotide).
Section 2 Pharmacognosy
269
Section 2 Pharmacognosy
270
Primary and secondary metabolites derived from carbon metabolism in plants
Inter-relationships of biosynthetic pathways leading to secondary constituents in plants
Biosynthesis of Aromatic Compounds
ShikimicAcidPathway:The shikmic acid pathway is a
keyintermediatefromcarbohydrateforthebiosynthesisof C6-C3units(phenylpropanederivative).Theshikimicacid
pathwayconvertssimplecarbohydrateprecursorsderived fromglycolysisandthepentosephosphatepathwaytothe
aromatic amino acids. The shikimic acid pathway is present
inplants,fungi,andbacteriabutisnotfoundinanimals.
Section 2 Pharmacognosy
271
Shikimic Acid Pathway
Amino acids: Aminoacidsoccurinplantsbothintheform
offreestate andasthebasicunits ofproteinsandother metabolites.Theyariseatvariouslevelsofglycolyticand
TCA systems.
Section 2 Pharmacognosy
272
Amino acids and its precursors
Amino acids Precursors
Glutamate family α-ketoglutarate Aspartate family Oxaloacetate Alanine–valine–leucine group Pyruvate Serine–glycine group 3-phosphoglycerate Aromatic amino acids Phosphoenolpyruvate
Erythrose-4-phosphate
Formation of Amino Acids
Biosynthesis of Glycosides
Theterm ‘glycoside’ is a verygeneral one which embracesall the many and varied combinations of sugarsandaglycones.Themetabolicprocessofglycoside formationessentially consists of two parts. The first partofbiosynthesisisthereactionsbymeansofwhich varioustypes of aglycones are formed,whereas the otherpart of biosynthesis process takes into account metabolicpathwayinvolvingcouplingofaglyconewith sugarmoiety.Thesynthesisofglycosidesinplantcells
involvesinteractionofnucleotideglycosidesuchasUDP­glucosewiththealcoholicorphenolicgroupofasecond compoundaglycone.Theprincipalpathwayofglycoside formationinvolvesthetransferofuridylyl group from uridinetriphosphate(UTP)tosugar-1-phosphateandthe
enzymes catalyzing this reaction are known as uridylyl
transferases.The subsequent reactioncontrolled by enzymaticsystemglycosyltransferasesinvolvestransfer ofsugarfromuridine diphosphate to aglycone moiety resultinginformationofglycoside.
Section 2 Pharmacognosy
273
Biosynthesis of Alkaloids
Alkaloid derived from ornithine: Ornithine is incorporated
intoboth pyrrolidine specifically and asymmetrically intopyrrolidineringoftropanenucleus,theα-carbonof ornithinebecomingtheC1oftropinenucleus.
Alkaloids derived from lysine: In biogenesisof the
anabasine,lupinine,andiso-pelletierineprecursorislysine.
Biosynthesis of Morphine and Codeine
Alkaloids derived from phenylalanine, tyrosine and related amino acids: These amino acids and their
decarboxylationproducts serve as the precursor for
ephedrine, colchicines and opium alkaloids.
Section 2 Pharmacognosy
274
Section 2 Pharmacognosy
275
Biosynthesis of Ephedrine
Section 2 Pharmacognosy
276
Section 2 Pharmacognosy
277
Biosynthesis of Ergometrine
Section 2 Pharmacognosy
278