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BIOMOLECULES
SHAHINA AKHTER
XI A
GULF ASIAN ENGLISH SCHOOL
BIOMOLECULES
1. ANALYSIS OF CHEMICAL COMPOSITION OF LIVING ORGANISMS
Take a living tissue, weigh & grind it in trichloroacidic acid
Thick slurry is filtered through cheese cloth
Filtrate
Retentate
Inorganic compounds ash analysis
Living tissue is weighed to get wet weight
This is dried dry weight
C CO2 + H2O
Ca, Mg, Na, K
2.BIOMOLECULES OF CELLS
CHEMISTRY
http://upload.wikimedia.org/wikipedia/commons/thumb/4/40/Ketone-group-2D-skeletal.svg/150px-Ketone-group-2D-skeletal.svg.pnghttp://www.daviddarling.info/images/aldehyde.pnghttp://www.hcs.ohio-state.edu/hcs300/gif/benz1.gifBIOLOGICAL
MICROMOLECULES
MACROMOLECULES
M < 1000 MICROMOLECULES
(i)Amino acids(ii)Sugars(iii)Nucleotides(iv)Lipids
M > 1000 BIOMACROMOLECULES
(i)Polysaccharides(ii)Nucleic acids(iii)Proteins
Acid-soluble fraction cytoplasmic composition
Acid-insoluble fraction macromolecules of cytoplasm + cell organelles
COMPONENTS
%
Water
Proteins
Nucleic acids
Carbohydrates
Lipids
Ions
70 9010 155 7About 3About 2About 1
3. AMINO ACIDS
http://homepages.ius.edu/dspurloc/c122/images/aminostrc.gifBasic amino acids
Lysine
(ii)Acidic amino acids Glutamic acid
(iii)Neutral amino acidsAlanine
http://0.tqn.com/d/chemistry/1/0/6/V/1/lysine.pnghttp://image.shutterstock.com/display_pic_with_logo/904822/98885087/stock-photo-amino-acid-glutamic-acid-structural-formula-98885087.jpghttp://0.tqn.com/d/chemistry/1/0/I/V/1/alanine.pngAromatic amino acids
http://0.tqn.com/d/chemistry/1/0/4/N/1/phenylalanine.jpgPhenyl alanine
4.SUGARS
Monosaccharides : simplest sugars, which cannot be hydrolysed further into smaller sugars
Composed of 3-7 C atoms :
(i) Triose (3C) (Glyceraldehyde)
(ii) Tetrose (4C) (Erythrose)
(iii) Pentose (5C) (Ribose)
(iv) Hexose (6C) (Glucose)
(v) Heptose (7C) (Sedoheptulose)
http://img.tfd.com/mgh/ceb/thumb/Structural-formula-for-x3b1-D-glucose.jpghttp://img.tfd.com/mgh/ceb/thumb/Structural-formula-for-x3b1-d-galactose.jpgGlucose
Galactose
Monosaccharides have either a free CHO / CO group reducing sugars
Oligosaccharides : when 2/ few monosaccharides are combined by glycosidic bonds
They are named as:
(i) Disaccharides (2) : Sucrose
(ii) Trisaccharides (3) : Arabinose
(iii) Tetrasaccharides (4) :Stachyose
(iv) Pentasaccharides (5) : Verbascose
http://img.tfd.com/mgh/ceb/thumb/Formula-for-maltose-x3b1-form-indicates-reducing-group.jpgMaltose
5.LIPIDS
Heterogenous group of organic compunds
Water insoluble but soluble in non-polar organic solvents
Lipids
Straight chain compounds
Fused hydrocarbon rings+ long hydrocarbon chain e.g, cholesterol
Simple lipids
Oil Fats Waxes
Phospholipids Glycolipids Sphingolipids
Compound lipids
http://www.npalab.com/chemistry/cholesterol/index_files/cholesterol-2d.pngCHOLESTEROL
Lipids fatty acid
COOH R ( -CH3 , -C2H5 , -CH2)
http://www.chemspider.com/ImagesHandler.ashx?id=960&w=200&h=200PALMITIC ACID
Fatty acids
Saturated fatty acids butyric acid
Unsaturated fatty acids linoleic acid
http://www.lookchem.com/UserFilesUpload/323.gifhttp://0.tqn.com/d/chemistry/1/0/b/K/1/Linoleic_acid.jpgSimple lipid glycerol
Formed by esterification of glycerol with fatty acids monoglycerides , diglycerides , triglycerides
Fats high m.p & remain soilds at room temp (Butter)
Oils low m.p & remain liquids at low room temp (Sunflower oil)
http://home.roadrunner.com/~lubehawk/BioHELP!/glycerol.jpghttp://img.tfd.com/mgh/ceb/thumb/709700SX.jpgPhospholipids when lipids have P & phosphorylated organic compounds e.g. lecithin
Brains have sphingolipids
http://www.medicinescomplete.com/mc/excipients/current/images/ExclecithinC001_default.pngPHOSPHOLIPID - LECITHIN
6.NUCLEOTIDES
Phosphorylated nucleosides adenylic acid, guanylic acid, thymidylic acid, cytidylic acid & uridylic acid
N base attached to pentose sugar adenosine, guanosine, thymidine, cytidine & uridine
http://library.thinkquest.org/27819/media/bases.gifPurine + pyridimine monomers
Higher nucleotides store energy in their high energy P bonds
Nicotinamide + riboflavin coenzymes
Coenzymes : non protein organic moiety of holoenzyme
7.PRIMARY & SECONDARY METABOLITES
PRIMARY
SECONDARY
IDENTIFIABLE FUNCTIONS
PRDTS OF CERTAIN METABOLIC PATHWAYS
PRIMARY METABOLITES amino acids, N bases, proteins, nucleic acids, etc.
SECONDARY METABOLITES
(i) Pigments : Anthocyanin, carotenoids
(ii) Drugs : Vinblastin, curcumin
(iii) Alkaloids : Morphine, codeine
(iv) Essential oils : Lemon grass oil
(v) Lectins : Concanavalin A
(vi) Terpenoids : Monoterpenes
(vii) Toxins : Abrin, Ricin
(viii) Polymeric Compounds : Rubber, cellulose, gums
8.BIOMACROMOLECULES
M > 1000 daltons
Found in acid insoluble fraction
POLYSACCHARIDES NUCLEIC ACIDS PROTEINS LIPIDS
9. POLYSACCHARIDES
HOMOPOLYSACCHARIDES(CELLULOSE , STARCH)
HETEROPOLYSACCHARIDES(CHITIN)
http://cavemanchemistry.com/oldcave/projects/twine/cellulose.gifMONOMER GLUCOSE
PRESENT IN PLANT CELL WALL
Starch Glycogen Inulin
GLUCOSE
GLUCOSE
FRUCTOSE
PLANTS
ANIMALS
STORAGE POLYSACCHARIDE
STORAGE POLYSACCHARIDE
http://www.braukaiser.com/wiki/images/1/15/Glycosidic_bond.gifhttp://2.bp.blogspot.com/-5gzIXKpfex4/T4E5EQzlTGI/AAAAAAAAAUQ/E3oaEEZSrUk/s1600/image002-717790.png
Amylose
http://www.rsc.org/Education/Teachers/Resources/cfb/images/amylose.gifhttp://t3.gstatic.com/images?q=tbn:ANd9GcSdDzt8-ayCqB0o2JnMGXsjDr9RpI-Th3PSEMFHBXJ_6Zbw4ZfKUa0r1UgNHAAmylopectin
http://www.rsc.org/Education/Teachers/Resources/cfb/images/amylopectin.gifhttp://i30.photobucket.com/albums/c349/wee-mama-xyz/graphs/Amylopectin1.jpg10.NUCLEIC ACIDS
DNA
RNA
http://www.ib.bioninja.com.au/_Media/phosphodiester_bond_med.jpeghttp://www.nature.com/scitable/content/24298/sadava_11_9_large_2.jpgRIBONUCLEIC ACID (RNA)
http://www.museumoftheearth.org/sites/halfshell/img/molec/RNA_lg.jpghttp://www.mun.ca/biology/scarr/Fg10_09b_revised.gif mRNA : Carries information from DNA to ribosome
Decides sequence of amino acids
tRNA: Carries an amino acid from cytoplasm to r ibosome
rRNA: Forms parts of ribosomes
Forms part of seat of protein synthesis
11.PROTEINS
Heteropolymers containing string/strings of amino acids
Types of proteins result from 20 amino acids
Depending on
(i) no. of amino acid residues
(ii)sequence of amino acids
STRUCTURE OF PROTEINS
(i) Primary structure
http://images.tutorvista.com/content/cellular-macromolecules/protein-primary-structure.jpeg(ii) SECONDARY STRUCTURE
http://www.abcte.org/files/previews/biology/BioMod%203%5B1%5D.3%20secondary%20structure.jpg(iii) TERTIARY STRUCTURE
http://upload.wikimedia.org/wikipedia/commons/thumb/b/bf/TRNA_all2.png/250px-TRNA_all2.png(iv) QUARTERNARY STRUCTURE
http://chemistry.umeche.maine.edu/MAT500/1bl8-2.jpgCLASSIFICATION
PROTEINS
FIBROUSPolypeptides arranged in parallel bundles (silk fibres, keratin & collagen)
GLOBULARPolypeptides become coiled & folded (albumin, globulin, haemoglobin )
http://www.nd.edu/~aseriann/fibglob.gifPROTEINS
SIMPLEComposed of amino acids(histones, albumins)
CONJUGATEPeptide chain & cofactor
http://www.precisionnutrition.com/wordpress/wp-content/uploads/2009/12/Figure-1-Histones-1024x1022.jpghttp://users.rcn.com/jkimball.ma.ultranet/BiologyPages/P/Peptide.gifCONJUGATE PROTEINS
Chromoproteins pigments along with amino acids (haemoglobin)
Lipoproteins lipids in their molecules (egg yolk)
Phosphoproteins phosphate grp with amino acids (casein of milk)
Metalloproteins contain metallic ion with amino acids (Zn carbonic anhydrase)
Glycoproteins contain carbohydrates with amino acids
Nucleoproteins contain nucleic acids with amino acids (virus)
PROTEINS FUNCTIONS
Collagen Intercellular/extracellular ground substance
Trypsin Enzyme to digest protein
Insulin A hormone that regulates glucose level
4.Gamma globulin Antibody, that fights against infections5.Receptors Proteins that receive stimulus/substance6.GLUT- T Regulates transport of glucose into cells
12.CONCEPT OF METABOLISM
METABOLIC PATHWAYS DYNAMIC STATE OF BODY CONSTITUENTS
LINEAR
CIRCULAR
http://www.pancreaticdiseasecenter.org/wp-content/uploads/2012/03/metabolomics_11.jpghttp://www.laetusinpraesens.org/docs/images/ching00a_files/image024.jpgMETABOLISM
ANABOLISMMore complex compounds are formed from simple ones (proteins synthesis)
CATABOLISMComplex substance is broken into 2 / more smaller substances (Digestion of proteins by peptides
13. ENZYMES
CHARACTERISTICS OF ENZYMES
Proteins that catalyse biochemical reactions in living cells
Each enzyme catalyses the reaction of 1 substrate
Each enzyme requires a specific pH & temp
They accelerate a reaction
SIMILARITIES BETWEEN ENZYMES & INORGANIC CATALYSTS
Catalysts remain unchanged at the end of the reaction & they can be used again
Required in far less quantities as compared to the substrate
Do not initiate a reaction, but rate of reaction by lowering activation energy
Do not alter eqm of a reversible reaction
Form short-lived complexes with substrates
DIFFERENCES B/W ENZYMES & INORGANIC CATALYSTS
NOMENCLATURE OF ENZYMES
Adding suffix ase to the substrate on which they act e.g.,sucrase , protease etc.
Acc. To physiological activity it catalyses e.g.,oxidase , dehydrogenases, decarboxylase etc.
Acc. To source from which they are obtained e.g., papain, bromelain etc.
Some have been named like ptyalin, trypsin etc .
CLASSIFICATION OF ENZYMES
CLASS 1 : OXIDOREDUCTASES
Catalyse oxidation /reduction of a substance
Cytochrome oxidase oxidises cytochromes
Glycolate oxidase oxidises glycolate
Sreduced + Soxidised Soxidised + Sreduced
CLASS 2 : TRANSFERASES
They catalyse transfer of specific groups from 1 substrate to another
Glutamate pyruvate transaminase
S G + S S + S- G
CLASS 3 : HYDROLASES
Catalyse breakdown of larger molecules into smaller molecules with addition of H2O
Amylase hydrolases starch
CLASS 4 : LYASES
Catalyse cleavage of specific covalent bonds & removal of specific groups , without the use of H2O
Histidine decarboxylase cleaves histidine into histamine & CO2
X Y
C C X Y + C = C
CLASS 5 : ISOMERASES
Catalyse rearrangement of atoms in a molecule to form isomers
Phosphohexose isomerase converts glucose 6-phosphate into fructose -6-phosphate
CLASS 6 : LIGASES
Catalyse covalent bonding b/w 2 substrates to form a large molecule, mostly involving utilisation of energy by hydrolysis of ATP
RuBP carboxylase catalyses the joining of RuBP & CO2 in photosynthetic C fixation
MECHANISM OF ENZYME ACTION (LOCK & KEY HYPOTHESIS)
http://upload.wikimedia.org/wikibooks/en/e/ee/Induced-fit_model.JPGCATALYTIC CYCLE :
Substrate binds to active site of enzyme
Binding of substrate induces the enzyme to alter its shape & fit more tightly around substrate
Active site of enzyme, now in close proximity of substrate breaks the chemical bonds of substrate & an enzyme-product complex is formed
Enzyme releases the product of reaction & the free enzyme is ready to take up another molecule of substrate
http://www.classofoods.com/fotos/F_enzyme_werking.gifFACTORS AFFECTING ENZYME ACTION
Temperature
http://www.bbc.co.uk/schools/gcsebitesize/science/images/add_edex_bio_enzyme-chart.jpgEffect of pH
Graph showing temperature and enzyme activity. Between 0 and 40C, enzyme activity increases steadily. It peaks at 40C (optimum temperature), then decreases rapidlyEffect of substrate concentration
http://t2.gstatic.com/images?q=tbn:ANd9GcTUhk0j-ujJOaxmCzIBC8SgGYMkr9fDN3r5O1dlw1zCxgztXvrriLHM_jXq-wEffects of chemicals
When binding of a chemical reduces / shuts off the enzyme activity, the chemical is called inhibitor.
INHIBITORS
COMPETITIVEWhen inhibitor closely resembles substrate in molecular structure & binds to active site of enzyme
NON-COMPETITIVE When inhibitor does not compete with substrate for active site
http://course1.winona.edu/sberg/ChemStructures/Suc-mal.gifhttp://karimedalla.files.wordpress.com/2012/10/competitive_inhibit_c_la_784.jpgFeed back inhibition: Enzyme activity is inhibited by prdt of same enzyme reaction
GLUCOSE-6-PHOSPHATE
INHIBITS ACTION OF HEXOKINASE
CATALYSES
PHOSPHORYLATION OF GLUCOSE
Co-factors
ENZYMES
SIMPLE ENZYMES
CONJUGATE ENZYMES
Made of 1/several polypeptide
Has non-protein moiety + polypeptide chain
http://student.ccbcmd.edu/~gkaiser/biotutorials/proteins/images/u4fg3.jpgCOFACTOR
PROSTHETIC GROUP
COENZYME
METAL IONS
TIGHTLY BOUND TO APOENZYME
BOUND TO APOENZYME DURING COURSE OF CATALYSIS
METAL IONS FORM CO-ORDINATION BONDS WITH SIDE CHAIN AT ACTIVE SITE OF ENZYME & SUBSTRATE
HAEM
NAD & NADP
Zn
I would like to express my special thanks of gratitude to my
teacher Mrs. Alarmelu Natchiar as well as our principal Mrs Nasreen
Banu who gave me the golden opportunity to do this wonderful
presentation on the topic BIOMOLECULES, which also helped me in
doing a lot of Research and i came to know about so many new
things
I am really thankful to them.
Secondly I would also like to thank my parents and friends who
helped me a lot in finishing this presentation within the limited
time.
I am making this presentation not only for marks but to also
increase my knowledge .
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