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4 Major types of biological macromolecules:1. Proteins - do the vast majority of work; cell structure2. Nucleic Acids- DNA and RNA3. Carbohydrates (or Polysaccharides) (sugars)4. Lipids (fats) - "not every lipid is a fat MC"Macromolecules - 26% of a cell- 60% of that is protein- Made up of MONOMERS (building blocks of Macromolecules)- proteins - amino acids- nucleic acids - nucleotides- polysaccharides - monosaccharides- lipids- fatty acids- Synthesized by DEHYDRATION SYNTHESIS/CONDENSATION reactions and broken down by HYDROLYSIS reactions  - Dehydration Synthesis - H20 is a byproduct; Potential Energy stored  - Hydrolysis - H20 is added and Energy is released  - Reversible reactions!!!!- All monomers are linked by covalent bonds;1. Polysaccharides/Carbohydrates  - made from condensation reactions bringing together monosaccharides  - uses:     1. energy sources - ex: glucose     2. structural molecules - chitin;cellulose     3. cell identification and recognition - surface markings on cells; sugars (ex: glycoproteins/glycolipids)  - "carbohydrate" can either mean polysaccharide or monosaccharide  - General form chemically:     - C2H202     - Cn(H20)n     ** # of Carbons = # of H20 Molecules!!  - Standard conventions for atoms in ring structures:     - Within the ring- if not told explicitly, it's Carbon (C)       - number carbons from left to right! :)     - Above or below the ring- it not told explicitly, it's Hydrogen (H)  - Monosaccharides typically found in lengths of 3, 5, or 6 carbons     - 6 Carbons = HEXOSE SUGAR       - ex: GLUCOSE - C6H12O6       - In linear form: C=O at Carbon #1 = ALDEHYDE -- so glucose is an Aldose sugar       - If C=O at Carbon #2 = KEYTONE -- ex: fructose       - If Hydrogen is AHHHbove the ring? - Alpha Glucose       - If Hydrogen is BEEElow the ring? - Beta Glucose          - Both are molecules of Glucose, but are different MCs     - 3 Carbons = TRIOSE SUGAR       - Glycerol: 3 Carbon Backbone w/ OH (Hydroxyl) on each carbon; the rest filled with Hydrogens       - But a glycerol MC with a C=O at Carbon #1 = GLYCERALDEHYDE - C3H6O3          - NEVER FOUND IN CIRCULAR FORM; always straight chain form because its not long enough     - 5 Carbons = PENTOSE SUGAR       - Ex: Ribose - C5H10O5  - Some monosaccharides have identical formulas but different structures - ISOMERS     - isomers of Glucose (C6H12O6):       -a-Mannose       -a-Galactose       - Fructose - just b/c it has a 5 member Carbon Ring doesn't make it a Pentose- COUNT CARBONS!!*  - Other Monosaccharides have similar formulas, similar structures, and related functions:       - TRICK B/C THEY LOOK LIKE ISOMERS!       - Ribose (C5H10O5) and Deoxyribose (C5H10O4) ---Examine Carefully!  - Two monosaccharides can be brought together to form a disaccharide via acovalent bond     - GLYCOSIDIC LINKAGE!!!!       - a-1,4 glycosidic linkage       - b-1,4 glycosidic linkage       - only care about Carbon #1, whether its in the alpha or beta configuration  - Maltose & Cellobiose, both monosaccharides are glucose, but not all disaccharides are the same monomers       - Ex: Lactose = glucose + galactose       - Ex: Sucrose = glucose + fructose  - The chemical formula for a disaccharide of hexose sugars is C12H22O11     - This differs because H2O IS LOST!! Lost in the condensation reaction  - Nomenclature:     - 1 monomer = monosaccharide     - 2 monomers = disaccharide     - several monomers = oligosaccharide (like a chain of 4 because "oglio" =few)     - Hundreds or thousands of monomers = polysaccharide  - Carbohydrates/Polysaccharides can be modified     - linkage of oligosaccharides to other macromolecules , such as a protein or a lipid       - when covalently linked to membrane proteins or lipids, carbohydratesact as recognition and identification MCs (chem markers)       - glycoproteins and glycolipids (BLOOD TYPING)     - addition of chemical groups, such as Phosphate (Pi) groups and amine groups (NH2)       - ex: glucose => glucoseAMINE , which can be chitin if further modified       - ex: galactose => galactosAMINE , joint/joint substances  - Polysaccharides serve as (1) chemical sources of energy or (2) structural compounds     - Cellulose     - Starch     - Glycogen     1. Cellulose       => PLANT CELL WALLS!       - the most abundant carbon-containing (organic) compound on the face of the Earth       - found in plant cell walls - the primary component in fact :D       - linear, unbranched polymer of glucose (fibril) - "just glucose linked to glucose" through b-1,4 glycosidic linkages          - glucose (b-1,4 glycosidic linkage)glucose (b-1,4 glycosidic linkage)glucose (b-1,4 glycosidic linkage)       - fibrils held together by hydrogen bonding between the individual fibrils |||||||||       - "by convention" the second molecule is upside down - "if it doesn't fit,it won't work".       - SO - "rotate #2 MC 180degrees"     2. Starch       => FOOD!       - found chiefly in seeds, fruits, tubers, roots, and stems ofplants; energy storage       - LOOSELY branched


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UIUC MCB 150 - Biological macromolecules

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