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Functional Groups and Macromolecules
Biochemistry Functional Groups and Macromolecules
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Carbon—The Backbone of Biological Molecules
All living organisms Are made up of chemicals based mostly on carbon due to its bonding ability All life considered “carbon based life-forms”
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Biochemistry Part 1 Functional Groups
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Vocab to know… Organic chemistry
the study of carbon compounds Organic compounds have carbon in them (& usually H) Exception: CO2 is considered INORGANIC Range from simple to big molecules
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Formation of Bonds w/ Carbon
Carbon atoms forms diverse molecules b/c carbon has 4 valence electrons bind to to 4 other atoms can form 4 covalent bonds with itself or other atoms very important in living things! Carbon has bonding versatility allows it to form many diverse molecules, including carbon skeletons (carbon “chains”)
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The electron configuration of carbon
Gives it covalent compatibility with many different elements H O N C Hydrogen (valence = 1) Oxygen (valence = 2) Nitrogen (valence = 3) Carbon (valence = 4) Figure 4.4
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Molecular Diversity Arising from Carbon Skeleton Variation
Carbon chains Form skeletons of most organic molecules Vary in length and shape Straight Branched Rings
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Fat droplets (stained red)
Hydrocarbons Consists of only C and H’s Ex: petroleum; lipid ‘tails’ A.k.a= fatty acids Found in many of cell’s organic molecules Ex: fat molecules, cell membranse Covalent bonding btw C-H nonpolar (hydrophoic) High energy storage 100 µm Fat droplets (stained red) Figure 4.6 A, B
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ISOMERS Isomers same molecular formula, but different structure & properties Have same # of atoms arranged differently 3 types of isomers structural~ differ in covalent bonding arrangement geometric~ differ in spatial arrangement Arise from inflexibility of double C bond cis (same side) vs. trans (opposite sides) enantiomers~ mirror images of each other Ex: used in pharmacological industry
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1 usually active; other inactive
Example of Isomers Straight vs. branched Cis vs. trans 1 usually active; other inactive Asymmetrical Carbon
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Enantiomers Are important in the pharmaceutical industry L-Dopa D-Dopa
(effective against Parkinson’s disease) D-Dopa (biologically inactive) Figure 4.8
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Functional Groups 7 different groups in biology
part of organic molecules involved in chemical rxns chemically reactive groups Each group behaves in a consistent fashion no matter where it is # & arrangement of groups helps give molecules unique, distinctive chemical properties
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Hydroxyl Group (-OH) H bonded to O Make alcohols & sugars
Functional Groups Hydroxyl Group (-OH) H bonded to O Make alcohols & sugars Makes things Polar soluble in water (attracts H20) hydrophilic
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Functional Groups 2. Carbonyl Group (C=O) C double bond to O
usually increase polarity and reactivity of organic molecules Aldehyde (at the end of C skeleton) Ketone (INSIDE Carbon skeleton) All sugars have this group
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Aldehyde **Think: all the way at the end! Ketone
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Functional Groups cont’d
3. Carboxyl Group (-COOH) O double bonded to C to hydroxyl Carboxylic acids (organic acids) Covalent bond between O and H Polar Dissociation H+ source (Makes acids) **Think: Carboxyl has a hydroxyl!
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Functional Groups cont’d
4. Amino Group (-NH2) N to 2 H atoms Acts as a base (+1) Also makes AMINO ACIDS Have both amino and carboxyl groups
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Functional Groups cont’d
5. Sulfhydral Group (-SH) sulfur bonded to H Makes disulfide bridges 2 sulfhydral groups can interact to stabilize protein structure
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Functional Groups cont’d
6. Phosphate Group (-PO4-3) Covalently attached by 1 of its O to the C skeleton Can transfer energy btw molecules Ex: ATP Important in biology Ex: DNA/RNA, cell membranes
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Functional Groups cont’d
7. Methyl Group (-CH3) Usually not as reactive as other groups Used in gene expression
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Male or Female!! Only one little itty bitty difference that separates the sexes
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