Functional Groups and Macromolecules Biochemistry Functional Groups and Macromolecules
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”
Biochemistry Part 1 Functional Groups
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
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”)
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
Molecular Diversity Arising from Carbon Skeleton Variation Carbon chains Form skeletons of most organic molecules Vary in length and shape Straight Branched Rings
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
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
1 usually active; other inactive Example of Isomers Straight vs. branched Cis vs. trans 1 usually active; other inactive Asymmetrical Carbon
Enantiomers Are important in the pharmaceutical industry L-Dopa D-Dopa (effective against Parkinson’s disease) D-Dopa (biologically inactive) Figure 4.8
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
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
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
Aldehyde **Think: all the way at the end! Ketone
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!
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
Functional Groups cont’d 5. Sulfhydral Group (-SH) sulfur bonded to H Makes disulfide bridges 2 sulfhydral groups can interact to stabilize protein structure
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
Functional Groups cont’d 7. Methyl Group (-CH3) Usually not as reactive as other groups Used in gene expression
Male or Female!! Only one little itty bitty difference that separates the sexes