Simplest carbs, also called simple sugars, with the formula (CH2O)n
Disaccharides
"Double sugars" consisting of 2 monosaccharides joined by condensation
Polysaccharides
Polymers made up of hundreds and thousands of monosaccharides either in the form of linear or branch, broken down through hydrolysis
Monosaccharides
glucose, fructose, galactose
Disaccharides
sucrose, maltose, lactose
Polysaccharides
starch, glycogen, cellulose
Monosaccharides
Consist of 3 - 7 carbon atoms
Aldoses
Monosaccharides with a terminal carbonyl group
Ketoses
Monosaccharides with an internal carbonyl group
Monosaccharide classification
Heptose, hexose, pentose, tetrose, triose (7 to 3 carbons)
Glucose
An aldohexose, have 6 carbons in a straight chain, ending in an aldehyde group
Monosaccharides have molecular formulae that are multiples of CH2O
Glucose and galactose are different due to the special arrangement around a symmetric carbon
Monosaccharides especially glucose are major nutrients for cells
In cellular respiration cells extract energy stored in glucose molecules
Carbon skeleton of monosaccharides serves as raw material for the synthesis of small organic molecules like amino acids and fatty acids
Unused glucose is generally incorporated as monomers into disaccharides or polysaccharides
Ribose with five carbons are building blocks for RNA and DNA molecules
Fructose
Ketose sugar, and fruit sugar, 1.5 times sweeter than sucrose but have low Glycemic Index
Isomers
Same molecular formula but different structures and properties
Enantiomers
Mirror images of each other with different properties
Alpha and beta glucose
2 most common isomers, similar ring structures and only the hydrogen (H) and hydroxyl (OH) groups on C1 are different
Alpha glucose molecules can combine to form starch, beta glucose can form cellulose</b>
Disaccharides
2 monosaccharides join together via condensation reaction that releases water and requires energy to form a glycosidic bond
Polysaccharides
Many monosaccharides linked together by glycosidic bonds, general formula (C6H10O5)n, insoluble and not sweet
Starch and glycogen
Provide energy storage
Cellulose
Provides plant support and rigidity
Amylose
Linear polymer of glucose, linked by α 1-4 bonds
Amylopectin
Branched polymer of glucose, branch out in α 1-6, every 24 to 30 units
Glycogen
Almost same structure as amylopectin but have more branches than them, every 8-12 glucose
Cellulose
Made from beta d-glucose polymer, found in plant cell walls
Chitin
Also made with beta d-glucose, found in insect shells
Bacterial cell wall
Made of n-acetylglucosamine and n-acetylmuramic acid and they repeat
Lipids
Also macromolecules, not soluble in water (covalent bond) but in soluble organic solvent like ether, 3 families - fat (triglycerides, triacylglycerols), phospholipids and steroids
Triglycerides
In 2 forms - fats (solid at room temp) and oils (liquid at room temp), formed from condensation process of glycerol and fatty acids
Saturated vs Unsaturated fatty acids
Presence of double bond affects how packed the fatty acids are, temperature affects saturation, addition of hydrogen (hydrogenation) will remove the double bond which make the plant oil solid
Functions of fat
Long-term energy storage, cushion for vital organs, insulation
Phospholipids
Only two tails, the last tail is attached to the phosphate group, have hydrophilic and hydrophobic tails, form a ball-like form when in contact with aqueous or water, main function is major component in plasma membrane