B1.1: Carbohydrates And Lipids Flashcards
(42 cards)
Chemical properties of carbon - bio molecules
In all four major categories:
Carb, lipids, proteins, nucleic acids
4 electrons on outer shell
-> allow large stable molecules
Carbon -> arrange themselves to form a huge variety of chemical compounds:
Bond to other atoms
- long branched chains (glycogen)
- long straight chain molecule (cellulose)
- cyclic single rings (thymine, uracil…)
- multiple rings (adenine, guanine)
- tetrahedral structure (different 3D shape, different properties)
Double and triple bonds -> unsaturated compounds
What are some common functional groups?
OH (hydroxyl)
COOH (carboxyl)
NH2 (amino/amine)
H2PO4 (phosphate)
What is a monomer?
Smaller units from which larger molecules are made
what is a polymer?
molecules made from a large number of monomers joined together in a chain
-> polymerization
What is a macromolecule?
Very large molecules
1000+ atoms -> high molecular mass
polymers can be macromolecules, but not all macromolecules are polymers
polymers must have repeating subunits
Form by condensation reaction
Formation of polysaccharide
formed when two hydroxyl groups on different monosaccharides interact to form a strong covalent bond called a glycosidic bond
Formation of polypeptide
formed when two amino acid monomers interact to form a strong covalent bond called a peptide bond
How are polymers digested?
Hydrolysis reaction (breaking down with water)
Covalent bonds in macromolecules -> broken when water added
-> the -H and -OH from the water molecule are used to form the functional groups of the products
Examples of hydrolysis reaction
- hydrolysis of glycosidic bonds in poly- or disaccharides to produce monosaccharides
- hydrolysis of peptide bonds in polypeptides to produce amino acids
- hydrolysis of ester bonds in triglycerides to produce three fatty acids and glycerol
Saccharide:
Bond type
General formula
Properties
Glycosidic bond (condensation reaction)
CnH2nOn
Colorless crystalline molecules
Soluble in water
Différent types of monosaccharides
Formed from varying numbers of C atoms
Triose -> 3 C
Pentose -> 5 C
Hexose -> 6 C
What is glucose?
Basic hexose monosaccharide sugar molecule that is used in respiration to produce ATP
Chemical store of energy
Formed in photosynthesis
C6H12O6
What is the difference between alpha and beta glucose?
Alpha -> OH on C1 below
Beta -> OH on C1 above
Properties of glucose
- stable structure due to covalent bonds
- soluble in water due to polar nature
- easily transportable due to water solubility
- source of chemical energy when bonds are broken
What is ribose?
Basic monosaccharide pentose sugar
Found in RNA
a similar version in DNA
-> deoxyribose: has H in place of one of the OH
What is maltose?
- maltose (malt sugar) is formed from two alpha glucose molecules joined by a 1-4 glycosidic bond
- plants
What is sucrose?
- sucrose (table sugar) is formed from alpha glucose and fructose joined by an alpha 1-4 glycosidic bond
- plants
What is lactose?
- lactose (milk sugar) is formed from galactose and alpha glucose joined by a beta 1-4 glycosidic bond
- animals
What are polysaccharides used as?
Structure or energy source
-> able to do both bc of differences between a and b bonds
Starch (plants -> energy)
Glucose (plants -> energy)
Glycogen (humans -> storage)
Why are carbs good for both energy storage and structure? (Using examples)
Ex: starch and glycogen -> energy storage
Compact
Insoluble
-> soluble molecules will dissolve in cell lowering the water potential and causing water to move into cell -> too much water -> animal cell burst
Ex: cellulose -> structure
Strong and durable
Insoluble and slightly elastic
Chemically inert
Properties and uses of starch
Major carb storage molecule in plants
Usually stored as intracellular starch grains in organelles -> plastids
-> chlorophyll/amyloplast
Starch produced from glucose -> photosynthesis
Broken down during respiration -> energy -> source of carbon from producing other molecules
Structure of starch
2 different structural units:
Amylose (10-30%)
Glucose molecules joined by a 1-4 glycosidic bonds
Unbranched structure -> compact helical structure -> resist digestion
Amylopecitin (70-90%)
Glucose molecules joined by a 1-4 glycosidic bonds
Also contains more a 1-6 glycosidic bonds
-> results in highly branched structure
-> many terminal glucose -> easily hydrolyzed (easy take or add)
Properties and uses of cellulose
Plant cell walls - most abundant organic polymer
Very strong, prevents cell from bursting when excess water
Long chains of b glucose molecules joined by beta 1-4 glycosidic bonds
Glucose chains -> rope-like microfibrils -> layered to form network
Structure of cellulose
polysaccharide made up of many beta glucose molecules
glucose molecules are linked by beta 1-4 glycosidic bonds
-> to from glycosidic with b glucose -> every alternate must be inverted
Long straight unbranched chains
Alternate pattern -> good tensile strength (structure)