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28 Cards in this Set

  • Front
  • Back

The central dogma

DNA --> RNA --> PROTEIN


The genetic flow of information

What is required for information containing biopolymers?

1. defined start


2. An atom with at least 3 bonding options


3. some residue


4. common backbone


5. different side chains


6. defined end

Elements of life

C, H, O, N, P, S


Small atomic radii


form strong covalent bonds

Unique properties of carbon

1. life depends on carbon


2. all major biopolymers have a carbon backbone


3. it is NOT the most abundant element on earth's crust


4. can bind to itself and form long chains (catenation)


5. forms 4 bonds


6. inert or kinetically stable to hydrolysis and oxidation

elements of earth's crust

1. O: 47%


2. Si: 28%


3. Al: 7.9%


4. Fe: 5%

What must an element do to form a polymer?

it must have at least 3 valence or bonding electrons --> requires 2 bonds

Organic reactions tend to be

under kinetic control versus thermodynamic control

Reactions are attractive for enzyme control when

the rate of the reaction is so slow due to high activation energy and it being thermodynamically favourable

thermodynamically favourable

from high energy, to low energy or from less stable, to more stable


the product has less energy than the reactant

covalent

equal electron distribution between the 2 atoms


H-H


C-C


C-H

Partial charges

asymmetrical electron distriution

ionic

full charge on each atom, exchanged/trasnferred

Major Biopolymers

1. lipids


2. carbohydrates

Functional groups

site of organic reactivity in a compound, include (the functional group is not the name but the atoms and bonds):


1. amine groups


2. amide groups


3. Alkenes


4. Methyl


5. alcohol


6. aldehyde


7. carbonyl


8. carboxylic acid


9. alkynes

Amine groups

ionic, basic, often positively charged at ph 7


H-N-H


Primary amines can be shown in text as: RNH2


Secondary amines can be shown in text as: R2NH


Tertiary amines can be shown in text as: R3N

amide groups

a derivative of carboxylic acids, polar but non-ionic


CONR


Primary amides can be shown in text as: RCONH2


Secondary amides have an alkyl or aryl group attached to the nitrogen: RCONHR


Tertiary amides have two alkyl or aryl group attached to the nitrogen: RCONR2

alkenes

Alkenes consist of a C=C double bond function.

Alkenes can be shown in text as:


Mono substituted: RCH=CH2


1,1-disubstituted: R2C=CH2


1,2-disubstituted: RCH=CHR


Alkenes are planar and there is no rotation about the C=C bond.


Alkenes are electron rich reactive centres and are susceptible to electrophilic addition.

Methyl

CH3

Alcohol

OH


Primary alcohols have an -OH function attached to an R-CH2- group.


Secondary alcohols have an -OH function attached to a R2CH- group.


Tertiary alcohols have an -OH function attached to a R3C- group.

aldehyde
Aldehydes have a hydrogen and an alkyl (or aromatic) group attached to a carbonyl function.

Aldehydes can be shown in text as: RCHO

carbonyl

The carbonyl group is a super function because many common functional groups are based on a carbonyl, including:

aldehydes, ketones, carboxylic acids, esters, amides, acyl (acid) chlorides, acid anhydrides

Carboxylic acid

Carboxylic acids have an alkyl or aromatic groups attached to a hydroxy-carbonyl function.

Carboxylic acids can be shown in text as: RCOOH

Information Biopolymers

1. Nucleic acids: DNA and RNA


2. Protein


3. A variety of monomers



Information biopolymers require

order


template


process of copying the template faithfully

information biopolymers: proteins

1 made up of 20 amino acids (differ in side chains R)


2. different chemical properties in side chains


3. amino acid sequence determines the structure and the structure determines the function


4. 50% of cell weight


5. give the cell its shape

proteins form

1. receptors


2. enzymes


3. hormones


4. growth factors


5. toxins


6. transporters


7. antibodies

peptide bond formation

1. via translation on ribosomes


2. catalyzed by rna


3. activated by atp first

the peptide bond

has 2 resonance structures


has a polarity with O being -ve and N being +ve


can't rotate due to a partial double bond character