Exam 4- Chapter 8 Part 1 Flashcards
Each DNA nucleotide building block consists of:
5-carbon sugar
phosphate group attached to 5-carbon sugar
Nitrogen base added to the 1’ carbon of the sugar
nucleotide pairing
A pairs with T to form 2 H bonds
C pairs with G to form 3 H bonds
What bond forms the sugar phosphate backbone of each strand
phosphodiester
Structure of DNA for bacteria
singular circular chromosome (no histones)
Structure of DNA for archaea
singular circular chromosome packaged around a histone
histone is tetramere
Structure of DNA for Eukarya
multiple linear chromosomes packaged around histones
histones are octomere
Relationship between DNA, RNA , protein
DNA is divided into genes
transcrition yields mRNA copy of specific genes
translation uses information from mRNA to synthesize protein
Griffiths experiment
Smooth (s) and rough (r) strains of S. pneumoniae
Heat killed S strains released something into the environment that R strains can pick up and become pathogenic
What caused S strains to have this transforming factor
capsule
What did Griffiths experiment tell us
There was some transforming factor that can be passed
pointed out that DNA could contribute hereditary information
Avery MacLeod and McCarty experiment
Took R strains with heat kille dS
had three plates, each with protease, RNase, or DNase
which degraded their respective molecule
What happened to protease plate
colonies still formed
There was still conversation
What happened to the RNase plate
colonies still formed
there was still conversion
What happened to DNase plate
no colonies formed
What was the purpose of Avery MacLeod and McCarty experiment
to determine if DNA, RNA, or protein was responsible for the transformation effect in Griffith’s experiment
Hershey Chase experiment
use radioactive labeling of protein or DNA component in bacteriophage
Let labeled phages infect bacterial cells
Only DNA-labeled phage when into bacterial cells
DnaA
binds to 9 base pair repeat in Ori-C and induces a conformational change
DnaB
helicase
unwinds double strand
DnaC
healicase loader
brings DnaB to where it needs to go
DNA gyrase
removes tension by knicking strand allowing DnaB to work better
DnaG
primase
lays down RNA primer to give free 3’ OH
SSB proteins
Stabilize single strands so they are not degraded and do not retwist
Okazki fragments
lagging strand still has to be transcribed from 5’-3’
Okazaki fragments allow this to still happen
DNA polymerase
high fidelity enzyme-proofreading
removes mismatched base by exonuclease activity