Chapter 10 - DNA Structure Flashcards
Central Dogma
DNA -> transcription-> RNA -> translation-> Proteins
hershey chase experiment
T2 virus = protein + DNA
attacks E. Coli bacteria
conclusion of transformation experiments
DNA is the genetic material for many viruses and prokaryotes
transformation
involves converting one line of bacteria/virus to another line
nucleic acid parts
nitrogenous base, 5-carbon sugar (pentose), phosphate group
polymers of nucleic acid
DNA & RNA
pyrimidines
one ring
cytosine, thymines, uracil
purines
have two rings
guanine and adenine
ribose
5 carbon sugar with a hydroxy group on carbon 2’
deoxyribose
5 carbon sugar with an H on carbon 2’
nucleoside
nitrogenous base attached to 1’ carbon of ribose or deoxyribose
nucleotide
nucleoside with a phosphate group attached to 5’ carbon
phosphodiester bonds
links adjacent nucleotides
oligonucleotide
shorter chain of nucleotides that consists of less than 20
polynucleotide
long chain of nucleotide, more than 20
watson and crick base pairs
C-G
A-T
watson and crick model
double helix (two polynucleotide chains coiled around a common axis)
B-DNA
right handed
most common form (in humans)
A-DNA
right handed helix, very compact
not known from living organisms
Z-DNA
left handed helix
12 bases per turn
C-G only
RNA structure
sugar is ribose
U-T, C-G
major function of RNA
expression of genes
can be genetic material of some viruses
PCR Steps
denature DNA
anneal primers
extend primers
PCR Steps
denature DNA
anneal primers
extend primers
tetranucleotide hypothesis
in any length of DNA, there is an equal number of bases in same repetitive order
A=T, C=G -> 25% of each
virulant
disease causing
QB bacteriophage
enzyme that directly copies RNA
reverse transcriptase
viral DNA -> reverse transcription -> DNA -> transcription -> viral mRNA -> viral protein
tobacco mosaic virus
transformation example
amplification of DNA
make clones of DNA
ex- PCR
DNA fractions
electrophoresis
base content analyses
sequencing
primers
specific sequence that matches target DNA (about 20 base pairs long)
part of PCR testing
what is needed for a PCR test
template DNA, primers, DNA polymerase, nucleotide, Mg+ buffer
DNA denaturing temp
95 degrees Celsius
needed to break Hydrogen bonds and separate the strands
primer annealing temp
60-65 degrees Celsius
strand elongation temp
70 degrees Celsius
denature DNA
breaking a DNA strand into single strands
anneal primers
enables primers to attach to a specific location
extend primers
extend the new DNA strands from the primers
product of first cycle of PCR
two new DNA molecules
cycle 2 of PCR
four new DNA molecules
DNA electrophoresis
separation of DNA fragments based on length
charge on DNA
negative