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DNase
enzyme treatment that eliminated DNA
components of nucleotide
pentose sugar
nitrogenous base
phosphate group
DNA polymerase 1
removes RNA primers using 5’-3’ exonuclease activity
DNA helicase
unwinds the DNA double helix ahead of the replication form
leading strand
synthesized toward the replication fork
lagging strand
synthesized away from the replication fork
codon
3 nucleotide mRNA sequence that specifies a single amino acid or stop signal
missense mutation
point mutation causes a single amino acid substitution in resulting protein
nonsense mutation
point mutation changes amino acid codon into a premature stop codon
silent mutation
alters nucleotide without changing encoded amino acid
frameshift mutation
results from deletion of nucleotides not divisible by 3
prototrophic bacterial strain
wild type strain capable of synthesizing all nutrients on minimal media
auxotrophic bacterial strain
mutant strain requiring specific nutritional supplements to grow
transformation
bacterial uptake of extracellular DNA from the environment
transduction
bacteriophage mediated transfer of bacterial DNA between cells
conjugation
plasmid mediated transfer of bacterial DNA from donor to recipient cell
hairpin loop
destabilizes transcription complex during rho-independent termination
A site
receives incoming aminoacyl tRNA molecules
P site
holds tRNA attaches to the growing peptide chain
release factor
binds to stop codons in A site to trigger translation termination
Kozak sequence
eukaryotic consensus sequence surrounds start codon aids translation initiation
B-galactosidase
encoded by Lac Z gene of Lac operon
Lac permease
encoded by Lac Y gene
allolactose
acts as inducer by inactivating the Lac repressor
restriction enzyme
recognizes foreign DNA that lacks hosts methylation pattern and cuts in
CRISPR
guides RNA directs CAS proteins to foreign DNA which is cleaved
single strand binding protein (SSBP)
stabilize separated DNA strands
RNA primase
makes short RNA primer needed to provide 3’ OH
DNA polymerase 3
main bacterial replicative polymerase
-35 region
coding strand; TTGACA
affects transcription initiation
-10 region
coding strand; TATAAT
affects transcription initiation
transcription start site
the first base copies into RNA; +1
dalgarno sequence
in mRNA 5’ UTR; AGGAGG
initiate translation binds complementary to 16s ribosomal subunit
translation start codon
ATG on coding DNA
I+
functional lac repressor (acts in trans)
I-
non functional repressor
O+
normal operator
Oc
constitutive operator mutation (acts only in cis)
Z+
functional B-galactoside
Z-
nonfunctional B-galactoside
Y+
functional permease
Y-
nonfunctional permease
Watson & Crick
proposed a molecular structure for DNA
Garrod
used inborn errors of metabolism to support idea that genes specify proteins
Pribnow
identified prokaryotic promoter sequence
Pribnow=promoter
Shine & Dalgarno
identified prokaryotic 5’ UTR sequence used for ribosome binding
Dalgarno=ribosome binding
Chargoff
found A=T C=G in DNA
Chargoff=base pairs
Jacob & Monod
determined mechanisms of Lac operon regulation
Franklin
generated X-ray patterns for DNA
Franklin=X-ray
Charpentier
demonstrated CRISPR - Cas 9 genome editing in eukaryotes
Charpentier= CRISPR