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DNA gyrase
Nics one of the chromosomes to relax the DNA supercoils ahead of the Replisome.
Helicase
Unwinds the double strands of DNA at the replication fork. (Unzips your genes)
Single Strand Binding Proteins
Decorate the lagging strand to prevent it from binding back to the original strand.
DNA primase
Adds a short piece of RNA primer that is complementary to the single-strand piece of DNA. The RNA strands have a 3’ hydroxyl group at the end. Gives DNA polymerases a starting point
DNA Polymerase 3 (leading strand)
Works towards the replication fork, 3’→5’, Continuously laying nucleotides down to create a complementary stand of DNA(3’→5’)
DNA Polymerase 3 (lagging strand)
Works in the opposite direction of the replication fork, makes the new strand of DNA in fragments. Reads the strand 3’→5’.
Okazaki Fragments
Have gaps where the original RNA primer was.
DNA polymerase 1
Responsible for filling the gaps on the Okazaki fragments where the RNA primer was removed. Leaves a gap between the newly put dna by DNA Pol 1 and the dna placed by the DNA Pol 3. (Corrects things)
DNA ligase
Bonds and makes the covalent, phosphodiester bond are to complete the new strand.
TER sites
Found in circular chromosomes. Recognized by Tus proteins that block the progress of the replication fork.
Telomerase
Found in eukaryotes, the ends of the linear chromosomes.
Tau protein
Holds the replisome together
Tus protein
tells the replication machinery that your done At the end of a circular chromosome
dnaA
Origin binding protein that binds to the origin
SeqA
binds to the origin during a 10 minute period, where nothing can happen to the DNA except DNA replication
MreB protein
form filamentous bands around the inside of the cell under cytoplasmic membrane to direct new cell wall to be made at certain locations
FtsI proteins
Transpeptidases that insert new peptidoglycan into expanding cell wall
Transglycosylases
From glycosidic bonds between sugars
Autolysins
Create small openings in existing cell wall
Autolysis
Spontaneous cell lysis
May occur if there is an error in inserting new cell wall material
Bactoprenol
Binds to the peptidoglycan precursor, facilitates transport through the cytoplasmic membrane. Lipid alcohol
Transpeptidation
Uses FtsI to form peptide bonds between pentapeptide of peptidoglycan precursor and tetrapeptide of an existing peptidoglycan unit. Happens between the 4th amino acid of the precursor and the third amino acid of the existing peptide. The 5th amino acid gets removed in the process.
Transglycosylase
Replaces the beta 1,4 glycosidic bond between N-acetylmoramic acid and N-acetylglucosamine on both sides of the precursor
LAG phase
Period of adjustment, when cells get introduced to a new growth medium.
Exponential phase
Cells are dividing (LOG phase)
Stationary phase
Cells stop dividing but are not dying
N=No 2^n
Final number of cells
g=t/n
Generation time
No
Initial number of cells
n
Number of generations
t
Time of exponential growth (either hours, or minutes)
Polycistronic mRNA
any time you have a coding sequence that represents multiple genes in RNA
Operon
DNA sequence were multiple genes are represented continuously without being interrupted by a terminator
Open reading frame
What gets translated, start codon to stop codon