Utilisateur
xtrachromosomal DNA elements found in all types of bacteria; often multiple plasmids per cell
Usually covalently closed, circular dsDNA; sometimes linear or ssDNA. vary greatly in size and sometimes resemble the chromosome.
Genes (proteins, RNAs) that provide specific advantages (e.g., antibiotic resistance)
They aid bacterial adaptation & evolution and are powerful tools in molecular biology
After the functions they encode (e.g., R plasmids = antibiotic resistance).
Standardized lab naming: “p” + creator initials + version (e.g., pUC19, pTR1)
Covalently closed, circular dsDNA, negatively supercoiled
supercoil stress relieved by protein binding and used to facilitate replication and transcription
Plasmids are small, allowing for selective precipitation of bacterial chromosome and other macromolecules
Lyse cells with detergent & base.
Precipitate chromosome & other macromolecules with salt solution.
Bind soluble plasmid DNA to column → wash → elute
An origin of replication (oriV).
They act as replicons — units of DNA with their own replication origin
Usually encode only 1 protein near oriV; other proteins are borrowed from the host
Common plasmid replication mechanism where replication starts at oriV using RNA primer that intiates DNAP replication, proceeds unidirectionally or bidirectionally around the plasmid
ColE1, RK2, F, P1 (also the mechanism for bacterial chromosomes, though not called theta there)
A replication mechanism producing ssDNA intermediates, later converted to dsDNA
A nick introduced by Rep protein at ds oriV (DSO), creating a 3′-OH for DNA Pol III extension, displacing the parental strand. lagging strand synthesis occurs on displaced strand. produces long concatemers in which the original parental dna seq is repeated many times
1. rep protein binds at ds oriV @ palindrome
2. causes formation of hairpin cruciform structure
3.nicking; rep covalently bounds by Tyr to 5'-PO4
4.DNA pol II extends 3'OH
5. rep transfers 5' PO4 to 3'OH to create circular ssDNA
6. host RNAP makes primer at ss oriV
7. DNA pol III replicates around ssDNA circle
8. DNA pol I removes RNA primer, replaces with DNA, ligases seals
By some phages, during bacterial conjugation, and in certain plasmids
Long concatemers (multiple repeated plasmid units)
The range of bacterial species a plasmid can replicate in
Replicates only in E. coli and close relatives (e.g., ColE1 plasmids: pBR322, pET, pUC)
Replicates in many Gram negatives and some Gram positives (e.g., RK2/RSF1010 derivatives such as pBBR1MCS)
Encode all proteins for replication (not dependent on host) and use promoter/translation (gene expression sequences) signals recognized by wide variety of machinery (promoters, translation, intiation sites)
Method to introduce plasmid into hosts + selectable marker trait (presentable phenotype encoded by plasmid to find in bacteria)
The number of copies of a plasmid per cell, tightly controlled
High copy number plasmids; only regulate replication once numbers get very high
Low copy number plasmids (as low as 1 per cell); replication must be tightly regulated
Inability of two plasmids to coexist stably in the same cell
Plasmids share the same replication control mechanism → not distinguished during replication → one lost randomly.
Plasmids share the same partitioning system → not distinguished during segregation → uneven distribution → one lost
A classification for plasmids that cannot coexist in the same cell (same incompatibility group).By testing if a plasmid is cured from strains already containing a plasmid of a known Inc group- must have easily measured trait so can detect plasmid presence.
sRNA interference with primer processing (ColE1-type).
Rep protein regulation via complementary RNA (R1-type).
Rep protein autoregulation & plasmid coupling (iterons/handcuffing) (pSC101-type)
RNA II normally forms replication primer. As plasmid copy number rises, sRNA RNA I accumulates → binds RNA II → prevents priming of replication
Rep protein required at oriV to seperate strands prior to replication. Rising copy number → sRNA accumulates --> CopA sRNA inhibits RepA translation, CopB repressor shuts off PrepA transcription
Replication occurs until copy number is controlled by CopA/CopB feedback. CopB repressor made and shuts off PrepA and then copA RNA made and binds repA transcript to inhibit translation.
Rep protein at high levels binds its own promoter (autorepression) and iteron sites on plasmids → plasmids are coupled together (“handcuffing”) to block replication
Low-copy plasmids must ensure each daughter cell inherits at least one copy
Par proteins (similar to bac chromosome segregation Par systems)
ParR binds centromere-like parC site.
ParM-ATP polymerizes (actin-like filament) under ParR:parC.
Filament pushes plasmids apart.
ATP hydrolysis → depolymerization resets system
ParA-ATP polymerizes along randomly on nucleoid DNA.
ParB binds parS site on plasmid.
ParB-parSattracted to ParA-ATP and stimulates ATP hydrolysis and depolymeriztion of ParA.
Depolymerization of parA, pulls plasmid and parB-parS across chromosome
R1-type = ParM pushes plasmids apart via actin-like filament polymerization.
P1/F-type = ParA pulls plasmid via depolymerization on nucleoid
R1; par C, Par R, ParM-ATP (at midpoint), pushes DNA apart- filament polymerizes to move DNA
P1/F: ParS, ParB, ParA-ATP (on nucleoid), pulls DNA apart- filament depolymerizes to move DNA
Partitioning systems.
Site-specific recombinases to resolve plasmid multimers.
Toxin-antitoxin systems (cell dies if plasmid lost).
plasmid cloning vectors
