Registration for a live webinar on 'Innovative Vaccines and Viral Pathogenesis: Insights from Recent Monkeypox Research' is now open.
See webinar detailsWe noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
- Introduction and General Properties of Plasmids
-
1. Introduction to plasmid biology
- Prof. Emeritus Don Clewell
-
2. General properties and applications of plasmids
- Prof. Emeritus Don Clewell
- Replication
-
3. Plasmids: copy number control by antisense RNAs
- Prof. Gerhart Wagner
-
4. Plasmid rolling-circle (RC) replication
- Prof. Saleem Khan
-
5. Replication of linear plasmids in bacteria
- Prof. George Chaconas
- Maintenance and Partitioning
-
6. Plasmid segregation and stability in bacteria
- Prof. Barbara Funnell
-
7. Plasmid stabilization by cell killing
- Prof. Keith Weaver
-
8. Dimer catastrophes and plasmid resolution
- Dr. David Summers
- Conjugation and Mobilization
-
9. The diversity of bacterial conjugation and mobilization systems
- Prof. Fernando de la Cruz
-
11. DNA processing in conjugative transfer
- Dr. Joel Schildbach
-
12. Agrobacterium tumefaciens
- Dr. Stephen Winans
- Genetic Traits Frequently Associated with Plasmids
-
13. Insertion sequences and DNA transposition
- Prof. William Reznikoff
-
14. Plasmids, integrons and the spread of antibiotic resistance
- Prof. Hatch Stokes
-
15. Virulence plasmids
- Prof. Julian Rood
- Eukaryotic Plasmids
-
16. The yeast plasmid: a highly persistent selfish DNA element
- Prof. Makkuni Jayaram
- Population Biology and Evolution
-
17. Evolution of plasmids and their role in bacterial diversity and adaptability
- Prof. Christopher Thomas
- Archived Lectures *These may not cover the latest advances in the field
-
19. Plasmid segregation and stability in bacteria
- Prof. Barbara Funnell
-
20. Replication of linear plasmids in bacteria
- Prof. George Chaconas
Printable Handouts
Navigable Slide Index
- Introduction
- Linear DNA in diverse bacteria
- The 'end replication' problem
- Solving the end replication problem
- Streptomyces
- Replication pathway for Adenovirus and Bacillus phage f29
- Streptomyces DNA replication
- A minimal pSLA2 replicon
- Cis and trans acting regions for pSLA2 replication
- Linear DNA replication intermediate
- Predicted secondary structure of S. lividans SLP2 plasmid end
- Patching by terminal protein
- The terminal proteins of Streptomyces
- Comparison of seven TP sequences
- Recruitment of TP
- Deoxynucleotidylation of TP and DNA synthesis
- Tap directs Tpg to its location and adds dCMP
- Streptomyces summary
- Borrelia
- The segmented genome of Borrelia burgdorferi
- Replication pathway for linear plasmids in Borrelia (1)
- Origin mapping by nascent strand analysis
- Origin location in the linear chromosome
- Plasmid maintenance proteins in B. baveriensis
- Minimal replicons
- Regions required for Ip17 replication
- The BBD14 (Family 62) and BBD21 (Family 32) proteins
- The telomere resolvase (ResT)
- Replication pathway for linear plasmids in Borrelia (2)
- Purification of recombinant B. burgdorferi ResT
- Assay for telomere resolution by ResT
- The telomeres
- Three classes of telomere in Bb. Cleavage between bp 3 and 4 in all
- Minimal substrate requirements
- How does DNA cleavage and ligation occur?
- Comparison of domains in 3 telomere resolvases
- Active site residues of telomere resolvases
- Mechanism of action of ResT: a 2-step transesterification
- Features of telomere resolvases
- How does hairpin formation occur?
- Alignment of hairpin binding molecules of Tn5 and Tn10 with ResT
- A composite active site promotes telomere resolution
- A composite active site
- Structure and function of telomere resolvases
- Genome plasticity in Borrelia
- Sequence scrambling in linear plasmids
- Telomere exchanges
- What causes high incidence of gene duplications and telomere exchanges in Borrelia species?
- ResT reversal using a plasmid substrate
- Telomere exchange by ResT-mediated telomere fusions
- Sequence scrambling near the B. burgdorferi telomeres
- Reversal of telomere resolution (telomere fusion)
- Conclusions: genome plasticity and ResT (1)
- Conclusions: genome plasticity and ResT (2)
- The end
Topics Covered
- Linear DNA replication in bacteria
- The ‘end replication’ problem
- Linear DNA replication in Streptomyces
- Linear DNA replication in Borrelia
- Telomere resolvase (ResT)
- Genome plasticity in Borrelia
- Sequence scrambling in linear plasmids
- Reversal of telomere resolution
- Covalently closed hairpin ends
Talk Citation
Chaconas, G. (2024, January 31). Replication of linear plasmids in bacteria [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 1, 2024, from https://doi.org/10.69645/YSNK2670.Export Citation (RIS)
Publication History
Financial Disclosures
- There are no commercial/financial matters to disclose.
A selection of talks on Microbiology
Transcript
Please wait while the transcript is being prepared...
0:00
The title of this
presentation is
Replication of Linear
Plasmids in Bacteria.
0:08
Let's begin our
discussion with a look at
the distribution of linear
DNA in the bacterial world.
This figure shows a tree of
relatedness for bacterial phyla,
in which phyla have
linear replicons.
Two things are immediately
obvious from this tree.
First, a few bacterial
phyla carry linear DNA.
Second, the ones that do
are not closely related.
Linear DNA has been found in
protobacteria, actinobacteria,
and spirochetes.
Three phyla that are
evolutionarily distant
from each other.
The observed linear DNA
has been found in the form
of bacterial chromosomes,
plasmids and Phages.
The reasons why linear
DNA in bacteria is
not a common occurrence is
discussed in the next slide.
1:01
Most bacterial plasmids
are circular molecules.
This simplifies the DNA
replication process.
With linear DNA molecules,
we encounter what
has been referred
to as the end
replication problem.
This was first noted by James
Watson in the early 1970s.
The problem results
from the fact
all DNA polymerases require
a primer to initiate
DNA synthesis.
As shown in this illustration,
when synthesis is complete
on the lagging strand,
and the RNA primer at
the five prime end of
the newly replicated
strand is removed,
we are left with a gap.
This gap cannot be filled in
de novo by a DNA polymerase,
and we are left with
unreplicated DNA at
the ends of the lagging strand
of linear DNA molecules.