Berkeley
From 2006.igem.org
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<h1>=== Berkeley iGEM Team ===<h2> | <h1>=== Berkeley iGEM Team ===<h2> | ||
| - | + | ||
| - | <h3>Professors:</h3 | + | <h3>Professors:</h3> |
| - | Adam Arkin | + | Adam Arkin |
Jay Keasling | Jay Keasling | ||
| - | + | ||
| - | + | <h3>GSIs:</h3> | |
| - | <h3>GSIs:</h3 | + | Jonathan Goler |
| - | Jonathan Goler | + | |
Justyn Jaworski | Justyn Jaworski | ||
| - | + | ||
| - | + | <h3>Members:</h3> | |
| - | <h3>Members:</h3 | + | Michael Chen |
| - | Michael Chen | + | Vlad Goldenberg |
| - | Vlad Goldenberg | + | Stephen Handley |
| - | Stephen Handley | + | Melissa Li |
| - | Melissa Li | + | Jonathan Sternberg |
| - | Jonathan Sternberg | + | Jay Su |
| - | Jay Su | + | Eddie Wang |
| - | Eddie Wang | + | |
Gabriel Wu | Gabriel Wu | ||
| - | + | ||
| - | + | ||
<h1>Addressable Bacterial Communication</h1> | <h1>Addressable Bacterial Communication</h1> | ||
We've been working on addressable bacterial communication via conjugation. The message being transferred is a gene locked using the Isaacs et al. riboregulator, and is sent in a packet mobilized by F-plasmid conjugation. This mobilized plasmid is sent to cells in the vicinity upon induction of the pBadAraC-controlled TraJF conjugation regulatory protein, expression of which triggers a cascade that constructs and uses F-plasmid conjugation machinery to send the packet plasmid. The message can only be unlocked by cells containing a trans activating key which acts to unlock the hairpin formed over the RBS by the cis-repressed riboregulator, where addressability is achieved by varying a 5 nucleotide region shared by the locks and keys. Upon receipt of the packet plasmid, the recipient cell turns on its own RP2-based conjugation machinery to send a similar acknowledgement packet back to the original cell, containing a genetic message locked and opened by a second addressed lock/key pair. | We've been working on addressable bacterial communication via conjugation. The message being transferred is a gene locked using the Isaacs et al. riboregulator, and is sent in a packet mobilized by F-plasmid conjugation. This mobilized plasmid is sent to cells in the vicinity upon induction of the pBadAraC-controlled TraJF conjugation regulatory protein, expression of which triggers a cascade that constructs and uses F-plasmid conjugation machinery to send the packet plasmid. The message can only be unlocked by cells containing a trans activating key which acts to unlock the hairpin formed over the RBS by the cis-repressed riboregulator, where addressability is achieved by varying a 5 nucleotide region shared by the locks and keys. Upon receipt of the packet plasmid, the recipient cell turns on its own RP2-based conjugation machinery to send a similar acknowledgement packet back to the original cell, containing a genetic message locked and opened by a second addressed lock/key pair. | ||
Revision as of 00:56, 3 November 2005
=== Berkeley iGEM Team ===
Contents |
Professors:
Adam Arkin Jay Keasling
GSIs:
Jonathan Goler Justyn Jaworski
Members:
Michael Chen Vlad Goldenberg Stephen Handley Melissa Li Jonathan Sternberg Jay Su Eddie Wang Gabriel Wu
<h1>Addressable Bacterial Communication</h1> We've been working on addressable bacterial communication via conjugation. The message being transferred is a gene locked using the Isaacs et al. riboregulator, and is sent in a packet mobilized by F-plasmid conjugation. This mobilized plasmid is sent to cells in the vicinity upon induction of the pBadAraC-controlled TraJF conjugation regulatory protein, expression of which triggers a cascade that constructs and uses F-plasmid conjugation machinery to send the packet plasmid. The message can only be unlocked by cells containing a trans activating key which acts to unlock the hairpin formed over the RBS by the cis-repressed riboregulator, where addressability is achieved by varying a 5 nucleotide region shared by the locks and keys. Upon receipt of the packet plasmid, the recipient cell turns on its own RP2-based conjugation machinery to send a similar acknowledgement packet back to the original cell, containing a genetic message locked and opened by a second addressed lock/key pair. </p>
We have used the lambda-red protocol to knock out the TraJ gene on the F plasmid so as to have total control over transfer via the pBadAraC promoter. Additionally, by knocking out the OriT nick region, we have marooned the F plasmid and its transfer machinery in the original cell so as to ensure only the packet is being sent.
Papers we've used/read
Haldimann, Wanner, "Conditional-Replication, Integration, Excision, and Retrieval Plasmid-Host Systems for Gene Structure-Function Studies of Bacteria"
Isaacs et al., "Engineered riboregulators enable post-transcriptional control of gene expression"
Jaenecke et al., "A stringently controlled expression system for analyzing lateral gene transfer between bacteria"
Knight, "Idempotent Vector Design for Standard Assembly of Biobricks"
Lawley et al., "F factor conjugation is a true type IV secretion system"
Miller et al., "F Factor Inhibition of Conjugal Transfer of broad host range plasmid RP4"
