Berkeley

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(Berkeley iGEM Team)
(Berkeley iGEM Team)
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Gabriel Wu
Gabriel Wu
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<h1>Addressable Bacterial Communication</h1>
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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.
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"Relevant Papers"
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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.
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<h1>Papers we've used/read</h1>
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"Addressable Bacterial Communication"<br>
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Haldimann, Wanner, "Conditional-Replication, Integration, Excision, and Retrieval Plasmid-Host Systems for Gene Structure-Function Studies of Bacteria"
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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, wherein 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.
+
Isaacs et al., "Engineered riboregulators enable post-transcriptional control of gene expression"
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Jaenecke et al., "A stringently controlled expression system for analyzing lateral gene transfer between bacteria"<br>
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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 valuable transfer machinery in the original cell so as to ensure only the packet is being sent.
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Knight, "Idempotent Vector Design for Standard Assembly of Biobricks"<br>
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Lawley et al., "F factor conjugation is a true type IV secretion system"<br>
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Miller et al., "F Factor Inhibition of Conjugal Transfer of broad host range plasmid RP4"<br>

Revision as of 00:50, 3 November 2005

Berkeley iGEM Team

Instructors:

Jay Keasling

Adam Arkin

Jonathan Goler

Justyn Jaworski

Members:

Michael Chen

Vlad Goldenberg

Stephen Handley

Melissa Li

Jonathan Sternberg

Jay Su

Eddie Wang

Gabriel Wu

Addressable Bacterial Communication

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 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"

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