• Introduction
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  • The Team
  • Photo Gallery
• Our Project
  • Results Summary
  • Selection System
  • In-Vitro Characterization
  • In-Vivo Characterization
  • Microfluidics
  • Data
  • Attributions
• Tools
  • Gibson Assembly
  • MITOMI
• Notebook
  • Protocols
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• Considerations
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• Acknowledgements
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Data

team, please check this page: [1]

Overview

Summary

There are three pillars that underlie our transcription factor development pipeline. The first pillar is a selection system which lyses cells containing strong matches between a transcription factor and its promoter and allows for the speedy recovery of the relevant DNA. The second pillar is an in vivo characterization system that uses two different reporter systems as a way to document the binding affinities of the TetR transcription factor and its promoter pTet. The third pillar is an in-vitro characterization system called MITOMI that allows for high-throughput analysis of DNA-protein interaction strengths.

In developing these three pillars, a number of parts were made. We have listed all of them and have highlighted our favorites.

Systems

Selection System: We cloned the Berkeley Lysis cassette (BBa_K112808) under control of the T7 promoter into a low copy number plasmid (pSB3K1, formerly BBa_I739202).

In Vivo Characterization: We cloned an RFP gene under control of T7 promoter variants (parts BBa_K613001 through BBa_K613012) into a low copy number plasmid (pSB3K1, formerly BBa_I739202). We also cloned TetR mutants (parts BBa_K613013 through BBa_K613019) into a a low copy number plasmid (pSB3K1, formerly BBa_I739202). Both sets of plasmids were thoroughly characterized using IPTG platereader experiments.

In Vitro Characterization:

Favourite parts

Our three favourite parts are TetR mutants, characterised in-vivo using our reporter systems, and in-vitro by MITOMI.

• BBa_K613015 TetR E37A W43S T141A mutant
• BBa_K613016 TetR P39K mutant
• BBa_K613017 TetR Y42F mutant

Pre-existing parts characterised

• BBa_K112808 Experience Page - The Berkeley Lysis Device: In developing our Lysis selection device, we characterised induction, and ran proof-of-principle experiments.

All other parts submitted

TetR Mutants

In addition to our three favourite tetR mutants, we created these four:

• K613013 V36F mutant
• K613014 V36F W43S mutant
• K613018 Y42F K108E mutant
• K613019 P39Q Y42M mutant

T7 Promoter variants

We submitted a family of T7 promoters with varying strength. Our lysis selection device uses what we refer to as the wild-type (100% reported strength) T7 Promoter:

• K613001 T7 Promoter, 100% reported strength

In addition, we submitted the following mutants:

Variants without additional lac operator (constitutive):

• BBa_K613002 T7 Promoter, 14% reported strength
• BBa_K613003 T7 Promoter, 30% reported strength
• BBa_K613004 T7 Promoter, 54% reported strength
• BBa_K613005 T7 Promoter, 80% reported strength
• BBa_K613006 T7 Promoter, 111% reported strength

Variants with additional lac operator (LacI repressed):

• BBa_K613007 T7 Promoter, LacI repressed, 100% reported strength
• BBa_K613008 T7 Promoter, LacI repressed, 14% reported strength
• BBa_K613009 T7 Promoter, LacI repressed, 30% reported strength
• BBa_K613010 T7 Promoter, LacI repressed, 54% reported strength
• BBa_K613011 T7 Promoter, LacI repressed, 80% reported strength
• BBa_K613012 T7 Promoter, LacI repressed, 111% reported strength

Medium-strength Plac

We submitted a new Plac promoter of medium strength. We characterized it with ATC inductions, using RFP as a readout.

• BBa_K613000 pLac promoter, medium strength