SynBERC:MIT/Calendar/2007-8-8: Difference between revisions

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==Wanted parts==
==Wanted parts==
* Expression biobrick plasmids
* Expression biobrick plasmids
** T7 promoter
** T7 promoter - may have patent issues but it has been tried and tested.
** T3
** T3
** SP6
** SP6
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* Transposase genes
* Transposase genes


* R6 origin plasmids
* Plasmid origins
** R6, P1, F, colE1


* chomosomal integration fragments
* chomosomal integration fragments

Revision as of 10:25, 8 August 2007

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Anyone in the synthetic biology community is welcome to attend.

Wednesday August 8, 2007 at 12:30pm EST

32-D463, MIT

Topic of discussion

Jason Kelly will be leading a discussion on how do we make BioBricks more useful for academic research labs. In this discussion, we will also be generating a list of "wanted" BioBrick parts.

Wanted parts

  • Expression biobrick plasmids
    • T7 promoter - may have patent issues but it has been tried and tested.
    • T3
    • SP6
    • T7 RNA polymerase containing strains
    • also T3, SP6 What are the patent issues on these?
  • Popular plasmids
    • Any requests through the SynBERC BB plasmid project? (Collin)
  • xre protein, promoters (subtilis)
  • antibiotic cassettes
    • Apramycin
    • Trimethoprim
  • Transposase genes
  • Plasmid origins
    • R6, P1, F, colE1
  • chomosomal integration fragments
    • choice of locations on the chromosome
  • cell killing enzymes
    • VSVG
  • protein export tags
    • phoA
  • protein purification tags, antibody epitopes
    • FLAG
    • 6HIS
    • Strep
    • GST
    • Chitin binding
    • MBP
  • protein solubility
    • maltose binding protein
  • protein splicing domains
  • surface display proteins
    • LPP/OmpA
    • Neisseria IgA1
  • New fluorescent proteins
    • EBFP2 blue
    • new red monomers
  • luminescent reporters
    • renilla
    • photuris
    • bacterial (Photorhabdus)
  • Promoters in reverse direction
  • Parts to enable custom insertions in the middle of devices (e.g. a set of alternate restriction sites that are also kept out of BBs (and BB plasmids) when possible to support using them for editing)
  • Add your wanted part here ...

Live Notes

Rocking the notetaking:

  • Audience: Asking about creating a 5-gene operon, something to do with the PZE system, interested in using BB methods to build permutations of the transcription logic
  • Audience: GST tags are key for surface plasmon resonance

Question: how do people keep track of plasmids and their constructs?

Problem: right now people do not have a way to import or export annotated sequence files from the registry.

Jason: one of the most useful functions of the Registry is documentation and archival of parts.

The Sauer lab just uses a notepad to keep track of plasmids.