Mini-bootcamp 2011

From MurrayWiki
Revision as of 17:38, 8 February 2011 by Murray (Talk | contribs)

Jump to: navigation, search

This page contains a description of the mini-bootcamp run in Feb 2011.

Group

Students
  • Jorge Goncalves
  • Jun Liu
  • Yuan Ye
  • Enoch Yeung
Part-time students
  • Elisa Franco
  • Richard Murray
Instructors
  • Emzo de los Santos
  • Joe Meyerowitz
  • Ophelia Venturelli
  • Vanessa Jonsson
Project advisor
  • Richard Murray

Project description

The goal of this project is to measure variability in gene expression that is relevant for synthetically designed circuits. The issue that we are trying to understand is now much variability arises for the expression of a given circuit under degrees of freedom that are typically not controlled in synthetic designs:

  • Location and orientation of circuit elements in the plasmid
  • Vectors used for expressing the circuit, including copy number and antibiotic resistance
  • Growth conditions (temperature, oxygen, media, growth phase)

To understand how these (and other) factors will affect circuit operation, a simple genetic circuit consisting of 2 reporters will be built and implemented in a variety of conditions. The dynamic response of the circuit will be measured, including cell-to-cell variability (via flow cytometry and microscopy).

Project objectives:

  • Construct a simple genetic circuit that tests the effects of putting different reporters in different configurations in a plasmid.
  • Characterize the differences (if any) in mean expression level of the circuits, possibly in multiple growth conditions, using a plate reader
  • Characterize differences in expression distributions using flow cytometry (FACS Calibur) and fluorescent microscopy
  • Perform in vitro testing of the constructs using the PURExpress kit and spectrofluorometer to check for differences in mean expression level

Lambda switch.png

  • Circuit layout: directions, ordering

Biobrick plasmid.png

  • (Cell strain)
  • Growth media: LB, M9/glycerol, M9/glucose
  • Induction level
  • Temperature

Schedule

Session 0: project discussion and lab tour

Session 1: cloning

Session 2: gels

Session 3: plate reader

Session 4: microscope

Session 5: spectrofluorometer

Session 6: flow cytometer