Team:Purdue/Characterization

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Characterization & Experimental Design

Meeting 7/2/12
List of What Needs to get Done this Week:
  • Research protocols on setting up and running experiments using biofilms
  • Research flow and static protocols for biofilms
  • Research ways to characterize silica matrix and acquire quantifiable data
  • Create timelines for each assay researched
  • Order reagents and get training on any equipment needed for assays
7/3/12
Researched stages of biofilm formation:

1. Initial Attachment - attachment occurs via van der waals forces

2. Irreversible Attachment - this is where the EPS forms

3. Maturation I - matrix formed with adhesion proteins

4. Maturation II - the full biofilm forms

5. Dispersion - bacteria released

Also researched shear stress modeling, chassis development, microsensors, and confocal microscopy assays. Research was done on different ways to characterize the silica coat. Three extremely helpful articles are listed below.
A powerpoint highlighting possible characterization methods is given here

After discussion with the team and our faculty advisor, Dr. Rickus, we have decided to use the scanning eletron microscopy (SEM), x-ray diffraction (XRD), and a live/dead assay (specifically, the Baclight Bacterial Viability Kit).

Contents

7/5/12

Researched possible competitors in the field of bioreactor filtration.

  • Hydro Engineering - produces "Hydrokleen", which is a bioreactor filtration system that would generally be used in industrial plants and acts as a water recycler.
  • Seven Trent Services - produces Tetra Amphidrone fixed sequencing Batch Biological Filter, a waste water treatment process that uses a biological filter to remove various pollutants
  • Kinetics - this company makes a range of water treatment processes and machines that can be used in industry as well as consumer markets
  • ABEC - produces bioreactors, but could not find more detail into what kind


7/8/12


Created a cell culture to have competent cells for a biofilm culture.</br>


Also did research into developing a static biofilm assay to test how well our bacteria makes biofilm before and after our transformation. <a href="http://media.wiley.com/CurrentProtocols/0471729256/0471729256-sampleUnit.pdf">"Growing and Analyzing Static Biofilms"</a> by Judisth H. Mernitt, Daniel E. Kadouri, and George A. O'Toole was helpful in determining how we would do this assay.</br>


7/9/12


Performed the <a href="https://2012.igem.org/Team:Purdue/Protocol#Stationary Phase"> Gorwth Rate Assay</a> on NEB Beta and DH5 Alpha E.coli strains to determine the time frame we will use to grow our static biofilms.A typical bacterial growth curve is shown below. This is what we expect our curves to look like. </br>
<img border="1" align="left" src="Bacterial_growth_curve.jpg" width="400" height="296"/>













Below is the results of the growth rate assay for NEB Beta and DH5 alpha. Overall, the plots show the expected shape with a lag, log, and stationary phase.

<img border="1" align="left" src="Growth_Rate_NEB_and_DH5.jpg" width="481" height="292"/>














Also worked out the lab plan for the rest of the week.</br>

7/10/12

We did the same <a href="https://2012.igem.org/Team:Purdue/Protocol#Stationary Phase"> Gorwth Rate Assay</a> as yesterday, but with the XL-10 Gold E.coli strain because we think it will work better for the biofilm purposes.</br>


Below is the results of the growth rate assay for XL-10 Gold. The plots show the expected shape with a lag, log, and stationary phase. <img border="1" src="Growth_Curve_XL10.jpg" width="482" height="292"/>

<a href="https://static.igem.org/mediawiki/2012/4/41/Bacteria_Growth_Rate.xls">Here </a> is the excel file containing all of the data from the three growth rate assays.


Also researched and developed the static biofilm assay that we can do to determine the biofilm rates of our non-transformed E.coli.</br>

7/13/12


Performed the <a href="https://2012.igem.org/Team:Purdue/Protocol#Static Biofilm"> Static Biofilm Assay</a>.</br>


Had a team meeting, discussed goals for the following week:</br>

  • Write out protocols and email them to the entire team for revisions
  • Plan a meeting to go through and troubleshoot the protocols together
  • Find a way to determine the optimized concentration of curli
  • Purchase all materials needed for future protocols


7/16/12


Researched how Membrane Aerated Bioreactor work and how we will use one for testing.</br>

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