Difference between revisions of "Team:SF Bay Area DIYBio/Results"

 
Line 1: Line 1:
 
{{SF_Bay_Area_DIYBio}}
 
{{SF_Bay_Area_DIYBio}}
 
+
__NOTOC__
 
==Accomplishments==
 
==Accomplishments==
  

Latest revision as of 13:14, 21 November 2015

Accomplishments

Researched UV sources and built UV exposure rig to mimic solar UV

  • UVA: 320-400nm. “Tanning” wavelengths. Long-term free radical damage
  • UVB: 280-320nm. Causes sunburn and direct DNA damage
  • UVC: 100-280nm. Rapid skin and retinal damage (e.g.: germicidal UV in BSC)

We want to mimic solar UV: broad-band UVA+UVB, but not UVC! After testing many UV sources, we settled on:

  • UVB basking lamp for pet reptiles
  • UVA nail curing lamp

Spectra.png

Determined exposure level needed for >4 log decrease in CFU

UV kill curve was generated for E.coli HB101, to establish baseline exposure for Directed Evolution

We also tested HB101 + pGLO plasmid, to check if GFP has a protective effect.

Kill Curve results.png

Demonstrated GFP is NOT an effective UV protectant for E.coli

4 log decrease in viable cells after 75min for HB101, 30min for pGLO

If anything, pGLO has a negative effect on UV resistance!

Synthesized and transformed A. variabilis shinorine biosynthesis genes

Submitted one gene (Ava_3856) to Parts Registry

Demonstrated that we produced UV absorbing compounds

MAA’s can be extracted with methanol:

  • Grow 20ml culture overnight in TSB
  • Spin down & wash in saline 2x
  • Extract in 2ml methanol at 4C overnight
  • Pellet at 10,000rpm, collect supernatant
  • Collect UV absorption spectrum:
    • E. coli HB101 (control)
    • HB101+Ava_3858-3855 (full shinorine pathway)
    • HB101+Ava_3858-3856 (up to mycosporine-glycine only)

UV Absorption Curve.png

Yay - we’re producing UV absorbing compounds! Further analysis will have to wait until we get our HPLC up and running...