Composite

Part:BBa_K410000

Designed by: Christina Graves, Scott Holmes   Group: iGEM10_GeorgiaTech   (2010-10-27)
Revision as of 19:17, 7 November 2010 by Debika89 (Talk | contribs)

Periplasmic Heat Generation


What it is: This part consists of hybB-ompA-AOX1A. HybB is a cold shock promoter. OmpA is a periplasmic targeting sequence, and AOX1A is a gene responsible for thermogenesis in the sacred lotus, a plant. What it does: Induces AOX1A expression in response to a cold shock. Here, we describe a "cold shock" as incubating E. coli between 20-30C for 10-12 hours. The part should produce a thermogenic response raising the temperature of the E. coli's immediate environment (plate or liquid cultures) above ambient temperature.


Usage and Biology

Characterization

Absolute Temperature Characterization

pSB1A3 containing biobrick part hybB-OmpA-AOX1a was transformed into E. coli BL21. Transformants were grown in 600 mL of LB media(+carbenicillin) at 37 degrees Celcius overnight. The solutions were centrifuged, the soft pellet collected, and resuspended in equivalent amount of fresh LB media(+carbenicillin). The cultures were then placed in a 10 degrees Celcius incubator for 1 hour. 75 mL were pipetted into three different insulated containers and placed in 15, 20 and 25 degrees Celcius incubators for 1 hour acclimation period. Temperatures were recorded at regular intervals using a thermistor. In addition to the pSB1A3 vector containing the biobrick part, a control (pSB1A3 vector with insert hybB-OmpA-mRFP) was also monitored. The graphs shown below illustrate absolute temperature change over time at different incubation temperatures. width: 150px

width: 200px

width: 250px

The graph below illustrated absolute temperature difference from initial temperature, when t=0.

Baseline.jpg

Cell Density and Growth Rate Monitoring

Two constructs (hybB -- ompA -- AOX1A, and hybB-ompA-mRFP)in vector pSB1A3 were transformed into E. coli BL21. The mRFP construct served as a control in this experiment, and an additional control of empty vector (psB1a3) was also transformed. Colonies were inoculated into LB and carbenicillin (100 mL) and incubated at 37 until the optical density reached 0.8. After the OD levels reached 0.8 for all cultures, flasks were transferred to 37, 30, 25, 20, or 15 degrees Celsius incubators (with agitation @ 210 rpm). Optical density was measured at regular intervals using a spectrometer. Data below is plotted on a logarithmic scale.

0D15.jpg

OD20.jpg;

OD25.jpg

OD30.jpg

OD37.jpg


Part Design


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 394
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


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Categories
Parameters
None