Composite

Part:BBa_K515102

Designed by: Atipat Patharagulpong   Group: iGEM11_Imperial_College_London   (2011-09-07)
Revision as of 01:26, 22 September 2011 by Nk2909 (Talk | contribs)

J23100 promoter - PA2652


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 710
    Illegal NgoMIV site found at 812
    Illegal AgeI site found at 118
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1019


This BioBrick has been sequence verified.

Background

Malate responding chemoreceptor originally found in Pseudomonas aeruginosa PA01[1] is a codon optimised translational subunit. This subunit BBa_K515002 contains optimised insulator and RBS sequence, its expression is under the control of constitutive promoter BBa_J23100. Device is used as an additional chemoreceptor for endogenous chemotaxis mechanism of E. coli. Device responds to L (-) malic acid, linear formula (HO2CCH2CH(OH)CO2H).

Device contains 15 bp insulator seuence, which ensures tunability of expression through easy switching of promoters. In addition, insulator sequence allows the translation initiation rate (TIR) of the ribosome binding site (RBS) to remain the same, when the promoter is replaced.

Device is compatible for motile strains of E. coli. It has been tested in E. coli DH5α strain, inserted in the vector backbone pSB1C3.

Experimental Data

Behavioral analysis of E. coli cells was used to identify functioning of this device. The analysis is based on the transient difference in velocities of bacteria capable of sensing chemoattractant, when exposed to attractant which is in comparison to control cells, that are unable to sense L (-) malic acid.

Figure 1: Probability density function of bacterial number at observed velocities. PA2652 cells exposed to 10 mM malate are more than 90% likely to be moving at just over 2 μm/s. PA2652 cells that were exposed to serine were 90% likely to be moving at velocity just over 2 μm/s. PA2652 cells that were not exposed to attractant were have likely to be found at velocity of Rising concentrations of serine were tested. a) 0 mM control - circular colony b) 0.01 mM - circular colony e) 0.1 mM - circular colony d) 1 mM - possible eliptical colony c) 10 mM - eliptical colony f) 100 mM - eliptical colony away from the attractant. Data collected by Imperial iGEM 2011.

References

[1] Alvarez-Ortega C and Harwood CS (2007) Identification of malate chemoreceptor in Pseudomonas aeruginosa by screening for chemotaxis defects in an energy taxis-deficient mutant. Applied and Environmental Microbiology 73 7793-7795.

[edit]
Categories
//cds/receptor
Parameters
chassisE. coli DH5α
controlJ23100
device_typeChemotaxis receptor
ligandsMalate
originP. aeruginosa
resistanceChloramphenicol