Team:Groningen/Project/WholeSystem

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Revision as of 09:57, 17 October 2009

Introduction

Cloning Strategy

Figure 1: Whole system, combining the bouyancy device on a pSB2K3 vector and the accumulation device on a pSB1AC3 vector

Results

Combining parts Bba-K190033 and Bba_K190038 was done by using a normal transformation protocol with both ampicillin and kanamycin as antibiotics. A buoyancy test was performed as described also using both ampicillin and kanmycin as antibiotics. Iptg was also added to the dayculture to induce the Bba_K190033 part. In exponential phase 10μM NaAsO2 was added to half of the samples. A restriction was done to check the transformation.

Restriction

Figure 1 shows that the transformation of both vectors succeeded.

Figure 1

The gel shows a 1Kb marker to the far left, after that two times a restriction with EcoR1 and Pst1 can be seen. This shows clearly fragments of 6000pb and 4500pb for the Bba_K190033 and fragments of 2000pb and 1300 bp for the Bba_K190038. The next two slots show non-restricted plasmids, two distinc bands can be seen clearly indicating the presence of two plasmids.

Buoyancy test

The buoyancy test elegantly shows that combining both an accumulation device and the gvp-buoyancy device allows buoyancy.

Figure 2

On the left the system without arsenic can be seen and on the right the system with arsenic is shown. It can be seen that the right sample floats. This indicates that the GlpF is transporting the arsenic inside the cells, the fMT accumulates it (otherwise the cells would be dead) and the gvp was induced by the arsenic so the cells start to float.

Conclusion