Team:Groningen/Project/Construct

From 2013.igem.org

(Difference between revisions)
Line 49: Line 49:
<h3>Promoter activity</h3>
<h3>Promoter activity</h3>
 +
 +
BBa_K108
<div align="left">  <!--you can use left/right or center to align the image-->
<div align="left">  <!--you can use left/right or center to align the image-->
<table  id="layout" width="100%"> <!--change the percentage to determine the size of your image-->
<table  id="layout" width="100%"> <!--change the percentage to determine the size of your image-->
Line 87: Line 89:
<tr>
<tr>
<td>
<td>
-
<font size="1">Figure 3: In (a) An overlay picture is shown from the phase-contrast and GFP-channel picture. In (b,c) The intensity in of ~40 cells in the GFP-channel, were analyzed from two pictures. The average intensity (AU) from the cells are plotted above with the standard deviation. In (b) a GFP from our group is shown and in (c)a biobricked GFP (BBa_E0840) is shown in a plot.</font>
+
<font size="1">Figure 3: In (a) An overlay picture is shown from the phase-contrast and GFP-channel picture. In (b,c) the intensity in of ~40 cells in the GFP-channel, were analyzed from two pictures. The average intensity (AU) from the cells are plotted above with the standard deviation. In (b) a GFP from our group is shown and in (c)a biobricked GFP (BBa_E0840) is shown in a plot. wt=wildtype, T0= before induction, T1,2,3=#h of induction with IPTG.</font>
</td>
</td>
</tr>
</tr>

Revision as of 13:06, 1 October 2013

Constructs

An amyE intergrational backbone

To transform B. subtilis with our developed biobricks we have improved the amyE intergrational backbone from Munich's iGEM team 2012 (BBa_K823023) that had no inducible promoter. We've added the HyperSpank IPTG inducible promoter from Rudner's Lab 2004. This promoter is placed right in front of the prefix, so any biobrick can be inserted in this backbone (BBa_K1085014) and can be induced with IPTG.

In figure 1 a close-up of the promoter is shown.

The HyperSpank promoter has a single nucleotide change (G->T) at the -1 position. This increases the expression levels but also causes leaky expression when IPTG is absence[1]. To improve repression, a second lacO operator site has been inserted 71 bp upstream of the first. (David Rudner, Harvard Medical School)

Figure 1: Hy_Spank promoter

Figure 2:

Promoter activity

BBa_K108
Figure 3
A:

B:

C:
Figure 3: In (a) An overlay picture is shown from the phase-contrast and GFP-channel picture. In (b,c) the intensity in of ~40 cells in the GFP-channel, were analyzed from two pictures. The average intensity (AU) from the cells are plotted above with the standard deviation. In (b) a GFP from our group is shown and in (c)a biobricked GFP (BBa_E0840) is shown in a plot. wt=wildtype, T0= before induction, T1,2,3=#h of induction with IPTG.





Silk concstructs


What kind of spider silk gene is it
What are general problems with this gene
Where did we get it from.
Codon optimisation, solved the problems.

Strep-tag


Why this is needed
For what purposes it comes in handy

Signal peptide


Why is it so important.
The use of existing pathway so not lots of trouble
The signal sequences are nice addition to the registry
how the pathway works and how the silk will be secreted