"
Team:Imperial College London/Project Chemotaxis Specifications
From 2011.igem.org
(Created page with "{{:Team:Imperial_College_London/Templates/Header}} {{:Team:Imperial_College_London/Templates/Chemotaxis}} <html> <body> <h1>Specifications</h1> <p>The chemotaxis module is respo...") |
|||
| Line 5: | Line 5: | ||
<body> | <body> | ||
<h1>Specifications</h1> | <h1>Specifications</h1> | ||
| - | <p>The chemotaxis module is responsible for ensuring that our bacteria move towards roots. For this, the bacteria need to be able to sense a common root exudate. We have chosen E. coli chemotaxis to be rewired towards malic acid (also referred to as malate), compound found in TCA cycle, which is | + | <p>The chemotaxis module is responsible for ensuring that our bacteria move towards roots. For this, the bacteria need to be able to sense a common root exudate. We have chosen <i>E. coli</i> chemotaxis to be rewired towards malic acid (also referred to as malate), a compound found in TCA cycle, which is released form the roots at low concentrations. Since <i>E. coli</i>, the chassis we are using for lab experiments, does not normally exhibit chemotaxis towards malate, we needed to engineer a malate-responsive sensor into the microbes that will enable them to perform chemotaxis towards roots.</p> |
| - | <p>Following chemotaxis towards the roots, our bacteria should be taken up into the roots. We want the bacteria to get taken up into the plant roots to ensure that the concentration of indole-3-acetic acid in the plant is increased. If the bacteria remained outside the roots, this goal may also be reached but | + | <p>Following chemotaxis towards the roots, our bacteria should be taken up into the roots. We want the bacteria to get taken up into the plant roots to ensure that the concentration of indole-3-acetic acid in the plant is increased. If the bacteria remained outside the roots, this goal may also be reached but it may be harder to increase internal IAA concentration. In addition, uptake of bacteria into the roots followed by secretion of chemicals presents a novel platform for modifying plants without genetically modifying the plant genomes. |
| - | In a paper published last year, Paungfoo-Lonhienne et al. showed that Arabidopsis and tomato plants are able to actively break down their cell wall to take up GFP-tagged E. coli and S. cerevisiae and use them as a source of nutrients. </p> | + | In a paper published last year, Paungfoo-Lonhienne et al. showed that <i>Arabidopsis</i> and tomato plants are able to actively break down their cell wall to take up GFP-tagged <i>E. coli</i> and <i>S. cerevisiae</i> and use them as a source of nutrients. </p> |
</body> | </body> | ||
</html> | </html> | ||
Revision as of 17:00, 18 September 2011
Module 1: Phyto-Route
Chemotaxis is the movement of bacteria based on attraction or repulsion of chemicals. Roots secrete a variety of compounds that E. coli are not attracted to naturally. Accordingly, we engineered a chemoreceptor into our chassis that can sense malate, a common root exudate, so that it can swim towards the root. Additionally, E. coli are actively taken up by plant roots, which will allow targeted IAA delivery into roots by our system.
Specifications
The chemotaxis module is responsible for ensuring that our bacteria move towards roots. For this, the bacteria need to be able to sense a common root exudate. We have chosen E. coli chemotaxis to be rewired towards malic acid (also referred to as malate), a compound found in TCA cycle, which is released form the roots at low concentrations. Since E. coli, the chassis we are using for lab experiments, does not normally exhibit chemotaxis towards malate, we needed to engineer a malate-responsive sensor into the microbes that will enable them to perform chemotaxis towards roots.
Following chemotaxis towards the roots, our bacteria should be taken up into the roots. We want the bacteria to get taken up into the plant roots to ensure that the concentration of indole-3-acetic acid in the plant is increased. If the bacteria remained outside the roots, this goal may also be reached but it may be harder to increase internal IAA concentration. In addition, uptake of bacteria into the roots followed by secretion of chemicals presents a novel platform for modifying plants without genetically modifying the plant genomes. In a paper published last year, Paungfoo-Lonhienne et al. showed that Arabidopsis and tomato plants are able to actively break down their cell wall to take up GFP-tagged E. coli and S. cerevisiae and use them as a source of nutrients.
