Revision as of 14:50, 21 October 2009

Meetings Calendar

Metal Sequester

Introduction

In order to take up and keep the cadmium from the soil efficiently, we needed to think about a way to cross-link the metal ions to intra-cellular proteins which would end up for the most of it in the spore. If the heavy metal ions were not cross linked to a "sponge protein", it could be lethal to the cell at lower concentration and the cell could end up sporulating too early, or even bursting in the soil, releasing all the heavy metal it has taken up.
From our meeting with Prof. Nigel Robinson on the 18th of March 2009, it was evident that the best way of getting cadmium into the spore is to express a metallothionein, which would 'soak up' the cadmium, which in turn would be trapped within the protein in the spore.

Novelty in this sub-project

To increase the efficiency of our system in sequestering the heavy metal cadmium from the soil, we divised a plan to make sure that most of the metal ions that have been taken in our B.subtilis cell is then rendered bio-unavailable by incorporating it into smtA metallothionein.

SmtA metallothionein protein from E. coli can bind to heavy metals [1,2,3]. They have a tendency to bind to cationic metal ions such as cadmium, copper, arsenic, mercury, silver.

It has been shown that in B.subtilis, in order to express a specific protein in the spore coat, it is possible to make a fusion protein with a spore coat protein called CotC, and a group have successfully expressed antigen proteins which are about the same size as our smtA metallothionein in order to make a vaccine. By fusing CotC spore coat protein from Bacillus subtilis, our smtA metallothionein can be localized to the spore coat, hence we can successfully trap most of the metals ions into the bacterial spores.

It is also fused with GFP reporter gene to see the spores using a microscope. The fusion protein expression will be controlled by sigK promoter which is activated by sporulation conditions.

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-It has been shown that in ''B.subtilis'', in order to express a specific protein in the spore coat, it is possible to make a fusion protein with a spore coat protein called ''CotC'', and a group have successfully expressed antigen proteins which are about the same size as our ''smtA'' metallothionein in order to make a vaccine. By fusing CotC spore coat protein from Bacillus subtilis, our ''smtA'' metallothionein can be localized to the spore coat, hence we can successfully trap most of the metals ions into the bacterial spores.
+It has been shown that in ''B.subtilis'', in order to express a specific protein in the spore coat, it is possible to make a fusion protein with a spore coat protein called ''CotC'', and a group have successfully expressed antigen proteins which are about the same size as our ''smtA'' metallothionein in order to make a vaccine. By fusing CotC spore coat protein from ''Bacillus subtilis'', our ''smtA'' metallothionein can be localized to the spore coat, hence we can successfully trap most of the metals ions into the bacterial spores.
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 <br>It is also fused with GFP reporter gene to see the spores using a microscope. The fusion protein expression will be controlled by sigK promoter which is activated by sporulation conditions.

Team:Newcastle/Metals

From 2009.igem.org

Revision as of 14:50, 21 October 2009

Metal Sequester

Introduction

Novelty in this sub-project

Modelling

BioBrick constructs

Lab Work Strategies

Other Presentations and Diagrams