Team:XMU-China/Project/Appoach

In December 2010, we began thinking about project for 2011 iGEM .We tried to get inspiration from materials provided by iGEM teams in past three years. And we put forward many ideas. For example, we could construct a kind of E.coli which can decompose and detect carbinol harming human body. Another example is that we try to make E.coli have magneto taxis. We collected papers about those ideas. One day，our instructor had Pu’er tea in his office，and said to us that this kind of tea isn’t bitter but sweet because it is fermented. One of team member felt interesting. What’s more, she found that the concentration of bacteria used for fermentation is the most important factor influencing taste of the tea. At present, the usual method controlling the concentration of bacteria is adjusting the concentration of the medium. We thought: if bacteria can keep the optimum concentration by itself, fermentation technology can be simplified.

Figure 1: From brainstorm to our project i-ccdB.

Design

We know that Vibrio fischeri is typical bacterium of quorum-sensing. This bacterium was shown to coordinate their behavior via the secretion of specific signaling molecules in a population density-dependent manner. Lux Box, luxR and luxI are key control elements of quorum-sensing mechanism in Vibrio fischeri. In 2004，Arnold’s lab published a paper in NATURE Magazine, Programmed population control by cell–cell communication and regulated killing. They have built and characterized a ‘population control’ circuit that autonomously regulates the density of an Escherichia coli population. The cell density is broadcasted and detected by elements from a bacterial quorum-sensing system, which in turn regulate the death rate. We wanted to go further in this direction and did more research that makes the concentration of E.coli keep at different levels.

Different subprojects

Our research attempted to decouple quorum-sensing mechanism in Vibrio fischeri, construct standard cell-cell communicating system, and analyze factors that influence communicating system on genetic level. Major works were listed as follows:

1. constructing standard programmed cell-death circuits

2. constructing a series of standard programmed cell-death circuits，which have different RBS sequences before splicing killer fusion gene lacZɑ-ccdB

3.using the method of site-directed mutagenesis to modify the promoter lux pR，changing its efficiency

4. performing these circuits

Aims

Bacteria concentration has significant impact on production of fermentation product. Product concentration is proportional with bacteria concentration at suitable special growth rate. The primary metabolite production is the case, such as amino acid and vitamin. However, for secondary metabolite production, such as antibiotic, the special growth rate should not be too high. Otherwise, it would generate negative impacts, such as fast consumption of nutrient substance, significant change of culture media, accumulation of toxic substance in culture media and significant decline of OD, which would alter the metabolic pathway of bacteria. We aimed at constructing a series of bacteria can maintain at the different concentration by itself. We hope that our work can introduce a new way which controls the concentration of bacteria for fermentation process control technology.

The Final Product

The device is designed to build a programmed bacterial death circuit, which is based on the quorum sensing system of Vibrio fischeri. The LuxI protein synthesizes a small, diffusible acyl-homoserinelactone (AHL) signaling molecule. The AHL accumulates as the cell density increases. At sufficiently high concentrations, it binds the LuxR, which induces the expression of the killer gene ccdB under the control of a promoter lux pR. Sufficiently high levels of CcdB which is a bacterial toxin that targets DNA gyrase cause cell death. Low cell density doesn’t have the ability to produce sufficient LuxR/AHL complex to activate the promoter lux pR. The programmed death circuit ends and the cell density increases. When the cells reach a certain concentration, the death circuit is restarted. Back and forth, the programmed death is achieved in the dynamic process of growth and death. In that way, the bacteria population is programmed to maintain one certain cell density. In order to control the expression of the killer protein ccdB, we designed a series of bacteria population-control devices using RBSs with different efficiency. The cell growth and fluorescent curves corresponding to different RBSs illustrate that the bacteria population was successfully controlled at different cell densities.