Team:WITS-CSIR SA/Project/Concept

The team this year has decided to create a microscopic biological communication network, in which there will be the transfer of data between bacterial populations as chemical signals. “Biotweet” provides a generic framework that will serve as the basis for the functioning of complex biological communication networks. This framework may be useful in various applications, including those of the medical and industrial sectors.

An integral component of any network is the establishment of the connections between the nodes of the network. These allow for the directed transport of data packets between specific nodes. We have, therefore, focused our efforts on constructing these abstract connections that would exist in our biological network: a challenging task, considering that bacterial cells cannot be linked by wires. Analogous to the transfer of data as electronic packets in a computer network, the concept of engineering bacteria to transport packets of chemical signals between bacterial populations arose. In this way, the bacteria themselves can form the network connections. In order to do this, we decided to reprogram the motility of bacteria, so that they will travel in a stimulus-directed fashion to points of the network, where they can send and receive signals. To ensure that the bacteria do not take a detour, and lose the data in the event that they encounter a natural stimulus, the stimuli that induce this chemotactic response would need to be specific to the application of the network and new to the bacteria. With these specifications in mind, we needed a way of manipulating the chemotaxis of bacteria that would allow for us to easily adapt the bacterial chemotactic response to the stimuli associated with any application.

We have therefore chosen to use riboswitches to control the expression of the flagella rotation regulator protein CheZ (Fig 1), and ultimately bacterial chemotaxis (Topps and Gallivan, 2007).

Riboswitches are ligand-inducible RNA protein expression regulators that are comprised of an aptamer domain and an expression platform (Gallivan, 2007). The aptamer is a sequence of nucleotides that is designed to specifically bind to ligands, while the expression platform consists of a ribosome binding site (RBS) and a downstream gene. When the specific ligand binds to the aptamer domain, the riboswitch undergoes a structural change. This results in the exposure of the RBS (that is otherwise hidden) and the expression of the downstream gene (Gallivan, 2007). Using this riboswitch mechanism, the expression of CheZ can be regulated in a ligand concentration-dependent manner, outside the control of the natural chemotaxis pathway. Topps and Gallivan (2007) demonstrated that these riboswitches can be used to reprogram the chemotactic response of bacteria, so that they move up a concentration gradient, towards the source of the stimulus that activates the riboswitch. This process is called pseudotaxis. By using these riboswitches, bacteria can theoretically be reprogrammed to respond to any stimulus, if the appropriate riboswitch is made. This provides the versatility needed for biological network connections to be established in any application. Furthermore, this eliminates the need to engineer novel chemoreceptors, which is particularly challenging due to the complexities that occur at the interface between the new chemoreceptor and the already existing downstream signalling proteins (Topps and Gallivan, 2007).