Innovative Methods for Selective Silencing of Microbial Signals Using Micro-Scavengers in Artificial Life Systems
Jitka Čejková, University of Chemistry and Technology, Prague, Czechia
The aim of our project is to develop innovative methods to modulate microbial communication by selectively silencing specific signalling substances within microbial environments. This approach, akin to silencing certain words in a conversation to observe the resulting changes, involves using micro-scavengers (MSSs) equipped with an active core, gating mechanism, and magnetic particles for remote manipulation. These MSSs will absorb signalling substances through mechanisms such as complexation of metal ions, adsorption of low-molecular-weight organic substances, and catalytic degradation. By periodically regenerating the scavengers via photocatalytic degradation, we will maintain their capacity for signal removal. This methodology allows for the investigation of phenomena such as quorum sensing (QS), where microorganisms gauge population size through signal concentration. The ability to disrupt QS can mitigate pathogenic behaviours or induce dormancy in microorganisms, offering potential applications in antifouling and preservation. Additionally, selective signal scavenging will enable the study of chemotaxis and can facilitate active microbial control, paving the way for unconventional applications like biocomputing. Our work aligns with the goals of the Molecular Communication Approaches for Wetware Artificial Life workshop, providing insights into the engineering of molecular communication to enhance the functionality and complexity of artificial life systems.
Asymmetrical Division in Populations of Protocells
Marco Villani [1,2] (speaker), Roberto Serra [1,2,3]
[1] University of Modena and Reggio Emilia, Italy; [2] European Centre for Living Technology, Venice, Italy; [3] Institute of Advanced Studies, University of Amsterdam, Netherlands
The growth of a protocell population that divides symmetrically requires the synchronization between the two processes of duplication of the genetic material and of fission of the lipid container. However, uneven division, where daughter protocells are of different sizes, often occurs. This work examines asymmetrical division, where each protocell produces two daughters of different sizes, making true synchronization impossible. The concept of homogeneous growth is introduced to ensure sustainable population growth. Various models of protocell growth and reproduction are considered, showing through simulations that homogeneous growth can occur in both Surface Reaction Models (where replicators are in the membrane) and Internal Reaction Models (where replicators are in the internal water phase) under different kinetic equations. The study suggests that the “chemical signature” of a protocell, defined by the ratios of replicators at fission time, is conserved through generations when linear kinetic equations are involved.
Programming Biological Systems with Synthetic Biology
Thomas Gorochowski, Royal Society University Research Fellow & Associate Professor of Biological Engineering,
School of Biological Sciences, University of Bristol, UK
I have always been fascinated by the possibility of reprogramming biology across scales using synthetic biology as a foundation. In this talk, I'll cover some of the diverse projects my lab has been working on in this area, covering the characterisation of genetic parts and regulatory circuits using sequencing technologies, to the spatial control of living collectives using light. I hope this scattering of science will give you a feeling for my broad scientific interests and demonstrate some of the exciting possibilities that synthetic biology approaches offer to harness biology in new ways.