Award details

Engineered security systems for environmental synthetic biology

Reference	BB/J019720/1
Principal Investigator / Supervisor	Professor Thomas Ellis
Co-Investigators / Co-Supervisors	Professor Guy-Bart Stan
Institution	Imperial College London
Department	Bioengineering
Funding type	Research
Value (£)	120,073
Status	Completed
Type	Research Grant
Start date	01/09/2012
End date	30/11/2013
Duration	15 months

Abstract

Synthetic biology applies the principles of engineering to biology and in doing so has advanced the pace of development in biotechnology, particularly in microbial systems. By-and-large most designs utilise plasmids in the engineering process and also for hosting the synthetic DNA constructs in the final application. While this is understandable from a technical perspective, it is undesirable from a safety aspect, as plasmids are inherently mobile DNA elements that are prone to spreading through diverse microbial populations through horizontal gene transfer (HGT), especially when they encode antibiotic resistance markers. For synthetic biology applications to be considered safe and gain regulatory approval a design-change is needed. For this reason, this proposal aims to provide crucial new security tools for synthetic biology. By designing, modelling and implementing several new 'security devices' using a parts-based approach, we will create multiple, redundant mutual-dependencies between modular plasmids and engineered E. coli cells and produce a kit that will be suitable for synthetic biology to be applied to real-world applications such as environmental biosensing. This will be a crucial step in allowing synthetic biology applications to be put to use in defence, energy, environment and health situations. The devices of our engineered system will be based on toxin-antitoxin (TA) systems (including those known to work in both gram-positive and gram-negative bacteria), as well as on auxotrophic selection systems and recently described tunable conditional origins of replication (CORs). To help assess our success and to inform our designs we will also develop a fluorescence-based assay to detect and measure HGT events between engineered bacteria and use measurements from this assay to derive a probabilistic model of HGT in such conditions.

Summary

This research seeks to provide crucial parts needed to advance the exciting new topic of synthetic biology in order to safely and securely realise biotechnology applications for health, environment and energy needs. Since 2000, the new field of synthetic biology has advanced the existing science of genetic modification by applying principles of engineering; design, simulation and testing. This approach has allowed us to predictably create exciting new technologies by modifying safe microbes to perform new tasks including computation, multi-input environmental sensing and efficient production of medicinal drugs and bioenergy. While research success in synthetic biology has been rapid, the transfer of this work into real applications used by society has been limited; we can build excellent cell biosensors for explosives, arsenic and other environmental pollutants but none have actually been put to use. Largely this is because synthetic biology creates genetically modified organisms (GMOs) and these are a regulatory hazard to deploy. The major concern is that engineered DNA of these GMOs will be transferred to natural microbes by a process called horizontal gene transfer (HGT) and that this will disrupt natural ecosystems. This concern is particularly apt when we work with bacteria such as E. coli, as in these organisms synthetic biologists typically engineer their systems to be maintained on DNA circles called plasmids, which are easy to work with but also rapidly shared among bacteria and usually confer resistance to antibiotics. To overcome this hurdle and allow safe application of synthetic biology in the environment, this research aims to use synthetic biology techniques to construct a new kind of plasmid system that is secured to the intended cell, does not confer antibiotic resistance and resists horizontal gene transfer into natural bacteria. The development of this will include an assay to measure HGT and a model simulation to predict the key factors involved.

Impact Summary

Synthetic biology is expected this decade to move from the demonstration of new technologies to being a major part of applied bioscience research and commercial biotechnology. In particular, synthetic biology promises innovative new solutions in the defence and security sector. Microbes can be reprogrammed to be low-cost intelligent biosensors that perform logic functions in order to report on environmental pathogens and pollutants. Microbes can also be reengineered to provide high-value chemical compounds such as fuels, therapeutics and novel biomaterials. In all of these cases, synthetic biology requires genetic modification (GM) of microbes, typically using engineered plasmids and bacteria such as E. coli. Because of this, very few demonstrated applications of synthetic biology have been actually used in the real-world. The safety and regulation concerns of introducing GM bacteria, especially those that encode antibiotic resistance, are the major barrier to synthetic biology yielding significant products. The project proposed here intends to have a major impact on the current reality of synthetic biology, which is that there are many good ideas - biosensors, biofuels, biomaterials - but very few real applications. Without confronting the issues of GM microbes the hype of this subject will not be justified and the many security and defence projects, as well as energy and health projects that the UK government will fund, will not stand a chance of realisation. The research of this project will look at, and address one of the chief concerns of GM microbes, which is the transfer of the synthetic DNA (typically plasmids) from the engineered cells to the millions of natural microbes in our ecosystem. By assaying this transfer and then using synthetic biology to design new devices and systems to prevent it, the research of this project seeks to generate a new set of tools that will have the impact of making synthetic biology secure. This impact will be significant - itwill accelerate the likelihood of synthetic biology being applied in the real world and will also improve the security of existing biotechnologies. In that respect, this research will benefit almost all current and future synthetic biology projects that utilise microbial systems and plasmids. Beyond research, this project will also impact on both educational training and the private commercial sector. The members of this project play an active role in the training and education of the next generation through synthetic biology teaching at Imperial and through the annual iGEM undergraduate competition. The results of the project described here will feed into both. The UK has had remarkable success in teaching parts-based synthetic biology, producing many world-class undergraduate projects, so investment in further research here in the UK is critical to retaining the best students in the country and building a successful UK biotechnology industry. The private sector is actively involved in synthetic biology and this project will impact on commercial biotechnology by creating a secure, safer alternative to out-dated plasmids currently in use and we expect that will aid acceptance by UK regulators. We will seek to form collaborations with UK and international partners through an established synthetic biology industry club that we run at Imperial College. In addition to this we also plan to work with our CSynBI partners based at LSE BIOS who are exploring the social, political, economic and ethical dimensions of synthetic biology and have requested funds in order to do this. We will look into the steps required for regulatory approval of typical synthetic biology applications - such as environmental biosensors - and assess how our project can answer the needs of the public. This will be greatly aided by a one-day workshop we intend to run looking at the regulation of synthetic biology applications.

Committee	Research Committee D (Molecules, cells and industrial biotechnology)
Research Topics	Microbiology, Synthetic Biology, Technology and Methods Development
Research Priority	Synthetic Biology, Technology Development for the Biosciences
Research Initiative	Joint Synthetic Biology Initiative (JSBI) [2011]
Funding Scheme	X – not Funded via a specific Funding Scheme

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