Engineered burden-based feedback for robust and optimised synthetic biology

合成生物学是一门令人兴奋的新学科，它通过严格地将工程设计原理应用于我们与生物系统的工作方式来加速新生物技术的研究和开发。合成生物学最突出的应用是合理修改和重新设计微生物等活生物体，以便在能源生产，生物医学，药物生产和食品技术等部门进行新的有效利用。开发和应用合成生物学的关键是合成生物学设计的严格量化，建模，分析和控制。通过使用这个工程框架，我们的目标是能够可靠地预测和鲁棒地控制工程生物系统将如何运行。尽管合成生物学在研究中取得了许多成功，但当新的合成遗传信息被添加到这些宿主细胞中时，仍然很难预测工程细胞的行为。其中一个主要原因是，新的合成基因给细胞增加了一个尚未量化的负担，特别是对常用的微生物，如大肠杆菌。杆菌这种负担效应是由于新基因需要资源来维持和发挥作用。这意味着引入的基因从宿主细胞生长和生存所需的资源中夺走了资源。通常，这样做的结果是合成生物学设计无法按照预期发挥作用，或者只能在一组狭窄的理想条件下发挥作用。本项目提出的工作旨在解决和利用合成生物学的未充分研究的影响，我们称之为负担。为了实现这一目标，我们将使用新的遗传工具来量化几种典型合成生物学设备的负担效应，并在充分表征的微生物E.因此，我们的研究结果对许多研究这种模式生物的研究人员是有用的。为了了解细胞如何自然地对负荷做出反应，我们将使用RNA测序的高分辨率工具来量化细胞在负荷时触发的基因表达变化。量化的负荷与响应于负荷的量化基因表达变化相结合，将为我们提供关键数据，这些数据可用于建立细胞如何对添加和使用的新合成基因作出反应的数学模型。该模型将允许合成生物学的未来应用，以预测合成系统将如何与其宿主细胞相互作用，从而为任何控制工程设计所固有的鲁棒性/性能折衷的严格优化打开大门。它还将允许新一代合成生物学设备自动考虑负担效应。为了证明这最后一点，该项目将使用我们对负担的量化理解来设计新型合成质粒载体，这些载体旨在通过考虑负担的反馈机制自动调节其拷贝数，从而作为通用的基于负担的控制器。我们将展示这些质粒系统如何通过构建和测试一种自我调节的生物夜灯来工作，这种夜灯在黑暗中发出生物荧光，而不会对生长造成任何重大损失。我们产生的新质粒系统将对合成生物学非常有价值，因为它们将允许合成设备和系统直接响应细胞健康，从而赋予它们未来在健康，能源和生物传感方面的应用所需的强大和可预测的行为。

Synthetic biology is an exciting new subject that is accelerating the research and development of new biotechnologies by rigorously applying engineering design principles to the way we work with biological systems. The most prominent application of synthetic biology is the rational modification and redesign of living organisms like microbes for new efficient use in sectors such as energy production, biomedicine, drug production and food technology. Crucial to developing and applying synthetic biology is the rigorous quantification, modelling, analysis and control of the synthetic biology designs. By using this engineering framework we aim to be able to reliably predict and robustly control how engineered biological systems will operate.Although synthetic biology has had numerous successes in research, it is still difficult to predict how engineered cells behave when new synthetic genetic information is added to these host cells. One of the major reasons for this is that new synthetic genes add an as-yet unquantified burden to cells, particularly to commonly used microbes like E. coli. This burden effect is due to the new genes requiring resources to be maintained and function. This means that the introduced genes take resources away from those needed by their host cell in order to grow and survive. Usually the result of this is the unpredictable failure of the synthetic biology design to behave as expected or the creation of designs that only function in a narrow set of ideal conditions.The work proposed in this project seeks to address and make use of the understudied effect of synthetic biology we know as burden. To achieve this goal, we will use novel genetic tools to quantify the effect of burden for several typical synthetic biology devices and do this work in the well-characterised microbe E. coli so that our results are useful to the many researchers who work with this model organism. To see how the cell naturally reacts to burden we will use the high-resolution tool of RNA sequencing to quantify the gene expression changes that a cell triggers when it is burdened. Quantified burden combined with the quantified gene expression changes in response to burden will together give us crucial data that can be used to build a mathematical model of how a cell reacts to new synthetic genes being added and used. This model will allow future applications of synthetic biology to predict how synthetic systems will interact with their host cells and therefore open the door for rigorous optimisation of the robustness/performance compromise inherent to any control engineering design. It will also allow for a new generation of synthetic biology devices that automatically account for the burden effect. To demonstrate this final point, this project will use our quantified understanding of burden to engineer novel synthetic plasmid vectors that are designed to auto-regulate their copy number via feedback mechanisms that take into account burden, thereby serving as general purpose burden-based controllers. We will show how these plasmid systems work by building and testing a self-regulating biological nightlight that emits bioluminescence in the dark without any significant loss in growth. The new plasmid systems we generate will be extremely valuable for synthetic biology as they will allow synthetic devices and systems to respond directly to cell health thereby endowing them with the robust and predictable behaviours needed for future applications in health, energy and biosensing.