Fast, cheap and somewhat in control
© BioMed Central Ltd 2006
Published: 30 August 2006
Efforts to manipulate living organisms have raised the question of whether engineering principles of hierarchy, abstraction and design can be applied to biological systems. Here, we consider the practical challenges to controlling living organisms that must be surmounted, or at least managed, if synthetic biology and cellular bioengineering are to be productive.
Manipulating biology through the ages
The natural world around us is not quite so natural. Over many generations, societies have engaged in a struggle to mold nature to serve the needs, real and perceived, of their members. From cultivating grains to mining coal, we have sought to address local and global demands for food, shelter, health, and convenience through technology guided by science. One of the earliest and most profound of human engineering inventions was biotechnology in the form of farming, starting about 12,000 years ago. This was later transformed into a true domestication of animal and plant species that might be defined as "genetic alteration through conscious or unconscious selection" . It provided the key foundation for the spread and stability of human societies and has become one of the most central and longest-lived sciences there is. In more modern times, a scientific/rational basis for domestication and control of biological organisms has been sought both to make breeding organisms for human purposes quicker and more successful, and to limit the spread of infectious disease and other invasive species. The eradication of smallpox and the near-eradication of polio stand as reminders of how advanced medical, industrial and social engineering can change the health of an entire world. The precision of molecular biology has led to a whole new form of domestication and industry. Launched by the first mass production of a human protein (somatostatin) in bacteria, industrial genetic engineering became one of the most transforming industries of the 20th century . After the introduction of genetically engineered herbicide- and insect-resistant crops in 1995, genetically engineered maize is now more than 20% of the US crop, and approximately 80% of the US soybean crop is now genetically engineered .
Engineered biological systems are being used to address a wide variety of society's needs. Examples include the production of insulin and more than 200 other biopharmaceuticals and countless natural products, industrial catalysts and bioenergy substrates such as sugars, ethanol, methane and hydrogen, in microbes, eukaryotic cells and higher organisms; engineered resistance, ripening, oil production and nutrient overexpression in plants ; and more exotic successes such as the use of cytokine-expressing Mycobacterium bovis BCG as an effective treatment for certain forms of bladder cancer . These successes have largely been 'one offs', however; each one is a special case, and while lessons were learned, they do not provide a definitive roadmap for the next advance. Could it be any different? Could each small success make the solution of major problems easier? The increasing number of such special cases, as well as society's growing need for solutions to energy and environmental problems, presages the need for a more rational and integrated approach to engineering biology.
We can learn lessons from other engineering fields. Products such as the personal computer and cellular phone have at their foundation deep fundamental theory and technology from solid-state physics, materials science, and computational and information theory. These foundations enable the predictable control of materials and processes through the application of physical laws to meet specific objectives. In addition, the industry surrounding these devices has defined a set of standards and protocols that make the parts and systems of these devices (often) interoperable, extensible and, most importantly, allow the efficient scale-up of manufacture and distribution of the technology. The practice of engineering has a broadly successful track record of addressing social needs (as well as creating additional problems) when applied to materials like silicon and steel, where the physical rules are known and the complexity is limited or very well controlled. Engineering as a practice has not, however, been successful in such endeavors as controlling the weather or avoiding natural disasters, due largely to the scale, complexity and uncertainty inherent to those problems. So we must ask: is the conventional paradigm of engineering appropriate for biology? Can we develop, or deal with, the lack of a coherent theoretical and physical foundation for living systems? Or is control of biology destined for the same fate as rainmaking?
Why should biology be engineerable?
Given the complexity of biology, an engineering approach based on design may seem an unlikely route to success. Living systems, unlike classical engineered systems, grow and evolve, and have material properties that are not easily controlled or predicted and that are often sensitive to their local environment. Indeed, traditionally directed evolution through selective breeding of, for example, pest-resistant or high-yield crops has been the main method for obtaining a desired outcome in biology. This is true at the bio-molecular level as well, in which creation of new function in proteins and nucleic acids is often accomplished through directed evolution rather than de novo design [6, 7]. The technology for direct, rational manipulation of an organism's DNA has improved in precision and efficiency, greatly increasing our ability to produce therapeutics, natural products, antibodies and enzymes in heterologous systems. Yet actually achieving, let alone optimizing, the production of a given target in a given system is still a time-consuming art driven by decades of empirical observation. Engineering of more complex behaviors will require a more principled understanding of biological system design.
Basic research over the past few decades has given us confidence that there is at least some organized structure to the workings of cells - a structure that may be altered or even rebuilt through an intelligent process of engineering. This view is emerging from multiple disciplines. Comparative genomics is helping to uncover the structure and evolution of the genome. Large-scale tracking of DNA expression, protein synthesis, molecular interactions and intermediates is revealing groups of molecules that work and play together. Fluorescent imaging of living cells is identifying time-dependent changes in protein activity and localization that correlate with behavior. Reconstitution of biochemical and biophysical processes from 'minimal systems' of proteins has built confidence that top-down and bottom-up approaches to biology meet somewhere in the middle. Systems biology has sought to integrate these results and data to reverse-engineer an understanding of biological network function and dynamics. Finally, the infrastructure for storing and disseminating information on biological systems, and for modeling them, has grown concurrently. In turn, this allows the rapid access and cross-comparison of information that is critical to establishing data quality and creating interoperability standards that will enable biologists to leverage their efforts and build scalable systems.
The key observation that biological systems exhibit some degree of modularity underlies the current belief that useful and 'engineerable' design principles exist . Whether at the level of protein motifs with similar binding properties or groups of proteins that carry out specific functions in a variety of distinct settings, the modular parts of biological systems are used and reused to generate and control the apparently complex behavior of living organisms. The bold question that was asked at the dawn of recombinant DNA research, and continues to be asked today, is whether a growing understanding of this modularity and new tools to manipulate it can be used to engineer new and useful behavior. Attempts to directly answer this question - and to think about its consequences - have resulted in the formation of a loose assembly of scientists, engineers, ethicists and other thinkers engaged in what has become known as 'synthetic biology'.
What sets synthetic biology apart from molecular biology and its closely allied fields of genetic and metabolic engineering is the ambition to formalize the process of designing cellular systems, in the way that traditional engineering disciplines have formalized design and manufacture, so that complex behaviors can be achieved for practical ends. Such behaviors will require larger biochemical circuits, typically encoded in DNA, for control. To achieve this, synthetic biologists look to move beyond the qualitative and often ad hoc engineering pathways that have underlain the slow progress to this point. The goal, instead, is to create a systematic engineering science founded on the standardization of a cellular 'chassis' - the types of parts available, their manufacture, their characterization and protocols for their interconnection - analogous to those that underlie and enable the scalability of mechanical, electrical and civil engineering. But the analogy with traditional engineering should not be taken too far, as there are challenges to engineering biology that no internal combustion engine or microprocessor has faced.
What are the engineering challenges?
Despite much effort, the dream of engineering biology has not yet led to simple and rapid construction of biological organisms that address specific problems. The reasons for this are twofold. One is the lack of a technology infrastructure that enables production of biological parts and easy assembly of these parts into systems, a challenge that has been addressed in a recent review . The second, which we focus on here, is the difficulty of predicting what biological components will do, even when the parts are readily obtainable and much is known about them individually . On this issue, lessons learned from engineering bridges, boats and planes are of little help, because the operating conditions under which biological systems function are significantly different from those of familiar macroscopic systems. Thermal fluctuations that drive stochastic behavior can typically be ignored or managed in traditional engineering, but often not in cells. And in situ evolutionary change in parts and control systems are simply not problems for inanimate objects - not so for biology. In fact, biology's success - its ability to grow and evolve new solutions and test fitness through competition - has depended on just those behaviors that frustrate predictability. Any engineering of biology to serve our needs must recognize, understand and manage this drive towards variation and the evolutionary competition with other organisms. Some of these issues are already under practical consideration in relation to genetically modified organisms .
Engineering exogenous protein or gene circuits into a new host organism also faces problems of integration due to 'parasitic' effects and cross-talk with existing pathways. Parasitic effects that arise due to direct interaction among new components or through indirect interactions via their effects on the organism into which they are introduced - the chassis - such as sickening it or draining inputs to other pathways, often play a dominant role in preventing circuit function. To be broadly useful, the features of a biological component and the organism into which it is introduced must be characterized such that its function is predictable. Most circuit designs rely, at least in part, in transferring natural components from other organisms into the host chassis. There are basic problems of adapting the part for operation in the new host by, for example, adjusting codon usage, and as the part did not coevolve with the other parts of the chassis it might cross-react with other components in unforeseen ways. Zarrinpar et al.  elegantly demonstrated this in yeast by showing that a yeast Pbs2 protein binds specifically to SH3 (Src homology 3) domains from yeast but is promiscuous with SH3 domains from other organisms. These issues are compounded when design moves away from the single cell and towards multicellularity, as some researchers are now attempting [13, 14].
To demonstrate the challenges of engineering biology to control behavior, we use two simple examples: one addresses how evolution could degrade biological circuit performance over time; and the other addresses how noise, possibly external to the system, can have dramatic effects on system behavior. In the first example, we borrow a model for competition between multiple strains of a microbe under nutrient-limiting conditions in continuous culture . We assume that there are two quasispecies of bacterium, one bearing a functional version of our synthetic biological circuit and the other carrying a disabled version created by deleterious mutation from the first. The deleterious mutation rate is a function of circuit size in base pairs (bp), basal mutation rate in base pairs per generation, the generation time itself, and a factor related to the specific circuit design, which gives the fraction of mutations leading to loss of function of the circuit. The basal mutation rate, m, in Escherichia coli is approximately 5.4 × 10-10 base-pairs per cell per generation; the fraction of mutations that actually disable the circuit, f, is a free parameter, which for this simulation we set to 1/1,000. The circuit size for a small two-gene circuit is approximately 2,000 bp. We vary this parameter in the following calculations, holding f constant for convenience, although, in reality, for each circuit design f is a variable. We also assume that having a functioning circuit places a metabolic load on the cell that slows its growth rate. This load has been observed experimentally in a number of cases, but there are few hard and fast rules [16–18]. A disabling mutation can release this load, leading to faster growth of the mutant population. The deleterious mutation rate sets a threshold above which, over time, the nonfunctional mutant population can outcompete the wild-type population.
The first of these two simple examples demonstrates that two of the key properties of a cellular chassis and its environment that need to be engineered are the basal mutation rate and the robustness to circuit load, which should, generally, both be minimized. Furthermore, the particular design choices made in part choice and in the mechanisms by which these parts are hooked together to make a system will affect the value of f, the deleterious mutation rate. The second of these examples shows how even a simple biochemical system can exhibit complex unintended behaviors if the environment in which it operates changes only its noise properties (even if the mean values stay the same). Thus a designed cell that is passing through uncertain or multiple environments will have to be designed to minimize or even to exploit these effects. In fact, outside bioreactors, engineered organisms - other than a few agricultural examples - survive poorly in real-world environments where conditions and competition with other organisms are less controlled . Both the cases described here demonstrate special considerations that must be applied to the engineering of biological systems in order to meet the challenges to the scalability of engineered organisms.
Immediate goals and future prospects
As we have for millennia, we are shaping the biological world to meet our needs. There are major problems that cry out for biologically engineered solutions, such as those in cell and tissue engineering, gene therapy, biologically derived materials, biocatalysis and natural product synthesis, optimization of agricultural yield and nutrition, pest and disease control and much more. Synthetic biology, with its focus on elucidating and harnessing design principles of living systems, aims to tackle these problems. But unlike other engineering disciplines, synthetic biology has not developed to the point where there are scalable and reliable approaches to finding solutions. Instead, the emerging applications are most often kludges that work, but only as individual special cases. They are solutions selected for being fast and cheap and, as a result, they are only somewhat in control (with apologies to Errol Morris).
Yet there is optimism in the field. Engineering biology is indeed a great challenge, but its potential benefits are even greater. Through the creative efforts of many investigators, solutions to robustness and noise suppression may be found - or we will at least understand why no solutions can be found. Further effort and investment are required to develop robust theories and computational infrastructure for biological circuit design and synthesis, to establish standards in measurement and information about circuits and their inter-operability, and to create new manufacturing technologies that allow production of large circuits, creation of novel chasses (with, for example, new genetic codes ), and environments for the development of artificial tissues. Excitement among those engaged in engineering biology stems from the fact that there are clear routes to progress on all of these fronts and from the incredible pull of the applications that are possible if these problems are solved.
We thank David Schaffer for a critical reading of the manuscript. In this work A.P.A. is supported by the Howard Hughes Medical Institute and was performed as part of the Virtual Institute for Microbial Stress and Survival  supported by the US Department of Energy, Office of Science, Office of Biological and Environmental Research, Genomics Program:GTL through contract DE-AC02-05CH11231 between Lawrence Berkeley National Laboratory and the US Department of Energy. D.A.F. acknowledges NSF and NIH funding during the course of this work.
- Janick J: Perspectives on New Crops and New Uses. Edited by: Janick J. 1999, Phoenix, Arizona: ASHS Press, 4: 104-110.
- Itakura K, Hirose T, Crea R, Riggs AD, Heyneker HL, Bolivar F, Boyer HW: Expression in Escherichia coli of a chemically synthesized gene for the hormone somatostatin. Science. 1977, 198: 1056-1063.PubMedView Article
- Adoption of Genetically Engineered Crops in the US. [http://www.ers.usda.gov/Data/BiotechCrops]
- Capell T, Christou P: Progress in plant metabolic engineering. Curr Opin Biotechnol. 2004, 15: 148-154. 10.1016/j.copbio.2004.01.009.PubMedView Article
- Kassouf W, Kamat AM: Current state of immunotherapy for bladder cancer. Expert Rev Anticancer Ther. 2004, 4: 1037-1046. 10.1586/1473722.214.171.1247.PubMedView Article
- Bloom JD, Meyer MM, Meinhold P, Otey CR, MacMillan D, Arnold FH: Evolving strategies for enzyme engineering. Curr Opin Struct Biol. 2005, 15: 447-452. 10.1016/j.sbi.2005.06.004.PubMedView Article
- Bornscheuer UT: Trends and challenges in enzyme technology. Adv Biochem Eng Biotechnol. 2005, 100: 181-203.PubMed
- Wolf DM, Arkin AP: Motifs, modules and games in bacteria. Curr Opin Microbiol. 2003, 6: 125-134. 10.1016/S1369-5274(03)00033-X.PubMedView Article
- Endy D: Foundations for engineering biology. Nature. 2005, 438: 449-453. 10.1038/nature04342.PubMedView Article
- Sprinzak D, Elowitz MB: Reconstruction of genetic circuits. Nature. 2005, 438: 443-448. 10.1038/nature04335.PubMedView Article
- Kirk TK, Carlson JE, Ellstrand N, Kapuscinski AR, Lumpkin TA, Magnus DC, Magraw DB, Nester EW, Peloquin JJ, Snow AA, et al: Biological Confinement of Genetically Engineered Organisms. 2004, Washington DC: National Academies Press
- Zarrinpar A, Park SH, Lim WA: Optimization of specificity in a cellular protein interaction network by negative selection. Nature. 2003, 426: 676-680. 10.1038/nature02178.PubMedView Article
- Basu S, Mehreja R, Thiberge S, Chen MT, Weiss R: Spatiotemporal control of gene expression with pulse-generating networks. Proc Natl Acad Sci USA. 2004, 101: 6355-6360. 10.1073/pnas.0307571101.PubMedPubMed CentralView Article
- Basu S, Gerchman Y, Collins CH, Arnold FH, Weiss R: A synthetic multicellular system for programmed pattern formation. Nature. 2005, 434: 1130-1134. 10.1038/nature03461.PubMedView Article
- Hansen SR, Hubbell SJ: Single-nutrient microbial competition: quantitative agreement between experimental and theoretically forecast outcomes. Science. 1980, 207: 1491-1493.PubMedView Article
- Flores S, de Anda-Herrera R, Gosset G, Bolivar FG: Growth-rate recovery of Escherichia coli cultures carrying a multicopy plasmid, by engineering of the pentose-phosphate pathway. Biotechnol Bioeng. 2004, 87: 485-494. 10.1002/bit.20137.PubMedView Article
- Neubauer P, Lin HY, Mathiszik B: Metabolic load of recombinant protein production: inhibition of cellular capacities for glucose uptake and respiration after induction of a heterologous gene in Escherichia coli. Biotechnol Bioeng. 2003, 83: 53-64. 10.1002/bit.10645.PubMedView Article
- Haddadin FT, Harcum SW: Transcriptome profiles for high-cell-density recombinant and wild-type Escherichia coli. Biotechnol Bioeng. 2005, 90: 127-153. 10.1002/bit.20340.PubMedView Article
- You L, Cox RS, Weiss R, Arnold FH: Programmed population control by cell-cell communication and regulated killing. Nature. 2004, 428: 868-871. 10.1038/nature02491.PubMedView Article
- McAdams HH, Arkin A: Towards a circuit engineering discipline. Curr Biol. 2000, 10: R318-R320. 10.1016/S0960-9822(00)00440-1.PubMedView Article
- Gerdes SY, Scholle MD, Campbell JW, Balazsi G, Ravasz E, Daugherty MD, Somera AL, Kyrpides NC, Anderson I, Gelfand MS, et al: Experimental determination and system level analysis of essential genes in Escherichia coli MG1655. J Bacteriol. 2003, 185: 5673-5684. 10.1128/JB.185.19.5673-5684.2003.PubMedPubMed CentralView Article
- Albert R, Jeong H, Barabasi AL: Error and attack tolerance of complex networks. Nature. 2000, 406: 378-382. 10.1038/35019019.PubMedView Article
- Swain PS, Elowitz MB, Siggia ED: Intrinsic and extrinsic contributions to stochasticity in gene expression. Proc Natl Acad Sci USA. 2002, 99: 12795-12800. 10.1073/pnas.162041399.PubMedPubMed CentralView Article
- Cai L, Friedman N, Xie XS: Stochastic protein expression in individual cells at the single molecule level. Nature. 2006, 440: 358-362. 10.1038/nature04599.PubMedView Article
- Pedraza JM, van Oudenaarden A: Noise propagation in gene networks. Science. 2005, 307: 1965-1969. 10.1126/science.1109090.PubMedView Article
- McAdams HH, Arkin A: Stochastic mechanisms in gene expression. Proc Natl Acad Sci USA. 1997, 94: 814-819. 10.1073/pnas.94.3.814.PubMedPubMed CentralView Article
- Weinberger LS, Burnett JC, Toettcher JE, Arkin AP, Schaffer DV: Stochastic gene expression in a lentiviral positive-feedback loop: HIV-1 Tat fluctuations drive phenotypic diversity. Cell. 2005, 122: 169-182. 10.1016/j.cell.2005.06.006.PubMedView Article
- Golding I, Paulsson J, Zawilski SM, Cox EC: Real-time kinetics of gene activity in individual bacteria. Cell. 2005, 123: 1025-1036. 10.1016/j.cell.2005.09.031.PubMedView Article
- Newman JR, Ghaemmaghami S, Ihmels J, Breslow DK, Noble M, DeRisi JL, Weissman JS: Single-cell proteomic analysis of S.cerevisiae reveals the architecture of biological noise. Nature. 2006, 441: 840-846. 10.1038/nature04785.PubMedView Article
- Raser JM, O'Shea EK: Control of stochasticity in eukaryotic gene expression. Science. 2004, 304: 1811-1814. 10.1126/science.1098641.PubMedPubMed CentralView Article
- Samoilov M, Plyasunov S, Arkin AP: Stochastic amplification and signaling in enzymatic futile cycles through noise-induced bistability with oscillations. Proc Natl Acad Sci USA. 2005, 102: 2310-2315. 10.1073/pnas.0406841102.PubMedPubMed CentralView Article
- Wolf DM, Vazirani VV, Arkin AP: Diversity in times of adversity: probabilistic strategies in microbial survival games. J Theor Biol. 2005, 234: 227-253. 10.1016/j.jtbi.2004.11.020.PubMedView Article
- Kussell E, Leibler S: Phenotypic diversity, population growth, and information in fluctuating environments. Science. 2005, 309: 2075-2078. 10.1126/science.1114383.PubMedView Article
- Thattai M, van Oudenaarden A: Stochastic gene expression in fluctuating environments. Genetics. 2004, 167: 523-530. 10.1534/genetics.167.1.523.PubMedPubMed CentralView Article
- Cases I, de Lorenzo V: Genetically modified organisms for the environment: stories of success and failure and what we have learned from them. Int Microbiol. 2005, 8: 213-222.PubMed
- Wang L, Xie J, Schultz PG: Expanding the genetic code. Annu Rev Biophys Biomol Struct. 2006, 35: 225-249. 10.1146/annurev.biophys.35.101105.121507.PubMedView Article
- VIMSS: Virtual Institute for Microbial Stress and Survival. [http://VIMSS.lbl.gov]