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The Multiplanetary Future of Plant Synthetic Biology

Department of Molecular Sciences, Macquarie University, Sydney NSW 2109, Australia
CSIRO Synthetic Biology Future Science Platform, Canberra ACT 2601, Australia
New South Wales Department of Primary Industries, Orange NSW 2800, Australia
Author to whom correspondence should be addressed.
Genes 2018, 9(7), 348;
Received: 30 May 2018 / Revised: 6 July 2018 / Accepted: 9 July 2018 / Published: 10 July 2018
(This article belongs to the Special Issue Emerging Applications in Synthetic Biology)


The interest in human space journeys to distant planets and moons has been re-ignited in recent times and there are ongoing plans for sending the first manned missions to Mars in the near future. In addition to generating oxygen, fixing carbon, and recycling waste and water, plants could play a critical role in producing food and biomass feedstock for the microbial manufacture of materials, chemicals, and medicines in long-term interplanetary outposts. However, because life on Earth evolved under the conditions of the terrestrial biosphere, plants will not perform optimally in different planetary habitats. The construction or transportation of plant growth facilities and the availability of resources, such as sunlight and liquid water, may also be limiting factors, and would thus impose additional challenges to efficient farming in an extraterrestrial destination. Using the framework of the forthcoming human missions to Mars, here we discuss a series of bioengineering endeavors that will enable us to take full advantage of plants in the context of a Martian greenhouse. We also propose a roadmap for research on adapting life to Mars and outline our opinion that synthetic biology efforts towards this goal will contribute to solving some of the main agricultural and industrial challenges here on Earth.

Graphical Abstract

1. Taking Full Advantage of Plants on Extraterrestrial Human Outposts

The exploration of space is one of the most inspiring areas of scientific research and a major driver of technological innovation. Achieving sustainable human presence on alien planetary bodies will expand our understanding of the cosmos, our capacity to investigate fundamental questions, such as the potential for life beyond our home planet, and will enable continued growth of the global economy. Space agencies such as NASA (National Aeronautics and Space Administration) and ESA (European Space Agency) as well as companies from the private sector like SpaceX share the common interest of moving forward the human exploration of deep space and launching the first manned missions to Mars in the near future [1,2,3]. A major factor limiting the expansion of human space exploration is the enormous logistical costs of launching and resupplying resources from Earth. Therefore, developing robust technologies to enable sustainable long-duration human operations in space will be of paramount importance in the coming years.
Human and plant life is intimately linked on planet Earth and so might be true on future extraterrestrial outposts. By supplying oxygen (O2), fixing carbon dioxide (CO2), and recycling waste and water (H2O), plants could contribute to sustaining bioregenerative life support systems [4,5], whilst also providing food and precursors for manufacturing medicines and materials on distant locations such as the Moon or Mars. Making the most of plants on-site would increase self-sufficiency during long-stay residence periods, hence minimizing risks and reducing the transportation of cargo and the deployment of resupply missions. However, because plants have evolved under the conditions of the terrestrial biosphere, substantial resources would need to be allocated if we aim to achieve efficient farming by mimicking Earth’s conditions in other planetary environments. Simple inputs like sunlight and liquid water could potentially be limited, beneficial microorganisms and nutrients might need to be implanted, and well-conditioned greenhouses capable of shielding plants from harmful ultraviolet (UV) and cosmic radiation would need to be built or transported. Considerable energy would also need to be allocated for maintaining additional controlled greenhouse conditions such as temperature, humidity, and pressure. In this context, despite continuous advances in space agriculture [6,7], bioengineering approaches aimed at reducing the burden of sustaining extraterrestrial greenhouses and improving plant performance under different planetary environments remain to be explored.
In this article, we extend the existing body of work on the use of microbes [8,9,10,11] and argue that synthetic biology will provide the means for outpacing terrestrial evolution to take full advantage of plants beyond Earth. We use the forthcoming human missions to Mars as a scenario to discuss a series of bioengineering undertakings that will enable plants to thrive in Martian growth facilities.

2. Refactoring Plants for Enhanced Performance on Mars

Mars is the most Earth-like of our neighboring planets and the next step for human planetary exploration. It is anticipated that in order to achieve long-duration habitation of the Martian surface, missions to the red planet will need to depart from complete reliance on shipped cargo and achieve a high level of self-sufficiency [8,11,12,13]. As described above, one way to move towards this goal would be to deploy special facilities designed to allow plants to survive the harsh environment of Mars [14,15]. A complementary approach would be to engineer plants for enhanced performance under Martian conditions, an endeavor that will require substantial modifications at multiple levels but will ultimately bring benefits in energy, water, and habitat-space use. In this section, we focus on potential plant synthetic biology solutions to a series of Martian challenges (Figure 1). Because recent studies indicate that the reduced gravity level on Mars of 0.38 g (compared to 1 g on Earth) may not be a major problem for plant growth and development [16], we will not discuss gravity in this article. For a description of the Martian environmental conditions, such as temperature and atmospheric and soil (i.e., regolith) composition, we refer the reader to two recent articles [8,9].

2.1. Enhancing Photosynthesis and Photoprotection

Light energy is essential for the photosynthesis process that allows plants to produce oxygen and new biomass from carbon dioxide and water. Plant light energy conversion efficiency is far from being optimal because photosynthetic organisms in the wild have been evolutionarily selected for reproductive success and not for high biomass production [17]. On Mars, where sunlight intensity is significantly lower than on Earth (~43% at comparable latitude and time of day [9]), and where the need of growing plants inside greenhouses will further reduce sunlight levels even if built with the best transparent materials, improved photosynthesis will likely constitute a major advance. Maximizing the use of natural sunlight would save considerable power resources that would have to be otherwise diverted to support artificial lighting [14]. Improving photosynthetic efficiency will, therefore, not only increase plant biomass production but will also translate into energy savings (Figure 1).
Plants harvest energy from a small proportion of the light spectrum, mainly in the wavelength range of 400–700 nm, and thus access only about 50% of the incident solar energy [17]. One promising target for improving plant use efficiency of sunlight would be to expand the region of the light spectrum used by photosynthesis via reengineering the light-harvesting antenna and reaction center complexes [17,18,19,20]. Expanding the spectral coverage of light harvesting towards the UV and/or the infrared regions will mean that photons from currently inaccessible wavelengths would be available for energizing plant growth. Since the absence of a significant ozone layer and low atmospheric pressure of Mars result in a higher surface flux of UV radiation [21], enabling the photosynthetic use of the UV region of the solar spectrum could prove particularly effective. Such a strategy, however, would require the use of UV-transparent greenhouses and also the realization of superior UV-protection mechanisms to minimize cell damage, conceivably by engineering highly efficient synthetic UV-dependent responses. Additionally, since UV is potentially damaging to DNA, RNA, proteins, and cellular metabolism, enhancing UV-tolerance would likely result in a better plant performance in general [22]. Along the same lines, as photooxidative stress occurs when the absorbed light energy exceeds that used in photosynthesis, engineering improved photoprotection mechanisms could further enhance the performance of the light-harvesting machinery [23], as recently demonstrated in tobacco (Nicotiana tabacum) plants [24].
One other ambitious approach for improving plant biomass production involves increasing the yield of photosynthetic carbon assimilation. There are numerous strategies that are currently being pursued towards this goal, from improving the catalytic activity of Rubisco (i.e., ribulose-1, 5-bisphosphate carboxylase/oxygenase, the CO2-fixing enzyme in photosynthesis) and implementing CO2-concentrating mechanisms to engineering photorespiration bypasses and installing synthetic carbon fixation pathways [20,25,26,27,28]. Among these strategies, building new-to-nature CO2-fixing pathways holds the most promise to improve photosynthetic light energy conversion, since it is arguably the approach that would be less likely limited by serendipitous evolutionary constraints [29,30]. Also, given that CO2 and O2 compete at the active site of Rubisco and that the atmospheric CO2/O2 ratio on Mars is enormously higher than on Earth [8], it is possible that carbon fixation by Rubisco on Mars could be highly effective.

2.2. Improving Drought and Cold Tolerance

Water will be a crucial resource for plants but also for many other applications in a Martian outpost [31]. Because water on Mars is mostly available in the form of ice [32], part of the energy budget of the outpost will need to be allocated for its extraction and recycling [31]. Also, if energetically expensive systems (e.g., hydroponics) were required to sustain plant growth, additional energy will need to be diverted for this purpose [6,15,33]. Developing plants that require less water per unit mass of production will, therefore, contribute to better water and energy management on Mars (Figure 1).
One way to improve drought tolerance would be to manipulate the opening and closure of stomatal pores, from which water is lost via transpiration. This approach has already been shown to reduce plant water loss [34] and could potentially be even more effective if the signaling pathways that adjust stomatal behavior in response to drought were rewired to achieve programmable functional insulation, hence minimizing growth penalties often derived from crosstalk between stress responses and developmental networks [35,36,37]. Other promising approaches would be to engineer plants of interest with crassulacean acid metabolism, which increases water-use efficiency and enables plants to inhabit water-limited environments such as semi-arid deserts [38]. More progressive synthetic biology approaches could even enable the engineering of drought-tolerance mechanisms analogous to those found in resurrection plants, extremophytes that can withstand severe drought conditions [39,40], or even more evolutionary distant organisms that can undergo anhydrobiosis and survive extreme desiccation [41,42].
Mitigating the low average temperature of Mars and its huge diurnal thermal variation [43] will be another key aspect that will require substantial energy allocation [14]. Engineering cold-hardy plants could help reduce the amount of energy allotted to meet the thermal requirements of Martian greenhouses (Figure 1). As with the case of improving drought tolerance, engineering plants of interest to exploit the protection mechanisms used by other organisms adapted to withstand low temperatures is a promising strategy. There are clear examples that cold tolerance can be enhanced by the expression of ice-binding proteins capable of inhibiting the growth of damaging ice crystals [44]. Increased levels of membrane unsaturated fatty acids and certain osmoprotectants (e.g., fructans) also lead to cold tolerance; hence manipulating their metabolism is also a particularly attractive target [45,46]. A more sophisticated strategy would be to design a dynamic multilevel cryoprotective response regulated, perhaps through the circadian clock [47], in such a way to anticipate the large temperature drop of the Martian night. Synthetic circadian regulation could enable optimal use of energy by timing the cryoprotective response with the diurnal solar oscillation [48]. Because the length of Mars day (~24.5 h) is similar to that of Earth (~24 h) [3] just minor adjustments of the plant circadian timing system might be required for optimal functioning.

2.3. Engineering High Yield and Functional Food

The limited size of the Martian greenhouses and the availability of indispensable plant nutrients like phosphorus and nitrogen will represent additional challenges for an agricultural system on Mars. Ideal plants should have high biomass productivity, high harvest indices, minimum horticultural requirements, and provide food for a functional diet [13,49] (Figure 1).
A possible solution to boost biomass productivity would be to achieve cultivation at very high plant density [50,51] by manipulation of the shade avoidance response [52], which can be detrimental to yield because carbon resources are redirected to stem or petiole elongation at the expense of biomass production [53]. Redesigning the plant development and architecture at different levels could also lead to crop variants with extraordinary harvest indices. This idea has recently been demonstrated in tomato (Solanum lycopersicum) plants engineered in a number of architectural traits resulting in improved productivity [54,55,56]. Moreover, engineering the root system architecture for optimal nutrient acquisition and increased fertilizer use efficiency could further translate to higher yields [57,58] (Figure 1). Changing the root system architecture to improve phosphorus uptake [59] could be particularly relevant on Mars, as it is unclear if phosphorus is readily available to sustain plant growth [8,60,61], in which case, it should be supplemented as a fertilizer.
Nitrogen, which is also an essential plant nutrient, is present on the surface of Mars in the form of nitrate [62] that could potentially be biochemically accessible to plants. Alternatively, nitrogen gas (N2) could be directly assimilated from the Martian atmosphere [8]. However, because the capacity to fix gaseous N2 is restricted to a specialized group of prokaryotes and does not occur in plants, one ambitious goal would be to endow plants with the capacity to directly assimilate atmospheric nitrogen (Figure 1). To this end, all the required microbial machinery for fixing nitrogen could be transferred into plants, a strategy that is currently being pursued by different laboratories and, although technically challenging, it is certainly within the capacity of modern synthetic biology [63,64,65,66,67,68]. However, given the huge difference in the atmospheric nitrogen content of Earth (~78%) and Mars (~2.7%) [9], such a transplanted microbial pathway might not work efficiently on Mars. Possible solutions to this challenge would be to exploit indigenous Martian nitrogen [62] to enrich greenhouse N2 concentration or to employ protein-engineering techniques to increase nitrogenase affinity and develop a N2-fixation pathway of high performance under low nitrogen concentration. Alternatives to endowing plants with the capacity to assimilate atmospheric nitrogen would be to engineer nitrogen fixation in root-associated microbes or to develop synthetic root-microbe symbiosis with microorganisms already capable of fixing nitrogen [69,70,71].
Another consideration for sustaining an extended human presence on Mars is that of producing nutritious food. Poor nutrition can cause detrimental effects on health and adversely affect physical and cognitive performance [72]. Plants could be central to maintaining good nutrition on long-duration manned space expeditions. For instance, the consumption of carotenoids, a group of isoprenoid compounds with activity as antioxidants and vitamin A precursors [73], has been identified as of particular interest for humans on space [49,74]. Unlike plants, which synthesize carotenoids in their plastids [75,76], humans do not produce carotenoids and have to incorporate them in their diets [73]. Because carotenoid accumulation in plants is the result of multiple processes [23,76,77], the combination of various bioengineering strategies, from manipulating the carotenoid biosynthesis and storage mechanisms to installing alternative carotenogenic pathways [76,78,79,80,81] holds potential to take the carotenoid content of crops to a new level. From a holistic point of view, the ultimate synthetic biology approach to make the most of plant-based food on Mars would be to develop multi-biofortified crops with improved nutritional properties [82,83,84] and enhanced quality traits (e.g., extended shelf life and reduced allergenicity) [85,86,87,88,89,90,91,92].

3. Tailoring Microorganisms to Complement and Facilitate Plant Life on Mars

The establishment and utilization of plants on Mars would benefit significantly from its use in conjunction with microorganisms. Besides their potential use to supply nitrogen as discussed above, engineered microbes would be necessary for the removal of toxic compounds from the Martian soil and its transformation from an arid and oligotrophic desert material into a nutrient-rich soil able to support plant growth (Figure 2). As in the case of plants, due to the drastically different environment in which these microbes would need to perform, synthetic biology will be essential for engineering desired functions. Once plants are established, microbes could be used to convert plant biomass into proteins and metabolites that serve as materials, chemicals, and medicines. By using plant sugars and biomass as versatile feedstock for bioprocessing, these resources could be made available on-demand at high rates, titers, and yields. It is important to note that an enormous array of microbes designed to perform a multitude of useful tasks could be transported to Mars with very little cargo-burden. In this section, we focus on crucial applications of microorganisms relating to the establishment and utilization of plants on Mars.

3.1. Conditioning Martian Soil for Plant Growth Using Microbes

Recent experiments have shown that several plant species are remarkably healthy when grown on Mars soil simulants [93]. Additional experiments simulating the gravitational conditions of Mars also suggest that soil-based agriculture would require about 90% less water than on Earth as a consequence of lower leaching rates [94]. As a whole, these results are encouraging for the prospect of utilizing Martian soil for growing plants on Mars. Towards this goal, microorganisms can be utilized to perform several critical tasks in the conditioning of Martian soil for plant growth.
First, we need to identify and learn from microorganisms capable of surviving Martian soil conditions with minimal nutritional requirements. The Antarctic Dry Valleys on Earth have some of the most comparable conditions to Mars, with extreme aridity, low temperatures, high radiation, and lack of nutrients [95,96]. It was recently found that a novel mode of metabolism facilitates bacterial persistence in these extreme conditions, whereby atmospheric trace levels of hydrogen (H2), CO2, and carbon monoxide (CO) provide energy and carbon to support microbial communities [97]. This type of metabolism, for example, could potentially be exploited by primary colonizing microbes designed to implement the first conditioning steps of the hyper-arid Marian soil. Critically, the required gases to sustain this type of chemotrophic growth could be made available directly from the Martian atmosphere and water electrolysis [8].
The Martian soil has been found to contain high levels of perchlorates [98]. Perchlorates are toxic to human hormone systems, and any soil used to grow plants for human consumption would need to have dramatically lowered perchlorate levels [99,100]. One way to achieve this would be to remove perchlorate salts with water; however, this would impose a burden on the valuable water and energy resources on Mars. An attractive alternative solution to this problem is to use biological removal of perchlorate by engineering CO2-utilizing bacteria to express perchlorate reduction enzymes. This would enable continued bioremediation over time and possibly contribute to bacterial growth. Alternatively, bacteria capable of complete perchlorate reduction [99] could be engineered for autotrophic carbon fixation, although this would be a far more complex feat. In addition to detoxifying Martian soil, the biological reduction of perchlorates would have the additional benefit of releasing water found as hydrated perchlorate salts [101], increasing soil moisture (Figure 2). To further improve soil water content, bacteria could be engineered to produce an extracellular polysaccharide or adhesive protein that would bind soil particles together and hence mitigate desiccation [102] (Figure 2).

3.2. Microbes for Metabolite and Protein Production from Plant Material

In recent years, a burgeoning bio-economy has emerged where the precision, reaction rates, and diversity of microbial biochemistry have been harnessed using synthetic biology to produce a multitude of industrial and consumer products. This economy is arising to create products that are either produced unsustainably from oil (e.g., chemicals) [103], inefficiently from plants and animals (e.g., medicines) [104] or that cannot be produced industrially in any other way (e.g., spider silk) [105]. The advantages of this paradigm will be even more pertinent on extraterrestrial outposts, where every resource must be consumed and/or produced as efficiently as possible. Additionally, any biomolecule that can be produced on-site and on-demand lowers the burden of having to be transported. Many of these valuable biomolecules should, if possible, be produced autotrophically using photosynthesis, acetogenesis, or methanogenesis from waste carbon dioxide and carbon monoxide [8,9,10,11,12]. However, these modes of metabolism have limitations in terms of the production rates, titers, and yields of specific products depending on the adenosine triphosphate (ATP) and redox requirements of a given production pathway [106,107,108]. Using aerobic heterotrophic catabolism of plant-derived sugars and biomass can circumvent these limitations due to greater ATP generation and redox flexibility per molecule of substrate. Such a production scenario could, therefore, be advantageous and compatible with growing plants on Mars. Using plant biomass to provide sugars for fermentation would also afford great versatility and adaptability, as the same renewable feedstock would serve as input to a variety of products as they are required. This mode of production would also enable the use of the highly developed synthetic biology and bio-production tools available in model organisms such as Escherichia coli and Saccharomyces cerevisiae.
Production of medicines on Mars will be particularly important to reduce cargo transport and avoid degradation of stored medicines by radiation and temperature variations [109]. Synthetic biology principles could be applied to efficiently and simultaneously produce many pharmaceutical molecules on-demand using both plant biofactories [110,111] and compact microbial bioreactors [112,113,114]. While plants are very attractive for the production of medicines for oral delivery because fermentation and purification processes can be avoided [115], microorganism such as Pichia pastoris are advantageous synthetic biology chassis organisms for a multitude of other applications due to their metabolic versatility and extensive gene-engineering tools [116]. P. pastoris could potentially be an ideal production host for medicines, metabolites, and materials on Mars and it also has the ability to grow on methanol as a sole carbon source. Methanol is a one-carbon alcohol that can be derived from the oxidation of methane or the reduction of CO/CO2 with H2 to give methane, and then methanol. Given that CO/CO2 and H2 can be obtained from the combustion of organic material such as inedible plant matter or human waste, the Martian atmosphere, and water electrolysis, methanol derived from these sources is a potentially versatile and easily storable carbon source for microbial production strains.

4. A Roadmap for Research on Adapting Life to Mars

Achieving the proposed goals of adapting plant and microbial life to thrive on a Martian environment in a timeframe compatible with the forthcoming human expeditions to the red planet will require novel approaches. We propose that this formidable challenge can be tackled by establishing a ‘Mars Biofoundry’, that is, an automated and versatile platform capable of expediting the engineering and high throughput phenotyping of biological systems adapted to the environmental conditions that will be encountered on Mars (Figure 3).
Biofoundries facilitate complex automated workflows to build, analyze, and optimize thousands of bioengineering designs in parallel, hence accelerating the exploration of enormous design-space in ways that are unfeasible with traditional approaches [117]. While the majority of current platforms operate with microorganisms, the Mars Biofoundry would also incorporate plants. Therefore, it should be capable of efficient engineering and screening of high-performing plants and microbes under simulated Martian conditions. This unique capacity would also help to identify plant species that would be best suited for Mars.
Direct engineering of plants, even if implementing the most advanced methods [118,119,120], might be impractical because of their lengthy regeneration times and the sheer size of facilities to house large-scale screens. A far more progressive approach would be to test plant-targeted bioengineering designs in heterologous organisms that would be easy to manipulate, capable of rapidly generating large populations, and suitable for massive functional analysis in parallel [64,121,122,123]. Microorganisms such as algae, yeast, and bacteria could be used to rapidly test an enormous array of circuit and pathway designs and, whenever possible, also as plant-proxies in screens simulating the conditions of Mars. Because traits linked to plant development are unlikely to be characterized in unicellular microorganism, the best-performing solutions would then be transferred into simple multicellular plant models such as Marchantia polymorpha and Physcomitrella patens [124,125] for additional characterization under simulated Martian greenhouse conditions (Figure 3). Further refinements in planta (e.g., traits related to functional or anatomical tissue differentiation) or via reiterative microbial engineering rounds could be implemented if necessary. The whole process of outsourcing the optimization of plant-targeted bioengineering designs to microbes could be completed in far less time and with only a fraction of the cost that would be required if pursuing the direct engineering of plants.
Ultimately, we envision that shakedown experiments could be performed within miniature growth facilities deployed on the surface of Mars every ~2 years by future frequent unmanned flights [3]. Remote monitoring of performance on Mars would provide critical knowledge to adjust the work of the biofoundry on Earth (Figure 3). Research on adapting life to Mars would also help to assess the risk of planetary biological contamination in case of accidental release [9] and would, therefore, be invaluable to design effective strategies aimed at reducing this risk.

5. From Earth to Mars and Back to Earth

The human exploration of Mars will be one of the greatest achievements of humanity and the first step of our multiplanetary journey. Developing the technology required for sustaining humans on another planet would lead to revolutionary advancements and fascinating scientific discoveries. Plants could contribute to this enterprise with great implications for Earth. A growing global population is leading to rising demand for food, which will require an increase in agricultural productivity without adverse environmental impact and without placing more land under cultivation [126]. Crop yields are already reaching capacity [127] and continuation with current agricultural technology will strain Earth’s ecosystem [128]. Improving plant traits useful for Mars such as those discussed earlier (Figure 1) will have far-reaching implications across the board for terrestrial agriculture. Advances in microbial-mediated soil conditioning, which will be required for facilitating plant life on Mars (Figure 2), and in the use of plant biomass as renewable feedstock for the manufacture of all kinds of products will respectively help improve crop yield and develop a truly sustainable industry on Earth. Establishing facilities such as the proposed Mars Biofoundry (Figure 3) will likely bring immense benefit to the turnaround time of plant research, hence having widespread implications for addressing the needs of food security and environmental protection but also advancing our understanding of plant biology. Ultimately, the main beneficiary of efforts to develop plants for Mars is Earth.

Author Contributions

B.L. conceived the article and defined its content. B.L., T.C.W., and H.D.G. discussed the outlined research and wrote the article.


Work by B.L. and T.C.W. is funded by the CSIRO Synthetic Biology Future Science Platform and Macquarie University. H.D.G. is supported by the New South Wales Department of Primary Industries, Australia.


We thank Ernesto Llamas from Sketching Science ( for contributing to the figures with digital drawings. We thank Jaime Martinez-Garcia (Centre for Research in Agricultural Genomics), Manuel Rodriguez-Concepcion (Centre for Research in Agricultural Genomics), and Natalie Curach (Macquarie University) for critical reading of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.


  1. Cichan, T.; Bailey, S.A.; Antonelli, T.; Jolly, S.D.; Chambers, R.P.; Clark, B.; Ramm, S.J. Mars Base Camp: An architecture for sending humans to Mars. New Space 2017, 5, 203–218. [Google Scholar] [CrossRef]
  2. Vernikos, J.; Walter, N.; Worms, J.C.; Blanc, S. THESEUS: The European research priorities for human exploration of space. NPJ Microgravity 2016, 2, 16034. [Google Scholar] [CrossRef] [PubMed][Green Version]
  3. Musk, E. Making humans a multi-planetary species. New Space 2017, 5, 46–61. [Google Scholar] [CrossRef]
  4. Fu, Y.; Li, L.; Xie, B.; Dong, C.; Wang, M.; Jia, B.; Shao, L.; Dong, Y.; Deng, S.; Liu, H.; et al. How to establish a Bioregenerative Life Support System for long-term crewed missions to the Moon or Mars. Astrobiology 2016, 16, 925–936. [Google Scholar] [CrossRef] [PubMed]
  5. Wolff, S.A.; Coelho, L.H.; Karoliussen, I.; Jost, A.I. Effects of the extraterrestrial environment on plants: Recommendations for future space experiments for the MELiSSA higher plant compartment. Life 2014, 4, 189–204. [Google Scholar] [CrossRef] [PubMed]
  6. Wheeler, R.M. Agriculture for space: People and places paving the way. Open Agric. 2017, 2, 14–32. [Google Scholar] [CrossRef]
  7. Zabel, P.; Bamsey, M.; Schubert, D.; Tajmar, M. Review and analysis of over 40 years of space plant growth systems. Life Sci. Space Res. 2016, 10, 1–16. [Google Scholar] [CrossRef] [PubMed]
  8. Menezes, A.A.; Cumbers, J.; Hogan, J.A.; Arkin, A.P. Towards synthetic biological approaches to resource utilization on space missions. J. R. Soc. Interface 2015, 12, 20140715. [Google Scholar] [CrossRef] [PubMed]
  9. Verseux, C.; Baque, M.; Lehto, K.; de Vera, J.P.P.; Rothschild, L.J.; Billi, D. Sustainable life support on Mars—The potential roles of cyanobacteria. Int. J. Astrobiol. 2016, 15, 65–92. [Google Scholar] [CrossRef]
  10. Way, J.C.; Silver, P.A.; Howard, R.J. Sun-driven microbial synthesis of chemicals in space. Int. J. Astrobiol. 2011, 10, 359–364. [Google Scholar] [CrossRef]
  11. Rothschild, L.J. Synthetic biology meets bioprinting: Enabling technologies for humans on Mars (and Earth). Biochem. Soc. Trans. 2016, 44, 1158–1164. [Google Scholar] [CrossRef] [PubMed]
  12. Menezes, A.A.; Montague, M.G.; Cumbers, J.; Hogan, J.A.; Arkin, A.P. Grand challenges in space synthetic biology. J. R. Soc. Interface 2015, 12, 20150803. [Google Scholar] [CrossRef] [PubMed][Green Version]
  13. Perchonok, M.H.; Cooper, M.R.; Catauro, P.M. Mission to Mars: Food production and processing for the final frontier. Annu. Rev. Food Sci. Technol. 2012, 3, 311–330. [Google Scholar] [CrossRef] [PubMed]
  14. Hublitz, I.; Henninger, D.L.; Drake, B.G.; Eckart, P. Engineering concepts for inflatable Mars surface greenhouses. Adv. Space Res. 2004, 34, 1546–1551. [Google Scholar] [CrossRef] [PubMed]
  15. Furfaro, R.; Gellenbeck, S.; Giacomelli, G.; Sadler, P. Mars-Lunar Greehouse (MLGH) prototype for bioregenerative life support systems: Current status and future efforts. In Proceedings of the 47th International Conference on Environmental Systems, Charleston, SC, USA, 16–20 July 2017. [Google Scholar]
  16. Kiss, J.Z. Plant biology in reduced gravity on the Moon and Mars. Plant Biol. 2014, 16, 12–17. [Google Scholar] [CrossRef] [PubMed]
  17. Blankenship, R.E.; Tiede, D.M.; Barber, J.; Brudvig, G.W.; Fleming, G.; Ghirardi, M.; Gunner, M.R.; Junge, W.; Kramer, D.M.; Melis, A.; et al. Comparing photosynthetic and photovoltaic efficiencies and recognizing the potential for improvement. Science 2011, 332, 805–809. [Google Scholar] [CrossRef] [PubMed]
  18. Dutta, P.K.; Lin, S.; Loskutov, A.; Levenberg, S.; Jun, D.; Saer, R.; Beatty, J.T.; Liu, Y.; Yan, H.; Woodbury, N.W. Reengineering the optical absorption cross-section of photosynthetic reaction centers. J. Am. Chem. Soc. 2014, 136, 4599–4604. [Google Scholar] [CrossRef] [PubMed]
  19. Grayson, K.J.; Faries, K.M.; Huang, X.; Qian, P.; Dilbeck, P.; Martin, E.C.; Hitchcock, A.; Vasilev, C.; Yuen, J.M.; Niedzwiedzki, D.M.; et al. Augmenting light coverage for photosynthesis through YFP-enhanced charge separation at the Rhodobacter sphaeroides reaction centre. Nat. Commun. 2017, 8, 13972. [Google Scholar] [CrossRef] [PubMed]
  20. Ort, D.R.; Merchant, S.S.; Alric, J.; Barkan, A.; Blankenship, R.E.; Bock, R.; Croce, R.; Hanson, M.R.; Hibberd, J.M.; Long, S.P.; et al. Redesigning photosynthesis to sustainably meet global food and bioenergy demand. Proc. Natl. Acad. Sci. USA 2015, 112, 8529–8536. [Google Scholar] [CrossRef] [PubMed]
  21. Cockell, C.S.; Catling, D.C.; Davis, W.L.; Snook, K.; Kepner, R.L.; Lee, P.; McKay, C.P. The ultraviolet environment of Mars: Biological implications past, present, and future. Icarus 2000, 146, 343–359. [Google Scholar] [CrossRef] [PubMed]
  22. Tohge, T.; Fernie, A.R. Leveraging natural variance towards enhanced understanding of phytochemical sunscreens. Trends Plant Sci. 2017, 22, 308–315. [Google Scholar] [CrossRef] [PubMed]
  23. Llorente, B. Regulation of carotenoid biosynthesis in photosynthetic organs. Subcell. Biochem. 2016, 79, 141–160. [Google Scholar] [PubMed]
  24. Kromdijk, J.; Glowacka, K.; Leonelli, L.; Gabilly, S.T.; Iwai, M.; Niyogi, K.K.; Long, S.P. Improving photosynthesis and crop productivity by accelerating recovery from photoprotection. Science 2016, 354, 857–861. [Google Scholar] [CrossRef] [PubMed][Green Version]
  25. Erb, T.J.; Zarzycki, J. Biochemical and synthetic biology approaches to improve photosynthetic CO2-fixation. Curr. Opin. Chem. Biol. 2016, 34, 72–79. [Google Scholar] [CrossRef] [PubMed]
  26. Giessen, T.W.; Silver, P.A. Engineering carbon fixation with artificial protein organelles. Curr. Opin. Biotechnol. 2017, 46, 42–50. [Google Scholar] [CrossRef] [PubMed]
  27. Liu, D.; Ramya, R.C.S.; Mueller-Cajar, O. Surveying the expanding prokaryotic Rubisco multiverse. FEMS Microbiol. Lett. 2017, 364. [Google Scholar] [CrossRef] [PubMed][Green Version]
  28. Xin, C.P.; Tholen, D.; Devloo, V.; Zhu, X.G. The benefits of photorespiratory bypasses: How can they work? Plant Physiol. 2015, 167, 574–585. [Google Scholar] [CrossRef] [PubMed]
  29. Erb, T.J.; Jones, P.R.; Bar-Even, A. Synthetic metabolism: Metabolic engineering meets enzyme design. Curr. Opin. Chem. Biol. 2017, 37, 56–62. [Google Scholar] [CrossRef] [PubMed]
  30. Schwander, T.; Schada von Borzyskowski, L.; Burgener, S.; Cortina, N.S.; Erb, T.J. A synthetic pathway for the fixation of carbon dioxide in vitro. Science 2016, 354, 900–904. [Google Scholar] [CrossRef] [PubMed][Green Version]
  31. Ralphs, M.; Franz, B.; Baker, T.; Howe, S. Water extraction on Mars for an expanding human colony. Life Sci. Space Res. 2015, 7, 57–60. [Google Scholar] [CrossRef] [PubMed]
  32. Dundas, C.M.; Bramson, A.M.; Ojha, L.; Wray, J.J.; Mellon, M.T.; Byrne, S.; McEwen, A.S.; Putzig, N.E.; Viola, D.; Sutton, S.; et al. Exposed subsurface ice sheets in the Martian mid-latitudes. Science 2018, 359, 199–201. [Google Scholar] [CrossRef] [PubMed]
  33. Barbosa, G.L.; Gadelha, F.D.; Kublik, N.; Proctor, A.; Reichelm, L.; Weissinger, E.; Wohlleb, G.M.; Halden, R.U. Comparison of land, water, and energy requirements of lettuce grown using hydroponic vs. conventional agricultural methods. Int. J. Environ. Res. Public Health 2015, 12, 6879–6891. [Google Scholar] [CrossRef] [PubMed]
  34. Glowacka, K.; Kromdijk, J.; Kucera, K.; Xie, J.; Cavanagh, A.P.; Leonelli, L.; Leakey, A.D.B.; Ort, D.R.; Niyogi, K.K.; Long, S.P. Photosystem II Subunit S overexpression increases the efficiency of water use in a field-grown crop. Nat. Commun. 2018, 9, 868. [Google Scholar] [CrossRef] [PubMed]
  35. Cabello, J.V.; Lodeyro, A.F.; Zurbriggen, M.D. Novel perspectives for the engineering of abiotic stress tolerance in plants. Curr. Opin. Biotechnol. 2014, 26, 62–70. [Google Scholar] [CrossRef] [PubMed]
  36. Paul, M.J.; Nuccio, M.L.; Basu, S.S. Are GM crops for yield and resilience possible? Trends Plant Sci. 2018, 23, 10–16. [Google Scholar] [CrossRef] [PubMed]
  37. Albert, R.; Acharya, B.R.; Jeon, B.W.; Zanudo, J.G.T.; Zhu, M.; Osman, K.; Assmann, S.M. A new discrete dynamic model of ABA-induced stomatal closure predicts key feedback loops. PLoS Biol. 2017, 15, e2003451. [Google Scholar] [CrossRef] [PubMed]
  38. Yang, X.; Cushman, J.C.; Borland, A.M.; Edwards, E.J.; Wullschleger, S.D.; Tuskan, G.A.; Owen, N.A.; Griffiths, H.; Smith, J.A.; De Paoli, H.C.; et al. A roadmap for research on crassulacean acid metabolism (CAM) to enhance sustainable food and bioenergy production in a hotter, drier world. New Phytol. 2015, 207, 491–504. [Google Scholar] [CrossRef] [PubMed][Green Version]
  39. Costa, M.C.D.; Farrant, J.M.; Oliver, M.J.; Ligterink, W.; Buitink, J.; Hilhorst, H.M.W. Key genes involved in desiccation tolerance and dormancy across life forms. Plant Sci. 2016, 251, 162–168. [Google Scholar] [CrossRef] [PubMed]
  40. Giarola, V.; Hou, Q.; Bartels, D. Angiosperm plant desiccation tolerance: Hints from transcriptomics and genome sequencing. Trends Plant Sci. 2017, 22, 705–717. [Google Scholar] [CrossRef] [PubMed]
  41. Mazin, P.V.; Shagimardanova, E.; Kozlova, O.; Cherkasov, A.; Sutormin, R.; Stepanova, V.V.; Stupnikov, A.; Logacheva, M.; Penin, A.; Sogame, Y.; et al. Cooption of heat shock regulatory system for anhydrobiosis in the sleeping chironomid Polypedilum vanderplanki. Proc. Natl. Acad. Sci. USA 2018, 115, E2477–E2486. [Google Scholar] [CrossRef] [PubMed]
  42. Yoshida, Y.; Koutsovoulos, G.; Laetsch, D.R.; Stevens, L.; Kumar, S.; Horikawa, D.D.; Ishino, K.; Komine, S.; Kunieda, T.; Tomita, M.; et al. Comparative genomics of the tardigrades Hypsibius dujardini and Ramazzottius varieornatus. PLoS Biol. 2017, 15, e2002266. [Google Scholar] [CrossRef] [PubMed]
  43. Schofield, J.T.; Barnes, J.R.; Crisp, D.; Haberle, R.M.; Larsen, S.; Magalhaes, J.A.; Murphy, J.R.; Seiff, A.; Wilson, G. The Mars Pathfinder atmospheric structure investigation/meteorology (ASI/MET) experiment. Science 1997, 278, 1752–1758. [Google Scholar] [CrossRef] [PubMed]
  44. Bredow, M.; Walker, V.K. Ice-binding proteins in plants. Front. Plant Sci. 2017, 8, 2153. [Google Scholar] [CrossRef] [PubMed]
  45. Megha, S.; Basu, U.; Kay, N.N.V. Metabolic engineering of cold tolerance in plants. Biocatal. Agric. Biotechnol. 2014, 3, 88–95. [Google Scholar] [CrossRef]
  46. Krasensky, J.; Jonak, C. Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. J. Exp. Bot. 2012, 63, 1593–1608. [Google Scholar] [CrossRef] [PubMed][Green Version]
  47. Harmer, S.L. The circadian system in higher plants. Annu. Rev. Plant Biol. 2009, 60, 357–377. [Google Scholar] [CrossRef] [PubMed]
  48. Dodd, A.N.; Salathia, N.; Hall, A.; Kevei, E.; Toth, R.; Nagy, F.; Hibberd, J.M.; Millar, A.J.; Webb, A.A. Plant circadian clocks increase photosynthesis, growth, survival, and competitive advantage. Science 2005, 309, 630–633. [Google Scholar] [CrossRef] [PubMed]
  49. Kyriacou, M.C.; De Pascale, S.; Kyratzis, A.; Rouphael, Y. Microgreens as a component of space life support systems: A cornucopia of functional food. Front. Plant Sci. 2017, 8, 1587. [Google Scholar] [CrossRef] [PubMed]
  50. Boccalandro, H.E.; Ploschuk, E.L.; Yanovsky, M.J.; Sanchez, R.A.; Gatz, C.; Casal, J.J. Increased phytochrome B alleviates density effects on tuber yield of field potato crops. Plant Physiol. 2003, 133, 1539–1546. [Google Scholar] [CrossRef] [PubMed]
  51. Lopez Pereira, M.; Sadras, V.O.; Batista, W.; Casal, J.J.; Hall, A.J. Light-mediated self-organization of sunflower stands increases oil yield in the field. Proc. Natl. Acad. Sci. USA 2017, 114, 7975–7980. [Google Scholar] [CrossRef] [PubMed][Green Version]
  52. Martinez-Garcia, J.F.; Gallemi, M.; Molina-Contreras, M.J.; Llorente, B.; Bevilaqua, M.R.; Quail, P.H. The shade avoidance syndrome in Arabidopsis: The antagonistic role of phytochrome a and B differentiates vegetation proximity and canopy shade. PLoS ONE 2014, 9, e109275. [Google Scholar] [CrossRef] [PubMed]
  53. Ganesan, M.; Lee, H.Y.; Kim, J.I.; Song, P.S. Development of transgenic crops based on photo-biotechnology. Plant Cell Environ. 2017, 40, 2469–2486. [Google Scholar] [CrossRef] [PubMed]
  54. Rodriguez-Leal, D.; Lemmon, Z.H.; Man, J.; Bartlett, M.E.; Lippman, Z.B. Engineering quantitative trait variation for crop improvement by genome editing. Cell 2017, 171, 470–480. [Google Scholar] [CrossRef] [PubMed]
  55. Soyk, S.; Lemmon, Z.H.; Oved, M.; Fisher, J.; Liberatore, K.L.; Park, S.J.; Goren, A.; Jiang, K.; Ramos, A.; van der Knaap, E.; et al. Bypassing negative epistasis on yield in tomato imposed by a domestication gene. Cell 2017, 169, 1142–1155. [Google Scholar] [CrossRef] [PubMed]
  56. Soyk, S.; Muller, N.A.; Park, S.J.; Schmalenbach, I.; Jiang, K.; Hayama, R.; Zhang, L.; Van Eck, J.; Jimenez-Gomez, J.M.; Lippman, Z.B. Variation in the flowering gene SELF PRUNING 5G promotes day-neutrality and early yield in tomato. Nat. Genet. 2017, 49, 162–168. [Google Scholar] [CrossRef] [PubMed]
  57. Khan, M.A.; Gemenet, D.C.; Villordon, A. Root system architecture and abiotic stress tolerance: Current knowledge in root and tuber crops. Front. Plant Sci. 2016, 7, 1584. [Google Scholar] [CrossRef] [PubMed]
  58. Kong, X.; Zhang, M.; De Smet, I.; Ding, Z. Designer crops: Optimal root system architecture for nutrient acquisition. Trends Biotechnol. 2014, 32, 597–598. [Google Scholar] [CrossRef] [PubMed]
  59. Heppell, J.; Talboys, P.; Payvandi, S.; Zygalakis, K.C.; Fliege, J.; Withers, P.J.; Jones, D.L.; Roose, T. How changing root system architecture can help tackle a reduction in soil phosphate (P) levels for better plant P acquisition. Plant Cell Environ. 2015, 38, 118–128. [Google Scholar] [CrossRef] [PubMed]
  60. Pasek, M. Early Mars: Without phosphate limits. Nat. Geosci. 2013, 6, 806–807. [Google Scholar] [CrossRef]
  61. Adcock, C.T.; Hausrath, E.M.; Forster, P.M. Readily available phosphate from minerals in early aqueous environments on Mars. Nat. Geosci. 2013, 6, 824–827. [Google Scholar] [CrossRef]
  62. Stern, J.C.; Sutter, B.; Freissinet, C.; Navarro-Gonzalez, R.; McKay, C.P.; Archer, P.D., Jr.; Buch, A.; Brunner, A.E.; Coll, P.; Eigenbrode, J.L.; et al. Evidence for indigenous nitrogen in sedimentary and aeolian deposits from the Curiosity rover investigations at Gale crater, Mars. Proc. Natl. Acad. Sci. USA 2015, 112, 4245–4250. [Google Scholar] [CrossRef] [PubMed]
  63. Allen, R.S.; Tilbrook, K.; Warden, A.C.; Campbell, P.C.; Rolland, V.; Singh, S.P.; Wood, C.C. Expression of 16 nitrogenase proteins within the plant mitochondrial matrix. Front. Plant Sci. 2017, 8, 287. [Google Scholar] [CrossRef] [PubMed]
  64. Buren, S.; Young, E.M.; Sweeny, E.A.; Lopez-Torrejon, G.; Veldhuizen, M.; Voigt, C.A.; Rubio, L.M. Formation of nitrogenase NifDK tetramers in the mitochondria of Saccharomyces cerevisiae. ACS Synth. Biol. 2017, 6, 1043–1055. [Google Scholar] [CrossRef] [PubMed]
  65. Yang, J.; Xie, X.; Yang, M.; Dixon, R.; Wang, Y.P. Modular electron-transport chains from eukaryotic organelles function to support nitrogenase activity. Proc. Natl. Acad. Sci. USA 2017, 114, E2460–E2465. [Google Scholar] [CrossRef] [PubMed]
  66. Buren, S.; Rubio, L.M. State of the art in eukaryotic nitrogenase engineering. FEMS Microbiol. Lett. 2018, 365. [Google Scholar] [CrossRef] [PubMed]
  67. Li, X.X.; Liu, Q.; Liu, X.M.; Shi, H.W.; Chen, S.F. Using synthetic biology to increase nitrogenase activity. Microb. Cell Fact. 2016, 15, 43. [Google Scholar] [CrossRef] [PubMed]
  68. Temme, K.; Zhao, D.; Voigt, C.A. Refactoring the nitrogen fixation gene cluster from Klebsiella oxytoca. Proc. Natl. Acad. Sci. USA 2012, 109, 7085–7090. [Google Scholar] [CrossRef] [PubMed]
  69. Rogers, C.; Oldroyd, G.E. Synthetic biology approaches to engineering the nitrogen symbiosis in cereals. J. Exp. Bot. 2014, 65, 1939–1946. [Google Scholar] [CrossRef] [PubMed][Green Version]
  70. Geddes, B.A.; Ryu, M.H.; Mus, F.; Costas, A.G.; Peters, J.W.; Voigt, C.A.; Poole, P. Use of plant colonizing bacteria as chassis for transfer of N2-fixation to cereals. Curr. Opin. Biotechnol. 2015, 32, 216–222. [Google Scholar] [CrossRef] [PubMed]
  71. Mus, F.; Crook, M.B.; Garcia, K.; Garcia Costas, A.; Geddes, B.A.; Kouri, E.D.; Paramasivan, P.; Ryu, M.H.; Oldroyd, G.E.D.; Poole, P.S.; et al. Symbiotic nitrogen fixation and the challenges to its extension to nonlegumes. Appl. Environ. Microbiol. 2016, 82, 3698–3710. [Google Scholar] [CrossRef] [PubMed]
  72. Bergouignan, A.; Stein, T.P.; Habold, C.; Coxam, V.; O’ Gorman, D.; Blanc, S. Towards human exploration of space: The THESEUS review series on nutrition and metabolism research priorities. NPJ Microgravity 2016, 2, 16029. [Google Scholar] [CrossRef] [PubMed][Green Version]
  73. Rodriguez-Concepcion, M.; Avalos, J.; Bonet, M.L.; Boronat, A.; Gomez-Gomez, L.; Hornero-Mendez, D.; Limon, M.C.; Melendez-Martinez, A.J.; Olmedilla-Alonso, B.; Palou, A.; et al. A global perspective on carotenoids: Metabolism, biotechnology, and benefits for nutrition and health. Prog. Lipid Res. 2018, 70, 62–93. [Google Scholar] [CrossRef] [PubMed]
  74. Cohu, C.M.; Lombardi, E.; Adams, W.W.; Demmig-Adams, B. Increased nutritional quality of plants for long-duration spaceflight missions through choice of plant variety and manipulation of growth conditions. Acta Astronaut. 2014, 94, 799–806. [Google Scholar] [CrossRef]
  75. Llorente, B.; D’Andrea, L.; Rodriguez-Concepcion, M. Evolutionary recycling of light signaling components in fleshy fruits: New insights on the role of pigments to monitor ripening. Front. Plant Sci. 2016, 7, 263. [Google Scholar] [CrossRef] [PubMed]
  76. Llorente, B.; Martinez-Garcia, J.F.; Stange, C.; Rodriguez-Concepcion, M. Illuminating colors: Regulation of carotenoid biosynthesis and accumulation by light. Curr. Opin. Plant Biol. 2017, 37, 49–55. [Google Scholar] [CrossRef] [PubMed]
  77. Sun, T.; Yuan, H.; Cao, H.; Yazdani, M.; Tadmor, Y.; Li, L. Carotenoid metabolism in plants: The role of plastids. Mol. Plant 2018, 11, 58–74. [Google Scholar] [CrossRef] [PubMed]
  78. D’Andrea, L.; Simon-Moya, M.; Llorente, B.; Llamas, E.; Marro, M.; Loza-Alvarez, P.; Li, L.; Rodriguez-Concepcion, M. Interference with Clp protease impairs carotenoid accumulation during tomato fruit ripening. J. Exp. Bot. 2018, 69, 1557–1568. [Google Scholar] [CrossRef] [PubMed]
  79. Llorente, B.; D’Andrea, L.; Ruiz-Sola, M.A.; Botterweg, E.; Pulido, P.; Andilla, J.; Loza-Alvarez, P.; Rodriguez-Concepcion, M. Tomato fruit carotenoid biosynthesis is adjusted to actual ripening progression by a light-dependent mechanism. Plant J. 2016, 85, 107–119. [Google Scholar] [CrossRef] [PubMed][Green Version]
  80. Majer, E.; Llorente, B.; Rodriguez-Concepcion, M.; Daros, J.A. Rewiring carotenoid biosynthesis in plants using a viral vector. Sci. Rep. 2017, 7, 41645. [Google Scholar] [CrossRef] [PubMed][Green Version]
  81. Zhou, X.; Welsch, R.; Yang, Y.; Alvarez, D.; Riediger, M.; Yuan, H.; Fish, T.; Liu, J.; Thannhauser, T.W.; Li, L. Arabidopsis OR proteins are the major posttranscriptional regulators of phytoene synthase in controlling carotenoid biosynthesis. Proc. Natl. Acad. Sci. USA 2015, 112, 3558–3563. [Google Scholar] [CrossRef] [PubMed][Green Version]
  82. Zhang, Y.; Butelli, E.; Alseekh, S.; Tohge, T.; Rallapalli, G.; Luo, J.; Kawar, P.G.; Hill, L.; Santino, A.; Fernie, A.R.; et al. Multi-level engineering facilitates the production of phenylpropanoid compounds in tomato. Nat. Commun. 2015, 6, 8635. [Google Scholar] [CrossRef] [PubMed][Green Version]
  83. Naqvi, S.; Zhu, C.; Farre, G.; Ramessar, K.; Bassie, L.; Breitenbach, J.; Perez Conesa, D.; Ros, G.; Sandmann, G.; Capell, T.; et al. Transgenic multivitamin corn through biofortification of endosperm with three vitamins representing three distinct metabolic pathways. Proc. Natl. Acad. Sci. USA 2009, 106, 7762–7767. [Google Scholar] [CrossRef] [PubMed][Green Version]
  84. Butelli, E.; Titta, L.; Giorgio, M.; Mock, H.P.; Matros, A.; Peterek, S.; Schijlen, E.G.; Hall, R.D.; Bovy, A.G.; Luo, J.; et al. Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors. Nat. Biotechnol. 2008, 26, 1301–1308. [Google Scholar] [CrossRef] [PubMed]
  85. Llorente, B.; Alonso, G.D.; Bravo-Almonacid, F.; Rodriguez, V.; Lopez, M.G.; Carrari, F.; Torres, H.N.; Flawia, M.M. Safety assessment of nonbrowning potatoes: Opening the discussion about the relevance of substantial equivalence on next generation biotech crops. Plant Biotechnol. J. 2011, 9, 136–150. [Google Scholar] [CrossRef] [PubMed]
  86. Llorente, B.; Rodriguez, V.; Alonso, G.D.; Torres, H.N.; Flawia, M.M.; Bravo-Almonacid, F.F. Improvement of aroma in transgenic potato as a consequence of impairing tuber browning. PLoS ONE 2010, 5, e14030. [Google Scholar] [CrossRef] [PubMed]
  87. Morris, J.; Hawthorne, K.M.; Hotze, T.; Abrams, S.A.; Hirschi, K.D. Nutritional impact of elevated calcium transport activity in carrots. Proc. Natl. Acad. Sci. USA 2008, 105, 1431–1435. [Google Scholar] [CrossRef] [PubMed][Green Version]
  88. Uluisik, S.; Chapman, N.H.; Smith, R.; Poole, M.; Adams, G.; Gillis, R.B.; Besong, T.M.; Sheldon, J.; Stiegelmeyer, S.; Perez, L.; et al. Genetic improvement of tomato by targeted control of fruit softening. Nat. Biotechnol. 2016, 34, 950–952. [Google Scholar] [CrossRef] [PubMed][Green Version]
  89. Chakraborty, S.; Chakraborty, N.; Agrawal, L.; Ghosh, S.; Narula, K.; Shekhar, S.; Naik, P.S.; Pande, P.C.; Chakrborti, S.K.; Datta, A. Next-generation protein-rich potato expressing the seed protein gene AmA1 is a result of proteome rebalancing in transgenic tuber. Proc. Natl. Acad. Sci. USA 2010, 107, 17533–17538. [Google Scholar] [CrossRef] [PubMed]
  90. Gallo, M.; Sayre, R. Removing allergens and reducing toxins from food crops. Curr. Opin. Biotechnol. 2009, 20, 191–196. [Google Scholar] [CrossRef] [PubMed]
  91. Zhang, Y.; Butelli, E.; De Stefano, R.; Schoonbeek, H.J.; Magusin, A.; Pagliarani, C.; Wellner, N.; Hill, L.; Orzaez, D.; Granell, A.; et al. Anthocyanins double the shelf life of tomatoes by delaying overripening and reducing susceptibility to gray mold. Curr. Biol. 2013, 23, 1094–1100. [Google Scholar] [CrossRef] [PubMed]
  92. Sanchez-Leon, S.; Gil-Humanes, J.; Ozuna, C.V.; Gimenez, M.J.; Sousa, C.; Voytas, D.F.; Barro, F. Low-gluten, nontransgenic wheat engineered with CRISPR/Cas9. Plant Biotechnol. J. 2018, 16, 902–910. [Google Scholar] [CrossRef] [PubMed]
  93. Wamelink, G.W.; Frissel, J.Y.; Krijnen, W.H.; Verwoert, M.R.; Goedhart, P.W. Can plants grow on Mars and the moon: A growth experiment on Mars and moon soil simulants. PLoS ONE 2014, 9, e103138. [Google Scholar] [CrossRef] [PubMed]
  94. Maggi, F.; Pallud, C. Martian base agriculture: The effect of low gravity on water flow, nutrient cycles, and microbial biomass dynamics. Adv. Space Res. 2010, 46, 1257–1265. [Google Scholar] [CrossRef]
  95. Cary, S.C.; McDonald, I.R.; Barrett, J.E.; Cowan, D.A. On the rocks: The microbiology of Antarctic Dry Valley soils. Nat. Rev. Microbiol. 2010, 8, 129–138. [Google Scholar] [CrossRef] [PubMed]
  96. Marchant, D.R.; Head, J.W. Antarctic dry valleys: Microclimate zonation, variable geomorphic processes, and implications for assessing climate change on Mars. Icarus 2007, 192, 187–222. [Google Scholar] [CrossRef][Green Version]
  97. Ji, M.; Greening, C.; Vanwonterghem, I.; Carere, C.R.; Bay, S.K.; Steen, J.A.; Montgomery, K.; Lines, T.; Beardall, J.; van Dorst, J.; et al. Atmospheric trace gases support primary production in Antarctic desert surface soil. Nature 2017, 552, 400–403. [Google Scholar] [CrossRef] [PubMed]
  98. Hecht, M.H.; Kounaves, S.P.; Quinn, R.C.; West, S.J.; Young, S.M.M.; Ming, D.W.; Catling, D.C.; Clark, B.C.; Boynton, W.V.; Hoffman, J.; et al. Detection of perchlorate and the soluble chemistry of Martian soil at the Phoenix Lander site. Science 2009, 325, 64–67. [Google Scholar] [CrossRef] [PubMed]
  99. Bardiya, N.; Bae, J.H. Dissimilatory perchlorate reduction: A review. Microbiol. Res. 2011, 166, 237–254. [Google Scholar] [CrossRef] [PubMed]
  100. Davila, A.F.; Willson, D.; Coates, J.D.; Mckay, C.P. Perchlorate on Mars: A chemical hazard and a resource for humans. Int. J. Astrobiol. 2013, 12, 321–325. [Google Scholar] [CrossRef]
  101. Martin-Torres, F.J.; Zorzano, M.P.; Valentin-Serrano, P.; Harri, A.M.; Genzer, M.; Kemppinen, O.; Rivera-Valentin, E.G.; Jun, I.; Wray, J.; Madsen, M.B.; et al. Transient liquid water and water activity at Gale crater on Mars. Nat. Geosci. 2015, 8, 357–361. [Google Scholar] [CrossRef]
  102. Maestre, F.T.; Sole, R.; Singh, B.K. Microbial biotechnology as a tool to restore degraded drylands. Microb. Biotechnol. 2017, 10, 1250–1253. [Google Scholar] [CrossRef] [PubMed][Green Version]
  103. Vickers, C.E.; Williams, T.C.; Peng, B.; Cherry, J. Recent advances in synthetic biology for engineering isoprenoid production in yeast. Curr. Opin. Chem. Biol. 2017, 40, 47–56. [Google Scholar] [CrossRef] [PubMed]
  104. Paddon, C.J.; Westfall, P.J.; Pitera, D.J.; Benjamin, K.; Fisher, K.; McPhee, D.; Leavell, M.D.; Tai, A.; Main, A.; Eng, D.; et al. High-level semi-synthetic production of the potent antimalarial artemisinin. Nature 2013, 496, 528–532. [Google Scholar] [CrossRef] [PubMed][Green Version]
  105. Xia, X.X.; Qian, Z.G.; Ki, C.S.; Park, Y.H.; Kaplan, D.L.; Lee, S.Y. Native-sized recombinant spider silk protein produced in metabolically engineered Escherichia coli results in a strong fiber. Proc. Natl. Acad. Sci. USA 2010, 107, 14059–14063. [Google Scholar] [CrossRef] [PubMed]
  106. Marcellin, E.; Behrendorff, J.B.; Nagaraju, S.; DeTissera, S.; Segovia, S.; Palfreyman, R.W.; Daniell, J.; Licona-Cassani, C.; Quek, L.E.; Speight, R.; et al. Low carbon fuels and commodity chemicals from waste gases- systematic approach to understand energy metabolism in a model acetogen. Green Chem. 2016, 18, 3020–3028. [Google Scholar] [CrossRef][Green Version]
  107. Schuchmann, K.; Muller, V. Autotrophy at the thermodynamic limit of life: A model for energy conservation in acetogenic bacteria. Nat. Rev. Microbiol. 2014, 12, 809–821. [Google Scholar] [CrossRef] [PubMed]
  108. Valgepea, K.; Lemgruber, R.D.P.; Meaghan, K.; Palfreyman, R.W.; Abdalla, T.; Heijstra, B.D.; Behrendorff, J.B.; Tappel, R.; Kopke, M.; Simpson, S.D.; et al. Maintenance of ATP homeostasis triggers metabolic shifts in gas-fermenting acetogens. Cell Syst. 2017, 4, 505–515. [Google Scholar] [CrossRef] [PubMed]
  109. Du, B.; Daniels, V.R.; Vaksman, Z.; Boyd, J.L.; Crady, C.; Putcha, L. Evaluation of physical and chemical changes in pharmaceuticals flown on space missions. AAPS J. 2011, 13, 299–308. [Google Scholar] [CrossRef] [PubMed]
  110. Loh, H.S.; Green, B.J.; Yusibov, V. Using transgenic plants and modified plant viruses for the development of treatments for human diseases. Curr. Opin. Virol. 2017, 26, 81–89. [Google Scholar] [CrossRef] [PubMed]
  111. Zhang, B.; Shanmugaraj, B.; Daniell, H. Expression and functional evaluation of biopharmaceuticals made in plant chloroplasts. Curr. Opin. Chem. Biol. 2017, 38, 17–23. [Google Scholar] [CrossRef] [PubMed]
  112. Cao, J.C.; Perez-Pinera, P.; Lowenhaupt, K.; Wu, M.R.; Purcell, O.; de la Fuente-Nunez, C.; Lu, T.K. Versatile and on-demand biologics co-production in yeast. Nat. Commun. 2018, 9, 77. [Google Scholar] [CrossRef] [PubMed]
  113. Perez-Pinera, P.; Han, N.R.; Cleto, S.; Cao, J.C.; Purcell, O.; Shah, K.A.; Lee, K.; Ram, R.; Lu, T.K. Synthetic biology and microbioreactor platforms for programmable production of biologics at the point-of-care. Nat. Commun. 2016, 7, 12211. [Google Scholar] [CrossRef] [PubMed][Green Version]
  114. Pardee, K.; Slomovic, S.; Nguyen, P.Q.; Lee, J.W.; Donghia, N.; Burrill, D.; Ferrante, T.; McSorley, F.R.; Furuta, Y.; Vernet, A.; et al. Portable, on-demand biomolecular manufacturing. Cell 2016, 167, 248–259. [Google Scholar] [CrossRef] [PubMed]
  115. Kwon, K.C.; Daniell, H. Low-cost oral delivery of protein drugs bioencapsulated in plant cells. Plant Biotechnol. J. 2015, 13, 1017–1022. [Google Scholar] [CrossRef] [PubMed][Green Version]
  116. Pena, D.A.; Gasser, B.; Zanghellini, J.; Steiger, M.G.; Mattanovich, D. Metabolic engineering of Pichia pastoris. Metab. Eng. 2018. [Google Scholar] [CrossRef]
  117. Chao, R.; Mishra, S.; Si, T.; Zhao, H. Engineering biological systems using automated biofoundries. Metab. Eng. 2017, 42, 98–108. [Google Scholar] [CrossRef] [PubMed]
  118. Shih, P.M.; Vuu, K.; Mansoori, N.; Ayad, L.; Louie, K.B.; Bowen, B.P.; Northen, T.R.; Loque, D. A robust gene-stacking method utilizing yeast assembly for plant synthetic biology. Nat. Commun. 2016, 7, 13215. [Google Scholar] [CrossRef] [PubMed][Green Version]
  119. Wu, Y.; You, L.; Li, S.; Ma, M.; Wu, M.; Ma, L.; Bock, R.; Chang, L.; Zhang, J. In vivo assembly in Escherichia coli of transformation vectors for plastid genome engineering. Front. Plant Sci. 2017, 8, 1454. [Google Scholar] [CrossRef] [PubMed]
  120. Altpeter, F.; Springer, N.M.; Bartley, L.E.; Blechl, A.E.; Brutnell, T.P.; Citovsky, V.; Conrad, L.J.; Gelvin, S.B.; Jackson, D.P.; Kausch, A.P.; et al. Advancing crop transformation in the era of genome editing. Plant Cell 2016, 28, 1510–1520. [Google Scholar] [CrossRef] [PubMed]
  121. Dann, M.; Leister, D. Enhancing (crop) plant photosynthesis by introducing novel genetic diversity. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2017, 372. [Google Scholar] [CrossRef] [PubMed]
  122. Nemhauser, J.L.; Torii, K.U. Plant synthetic biology for molecular engineering of signalling and development. Nat. Plants 2016, 2, 16010. [Google Scholar] [CrossRef] [PubMed][Green Version]
  123. Leister, D. Experimental evolution in photoautotrophic microorganisms as a means of enhancing chloroplast functions. Essays Biochem. 2018, 62, 77–84. [Google Scholar] [CrossRef] [PubMed]
  124. Boehm, C.R.; Pollak, B.; Purswani, N.; Patron, N.; Haseloff, J. Synthetic botany. Cold Spring Harb. Perspect. Biol. 2017, 9, a023887. [Google Scholar] [CrossRef] [PubMed]
  125. Reski, R.; Bae, H.; Simonsen, H.T. Physcomitrella patens, a versatile synthetic biology chassis. Plant Cell Rep. 2018. [Google Scholar] [CrossRef] [PubMed]
  126. Food and Agriculture Organization of the United Nations. The Future of Food and Agriculture—Trends and Challenges; Food and Agriculture Organization of the United Nations: Rome, Italy, 2017. [Google Scholar]
  127. Mueller, N.D.; Gerber, J.S.; Johnston, M.; Ray, D.K.; Ramankutty, N.; Foley, J.A. Closing yield gaps through nutrient and water management. Nature 2012, 490, 254–257. [Google Scholar] [CrossRef] [PubMed]
  128. Hunter, M.C.; Smith, R.G.; Schipanski, M.E.; Atwood, L.W.; Mortensen, D.A. Recalibrating targets for sustainable intensification. Bioscience 2017, 67, 386–391. [Google Scholar] [CrossRef]
Figure 1. Synthetic biology applied for enhancing plant performance. Different traits that can be engineered simultaneously to take full advantage of plants on Mars (and Earth).
Figure 1. Synthetic biology applied for enhancing plant performance. Different traits that can be engineered simultaneously to take full advantage of plants on Mars (and Earth).
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Figure 2. Engineering microorganisms to facilitate plant life on Mars. This conceptual microbe scavenges atmospheric hydrogen (H2) and carbon dioxide (CO2), and it is customized to condition Martian soil for plant growth by reducing soil perchlorate salts (MgClO4 and CaClO4) and increasing soil moisture. H2O: water; Cl: chlorine; Ca2+: calcium; and Mg2+: magnesium.
Figure 2. Engineering microorganisms to facilitate plant life on Mars. This conceptual microbe scavenges atmospheric hydrogen (H2) and carbon dioxide (CO2), and it is customized to condition Martian soil for plant growth by reducing soil perchlorate salts (MgClO4 and CaClO4) and increasing soil moisture. H2O: water; Cl: chlorine; Ca2+: calcium; and Mg2+: magnesium.
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Figure 3. Schematic roadmap for research on adapting life to Mars. The Mars Biofoundry integrates the design of synthetic biology approaches (A) with an automated platform for implementing bioengineering designs in plants and microbes (B) and a facility for high-throughput phenotyping under simulated Martian conditions (C). The process iterates as a design-build-test cycle. Eventually, engineered organisms could be periodically transported to Mars (D) to perform experiments within miniature growth facilities (E). Remote monitoring of performance on Mars (F) would provide critical knowledge to adjust the work carried out at the biofoundry on Earth.
Figure 3. Schematic roadmap for research on adapting life to Mars. The Mars Biofoundry integrates the design of synthetic biology approaches (A) with an automated platform for implementing bioengineering designs in plants and microbes (B) and a facility for high-throughput phenotyping under simulated Martian conditions (C). The process iterates as a design-build-test cycle. Eventually, engineered organisms could be periodically transported to Mars (D) to perform experiments within miniature growth facilities (E). Remote monitoring of performance on Mars (F) would provide critical knowledge to adjust the work carried out at the biofoundry on Earth.
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Llorente, B.; Williams, T.C.; Goold, H.D. The Multiplanetary Future of Plant Synthetic Biology. Genes 2018, 9, 348.

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Llorente B, Williams TC, Goold HD. The Multiplanetary Future of Plant Synthetic Biology. Genes. 2018; 9(7):348.

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Llorente, Briardo, Thomas C. Williams, and Hugh D. Goold. 2018. "The Multiplanetary Future of Plant Synthetic Biology" Genes 9, no. 7: 348.

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