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For millennia, humanity has depended on photosynthesis to cultivate crops and feed a growing population. However, the escalating challenges of climate change and global hunger now compel us to surpass the efficiency limitations of photosynthesis. Here, we propose the adoption of an electro-agriculture (electro-ag) framework that combines CO2 electrolysis with biological systems to enhance food production efficiency. Adopting a food system based entirely on electro-ag could reduce United States agricultural land use by 88%, freeing nearly half of the country’s land for ecosystem restoration and natural carbon sequestration. Electro-ag bypasses traditional photosynthesis, enabling food cultivation in non-arable urban centers, arid deserts, and even outer space environments. We offer a new strategy that improves energy efficiency by an order of magnitude compared with photosynthesis, along with essential guidance for developing electro-ag focused on staple crops, to maximize benefits for regions facing food insecurity. This innovative approach to agriculture holds significant promise in reducing environmental impacts, streamlining supply chains, and addressing the global food crisis. 

Plant cellular agriculture aims to disrupt the way plant derived products are produced. Plant cell cultures are typically grown with sucrose as the primary carbon and energy source, but alternative carbon sources may have advantages over sucrose including less strain on food systems, lower costs, and more sustainable sourcing. Here we review carbon and energy sources that may serve as alternatives to sucrose in the cultivation of plant cell cultures. We identified acetate as a promising candidate and took the first steps to evaluate its potential for use in growing tobacco plant cell cultures. When added to media containing sucrose, acetate concentrations above 8 mM completely inhibit growth. Lower concentrations of acetate (2-4 mM) can support an increase in dry weight without sucrose but do not provide enough energy for substantial growth.¹³C labeling indicates that tobacco plant cell cultures can incorporate carbon from exogenous acetate into proteins and carbohydrates. Analysis of transcriptome data showed that genes encoding glyoxylate cycle enzymes are expressed at very low levels compared to genes from the TCA cycle and glycolysis. Adaptive laboratory evolution experiments were able to increase tobacco cell cultures tolerance to acetate, demonstrating the potential for this type of approach going forward. Overall, our results indicate that acetate can be metabolized by plant cell cultures and suggest that further adaptive laboratory evolution or strain engineering efforts may enable acetate to serve as a sole carbon and energy source for tobacco plant cell cultures. This assessment of acetate provides a framework for evaluating other carbon and energy sources for plant cell cultures, efforts that will help reduce the costs and environmental impact, and increase the commercial potential of plant cellular agriculture. 

Abstract Artificial photosynthesis systems are proposed as an efficient alternative route to capture CO 2 to produce additional food for growing global demand. Here a two-step CO 2 electrolyser system was developed to produce a highly concentrated acetate stream with a 57% carbon selectivity (CO 2 to acetate), allowing its direct use for the heterotrophic cultivation of yeast, mushroom-producing fungus and a photosynthetic green alga, in the dark without inputs from biological photosynthesis. An evaluation of nine crop plants found that carbon from exogenously supplied acetate incorporates into biomass through major metabolic pathways. Coupling this approach to existing photovoltaic systems could increase solar-to-food energy conversion efficiency by about fourfold over biological photosynthesis, reducing the solar footprint required. This technology allows for a reimagination of how food can be produced in controlled environments.