About This Project
Enhancing photosynthesis can help mitigate greenhouse gases, but plants and algae use only visible light (400-700 nm), leaving much of the light spectrum untapped. This project introduces chlorophyll f, a pigment that absorbs far-red light (700-800 nm), into a plant, enabling greater photosynthetic efficiency that boosts biomass growth and CO2 sequestration. This bioengineering approach supports the Homeworld Collective’s mission to develop synthetic biology solutions for CO2 removal.
Ask the Scientists
Join The DiscussionMotivating Factor
Photosynthesis forms the basis for higher life on Earth and is the primary mechanism for global carbon sequestration, converting atmospheric CO2 into biomass. Photosynthetic efficiency, however, is limited by the range of light wavelengths that photosynthetic organisms can use for energy conversion [1], thus limiting natural carbon sequestration. Most photosynthetic organisms use visible light (400-700 nm) which accounts for ~50% of solar energy. Therefore, a significant portion of available light remains unused, especially when visible light is attenuated due to shading [2]. This reduces the potential for carbon sequestration and biomass production, which in turn constrains efforts to address rising CO2 levels and global energy demands. Expanding and tuning the spectral range of light absorption in photosynthetic organisms could significantly enhance photosynthetic efficiency [3, 4], contributing to scalable greenhouse gas removal strategies.
Specific Bottleneck
At the heart of photosynthesis are two protein complexes that harvest light and convert it to chemical energy, called photosystems I and II (PSI and PSII) [5]. A key bottleneck in improving photosynthetic efficiency is the competition between the two for the same range of visible light photons [4]. This competition results in inefficient energy utilization and limits overall photosynthetic output. In plant canopies where lower levels receive minimal light, this inefficiency is exacerbated. Recent discoveries have shown that some photosynthetic microorganisms, called cyanobacteria, have evolved mechanisms to overcome this limitation by altering their photosystems to additionally use light between 700 and 800 nm [6], called far-red light, but this adaptation is not observed in any plants. Our challenge lies in engineering plants to exhibit properties similar to those allowing for far-red light absorption in the unique cyanobacteria, which would improve overall photosynthesis.
Actionable Goals
To address this bottleneck, we aim to engineer plants with expanded light absorbance capabilities by leveraging known known far-red light photoacclimation mechanisms in cyanobacteria. This involves:
- Introducing and optimizing the biosynthetic pathway for a far-red light-absorbing chlorophyll (chlorophyll f) into a plant.
- Testing whether and where chlorophyll f binds nonspecifically to the photosystems and if it leads to far-red light absorption.
- Engineering the plant photosystems to bind chlorophyll f at specific locations that allows for photochemistry.
- Evaluating the impact of these modifications on photosynthetic efficiency and biomass yield in controlled conditions.
By achieving these goals, we can significantly enhance the capacity of plants to capture and convert light energy, providing a viable pathway for improving biological CO2 sequestration.
Budget
·Personnel: Funds one research scientist for genetic engineering, protein analysis, and photosynthetic assays.
·Molecular biology reagents: Provides necessary materials like plasmids, transformation kits, and sequencing tools for optimizing chlorophyll f biosynthesis in Arabidopsis.
·Culturing and growth monitoring equipment: Supports the controlled growth of plants under variable light conditions, ensuring accurate measurement of photosynthetic efficiency and biomass yield.
·Spectroscopic and photosynthetic efficiency analysis: Covers the cost of equipment for analyzing photosynthetic performance (fluorometry, gas exchange) and structural validation (cryogenic electron microscopy) to assess chlorophyll f integration and impact on carbon sequestration.
·Indirect costs at 10% allowable rate
Meet the Team
Team Bio
Our team’s expertise spans photosynthesis, genetic engineering, structural biology, and spectroscopy. I, along with Gaozhong, Nikki, Himanshu, and Chris B., all hold PhDs in biochemistry with a focus on photosynthesis. Gaozhong has 25+ years of experience and expertise in genetic manipulation, Nikki specializes in spectroscopy, Himanshu in genetics, Chris B. in microscopy, and I am a structural biologist. Our graduate student and undergraduates also bring valuable energy and contributions.
Christopher Gisriel
My path to biochemistry began after high school when I joined the U.S. Army and served a tour of duty in Afghanistan. After my time in the military, I attended community college, where I discovered my passion for chemistry and biology. This interest led me to transfer to Arizona State University (ASU), where I completed my B.S. in biochemistry. During my time at ASU, I had the opportunity to work in a research laboratory, and that experience solidified my decision to pursue a career in scientific research.
I went on to earn my Ph.D. in biochemistry, where my research focused on structural biology and photosynthetic protein complexes. A major part of my graduate work involved solving the first molecular structure of a Type I anoxygenic reaction center, which gave crucial insights into the evolution of photosynthesis. My academic achievements were recognized when I was named a 2017 CLAS Leader and Outstanding Graduate by ASU’s College of Liberal Arts and Sciences.
I continued to build my expertise through postdoctoral positions at ASU and Yale University. At ASU’s Biodesign Center for Applied Structural Discovery, I worked on X-ray Free Electron Laser crystallography and cryo-electron microscopy. At Yale, I studied far-red light photoacclimation and water oxidation in photosystem II.
In Fall 2024, I opened my independent lab at the University of Wisconsin-Madison’s Department of Biochemistry. My group's research focuses on understanding and engineering photosynthetic protein complexes to improve photosynthetic efficiency and contribute to global carbon sequestration efforts.
Additional Information
Bibliography
1. X.-G. Zhu, S. P. Long, D. R. Ort, Improving photosynthetic efficiency for greater yield. Annual Review of Plant Biology 61, 235–261 (2010).
2. N. P. R. Anten, Optimal photosynthetic characteristics of individual plants in vegetation stands and implications for species coexistence. Annals of Botany 95, 495–506 (2005).
3. M. Chen, R. E. Blankenship, Expanding the solar spectrum used by photosynthesis. Trends in Plant Science 16, 427–431 (2011).
4. R. E. Blankenship, D. M. Tiede, J. Barber, G. W. Brudvig, G. Fleming, M. Ghirardi, M. R. Gunner, W. Junge, D. M. Kramer, A. Melis, T. A. Moore, C. C. Moser, D. G. Nocera, A. J. Nozik, D. R. Ort, W. W. Parson, R. C. Prince, R. T. Sayre, Comparing photosynthetic and photovoltaic efficiencies and recognizing the potential for improvement. Science (New York, N.Y.) 332, 805–9 (2011).
5. R. E. Blankenship, Molecular Mechanisms of Photosynthesis (John Wiley & Sons, Ltd., Southern Gate, 2021). 6. E. Elias, T. J. Oliver, R. Croce, Oxygenic photosynthesis in far-red light: Strategies and mechanisms. Annual Review of Physical Chemistry, doi: https://doi.org/10.1146/annure... (2024).
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