BBSRC-NSF/BIO: Engineering an algal pyrenoid into higher plants to enhance yields

Lead Research Organisation: University of Edinburgh
Department Name: Sch of Biological Sciences

Abstract

Abstracts are not currently available in GtR for all funded research. This is normally because the abstract was not required at the time of proposal submission, but may be because it included sensitive information such as personal details.

Technical Summary

This project aims to enhance the growth of the model C3 plant Arabidopsis by introducing a minimal CO2-concentrating mechanism (CCM) based on the pyrenoid of the green alga Chlamydomonas reinhardtii. CCMs enhance growth by delivering a high concentration of CO2 to the primary carboxylation enzyme Rubisco, which increases the catalytic rate of CO2 uptake by Rubisco and suppresses photorespiration. The algal CCM enhances CO2 uptake in nearly all eukaryotic algae and works by actively pumping CO2 into the pyrenoid matrix, a dense aggregate of Rubisco. Pyrenoids are traversed by modified photosynthetic thylakoid membranes, which are called pyrenoid tubules. These pyrenoid tubules are thought to deliver concentrated CO2 to Rubisco through the activity of a specialised carbonic anhydrase that leverages the low pH inside the thylakoid lumen to convert bicarbonate into CO2. The bicarbonate enters the tubules from the surrounding stroma via bicarbonate transporters in the thylakoid.

Together our labs have recently discovered the core components required for correct pyrenoid function and we aim to engineer these into Arabidopsis with the aim to reconstitute a functional synthetic pyrenoid. The project consists of three experimental aims and one computational modelling aim, with each aim supported by targeted experiments in Chlamydomonas (see details in Objectives). We aim to i) reconstitute Rubisco aggregation by expressing the algal protein EPYC1, which links Rubisco to form the pyrenoid matrix, ii) cluster the matrix around thylakoid membranes containing bicarbonate transporters by expressing two membrane proteins that bind Rubisco, and iii) express and localise a carbonic anhydrase to the thylakoid membranes that traverse the pyrenoid matrix. Our efforts to engineer a pyrenoid into Arabidopsis will push the boundaries of plant synthetic biology and will advance our fundamental understanding of the principles that underpin the functioning of the algal CCM.

Planned Impact

Who will benefit from this research? In the short to medium term, the fundamental aspects of the research will benefit academics and researchers in all fields of plant research based in the UK, US and internationally. Particularly, this work will be of interest to researchers focused on enhancing food security by improving photosynthesis, including members of the international RIPE and C4 Rice Project consortia. It will also be of considerable interest to metabolic engineers and metabolic modellers. Medium to long term benefiters will include members of the agro-industry including biotechnologists and plant breeders seeking to increase plant productivity and/or harvest index, along with Multinational and Government Agencies who can use results to strategize future funding in areas of high potential impact (e.g. GCRF). During the research, the PDRAs and undergraduates working on the project will benefit considerably from training. The general public will also benefit from planned outreach activities.

How will they benefit from the research? Academics and researchers will receive comprehensive new information about the CCM of algae, requirements for CO2 concentration in higher plant chloroplasts, and mechanisms of assembly of supra-molecular complexes. Researchers will have access at the point of publication to new Chlamydomonas and plant expression constructs and lines, novel Arabidopsis material with altered primary carbon assimilation and models describing the relationship between the spatial distributions of inorganic carbon substrates and enzymes and the process of CO2 assimilation in algae. Agro-industry will receive information to underpin rational approaches to increase plant productivity, and relevant new genes and modelling methodologies. The agricultural community will benefit in the longer term from sustainable crop improvements enabled by our research. The PDRAs will receive a wide range of training in molecular biology, plant physiology, synthetic biology, and professional skills, with opportunities to attend training courses and opportunities to interact closely with researchers on an international scale. They will also receive training in transferable skills such as presentation and dissemination of results, and grant-writing. Our research findings relate to issues of public interest including sustainable crop production, global food security and atmospheric and climate change. The research also has wide educational value, at all levels through schools and Universities.

How will we ensure they benefit from the research? We will publish results in high-impact journals in a timely fashion with open access. We will present research results at international meetings and institutions and use social media and lab websites to promote new findings ahead of and during publication. We will submit materials, data and models to relevant international depositories. We will exploit extensive existing contacts of the PIs with other academics with relevant research interests as soon as any exploitable results/materials are generated. We will make informal contacts with biotechnologists as soon as exploitable results are generated; recognise and protect IP to ensure wise and fruitful exploitation. Collectively, we have vibrant contacts with relevant industries. We will provide mentoring to ensure uptake of PDRA training schemes, including regular progress reviews and career development plans, participation in the dissemination of results, and understanding of the wider implications and applications of the research. Results will be used as part of our regular engagement with non-academic audiences, e.g. local interest groups, schools, local and national science showcases, media. We will involve undergraduate students by providing laboratory summer secondments and discussing our research in teaching material. We will seek opportunities to inform the work of charitable bodies and governmental agencies.

Publications

10 25 50
 
Description 2020 March.
Since the start of the award (Sept 2019), the work from this grant has already contributed to two key publications in the high impact journal PNAS (Itakura et al. 2019. A Rubisco-binding protein is required for normal pyrenoid number and starch sheath. https://doi.org/10.1073/pnas.1904587116) outlining the discovery of a new pyrenoid protein and in JXB (Atkinson et al., 2019. The pyrenoidal linker protein EPYC1 phase separates with hybrid Arabidopsis-Chlamydomonas Rubisco through interactions with the algal Rubisco small subunit. https://doi.org/10.1093/jxb/erz275), where we detailed the residues involved in aggregating Rubisco with the pyrenoid linker protein EPYC1.


2021 March.
Despite the disruptions during COVID lockdown, we have made good progress on several of our aims.
Aim 1: Reconstitute a pyrenoid matrix in higher plants. We have made significant progress on understanding the interactions between EPYC1 and Rubisco, and successfully assembled a proto-pyrenoid condensate in Arabidopsis. This work has contributed to two high impact publications in Nature Plants (He et al., 2020. The structural basis of Rubisco phase separation in the pyrenoid. https://doi.org/10.1038/s41477-020-00811-y) and Nature Communications (Atkinson et al. 2020. Condensation of Rubisco into a proto-pyrenoid in higher plant chloroplasts. https://doi.org/10.1038/s41467-020-20132-0). Furthermore, we have produced Rubisco SSU CRISPR lines that allow us to further reduce Rubisco levels and modify the small subunit of Rubisco in Arabidopsis. This work has also been published in the Journal of Experimental Botany (Khumsupan et al. 2020. Generating and characterising single- and multi-gene mutants of the Rubisco small subunit family in Arabidopsis. doi:10.1093/jxb/eraa316).

Aim 2: Place the matrix around thylakoids containing HCO3- transporters. We are currently working on Aim 2.2 (Express thylakoid-localised Rubisco-binding proteins in matrix-forming Arabidopsis) and Aim 2.3 (Add thylakoid HCO3- transporters). For Aim 2.2 we have successfully targetted RBMP1 (BST4) and RBMP2 to the chloroplast in Arabidopsis and are further characterising the impact of these modifications. Similarly, for Aim 2.3 we have successfully targetted BST1, BST2 and BST3 to the chloroplast in Arabidopsis and are further characterising the impact of these modifications. Recent work in collaboration with the Mackinder Lab (York) and Blatt Lab (Glasgow) has confirmed that BST1 is a HCO3- channel. We are currently examining the formation of multimeric complexes of BST1-3 in Chlamydomonas and Arabidopsis.

Aim 3: Put the pyrenoidal carbonic anhydrase into the thylakoid lumen. We have successfully targetted CAH3 to the chloroplast in Arabidopsis and are currently confirming if CAH3 is localised in the thylakoid lumen. We are also examining the potential CA activities of LCIB and LCIC in planta and interactions between LCIB and LCIC.


2021 March.
Despite continued disruptions caused due to COVID, we have made good progress on several of our aims.
Aim 1: Reconstitute a pyrenoid matrix in higher plants. We have now generated Rubisco SSU CRISPR lines in Arabidopsis expressing CrRbcS2 and EPYC1. As with previous work, these lines have produced proto-pyrenoid condensates. Preliminary work indicates that the condensates are larger, likely due to the higher ratio of Chlamydomonas RbcS vs native RbcS. We have now also produced Rubisco SSU CRISPR lines in tobacco to develop tobacco as a new crop-based system for introducing the Chlamydomonas CCM. This work has been published in the Frontiers in Genome Editing (Donovan al. 2020. CRISPR-Cas9-mediated mutagenesis of the Rubisco small subunit family in Nicotiana tabacum. https://doi.org/10.3389/fgeed.2020.605614). Line 4 from this study is currently being transformed with Chlamydomonas RbcS2 and EPYC1.

Aim 2: Place the matrix around thylakoids containing HCO3- transporters. We are currently working on Aim 2.2 (Express thylakoid-localised Rubisco-binding proteins in matrix-forming Arabidopsis) and Aim 2.3 (Add thylakoid HCO3- transporters). For Aim 2.2 we have successfully targeted RBMP1 (BST4) and RBMP2 to the chloroplast in Arabidopsis and are further characterising the impact of these modifications. Expression of RBMP2 has remained low following transformation, and the further reduced/absent in subsequent generations. Co-expression with proto-pyrenoid condensates shows no obvious co-localisation. Thus, we chose to focus more on RBMP1. RBMP1 localises to the thylakoid membrane and expression lines show normal growth phenotype in WT Arabidopsis, but reduced growth in mutant lines expressing CrRbcS2. Furthermore, RBMP1 is enriched in the proto-pyrenoid condensates. We are currently exploring the physiology of the generated RBMP1 expression lines. A newly identified protein SAGA3, discovered in the Jonikas lab as a potential regulator of thylakoid matrix biogenesis in Chlamydomonas, is also currently being expressed in Arabidopsis.
For Aim 2.3 we have progressing towards T3 generation plants for BST1, BST2 and BST3. Preliminary analysis of BST1 and BST2 indicates a slight growth phenotype. Native gel analyses of BST1, BST2 and BST3 in plants and Chlamydomonas indicate that these proteins form a decameric complex both in Chlamydomonas and in planta. We are currently attempting to purify sufficient BST1 protein from N. benth for cryo-EM based structural analysis.

Aim 3: Put the pyrenoidal carbonic anhydrase into the thylakoid lumen. Our initial attempts to target CAH3 to the thylakoid lumen in Arabidopsis were not successful, so we screened several additional native thylakoid transit peptides-CAH3 fusions in N. benth. We identified two strong candidates and transformed these into Arabidopsis. Immunoblots of the T1 generation indicate good expression levels - we will shortly confirm localisation. We have also produced several stable Arabidopsis lines (WT and quadruple native CA mutants) expressing LCIB and LCIC to determine if these proteins have CA activity when expressed in planta. This work is ongoing.

Aim 4: Generate a predictive model of the algal CCM. Recently the Jonikas lab and our new CAPP collaborator Prof. Ned Wingreen, Princeton) have produced a predictive model of the algal CCM. We are currently using this to guide our latest engineering efforts, including transformation of CAH3 into lines expressing BST1 and generation of a starch sheath around the proto-pyrenoid. The latter efforts have involved expression of SAGA1 and SAGA2, which both localise around the proto-pyrenoid condensate. TEM analysis has indicated starch aggregation around the condensate.


2022 March.
Aim 1: Reconstitute a pyrenoid matrix in higher plants. Tobacco line 4 was transformed with Chlamydomonas RbcS2 (CrSSU) and EPYC1, and similarly in Arabidopsis, Line 4 was complemented by CrSSU and condensates were observed with co-expression of EPYC1. We are currently progressing these lines to homozygosity for CrSSU and EPYC1.

Aim 2: Place the matrix around thylakoids containing HCO3- transporters. For Aim 2.2 (Express thylakoid-localised Rubisco-binding proteins in matrix-forming Arabidopsis) we have found that RBMP1 is not able to draw thylakoid membranes into the proto-pyrenoid condensate. Further work has indicated that RBMP1 is likely involved in regulating oxidative stress within the pyrenoid in Chlamydomonas and is not a critical tethering protein for pyrenoid assembly. This work is currently being prepared for publication. In the past year we have focused on SAGA3 (now renamed MITH1). We have observed that co-expression of proteins SAGA1 and MITH1 are sufficient to draw thylakoid membranes into the proto-pyrenoid matrix. This work is currently under review for publication.

For Aim 2.3 We have not found any significant differences in growth for plants expressing BST1, BST2 or BST3. This is consistent with the predictions of the recent model of the Chlamydomonas CCM be Fei et al. 2022 (Nature Plants) publish by Co-I Martin Jonikas (see Aim 4). We have been unsuccessful with attempts to purify BST1 protein from N. benth for cryo-EM based structural analysis. Currently we are working towards co-expression of BST1, which has been shown to be a bicarbonate channel by collaborative work with the Mackinder/Blatt labs, with CAH3 (see Aim 3) to examine if expressing these components together has any impact on growth. This is a key step to inform interpretation of later mutants, specifically, the assembly of all six key components that are predicted to be required for a functional CCM (CrSSU, EPYC1, BST1, CAH3, SAGA1, MITH1). THe generation of plants lines expressing all six of the latter components is ongoing.

Aim 3: Put the pyrenoidal carbonic anhydrase into the thylakoid lumen. We have identified a native Arabidopisis thylakoid transit peptide (At-TP) that when fused to mature CAH3 results in localisation to the thylakoid lumen. We have generated stable Arabidopisis lines expressing At-TP:CAH3 and have confirmed localisation to the lumen through fractionation and immunoblotting. Furthermore we have confirmed that At-TP:CAH3 retains CA activity in planta. We have generated several plant lines and constructs to further explore LCIB and LCIC and point mutations variants of these proteins to determine if these proteins have CA activity. However, as our model (Aim 4) indicates that these components are not necessary for assembling a functional CCM, we have decided to pause work on them and focus on the six key components above.

Aim 4: Generate a predictive model of the algal CCM. Following on from 2021, work on SAGA1 and SAGA2 is currently being prepared for publication. TEM and 3View serial block face imaging (in collaboration with David Seung, JIC) has been used to characterise how expression of SAGA1 and SAGA2 leads to starch aggregation around the protopyrenoid condensate in plants expressing CrSSU and EPYC1. We expect this work will lay the foundation for building a starch sheath around the proto-pyrenoid, which is a key requirement for increasing the efficiency of a functional pyrenoid-based CCM.
Exploitation Route The outcomes of this work will inform all future studies aimed at engineering the algal CO2 concentrating mechanism into higher plants to enhance photosynthetic efficiencies and biomass yields.

We have been invited to submit a full grant application to the Gates Foundation (AgDev) to progress this work in Arabidopsis and into crop species.
he Gates Foundation (AgOne) has patented work associated with assembly of the proto-pyrenoid.

New PhD student in my lab Ella Catheral (co-supervisor Elizabete Carmo-Silva) is working towards engineering the algal CCM into rice.
PhD student Yuwei Mao (previously PDRA Dr Aranzazú Díaz Ramos) is collaborating with Dr James Barrett (Mackinder lab) to investigate the molecular aspects of Rubisco-based pyrenoid formation in hornworts and other algae, such as Chlorella.
PhD student Yuwei Mao is collaborating with Dr Laura Gunn (Cornell) to investigate the molecular aspects of Rubisco-based pyrenoid formation in hornworts.
Sectors Agriculture, Food and Drink,Education,Manufacturing, including Industrial Biotechology

URL http://mccormick.bio.ed.ac.uk/
 
Description 2020: publication of our work a high impact factor journal (Nature Plants) resulted in press release (https://www.sciencedaily.com/releases/2015/11/151116112048.htm) and coverage on several science news websites. 2020: publication of our work a high impact factor journal (Nature Communications) resulted in press release (https://www.ed.ac.uk/biology/news-events/news-2020/algae-superpowers-could-provide-major-boost-to-foo) and coverage on several science news websites. 2021 Publication presentation online at JRNLclub (https://jrnlclub.org/research-films/condensation-of-rubisco-into-a-proto-pyrenoid-in-higher-plant-chloroplasts). 2021 Changing World Conversations: The future of food (COP26). (https://media.ed.ac.uk/media/4.4.1%20CSE%20Alistair/1_imnz33x8) 2022 Engaged with general public , students, researchers and industry during the Scotland BioEconomy Week 2022 (https://www.ibioic.com/events-database/ask-a-plant-biotechnologis)
First Year Of Impact 2020
Sector Agriculture, Food and Drink
Impact Types Cultural,Societal

 
Description Participation in SULSA theme committee - Development and Regulation
Geographic Reach National 
Policy Influence Type Participation in a guidance/advisory committee
 
Description Rewriting The Genetic Code: The Algal Plastome As A Testbed For Basic And Applied Studies
Amount £3,146,402 (GBP)
Funding ID BB/W003538/1 
Organisation Biotechnology and Biological Sciences Research Council (BBSRC) 
Sector Public
Country United Kingdom
Start 04/2022 
End 03/2027
 
Description The York Physics of Pyrenoids Project (YP3): Nanostructured Biological LLPS:Next-Level-Complexity Physics of CO2-fixing Organelles
Amount £2,488,444 (GBP)
Funding ID EP/W024063/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 04/2022 
End 03/2025
 
Title Image data of pyrenoids in Chlamydomonas and proto-pyrenoid condensates in higher plant chloroplasts 
Description A collection of image data from the manuscript 'Condensation of Rubisco into a proto-pyrenoid in higher plant chloroplasts' by Nicky Atkinson, Yuwei Mao, Kher Xing Chan and Alistair J. McCormick. The .zip file contains raw data for Figure 1 (confocal and TEM images in Arabidopsis and Chlamydomonas), Figure 3e (Immunogold TEM images of proto-pyrenoid condensates in Arabidopsis) and Supplementary Figure 2c (TEM Images of pyrenoids in wild-type Chlamydomonas cells). 
Type Of Material Database/Collection of data 
Year Produced 2020 
Provided To Others? Yes  
Impact Accompanying dataset to high impact publication in Nature Communications. Supporting data for Patent application. 
URL https://doi.org/10.7488/ds/2945
 
Title PYRENOID-LIKE STRUCTURES 
Description Aspects of the present disclosure relate to genetically altered plants having a modified Rubisco and further having a modified Essential Pyrenoid Component 1 (EPYC1) for formation of an aggregate of modified Rubisco and EPYC1 polypeptides. Other aspects of the present disclosure relate to methods of making such plants as well as cultivating these genetically altered plants. 
IP Reference WO2021023982 
Protection Patent / Patent application
Year Protection Granted 2021
Licensed No
Impact We are in current talks with the Bill and Melinda Gates foundation about further funding related to this patent.
 
Title RUBISCO-BINDING PROTEIN MOTIFS AND USES THEREOF 
Description Described herein are chimeric polypeptides that include one or more Rubisco-binding motifs (RBMs) and a heterologous polypeptide. Additional aspects of the present disclosure provide genetically altered plants having a chimeric polypeptide including one or more Rubisco-binding motifs (RBMs) and a heterologous polypeptide. Further aspects of the present disclosure relate to genetically altered plants having a stabilized polypeptide including two or more RBMs and one or both of an algal Rubisco-binding membrane protein (RBMP) and a Rubisco small subunit (SSU) protein. Other aspects of the present disclosure relate to methods of making such chimeric polypeptides and plants, as well as cultivating these genetically altered plants. 
IP Reference WO2021025962 
Protection Patent granted
Year Protection Granted 2021
Licensed No
Impact We are in current talks with the Bill and Melinda Gates foundation about further funding related to this patent.
 
Description Condensing Rubisco into a proto-pyrenoid in plant chloroplasts - 1st International BioDesign Research Conference 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact The conference features a selection of world specialists working on BioDesign Research areas including 6 Nobel laureates. It's goals were to showcase the latest achievements and research progress in the field of Biosystems Design and Synthetic Biology, to foster communication and interdisciplinary collaboration among scientists, and to promote interactions between academia and industry, and to facilitate graduate student and postdoc training.
Year(s) Of Engagement Activity 2020
URL https://www.biodesign-conference.com/
 
Description Edinburgh Plant Science - Early career researchers meeting 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Postgraduate students
Results and Impact The meeting provided PhD students, postdocs and young PIs in the Edinburgh Plant Science community to to get to know the partner institutes better and present their research. McCormick introduced the meeting and was on a group discussion panel discussing the processes in progressing from PhD, to PostDoc and to PI.
Year(s) Of Engagement Activity 2020
URL http://www.edinburghplantscience.com/news/invitation-our-early-career-researcher-ecr-meeting
 
Description How to build an algal pyrenoid into Arabidopsis - 3rd International Conference on Plant Synthetic Biology 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact The 3rd International Conference on Plant Synthetic Biology brought together scientists and engineers from universities, industry and government working in all aspects of plant synthetic biology, plant bioengineering and plant biotechnology.
Year(s) Of Engagement Activity 2019
URL https://www.aiche.org/sbe/conferences/international-conference-on-plant-synthetic-biology-and-bioeng...
 
Description Introducing an algal pyrenoid into higher plants to enhance CO2 assimilation - Gordon Research Conference 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact The Gordon Research Conference (GRC), CO2 Assimilation in Plants from Genome to Biome, is among the most critical forums for bringing together the top plant scientists in the world, along with rising early-career scientists, to share and discuss the critical advances on this grand challenge. At this meeting scientists presented and discussed cutting edge, often unpublished research, that is geared toward the new "green revolution" and that will develop ideas and collaborations to guide and support research on carbon aspects of photosynthesis for years to come.
Year(s) Of Engagement Activity 2019
URL https://www.grc.org/co2-assimilation-in-plants-from-genome-to-biome-conference/2019/
 
Description Invited Talk (Oxford University) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach Regional
Primary Audience Professional Practitioners
Results and Impact Gave a research presentation to the Oxford Plant Biology department. ~70 people attended. Exposed me to research at Oxford and potential future collaboration opportunities.
Year(s) Of Engagement Activity 2021
 
Description Invited Talk (University of York) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Professional Practitioners
Results and Impact Gave a research presentation to the University of York Biology department. ~70 people attended. Opportunity to disseminate research and to discuss future potential future collaboration opportunities at York.
Year(s) Of Engagement Activity 2022
URL https://www.york.ac.uk/biology/news-events/seminars/plant-biology/2022-23/dralistairmccormick-autumn...
 
Description Invited talk (CCM10 conference, Princeton, USA) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact This was an invited talk at the tenth International Conference on Inorganic Carbon Acquisition by Aquatic Photosynthetic Organisms, better known as CCM10. CCM10 had a diverse array of talks and posters. There were 110 attendees giving 45 talks and presenting 28 posters. Outcomes included fututre collaboration activities, funding opportunities, and involvement in co-editing a journal special issue for the conference proceedings in Photosynthesis Research.
Year(s) Of Engagement Activity 2022
URL http://ccm10.princeton.edu
 
Description Invited talk (Rubisco Symposium, University of Illinois at Urbana-Champaign, USA) 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact The symposium celebrated and highlighted the centrality of Bill Ogren's discovery of Rubisco oxygenase activity, which launched whole new fields of inquiry and whole new levels of understanding literally encompassing the enzyme to the globe. The speakers represented leaders in research on environmental dynamics from the microbial to the global that Ogren's discovery has fundamentally impacted.
Year(s) Of Engagement Activity 2022
URL https://www.calendars.illinois.edu/detail/7?eventId=33431179
 
Description Science communication article on algal CO2 concentrating mechanisms and potential engineering into higher plants (Charlotte Walker) 
Form Of Engagement Activity A magazine, newsletter or online publication
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Public/other audiences
Results and Impact Popular science article published in the Marine Biologist magazine on algal CO2 concentrating mechanisms and their potential for engineering into higher plants. Also created illustrative content to accompany article.
Year(s) Of Engagement Activity 2020
URL https://www.mba.ac.uk/marine-biologist
 
Description Scientists solve the mystery behind an enigmatic organelle, the pyrenoid - press release 
Form Of Engagement Activity A press release, press conference or response to a media enquiry/interview
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Postgraduate students
Results and Impact Press release for Nature Plants publication
Year(s) Of Engagement Activity 2020
URL https://molbio.princeton.edu/news/jonikas-lab-researchers-have-learned-how-enigmatic-organelle-pyren...
 
Description Transplanting the pyrenoid: towards introducing an algal CO2-concentrating mechanism into higher plants - Invited seminar Sheffield University 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Undergraduate students
Results and Impact Recorded invited seminar attended by student at staff at the University of Sheffield. Due to the broad interest of the seminar, a request was made to provide the seminar as a teaching tool for subsequent Sheffield MSc courses.
Year(s) Of Engagement Activity 2020
 
Description Workshop facilitator for Food Standards Agency and N8 Agrifood (Charlotte Walker) 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Other audiences
Results and Impact Workshop facilitator for a FSA and N8 Agrifood on GM and GE in food and feed. Participants were scientists, industry professionals and policy makers.
Year(s) Of Engagement Activity 2021