TY - JOUR
T1 - Installation of C4 photosynthetic pathway enzymes in rice using a single construct
AU - Ermakova, Maria
AU - Arrivault, Stéphanie
AU - Giuliani, Rita
AU - Danila, Florence
AU - Alonso-Cantabrana, Hugo
AU - Vlad, Daniela
AU - Ishihara, Hirofumi
AU - Feil, Regina
AU - Guenther, Manuela
AU - Borghi, Gian Luca
AU - Covshoff, Sarah
AU - Ludwig, Martha
AU - Cousins, Asaph B.
AU - Langdale, Jane A.
AU - Kelly, Steven
AU - Lunn, John E.
AU - Stitt, Mark
AU - von Caemmerer, Susanne
AU - Furbank, Robert T.
N1 - Funding Information:
This work was funded by a C4 Rice Project grant from Bill & Melinda Gates Foundation to the University of Oxford (2015–2019; OPP1129902), Max Planck Society (SA, HI, RF, MG, JEL, MS) and Australian Research Council (DP150101037 to ML, JEL, MS and CE140100015). Work in the SK laboratory was supported by the European Union’s Horizon 2020 research and innovation programme under grant agreement number 637765; SK is a Royal Society University Research Fellow. We thank Riya Kuruvilla, Xueqin Wang and Soumi Bala for technical support and Robert Sharwood and Spencer Whitney for the gifts of antibodies. We thank the Australian Plant Phenomics Facility supported under the National Collaborative Research Infrastructure Strategy of the Australian Government and CSIRO Black Mountain MicroImaging Centre.
Funding Information:
This work was funded by a C4 Rice Project grant from Bill & Melinda Gates Foundation to the University of Oxford (2015–2019; OPP1129902), Max Planck Society (SA, HI, RF, MG, JEL, MS) and Australian Research Council (DP150101037 to ML, JEL, MS and CE140100015). Work in the SK laboratory was supported by the European Union’s Horizon 2020 research and innovation programme under grant agreement number 637765; SK is a Royal Society University Research Fellow. We thank Riya Kuruvilla, Xueqin Wang and Soumi Bala for technical support and Robert Sharwood and Spencer Whitney for the gifts of antibodies. We thank the Australian Plant Phenomics Facility supported under the National Collaborative Research Infrastructure Strategy of the Australian Government and CSIRO Black Mountain MicroImaging Centre.
Publisher Copyright:
© 2020 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.
PY - 2021/3
Y1 - 2021/3
N2 - Introduction of a C4 photosynthetic mechanism into C3 crops offers an opportunity to improve photosynthetic efficiency, biomass and yield in addition to potentially improving nitrogen and water use efficiency. To create a two-cell metabolic prototype for an NADP-malic enzyme type C4 rice, we transformed Oryza sativa spp.japonica cultivar Kitaake with a single construct containing the coding regions of carbonic anhydrase, phosphoenolpyruvate (PEP) carboxylase, NADP-malate dehydrogenase, pyruvate orthophosphate dikinase and NADP-malic enzyme from Zea mays, driven by cell-preferential promoters. Gene expression, protein accumulation and enzyme activity were confirmed for all five transgenes, and intercellular localization of proteins was analysed. 13CO2 labelling demonstrated a 10-fold increase in flux though PEP carboxylase, exceeding the increase in measured in vitro enzyme activity, and estimated to be about 2% of the maize photosynthetic flux. Flux from malate via pyruvate to PEP remained low, commensurate with the low NADP-malic enzyme activity observed in the transgenic lines. Physiological perturbations were minor and RNA sequencing revealed no substantive effects of transgene expression on other endogenous rice transcripts associated with photosynthesis. These results provide promise that, with enhanced levels of the C4 proteins introduced thus far, a functional C4 pathway is achievable in rice.
AB - Introduction of a C4 photosynthetic mechanism into C3 crops offers an opportunity to improve photosynthetic efficiency, biomass and yield in addition to potentially improving nitrogen and water use efficiency. To create a two-cell metabolic prototype for an NADP-malic enzyme type C4 rice, we transformed Oryza sativa spp.japonica cultivar Kitaake with a single construct containing the coding regions of carbonic anhydrase, phosphoenolpyruvate (PEP) carboxylase, NADP-malate dehydrogenase, pyruvate orthophosphate dikinase and NADP-malic enzyme from Zea mays, driven by cell-preferential promoters. Gene expression, protein accumulation and enzyme activity were confirmed for all five transgenes, and intercellular localization of proteins was analysed. 13CO2 labelling demonstrated a 10-fold increase in flux though PEP carboxylase, exceeding the increase in measured in vitro enzyme activity, and estimated to be about 2% of the maize photosynthetic flux. Flux from malate via pyruvate to PEP remained low, commensurate with the low NADP-malic enzyme activity observed in the transgenic lines. Physiological perturbations were minor and RNA sequencing revealed no substantive effects of transgene expression on other endogenous rice transcripts associated with photosynthesis. These results provide promise that, with enhanced levels of the C4 proteins introduced thus far, a functional C4 pathway is achievable in rice.
KW - C photosynthesis
KW - metabolic engineering
KW - rice
UR - http://www.scopus.com/inward/record.url?scp=85093919262&partnerID=8YFLogxK
U2 - 10.1111/pbi.13487
DO - 10.1111/pbi.13487
M3 - Article
C2 - 33016576
AN - SCOPUS:85093919262
SN - 1467-7644
VL - 19
SP - 575
EP - 588
JO - Plant Biotechnology Journal
JF - Plant Biotechnology Journal
IS - 3
ER -