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Baccolini, C.

Publications and source records attributed to Baccolini, C..

2 recordsLinked to original sources

C4 photosynthetic pathway fluxes in transgenic rice plants

Most land plants photosynthesize using the C3 pathway, in which ribulose bisphosphate carboxylase/oxygenase (Rubisco) fixes CO2 into 3-carbon acids. The C4 pathway, a biochemical CO2-concentrating mechanism that operates in the context of specialized leaf anatomy to concentrate CO2 around Rubisco, is more efficient. Introduction of the C4 pathway into the C3 crop rice could increase yield by 50%. Expression of five C4 enzymes in transgenic rice previously led to flux through the first step. However, there was no evidence for flux later in the cycle. Here we developed new transgenic rice lines and novel protocols to detect C4 cycle activity: CO2 fixation into C4 acids by carboxylation of a C3 compound, decarboxylation, refixation of CO2 by Rubisco, and regeneration of the C3 donor. We demonstrate that these four core C4 reactions are operating in rice, establishing the in vivo flux framework needed to progress towards a functional carbon-concentrating mechanism

plant biology↗

Exploring the diversity of the CO2-concentrating mechanism (CCM) in different C4 subtypes

C4 plants have traditionally been classified into NADP-malic enzyme (NADP-ME), NAD-malic enzyme (NAD-ME) and PEP carboxykinase (PEPCK) subtypes based on the predominant C4-acid decarboxylating enzyme. To investigate the relative contributions of malate and aspartate to C4-pathway fluxes in each subtype, we performed 13CO2 pulse and pulse-chase labelling experiments on four C4 grass species: Zea mays and Setaria viridis (NADP-ME), Panicum miliaceum (NAD-ME) and Megathyrsus maximus (PEPCK). Only a proportion (8-50%) of the total malate pool in the leaves is photosynthetically active whereas essentially all of the aspartate pool is photosynthetically active. Estimates of metabolic fluxes indicate that approximately two thirds of the C4 pathway flux is via malate in Z. mays and the remaining third via aspartate, while in S. viridis 50% of the flux is via malate and 50% via aspartate. In P. miliaceum and M. maximus, 91% and 85% of the flux is via aspartate and the remaining 5% and 15% via malate, respectively. The results reveal greater complexity of C4 pathway fluxes than is usually represented in textbook diagrams, and demonstrate the feasibility of using non-radioactive 13CO2 in pulse-chase labelling experiments to study C4 photosynthesis and to detect C4 pathway fluxes in C3 plants engineered to perform C4 photosynthesis. Highlight StatementPhotosynthetic fluxes in C4 species are more complex than most textbook models show, with malate and aspartate both carrying C4 cycle fluxes in all three subtypes (NADP-ME, NAD-ME and PEPCK).

plant biology↗