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Biology subjects

Cheung, C. Y. M.

Publications and source records attributed to Cheung, C. Y. M..

2 recordsLinked to original sources

A multi-phase flux balance model reveals flexibility of guard cell central carbon metabolism

Experimental research in guard cell metabolism has revealed the roles of the accumulation of various metabolites in guard cell function, but a comprehensive understanding of their metabolism over the diel cycle is still incomplete, given the limitations of current experimental methods. In this study, we constructed a four-phase flux balance model of guard cell metabolism to investigate the changes in guard cell metabolism over the diel cycle, including the day and night and stomata opening and closing. Our model demonstrated the metabolic flexibility in guard cells, showing that multiple metabolic processes can contribute to the synthesis and metabolism of malate and sucrose as osmolytes during stomatal opening and closing. We showed that guard cells can adapt to varying light availability and sucrose uptake from the apoplast during the day by operating in a mixotrophic mode with a switch between sucrose synthesis via the Calvin-Benson cycle and sucrose degradation via the oxidative pentose phosphate pathway. During stomatal opening, our model predicted an alternative flux mode of the Calvin-Benson cycle with all dephosphorylating steps diverted to diphosphate--fructose-6-phosphate 1-phosphotransferase to produce PPi, which is used to pump protons across the tonoplast for the accumulation of osmolytes. An analysis of the energetics of the use of different osmolytes in guard cells showed that malate and Cl- are similarly efficient as the counterion of K+ during stomatal opening. Significance statementThis work presents the first four-phase metabolic model for predicting guard cell metabolism over the diel cycle, which predicted an alternative flux model of the Calvin-Benson cycle that maximises the production of PPi during stomatal opening. While multiple metabolic processes were shown be important in synthesising and metabolising osmolytes in guard cells of different experimental systems, our model demonstrated that these processes can operate simultaneously and at different rates depending on conditions.

plant biology

Metabolic modelling of CAM cycling, CAM idling and the C3-CAM continuum

The evolution of Crassulacean acid metabolism (CAM) is thought to be along a C3-CAM continuum including multiple variations of CAM such as CAM cycling and CAM idling. Here, we applied large-scale constraint-based modelling to investigate the metabolism and energetics of plants operating in C3, CAM, CAM cycling and CAM idling. Our modelling results suggested that CAM cycling and CAM idling could be potential evolutionary intermediates in CAM evolution by establishing a starch/sugar-malate cycle. Our model analysis showed that by varying CO2 exchange during the light period, as a proxy of stomatal conductance, there exists a C3-CAM continuum with gradual metabolic changes, supporting the notion that evolution of CAM from C3 could occur solely through incremental changes in metabolic fluxes. Along the C3-CAM continuum, our model predicted changes in metabolic fluxes not only through the starch/sugar-malate cycle that is involved in CAM photosynthetic CO2 fixation but also other metabolic processes including the mitochondrial electron transport chain and the tricarboxylate acid cycle at night. These predictions could guide engineering efforts in introducing CAM into C3 crops for improved water use efficiency.

biochemistry