Abstract

Crassulacean acid metabolism (CAM) is one of the three photosynthetic pathways in higher plants and is characterized by high water use efficiency. This mainly relies on major nocturnal CO2 fixation sustained by degradation of storage carbohydrate such as starch to provide phosphoenolpyruvate (PEP) and energy. In contrast to C3 plants where starch is mainly degraded by the hydrolytic route, different observations suggested the phosphorolytic route to be a major pathway for starch degradation in CAM plants. To elucidate the interplay and relevant contributions of the phosphorolytic and hydrolytic pathways for starch degradation in CAM, we assessed diel patterns for metabolites and enzymes implicated in both the hydrolytic route (β-amylase, DPE1, DPE2, maltase) and the phosphorolytic route (starch phosphorylase) of starch degradation in the CAM orchid Phalaenopsis “Edessa.” By comparing the catalytic enzyme activities and starch degradation rates, we showed that the phosphorolytic pathway is the major route to accommodate nocturnal starch degradation and that measured activities of starch phosphorylase perfectly matched calculated starch degradation rates in order to avoid premature exhaustion of starch reserves before dawn. The hydrolytic pathway seemed hampered in starch processing not by β-amylase but through insufficient catalytic capacity of both DPE2 and maltase. These considerations were further corroborated by measurements of enzyme activities in the CAM model plant Kalanchoë fedtschenkoi and strongly contradict with the situation in the C3 plant Arabidopsis. The data support the view that the phosphorolytic pathway might be the main route of starch degradation in CAM to provide substrate for PEP with additional hydrolytic starch breakdown to accommodate mainly sucrose synthesis.

Highlights

  • Crassulacean acid metabolism (CAM) is one of the three photosynthetic pathways present in higher plants and is characterized by an optimized water use efficiency (WUE) by taking up CO2 predominantly at night when evapotranspiration rates are low

  • To account for the observed gradual decrease in starch degradation rate towards the end of the night in the leaves of Phalaenopsis “Edessa” we considered two starch degradation rates in our study i.e. (1) 67 ± 13 nmol g-1FW min-1 from ZT12 to ZT20 and (2) 38 ± 6 nmol g-1FW min-1 from ZT20 to ZT24 (Figure 1)

  • In Phalaenopsis “Edessa” nocturnal starch breakdown during the 4 final hours was reduced with ca. 33% and accompanied by a threefold reduction in nocturnal CO2 fixation and malic acid accumulation (Figure 1)

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Summary

Introduction

Crassulacean acid metabolism (CAM) is one of the three photosynthetic pathways present in higher plants and is characterized by an optimized water use efficiency (WUE) by taking up CO2 predominantly at night when evapotranspiration rates are low. It is convenient to recognize four distinct phases of gas exchange in CAM plants, which are used to describe the photosynthetic performance. At the start of the day, in Phase II, stomata will gradually close and external CO2 is mainly fixed by ribulose-1,5bisphosphate carboxylase-oxygenase (rubisco). Gas exchange is curtailed by stomatal closure during the middle of the day (Phase III), thereby reducing transpirational water losses and improving WUE. During this phase, malic acid exits the vacuole and decarboxylation releases CO2 which is re-fixed by rubisco. In Phase IV stomata open again towards the end of the day and external CO2 is mainly sequestered via rubisco (Osmond, 1978)

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