e-book Carbohydrate Reserves in Plants - Synthesis and Regulation (Developments in Crop Science)

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Notably, while transcripts of these enzymes undergo large diurnal changes, the levels of the encoded proteins do not change significantly over the course of a single day Smith et al.

Plant Breeding for Disease Resistance

Moreover, it has been estimated that it would take days for a change in transcript levels to significantly affect the levels of most of these enzymes Gibon et al. These facts, along with the immediate adjustment of the degradation rate to unexpected perturbations, strongly suggest that the underlying mechanism operates at a post-translational level, possibly through protein modifications, rather than at the level of transcription.

Based on these experimental results, mathematical models have recently been developed, analysing the mechanisms that could underlie the computation of the appropriate starch degradation rate and how this operation is controlled by the circadian clock. Many unanswered questions remain, but the models have already produced a number of predictions, some of which have been experimentally verified, and paved the way for the design of future targeted experiments that can potentially identify key regulators of starch degradation.

In this review we briefly describe the models, illustrate what they have contributed, and clarify which aspects need further investigation. The most striking aspect of the starch degradation process is its ability to immediately compensate for unexpected changes in the length of the night or the amount of starch available to degrade.

As recently proposed Scialdone et al. In this way, the appropriate starch degradation rate can be computed. As discussed above, the mechanism is expected to operate at a post-translational level. In the simplest scenario, information about starch and time is encoded in two diffusible molecules in the chloroplasts, respectively called S and T. The experimental evidence suggests the basic features that these two molecules must have.

Hexose Kinases and Their Role in Sugar-Sensing and Plant Development

The concentration of molecule S should be proportional to the amount of starch present in the chloroplast. This allows a simple and independent measure of the starch accumulated in the granules, much of which is within the granule matrix and is therefore presumably inaccessible to the enzymes involved in starch degradation. S and T must interact in such a way as to produce a starch degradation rate proportional to the ratio of their concentrations and equal to the ratio between the chloroplastic starch content and the expected time to dawn, i.

Digital implementation of such an arithmetic operation is prohibitively complex. However, chemical kinetics offers much simpler interaction schemes that can implement arithmetic division in an analog fashion. Simple calculations show that under certain conditions that can be explicitly determined, this mechanism leads to a degradation rate proportional to the ratio between the concentrations of S and T and equal to the amount of chloroplastic starch divided by the expected time to dawn. Moreover, this model can fit very well all the available data Scialdone et al.

Other conceptually similar implementations are also possible, and while the details of the mechanism could differ e. For instance, the model shows that the mechanism is so robust that it can accommodate perturbations even more extreme that those previously tested, such as an unexpected period of light occurring in the middle of the night. This prediction was indeed verified, as it was shown that the starch degradation rate was correctly recomputed after a night-time light period of 5 h Scialdone et al. Furthermore, another prediction concerns the properties of starch-excess mutants i.

Such mutants should still degrade starch linearly with time but consume a fixed percentage of starch during the night, regardless of the starch content at the beginning of the night. This prediction was also experimentally confirmed, with starch degradation mutants like lsf1 and sex4 Comparot-Moss et al. The identity of the hypothesized S and T molecules is still to be discovered. However, there are experimental clues on where they could be acting. The addition of phosphate groups is thought to allow access for starch degrading enzymes, with subsequent removal of the phosphate groups needed for full starch polymer degradation.

This hypothesis is supported by evidence that the level of phosphate per unit mass of starch is not constant during the day, but rather reaches a maximum around dusk, in dynamics which resembles the behavior predicted for the S molecule concentration Scialdone et al. Whether the starch phosphate content mirrors the total amount of starch, or the time to expected dawn, is a question that can be clarified using model predictions. According to the model, in plants that are subjected to an unexpected increase in light intensity, the starch phosphate levels would reach a higher value with respect to the control if the starch phosphate levels were proportional to starch reserves.

However, the phosphate levels would be unaltered relative to the control if starch phosphate levels were alternatively proportional to the time to expected dawn. Another interesting result concerns the phenotype of the mutant lacking PWD.

Plant Storage Products (Carbohydrates, Oils and Proteins)

Such a mutant maintains linear starch degradation with time during the night, but is not able to adjust the degradation rate to an unexpectedly early night. This result suggests that PWD could be part of the molecular machinery that sets the degradation rate Scialdone et al. Additional experiments will be required to test the behavior of the pwd mutant under different conditions e.

The models could then help to interpret these results in order to uncover the exact role of this enzyme. Conversely, GWD has been shown to have little influence over the control of flux in starch degradation, and, in particular, its redox regulation is not necessary for the computation of the appropriate starch degradation rate Skeffington et al.


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Alternative hypotheses have recently been investigated into how the circadian clock exerts control over starch turnover. The analysis combined models of the Arabidopsis circadian clock with the arithmetic division model described above Seaton et al.

The first question posed was how information about the time to expected dawn is encoded in the dynamics of the T molecule, and, in turn, the role of the T molecule in the starch degradation process. Another possibility is that the T concentration increases with time during the day, approximately tracking the time since last dawn. In this case, in order to implement arithmetic division between starch levels and the time to dawn, T must promote starch degradation Scialdone et al. Possible regulatory schemes capable of producing these T dynamics by using circadian clock components are shown in Seaton et al.

Models with a light-gated regulation of starch degradation, where the rate is set at each light-dark transition were also analyzed, as opposed to models with a continuous computation of the starch degradation rate throughout the night. These different scenarios were combined together in model variants, also considering the possibility that starch synthesis might be under the control of the circadian clock. All the model variants explored in Seaton et al. The main differences between them consisted of the phenotypes predicted in the presence of circadian clock mutations.

The general conclusion was that models with a light-gated control of starch degradation are more robust to circadian clock mutations than models based on a continuous calculation of the starch degradation rate. On the other hand, if the degradation rate is fixed at dusk, it would not be possible to adjust for fluctuations in reaction rates that could occur at night and cause too rapid or too slow a starch turnover. Robustness to both circadian clock mutations and noise in reaction rates could be combined in a mechanism with an intermediate level of clock control, where the degradation rate is still continuously computed but the T molecule is controlled by the clock only during the day and decays linearly with time at night Seaton et al.

One possible way to rule out a pure light-gated response, would be to test for the presence of non-linear starch profiles at night in the wild-type. Even though some experiments hint at non-linear dynamics, especially around the time of expected dawn Scialdone et al. Several lines of evidence suggest concerted control of both starch degradation and synthesis. In long days, a comparatively slower starch synthesis rate is associated with more rapid starch degradation, with the opposite pattern occurring in short days Gibon et al.

Moreover, plants that run out of starch after an extended night, synthesize more starch during the next day Gibon et al. A recent phenomenological model has investigated this issue, employing sinusoidal cycles governed by the circadian clock for the rates of sucrose export, starch degradation and starch synthesis.

This is the form generated by the arithmetic division model through the interaction between the S and T molecules. Sucrose starvation was also analyzed when one or two among the three rates were constant, where it was shown that regulation of the starch degradation rate was the most important to achieve minimization of sucrose starvation Feugier and Satake, Although these conclusions are potentially interesting, the initial assumptions of this model may be too simplistic, as there is little good evidence that the starch synthesis rate is directly under the control of the circadian clock.

Indeed, the partitioning of photoassimilate between starch and sucrose is likely to be controlled by multiple mechanisms that may be quite distinct from those ensuring a constant supply of sucrose from starch at night Mugford et al.

How plants manage food reserves at night: quantitative models and open questions

Moreover, it seems unlikely that, as speculated in Feugier and Satake , plants can adjust to different photoperiods through alteration of the phases of clock-dependent metabolic rates, given observations suggesting that there is little change in clock components' phases with photoperiod Edwards et al.

A model exploring the molecular mechanisms that could couple starch degradation to other processes in the plant's metabolism has recently been proposed Pokhilko et al. This model includes several modules describing metabolism, the circadian clock and interactions between the two. While starch degradation is described by the arithmetic division model, the existence of a molecule I is hypothesized, which controls the fraction of photosynthate allocated to starch synthesis. The levels of this molecule I are assumed to increase with increasing levels of carbon starvation.

In this picture, since regulation of the starch degradation rate imposes a depletion of carbon reserves at the time of expected dawn, an unexpectedly prolonged night would be accompanied by a period of starvation and a consequent increase in the levels of the I molecule. This would then induce a higher starch synthesis rate during the following light period, as experimentally observed see above and Gibon et al.

The model predicts the characteristics and behaviors of I and of the other presumptive molecular regulators under a number of conditions. Comparisons with experimental data then allowed identification of candidates for some of these molecules Pokhilko et al. SnRK1, a kinase that plays an important role in the sucrose synthesis pathway by modulating activity of sucrose-phosphate synthase and F26P phosphatase, was identified as a candidate for I.

This prediction could be validated experimentally by, e. However, how the levels of these proteins and not just transcripts change, and the role of their post-translational modifications, would need to be assessed in order to confirm these putative functions. Regulation of carbohydrate availability at night is a crucial aspect of plant metabolism.

How plants manage food reserves at night: quantitative models and open questions

This is particularly true for annual species like Arabidopsis , which complete their life cycle in a year and are under strong selective pressure to optimize carbon utilization for the maximization of seed production. In such a mechanism a central role is played by the circadian clock, and there are suggestions that the regulation of starch degradation is the clock's major contribution to the optimization of plant productivity Graf and Smith, Mathematical modeling is helping to unravel the molecular mechanisms that control starch degradation by generating hypotheses and testable predictions.

This approach has been particularly useful in providing a starting point for future experiments for a process whose underlying mechanism was previously completely mysterious. The arithmetic division computation that produces the appropriate starch degradation rate is thought to occur at a post-translational level.

Hence it will probably be necessary to analyse the dynamics of the relevant post-translational modifications in order to shed light on the identity of the molecules that implement the computation Skeffington et al. Models could then be refined to incorporate additional biochemical details to aid the interpretation and design of new experiments. However, some model predictions are already supported by experiments, such as the response to previously untested environmental perturbations.

Mutants that accumulate abnormally high e. In particular, the starch degradation pattern of some starch-excess mutants was used to confirm predictions from the models see above and Scialdone et al. Other predictions yet to be tested will help to elucidate important questions, such as whether the computation of the starch degradation rate is a one-off event occurring at dusk or whether it happens continuously during the night, and what is the role for cycles of starch phosphate content. Models have also helped to identify molecules that could have important regulatory functions e.

There have also been efforts to combine models for starch degradation and other aspects of plant metabolism with models at higher scales e. The eventual goal here is to construct multiscale models that could provide new insights in plant behavior and help direct plant bioengineering Chew et al.

Essentially all plants manufacture and store starch during daylight hours, breaking it down during the night, irrespective of the type of photosynthesis used: Furthermore, evidence suggests that a similarly tight control of starch degradation linear in time takes place both in plants having the same type of photosynthesis as Arabidopsis like Brachypodium distachyon , see Scialdone et al. While the biochemical details could differ, models based on the same general concepts could therefore be used to describe starch metabolism in a wide range of cases.

Similar mechanisms that allow optimization of the use of limited resources could also be operating in other biological processes Scialdone et al.