scholarly journals A dual-targeted purple acid phosphatase in Arabidopsis thaliana moderates carbon metabolism and its overexpression leads to faster plant growth and higher seed yield

2012 ◽  
Vol 194 (1) ◽  
pp. 206-219 ◽  
Author(s):  
Feng Sun ◽  
Pui Kit Suen ◽  
Youjun Zhang ◽  
Chao Liang ◽  
Chris Carrie ◽  
...  
Antioxidants ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 935
Author(s):  
Zhou Xu ◽  
Renshan Zhang ◽  
Meijing Yang ◽  
Yee-Song Law ◽  
Feng Sun ◽  
...  

Energy metabolism in plant cells requires a balance between the activities of chloroplasts and mitochondria, as they are the producers and consumers of carbohydrates and reducing equivalents, respectively. Recently, we showed that the overexpression of Arabidopsis thaliana purple acid phosphatase 2 (AtPAP2), a phosphatase dually anchored on the outer membranes of chloroplasts and mitochondria, can boost the plant growth and seed yield of Arabidopsis thaliana by coordinating the activities of both organelles. However, when AtPAP2 is solely overexpressed in chloroplasts, the growth-promoting effects are less optimal, indicating that active mitochondria are required for dissipating excess reducing equivalents from chloroplasts to maintain the optimal growth of plants. It is even more detrimental to plant productivity when AtPAP2 is solely overexpressed in mitochondria. Although these lines contain high level of adenosine triphosphate (ATP), they exhibit low leaf sucrose, low seed yield, and early senescence. These transgenic lines can be useful tools for studying how hyperactive chloroplasts or mitochondria affect the physiology of their counterparts and how they modify cellular metabolism and plant physiology.


2012 ◽  
Vol 63 (18) ◽  
pp. 6531-6542 ◽  
Author(s):  
Whitney D. Robinson ◽  
Joonho Park ◽  
Hue T. Tran ◽  
Hernan A. Del Vecchio ◽  
Sheng Ying ◽  
...  

2019 ◽  
Author(s):  
Wheaton L. Schroeder ◽  
Rajib Saha

AbstractStoichiometric Models of metabolism have proven valuable tools for increased understanding of metabolism and accuracy of synthetic biology interventions to achieve desirable phenotypes. Such models have been used in conjunction with optimization-based and have provided “snapshot” views of organism metabolism at specific stages of growth, generally at exponential growth. This approach has limitations in that metabolic history of the modeled system cannot be studied. The inability to study the complete metabolic history has limited stoichiometric metabolic modeling only to the static investigations of an inherently dynamic process. In this work, we have sought to address this limitation by introducing an optimization-based computational framework and applying to a stoichiometric model of the model plant Arabidopsis thaliana of four linked sub-models of leaf, root, seed, and stem tissues which models the core carbon metabolism through the lifecycle of arabidopsis (named as p-ath780). Uniquely, this framework and model considers diurnal metabolism, changes in tissue mass, carbohydrate storage, and loss of plant mass to senescence and seed dispersal. p-ath780 provide “snapshots” of core-carbon metabolism at one hour intervals of growth, in order to show the evolution of metabolism and whole-plant growth across the lifecycle of a single representative plant. Further, it can simulate important growth stages including seed germination, leaf development, flower production, and silique ripening. The computational framework has shown broad agreement with published experimental data in tissue mass yield, maintenance cost, senescence cost, and whole-plant growth checkpoints. Having focused on core-carbon metabolism, it serves as a scaffold for lifecycle models of other plant systems, to further increase the sophistication of in silico metabolic modeling, and to increase the range of hypotheses which can be investigated in silico. As an example, we have investigated the effect of alternate growth objectives on this plant over the lifecycle.Author SummaryIn an attempt to study the evolution of metabolism across the lifecycle of plants, in this work we have created an optimization-based framework for the in silico modeling of plant metabolism across the lifecycle of a model plant. We then applied this framework to four core-carbon tissue-level (namely, leaf, root, seed, and stem) stoichiometric models of the model plant species Arabidopsis thaliana, and further informed this framework with a wide array of published in vivo data to increase model and framework accuracy. Unique to the p-ath780 model, comparted to other models of plant metabolism, is the simultaneous considerations of diurnal metabolism, carbohydrate storage, changes in tissue mass (including losses), and changes in metabolism with respect to plant growth stage. This provides a more complete picture of plant metabolism and allows for a wider array of future studies of plant metabolism, particularly since we have only modeled the core carbon metabolism of A. thaliana, allowing this work to serve as a framework for studies of other plant systems.


IUCrJ ◽  
2014 ◽  
Vol 1 (2) ◽  
pp. 101-109 ◽  
Author(s):  
Svetlana Vladimirovna Antonyuk ◽  
Mariusz Olczak ◽  
Teresa Olczak ◽  
Justyna Ciuraszkiewicz ◽  
Richard William Strange

Phosphatases function in the production, transport and recycling of inorganic phosphorus, which is crucial for cellular metabolism and bioenergetics, as well as in bacterial killing, since they are able to generate reactive oxygen speciesviaFenton chemistry. Diphosphonucleotide phosphatase/phosphodiesterase (PPD1), a glycoprotein plant purple acid phosphatase (PAP) from yellow lupin seeds, contains a bimetallic Fe–Mn catalytic site which is most active at acidic pH. Unlike other plant PAPs, PPD1 cleaves the pyrophosphate bond in diphosphonucleotides and the phosphodiester bond in various phosphodiesters. The homohexameric organization of PPD1, as revealed by a 1.65 Å resolution crystal structure and confirmed by solution X-ray scattering, is unique among plant PAPs, for which only homodimers have previously been reported. A phosphate anion is bound in a bidentate fashion at the active site, bridging the Fe and Mn atoms in a binding mode similar to that previously reported for sweet potato PAP, which suggests that common features occur in their catalytic mechanisms. The N-terminal domain of PPD1 has an unexpected and unique fibronectin type III-like fold that is absent in other plant PAPs. Here, thein vitroDNA-cleavage activity of PPD1 is demonstrated and it is proposed that the fibronectin III-like domain, which `overhangs' the active site, is involved in DNA selectivity, binding and activation. The degradation of DNA by PPD1 implies a role for PPD1 in plant growth and repair and in pathogen defence.


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