journal article·2022-06-19Open access

Mechanisms Regulating Energy Homeostasis in Plant Cells and Their Potential to Inspire Electrical Microgrids Models

Nobuhiro Suzuki, Shunsuke Shigaki, Mai Yunose, Nicholas Raditya Putrawisesa, Sho Hogaki, Maria Carmela Di Piazza

Biomimetics· Volume 7· Issue 2

Abstract

In this paper, the main features of systems that are required to flexibly modulate energy states of plant cells in response to environmental fluctuations are surveyed and summarized. Plant cells possess multiple sources (chloroplasts and mitochondria) to produce energy that is consumed to drive many processes, as well as mechanisms that adequately provide energy to the processes with high priority depending on the conditions. Such energy-providing systems are tightly linked to sensors that monitor the status of the environment and inside the cell. In addition, plants possess the ability to efficiently store and transport energy both at the cell level and at a higher level. Furthermore, these systems can finely tune the various mechanisms of energy homeostasis in plant cells in response to the changes in environment, also assuring the plant survival under adverse environmental conditions. Electrical power systems are prone to the effects of environmental changes as well; furthermore, they are required to be increasingly resilient to the threats of extreme natural events caused, for example, by climate changes, outages, and/or external deliberate attacks. Starting from this consideration, similarities between energy-related processes in plant cells and electrical power grids are identified, and the potential of mechanisms regulating energy homeostasis in plant cells to inspire the definition of new models of flexible and resilient electrical power grids, particularly microgrids, is delineated. The main contribution of this review is surveying energy regulatory mechanisms in detail as a reference and helping readers to find useful information for their work in this research field.
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Research context

OpenAlex topics: Photosynthetic Processes and Mechanisms · Plant and Biological Electrophysiology Studies · Plant Molecular Biology Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, 7-1 Kioi-Cho, Chiyoda, Tokyo 102-8554, Japan

Department of System Innovation, Osaka University, 1-2 Machikaneyama-Cho, Toyonaka, Osaka 560-0043, Japan

Istituto di Ingegneria del Mare (INM), Consiglio Nazionale delle Ricerche (CNR), Via Ugo La Malfa 153, 90146 Palermo, Italy

References (100+)

Show source-provided references
1. Song, Y., Alyafei, M.S., Masmoudi, K., Jaleel, A., and Ren, M. (2021). Contributions of TOR Signaling on Photosynthesis. Int. J. Mol. Sci., 22.10.3390/ijms22168959 ↗
2. A new take on organelle-mediated stress sensing in plants10.1111/nph.17333 ↗
3. Mitochondrial redox systems as central hubs in plant metabolism and signaling10.1093/plphys/kiab101 ↗
4. González, M.C., Francisco, J.C., Sahrawy, M., and Serrato, A.J. (2021). Current Knowledge on Mechanisms Preventing Photosynthesis Redox Imbalance in Plants. Antioxidants, 10.10.3390/antiox10111789 ↗
5. Shi, Y., Ke, X., Yang, X., Liu, Y., and Hou, X. (2002). Plants response to light stress. J. Genet. Genom., in press.
6. GUN1 involvement in the redox changes occurring during biogenic retrograde signaling
7. Alternative oxidase (AOX) 1a and 1d limit proline-induced oxidative stress and aid salinity recovery in Arabidopsis10.1093/plphys/kiab578 ↗
8. Responses of genes of DNA repair, alternative oxidase, and pro-/antioxidant state in Arabidopsis thaliana with altered expression of AOX1a to gamma irradiation10.1080/09553002.2022.1998712 ↗
9. Respiration During Photosynthesis10.1146/annurev.pp.46.060195.000401 ↗
10. Beneficial interactions of mitochondrial metabolism with photosynthetic carbon assimilation10.1016/j.tplants.2003.09.015 ↗
11. Sink regulation of photosynthesis10.1093/jexbot/52.360.1383 ↗
12. Arabidopsis and primary photosynthetic metabolism-more than the icing on the cake10.1111/j.1365-313X.2010.04142.x ↗
13. The importance of energy balance in improving photosynthetic productivity10.1104/pp.110.166652 ↗
14. UCP1 and AOX1a contribute to regulation of carbon and nitrogen metabolism and yield in Arabidopsis under low nitrogen stress10.1007/s00018-021-04036-w ↗
15. The Mitochondrial Respiratory Chain Maintains the Photosynthetic Electron Flow in Arabidopsis thaliana Leaves under High-Light Stress10.1093/pcp/pcz193 ↗
16. Differential modulation of photosynthesis, ROS and antioxidant enzyme activities in stress-sensitive and-tolerant rice cultivars during salinity and drought upon restriction of COX and AOX pathways of mitochondrial oxidative electron transport10.1016/j.jplph.2021.153583 ↗
17. Alternative photosynthesis pathways drive the algal CO(2)-concentrating mechanism10.1038/s41586-022-04662-9 ↗
18. The ER Is a Common Mediator for the Behavior and Interactions of Other Organelles10.3389/fpls.2022.846970 ↗
19. Transport, functions, and interaction of calcium and manganese in plant organellar compartments10.1093/plphys/kiab122 ↗
20. Networked Microgrids for Enhancing the Power System Resilience10.1109/JPROC.2017.2685558 ↗
21. Mar, A., Pereira, P., and Martins, J.F. (2019). A Survey on Power Grid Faults and Their Origins: A Contribution to Improving Power Grid Resilience. Energies, 12.10.3390/en12244667 ↗
22. Bio-inspired design for robust power grid networks10.1016/j.apenergy.2019.113349 ↗
23. Biologically inspired modelling of smart grid for dynamic power-flow control under power failure10.1504/IJAACS.2018.095307 ↗
24. Kooijman, B. (2009). Dynamic Energy Budget Theory for Metabolic Organisation, Cambridge University Press. [3rd ed.].10.1017/CBO9780511805400 ↗
25. Einarsson, B. (2011). An Interacting Particle Model and Dynamic Energy Budget Theory: Analysis and Applications. [Ph.D. Thesis, University of Iceland].
26. Nguyen, T.-H., Nguyen, L.V., Jung, J.J., Agbehadji, I.E., Frimpong, S.O., and Millham, R.C. (2020). Bio-Inspired Approaches for Smart Energy Management: State of the Art and Challenges. Sustainability, 12.10.3390/su12208495 ↗
27. Predicting Population Dynamics from the Properties of Individuals: A Cross-Level Test of Dynamic Energy Budget Theory10.1086/669904 ↗
28. A Biological approach for energy management in smart grid and hybrid energy storage systems
29. Venayagamoorthy, G.K. (2009, January 26–30). Potentials and promises of computational intelligence for smart grids. Proceedings of the 2009 IEEE Power & Energy Society General Meeting, Calgary, AB, Canada.10.1109/PES.2009.5275179 ↗
30. Reviewing homeostasis of sustainable energy systems: How reactive and predictive homeostasis can enable electric utilities to operate distributed generation as part of their power supply services10.1016/j.rser.2017.06.094 ↗
31. A cascade hybrid PSO feed-forward neural network model of a biomass gasification plant for covering the energy demand in an AC microgrid10.1016/j.enconman.2021.113896 ↗
32. Ullah, K., Jiang, Q., Geng, G., Rahim, S., and Khan, R.A. (2022). Optimal Power Sharing in Microgrids Using the Artificial Bee Colony Algorithm. Energies, 15.10.3390/en15031067 ↗
33. Sertic, G. (2021, September 20). Nature’s Blueprint: Solar Cells Inspired by Plant Cells. Available online: https://www.yalescientific.org/2015/11/natures-blueprint-solar-cells-inspired-by-plant-cells/.
34. Pollen tube growth: Where does the energy come from?10.4161/15592324.2014.977200 ↗
35. Kiyono, H., Katano, K., and Suzuki, N. (2021). Links between Regulatory Systems of ROS and Carbohydrates in Reproductive Development. Plants, 10.10.3390/plants10081652 ↗
36. A Genetic Analysis of Chloroplast Division and Expansion in Arabidopsis thaliana10.1104/pp.104.1.201 ↗
37. arc6, a Fertile Arabidopsis Mutant with Only Two Mesophyll Cell Chloroplasts10.1104/pp.106.3.1169 ↗
38. How do plants make mitochondria?10.1007/s00425-012-1762-3 ↗
39. Chloroplast Retrograde Regulation of Heat Stress Responses in Plants10.3389/fpls.2016.00398 ↗
40. Connecting Chlorophyll Metabolism with Accumulation of the Photosynthetic Apparatus10.1016/j.tplants.2020.12.005 ↗
41. A central integrator of transcription networks in plant stress and energy signalling10.1038/nature06069 ↗
42. Multifaceted Roles of Plant Autophagy in Lipid and Energy Metabolism10.1016/j.tplants.2020.05.004 ↗
43. Degradation of Lipid Droplets in Plants and Algae-Right Time, Many Paths, One Goal10.3389/fpls.2020.579019 ↗
44. Snf1-RELATED KINASE1-Controlled C/S(1)-bZIP Signaling Activates Alternative Mitochondrial Metabolic Pathways to Ensure Plant Survival in Extended Darkness10.1105/tpc.17.00414 ↗
45. Mitophagy in plants10.1016/j.bbagen.2021.129916 ↗
46. Protein Kinase Signaling Pathways in Plant-Colletotrichum Interaction10.3389/fpls.2021.829645 ↗
47. The magic ‘hammer’ of TOR: The multiple faces of a single pathway in the metabolic regulation of plant growth and development10.1093/jxb/ery459 ↗
48. Sakr, S., Wang, M., Dédaldéchamp, F., Perez-Garcia, M.D., Ogé, L., Hamama, L., and Atanassova, R. (2018). The Sugar-Signaling Hub: Overview of Regulators and Interaction with the Hormonal and Metabolic Network. Int. J. Mol. Sci., 19.10.3390/ijms19092506 ↗
49. Ribosome and transcript copy numbers, polysome occupancy and enzyme dynamics in Arabidopsis
50. Diurnal changes of polysome loading track sucrose content in the rosette of wild-type arabidopsis and the starchless pgm mutant10.1104/pp.112.212258 ↗
51. Differential TOR activation and cell proliferation in Arabidopsis root and shoot apexes10.1073/pnas.1618782114 ↗
52. The Arabidopsis Circadian Clock and Metabolic Energy: A Question of Time10.3389/fpls.2021.804468 ↗
53. Dynamic epigenetic modifications in plant sugar signal transduction10.1016/j.tplants.2021.10.009 ↗
54. SnRK1 activation, signaling, and networking for energy homeostasis10.1016/j.pbi.2019.03.006 ↗
55. The SnRK1 Kinase as Central Mediator of Energy Signaling between Different Organelles10.1104/pp.17.01404 ↗
56. An abscisic acid-responsive protein interaction network for sucrose non-fermenting related kinase1 in abiotic stress response10.1038/s42003-020-0866-8 ↗
57. SnRK1 isoforms AKIN10 and AKIN11 are differentially regulated in Arabidopsis plants under phosphate starvation
58. The plant energy sensor: Evolutionary conservation and divergence of SnRK1 structure, regulation, and function10.1093/jxb/erw416 ↗
59. Plant glucose transporter structure and function10.1007/s00424-020-02449-3 ↗
60. Starch granule initiation in Arabidopsis thaliana chloroplasts10.1111/tpj.15359 ↗
61. Dynamic changes in the starch-sugar interconversion within plant source and sink tissues promote a better abiotic stress response10.1016/j.jplph.2019.01.007 ↗
62. Starch degradation
63. The diurnal metabolism of leaf starch10.1042/BJ20061393 ↗
64. Quantitative measurement of specific biomarkers for protein oxidation, nitration and glycation in Arabidopsis leaves10.1111/j.1365-313X.2009.03898.x ↗
65. Glyoxalase I--structure, function and a critical role in the enzymatic defence against glycation10.1042/bst0311343 ↗
66. Glycation by ascorbic acid causes loss of activity of ribulose-1,5-bisphosphate carboxylase/oxygenase and its increased susceptibility to proteases10.1093/pcp/pcf162 ↗
67. Plant monounsaturated fatty acids: Diversity, biosynthesis, functions and uses10.1016/j.plipres.2021.101138 ↗
68. Comparative evolutionary ecology of seed size10.1016/0169-5347(92)90006-W ↗
69. Miray, R., Kazaz, S., To, A., and Baud, S. (2021). Molecular Control of Oil Metabolism in the Endosperm of Seeds. Int. J. Mol. Sci., 22.10.3390/ijms22041621 ↗
70. Seed storage oil mobilization10.1146/annurev.arplant.59.032607.092938 ↗
71. Bryant, D.A. (1994). Chloroplast Origins and Evolution. The Molecular Biology of Cyanobacteria, Springer.10.1007/978-94-011-0227-8 ↗
72. Mitochondrial function as a therapeutic target in heart failure10.1038/nrcardio.2016.203 ↗
73. The plastid transcription machinery and its coordination with the expression of nuclear genome: Plastid-Encoded Polymerase, Nuclear-Encoded Polymerase and the Genomes Uncoupled 1-mediated retrograde communication10.1098/rstb.2019.0399 ↗
74. Plant mitochondria—Past, present and future10.1111/tpj.15495 ↗
75. Jamsheer, M., Jindal, S., Sharma, M.A., Sharma, M., Sivaj, S., Thomas, C., and Laxmi, A. (2020). A negative feedback loop of the TOR signaling moderates growth and enables rapid sensing of stress signals in plants. bioRxiv.10.1101/2020.09.06.284745 ↗
76. Glucose-TOR signalling reprograms the transcriptome and activates meristems10.1038/nature12030 ↗
77. A Conserved Upstream Open Reading Frame Mediates Sucrose-Induced Repression of Translation10.1105/tpc.019349 ↗
78. TOR and S6K1 promote translation reinitiation of uORF-containing mRNAs via phosphorylation of eIF3h10.1038/emboj.2013.61 ↗
79. Auxin-dependent cell division and cell elongation. 1-Naphthaleneacetic acid and 2,4-dichlorophenoxyacetic acid activate different pathways10.1104/pp.104.053843 ↗
80. How do sugars regulate plant growth and development? New insight into the role of trehalose-6-phosphate10.1093/mp/sss120 ↗
81. Auxin and Cellular Elongation10.1104/pp.15.01863 ↗
82. Abscisic Acid and abiotic stress signaling10.4161/psb.2.3.4156 ↗
83. Hussain, Q., Asim, M., Zhang, R., Khan, R., Farooq, S., and Wu, J. (2021). Transcription Factors Interact with ABA through Gene Expression and Signaling Pathways to Mitigate Drought and Salinity Stress. Biomolecules, 11.10.3390/biom11081159 ↗
84. Plant Hormone-Mediated Regulation of Heat Tolerance in Response to Global Climate Change10.3389/fpls.2020.627969 ↗
85. Zhao, Y., Zhang, W., Abou-Elwafa, S.F., Shabala, S., and Xu, L. (2021). Understanding a Mechanistic Basis of ABA Involvement in Plant Adaptation to Soil Flooding: The Current Standing. Plants, 10.10.3390/plants10101982 ↗
86. Soma, F., Takahashi, F., Yamaguchi-Shinozaki, K., and Shinozaki, K. (2021). Cellular Phosphorylation Signaling and Gene Expression in Drought Stress Responses: ABA-Dependent and ABA-Independent Regulatory Systems. Plants, 10.10.3390/plants10040756 ↗
87. Atif, R.M., Shahid, L., Waqas, M., Ali, B., Rashid, M.A.R., Azeem, F., Nawaz, M.A., Wani, S.H., and Chung, G. (2019). Insights on Calcium-Dependent Protein Kinases (CPKs) Signaling for Abiotic Stress Tolerance in Plants. Int. J. Mol. Sci., 20.10.3390/ijms20215298 ↗
88. Function of ABA in Stomatal Defense against Biotic and Drought Stresses10.3390/ijms160715251 ↗
89. Transcriptome responses to combinations of stresses in Arabidopsis10.1104/pp.112.210773 ↗
90. The Botany Array Resource: E-Northerns, Expression Angling, and promoter analyses10.1111/j.1365-313X.2005.02437.x ↗
91. Temporal-spatial interaction between reactive oxygen species and abscisic acid regulates rapid systemic acclimation in plants10.1105/tpc.113.114595 ↗
92. Translational Components Contribute to Acclimation Responses to High Light, Heat, and Cold in Arabidopsis10.1016/j.isci.2020.101331 ↗
93. Cold sensitivity of mitochondrial ATP synthase restricts oxidative phosphorylation in Arabidopsis thaliana10.1111/nph.15509 ↗
94. Sucrose transporters of higher plants
95. The Malus domestica sugar transporter gene family: Identifications based on genome and expression profiling related to the accumulation of fruit sugars10.3389/fpls.2014.00569 ↗
96. Ethylene Role in Plant Growth, Development and Senescence: Interaction with Other Phytohormones10.3389/fpls.2017.00475 ↗
97. Cell Wall Remodeling in Abscission Zone Cells during Ethylene-Promoted Fruit Abscission in Citrus
98. Integration of electric, calcium, reactive oxygen species and hydraulic signals during rapid systemic signaling in plants10.1111/tpj.15360 ↗
99. ROS as key players in plant stress signalling10.1093/jxb/ert375 ↗
100. The path of the smart grid10.1109/MPE.2009.934876 ↗