Engineering Strategies to Boost Crop Productivity by Cutting Respiratory Carbon Loss[OPEN]
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Mark Stitt | Andrew D. Hanson | A. Harvey Millar | Arren Bar-Even | Lee J. Sweetlove | Stephen D. Tyerman | A. Millar | M. Stitt | A. Bar‐Even | L. Sweetlove | A. Hanson | S. Tyerman | J. Amthor | Jeffrey S. Amthor
[1] A. Fernie,et al. Next-generation strategies for understanding and influencing source-sink relations in crop plants. , 2018, Current opinion in plant biology.
[2] J. H. M. Thornley,et al. Modelling the Components of Plant Respiration: Some Guiding Principles , 2000 .
[3] D. Ort,et al. How Do We Improve Crop Production in a Warming World? , 2010, Plant Physiology.
[4] P. Reich,et al. Thermal limits of leaf metabolism across biomes , 2017, Global change biology.
[5] M. Stitt,et al. Quantifying Protein Synthesis and Degradation in Arabidopsis by Dynamic 13CO2 Labeling and Analysis of Enrichment in Individual Amino Acids in Their Free Pools and in Protein1[OPEN] , 2015, Plant Physiology.
[6] M. Stitt,et al. Downregulation of pyrophosphate: d-fructose-6-phosphate 1-phosphotransferase activity in sugarcane culms enhances sucrose accumulation due to elevated hexose-phosphate levels , 2009, Planta.
[7] A. Lamouri,et al. Parkinsonism-associated Protein DJ-1/Park7 Is a Major Protein Deglycase That Repairs Methylglyoxal- and Glyoxal-glycated Cysteine, Arginine, and Lysine Residues , 2014, The Journal of Biological Chemistry.
[8] A. Ferraz,et al. Chemical composition and enzymatic digestibility of sugarcane clones selected for varied lignin content , 2011, Biotechnology for biofuels.
[9] C. Foyer,et al. Photosynthesis solutions to enhance productivity , 2017, Philosophical Transactions of the Royal Society B: Biological Sciences.
[10] Q. Shen,et al. Overexpression of a pH-sensitive nitrate transporter in rice increases crop yields , 2016, Proceedings of the National Academy of Sciences.
[11] M. Rossignol,et al. Nitrate Efflux at the Root Plasma Membrane: Identification of an Arabidopsis Excretion Transporter[W] , 2007, The Plant Cell Online.
[12] C. Masclaux-Daubresse,et al. Source and sink mechanisms of nitrogen transport and use. , 2018, The New phytologist.
[13] R. Kallenbach,et al. Comparison of acetyl bromide lignin with acid detergent lignin and Klason lignin and correlation with in vitro forage degradability , 2015 .
[14] M. Tester,et al. AtNPF2.5 Modulates Chloride (Cl−) Efflux from Roots of Arabidopsis thaliana , 2017, Front. Plant Sci..
[15] W. F. Hunt,et al. Respiration Modelling and Hypothesis Testing with a Dynamic Model of Sugar Beet Growth , 1979 .
[16] I. Haferkamp,et al. Nonmitochondrial ATP/ADP Transporters Accept Phosphate as Third Substrate , 2008, Journal of Biological Chemistry.
[17] W. Winiwarter,et al. How a century of ammonia synthesis changed the world , 2008 .
[18] J. Raven. TANSLEY REVIEW No. 2: REGULATION OF PH AND GENERATION OF OSMOLARITY IN VASCULAR PLANTS: A COST-BENEFIT ANALYSIS IN RELATION TO EFFICIENCY OF USE OF ENERGY, NITROGEN AND WATER. , 1985, The New phytologist.
[19] B. Eser,et al. From Suicide Enzyme to Catalyst: The Iron-Dependent Sulfide Transfer in Methanococcus jannaschii Thiamin Thiazole Biosynthesis. , 2016, Journal of the American Chemical Society.
[20] J. Förster,et al. Highly Active and Specific Tyrosine Ammonia-Lyases from Diverse Origins Enable Enhanced Production of Aromatic Compounds in Bacteria and Saccharomyces cerevisiae , 2015, Applied and Environmental Microbiology.
[21] Mauricio S. Antunes,et al. Engineering synthetic regulatory circuits in plants. , 2018, Plant science : an international journal of experimental plant biology.
[22] Mark Stitt,et al. Circadian, Carbon, and Light Control of Expansion Growth and Leaf Movement1[OPEN] , 2017, Plant Physiology.
[23] P. Finnegan,et al. A GmAOX2b antisense gene compromises vegetative growth and seed production in soybean , 2012, Planta.
[24] Y. Tsay,et al. Mutation of the Arabidopsis NRT1.5 Nitrate Transporter Causes Defective Root-to-Shoot Nitrate Transport[W][OA] , 2008, The Plant Cell Online.
[25] M. Stitt,et al. Carbon Supply and the Regulation of Cell Wall Synthesis. , 2018, Molecular plant.
[26] B. Friguet,et al. Protein damage, repair and proteolysis. , 2014, Molecular aspects of medicine.
[27] C. Maurel,et al. A receptor-like kinase mutant with absent endodermal diffusion barrier displays selective nutrient homeostasis defects , 2014, eLife.
[28] Steven A. Hill,et al. Fluxes of carbohydrate metabolism in ripening bananas , 1993, Planta.
[29] C. Pollock,et al. Invertase in leaves: Conundrum or control point? , 1999 .
[30] J. Feijó,et al. GABA signalling modulates plant growth by directly regulating the activity of plant-specific anion transporters , 2015, Nature communications.
[31] R. Sederoff,et al. Lignin and Biomass: A Negative Correlation for Wood Formation and Lignin Content in Trees1 , 2010, Plant Physiology.
[32] W. Plaxton,et al. THE ORGANIZATION AND REGULATION OF PLANT GLYCOLYSIS. , 1996, Annual review of plant physiology and plant molecular biology.
[33] M. Stitt,et al. Photosynthate partitioning to starch in Arabidopsis thaliana is insensitive to light intensity but sensitive to photoperiod due to a restriction on growth in the light in short photoperiods. , 2017, Plant, cell & environment.
[34] M. Hodges,et al. Respiratory carbon fluxes in leaves. , 2012, Current opinion in plant biology.
[35] Bruce A Kerwin,et al. Characterization of site-specific glycation during process development of a human therapeutic monoclonal antibody. , 2011, Journal of pharmaceutical sciences.
[36] C. Foyer,et al. A role for 'futile cycles' involving invertase and sucrose synthase in sucrose metabolism of tomato fruit. , 2001, Journal of experimental botany.
[37] E. Harel,et al. Genetic Engineering of Plant Secondary Metabolism , 2013, Recent Advances in Phytochemistry.
[38] J. Amthor. The McCree-de Wit-Penning de Vries-Thornley Respiration Paradigms: 30 Years Later , 2000 .
[39] G. Khush. Green revolution: the way forward , 2001, Nature Reviews Genetics.
[40] A. Arkin,et al. Stochastic amplification and signaling in enzymatic futile cycles through noise-induced bistability with oscillations. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[41] S. Huber. Biochemical Mechanism for Regulation of Sucrose Accumulation in Leaves during Photosynthesis. , 1989, Plant physiology.
[42] T. Rees,et al. Turnover of starch and sucrose in roots of Pisum sativum , 1988 .
[43] L. Willmitzer,et al. Leaf-Specific Antisense Inhibition of Starch Biosynthesis in Transgenic Potato Plants Leads to an Increase in Photoassimilate Export from Source Leaves during the Light Period , 1995 .
[44] Rico Schmidt,et al. Global proteomic analysis of advanced glycation end products in the Arabidopsis proteome provides evidence for age-related glycation hot spots , 2017, The Journal of Biological Chemistry.
[45] A. J. Cairns,et al. Absence of turnover and futile cycling of sucrose in leaves of Lolium temulentum L.: implications for metabolic compartmentation , 2004, Planta.
[46] A. S. Raghavendra,et al. Beneficial interactions of mitochondrial metabolism with photosynthetic carbon assimilation. , 2003, Trends in plant science.
[47] C. Y. M. Cheung,et al. A Dynamic Multi-Tissue Flux Balance Model Captures Carbon and Nitrogen Metabolism and Optimal Resource Partitioning During Arabidopsis Growth , 2018, Front. Plant Sci..
[48] D. Bush,et al. Transgenic approaches to altering carbon and nitrogen partitioning in whole plants: assessing the potential to improve crop yields and nutritional quality , 2015, Front. Plant Sci..
[49] J. Katz,et al. Futile cycling in glucose metabolism , 1978 .
[50] M. Stitt,et al. Growth rate correlates negatively with protein turnover in Arabidopsis accessions , 2017, The Plant journal : for cell and molecular biology.
[51] A. Millar,et al. Proteins with High Turnover Rate in Barley Leaves Estimated by Proteome Analysis Combined with in Planta Isotope Labeling1[W][OPEN] , 2014, Plant Physiology.
[52] R. Sage,et al. The temperature response of C(3) and C(4) photosynthesis. , 2007, Plant, cell & environment.
[53] Jeff Baldock,et al. Variability in harvest index of grain crops and potential significance for carbon accounting: examples from Australian agriculture , 2010 .
[54] M. Stitt,et al. Sucrose is metabolised by sucrose synthase and glycolysis within the phloem complex of Ricinus communis L. seedlings , 1993, Planta.
[55] T. Bouma,et al. Analysis of root respiration of Solanum tuberosum as related to growth, ion uptake and maintenance of biomass. , 1996 .
[56] V. Demidchik,et al. Stress-induced electrolyte leakage: the role of K+-permeable channels and involvement in programmed cell death and metabolic adjustment. , 2014, Journal of experimental botany.
[57] Dominique Rolin,et al. A New Substrate Cycle in Plants. Evidence for a High Glucose-Phosphate-to-Glucose Turnover from in Vivo Steady-State and Pulse-Labeling Experiments with [13C]Glucose and [14C]Glucose1 , 2005, Plant Physiology.
[58] W. Gruissem,et al. Quantifying Protein Synthesis and Degradation in Arabidopsis , 2015 .
[59] Hailin Zhang,et al. Chemical Characterization of Cotton Plant Parts for Multiple Uses , 2017 .
[60] E. Martinoia,et al. Identification of a Probable Pore-Forming Domain in the Multimeric Vacuolar Anion Channel AtALMT91[W][OPEN] , 2013, Plant Physiology.
[61] Hiroshi A. Maeda. Lignin biosynthesis: Tyrosine shortcut in grasses , 2016, Nature Plants.
[62] A. Millar,et al. Diurnal Changes in Mitochondrial Function Reveal Daily Optimization of Light and Dark Respiratory Metabolism in Arabidopsis* , 2010, Molecular & Cellular Proteomics.
[63] Stephen Sitch,et al. Implications of improved representations of plant respiration in a changing climate , 2017, Nature Communications.
[64] U. Roessner,et al. The response of the maize nitrate transport system to nitrogen demand and supply across the lifecycle. , 2013, The New phytologist.
[65] J. Amthor. Efficiency of lignin biosynthesis: a quantitative analysis. , 2003, Annals of botany.
[66] J. Lynch,et al. Spatiotemporal variation of nitrate uptake kinetics within the maize (Zea mays L.) root system is associated with greater nitrate uptake and interactions with architectural phenes , 2016, Journal of experimental botany.
[67] J. R. Wood,et al. Starch Biosynthesis in Developing Wheat Grain : Evidence against the Direct Involvement of Triose Phosphates in the Metabolic Pathway. , 1988, Plant physiology.
[68] M. Stitt. Pyrophosphate as an Energy Donor in the Cytosol of Plant Cells: an Enigmatic Alternative to ATP , 1998 .
[69] A. Millar,et al. Protein Degradation Rate in Arabidopsis thaliana Leaf Growth and Development[OPEN] , 2017, Plant Cell.
[70] M. Stitt,et al. Mitochondrial oxidative phosphorylation participating in photosynthetic metabolism of a leaf cell , 1988 .
[71] S. Tyerman,et al. Root Hydraulic and Aquaporin Responses to N Availability , 2017 .
[72] R. Loomis,et al. Yield Potential, Plant Assimilatory Capacity, and Metabolic Efficiencies , 1999 .
[73] B. Lacombe,et al. Substrate (un)specificity of Arabidopsis NRT1/PTR FAMILY (NPF) proteins , 2017, Journal of experimental botany.
[74] S. Long,et al. What have we learned from 15 years of free-air CO2 enrichment (FACE)? A meta-analytic review of the responses of photosynthesis, canopy properties and plant production to rising CO2. , 2004, The New phytologist.
[75] L. Kochian,et al. The ALMT Family of Organic Acid Transporters in Plants and Their Involvement in Detoxification and Nutrient Security , 2016, Front. Plant Sci..
[76] Xin Zhang,et al. Pyrophosphate: fructose-6-phosphate 1-phosphotransferase (PFP) regulates carbon metabolism during grain filling in rice , 2016, Plant Cell Reports.
[77] W. Boerjan,et al. Lignin biosynthesis. , 2003, Annual review of plant biology.
[78] E. Schaftingen,et al. Enzymatic repair of Amadori products , 2010, Amino Acids.
[79] D. Fell,et al. A Diel Flux Balance Model Captures Interactions between Light and Dark Metabolism during Day-Night Cycles in C3 and Crassulacean Acid Metabolism Leaves1[C][W][OPEN] , 2014, Plant Physiology.
[80] Zishan Zhang,et al. Contribution of the Alternative Respiratory Pathway to PSII Photoprotection in C3 and C4 Plants. , 2017, Molecular plant.
[81] R. Loomis,et al. Maximum Crop Productivity: An Extimate 1 , 1963 .
[82] R. Dixon,et al. Role of bifunctional ammonia-lyase in grass cell wall biosynthesis , 2016, Nature Plants.
[83] L. Heide,et al. Genetic Engineering of Plant Secondary Metabolism (Accumulation of 4-Hydroxybenzoate Glucosides as a Result of the Expression of the Bacterial ubiC Gene in Tobacco) , 1996, Plant physiology.
[84] B. Usadel,et al. Arabidopsis and primary photosynthetic metabolism - more than the icing on the cake. , 2010, The Plant journal : for cell and molecular biology.
[85] F. D. Vries,et al. The cost of maintenance processes in plant cells , 1975 .
[86] Thomas D. Niehaus,et al. Redesigning thiamin synthesis: Prospects and potential payoffs. , 2018, Plant science : an international journal of experimental plant biology.
[87] H. Lambers,et al. Effect of respiratory homeostasis on plant growth in cultivars of wheat and rice , 2004 .
[88] M. Gilliham,et al. Chloride: not simply a ‘cheap osmoticum’, but a beneficial plant macronutrient , 2017, Journal of experimental botany.
[89] John A. Raven,et al. RNA function and phosphorus use by photosynthetic organisms , 2013, Front. Plant Sci..
[90] A. Fernie,et al. Not just a circle: flux modes in the plant TCA cycle. , 2010, Trends in plant science.
[91] J. Berry,et al. Beyond SHAM and cyanide : opportunities for studying the alternative oxidase in plant respiration using oxygen isotope discrimination , 1995 .
[92] J. Amthor. From sunlight to phytomass: on the potential efficiency of converting solar radiation to phyto-energy. , 2010, The New phytologist.
[93] H. Lambers,et al. The contribution of roots and shoots to whole plant nitrate reduction in fast- and slow-growing grass species. , 2002, Journal of experimental botany.
[94] P. Chourey,et al. Genetic evidence that the two isozymes of sucrose synthase present in developing maize endosperm are critical, one for cell wall integrity and the other for starch biosynthesis , 1998, Molecular and General Genetics MGG.
[95] M. Stitt,et al. A study of the rate of recycling of triose phosphates in heterotrophic Chenopodium rubrum cells, potato tubers, and maize endosperm , 2004, Planta.
[96] M. Stitt,et al. Leaf Starch Turnover Occurs in Long Days and in Falling Light at the End of the Day1[OPEN] , 2017, Plant Physiology.
[97] Mark Stitt,et al. Sucrose synthase catalyses a readily reversible reaction in vivo in developing potato tubers and other plant tissues , 1993, Planta.
[98] Y. Tsay,et al. Nitrate Transport, Signaling, and Use Efficiency. , 2018, Annual review of plant biology.
[99] A. Millar,et al. Online oxygen kinetic isotope effects using membrane inlet mass spectrometry can differentiate between oxidases for mechanistic studies and calculation of their contributions to oxygen consumption in whole tissues. , 2014, Analytical chemistry.
[100] Patrik R. Jones,et al. Synthetic metabolism: metabolic engineering meets enzyme design. , 2017, Current opinion in chemical biology.
[101] S. Tyerman,et al. Maize NPF6 Proteins Are Homologs of Arabidopsis CHL1 That Are Selective for Both Nitrate and Chloride , 2017, Plant Cell.
[102] Joshua S Yuan,et al. Redesigning photosynthesis to sustainably meet global food and bioenergy demand , 2015, Proceedings of the National Academy of Sciences.
[103] L. Garcia,et al. Intracellular transport and compartmentation of phosphate in plants. , 2017, Current opinion in plant biology.
[104] S. Long,et al. Review Tansley Review , 2022 .
[105] J. Amthor. Respiration and crop productivity , 2004, Plant Growth Regulation.
[106] T. Whitlow,et al. An improved method for using electrolyte leakage to assess membrane competence in plant tissues. , 1992, Plant physiology.
[107] H. H. Laar,et al. Products, requirements and efficiency of biosynthesis: a quantitative approach. , 1974, Journal of theoretical biology.
[108] A. Weber,et al. Engineering C4 photosynthesis into C3 chassis in the synthetic biology age. , 2016, The Plant journal : for cell and molecular biology.
[109] S. Chaillou,et al. Nitrate transport and signalling in Arabidopsis. , 2014, Journal of experimental botany.
[110] F. Podestá,et al. The Functional Organization and Control of Plant Respiration , 2006 .
[111] A. Millar,et al. Protein turnover in plant biology , 2015, Nature Plants.
[112] M. Stitt,et al. Transgenic potato plants with strongly decreased expression of pyrophosphate:fructose-6-phosphate phosphotransferase show no visible phenotype and only minor changes in metabolic fluxes in their tubers , 1993, Planta.
[113] D. E. Van Dyk,et al. Metabolic Engineering of the Chloroplast Genome Using the Echerichia coli ubiC Gene Reveals That Chorismate Is a Readily Abundant Plant Precursor for p-Hydroxybenzoic Acid Biosynthesis1 , 2004, Plant Physiology.
[114] A. Millar,et al. Organization and regulation of mitochondrial respiration in plants. , 2011, Annual review of plant biology.
[115] M. Stitt,et al. Tobacco transformants with strongly decreased expression of pyrophosphate:fructose-6-phosphate expression in the base of their young growing leaves contain much higher levels of fructose-2,6-bisphosphate but no major changes in fluxes , 2001, Planta.
[116] K. Adolfsen,et al. Futile cycling increases sensitivity toward oxidative stress in Escherichia coli. , 2015, Metabolic engineering.
[117] K. Lindsey,et al. Can genetic manipulation of plant nitrogen assimilation enzymes result in increased crop yield and greater N-use efficiency? An assessment , 2004 .
[118] S. Tyerman,et al. Root Ideotype Influences Nitrogen Transport and Assimilation in Maize , 2018, Front. Plant Sci..
[119] A. Igamberdiev,et al. The origin of cytosolic ATP in photosynthetic cells. , 2016, Physiologia plantarum.
[120] A. Millar,et al. Opportunities for wheat proteomics to discover the biomarkers for respiration-dependent biomass production, stress tolerance and cytoplasmic male sterility. , 2016, Journal of proteomics.
[121] P. Dorrestein,et al. Saccharomyces cerevisiae THI4p is a suicidal thiamin thiazole synthase , 2010, Nature.
[122] L. Kochian,et al. Not all ALMT1-type transporters mediate aluminum-activated organic acid responses: the case of ZmALMT1 - an anion-selective transporter. , 2007, The Plant journal : for cell and molecular biology.
[123] M. Tester,et al. Structural variations in wheat HKT1;5 underpin differences in Na+ transport capacity , 2018, Cellular and Molecular Life Sciences.
[124] Mark Stitt,et al. Subcellular compartmentation of pyrophosphate and alkaline pyrophosphatase in leaves , 1987 .
[125] M. Bowman,et al. Structural determinants and modulation of substrate specificity in phenylalanine-tyrosine ammonia-lyases. , 2006, Chemistry & biology.
[126] Pyrophosphate: fructose-6-phosphate 1-phosphotransferase is involved in the tolerance of Arabidopsis seedlings to salt and osmotic stresses , 2014, In Vitro Cellular & Developmental Biology - Plant.
[127] Wei-Hua Wu,et al. NRT1.5/NPF7.3 Functions as a Proton-Coupled H+/K+ Antiporter for K+ Loading into the Xylem in Arabidopsis[OPEN] , 2017, Plant Cell.
[128] Christian R. Boehm,et al. Synthetic Botany. , 2017, Cold Spring Harbor perspectives in biology.
[129] Rico Schmidt,et al. Maillard Proteomics: Opening New Pages , 2017, International journal of molecular sciences.
[130] L. Willmitzer,et al. Evidence of the crucial role of sucrose synthase for sink strength using transgenic potato plants (Solanum tuberosum L.). , 1995, The Plant journal : for cell and molecular biology.
[131] M. Andrews. The partitioning of nitrate assimilation between root and shoot of higher plants , 1986 .
[132] R M Gifford,et al. Crop Productivity and Photoassimilate Partitioning , 1984, Science.
[133] D. Charles-Edwards. Efficiency and Expediency in Plant Growth , 1975 .
[134] J. Bailey-Serres,et al. Water-deficit-induced translational control in Nicotiana tabacum , 2003 .
[135] P. Falkowski,et al. Protein interactions limit the rate of evolution of photosynthetic genes in cyanobacteria. , 2005, Molecular biology and evolution.
[136] Guohua Xu,et al. Plant nitrogen assimilation and use efficiency. , 2012, Annual review of plant biology.
[137] C. Körner. Paradigm shift in plant growth control. , 2015, Current opinion in plant biology.
[138] S. Tyerman,et al. Aluminum-Activated Malate Transporters Can Facilitate GABA Transport[OPEN] , 2018, Plant Cell.
[139] J. Porter,et al. Crop responses to climatic variation , 2005, Philosophical Transactions of the Royal Society B: Biological Sciences.
[140] A. Hawkins. Protein Turnover: A Functional Appraisal , 1991 .
[141] M. Stitt,et al. A “futile” cycle of sucrose synthesis and degradation is involved in regulating partitioning between sucrose, starch and respiration in cotyledons of germinating Ricinus communis L. seedlings when phloem transport is inhibited , 1991, Planta.
[142] A. Glass. Nitrogen Use Efficiency of Crop Plants: Physiological Constraints upon Nitrogen Absorption , 2003 .
[143] J. Boyer,et al. Sugar input, metabolism, and signaling mediated by invertase: roles in development, yield potential, and response to drought and heat. , 2010, Molecular plant.
[144] J. Bonner. The Upper Limit of Crop Yield: This classical problem may be analyzed as one of the photosynthetic efficiency of plants in arrays. , 1962, Science.
[145] A. Maule,et al. Normal growth of Arabidopsis requires cytosolic invertase but not sucrose synthase , 2009, Proceedings of the National Academy of Sciences.
[146] P. Tillard,et al. Arabidopsis NRT1.1 is a bidirectional transporter involved in root-to-shoot nitrate translocation. , 2013, Molecular plant.
[147] Ulrich Schurr,et al. Diel time-courses of leaf growth in monocot and dicot species: endogenous rhythms and temperature effects , 2010, Journal of experimental botany.
[148] Benjamin Birami,et al. Diurnal periodicity of assimilate transport shapes resource allocation and whole‐plant carbon balance , 2018, The Plant journal : for cell and molecular biology.
[149] F. Salamini,et al. Plant biotechnology and breeding: allied for years to come. , 2003, Trends in plant science.
[150] U. Heber. Energy coupling in chloroplasts , 1976, Journal of bioenergetics and biomembranes.
[151] A. Kingston-Smith. Review article. Invertase in leaves: conundrum or control point? , 1999 .
[152] J. Zarzycki,et al. Biochemical and synthetic biology approaches to improve photosynthetic CO2-fixation. , 2016, Current opinion in chemical biology.