Multiscale Metabolic Modeling of C4 Plants: Connecting Nonlinear Genome-Scale Models to Leaf-Scale Metabolism in Developing Maize Leaves

C4 plants, such as maize, concentrate carbon dioxide in a specialized compartment surrounding the veins of their leaves to improve the efficiency of carbon dioxide assimilation. Nonlinear relationships between carbon dioxide and oxygen levels and reaction rates are key to their physiology but cannot be handled with standard techniques of constraint-based metabolic modeling. We demonstrate that incorporating these relationships as constraints on reaction rates and solving the resulting nonlinear optimization problem yields realistic predictions of the response of C4 systems to environmental and biochemical perturbations. Using a new genome-scale reconstruction of maize metabolism, we build an 18000-reaction, nonlinearly constrained model describing mesophyll and bundle sheath cells in 15 segments of the developing maize leaf, interacting via metabolite exchange, and use RNA-seq and enzyme activity measurements to predict spatial variation in metabolic state by a novel method that optimizes correlation between fluxes and expression data. Though such correlations are known to be weak in general, we suggest that developmental gradients may be particularly suited to the inference of metabolic fluxes from expression data, and we demonstrate that our method predicts fluxes that achieve high correlation with the data, successfully capture the experimentally observed base-to-tip transition between carbon-importing tissue and carbon-exporting tissue, and include a nonzero growth rate, in contrast to prior results from similar methods in other systems.

[1]  B. Halliwell Photorespiration , 2017, Methods in Molecular Biology.

[2]  Lukas A. Mueller,et al.  The Sol Genomics Network (SGN)—from genotype to phenotype to breeding , 2014, Nucleic Acids Res..

[3]  Christopher R. Myers,et al.  A robust and efficient method for estimating enzyme complex abundance and metabolic flux from expression data , 2014, Comput. Biol. Chem..

[4]  Justin Elser,et al.  VitisCyc: a metabolic pathway knowledgebase for grapevine (Vitis vinifera) , 2014, Front. Plant Sci..

[5]  J. Schwender,et al.  Transcript abundance on its own cannot be used to infer fluxes in central metabolism , 2014, Front. Plant Sci..

[6]  Mark Stitt,et al.  Comparative analyses of C4 and C3 photosynthesis in developing leaves of maize and rice , 2014, Nature Biotechnology.

[7]  Margaret N. Simons,et al.  Assessing the Metabolic Impact of Nitrogen Availability Using a Compartmentalized Maize Leaf Genome-Scale Model1[C][W][OPEN] , 2014, Plant Physiology.

[8]  Elhanan Borenstein,et al.  Emergent Biosynthetic Capacity in Simple Microbial Communities , 2014, PLoS Comput. Biol..

[9]  G. Katul,et al.  Increasing water use efficiency along the C3 to C4 evolutionary pathway: a stomatal optimization perspective , 2014, Journal of experimental botany.

[10]  L. Ponnala,et al.  Correlation of mRNA and protein abundance in the developing maize leaf. , 2014, The Plant journal : for cell and molecular biology.

[11]  H. Griffiths,et al.  Acclimation to low light by C4 maize: implications for bundle sheath leakiness. , 2014, Plant, cell & environment.

[12]  Yaqing Si,et al.  Developmental dynamics of Kranz cell transcriptional specificity in maize leaf reveals early onset of C4-related processes , 2014, Journal of experimental botany.

[13]  T. Brutnell,et al.  A Limited Role for Carbonic Anhydrase in C4 Photosynthesis as Revealed by a ca1ca2 Double Mutant in Maize1[W][OPEN] , 2014, Plant Physiology.

[14]  Daniel Machado,et al.  Systematic Evaluation of Methods for Integration of Transcriptomic Data into Constraint-Based Models of Metabolism , 2014, PLoS Comput. Biol..

[15]  A. Weber,et al.  Three distinct biochemical subtypes of C4 photosynthesis? A modelling analysis , 2014, Journal of experimental botany.

[16]  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.

[17]  Ali R. Zomorrodi,et al.  d-OptCom: Dynamic multi-level and multi-objective metabolic modeling of microbial communities. , 2014, ACS synthetic biology.

[18]  Yu Wang,et al.  Elements Required for an Efficient NADP-Malic Enzyme Type C4 Photosynthesis1[C][W][OPEN] , 2014, Plant Physiology.

[19]  Costas D. Maranas,et al.  k-OptForce: Integrating Kinetics with Flux Balance Analysis for Strain Design , 2014, PLoS Comput. Biol..

[20]  C. Raines,et al.  The CP12 protein family: a thioredoxin-mediated metabolic switch? , 2014, Front. Plant Sci..

[21]  Ping Zheng,et al.  The Genome Database for Rosaceae (GDR): year 10 update , 2013, Nucleic Acids Res..

[22]  Dan M. Bolser,et al.  Gramene 2013: comparative plant genomics resources , 2013, Nucleic Acids Res..

[23]  Susumu Goto,et al.  Data, information, knowledge and principle: back to metabolism in KEGG , 2013, Nucleic Acids Res..

[24]  P. Mendes,et al.  Systematic Construction of Kinetic Models from Genome-Scale Metabolic Networks , 2013, PloS one.

[25]  Anton Nekrutenko,et al.  Ten Simple Rules for Reproducible Computational Research , 2013, PLoS Comput. Biol..

[26]  Björn H. Junker,et al.  Multiscale Metabolic Modeling: Dynamic Flux Balance Analysis on a Whole-Plant Scale1[W][OPEN] , 2013, Plant Physiology.

[27]  Martin J. Lercher,et al.  Predicting C4 Photosynthesis Evolution: Modular, Individually Adaptive Steps on a Mount Fuji Fitness Landscape , 2013, Cell.

[28]  F. Bruggeman,et al.  Community Flux Balance Analysis for Microbial Consortia at Balanced Growth , 2013, PloS one.

[29]  D. Fell,et al.  Responses to Light Intensity in a Genome-Scale Model of Rice Metabolism1[C][W][OA] , 2013, Plant Physiology.

[30]  H. Griffiths,et al.  You're so vein: bundle sheath physiology, phylogeny and evolution in C3 and C4 plants. , 2013, Plant, cell & environment.

[31]  Jennifer L. Reed,et al.  Mechanistic analysis of multi-omics datasets to generate kinetic parameters for constraint-based metabolic models , 2013, BMC Bioinformatics.

[32]  Ronan M. T. Fleming,et al.  Systems-level characterization of a host-microbe metabolic symbiosis in the mammalian gut , 2013, Gut microbes.

[33]  S. Zeeman,et al.  Starch Metabolism in Arabidopsis , 2012, The arabidopsis book.

[34]  A. Hoppe What mRNA Abundances Can Tell us about Metabolism , 2012, Metabolites.

[35]  Susanne von Caemmerer,et al.  The Development of C4 Rice: Current Progress and Future Challenges , 2012, Science.

[36]  Neil Swainston,et al.  Improving metabolic flux predictions using absolute gene expression data , 2012, BMC Systems Biology.

[37]  J. Hibberd,et al.  Integrating C4 photosynthesis into C3 crops to increase yield potential. , 2012, Current opinion in biotechnology.

[38]  Bernhard O. Palsson,et al.  A road map for the development of community systems (CoSy) biology , 2012, Nature Reviews Microbiology.

[39]  Yixin Chen,et al.  Integrating Flux Balance Analysis into Kinetic Models to Decipher the Dynamic Metabolism of Shewanella oneidensis MR-1 , 2012, PLoS Comput. Biol..

[40]  Costas D. Maranas,et al.  OptCom: A Multi-Level Optimization Framework for the Metabolic Modeling and Analysis of Microbial Communities , 2012, PLoS Comput. Biol..

[41]  Peter D. Karp,et al.  Construction and completion of flux balance models from pathway databases , 2012, Bioinform..

[42]  E. Ruppin,et al.  Reconstruction of Arabidopsis metabolic network models accounting for subcellular compartmentalization and tissue-specificity , 2011, Proceedings of the National Academy of Sciences.

[43]  Jason A. Papin,et al.  Metabolic network reconstruction of Chlamydomonas offers insight into light-driven algal metabolism , 2011, Molecular systems biology.

[44]  C. Maranas,et al.  Zea mays iRS1563: A Comprehensive Genome-Scale Metabolic Reconstruction of Maize Metabolism , 2011, PloS one.

[45]  T. Nelson The grass leaf developmental gradient as a platform for a systems understanding of the anatomical specialization of C(4) leaves. , 2011, Journal of experimental botany.

[46]  R. Sage,et al.  The C(4) plant lineages of planet Earth. , 2011, Journal of experimental botany.

[47]  R. Furbank Evolution of the C(4) photosynthetic mechanism: are there really three C(4) acid decarboxylation types? , 2011, Journal of experimental botany.

[48]  A. Weber,et al.  Connecting the plastid: transporters of the plastid envelope and their role in linking plastidial with cytosolic metabolism. , 2011, Annual review of plant biology.

[49]  Radhakrishnan Mahadevan,et al.  Genome-scale dynamic modeling of the competition between Rhodoferax and Geobacter in anoxic subsurface environments , 2011, The ISME Journal.

[50]  Ronan M. T. Fleming,et al.  Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox v2.0 , 2007, Nature Protocols.

[51]  A. Weber,et al.  Transport Processes: Connecting the Reactions of C 4 Photosynthesis , 2011 .

[52]  J. Liao,et al.  Reducing the allowable kinetic space by constructing ensemble of dynamic models with the same steady-state flux. , 2011, Metabolic engineering.

[53]  Java Binding,et al.  GNU Linear Programming Kit , 2011 .

[54]  Peter D. Karp,et al.  Pathway Tools version 13.0: integrated software for pathway/genome informatics and systems biology , 2015, Briefings Bioinform..

[55]  Robert Turgeon,et al.  The developmental dynamics of the maize leaf transcriptome , 2010, Nature Genetics.

[56]  B. Palsson,et al.  Large-scale in silico modeling of metabolic interactions between cell types in the human brain , 2010, Nature Biotechnology.

[57]  H. Griffiths,et al.  Can the progressive increase of C₄ bundle sheath leakiness at low PFD be explained by incomplete suppression of photorespiration? , 2010, Plant, cell & environment.

[58]  L. Quek,et al.  C4GEM, a Genome-Scale Metabolic Model to Study C4 Plant Metabolism1[W][OA] , 2010, Plant Physiology.

[59]  B. Palsson,et al.  Insight into human alveolar macrophage and M. tuberculosis interactions via metabolic reconstructions , 2010, Molecular systems biology.

[60]  Radhakrishnan Mahadevan,et al.  Genome-scale metabolic modeling of a clostridial co-culture for consolidated bioprocessing. , 2010, Biotechnology journal.

[61]  J. Hibberd,et al.  The regulation of gene expression required for C4 photosynthesis. , 2010, Annual review of plant biology.

[62]  Jeffrey D Orth,et al.  What is flux balance analysis? , 2010, Nature Biotechnology.

[63]  Neema Jamshidi,et al.  Mass action stoichiometric simulation models: incorporating kinetics and regulation into stoichiometric models. , 2010, Biophysical journal.

[64]  Cristiana G O Dal'molin,et al.  C4GEM - Genome-Scale Metabolic Model to study C4 plant metabolism , 2010 .

[65]  A. Weber,et al.  Chapter 11 Transport Processes: Connecting the Reactions of C4 Photosynthesis , 2010 .

[66]  B. Palsson,et al.  A protocol for generating a high-quality genome-scale metabolic reconstruction , 2010 .

[67]  Neil Swainston,et al.  Towards a genome-scale kinetic model of cellular metabolism , 2010, BMC Systems Biology.

[68]  L. Quek,et al.  AraGEM, a Genome-Scale Reconstruction of the Primary Metabolic Network in Arabidopsis1[W] , 2009, Plant Physiology.

[69]  Desmond S. Lun,et al.  Interpreting Expression Data with Metabolic Flux Models: Predicting Mycobacterium tuberculosis Mycolic Acid Production , 2009, PLoS Comput. Biol..

[70]  B. Petitpierre,et al.  Evolutionary Insights on C4 Photosynthetic Subtypes in Grasses from Genomics and Phylogenetics , 2009, Genome biology and evolution.

[71]  M. Steup,et al.  Eukaryotic starch degradation: integration of plastidial and cytosolic pathways. , 2009, Journal of experimental botany.

[72]  J. Hibberd The evolution of C4 photosynthesis , 2009 .

[73]  C. Foyer,et al.  Photorespiratory metabolism: genes, mutants, energetics, and redox signaling. , 2009, Annual review of plant biology.

[74]  Qi Sun,et al.  PPDB, the Plant Proteomics Database at Cornell , 2008, Nucleic Acids Res..

[75]  D. Fell,et al.  A Genome-Scale Metabolic Model of Arabidopsis and Some of Its Properties , 2009 .

[76]  John A. Morgan,et al.  BMC Systems Biology BioMed Central Research article , 2009 .

[77]  P. Sowiński,et al.  On the mechanism of C4 photosynthesis intermediate exchange between Kranz mesophyll and bundle sheath cells in grasses. , 2008, Journal of experimental botany.

[78]  Michael Hucka,et al.  LibSBML: an API Library for SBML , 2008, Bioinform..

[79]  D. Broomhead,et al.  Something from nothing − bridging the gap between constraint‐based and kinetic modelling , 2007, The FEBS journal.

[80]  Lloyd W. Sumner,et al.  MedicCyc: a biochemical pathway database for Medicago truncatula , 2007, Bioinform..

[81]  T. Shikanai,et al.  Cyclic electron transport around photosystem I: genetic approaches. , 2007, Annual review of plant biology.

[82]  Christopher R. Myers,et al.  Python Unleashed on Systems Biology , 2007, Computing in Science & Engineering.

[83]  D. Stahl,et al.  Metabolic modeling of a mutualistic microbial community , 2007, Molecular systems biology.

[84]  Seth Debolt,et al.  Ascorbate as a biosynthetic precursor in plants. , 2007, Annals of botany.

[85]  Ronan M. T. Fleming,et al.  Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox v2.0 , 2007, Nature Protocols.

[86]  A. Weber,et al.  Plant peroxisomes respire in the light: some gaps of the photorespiratory C2 cycle have become filled--others remain. , 2006, Biochimica et biophysica acta.

[87]  Lorenz T. Biegler,et al.  On the implementation of an interior-point filter line-search algorithm for large-scale nonlinear programming , 2006, Math. Program..

[88]  Stephen P. Boyd,et al.  Convex Optimization , 2004, Algorithms and Theory of Computation Handbook.

[89]  C. Schnarrenberger Characterization and compartmentation, in green leaves, of hexokinases with different specificities for glucose, fructose, and mannose and for nucleoside triphosphates , 1990, Planta.

[90]  F. Sato,et al.  Differential use of two cyclic electron flows around photosystem I for driving CO2-concentration mechanism in C4 photosynthesis. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[91]  Carolyn J. Lawrence-Dill,et al.  Comparative Plant Genomics Resources at PlantGDB1 , 2005, Plant Physiology.

[92]  V. Franceschi,et al.  Calcium oxalate in plants: formation and function. , 2005, Annual review of plant biology.

[93]  Stephen H. Bryant,et al.  CD-Search: protein domain annotations on the fly , 2004, Nucleic Acids Res..

[94]  Tsuyoshi Endo,et al.  Cyclic electron flow around photosystem I is essential for photosynthesis , 2004, Nature.

[95]  C. Foyer,et al.  Measurement of the ascorbate content of spinach leaf protoplasts and chloroplasts during illumination , 1983, Planta.

[96]  R. Furbank,et al.  The C4 pathway: an efficient CO2 pump , 2004, Photosynthesis Research.

[97]  R. Mahadevan,et al.  The effects of alternate optimal solutions in constraint-based genome-scale metabolic models. , 2003, Metabolic engineering.

[98]  B. Palsson,et al.  An expanded genome-scale model of Escherichia coli K-12 (iJR904 GSM/GPR) , 2003, Genome Biology.

[99]  Hiroaki Kitano,et al.  The systems biology markup language (SBML): a medium for representation and exchange of biochemical network models , 2003, Bioinform..

[100]  R. Furbank,et al.  The C(4) pathway: an efficient CO(2) pump. , 2003, Photosynthesis research.

[101]  J. Allen Cyclic, pseudocyclic and noncyclic photophosphorylation: new links in the chain. , 2003, Trends in plant science.

[102]  F. Doyle,et al.  Dynamic flux balance analysis of diauxic growth in Escherichia coli. , 2002, Biophysical journal.

[103]  A. Hanson,et al.  ONE-CARBON METABOLISM IN HIGHER PLANTS. , 2001, Annual review of plant physiology and plant molecular biology.

[104]  A. Doulis,et al.  Determination of glycerolipid composition of rice and maize tissues using solid-phase extraction. , 2000, Biochemical Society transactions.

[105]  S. Brunak,et al.  Predicting subcellular localization of proteins based on their N-terminal amino acid sequence. , 2000, Journal of molecular biology.

[106]  G. Pastori,et al.  Ascorbate biosynthesis in mitochondria is linked to the electron transport chain between complexes III and IV. , 2000, Plant physiology.

[107]  S. V. Caemmerer,et al.  Biochemical models of leaf photosynthesis. , 2000 .

[108]  T. Sharkey,et al.  Photosynthesis : physiology and metabolism , 2000 .

[109]  M. J. Pimenta,et al.  S-Methylmethionine Plays a Major Role in Phloem Sulfur Transport and Is Synthesized by a Novel Type of Methyltransferase , 1999, Plant Cell.

[110]  K. Asada,et al.  THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons. , 1999, Annual review of plant physiology and plant molecular biology.

[111]  Chen,et al.  Phosphoenolpyruvate carboxykinase is involved in the decarboxylation of aspartate in the bundle sheath of maize , 1999, Plant physiology.

[112]  Hiroyuki Ogata,et al.  KEGG: Kyoto Encyclopedia of Genes and Genomes , 1999, Nucleic Acids Res..

[113]  R. Brown,et al.  Agronomic Implications of C4 Photosynthesis , 1999 .

[114]  G. Edwards,et al.  3 – The Biochemistry of C4 Photosynthesis , 1999 .

[115]  John Shanklin,et al.  DESATURATION AND RELATED MODIFICATIONS OF FATTY ACIDS1. , 1998, Annual review of plant physiology and plant molecular biology.

[116]  M. Suter,et al.  Cyst(e)ine is the transport metabolite of assimilated sulfur from bundle-sheath to mesophyll cells in maize leaves , 1998, Plant physiology.

[117]  C. Benning,et al.  The role of UDP-glucose epimerase in carbohydrate metabolism of Arabidopsis. , 1998, The Plant journal : for cell and molecular biology.

[118]  C. Foyer A Molecular Approach To Primary Metabolism In Higher Plants , 1997 .

[119]  N. Smirnoff THE FUNCTION AND METABOLISM OF ASCORBIC ACID IN PLANTS , 1996 .

[120]  J. Harwood Recent advances in the biosynthesis of plant fatty acids. , 1996, Biochimica et biophysica acta.

[121]  Saeed R. Khan Calcium Oxalate in Biological Systems , 1995 .

[122]  E. Heinz,et al.  A cytochrome-b5-containing fusion protein similar to plant acyl lipid desaturases. , 1995, European journal of biochemistry.

[123]  J. Ohlrogge,et al.  Lipid biosynthesis. , 1995, The Plant cell.

[124]  K. Gibson Palmitoleate formation by soybean stearoyl-acyl carrier protein desaturase. , 1993, Biochimica et biophysica acta.

[125]  J. Ray,et al.  Germin, a protein marker of early plant development, is an oxalate oxidase. , 1993, The Journal of biological chemistry.

[126]  H. Hayashi,et al.  Collection and Chemical Composition of Pure Phloem Sap from Zea mays L. , 1990 .

[127]  M. D. Hatch,et al.  Metabolite diffusion into bundle sheath cells from c(4) plants: relation to c(4) photosynthesis and plasmodesmatal function. , 1988, Plant physiology.

[128]  M. D. Hatch,et al.  C4 photosynthesis: a unique elend of modified biochemistry, anatomy and ultrastructure , 1987 .

[129]  T. Elthon,et al.  Proline Oxidation in Corn Mitochondria : Involvement of NAD, Relationship to Ornithine Metabolism, and Sidedness on the Inner Membrane. , 1982, Plant physiology.

[130]  D. Lewis,et al.  MANNOSE AND GREEN PLANTS: OCCURRENCE, PHYSIOLOGY AND METABOLISM, AND USE AS A TOOL TO STUDY THE ROLE OF ORTHOPHOSPHATE , 1977 .

[131]  M. Rumsby,et al.  Plastid differentiation, acyl lipid, and Fatty Acid changes in developing green maize leaves. , 1973, Plant physiology.

[132]  O. Hayaishi,et al.  ENZYMATIC FORMATION OF OXALATE AND ACETATE FROM OXALOACETATE , 1956 .