Assessing the Metabolic Impact of Nitrogen Availability Using a Compartmentalized Maize Leaf Genome-Scale Model

被引:72
作者
Simons, Margaret [1 ]
Saha, Rajib [1 ]
Amiour, Nardjis [3 ]
Kumar, Akhil [2 ]
Guillard, Lenaig [3 ]
Clement, Gilles [3 ]
Miquel, Martine [3 ]
Li, Zhenni [3 ]
Mouille, Gregory [3 ]
Lea, Peter J. [4 ]
Hirel, Bertrand [3 ]
Maranas, Costas D. [1 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Huck Inst Life Sci, Dept Bioinformat & Genom, University Pk, PA 16802 USA
[3] INRA, Inst Jean Pierre Bourgin, Ctr Versailles Grignon,Unite Mixte Rech 1318, Agro ParisTech,Equipe Recherce Labellis,Ctr Natl, F-78026 Versailles, France
[4] Univ Lancaster, Lancaster Environm Ctr, Lancaster LA1 4YQ, England
关键词
BUNDLE-SHEATH-CELLS; C-4; PHOTOSYNTHESIS; ESCHERICHIA-COLI; USE EFFICIENCY; FUNCTIONAL-DIFFERENTIATION; GLOBAL RECONSTRUCTION; BIOSYNTHETIC-PATHWAY; GENETIC-VARIABILITY; MUTANTS DEFICIENT; DRAFT SEQUENCE;
D O I
10.1104/pp.114.245787
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Maize (Zea mays) is an important C4 plant due to its widespread use as a cereal and energy crop. A second-generation genome-scale metabolic model for the maize leaf was created to capture C4 carbon fixation and investigate nitrogen (N) assimilation by modeling the interactions between the bundle sheath and mesophyll cells. The model contains gene-protein-reaction relationships, elemental and charge-balanced reactions, and incorporates experimental evidence pertaining to the biomass composition, compartmentalization, and flux constraints. Condition-specific biomass descriptions were introduced that account for amino acids, fatty acids, soluble sugars, proteins, chlorophyll, lignocellulose, and nucleic acids as experimentally measured biomass constituents. Compartmentalization of the model is based on proteomic/transcriptomic data and literature evidence. With the incorporation of information from the MetaCrop and MaizeCyc databases, this updated model spans 5,824 genes, 8,525 reactions, and 9,153 metabolites, an increase of approximately 4 times the size of the earlier iRS1563 model. Transcriptomic and proteomic data have also been used to introduce regulatory constraints in the model to simulate an N-limited condition and mutants deficient in glutamine synthetase, gln1-3 and gln1-4. Model-predicted results achieved 90% accuracy when comparing the wild type grown under an N-complete condition with the wild type grown under an N-deficient condition.
引用
收藏
页码:1659 / 1674
页数:16
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