Unveiling organ-specific metabolism of <i>Citrus clementina</i>

Understanding plant response to environmental factors such as temperature, drought, diseases, and carbon-to-nitrogen (C:N) ratio is essential for crop resilience, quality, and adaptation to climate change. Here, we present <i>i</i>Citrus2616, a high-resolution organ-specific genome-scale metabolic model for <i>Citrus clementina</i>, comprising 2,616 genes, 8,653 metabolites, and 10,654 reactions. The model integrates organ-specific metabolomics data, i.e., leaf, stem, and root, and predicts plant responses to different conditions with high accuracy. Lower C:N ratios showed higher growth rates compared to higher C:N ratios, suggesting an inverse relationship between growth and C:N ratios. Simulations show that polymers such as starch and hemicellulose increased 4-fold under mixotrophic compared to phototrophic conditions, contributing to enhanced rigidity of cell walls, thus improving mechanical and drought stress. Furthermore, <i>i</i>Citrus2616 revealed higher production of specialized metabolites such as flavonoids in the presence of specific nutrients. Additionally, transcriptomics data from symptomatic and asymptomatic leaf and root tissues across four seasons (winter, spring, fall, and summer) during Huanglongbing infection (citrus greening) were integrated into the model. This integration revealed tissue-specific metabolic adaptations, including shifts in energy allocation, secondary metabolite production, and stress-response pathways under biotic stress. These findings underscore the utility of <i>i</i>Citrus2616 in elucidating the metabolic underpinnings of biotic and abiotic stress resilience and could aid in improving crop productivity and quality, thereby meeting escalating market demands.

Authors

Institutions

Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-07-16
DOI
https://doi.org/10.1073/pnas.2503406122
Citations
3
Primary Topic
Microbial Metabolic Engineering and Bioproduction
Type
article
Field-Weighted Citation Impact
2.42

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Unveiling organ-specific metabolism of Citrus clementina

Anurag Passi, Juan D. Tibocha‐Bonilla, Beth B. Peacock, Amanda R. Hale et al.
3 citations
Proceedings of the National Academy of Sciences
Microbial Metabolic Engineering and Bioproduction
2.42
article

Unveiling organ-specific metabolism of Citrus clementina

Anurag Passi, Juan D. Tibocha‐Bonilla, Beth B. Peacock, Amanda R. Hale, James Borneman, Rodrigo Santibáñez, Karsten Zengler, Diego Tec-Campos, Cristal Zúñiga, Manish Kumar
article en
3 citations

Abstract

Understanding plant response to environmental factors such as temperature, drought, diseases, and carbon-to-nitrogen (C:N) ratio is essential for crop resilience, quality, and adaptation to climate change. Here, we present <i>i</i>Citrus2616, a high-resolution organ-specific genome-scale metabolic model for <i>Citrus clementina</i>, comprising 2,616 genes, 8,653 metabolites, and 10,654 reactions. The model integrates organ-specific metabolomics data, i.e., leaf, stem, and root, and predicts plant responses to different conditions with high accuracy. Lower C:N ratios showed higher growth rates compared to higher C:N ratios, suggesting an inverse relationship between growth and C:N ratios. Simulations show that polymers such as starch and hemicellulose increased 4-fold under mixotrophic compared to phototrophic conditions, contributing to enhanced rigidity of cell walls, thus improving mechanical and drought stress. Furthermore, <i>i</i>Citrus2616 revealed higher production of specialized metabolites such as flavonoids in the presence of specific nutrients. Additionally, transcriptomics data from symptomatic and asymptomatic leaf and root tissues across four seasons (winter, spring, fall, and summer) during Huanglongbing infection (citrus greening) were integrated into the model. This integration revealed tissue-specific metabolic adaptations, including shifts in energy allocation, secondary metabolite production, and stress-response pathways under biotic stress. These findings underscore the utility of <i>i</i>Citrus2616 in elucidating the metabolic underpinnings of biotic and abiotic stress resilience and could aid in improving crop productivity and quality, thereby meeting escalating market demands.

Proceedings of the National Academy of SciencesVol. 122(29)
University of California, Riverside (US), Constructor University (DE), University of California System (US), University of California San Diego (US), Institute for Learning Innovation (US), Autonomous University of Yucatán (MX), La Jolla Bioengineering Institute (US), Plant (United States) (US)
California Department of Food and Agriculture, National Institute of Food and Agriculture
Openalex Percentile: Top 11%
Microbial Metabolic Engineering and Bioproduction
2.42
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.