Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/15710
Título: Integration of C1 and C2 metabolism in trees
Autor: Jardine, Kolby J.
Souza, Vinícius Fernandes de
Oikawa, Patricia Yoshino
Higuchi, Niro
Bill, Markus
Porras, Rachel C.
Niinemets, Ülo
Chambers, Jeffrey Quintin
Palavras-chave: Acetic Acid
Carbon-13
Carbon Dioxide
Formaldehyde
Formic Acid
Glycine
Isoprene
Methanol
1,3 Butadiene Derivative
Carbon
Carbon-13
Formic Acid Derivative
Hemiterpene
Pentane
Volatile Organic Compound
Carbon Metabolism
Chloroplast
Inga Edulis
Isotope Labeling
Mass Fragmentography
Mass Spectrometry
Metabolite
Nonhuman
Photorespiration
Plant Growth
Plant Leaf
Proton Transfer Reaction Mass Spectrometry
Proton Transport
Quantitative Analysis
Reassimilation
Tree
Chemistry
Metabolism
Tree
Butadienes
Carbon
Carbon Isotopes
Formaldehyde
Formates
Hemiterpenes
Isotope Labeling
Metabolic Networks And Pathways
Methanol
Pentanes
Trees
Volatile Organic Compounds
Data do documento: 2017
Revista: International Journal of Molecular Sciences
É parte de: Volume 18, Número 10
Abstract: C1 metabolism in plants is known to be involved in photorespiration, nitrogen and amino acid metabolism, as well as methylation and biosynthesis of metabolites and biopolymers. Although the flux of carbon through the C1 pathway is thought to be large, its intermediates are difficult to measure and relatively little is known about this potentially ubiquitous pathway. In this study, we evaluated the C1 pathway and its integration with the central metabolism using aqueous solutions of13C-labeled C1 and C2 intermediates delivered to branches of the tropical species Inga edulis via the transpiration stream. Delivery of [13C]methanol and [13C]formaldehyde rapidly stimulated leaf emissions of [13C]methanol, [13C]formaldehyde, [13C]formic acid, and13CO2, confirming the existence of the C1 pathway and rapid interconversion between methanol and formaldehyde. However, while [13C]formate solutions stimulated emissions of13CO2, emissions of [13C]methanol or [13C]formaldehyde were not detected, suggesting that once oxidation to formate occurs it is rapidly oxidized to CO2 within chloroplasts.13C-labeling of isoprene, a known photosynthetic product, was linearly related to13CO2 across C1 and C2 ([13C2]acetate and [2-13C]glycine) substrates, consistent with reassimilation of C1, respiratory, and photorespiratory CO2. Moreover, [13C]methanol and [13C]formaldehyde induced a quantitative labeling of both carbon atoms of acetic acid emissions, possibly through the rapid turnover of the chloroplastic acetyl-CoA pool via glycolate oxidation. The results support a role of the C1 pathway to provide an alternative carbon source for glycine methylation in photorespiration, enhance CO2 concentrations within chloroplasts, and produce key C2 intermediates (e.g., acetyl-CoA) central to anabolic and catabolic metabolism. © 2017 by the authors. Licensee MDPI, Basel, Switzerland.
DOI: 10.3390/ijms18102045
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