Citation
Mongélard, Gaëlle, et al. "Measurement of Carbon Flux Through the MEP Pathway for Isoprenoid Synthesis By (31)P-NMR Spectroscopy After Specific Inhibition of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate Reductase. Effect of Light and Temperature." Plant, Cell & Environment, vol. 34, no. 8, 2011, pp. 1241-7.
Mongélard G, Seemann M, Boisson AM, et al. Measurement of carbon flux through the MEP pathway for isoprenoid synthesis by (31)P-NMR spectroscopy after specific inhibition of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate reductase. Effect of light and temperature. Plant Cell Environ. 2011;34(8):1241-7.
Mongélard, G., Seemann, M., Boisson, A. M., Rohmer, M., Bligny, R., & Rivasseau, C. (2011). Measurement of carbon flux through the MEP pathway for isoprenoid synthesis by (31)P-NMR spectroscopy after specific inhibition of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate reductase. Effect of light and temperature. Plant, Cell & Environment, 34(8), 1241-7. https://doi.org/10.1111/j.1365-3040.2011.02322.x
Mongélard G, et al. Measurement of Carbon Flux Through the MEP Pathway for Isoprenoid Synthesis By (31)P-NMR Spectroscopy After Specific Inhibition of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate Reductase. Effect of Light and Temperature. Plant Cell Environ. 2011;34(8):1241-7. PubMed PMID: 21443577.
TY - JOUR
T1 - Measurement of carbon flux through the MEP pathway for isoprenoid synthesis by (31)P-NMR spectroscopy after specific inhibition of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate reductase. Effect of light and temperature.
AU - Mongélard,Gaëlle,
AU - Seemann,Myriam,
AU - Boisson,Anne-Marie,
AU - Rohmer,Michel,
AU - Bligny,Richard,
AU - Rivasseau,Corinne,
Y1 - 2011/04/26/
PY - 2011/3/30/entrez
PY - 2011/3/30/pubmed
PY - 2011/12/13/medline
SP - 1241
EP - 7
JF - Plant, cell & environment
JO - Plant Cell Environ
VL - 34
IS - 8
N2 - The methylerythritol 4-phosphate (MEP) and the mevalonate pathways are the unique synthesis routes for the precursors of all isoprenoids. An original mean to measure the carbon flux through the MEP pathway in plants is proposed by using cadmium as a total short-term inhibitor of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate (MEcDP) reductase (GcpE) and measuring the accumulation rate of its substrate MEcDP by (31) P-NMR spectroscopy. The MEP pathway metabolic flux was determined in spinach (Spinacia oleracea), pea (Pisum sativum), Oregon grape (Mahonia aquifolium) and boxwood (Buxus sempervirens) leaves. In spinach, flux values were compared with the synthesis rate of major isoprenoids. The flux increases with light intensity (fourfold in the 200-1200 µmol m(-2) s(-1) PPFR range) and temperature (sevenfold in the 25-37 °C range). The relationship with the light and the temperature dependency of isoprenoid production downstream of the MEP pathway is discussed.
SN - 1365-3040
UR - https://www.unboundmedicine.com/medline/citation/21443577/Measurement_of_carbon_flux_through_the_MEP_pathway_for_isoprenoid_synthesis_by__31_P_NMR_spectroscopy_after_specific_inhibition_of_2_C_methyl_d_erythritol_24_cyclodiphosphate_reductase__Effect_of_light_and_temperature_
L2 - https://doi.org/10.1111/j.1365-3040.2011.02322.x
DB - PRIME
DP - Unbound Medicine
ER -