Changes in δ¹³C of dark respired CO₂ and organic matter of different organs during early ontogeny in peanut plants

References

• Cernusak LA, Tcherkez G, Keitel C, Cornwell WK, Santiago LS, Knohl A, Barbour MM, Williams DG, Reich PB, Ellsworth DS, Dawson TE, Griffiths HG, Farquhar GD, Wright IJ. Why are non-photosynthetic tissues generally 13C enriched compared with leaves in C3 plants? Review and synthesis of current hypotheses. Funct Plant Biol. 2009;36:199–213. doi: 10.1071/FP08216
   PubMed Web of Science ®Google Scholar
• Ghashghaie J, Badeck FW. Tansley review: opposite carbon isotope fractionation during dark respiration in roots vs leaves – a review. New Phytol. 2014;201:751–769. doi: 10.1111/nph.12563
   PubMed Web of Science ®Google Scholar
• Werner C, Gessler A. Diel variations in the carbon isotope composition of respired CO2 and associated carbon sources – a review of dynamics and mechanisms. Biogeosciences. 2011;8:2437–2459. doi: 10.5194/bg-8-2437-2011
   Web of Science ®Google Scholar
• Badeck FW, Tcherkez G, Nogués S, Piel C, Ghashghaie J. Post-photosynthetic fractionation of stable carbon isotopes between plant organs – a widespread phenomenon. Rapid Commun Mass Sp. 2005;19:1381–1391. doi: 10.1002/rcm.1912
   PubMed Web of Science ®Google Scholar
• Badeck FW, Fontaine JL, Dumas F, Ghashghaie J. Consistent patterns in leaf lamina and leaf vein C isotope composition across 10 herbs and tree species. Rapid Commun Mass Sp. 2009;23:2455–2460. doi: 10.1002/rcm.4054
   PubMed Web of Science ®Google Scholar
• Bathellier C, Badeck FW, Couzi P, Harscoët S, Mauve C, Ghashghaie J. Divergence in δ13C of dark respired CO2 and bulk organic matter occurs during the transition between heterotrophy and autotrophy in Phaseolus vulgaris L. plants. New Phytol. 2008;177:406–418.
   PubMed Web of Science ®Google Scholar
• Lamade E, Setyio IE, Girard S, Ghashghaie J. Changes in 13C/12C of oil palm leaves to understand the use of carbon during their passage from heterotrophy to autotrophy. Rapid Commun Mass Sp. 2009;23:2586–2596. doi: 10.1002/rcm.4169
   PubMed Web of Science ®Google Scholar
• Ghashghaie J, Badeck FW, Lanigan G, Nogués S, Tcherkez G, Deléens E, Cornic G, Griffiths H. Carbon isotope discrimination during dark respiration and photorespiration in C3 plants. Phytochem Rev. 2003;2:145–161. doi: 10.1023/B:PHYT.0000004326.00711.ca
   Google Scholar
• Rossmann A, Butzenlechner M, Schmidt H-L. Evidence for a non-statistical carbon isotope distribution in natural glucose. Plant Physiol. 1991;96:609–614. doi: 10.1104/pp.96.2.609
   PubMed Web of Science ®Google Scholar
• Tcherkez G, Nogués S, Bleton J, Cornic G, Badeck FW, Ghashghaie J. Metabolic origin of carbon isotope composition of leaf dark-respired CO2 in French bean. Plant Physiol. 2003;131:237–244. doi: 10.1104/pp.013078
   PubMed Web of Science ®Google Scholar
• Bathellier C, Tcherkez G, Bligny R, Gout E, Cornic G, Ghashghaie J. Metabolic origin of δ13C of respired CO2 from the roots of Phaseolus vulgaris. New Phytol. 2009;181:387–399. doi: 10.1111/j.1469-8137.2008.02679.x
   PubMed Web of Science ®Google Scholar
• Gessler A, Tcherkez G, Karyanto O, Keitel C, Ferrio JP, Ghashghaie J, Kreuzwieser J, Farquhar GD. On the metabolic origin of the carbon isotope composition of CO2 evolved from darkened light-adapted leaves in Ricinus communis. New Phytol. 2009;181:374–386. doi: 10.1111/j.1469-8137.2008.02672.x
   PubMed Web of Science ®Google Scholar
• Barbour MM, McDowell NG, Tcherkez G, Bickford CP, Hanson DT. A new measurement technique reveals rapid post-illumination changes in the carbon isotope composition of leaf-respired CO2. Plant Cell Environ. 2007;30:469–482. doi: 10.1111/j.1365-3040.2007.01634.x
   PubMed Web of Science ®Google Scholar
• Luettge U. Fat – carbohydrate – protein: storage in plant seeds. Lipid Technol. 2013;25:79–81. doi: 10.1002/lite.201300266
   Google Scholar
• Sebei K, Gnouma A, Herchi W, Sakouhi F, Boukhchina S. Lipids, proteins, phenolic composition, antioxidant and antibacterial activities of seeds of peanuts (Arachis hypogaea L.) cultivated in Tunisia. Biol Res. 2013;46:257–263. doi: 10.4067/S0716-97602013000300006
   PubMed Web of Science ®Google Scholar
• Eastmond PJ, Graham IA. Re-examining the role of the glyoxylate cycle in oilseeds. Trends Plant Sci. 2001;6:72–77. doi: 10.1016/S1360-1385(00)01835-5
   PubMed Web of Science ®Google Scholar
• Voet D, Voet JG. Biochemistry. 4th ed. Hoboken, NJ: Wiley; 2011. Chapter 23, Other pathways of carbohydrate metabolism; p. 871–881.
   Google Scholar
• Falk KL, Behal RH, Xiang CB, Oliver DJ. Metabolic bypass of the tricarboxylic acid cycle during lipid mobilization in germinating oilseeds – Regulation of NAD(+)-dependent isocitrate dehydrogenase versus fumarase. Plant Physiol. 1998;117:473–481. doi: 10.1104/pp.117.2.473
   PubMed Web of Science ®Google Scholar
• Smith BN. Carbon isotope ratios of respired CO2 from castor bean, peanut, pea, radish, squash, sunflower and wheat seedlings. Plant Cell Physiol. 1971;12:451–455.
   Web of Science ®Google Scholar
• Luo Y-H, da Silveira L, Sternberg L. Alterations in δ13C values of seedling cellulose associated with respiration during germination. Phytochemistry. 1994;35:877–880. doi: 10.1016/S0031-9422(00)90630-7
   Web of Science ®Google Scholar
• Meier U. Growth stages of mono-and dicotyledonous plants: BBCH Monograph. Federal Biological Research Centre for Agriculture and Forestry; 2001. p. 158. Available from: http://www.bba.de/veroeff/bbch/bbcheng.pdf
   Google Scholar
• R Core Team. R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2014. Available from: http://www.R-project.org/
   Google Scholar
• Botha FC, Potgieter GP, Botha AM. Respiratory metabolism and gene-expression during seed-germination. Plant Growth Regul. 1992;11:211–224. doi: 10.1007/BF00024560
   Web of Science ®Google Scholar
• Rosental L, Nonogaki H, Fait A. Activation and regulation of primary metabolism during seed germination. Seed Sci Res. 2014;24:1–15. doi: 10.1017/S0960258513000391
   Web of Science ®Google Scholar
• Jacks TJ, Yatsu LY, Altschul AM. Isolation and characterization of peanut spherosomes. Plant Physiol. 1967;42:585–597. doi: 10.1104/pp.42.4.585
   PubMed Web of Science ®Google Scholar
• Allfrey JM, Northcote DH. Effects of axis and plant hormones on mobilization of storage materials in ground-nut (Arachis hypogaea) during germination. New Phytol. 1977;78:547–563. doi: 10.1111/j.1469-8137.1977.tb02158.x
   Web of Science ®Google Scholar
• Basha SMM, Cherry JP. Proteolytic-enzyme activity and storage protein degradation in cotyledons of germinating peanut (Arachis hypogaea L.) seeds. J Agric Food Chem. 1978;26:229–234. doi: 10.1021/jf60215a045
   PubMed Web of Science ®Google Scholar
• Tcherkez G, Farquhar GD, Badeck FW, Ghashghaie J. Theoretical considerations about carbon isotope distribution in glucose of C3 plants. Funct Plant Biol. 2004;31:857–877. doi: 10.1071/FP04053
   PubMed Web of Science ®Google Scholar
• Gilbert A, Robins RJ, Remaud GS, Tcherkez G. Intramolecular 13C pattern in hexoses from autotrophic and heterotrophic C3 plant tissues. Proc Nat Acad Sci USA. 2012;109:18204–18209. doi: 10.1073/pnas.1211149109
   PubMed Web of Science ®Google Scholar
• Monson KD, Hayes JM. Biosynthetic control of the natural abundance of C-13 at specific positions within fatty-acids in Escherichia coli – evidence regarding the coupling of fatty-acid and phospholipid-synthesis. J Biol Chem. 1980;255:1435–1441.
   Web of Science ®Google Scholar
• Vogler EA, Hayes JM. Carbon isotopic compositions of carboxyl groups of biosynthesized fatty acids. Phys Chem Earth. 1980;12:697–704. doi: 10.1016/0079-1946(79)90150-2
   Google Scholar
• Ballentine DC, Macko SA, Turekian VC. Variability of stable carbon isotopic compositions in individual fatty acids from combustion of C4 and C3 plants: implications for biomass burning. Chem Geol. 1998;152:151–161. doi: 10.1016/S0009-2541(98)00103-X
   Web of Science ®Google Scholar
• Chikaraishi Y, Naraoka H, Poulson SR. Carbon and hydrogen isotopic fractionation during lipid biosynthesis in a higher plant (Cryptomeria japonica). Phytochemistry. 2004;65:323–330. doi: 10.1016/j.phytochem.2003.12.003
   PubMed Web of Science ®Google Scholar
• Chikaraishi Y, Naraoka H, Poulson SR. Hydrogen and carbon isotopic fractionations of lipid biosynthesis among terrestrial (C3, C4 and CAM) and aquatic plants. Phytochemistry. 2004;65:1369–1381. doi: 10.1016/j.phytochem.2004.03.036
   PubMed Web of Science ®Google Scholar
• Huang Y, Eglinton G, Ineson P, Bol R, Harkness DD. The effects of nitrogen fertilisation and elevated CO2 on the lipid biosynthesis and carbon isotopic discrimination in birch seedlings (Betula pendula). Plant Soil. 1999;216:35–45. doi: 10.1023/A:1004771431093
   Web of Science ®Google Scholar
• Wiesenberg GLB, Schwarzbauer J, Schmidt MWI, Schwark L. Plant and soil lipid modification under elevated atmospheric CO2 conditions: II. Stable carbon isotopic values (δ13C) and turnover. Organ Geochem. 2008;39:103–117. doi: 10.1016/j.orggeochem.2007.09.006
   Web of Science ®Google Scholar
• Bowsher C, Steer M, Tobin A. Plant biochemistry. 1st ed. New York: Garland Science, Taylor & Francis Group, LLC; 2008. p. 329–333.
   Google Scholar
• Taiz L, Zeiger E. Plant physiology. 4th ed. Sunderland, McA: Sibauer Associates; 2006. Chapter 11, Respiration and lipid metabolism. p. 253–288.
   Google Scholar
• Schmidt H-L. Fundamentals and systematics of the non-statistical distributions of isotopes in natural compounds. Naturwissenschaften. 2003;90:537–552. doi: 10.1007/s00114-003-0485-5
   PubMed Web of Science ®Google Scholar
• Melzer E, O'Leary MH. Aspartic-acid synthesis in C3 plants. Planta. 1991;185:368–371. doi: 10.1007/BF00201058
   PubMed Web of Science ®Google Scholar
• Hayes JM. Fractionation of the isotopes of carbon and hydrogen in biosynthetic processes. In: Valley JW, Cole DR, editors. Stable isotope geochemistry. Vol. 43, reviews in mineralogy and geochemistry. Washington, DC: Mineralogical Society of America; 2001. p. 225–278.
   Google Scholar
• Abelson PH, Hoering TC. Carbon isotope fractionation of amino acids by photosynthetic organisms. Proc Nat Acad Sci USA. 1961;47:623–632. doi: 10.1073/pnas.47.5.623
   PubMed Web of Science ®Google Scholar
• Gleixner G, Danier HJ, Werner RA, Schmidt H-L. Correlations between 13C content of primary and secondary plant products in different cell compartments and that in decomposing basidiomycetes. Plant Physiol. 1993;102:1287–1290.
   PubMed Web of Science ®Google Scholar
• Gleixner G, Scrimgeour C, Schmidt H-L, Viola R. Stable isotope distribution in the major metabolites of source and sink organs of Solanum tuberosum L. – A powerful tool in the study of metabolic partitioning in intact plants. Planta. 1998;207:241–245. doi: 10.1007/s004250050479
   Web of Science ®Google Scholar
• Schmidt H-L, Gleixner G. Carbon isotope effect on key reactions in plant metabolism and 13C-patterns in natural compounds. In: Griffiths H, editor. Stable isotopes, integration of biological, ecological and geochemical processes. Abingdon: BIOS Scientific Publishers; 1998. p. 13–25.
   Google Scholar
• Butzenlechner M, Thimet S, Kempe K, Kexel H, Schmidt H-L. Inter- and intramolecular isotopic correlations in some cyanogenic glycosides and glucosinolates and their practical importance. Phytochemistry. 1996;43:585–592. doi: 10.1016/0031-9422(96)00290-7
   Web of Science ®Google Scholar
• Melzer A, Schmidt H-L. Carbon isotope effects on the pyruvate dehydrogenase reaction and their importance for relative carbon-13 depletion in lipids. J Biol Chem. 1987;262:8159–8164.
   PubMed Web of Science ®Google Scholar
• Monson KD, Hayes JM. Biosynthetic control of the natural abundance of carbon 13 at specific positions within fatty-acids in Saccharomyces cerevisiae – Isotopic fractionations in lipid synthesis as evidence for peroxisomal regulation. J Biol Chem. 1982;257:5568–5575.
   PubMed Web of Science ®Google Scholar
• Monson KD, Hayes JM. Carbon isotopic fractionation in the biosynthesis of bacterial fatty-acids – Ozonolysis of unsaturated fatty-acids as a means of determining the intramolecular distribution of carbon isotopes. Geochim Cosmochim Acta. 1982;46:139–149. doi: 10.1016/0016-7037(82)90241-1
   Web of Science ®Google Scholar
• Weilacher T, Gleixner G, Schmidt H-L. Carbon isotope pattern in purine alkaloids a key to isotope discriminations in C1 compounds. Phytochemistry. 1996;41:1073–1077. doi: 10.1016/0031-9422(95)00757-1
   Web of Science ®Google Scholar