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. 1976 Mar;57(3):375–381. doi: 10.1104/pp.57.3.375

Studies on Lipid Synthesis and Degradation in Developing Soybean Cotyledons 1

Richard F Wilson a,2, Robert W Rinne a
PMCID: PMC542029  PMID: 16659486

Abstract

The metabolic activity of individual lipid classes found in developing soybean cotyledons (Glycine max.) is estimated by determining the degradation rate of the compound under given conditions. Pulse-labeling and dual substrate labeling are used to evaluate this parameter. These studies indicate first order decay kinetics for phosphatidic acid, phosphatidylinositol, phosphatidylcholine, phosphatidylethanolamine, N-acyl-phosphatidylethanolamine, diglyceride, and zero order kinetics for triglyceride in cotyledons var. “Harosoy 63” at 30 days after flowering. Decay coefficients for acyl groups and lipid-glycerol moieties within specific lipid classes from either method are comparable. Half-life (t½) calculations from the decay coefficients indicate extremely rapid turn-over rates (0.08 to 3.4 hours at 25 C) and suggest similar turnover rates of acyl groups and lipid-glycerol in diglyceride and all phospholipids except N-acylphosphatidylethanolamine where acyl groups are replaced independent of the glycerol moiety. These experiments reveal not only different metabolic activity between lipid components of soybean cotyledons, but also describe a new method for measuring lipid turnover in plants.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arias I. M., Doyle D., Schimke R. T. Studies on the synthesis and degradation of proteins of the endoplasmic reticulum of rat liver. J Biol Chem. 1969 Jun 25;244(12):3303–3315. [PubMed] [Google Scholar]
  2. Curstedt T., Sjövall J. Biosynthetic pathways and turnover of individual biliary phosphatidylcholines during metabolism of (1,1-2H2)ethanol in the rat. Biochim Biophys Acta. 1974 Nov 18;369(2):173–195. doi: 10.1016/0005-2760(74)90250-1. [DOI] [PubMed] [Google Scholar]
  3. Dehlinger P. J., Schimke R. T. Size distribution of membrane proteins of rat liver and their relative rates of degradation. J Biol Chem. 1971 Apr 25;246(8):2574–2583. [PubMed] [Google Scholar]
  4. Kagawa T., Lord J. M., Beevers H. The origin and turnover of organelle membranes in castor bean endosperm. Plant Physiol. 1973 Jan;51(1):61–65. doi: 10.1104/pp.51.1.61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Roughan P. G. Turnover of the glycerolipids of pumpkin leaves. The importence of phosphatidylcholine. Biochem J. 1970 Mar;117(1):1–8. doi: 10.1042/bj1170001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Wilson R. F., Rinne R. W. Effect of freezing and cold storage on phospholipids in developing soybean cotyledons. Plant Physiol. 1976 Feb;57(2):270–273. doi: 10.1104/pp.57.2.270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Wilson R. F., Rinne R. W. Phospholipids in the developing soybean seed. Plant Physiol. 1974 Nov;54(5):744–747. doi: 10.1104/pp.54.5.744. [DOI] [PMC free article] [PubMed] [Google Scholar]

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