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. 1997 Feb;113(2):549–557. doi: 10.1104/pp.113.2.549

Characterization of the Glycerolipid Composition and Biosynthetic Capacity of Pea Root Plastids.

L Xue 1, L M McCune 1, K F Kleppinger-Sparace 1, M J Brown 1, M K Pomeroy 1, S A Sparace 1
PMCID: PMC158171  PMID: 12223625

Abstract

The glycerolipid composition of pea (Pisum sativum L.) root plastids and their capacity to synthesize glycerolipids from [UL-14C]glycerol-3-phosphate were determined. Pea root plastids primarily consist of monogalactosyldiacylglycerol, triacylglycerol, phosphatidylcholine, digalactosyldiacylglycerol, and diacylglycerol. Maximum rates of total glycerolipid biosynthesis were obtained in the presence of 2.4 mM glycerol-3-phosphate, 15 mM KHCO3, 0.2 mM sodium-acetate, 0.5 mM each of NADH and NADPH, 0.05 mM coenzyme A, 2 mM MgCl2, 1 mM ATP, 0.1 M Bis-Tris propane (pH 7.5), and 0.31 M sorbitol. Glycerolipid biosynthesis was completely dependent on exogenously supplied ATP, coenzyme A, and a divalent cation, whereas the remaining cofactors improved their activity from 1.3- to 2.4-fold. Radioactivity from glycerol-3-phosphate was recovered predominantly in phosphatidic acid, phosphatidylglycerol, diacylglycerol, and triacylglycerol with lesser amounts in phosphatidylcholine and monoacylglycerol. The proportions of the various radiolabeled lipids that accumulated were dependent on the pH and the concentration of ATP and glycerol-3-phosphate. The data presented indicate that pea root plastids can synthesize almost all of their component glycerolipids and that glycerolipid biosynthesis is tightly coupled to de novo fatty acid biosynthesis. pH and the availability of ATP may have important roles in the regulation of lipid biosynthesis at the levels of phosphatidic acid phosphatase and in the reactions that are involved in phosphatidylglycerol and triacylglycerol biosynthesis.

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Selected References

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  1. Alban C., Joyard J., Douce R. Comparison of glycerolipid biosynthesis in non-green plastids from sycamore (Acer pseudoplatanus) cells and cauliflower (Brassica oleracea) buds. Biochem J. 1989 May 1;259(3):775–783. doi: 10.1042/bj2590775. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BLIGH E. G., DYER W. J. A rapid method of total lipid extraction and purification. Can J Biochem Physiol. 1959 Aug;37(8):911–917. doi: 10.1139/o59-099. [DOI] [PubMed] [Google Scholar]
  3. Bertrams M., Heinz E. Positional Specificity and Fatty Acid Selectivity of Purified sn-Glycerol 3-Phosphate Acyltransferases from Chloroplasts. Plant Physiol. 1981 Sep;68(3):653–657. doi: 10.1104/pp.68.3.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Heinz E., Roughan P. G. Similarities and differences in lipid metabolism of chloroplasts isolated from 18:3 and 16:3 plants. Plant Physiol. 1983 Jun;72(2):273–279. doi: 10.1104/pp.72.2.273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Joyard J., Douce R. Characterization of phosphatidate phosphohydrolase activity associated with chloroplast envelope membranes. FEBS Lett. 1979 Jun 1;102(1):147–150. doi: 10.1016/0014-5793(79)80947-3. [DOI] [PubMed] [Google Scholar]
  6. Kleinig H., Liedvogel B. Fatty acid synthesis by isolated chromoplasts from the daffodil. [14C]Acetate incorporation and distribution of labelled acids. Eur J Biochem. 1978 Feb;83(2):499–505. doi: 10.1111/j.1432-1033.1978.tb12116.x. [DOI] [PubMed] [Google Scholar]
  7. Kleppinger-Sparace K. F., Moore T. S. Biosynthesis of Cytidine 5'-Diphosphate-diacylglycerol in Endoplasmic Reticulum and Mitochondria of Castor Bean Endosperm. Plant Physiol. 1985 Jan;77(1):12–15. doi: 10.1104/pp.77.1.12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kleppinger-Sparace K. F., Stahl R. J., Sparace S. A. Energy requirements for Fatty Acid and glycerolipid biosynthesis from acetate by isolated pea root plastids. Plant Physiol. 1992 Feb;98(2):723–727. doi: 10.1104/pp.98.2.723. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kuiper P. J., Stuiver B. Cyclopropane Fatty acids in relation to earliness in spring and drought tolerance in plants. Plant Physiol. 1972 Mar;49(3):307–309. doi: 10.1104/pp.49.3.307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lord J. M., Kagawa T., Moore T. S., Beevers H. Endoplasmic reticulum as the site of lecithin formation in castor bean endosperm. J Cell Biol. 1973 Jun;57(3):659–667. doi: 10.1083/jcb.57.3.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Moore T. S. Phosphatidylglycerol synthesis in castor bean endosperm: kinetics, requirements, and intracellular localization. Plant Physiol. 1974 Aug;54(2):164–168. doi: 10.1104/pp.54.2.164. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Mudd J. B., Dezacks R. Synthesis of phosphatidylglycerol by chloroplasts from leaves of Spinacia oleracea L. (spinach). Arch Biochem Biophys. 1981 Jul;209(2):584–591. doi: 10.1016/0003-9861(81)90316-7. [DOI] [PubMed] [Google Scholar]
  13. Qi Q., Kleppinger-Sparace K. F., Sparace S. A. The Utilization of Glycolytic Intermediates as Precursors for Fatty Acid Biosynthesis by Pea Root Plastids. Plant Physiol. 1995 Feb;107(2):413–419. doi: 10.1104/pp.107.2.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sparace S. A., Mudd J. B. Phosphatidylglycerol synthesis in spinach chloroplasts: characterization of the newly synthesized molecule. Plant Physiol. 1982 Nov;70(5):1260–1264. doi: 10.1104/pp.70.5.1260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Stahl R. J., Sparace S. A. Characterization of Fatty Acid biosynthesis in isolated pea root plastids. Plant Physiol. 1991 Jun;96(2):602–608. doi: 10.1104/pp.96.2.602. [DOI] [PMC free article] [PubMed] [Google Scholar]

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