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. 1966 Feb;41(2):328–334. doi: 10.1104/pp.41.2.328

Chloroplast Fatty Acid Transformations in Nitrogen-Deficient and Senescent Tissues 1

David W Newman 1
PMCID: PMC1086341  PMID: 16656258

Abstract

The fatty acids of plastids from several types of mineral-deficient and senescent tissues were analyzed. Incorporation of acetate into long-chain fatty acids of leaf tissue and of plastids from nitrogen-deficient and normal plants was determined. In general, the senescent and nitrogen-deficient chloroplasts contained a higher ratio of saturates to unsaturates than did plastids from younger tissues and from tissues grown on a complete nutrient.

Nitrogen-deficient leaf tissue and plastids were capable of rapidly incorporating acetate into some of the fatty acids, especially palmitic and oleic acids. However, the comparative rate of acetate incorporation into linolenic acid in nitrogen-deficient chlorophyllous tissue was less than in tissue grown on a complete nutrient. With the addition of UDP-glucose to a reaction mixture containing added cofactors for noncyclic photosynthetic phosphorylation the relative incorporation of acetate into linolenate as compared to palmitate was increased in both the nitrogen-deficient and normal leaf tissue. This would indicate that nitrogen-deficient tissues have the enzymic systems for forming long-chain fatty acids but that the reduced photosynthesis limits the amount of precursors for the formation of lipids, especially galactolipids. However, nothing is known about the rate of fatty acid degradation under these conditions.

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Selected References

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

  1. Bloch K. E., Chano S. B. Galactolipids and Photosynthetic Oxygen Evolution. Science. 1964 May 1;144(3618):560–560. doi: 10.1126/science.144.3618.560-a. [DOI] [PubMed] [Google Scholar]
  2. HARRIS R. V., JAMES A. T. CONVERSION OF OLEIC ACID INTO LINOLEIC ACID BY A SUBCELLULAR SYSTEM OF CHLORELLA VULGARIS. Biochem J. 1965 Feb;94:15C–16C. doi: 10.1042/bj0940015c. [DOI] [PubMed] [Google Scholar]
  3. KATES M. Effects of solvents and surface-active agents on plastid phosphatidase C activity. Can J Biochem Physiol. 1957 Feb;35(2):127–142. [PubMed] [Google Scholar]
  4. MUDD J. B., MCMANUS T. T. RELATIONSHIP OF THE SYNTHESES OF LIPID AND WATER SOLUBLE ACIDS BY CHLOROPLAST PREPARATIONS. Plant Physiol. 1965 Mar;40:340–344. doi: 10.1104/pp.40.2.340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Neufeld E. F., Hall C. W. Formation of galactolipids by chloroplasts. Biochem Biophys Res Commun. 1964;14:503–508. doi: 10.1016/0006-291x(64)90259-1. [DOI] [PubMed] [Google Scholar]
  6. ROSENBERG A., PECKER M. LIPID ALTERATIONS IN EUGLENA GRACILIS CELLS DURING LIGHT-INDUCED GREENING. Biochemistry. 1964 Feb;3:254–258. doi: 10.1021/bi00890a019. [DOI] [PubMed] [Google Scholar]
  7. SASTRY P. S., KATES M. Lipid components of leaves. III. Isolation and characterization of mono- and digalactosyl diglycerides and lecithin. Biochim Biophys Acta. 1963 Apr 23;70:214–216. doi: 10.1016/0006-3002(63)90744-3. [DOI] [PubMed] [Google Scholar]
  8. STUMPF P. K., BOVE J. M., GOFFEAU A. Fat metabolism in higher plants. XX. Relation of fatty acid synthesis and photophosphorylation in lettuce chloroplast. Biochim Biophys Acta. 1963 Jun 18;70:260–270. doi: 10.1016/0006-3002(63)90750-9. [DOI] [PubMed] [Google Scholar]
  9. STUMPF P. K., JAMES A. T. Light-stimulated enzymic synthesis of oleic and palmitic acids by lettuce-chloroplast preparations. Biochim Biophys Acta. 1962 Feb 26;57:400–402. doi: 10.1016/0006-3002(62)91143-5. [DOI] [PubMed] [Google Scholar]
  10. STUMPF P. K., JAMES A. T. The biosynthesis of long-chain fatty acids by lettuce chloroplast preparations. Biochim Biophys Acta. 1963 Feb 19;70:20–32. doi: 10.1016/0006-3002(63)90715-7. [DOI] [PubMed] [Google Scholar]

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