Phospholipase activity during plant growth and development and in response to environmental stress

Trends in Plant Science

Volumn 3, Issue 11, 1998, Pages 419-426

  Chapman, Kent D ^a  

^a UNIVERSITY OF NORTH TEXAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0031741822     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1360-1385(98)01326-0     Document Type: Review

References (63)

1. Singer S.J., Nicolson G.L. The fluid-mosaic model of structure of cell membranes. Science. 175:1972;720-731.
2. Morita N.et al. Evidence for a glycosylphosphatidylinositol-anchored alkaline phosphatase in the aquatic plant Spirodella oligorrhiza. Biochim. Biophys. Acta. 1290:1996;53-62.
3. Ohlrogge J.B., Browse J.A. Lipid biosynthesis. Plant Cell. 7:1995;957-970.
4. Shanklin J., Cahoon E.B. Desaturation and modifications of fatty acids. Annu. Rev. Plant Physiol. Plant Mol. Biol. 49:1998;611-641.
5. Munnik T., Irvine R.F., Musgrave A. Phospholipid signalling in plants. Biochim. Biophys. Acta. 1389:1998;222-272.
6. van de Loo, F.J., Fox, B.G. and Sommerville C. (1993) Unusual fatty acids, in Lipid Metabolism in Plants (Moore, T.S., Jr, ed.), pp. 91-126, CRC Press.
7. Bafor M.et al. Ricinoleic acid biosynthesis and triacylglycerol assembly in microsomal preparations from developing castor-bean endosperm. Biochem. J. 280:1991;507-514.
8. Bafor M.et al. Biosynthesis of vernoleate (cis-12-epoxyoctadeca-cis-9-enoate) in microsomal preparations from developing endosperm of Euphorbia lagascae. Arch. Biochem. Biophys. 303:1993;145-151.
9. Stahl U., Banas A., Stymne S. Plant microsomal acyl hydrolases have selectivities for uncommon fatty acids. Plant Physiol. 107:1995;953-962.
10. Stahl, U. et al. (1997) Purification and characterization of a microsomal phospholipase A2 from developing elm seeds, in Physiology, Biochemistry and Molecular Biology of Plant Lipids (Williams, J.P., Khan, M.U. and Lem, N.W., eds), pp. 244-246, Kluwer.
11. 2 from developing seeds of elm. Plant Physiol. 117:1998;197-205.
12. Wang, X. (1993) Phospholipases, in Lipid Metabolism in Plants (Moore, T.S., Jr, ed.), pp. 499-520, CRC Press.
13. Dyer J.H., Ryu S.B., Wang X. Multiple forms of phospholipase D following germination and during leaf development of castor bean. Plant Physiol. 105:1994;715-724.
14. Ueki J.et al. Purification and characterization of phospholipase D (PLD) from rice (Oryza sativa L.) and cloning of cDNA for PLD from rice and maize (Zea mays L.). Plant Cell Physiol. 36:1995;903-914.
15. Ryu S.B., Zheng L., Wang X. Changes in phospholipase D expression in soybeans during seed development and germination. J. Am. Oil Chem. Soc. 73:1996;1171-1176.
16. Ritchie S., Gilroy S. Abscisic acid signal transduction in barley aleurone is mediated by phospholipase D activity. Proc. Natl. Acad. Sci. U. S. A. 95:1998;2697-2702.
17. Pappan, K. and Wang, X. (1998) Molecular, biochemical, and physiological characterization of plant phospholipase D, Biochim. Biophys. Acta (in press).
18. Qin W., Pappan K., Wang X. Molecular heterogeneity of phospholipase D: cloning of PLDγ and regulation of PLDγ, -β, and -α by polyphosphoinositides and calcium. J. Biol. Chem. 272:1997;28267-28273.
19. Pappan K.et al. Substrate selectivities and lipid modulation of plant phospholipase Dα, -β, and -γ Arch. Biochem. Biophys. 353:1998;131-140.
20. 2 activity by auxin in suspension-cultured parsley and soybean cells, Plant J. (in press).
21. 2 by auxin and mastoparan in hypocotyl segments from zucchini and sunflower. J. Plant Physiol. 145:1995;483-490.
22. 2 inhibitors. Implications for auxin-induced signal transduction. Planta. 202:1997;462-469.
23. 2 by auxin in microsomes from suspension-cultured soybean cells is receptor-mediated and influenced by nucleotides. Planta. 191:1993;515-523.
24. Wang X., Xu L., Zheng L. Cloning and expression of phosphatidylcholine-hydrolysing phospholipase D from Ricinus communis L. J. Biol. Chem. 269:1994;20312-20317.
25. Singer W.D., Brown H.A., Sternweiss P.C. Regulation of eukaryotic phosphatidylinositol-specific phospholipase C and phospholipase D. Annu. Rev. Biochem. 66:1997;475-509.
26. Fan L., Zheng S., Wang X. Antisense suppression of phospholipase Dα retards abscisic acid- and ethylene-promoted senescence of postharvest Arabidopsis leaves. Plant Cell. 9:1997;2183-2196.
27. Thompson, J.E. (1988) The molecular basis for membrane deterioration during senescence, in Senescence and Aging in Plants (Nooden, L.D. and Leopold, A.C., eds), pp. 51-81, Academic Press.
28. Jandus J.et al. Phospholipase D during tomato fruit ripening. Plant Physiol. Biochem. 35:1997;123-128.
29. Vick, B.A. (1993) Oxygenated fatty acids of the lipoxygenase pathway, in Lipid Metabolism in Plants (Moore, T.S., Jr, ed.), pp. 167-194, CRC Press.
30. Lee S.H.et al. Ethylene-mediated phospholipid catabolism pathway in glucose-starved carrot suspension cells. Plant Physiol. 116:1998;223-229.
31. Venable M.E., Blobe G.C., Obeid L.M. Identification of a defect in the phospholipase D/diacylglycerol pathway in cellular senescence. J. Biol. Chem. 269:1994;26040-26044.
32. Creelman R.A., Mullet J.E. Biosynthesis and action of jasmonates in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48:1997;355-381.
33. Cote, G.C., Yueh, Y.G. and Crain, R.C. (1996) Phosphoinositide turnover and its role in plant signal transduction, in Subcellular Biochemistry, Volume 26: myo-Inositol Phosphates, Phosphoinositides, and Signal Transduction (Biswas, B.B. and Biswas, S., eds), pp. 317-343, Plenum Press.
34. Einspahr K.J., Thompson G.A. Jr. Transmembrane signalling via phosphatidylinositol 4,5-bisphosphate hydrolysis in plants. Plant Physiol. 93:1990;361-366.
35. Low, P.S. and Schroeder, A.T. (1997) Signal transduction pathways of the plant oxidative burst, in Plant-Microbe Interactions Vol. 3 (Stacey, G. and Keen, N.T., eds), pp. 35-52, Chapman & Hall.
36. Chapman K.D.et al. N-Acylethanolamines: formation and molecular composition of a new class of plant lipids. Plant Physiol. 116:1998;1163-1168.
37. Lee S.M.et al. Systemic elevation of phosphatidic acid and lysophospholipid levels in wounded plants. Plant J. 12:1997;547-556.
38. Needleman P.et al. Arachidonic acid metabolism. Annu. Rev. Biochem. 55:1986;69-102.
39. Conconi A.et al. Intracellular levels of free linolenic and linoleic acids increase in tomato leaves in response to wounding. Plant Physiol. 111:1996;797-803.
40. Ryu S.B., Wang X. Activation of phospholipase D and the possible mechanism of activation in wound-induced lipid hydrolysis in castor leaves. Biochim. Biophys. Acta. 1303:1996;243-250.
41. Ryu, S.B. and Wang, X. (1998) Increases in free linolenic and linoleic acids associated with phospholipase D-mediated hydrolysis of phospholipids in wounded castor bean leaves, Biochim. Biophys. Acta (in press).
42. Lee, Y. et al. (1996) Phospholipid metabolism and light regulation of stomatal opening and leaf movement, in Regulation of Plant Growth and Development by Light (Briggs, W.R., Heath, R.L. and Tobin, E.M., eds), pp. 89-97, American Society of Plant Physiologists.
43. Moran N., Yueh Y.G., Crain R.C. Signal transduction and cell volume regulation in plant leaflet movement. News Physiol. Sci. 11:1996;108-114.
44. Chen, Q., Brglez, I. and Boss, W.F. (1991) Inositol phospholipids as plant second messengers, in Molecular Biology of Plant Development (Jenkins, G. and Schulch, W., eds), pp. 159-175, Company of Biologists, Cambridge.
45. Cho M.H.et al. The effects of mastoparan on the carrot cell plasma membrane polyphosphoinositide phospholipase C. Plant Physiol. 107:1995;845-856.
46. Cho M.H.et al. Changes in phosphatidylinositol metabolism in response to hyperosmotic stress in Daucus carota L. cells grown in suspension culture. Plant Physiol. 103:1993;637-647.
47. Hirayama T.et al. A gene encoding a phosphatidylinositol-specific phospholipase C is induced by dehydration and salt stress in Arabidopsis thaliana. Proc. Natl. Acad. Sci. U. S. A. 92:1995;3903-3907.
48. Mikami, K. et al. (1998) A gene encoding phosphatidylinositol-4-phosphate 5-kinase is induced by water stress and abscisic acid in Arabidopsis thaliana, Plant J. (in press).
49. Hartweck L.M., Llewellyn D.J., Dennis E.S. The Arabidopsis thaliana genome has multiple divergent forms of phosphatidylinositol-specific phospholipase C. Gene. 202:1997;151-156.
50. Young S.A., Wang X., Leach J.E. Changes in the plasma membrane distribution of rice phospholipase D during resistant interactions with Xanthomonas oryzae pv oryzae. Plant Cell. 8:1996;1079-1090.
51. Lamb C., Dixon R.A. The oxidative burst in plant disease resistance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48:1997;251-275.
52. Alvarez M.E.et al. Reactive oxygen intermediates mediate a systemic signal network in the establishment of plant immunity. Cell. 92:1998;773-784.
53. 2+-binding motifs. Plant Cell. 10:1998;255-266.
54. Chandra S., Heinstein P., Low P.S. Activation of phospholipase A by plant defense elicitors. Plant Physiol. 110:1996;979-986.
55. Roy S.et al. Phospholipase activity and phospholipid patterns in tobacco cells treated with fungal elicitor. Plant Sci. 107:1995;17-25.
56. Legendre L.et al. Phospholipase C activation during elicitation of the oxidative burst. J. Biol. Chem. 268:1993;24559-24563.
57. Atkinson M.M. Molecular mechanisms of pathogen recognition by plants. Adv. Plant Pathol. 10:1993;35-64.
58. Chapman K.D., Sprinkle W.B. Developmental, tissue-specific, and environmental factors regulate the biosynthesis of N-acylphosphatidylethanolamine in cotton (Gossypium hirsutum L.). Plant Physiol. 116:1996;1163-2268.
59. Sandoval J.A.et al. N-Acylphosphatidylethanolamine in dry and imbibing cottonseeds: amounts, molecular species, and enzymatic synthesis. Plant Physiol. 109:1995;269-275.
60. Schmid H.H.O., Schmid P.C., Natarajan V. The N-acylation-phosphodiesterase pathway and cell signalling. Chem. Phys. Lipids. 80:1996;133-142.
61. Stefano G.B., Liu Y., Goligorsky M.S. Cannabinoid receptors are coupled to nitric oxide release in invertebrate immunocytes, microglia, and human monocytes. J. Biol. Chem. 271:1996;19238-19242.
62. Delledonne M.et al. Nitric oxide functions as a signal in plant disease resistance. Nature. 394:1998;585-588.
63. Munnik, T. et al. (1998) Detailed analysis of the turnover of polyphosphoinositides and phosphatidic acid upon activation of phospholipase C and -D in Chlamydomonas cells with non-permeabilizing concentrations of mastoparan, Planta (in press).