Abscisic acid promotes accumulation of toxin ODAP in relation to free spermine level in grass pea seedlings (Lathyrus sativus L.)

Plant Physiology and Biochemistry

Volumn 44, Issue 2-3, 2006, Pages 161-169

  Xiong, You Cai ^a,c   Xing, Geng Mei ^b   Li, Feng Min ^a,c   Wang, Shao Ming ^d   Fan, Xian Wei ^a   Li, Zhi Xiao ^a   Wang, Ya Fu ^a  

^a LANZHOU UNIVERSITY   (China)

^b INSTITUTE OF HIGH ENERGY PHYSICS   (China)

^c INSTITUTE OF SOIL AND WATER CONSERVATION   (China)

^d SHIHEZI UNIVERSITY   (China)

Author keywords

N oxalyl l , diaminopropionic acid (ODAP); abscisic acid (ABA); drought stress; Grass pea; polyamines

Indexed keywords

ABSCISIC ACID; DIAMINO ACID; MACROGOL DERIVATIVE; OXALYLDIAMINOPROPIONIC ACID; PHYTOHORMONE; SPERMINE; WATER;

ARTICLE; DRUG EFFECT; LATHYRUS; METABOLISM; SEEDLING; TIME;

ABSCISIC ACID; AMINO ACIDS, DIAMINO; LATHYRUS; PLANT GROWTH REGULATORS; POLYETHYLENE GLYCOLS; SEEDLING; SPERMINE; TIME FACTORS; WATER;

LATHYRUS; LATHYRUS SATIVUS; PISUM SATIVUM;

EID: 33744785941     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2006.03.002     Document Type: Article

References (44)

1. Praveen S., Johari R.P., and Mehta S.L. Cloning and expression of OX-DAPRO degrading genes from soil microbe. J. Plant Biochem. Biotechno. 3 (1994) 25-29
2. Siddique K.H.M., Loss S.P., Herwig S.P., and Wilson J.M. Growth, yield and neurotoxin (ODAP) concentration of three Lathyrus species in Mediterranean-type environments of Western Australia. Aust. J. Exp. Agric. 36 (1996) 209-218
3. Rosa M.J.S., Ferreira R.B., and Teixeira A.R. Storage proteins from Lathyrus sativus seeds. J. Agric. Food Chem. 48 (2000) 5432-5439
4. Malathi K., Padmanabhan G., and Sharma P.S. Biosynthesis of β-N-oxalyl-l-α,β-diaminopropionic acid, the Lathyrus sativus neurotoxin. Phytochem. 9 (1970) 1603-1610
5. Sinha R.R., Das K., and Sen S.K. Plant regeneration from stem-derived callus of the seed legume Lathyrus sativus L. Plant Cell Tissue Org. Cult. 2 (1983) 67-76
6. Chen X., Wang F., Chen Q., Qin X.C., and Li Z.X. Analysis of neurotoxin 3-N-oxalyl-l-2, 3-diaminopropionic acid and its α-isomer in Lathyrus sativus by high-performance liquid chromatography with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) derivatisation. J. Agric. Food Chem. 48 (2000) 3383-3386
7. Guo J.Y., Yuan J.M., and Kang D. Clinical study on motor-neuron injury induced by Lathyrus sativus toxin. Chinese Neurology 30 4 (1997) 223-226 (In Chinese with English abstract)
8. Getahun H., Mekonnen A., Teklehaimanot R., and Lambein F. Epidemic of neurolathyrism in Ethiopia. Lancet 354 9175 (1999) 306-307
9. Mehta S.L., Ali K., and Barna K.S. Somaclonal variation in a food legume-Lathyrus sativus. J. Plant Biochem. Biotechnol. 3 (1994) 73-77
10. Nadolska-Orczyk A., and Orczyk W. Study of the factors influencing Agrobacterium-mediated transformation of pea (Pisum sativum L.). Mol. Breed. 6 (2000) 185-194
11. Tadesse W., Wollelie M., and Yohannes D. Identification of alternative crops for grass pea. In: Teklehaimanot R., and Lambein F. (Eds). Lathyrus and lathyrism: A Decade of Progress (1997), University of Ghent, Belgium 12-15
12. Spencer P.S., and Palmer V. Lathyrus sativus and lathyrism research: A global experience in applied neurotoxicology. Lathyrus and Lathyrism Newsletter (1989), Third World Medical Research Foundation, New York 1-8
13. Campbell C.G. Improvement of Lathyrus sativus. In: Spencer P.S. (Ed). The Grasspeas Threat and Promise. Proceedings of the International Network for Improvement of Lathyrus sativus and Erradication of Lathyrism (INILSEL) workshop, London, May 1988 (1988), Third World Medical Research Foundation, New York 139-146
14. Zambre M., Chowdhury B., Kuo Y.H., Van Montagu M., Angenon G., and Lambein F. Prolific regeneration of fertile plants from green nodular callus induced from meristematic tissues in Lathyrus sativus L. (grass pea). Plant Sci. 163 (2002) 1107-1112
15. Zhou G.K., Kong Y.Z., Cui K.R., Li Z.X., and Wang Y.F. Hydroxyl radical scavenging activity of β-N-oxalyl-l-α,β-diaminopropionic acid. Phytochem 58 (2001) 759-762
16. Xing G.S., Cui K.R., Li J., Wang Y.F., and Li Z.X. Water stress and accumulation of β-N-oxalyl-l-α,β-diaminopropionic acid in grass pea (Lathyrus sativus L.). J. Agric. Food Chem. 49 (2001) 216-220
17. Lambein F., Kuo Y.H., Ikegami F., and Murakoshi I. Toxic and non-toxic nonprotein amino acids in the Vicieae. In: Lubec G., and Rosenthal G.A. (Eds). Amino acids: chemistry, biology and medicine (1990), ESCOM, Leiden 21-28
18. Malathi K.A., Padmanaban G., and Sarma P.S. Biosnthesis of β-N-oxalyl-l-a,β-diaminopropionic acid, the Lathyrus sativus neurotoxin. Phytochem. 9 (1970) 1603-1610
19. Zhang D.W., Xing G.M., Xu H., Yan Z.Y., Wang C.Y., Wang Y.F., and Li Z.X. Relationship between oxalic acid and the metabolism of β-N-oxalyl-l-a,β-diaminopropionic acid (ODAP) in grass pea (Lathyrus sativus L.), Israel. J. Plant Sci. 53 (2005)
20. Bolweell P.P., Page A., Pislewska M., and Wojtaszek P. Pathogenic infection and the oxidative defences in plant apoplast. Protoplasma 217 (2001) 20-32
21. Bagni N., and Torrigiani P. Polyamines: a new class of growth substances. In: Karssen C.M., van Loon L.C., and Vreugdenhil D. (Eds). Progress in plant growth regulation (1992), Kluwer Academic Publishers, Dordrecht 264-275
22. Galston A.W., and Kaur-Sawhney R. Polyamines as endogenous growth regulators. In: Davies P.J. (Ed). Plant hormones: physiology, biochemistry and molecular biology (1995), Kluwer Academic Publishers, Dordrecht 158-178
23. Liu H.P., Dong B.H., Zhang Y.Y., Liu Z.P., and Liu Y.L. Relationship between osmotic stress and the levels of free, conjugated and bound polyamines in leaves of wheat seedlings. Plant Sci. 166 (2004) 1261-1267
24. Li C.Z., and Wang G.X. Interactions between reactive oxygen species, ethylene and polyamines in leaves of Glycyrrhiza inflata seedlings under root osmotic stress. Plant Growth Regul. 42 (2004) 55-60
25. Aziz A., and Larher F. Changes in polyamine titers associated with the proline response and osmotic adjustment of rape leaf discs submitted to osmotic stress. Plant Sci. 112 (1996) 175-186
26. Tadesse W. Stability of grass pea (Lathyrus sativus L.) varieties for ODAP content and grain yield in Ethiopia. Lathyrus Lathyrism Newsletter 3 (2003) 32-34
27. Creelman R.A., Mason H.S., Bensen R.J., Boyer J.S., and Mullet J.E. Water deficit and abscisic acid cause differential inhibition of shoot versus root growth in soybean seedlings. Plant Physiol. 92 (1990) 205-214
28. Colorado P., Rodriguez A., Nicolas G., and Rodriguez D. Abscisic acid and stress regulate gene expression during germination of chick-pea seeds: possible role of calcium. Physiol. Plant 91 (1994) 461-467
29. Slocum R.D., Kaur-Sawhney R., and Galston A.W. The physiology and biochemistry of polyamines in plant. Arch. Biochem. Biophys. 235 (1984) 283-303
30. Borrell A., Carbonell L., Farras R., Puig-Parellada P., and Tiburcio A.F. Polyamines inhibited lipid peroxidation in senescing oat leaves. Physiol. Plant 99 (1997) 385-390
31. Guo F., and Tang X.H. Polyamines in rice embryo and endosperm during their development. Acta Phytophysiol. Sinica 16 (1990) 173-178 (In Chinese with English abstract)
32. Zhang J., Xing G.M., Yan Z.Y., and Li Z.X. β-N-oxalyl-l-α,β-diaminopropionic acid protects the activity of glycolate oxidase in Lathyrus sativus seedlings under high light. Rus. J. Plant Physiol. 50 (2003) 618-622
33. Zeevaart J.A.D., and Creelman R.A. Metabolism and physiology of abscisic acid. Annu. Rev. Plant Physiol. 39 (1988) 439-473
34. Jiang M.Y., and Zhang J.H. Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulation the activity of antioxidant enzymes in maize leaves. J. Exp. Bot. 53 (2002) 2401-2410
35. Islam M.A., Blake T.J., Kocacinar F., and Lada R. Ambiol, spermine, and aminoethoxyvinylglycine prevent water stress and protect membrances in Pinus strobes L. under drought. Trees (Berl.) 17 (2003) 278-284
36. Foyer C.H., Descourvieres P., and Kunert K.J. Protection against oxygen radicals: important defense mechanism studied in transgenic plants. Plant Cell Environ. 17 (1994) 507-523
37. Tiburcio A.F., Altabella T., Borrel T., and Masgrau C. Polyamines metabolism and its regulation. Physiol. Plant 100 (1997) 664-674
38. Benavides M.P., Gallego S.M., Comba M.E., and Tomaro M.L. Relationship between polyamines and paraquat toxicity in sunflower leaf discs. Plant Growth Regul. 31 (2000) 215-224
39. Tadolini B., Cabrini L., Landi L., Varani E., and Pasquali P. Polyamine binding to phospolipid vesicles and inhibition of lipid peroxidation. Biochem Biophys. Res. Com. 122 (1984) 550-555
40. Drolet G., Dumbroff E.B., Legge R.L., and Thompson J.E. Radical scavenging proterties of polyamines. Phytochem. 25 (1986) 367-371
41. Bors W., Langebartels C., Michel C., and Sandermann H. Polyamiens as readical scavengers and protectants against ozone damage. Phytochem. 28 (1989) 1589-1595
42. Mou J.M., and Pan R.P. The role of polyamines in biological synthesis of DNA. Prog. Biochem. Biophys. 16 (1989) 359-361 (in Chinese with English abstract)
43. Wang F., Chen X., Qian C., Qin X., and Li Z. Determination of Neurotoxin 3-N-oxalyl-2,3-diamino-propionic acid and nonprotein amino acids in Lathyrus sativus by PRECOLUMN derivatization with 1-fluoro-2,4-dinitrobenzene. J. Chromatogr. 883 (2000) 113-118
44. Flores H.E., and Galston A.W. Analysis of polyamines in higher plants by high performance liquid chromatography. Plant Physiol. 69 (1982) 701-706