Possible Involvement of Lipid Peroxidation in Cooled Tulip Bulbs

Lipid peroxides and their conversion products are active in various physiological processes in growth and development. Physiological role of lipid metabolism in dormancy and dormancy release in tulip bulbs is unknown. We found in tulip leaves high level of free and bound C18:3 and C18:2 acids and small amounts of C18:1, C18:0, C16:1, C16:0, C14:0, C12:0 acids. In our studies the level of lipid peroxides was determined in leaves, anthers and basal plate of uncooled and cooled tulip bulbs ‘Apeldoorn’ as a concentration of MDA, using a modified thiobarbituric acid–malondialdehyde (TBA–MDA) assay. The MDA level was lower in anthers than in leaves and basal plate. During 8 weeks of bulbs storage no changes in lipid peroxidation levels were found, with the exception of 3 rd leaf at which a decrease was noted. After 8 weeks of bulbs storage, lipid peroxidation increased in all samples. However, there were no differences in MDA levels between samples from uncooled and cooled bulbs. It seems that in tulip bulbs lipid peroxidation was independent to temperature of bulbs storage. These results indicated that lipid peroxidation is probable not involved in dormancy and dormancy release in tulip bulbs.

[1]  H. Rogers,et al.  Characterization of a Novel Lipoxygenase-Independent Senescence Mechanism in Alstroemeria peruviana Floral Tissue1 , 2002, Plant Physiology.

[2]  C. Wasternack,et al.  Lipoxygenase-dependent degradation of storage lipids. , 2001, Trends in plant science.

[3]  D. Hannapel,et al.  Lipoxygenase Is Involved in the Control of Potato Tuber Development , 2001, Plant Cell.

[4]  M. Hamberg,et al.  The lipoxygenase pathway in tulip (Tulipa gesneriana): detection of the ketol route. , 2000, The Biochemical journal.

[5]  A. Fischer,et al.  Protein dynamics, activity and cellular localization of soybean lipoxygenases indicate distinct functional roles for individual isoforms. , 1999, The Plant journal : for cell and molecular biology.

[6]  C. Forney,et al.  Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds , 1999, Planta.

[7]  M. Esquerré-Tugayé,et al.  The incompatible interaction between Phytophthora parasitica var. nicotianae race 0 and tobacco is suppressed in transgenic plants expressing antisense lipoxygenase sequences. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[8]  R. Creelman,et al.  BIOSYNTHESIS AND ACTION OF JASMONATES IN PLANTS. , 1997, Annual review of plant physiology and plant molecular biology.

[9]  A. Handa,et al.  Molecular Cloning of a Ripening-Specific Lipoxygenase and Its Expression during Wild-Type and Mutant Tomato Fruit Development , 1997, Plant physiology.

[10]  M. Rickauer,et al.  Lipoxygenase Gene Expression in the Tobacco-Phytophthora parasitica nicotianae Interaction , 1996, Plant physiology.

[11]  J. Browse,et al.  Intracellular Levels of Free Linolenic and Linoleic Acids Increase in Tomato Leaves in Response to Wounding , 1996, Plant physiology.

[12]  R. Van der Hoeven,et al.  Visualization of differential gene expression using a novel method of RNA fingerprinting based on AFLP: analysis of gene expression during potato tuber development. , 1996, The Plant journal : for cell and molecular biology.

[13]  D. M. Saravitz,et al.  The Differential Expression of Wound-Inducible Lipoxygenase Genes in Soybean Leaves , 1996, Plant physiology.

[14]  M. Melan,et al.  The LOX1 Gene of Arabidopsis Is Temporally and Spatially Regulated in Germinating Seedlings , 1994, Plant physiology.

[15]  F. Rook,et al.  Carbohydrate Status of Tulip Bulbs during Cold-Induced Flower Stalk Elongation and Flowering , 1994, Plant physiology.

[16]  C. Kollöffel,et al.  Soluble and insoluble invertase activity in elongating Tulipa gesneriana flower stalks , 1993 .

[17]  J. Franssen,et al.  CHALCONES: A POSSIBLE PARAMETER TO TEST THE COLD DURATION OF TULIP (TULIPA GESNERIANA CV. APELDOORN) BULBS? , 1992 .

[18]  L. Plas,et al.  Use of polarized fluorescence spectroscopy to measure fluidity of mitochondrial membranes from cold-treated tulip bulbs. , 1992 .

[19]  C. Kollöffel,et al.  CHANGES IN FREE POLYAMINE CONTENTS IN TULIP BULBS CV.APELDOORN DURING DRY STORAGE , 1992 .

[20]  C. Kollöffel,et al.  Temperature dependent redistribution of organic nitrogen during ‘dry' storage of tulip bulbs cv. Apeldoorn , 1992 .

[21]  E. Farmer,et al.  Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors. , 1992, The Plant cell.

[22]  J. Siedow PLANT LIPOXYGENASE: STRUCTURE AND FUNCTION , 1991 .

[23]  N. Gorin,et al.  Further studies on the use of free amino acids in anthers from tulip bulbs cultivar 'Apeldoorn' as indicators about cold treatment at 5°C. , 1990 .

[24]  N. Gorin,et al.  Changes in the contents of four free amino acids in anthers from tulip bulbs cultivar ‘Apeldoorn’, stored at 5 or 17°C, as criteria related to cold treatment , 1989 .

[25]  P. Reddanna,et al.  Isolation and characterization of 5-lipoxygenase from tulip bulbs. , 1988, Biochemical and biophysical research communications.

[26]  T. Ohyama,et al.  Effect of cold storage treatment for forcing bulbs on the C and N metabolism of tulip plants , 1988 .

[27]  G. Grevers,et al.  Criteria related to precooling of tulip bulbs cv.Apeldoorn at 5°c , 1986 .

[28]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[29]  N. Gorin,et al.  Starch content of freeze-dried anthers and α-amylase activity of their extracts as criteria that dry-stored bulbs (Tulipa gesneriana, L.) cultivar ‘Apeldoorn’ have been exposed to 5°C , 1985 .

[30]  L. D. Metcalfe,et al.  Rapid Preparation of Fatty Acid Esters from Lipids for Gas Chromatographic Analysis. , 1966 .