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15S-Lipoxygenase metabolism in the marine diatom Pseudo-nitzschia delicatissima.
- Source :
- New Phytologist; Sep2009, Vol. 183 Issue 4, p1064-1071, 8p, 1 Diagram, 4 Graphs
- Publication Year :
- 2009
-
Abstract
- • In recent years, oxylipins (lipoxygenase-derived oxygenated fatty acid products) have been reported in several bloom-forming marine diatoms. Despite increasing attention on the ecophysiological role of these molecules in marine environments, their biosynthesis is largely unknown in these microalgae. • Biochemical methods, including tandem mass spectrometry, nuclear magnetic resonance and radioactive probes were used to identify structures, enzymatic activities and growth-dependent modulation of oxylipin biosynthesis in the pennate diatom Pseudo-nitzschia delicatissima. • Three major compounds, 15S-hydroxy-(5 Z,8 Z,11 Z,13 E,17 Z)-eicosapentaenoic acid (15S-HEPE), 15-oxo-5Z,9 E,11 E,13 E-pentadecatetraenoic acid and 13,14- threo-13 R-hydroxy-14 S,15 S- trans-epoxyeicosa-5 Z,8 Z,11 Z,17 Z-tetraenoic acid (13,14-HEpETE), were produced by three putative biochemical pathways triggered by eicosapentaenoic acid-dependent 15S lipoxygenase. Oxylipin production increases along the growth curve, with remarkable changes that precede the demise of the culture. At least one of the compounds, namely 15-oxoacid, is formed only in the stationary phase immediately before the collapse of the culture. • Synthesis and regulation of phyco-oxylipins seem to correspond to a signaling mechanism that governs adaptation of diatoms along the growth curve until bloom termination. Factors triggering the process are unknown but synthesis of 15-oxoacid, constrained within a time-window of a few days just before the collapse of the culture, implies the involvement of a physiological control not directly dependent on distress or death of diatom cells. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 0028646X
- Volume :
- 183
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- New Phytologist
- Publication Type :
- Academic Journal
- Accession number :
- 43609442
- Full Text :
- https://doi.org/10.1111/j.1469-8137.2009.02887.x