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Estimation of Lipid Hydroperoxide Levels in Tropical Marine Macroalgae

  • Puja Kumari
  • , Ravindra Pal Singh
  • , A. J. Bijo
  • , C. R.K. Reddy
  • , Bhavanath Jha

Publikation: Article › Begutachtung

8 Zitate (Scopus)

Abstract

The incipient levels of lipid hydroperoxides (LHPOs) were determined in selected green, brown, and red macroalgae by the FOX assay using hydroperoxy HPLC mix. The LHPOs contents varied between the investigated species and showed relatively low values in this study. Among the greens, it varied from 12 ± 6.2 μg · g-1 (Codium sursum) to 31.5 ± 2.8 μg · g-1 (Ulva lactuca), whereas in reds, from 5.7 ± 1.6 μg · g-1 (Gracilaria corticata) to 46.2 ± 6 μg · g-1 (Sarconema filiforme), and in browns, from 4.6 ± 4.4 μg · g-1 (Dictyota bartayresiana) to 79 ± 5.0 μg · g-1 (Sargassum tenerrimum), on fresh weight basis. These hydroperoxides represented a minor fraction of total lipids and ranged from 0.04% (S. swartzii) to 1.1% (S. tenerrimum) despite being a rich source of highly unsaturated fatty acids. The susceptibility of peroxidation was assessed by specific lipid peroxidazibility (SLP) values for macroalgal tissues. The LHPO values were found to be independent of both the PUFAs contents and their degree of unsaturation (DBI), as evident from the PCA analysis. SLP values were positively correlated with the LHPOs and negatively with DBI. The FOX assay gave ≥20-fold higher values for LHPOs as compared to the TBARS method for all the samples investigated in this study. Furthermore, U. lactuca cultured in artificial seawater (ASW) enriched with nutrients (N, P, and NP) showed a sharp decline in LHPOs contents relative to those cultured in ASW alone P ≤ 0.05. It is inferred from this study that the FOX assay is an efficient, rapid, sensitive, and inexpensive technique for detecting the incipient lipid peroxidation in macroalgal tissues.
OriginalspracheEnglish
Seiten (von - bis)1362-1373
Seitenumfang12
FachzeitschriftJournal of Phycology
Jahrgang48
Ausgabenummer6
Frühes Online-Datum9 Aug. 2012
DOIs
PublikationsstatusPublished - 1 Dez. 2012

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