2014
DOI: 10.1007/s10811-014-0381-8
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Metabolic profile of the brown macroalga Sargassum cymosum (Phaeophyceae, Fucales) under laboratory UV radiation and salinity conditions

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Cited by 18 publications
(24 citation statements)
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“…Due to tidal exposure, intertidal macroalgae are constantly exposed to fluctuating environmental stresses such as high temperature, desiccation and high radiation levels (PAR and UV radiation) (Sampath-Wiley et al 2008) that could easily lead to the formation and accumulation of free radicals and reactive species, triggering oxidative stress. Photobiological studies in macroalgae indicate diverse physiological disturbances in response to UV radiation, including alterations in growth and development (Altamirano et al 2003, Gao and Xu 2008, Navarro et al 2016, pigment degradation (Heo and Jeon 2009), dynamic or chronic photoinhibition of photosynthesis (Barufi et al 2011, Ayres-Ostrock and Plastino 2014, Figueroa et al 2014, protein and DNA damage (Buma et al 2001, Kumar et al 2004, decrease in lipid/fatty acid content (Khotimchenko andYakovleva 2005, Liang et al 2006), inhibition of enzyme activity (Lee and Shiu 2009), alterations in polyamines content (Polo et al 2014b), and modifications in cellular organization and ultrastructure (Holzinger and Lütz 2006, Polo et al 2014a, Schmidt et al 2015. As a photoprotective mechanism against UV radiation, especially UVB, macroalgae can increase the production of UV-absorbing compounds such as mycosporine-like amino acids, phenolic compounds and carotenoids, which play protective roles by mitigating the damage caused by the increase in reactive species (Ruhland et al 2007), therefore giving advantages that enable macroalgae to survive in the presence of UV radiation.…”
Section: Introductionmentioning
confidence: 99%
“…Due to tidal exposure, intertidal macroalgae are constantly exposed to fluctuating environmental stresses such as high temperature, desiccation and high radiation levels (PAR and UV radiation) (Sampath-Wiley et al 2008) that could easily lead to the formation and accumulation of free radicals and reactive species, triggering oxidative stress. Photobiological studies in macroalgae indicate diverse physiological disturbances in response to UV radiation, including alterations in growth and development (Altamirano et al 2003, Gao and Xu 2008, Navarro et al 2016, pigment degradation (Heo and Jeon 2009), dynamic or chronic photoinhibition of photosynthesis (Barufi et al 2011, Ayres-Ostrock and Plastino 2014, Figueroa et al 2014, protein and DNA damage (Buma et al 2001, Kumar et al 2004, decrease in lipid/fatty acid content (Khotimchenko andYakovleva 2005, Liang et al 2006), inhibition of enzyme activity (Lee and Shiu 2009), alterations in polyamines content (Polo et al 2014b), and modifications in cellular organization and ultrastructure (Holzinger and Lütz 2006, Polo et al 2014a, Schmidt et al 2015. As a photoprotective mechanism against UV radiation, especially UVB, macroalgae can increase the production of UV-absorbing compounds such as mycosporine-like amino acids, phenolic compounds and carotenoids, which play protective roles by mitigating the damage caused by the increase in reactive species (Ruhland et al 2007), therefore giving advantages that enable macroalgae to survive in the presence of UV radiation.…”
Section: Introductionmentioning
confidence: 99%
“…Under a combined stress of varying salinity and increased UV radiation the brown algae Sargassum cymosum , like the above‐mentioned red alga Grateloupia doryphora, displayed greater tolerance to salinity than to UV stress (Polo et al. ). Interestingly, decreasing free PUT and SPD levels were reported, compared to the generally reported increase in these PAs.…”
Section: Functions Of Polyaminesmentioning
confidence: 99%
“…This may account for the alga's ability to acclimatize to moderate saline stress (Garc ıa-Jim enez et al 2007) as lipid peroxidation, inhibition of ethylene synthesis and proteolytic attack can be prevented by PAs binding to thylakoid membranes in higher plants (Besford et al 1993). Under a combined stress of varying salinity and increased UV radiation the brown algae Sargassum cymosum, like the abovementioned red alga Grateloupia doryphora, displayed greater tolerance to salinity than to UV stress (Polo et al 2014). Interestingly, decreasing free PUT and SPD levels were reported, compared to the generally reported increase in these PAs.…”
Section: Functions Of Polyaminesmentioning
confidence: 99%
“…These secondary metabolites have been analysed in marine plants using a targeted metabolite approach with a RP-HPLC based system coupled with fluorescence detection after derivatization of plant crude extract with either dansylchloride or benzoylchloride [36,123]. In marine plants, the function of PAs has been examined in cell division, maturation of reproductive structures and callus induction [124]; however, their function as stress alleviators against salinity, desiccation stress and metal toxicity has only recently been recognized [34][35][36]123,[125][126][127][128]. For example, a hyposaline shock to Grateloupia turuturu has been shown to accumulate free Put, Spd and Spm together with a significant decrease in transglutaminase activity and an increase in arginine-dependent PA synthesis [125].…”
mentioning
confidence: 99%
“…The red seaweed Pyropia cinnamomea compensates for UV stress by increasing PA levels, especially bound-soluble and bound-insoluble PAs via the arginine-dependent PA synthesis pathway [123]. Similarly, the higher ratio of Put/Spd, together with a high level of phenolics in Sargassum cymosum when exposed to UVA + UVB radiation suggests that their binding to phenolic molecules results in stabilising the primary cell wall by cross-linking it to cellular components such as polysaccharide-bound phenols [128]. Further, accumulation of GABA possibly from Put degradation via diamine and/or polyamine oxidase activities (DAO and/or PAO) during hypersalinity stress in E. siliculosus has also been documented (Fig.…”
mentioning
confidence: 99%