“…The content of long-chain fatty acids in most seed oils and shoot tissues of edible plants is much lower than that observed in S. ambigua meal (Guil et al 1996, Dubois et al 1987, although it has been shown that plants from the Chenopodiaceae family (e.g. sugar beet, spinach) and salt-tolerant plants have a high content of C22 and C24 in their shoots and roots (Misra et al 1987, Imai et al 2004, Agoramoorthy et al 2007, Ivanova et al 2009). For example, the amount of behenic acid (C22:0) reported in shoots of S. europaea ranged from 1.2-2.5% (Guil et al 1996, Ivanova et al 2000, 2009 and for heneicosanoic acid (C21:1) reached up to 34.8% of the total lipids in Suaeda maritima leaves (Ivanova et al 2009).…”
Section: Methodsmentioning
confidence: 91%
“…The percentage of saturated lipids in S. ambigua meal is higher than that of vegetable oils with a MUFA nutritional profile (sensu Dubois et al 2007), presenting about 13.4 and 36.4% of total fatty acids, and including oils from rice, peanut, oat and Jatropha. S. ambigua meal saturated lipid values are also higher than those found in shoots of edible glycophytes, which have a value usually lower than 20% of the total lipids (Guil et al 1996), as follows: in fertile shoots of S. europaea (16.8-32.0%; Kulis et al 2010, Guil et al 1996, Ivanova et al 2009), in vegetative shoots of S. persica (20.7-21.4%) and S. fruticosa (22.3-25.0%) (Ventura et al 2011). Several authors highlighted the adaptive value for halophytes of high content of saturated lipids in decreased membrane permeability for Na + ions (Leach et al Ivanova et al 2000Ivanova et al , 2009, thus preventing the Na + intake into cells from the environment and also acting as osmotic barriers against the water loss and washing out of water-soluble nutrients and osmoregulators from the cytoplasm.…”
Section: Methodsmentioning
confidence: 99%
“…S. ambigua meal saturated lipid values are also higher than those found in shoots of edible glycophytes, which have a value usually lower than 20% of the total lipids (Guil et al 1996), as follows: in fertile shoots of S. europaea (16.8-32.0%; Kulis et al 2010, Guil et al 1996, Ivanova et al 2009), in vegetative shoots of S. persica (20.7-21.4%) and S. fruticosa (22.3-25.0%) (Ventura et al 2011). Several authors highlighted the adaptive value for halophytes of high content of saturated lipids in decreased membrane permeability for Na + ions (Leach et al Ivanova et al 2000Ivanova et al , 2009, thus preventing the Na + intake into cells from the environment and also acting as osmotic barriers against the water loss and washing out of water-soluble nutrients and osmoregulators from the cytoplasm. Additionally, high content of palmitic acid (56% of total fatty acids) in hexane leaf extract of the mangrove bush Excoecaria agallocha was related to antibacterial and antifungal activities observed against a total of 11 microorganisms (Agoramoorthy et al 2007).…”
Section: Methodsmentioning
confidence: 99%
“…The non-detection of linolenic-ω3 acid (18:3) Fifty six percent of the identified lipids in S. ambigua meal were saturated, and palmitic acid (C16:0) was the main fraction (19.8%). Part of this content comes from S. ambigua seeds that are rich in saturated fatty acids (D'Oca et al 2012), another significant part probably originated from C16:0 enriching phospholipids of cell membranes and glycerolipids of chloroplast membranes (Imai et al 2004, Ivanova et al 2009). The percentage of saturated lipids in S. ambigua meal is higher than that of vegetable oils with a MUFA nutritional profile (sensu Dubois et al 2007), presenting about 13.4 and 36.4% of total fatty acids, and including oils from rice, peanut, oat and Jatropha.…”
Section: Methodsmentioning
confidence: 99%
“…Sarcocornia perennis). Similar to their seeds, fatty acid composition of shoots of Salicornia and Sarcocornia species is dominated by polyunsaturated acids with 16 and 18 carbons, but a significant amount of saturated acids are also present (Imai et al 2004, Kulis et al 2010, Ventura et al 2011, and most of the lipids found in shoots are phospholipids (Ivanova et al 2000(Ivanova et al , 2009. EPAGRI (2008) reported the presence of β-sitosterol and stigmasterol in shoots of S. ambigua.…”
Sarcocornia ambigua is a perennial glasswort, native of South America and a potential new seed-oil crop and forage for direct irrigation with salt water. Small seeds develop inside fertile segments of its cylindrical leafless shoots and, at the harvest, seeds are typically mixed with remnant cellulose material difficult to separate. This work evaluated different extraction methods and the composition of total esterified fatty acids in a meal of ground fertile shoots of S. ambigua, seeking for an alternative primary matter and larger yield of total lipids. The highest lipid yield was obtained with a chloroform:methanol mixture (2:1)(v/v) (5.2% of dry weight). The most abundant polyunsaturated fatty acids in the meal were linoleic acid (C18:2; 21.4%) and oleic acid (C18:1; 18.3%). Fifty six percent of the lipids in S. ambigua meal were saturated and palmitic acid (C16:0) was the main fraction (19.8%). Long-chain fatty acids (≥ C20) represented 29.5% of the lipids. Most abundant long-chain fatty acids were behenic acid (C22:0; 7.1%), lignoceric acid (C24:0; 5.3%) and montanic acid (C28:0; 4.0%). The percentage of saturated lipids in S. ambigua meal was higher than that of vegetable oils with a MUFA nutritional profile and some of these lipids have known bioactive properties.
“…The content of long-chain fatty acids in most seed oils and shoot tissues of edible plants is much lower than that observed in S. ambigua meal (Guil et al 1996, Dubois et al 1987, although it has been shown that plants from the Chenopodiaceae family (e.g. sugar beet, spinach) and salt-tolerant plants have a high content of C22 and C24 in their shoots and roots (Misra et al 1987, Imai et al 2004, Agoramoorthy et al 2007, Ivanova et al 2009). For example, the amount of behenic acid (C22:0) reported in shoots of S. europaea ranged from 1.2-2.5% (Guil et al 1996, Ivanova et al 2000, 2009 and for heneicosanoic acid (C21:1) reached up to 34.8% of the total lipids in Suaeda maritima leaves (Ivanova et al 2009).…”
Section: Methodsmentioning
confidence: 91%
“…The percentage of saturated lipids in S. ambigua meal is higher than that of vegetable oils with a MUFA nutritional profile (sensu Dubois et al 2007), presenting about 13.4 and 36.4% of total fatty acids, and including oils from rice, peanut, oat and Jatropha. S. ambigua meal saturated lipid values are also higher than those found in shoots of edible glycophytes, which have a value usually lower than 20% of the total lipids (Guil et al 1996), as follows: in fertile shoots of S. europaea (16.8-32.0%; Kulis et al 2010, Guil et al 1996, Ivanova et al 2009), in vegetative shoots of S. persica (20.7-21.4%) and S. fruticosa (22.3-25.0%) (Ventura et al 2011). Several authors highlighted the adaptive value for halophytes of high content of saturated lipids in decreased membrane permeability for Na + ions (Leach et al Ivanova et al 2000Ivanova et al , 2009, thus preventing the Na + intake into cells from the environment and also acting as osmotic barriers against the water loss and washing out of water-soluble nutrients and osmoregulators from the cytoplasm.…”
Section: Methodsmentioning
confidence: 99%
“…S. ambigua meal saturated lipid values are also higher than those found in shoots of edible glycophytes, which have a value usually lower than 20% of the total lipids (Guil et al 1996), as follows: in fertile shoots of S. europaea (16.8-32.0%; Kulis et al 2010, Guil et al 1996, Ivanova et al 2009), in vegetative shoots of S. persica (20.7-21.4%) and S. fruticosa (22.3-25.0%) (Ventura et al 2011). Several authors highlighted the adaptive value for halophytes of high content of saturated lipids in decreased membrane permeability for Na + ions (Leach et al Ivanova et al 2000Ivanova et al , 2009, thus preventing the Na + intake into cells from the environment and also acting as osmotic barriers against the water loss and washing out of water-soluble nutrients and osmoregulators from the cytoplasm. Additionally, high content of palmitic acid (56% of total fatty acids) in hexane leaf extract of the mangrove bush Excoecaria agallocha was related to antibacterial and antifungal activities observed against a total of 11 microorganisms (Agoramoorthy et al 2007).…”
Section: Methodsmentioning
confidence: 99%
“…The non-detection of linolenic-ω3 acid (18:3) Fifty six percent of the identified lipids in S. ambigua meal were saturated, and palmitic acid (C16:0) was the main fraction (19.8%). Part of this content comes from S. ambigua seeds that are rich in saturated fatty acids (D'Oca et al 2012), another significant part probably originated from C16:0 enriching phospholipids of cell membranes and glycerolipids of chloroplast membranes (Imai et al 2004, Ivanova et al 2009). The percentage of saturated lipids in S. ambigua meal is higher than that of vegetable oils with a MUFA nutritional profile (sensu Dubois et al 2007), presenting about 13.4 and 36.4% of total fatty acids, and including oils from rice, peanut, oat and Jatropha.…”
Section: Methodsmentioning
confidence: 99%
“…Sarcocornia perennis). Similar to their seeds, fatty acid composition of shoots of Salicornia and Sarcocornia species is dominated by polyunsaturated acids with 16 and 18 carbons, but a significant amount of saturated acids are also present (Imai et al 2004, Kulis et al 2010, Ventura et al 2011, and most of the lipids found in shoots are phospholipids (Ivanova et al 2000(Ivanova et al , 2009. EPAGRI (2008) reported the presence of β-sitosterol and stigmasterol in shoots of S. ambigua.…”
Sarcocornia ambigua is a perennial glasswort, native of South America and a potential new seed-oil crop and forage for direct irrigation with salt water. Small seeds develop inside fertile segments of its cylindrical leafless shoots and, at the harvest, seeds are typically mixed with remnant cellulose material difficult to separate. This work evaluated different extraction methods and the composition of total esterified fatty acids in a meal of ground fertile shoots of S. ambigua, seeking for an alternative primary matter and larger yield of total lipids. The highest lipid yield was obtained with a chloroform:methanol mixture (2:1)(v/v) (5.2% of dry weight). The most abundant polyunsaturated fatty acids in the meal were linoleic acid (C18:2; 21.4%) and oleic acid (C18:1; 18.3%). Fifty six percent of the lipids in S. ambigua meal were saturated and palmitic acid (C16:0) was the main fraction (19.8%). Long-chain fatty acids (≥ C20) represented 29.5% of the lipids. Most abundant long-chain fatty acids were behenic acid (C22:0; 7.1%), lignoceric acid (C24:0; 5.3%) and montanic acid (C28:0; 4.0%). The percentage of saturated lipids in S. ambigua meal was higher than that of vegetable oils with a MUFA nutritional profile and some of these lipids have known bioactive properties.
Coastal wetlands are highly efficient ‘blue carbon’ sinks which contribute to mitigating climate change through the long-term removal of atmospheric CO2 and capture of carbon (C). Microorganisms are integral to C sequestration in blue carbon sediments and face a myriad of natural and anthropogenic pressures yet their adaptive responses are poorly understood. One such response in bacteria is the alteration of biomass lipids, specifically through the accumulation of polyhydroxyalkanoates (PHAs) and alteration of membrane phospholipid fatty acids (PLFA). PHAs are highly reduced bacterial storage polymers that increase bacterial fitness in changing environments. In this study, we investigated the distribution of microbial PHA, PLFA profiles, community structure and response to changes in sediment geochemistry along an elevation gradient from intertidal to vegetated supratidal sediments. We found highest PHA accumulation, monomer diversity and expression of lipid stress indices in elevated and vegetated sediments where C, nitrogen (N), PAH and heavy metals increased, and pH was significantly lower. This was accompanied by a reduction in bacterial diversity and a shift to higher abundances of microbial community members favouring complex C degradation. Results presented here describe a connection between bacterial PHA accumulation, membrane lipid adaptation, microbial community composition and polluted C rich sediments.
Graphical Abstract
Geochemical, microbiological and polyhydroxyalkanoate (PHA) gradient in a blue carbon zone.
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