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While focus in oil-producing microalgae is normally on nutrient deficiency, we addressed the seasonal variations of lipid content and composition in large-scale cultivation. Lipid content, fatty acid profiles and mono-di-and triglycerides (MAGs, DAGs, and TAGs) were analyzed during May 2007-May 2009 in Nannochloropsis oculata grown outdoors in closed vertical flat panels photobioreactors. Total lipids (TL) ranged from 11% of dry weight (DW) in winter to 30% of DW in autumn. 50% of the variation in TL could be explained by light and temperature. As the highest lipid content was recorded during autumn indicating an optimal, non-linear, response to light and temperature we hypothesize that enhanced thylakoid stacking under reduced light conditions resulted in more structural lipids, concomitantly with the increase in glycerides due to released photo-oxidative stress. The relative amount of monounsaturated fatty acids (MUFA) increased during autumn. This suggested a synthesis, either of structural fatty acids as MUFA, or a relative increase of C16:1 incorporated into TAGs and DAGs. Our results emphasize the significant role of environmental conditions governing lipid content and OPEN ACCESSEnergies 2012, 5 1578 composition in microalgae that have to be considered for correct estimation of algal oil yields in biodiesel production.

: Quinolones and a phosphatidyl glyceride were isolated from the sponge-associated bacterial strain Pseudomonas sp. Structures were elucidated by spectroscopic analysis and chemical transformations.

Total lipid and phospholipid recovery as well as amino acid quality and composition from cuttlefish (Sepia officinalis) and sardine (Sardina pilchardus) were compared. Enzymatic hydrolyses were performed using the three proteases Protamex, Alcalase, and Flavourzyme by the pH-stat method (24 h, pH 8, 50 degrees C). Three fractions were generated: an insoluble sludge, a soluble aqueous phase, and an oily phase. For each fraction, lipids, phospholipids, and proteins were quantified. Quantitative and qualitative analyses of the raw material and hydrolysates were performed. The degree of hydrolysis (DH) for cuttlefish viscera was 3.2% using Protamex, 6.8% using Flavourzyme, and 7% using Alcalase. DH for sardine viscera was 1.9% (using Flavourzyme), 3.1% (using Protamex) and 3.3% (using Alcalase). Dry matter yields of all hydrolysis reactions increased in the aqueous phases. Protein recovery following hydrolysis ranged from 57.2% to 64.3% for cuttlefish and 57.4% to 61.2% for sardine. Tissue disruption following protease treatment increased lipid extractability, leading to higher total lipid content after hydrolysis. At least 80% of the lipids quantified in the raw material were distributed in the liquid phases for both substrates. The hydrolysed lipids were richer in phospholipids than in the lipids extracted by classical chemical extraction, especially after Flavourzyme hydrolysis for cuttlefish and Alcalase hydrolysis for sardine. The total amino acid content differed according to the substrate and the enzyme used. However, regardless of the raw material or the protease used, hydrolysis increased the level of essential amino acids in the hydrolysates, thereby increasing their potential nutritional value for feed products.