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There has been growing interest in the use of microalgae for the production of biofuels, but production costs continue to be too high to compete with fossil fuel prices. One of the main limitations for photobioreactor productivity is light shielding, especially at high cell densities. The growth of the green microalga Chlorella sorokiniana, a robust industrial species, has been evaluated under different trophic conditions with traditional carbon sources, such as glucose and sucrose, and alternative low cost carbon sources, such as carob pod extract, industrial glycerol and acetate-rich oxidized wine waste lees. The mixotrophic cultivation of this microalga with wine waste lees alleviated the problems of light shielding observed in photoautotrophic cultures, improving specific growth rate (0.052 h-1) compared with the other organic sources. The fed-batch mixotrophic culture of Chlorella sorokiniana in a 2 L stirred tank reactor, with optimized nutritional conditions, 100 mM of acetate coming from the oxidized wine waste lees and 30 mM of ammonium, produced an algal biomass concentration of 11 gL-1 with a lipid content of 38% (w/w). This fed-batch strategy has been found to be a very effective means to enhance the biomass and neutral lipid productivity.

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The carotenoid biosynthesis pathway catalyses the synthesis of essential pigments that are crucial for light harvesting and photoprotection in photosynthetic organisms. It allows the production of several commercially important compounds and is the target of many herbicides. In the present work we studied the influence of light on the carotenoid composition and the expression of genes encoding the main steps of the pathway in the freshwater microalga Chlamydomonas reinhardtii. We observed that there is an activation of the xanthophyll cycle in response to high light, but also in response to other stress conditions, such as nitrogen starvation, which has not been reported previously. We analysed the expression level of (1) genes encoding the two first enzymes of the pathway, phytoene synthase and phytoene desaturase; (2) the enzymes responsible for the cyclization of lycopene, lycopene -cyclase and lycopene "-cyclase; (3) zeaxanthin epoxidase, which catalyses the epoxidation of zeaxanthin; and (4) the three known carotene hydroxylases, directly involved in the synthesis of xanthophylls from and -carotene. Measurements of carotenoid content in the presence of inhibitors of protein and carotenoid synthesis suggest that only one of the two possible routes for the synthesis of zeaxanthin upon transference to high light, either the de novo synthesis of carotenoids or the interconversion of violaxanthin and zeaxanthin, is dependent on protein synthesis. The high increase in the transcript levels of the cytochrome-dependent carotene -and "-hydroxylases in response to high light suggests an important role of these enzymes in regulation of xanthophyll synthesis upon light stress. These conclusions may be of high interest if efficient engineering of the pathway is to be accomplished.