The combination of uridine and nitrogen-deprivation promotes the efficient formation of astaxanthin-rich motile cells in Haematococcus pluvialis

In this study, the energy balance of two microalgae-to-biofuel concepts, one via a so called "dry route" (oil extraction from dried algae) and one via a "wet route" (oil extraction in the water phase), are assessed. Both routes are intended to convert the chemical energy contained in the microalgae into high-value biofuels with minimal fossil energy consumption. The analysis shows that the drying process in the dry route and the oil extraction process in the wet route consume a significant amount of energy. By coupling waste heat from a nearby power plant to the process, the energy balance can be improved and a potential fossil energy ratio (FER) up to 2.38 and 1.82 can be reached for the dry and wet route, respectively. The results indicate that based on current available technologies, the dry route has higher FER and the wet route has more potential in producing high valuable biofuels. Copyright © 2011 Elsevier Ltd. All rights reserved.

Summary The green alga Chlamydomonas reinhardtii does not synthesize high‐value ketocarotenoids like canthaxanthin and astaxanthin; however, a β‐carotene ketolase (CrBKT) can be found in its genome. CrBKT is poorly expressed, contains a long C‐terminal extension not found in homologues and likely represents a pseudogene in this alga. Here, we used synthetic redesign of this gene to enable its constitutive overexpression from the nuclear genome of C. reinhardtii. Overexpression of the optimized CrBKT extended native carotenoid biosynthesis to generate ketocarotenoids in the algal host causing noticeable changes the green algal colour to reddish‐brown. We found that up to 50% of native carotenoids could be converted into astaxanthin and more than 70% into other ketocarotenoids by robust CrBKT overexpression. Modification of the carotenoid metabolism did not impair growth or biomass productivity of C. reinhardtii, even at high light intensities. Under different growth conditions, the best performing CrBKT overexpression strain was found to reach ketocarotenoid productivities up to 4.3 mg/L/day. Astaxanthin productivity in engineered C. reinhardtii shown here might be competitive with that reported for Haematococcus lacustris (formerly pluvialis) which is currently the main organism cultivated for industrial astaxanthin production. In addition, the extractability and bio‐accessibility of these pigments were much higher in cell wall‐deficient C. reinhardtii than the resting cysts of H. lacustris. Engineered C. reinhardtii strains could thus be a promising alternative to natural astaxanthin producing algal strains and may open the possibility of other tailor‐made pigments from this host.