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Oxygenic photosynthetic organisms use solar energy to split water (H2O) into protons (H+), electrons (e-), and oxygen. A select group of photosynthetic microorganisms, including the green alga Chlamydomonas reinhardtii, has evolved the additional ability to redirect the derived H+ and e- to drive hydrogen (H2) production via the chloroplast hydrogenases HydA1 and A2 (H2 ase). This process occurs under anaerobic conditions and provides a biological basis for solar-driven H2 production. However, its relatively poor yield is a major limitation for the economic viability of this process. To improve H2 production in Chlamydomonas, we have developed a new approach to increase H+ and e- supply to the hydrogenases. In a first step, mutants blocked in the state 1 transition were selected. These mutants are inhibited in cyclic e- transfer around photosystem I, eliminating possible competition for e- with H2ase. Selected strains were further screened for increased H2 production rates, leading to the isolation of Stm6. This strain has a modified respiratory metabolism, providing it with two additional important properties as follows: large starch reserves (i.e. enhanced substrate availability), and a low dissolved O2 concentration (40% of the wild type (WT)), resulting in reduced inhibition of H2ase activation. The H2 production rates of Stm6 were 5-13 times that of the control WT strain over a range of conditions (light intensity, culture time, +/- uncoupler). Typically, approximately 540 ml of H2 liter(-1) culture (up to 98% pure) were produced over a 10-14-day period at a maximal rate of 4 ml h(-1) (efficiency = approximately 5 times the WT). Stm6 therefore represents an important step toward the development of future solar-powered H2 production systems.

With increasing concerns about the world’s crude oil consumption, alternative fuels based on renewable resources attract more and more attention. Microalgae have been proposed to be one of the most sustainable feedstocks for the production of lipid-based biodiesel. Naturally occurring, high-lipid producing microalgae strains can be domesticated and further genetically improved in order to redirect metabolite fluxes towards increased lipid contents. This review summarizes the current knowledge about metabolic engineering of microalgae in order to increase the cellular lipid content, with an emphasis on triacylglycerols for the production of biofuels. Additionally, it outlines the contribution of systems biology and genome-scale metabolic pathway modeling, as well as their potential impact in the future.

Net carbon sinks capable of avoiding dangerous perturbation of the climate system and preventing ocean acidification have been identified, but they are likely to be limited by resource constraints (Nature 463:747-756, 2010). Land scarcity already creates tension between food security and bioenergy production, and this competition is likely to intensify as populations and the effects of climate change expand. Despite research into microalgae as a next-generation energy source, the land-sparing consequences of alternative sources of livestock feed have been overlooked. Here we use the FeliX model to quantify emissions pathways when microalgae is used as a feedstock to free up to 2 billion hectares of land currently used for pasture and feed crops. Forest plantations established on these areas can conceivably meet 50 % of global primary energy demand, resulting in emissions mitigation from the energy and LULUC sectors of up to 544 [Formula: see text] 107 PgC by 2100. Further emissions reductions from carbon capture and sequestration (CCS) technology can reduce global atmospheric carbon concentrations close to preindustrial levels by the end of the present century. Though previously thought unattainable, carbon sinks and climate change mitigation of this magnitude are well within the bounds of technological feasibility.

Rapid induction of lipid accumulation in microalgae is an important prerequisite towards the use of microalgae as a feedstock for biodiesel production. In this study, we present a novel approach to induce lipids in Chlorella sp. within 24 h by short-term UV-C radiation (UVR) stress at different energy intensities ranging from 0 to 1000 mJ/cm2. Increase in the lipid fluorescence was measured by Nile red staining and fluorescence-activated cell sorting analysis followed by gas chromatography-mass spectrometry. Lipid fluorescence was significantly increased in cultures radiated at or above 250 mJ/cm2 compared to the mock-treated control cultures. Lower dosages at 100 and 250 mJ/cm2 led to a near doubling of total fatty acids, with a significant increase in unsaturated fatty acids and also most saturated fatty acids. This study provides a protocol for rapid lipid induction of microalgal cells by UV-C and the possible impact of UV-C radiation on fatty acid metabolism.

Mutagenesis and selection of microalgae can be used for accelerated breeding of elite strains, providing a significant advantage over genetic engineering as prior biochemical and genetic information is not required. Ultraviolet (UV)-C-induced mutagenesis combined with fluorescence-activated cell sorting (FACS) and microtiter plate reader cell density screening was used to produce Tetraselmis suecica strains with increased lipid contents without compromising on cell growth. After five rounds of mutation-selection, two dosages of UV-C (50 and >98 % lethality) yielded two improved strains (M5 and M24) that produced significantly more neutral lipids (increases of 114 and 123 %, respectively). This study highlights that repeated UV-C mutagenesis and high-throughput selection for cell growth can be a viable combined approach to improve lipid productivity in microalgae. These maybe used as elite strains for future breeding programs and as potential feedstock for biodiesel production.