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The brown seaweed Ectocarpus siliculosus is an emerging model species distributed worldwide in temperate coastal ecosystems. Over 1500 strains of E. siliculosus are available in culture from a broad range of geographic locations and ecological niches. To elucidate the molecular mechanisms underlying its capacity to cope with different environmental and biotic stressors, genomic and transcriptomic studies are necessary; this requires the co-isolation of genomic DNA and total RNA. In brown algae, extraction of nucleic acids is hindered by high concentrations of secondary metabolites that co-precipitate with nucleic acids. Here, we propose a reliable, rapid and cost-effective procedure for the co-isolation of high-quality nucleic acids using small quantities of biomass (25-, 50- and 100 mg) from strains of E. siliculosus (RHO12; LIA4A; EC524 and REP10-11) isolated from sites with different environmental conditions. The procedure employs a high pH extraction buffer (pH 9.5) which contains 100 mM Tris-HCl and 150 mM NaCl, with the addition of 5 mM DTT and 1% sarkosyl to ensure maximum solubility of nucleic acids, effective inhibition of nuclease activity and removal of interfering contaminants (e.g. polysaccharides, polyphenols). The use of sodium acetate together with isopropanol shortened precipitation time and enhanced the yields of DNA/RNA. A phenol:chlorophorm:isoamyl alcohol step was subsequently used to purify the nucleic acids. The present protocol produces high yields of nucleic acids from only 25 mg of fresh algal biomass (0.195 and 0.284 µg mg(-1) fresh weigh of RNA and DNA, respectively) and the high quality of the extracted nucleic acids was confirmed through spectrophotometric and electrophoretic analyses. The isolated RNA can be used directly in downstream applications such as RT-PCR and the genomic DNA was suitable for PCR, producing reliable restriction enzyme digestion patterns. Co-isolation of DNA/RNA from different strains indicates that this method is likely to have wider applications for intra- and inter-specific studies on other brown algae.

The present study describes a simple process for recovering a stream of products sequentially including bioethanol from the fresh biomass of the red seaweed Gracilaria corticata. From processing of 100 g fresh biomass (~12.2 g dry), 166 ± 3 µg/g R-phycoerytrin, 126 ± 4 µg/g R-phycocyanin can be realized on fresh weight basis, and 1.41 ± 0.03% crude lipid, 22.45 ± 0.53% agar, 12.39 ± 0.85% soil conditioner, 2.89 ± 0.04% bioethanol on dry weight basis along with 318 ± 3 ml of mineral rich liquid with possible fertilizer applications. The advantages of this process are complete utilization of feedstock without compromising the yield and quality of products, reusability of solvents and no solid waste. Further, the products recovered from one ton fresh biomass were found to have an estimated market value of USD 1051 while processing cost including raw material as 241 USD, a fourfold value addition of feedstock.

Algae, as a feedstock with minimum land footprint, is considered a promising biomass for sustainable fuels, chemicals, and materials. Unlike lignocellulosic biomass, algae consist mainly of lipids, carbohydrates, and proteins. This review focusses on the bio-oil and biochar co-products of algae-pyrolysis and presents the current state-of-the-art in the pyrolysis technologies and key applications of algal biochar. Algal biochar holds potential to be a cost-effective fertilizer, as it has high P, N and other nutrient contents. Beyond soil applications, algae-derived biochar has many other applications, such as wastewater-treatment, due to its porous structure and strong ion-exchange capacity. High specific capacitance and stability also make algal biochar a potential supercapacitor material. Furthermore, algal biochar can be great catalysts (or catalyst supports). This review sheds light on a wide range of algae-pyrolysis related topics, including advanced-pyrolysis techniques and the potential biochar applications in soil amendment, energy storage, catalysts, chemical industries, and wastewater-treatment plants.

A culture system for the edible, red seaweed, Gracilaria parÕispora Abbott long ogo , was Ž . developed in Hawaii that utilized a hatchery to produce tetrasporophyte and gametophyte life stages of the seaweed, reef growout of sporelings to harvest size adults, and multiplication of the harvested thalli in floating cages prior to sale. A central cooperative operated the hatchery and floating cages, and marketed the product. Sporelings from the hatchery were distributed to coastal residents who established patches of seaweed on the reef and sold their harvest to the cooperative. Mean relative growth rate of seaweed in the cages over 52 weeks was 2.64% dy1 and productivity y2 y1 was 14.8 g m d dry weight , within the range of intensive culture systems. Cage cultures Ž . were not sensitive to water motion over the range of 4–14 cm sy1 but growth and productivity tended to be higher in summer and spring than in winter. The culture system potentially overcomes problems that have hindered development of a sustainable supply of this species: low availability of wild stocks due to overharvesting; low productivity of spore cultures; and deterioration of vegetative cultures over time. Some of the elements may be applicable to other areas where wild stocks of Gracilaria have been overharvested.