Abstract:
A method for culturing microorganism which produces EPA (eicosapentaenoic acid) is provided to ensure optical condition of culturing in culture temperature, stirring rate, and NaCl concentration. A method for culturing microorganism which produces EPA comprises: a first step of isolating a strain having EPA productivity; a second step of sub-culturing strain and cooling at 1~20°C; a third step of measuring and identifying EPA productivity of strain; and a fourth step of adding media at 1~50 °C and 10~300 rpm and culturing.
Abstract:
A composition of a feed for fish farming separated from liquid waste from mackerel processing capable of using a protein source as a substitute for fish meal is provided to replace the fish meal which is the protein source of the feed for fish farming. A composition of a feed for fish farming is separated from the mackerels processing waste water and includes the water-soluble protein usable as fish meal substitution protein. The mackerels processing waste water is the waste water coming from the mackerels processing plant. The water-soluble protein is separated from the mackerels processing waste water through isoelectric precipitation. The water-soluble protein is added so that it become 30 percent of the total fish meal. The mackerels comprises one or more mackerelses selected from the group of the Scomber japonicus and Scomber australasicus.
Abstract:
A method for culturing a microalgae using deep sea water is provided to dramatically increase the amount of the microalgae and shorten culture time. A method for culturing a microalgae using deep sea water comprises: a first step of preparing f/2 medium containing deep sea water; a second step of culturing in an Erlenmeyer flask at 1-2000 lux and 10-30°C for 1-15 days; and a third step of adding medium of the first step and adjusting the air amount (30 L/min) without carbon for 1-30 days. The deep sea water is from east sea. The microalgae is cyanophyceae, bacillariophyceae, or dinoflagellate.