<i>Macrocystis pyrifera</i> Extract Residual as Nutrient Source for the Production of Sophorolipids Compounds by Marine Yeast <i>Rhodotorula rubra</i>
Allison Leyton,
Michael Araya,
Fadia Tala,
Liset Flores,
María Elena Lienqueo,
Carolina Shene
Affiliations
Allison Leyton
Center for Biotechnology and Bioengineering (CeBiB), Center of Food Biotechnology and Bioseparations, BIOREN and Department of Chemical Engineering, Universidad de La Frontera, Francisco Salazar 01145, Temuco 4780000, Chile
Michael Araya
Centro de Investigación y Desarrollo Tecnológico de Algas y otros Recursos Biológicos (CIDTA), Facultad de Ciencias Marinas, Universidad Católica del Norte, Coquimbo 17811421, Chile
Fadia Tala
Centro de Investigación y Desarrollo Tecnológico de Algas y otros Recursos Biológicos (CIDTA), Facultad de Ciencias Marinas, Universidad Católica del Norte, Coquimbo 17811421, Chile
Liset Flores
Center for Biotechnology and Bioengineering (CeBiB), Center of Food Biotechnology and Bioseparations, BIOREN and Department of Chemical Engineering, Universidad de La Frontera, Francisco Salazar 01145, Temuco 4780000, Chile
María Elena Lienqueo
Center for Biotechnology and Bioengineering (CeBiB), Department of Chemical Engineering, Biotechnology and Materials, Universidad de Chile, Beauchef 851, Santiago 8370459, Chile
Carolina Shene
Center for Biotechnology and Bioengineering (CeBiB), Center of Food Biotechnology and Bioseparations, BIOREN and Department of Chemical Engineering, Universidad de La Frontera, Francisco Salazar 01145, Temuco 4780000, Chile
Seaweed processing generates liquid fraction residual that could be used as a low-cost nutrient source for microbial production of metabolites. The Rhodotorula strain is able to produce antimicrobial compounds known as sophorolipids. Our aim was to evaluate sophorolipid production, with antibacterial activity, by marine Rhodotorula rubra using liquid fraction residual (LFR) from the brown seaweed Macrocystis pyrifera as the nutrient source. LFR having a composition of 32% w/w carbohydrate, 1% w/w lipids, 15% w/w protein and 52% w/w ash. The best culture condition for sophorolipid production was LFR 40% v/v, without yeast extract, artificial seawater 80% v/v at 15 °C by 3 growth days, with the antibacterial activity of 24.4 ± 3.1 % on Escherichia coli and 21.1 ± 3.8 % on Staphylococcus aureus. It was possible to identify mono-acetylated acidic and methyl ester acidic sophorolipid. These compounds possess potential as pathogen controllers for application in the food industry.