Microalgae

CSIRO Marine Research logo

CSIRO Collection
of Living Microalgae
Strain Database
Methods for Culturing Microalgae
CSIRO Microalgae
Supply Service
Research
Biotechnology
Aquaculture
Environment
Contacts
Home
 

>CSIRO HOME

CSIRO microalgae research

research - biotechnology

Microalgae are a largely untapped reservoir of novel and valuable bioactive compounds. Current research includes investigating the production of fatty acids, pigments, vitamins and other bioactive compounds by microalgae. Industry applications include nutraceuticals, pharmaceuticals, aquaculture and agricultural applications.

Growth and biomass

Microalgae are grown using different culture systems to optimise growth and production of biomass and bioactive molecules. This is essential for applications in aquaculture and biotechnology. As part of a collaboration with University of Florence, photobioreactor technology is used to grow microalgae including novel strains.

Applications:

Omega 3 polyunsaturated fatty acids (PUFA)

Nutraceuticals: Docosahexaenoic acid [DHA, 22:6(n-3)] and eicosapentaeneoic acid [EPA, 20:5(n-3)] are essential polyunsaturated fatty acids (PUFA) in the human diet. These PUFA may reduce the risk of coronary heart disease and alleviate inflammatory diseases. Some microalgae and thraustochytrids are a rich source of these PUFA.

Pharmaceutical leads: DHA and other novel bioactive PUFA can be chemically modified by adding or changing functional groups within different regions in the molecule (combinatorial chemistry) in order to enhance/change the bioactivity and hence lead to the synthesis of new pharmaceuticals. Other unusual fatty acids are likely to be bioactive.

Aquaculture: Microalgae are used as essential live feeds and supplements in the aquaculture of larval and juvenile animals including oyster spat, juvenile abalone, finfish larvae and rotifer.

Other applications: Antimicrobials, antifungals, agrochemicals and cosmetics

Chemical screening of fatty acids and novel/unusual lipids:

Thin-layer chromotography with flame ionization detection (TLC-FID) of total lipid extracts is used to quantify lipid classes: polar lipid, triglycerides, sterols, free fatty acids, steryl esters and HBI.

Gas chromotography (GC) is used to quantify fatty acids, hydroxy fatty acids, sterols and hydrocarbons. While gas chromotography-mass spectrometry (GC-MS) is used for structural elucidation of PUFA using electron impact (EI) and chemical ionization (C) conditions of fatty acid methyl ester (FAME). Location of double bond positions is achieved by EI GC-MS of dimethyl oxazoline (DMOX).

Last updated 26/08/04

Last updated 19/03/09 | Legal Notice and Disclaimer | Copyright