Palm Oil Mill Effluent for Lipid Production by the Diatom <i>Thalassiosira pseudonana</i>
Karthick Murugan Palanisamy,
Gaanty Pragas Maniam,
Ahmad Ziad Sulaiman,
Mohd Hasbi Ab. Rahim,
Natanamurugaraj Govindan,
Yusuf Chisti
Affiliations
Karthick Murugan Palanisamy
Algae Biotechnology Laboratory, Faculty of Industrial Sciences and Technology, Universiti Malaysia Pahang, Lebuhraya Tun Razak, Gambang, Kuantan 26300, Pahang, Malaysia
Gaanty Pragas Maniam
Algae Biotechnology Laboratory, Faculty of Industrial Sciences and Technology, Universiti Malaysia Pahang, Lebuhraya Tun Razak, Gambang, Kuantan 26300, Pahang, Malaysia
Ahmad Ziad Sulaiman
Faculty of Bioengineering and Technology, Universiti Malaysia Kelantan, Jeli 17600, Kelantan, Malaysia
Mohd Hasbi Ab. Rahim
Algae Biotechnology Laboratory, Faculty of Industrial Sciences and Technology, Universiti Malaysia Pahang, Lebuhraya Tun Razak, Gambang, Kuantan 26300, Pahang, Malaysia
Natanamurugaraj Govindan
Algae Biotechnology Laboratory, Faculty of Industrial Sciences and Technology, Universiti Malaysia Pahang, Lebuhraya Tun Razak, Gambang, Kuantan 26300, Pahang, Malaysia
Yusuf Chisti
School of Engineering, Massey University, Private Bag 11 222, Palmerston North 4442, New Zealand
Biomass and lipid production by the marine centric diatom Thalassiosira pseudonana were characterized in media based on palm oil mill effluent (POME) as a source of key nutrients. The optimal medium comprised 20% by volume POME, 80 µM Na2SiO3, and 35 g NaCl L−1 in water at pH ~7.7. In 15-day batch cultures (16:8 h/h light–dark cycle; 200 µmol photons m−2 s−1, 26 ± 1 °C) bubbled continuously with air mixed with CO2 (2.5% by vol), the peak concentration of dry biomass was 869 ± 14 mg L−1 corresponding to a productivity of ~58 mg L−1 day−1. The neutral lipid content of the biomass was 46.2 ± 1.1% by dry weight. The main components of the esterified lipids were palmitoleic acid methyl ester (31.6% w/w) and myristic acid methyl ester (16.8% w/w). The final biomass concentration and the lipid content were affected by the light–dark cycle. Continuous (24 h light) illumination at the above-specified irradiance reduced biomass productivity to ~54 mg L−1 day−1 and lipid content to 38.1%.