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Screening and comparative metabolic profiling of high lipid content microalgae strains for application in wastewater treatment

•Micractinium sp. IC-76 has 36.29 ± 0.11% of lipids and 71.9% of SFA and MUFA.•The efficiency of N-NH4 and P-PO4 removal is 96.4 ± 0.7 and 77.8 ± 5.6%, respectively.•Strain IC-76 in the stationary phase has high intracellular concentration of sucrose.•Strain IC-76 has the highest content of metaboli...

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Bibliographic Details
Published in:Bioresource technology 2018-02, Vol.250, p.538-547
Main Authors: Piligaev, A.V., Sorokina, K.N., Shashkov, M.V., Parmon, V.N.
Format: Article
Language:English
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Summary:•Micractinium sp. IC-76 has 36.29 ± 0.11% of lipids and 71.9% of SFA and MUFA.•The efficiency of N-NH4 and P-PO4 removal is 96.4 ± 0.7 and 77.8 ± 5.6%, respectively.•Strain IC-76 in the stationary phase has high intracellular concentration of sucrose.•Strain IC-76 has the highest content of metabolites of carbohydrate metabolism.•Changes in major biochemical cycles are also associated with lipid accumulation. New strains of green microalgae were isolated and screened for growth and the production of lipids from municipal wastewater. It was shown that the strain Micractinium sp. IC-76 has a biomass productivity of 37.18 ± 4.12 mg L−1 d−1 and a lipid content of 36.29 ± 0.11%, with a total content of saturated and monounsaturated fatty acids of 71.9%. The efficiency of nitrogen (N-NH4) and phosphorus (P-PO4) removal was 96.4 ± 0.7 and 77.8 ± 5.6%, respectively. The metabolic differences at the exponential and stationary phases of growth between the closely related strains with different patterns of lipid accumulation were revealed via gas chromatography mass spectrometry metabolic profiling. The strain Micractinium sp. IC-76 in the stationary phase of growth shows a significant difference in carbohydrate metabolism, especially sucrose concentration. High lipid induction during cultivation in wastewater was also driven by changes in the biosynthesis of amino acids, fatty acids and the tricarboxylic acid cycle.
ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2017.11.063