Carbon nanotubes (CNTs), α-Fe₂O₃ nanoparticles (nano Fe₂O₃) and MgO nanoparticles (nano MgO) were evaluated for the effects on algae growth and lipid production. Nano Fe₂O₃ promoted cell growth in the range of 0–20 mg·L⁻¹. CNTs, nano Fe₂O₃ and nano MgO inhibited cell growth of Scenedesmus obliquus at 10, 40 and 0.8 mg·L⁻¹ respectively. Neutral lipid and total lipid content increased with the increasing concentration of all tested nanoparticles. The maximum lipid productivity of cultures exposed to CNTs, nano Fe₂O₃ and nano MgO was observed at 5 mg·L⁻¹, 5 mg·L⁻¹ and 40 mg·L⁻¹, with the improvement by 8.9%, 39.6% and 18.5%. High dose exposure to nanoparticles limited increase in lipid productivity, possibly due to the repression on cell growth caused by nanoparticles-catalyzed reactive oxygen species (ROS) generation, finally leading to reduction in biomass and lipid production. Reduced accumulation of fatty acids of C18:3n3, C18:3n6 and C20:2 was observed in cells exposed to nanoparticles.

Microalgae cultivation on tannery wastewater (TWW) has been examined in some studies as a possible biological application to reduce contamination load and discharge effluents safely. However, Growth aspects, different tolerate strains and enriching the medium were not well investigated. In our study we applied Scenedesmus sp., Chlorella variabilis and Chlorella sorokiniana with different TWW concentrations. C. sorokiniana and C. variabilis cell density, chlorophyll, and sugar content grew substantially as compared to control. C.sorokiniana biomass and total lipids folded three and two times in 25% and 40% TWW, respectively as compared to control. Scenedesmus sp. showed longer lag phase and lower performance compared to the other two strains. Kelp waste extract (KWE) was added to balance the nutrients supply for C. sorokiniana, of which growth and effluents indicators were then greatly promoted in all concentrations. As the lag phase was shortened from 8 to 4 days in 60% concentration, subsequently, chlorophyll, carbohydrates, biomass and total lipids appreciated by 184%, 400%, 162% and 135%, respectively. Furthermore, the COD and ammonium removals improved by 51% and 45%, respectively. These outcomes emphasize the suitability of using TWW for microalgae cultivation with the suitable concentration while adding kelp waste extract for further enhancement.

The arctic strain of Chlorella sp. (Chlorella-Arc) exists in the coldest and driest arctic ecosystems, and it is a new resource of active polysaccharides. The extraction of crude polysaccharide from Chlorella-Arc was optimized using the response surface methodology. A crude polysaccharide yield of approximately 9.62 ± 0.11% dry weight was obtained under these optimized conditions. Three fractions (P-I, P-II, and P-III) were present after purification by 2-diethylaminoethanol Sepharose Fast Flow and Sephadex G-100 chromatography. The P-IIa fraction demonstrated significant antioxidant activities. Moreover, P-IIa was an α- and β-type heteropolysaccharide with a pyran group and contained variable amounts of rhamnose, arabinose, glucose, and galactose based on fourier-transform infrared spectroscopy, high-performance liquid chromatography, and ¹H and ¹³C nuclear magnetic resonance imaging. Production of high amounts of polysaccharide may allow further exploration of the microalgae Chlorella-Arc as a natural antioxidant.

Microalgae identification is extremely difficult. The efficiency of DNA barcoding in microalgae identification involves ideal gene markers and approaches employed, which however, is still under the way. Although Scenedesmus has obtained much research in producing lipids its identification is difficult. Here we present a comprehensive coalescent, distance and character-based DNA barcoding for 118 Scenedesmus strains based on rbcL, tufA, ITS and 16S. The four genes, and their combined data rbcL + tufA + ITS + 16S, rbcL + tufA and ITS + 16S were analyzed by all of GMYC, P ID, PTP, ABGD, and character-based barcoding respectively. It was apparent that the three combined gene data showed a higher proportion of resolution success than the single gene. In comparison, the GMYC and PTP analysis produced more taxonomic lineages. The ABGD generated various resolution in discrimination among the single and combined data. The character-based barcoding was proved to be the most effective approach for species discrimination in both single and combined data which produced consistent species identification. All the integrated results recovered 11 species, five out of which were revealed as potential cryptic species. We suggest that the character-based DNA barcoding together with other approaches based on multiple genes and their combined data could be more effective in microalgae diversity revelation.

The biofuels are receiving considerable attention as a substitute for petro diesel. For microalgae, the cell density or biomass and lipid contents are key components for biodiesel production. This study was conducted to develop favorable culture conditions for Dunaliella salina to maximize its biomass and lipid accumulation. The effect of salinity (0.5 to 2.5 M NaCl) on the cell population, biochemical composition, and lipid output of Dunaliella salina was examined under a controlled environment for 21 days. Maximum growth (6.57 × 10⁷ to 7.17 × 10⁷cells mL⁻¹) potentials were observed at 1.5 to 2 M NaCl. The photosynthetic pigments and carbohydrates also showed trends similar to growth. The maximum carotenoid level (5.16 mg L⁻¹) was recorded at 2 M NaCl. Almost all physicochemical parameters increased with increases in salinity, biomass (1231.66 ± 1.26 mg L⁻¹) and lipid content (248.33 mg L⁻¹), as recorded at 2 M NaCl. Based on fluorescence intensity, the highest values (11.84 × 10⁷cells/ml) of neutral lipids and total lipids (22.28%) were recorded at optimum salinity levels. The present study suggests that a high biomass and lipid accumulation of Dunaliella salina SA 134 could be obtained at the 2 M NaCl level.