Cohesive phycoremediation of pyrene by freshwater microalgae Selenastrum sp. and biodiesel production and its assessment.


Journal

Environmental geochemistry and health
ISSN: 1573-2983
Titre abrégé: Environ Geochem Health
Pays: Netherlands
ID NLM: 8903118

Informations de publication

Date de publication:
07 Jun 2024
Historique:
received: 05 03 2024
accepted: 23 04 2024
medline: 8 6 2024
pubmed: 8 6 2024
entrez: 7 6 2024
Statut: epublish

Résumé

In this study, the freshwater microalgae Selenastrum sp. was assessed for the effective degradation of pyrene and simultaneous production of biodiesel from pyrene-tolerant biomass. The growth of algae was determined based on the cell dry weight, cell density, chlorophyll content, and biomass productivity under different pyrene concentrations. Further, lipids from pyrene tolerant culture were converted into biodiesel by acid-catalyzed transesterification, which was characterized for the total fatty acid profile by gas chromatography. Increased pyrene concentration revealed less biomass yield and productivity after 20 days of treatment, indicating potent pyrene biodegradation by Selenastrum sp. Biomass yield was unaffected till the 20 mg/L pyrene. A 95% of pyrene bioremediation was observed at 20 days of culturing. Lipid accumulation of 22.14%, as evident from the estimation of the total lipid content, indicated a marginal increase in corroborating pyrene stress in the culture. Fatty acid methyl esters yield of 63.06% (% per 100 g lipids) was noticed from the pyrene tolerant culture. Moreover, fatty acid profile analysis of biodiesel produced under 10 mg/L and 20 mg/L pyrene condition showed escalated levels of desirable fatty acids in Selenastrum sp., compared to the control. Further, Selenastrum sp. and other freshwater microalgae are catalogued for sustainable development goals attainment by 2030, as per the UNSDG (United Nations Sustainable Development Goals) agenda. Critical applications for the Selenastrum sp. in bioremediation of pyrene, along with biodiesel production, are enumerated for sustainable and renewable energy production and resource management.

Identifiants

pubmed: 38849628
doi: 10.1007/s10653-024-02012-4
pii: 10.1007/s10653-024-02012-4
doi:

Substances chimiques

Pyrenes 0
Biofuels 0
pyrene 9E0T7WFW93
Fatty Acids 0
Water Pollutants, Chemical 0
Chlorophyll 1406-65-1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

225

Subventions

Organisme : King Saud University
ID : RSP2024R218

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature B.V.

Références

Aldaby, E. S. E., & Mawad, A. M. M. (2019). Pyrene biodegradation capability of two different microalgal strains. Global Nest Journal, 21(3), 290–295.
Anto, S., Premalatha, M., & Mathimani, T. (2022). Tertiary amine as an efficient CO
doi: 10.1016/j.chemosphere.2021.132442
Bharathi, D., Lee, J., Albeshr, M. F., Alrefaei, A. F., Le, T. T., & Mathimani, T. (2023). Enhanced photocatalytic degradation of polycyclic aromatic hydrocarbon by graphitic carbonitride-nickel (g-C
doi: 10.1016/j.chemosphere.2023.140464
Chan, S. M. N., Luan, T., Wong, M. H., & Tam, N. F. Y. (2006). Removal and biodegradation of polycyclic aromatic hydrocarbons by Selenastrum capricornutum. Environmental Toxicology and Chemistry: An International Journal, 25(7), 1772–1779.
doi: 10.1897/05-354R.1
Chen, Q., Li, Z., Li, Y., Liu, M., Wu, Y., Chen, Z., & Zhu, B. (2024). Biodegradation of benzo [a] pyrene by a marine Chlorella vulgaris LH-1 with heterotrophic ability. Marine Pollution Bulletin, 198, 115848.
doi: 10.1016/j.marpolbul.2023.115848
de Llasera, M. G., Pérez, A. F., Marín, G. P., & Calva, E. B. (2022). First evidence of extracellular enzymatic degradation of benzo (a) pyrene by the phytoplankton species Selenastrum capricornutum and the influence of temperature. Environmental Advances, 8, 100246.
doi: 10.1016/j.envadv.2022.100246
Dell’Anno, F., Rastelli, E., Sansone, C., Brunet, C., Ianora, A., & Dell’Anno, A. (2021). Bacteria, fungi and microalgae for the bioremediation of marine sediments contaminated by petroleum hydrocarbons in the omics era. Microorganisms, 9(8), 1695.
doi: 10.3390/microorganisms9081695
García, M. M., & de Llasera, M. P. G. (2024). Benzo (k) fluoranthene and benzo (b) fluoranthene degradation by Selenastrum capricornutum and identification of metabolites using HPLC-FD and HPLC-ESI-QqQ-MS/MS. Journal of Hazardous Materials, 465, 133444.
doi: 10.1016/j.jhazmat.2024.133444
García de Llasera, M. P., Olmos-Espejel, J. D. J., Díaz-Flores, G., & Montaño-Montiel, A. (2016). Biodegradation of benzo (a) pyrene by two freshwater microalgae Selenastrum capricornutum and Scenedesmus acutus: A comparative study useful for bioremediation. Environmental Science and Pollution Research, 23, 3365–3375.
doi: 10.1007/s11356-015-5576-2
Hoekman, S. K., Broch, A., Robbins, C., Ceniceros, E., & Natarajan, M. (2012). Review of biodiesel composition, properties, and specifications. Renewable and Sustainable Energy Reviews, 16(1), 143–169.
doi: 10.1016/j.rser.2011.07.143
Hoque, M. Z., Anand, D., Musa, M. M., Nzila, A., Guerriero, G., & Ahmad, I. (2023). Enhanced biodegradation of phenanthrene and anthracene using a microalgal-bacterial consortium. Frontiers in Microbiology, 14, 1227210.
doi: 10.3389/fmicb.2023.1227210
Jitae, K., Pham, T. H., Heesun, Y., Nguyen, M. V., & Taeyoung, K. (2024). Improved photocatalytic oxidation of micropollutant in wastewater by solar light: Assisted palladium-doped graphitic carbon nitride. Environmental Geochemistry and Health, 46(3), 76.
doi: 10.1007/s10653-023-01834-y
Kalaiselvan, N., Al-Ansari, M. M., & Mathimani, T. (2024). Biodiesel production from the Scenedesmus sp. and utilization of pigment from de-oiled biomass as sensitizer in the dye-sensitized solar cell (DSSC) for performance enhancement. Environmental Research, 251, 118726.
doi: 10.1016/j.envres.2024.118726
Kalaiselvan, N., & Mathimani, T. (2022). Design and fabrication of box-type passive solar dryer (BTPSD) with thermal insulation material for valorizing biomass and neutral lipids of marine Chlorella vulgaris for biodiesel application. Scientific Reports, 12(1), 6046.
doi: 10.1038/s41598-022-09665-0
Ke, L., Luo, L., Wang, P., Luan, T., & Tam, N. F. Y. (2010). Effects of metals on biosorption and biodegradation of mixed polycyclic aromatic hydrocarbons by a freshwater green alga Selenastrum capricornutum. Bioresource Technology, 101(18), 6950–6961.
doi: 10.1016/j.biortech.2010.04.011
Li, X., Cai, F., Luan, T., Lin, L., & Chen, B. (2019). Pyrene metabolites by bacterium enhancing cell division of green alga Selenastrum capricornutum. Science of the Total Environment, 689, 287–294.
doi: 10.1016/j.scitotenv.2019.06.162
Luo, S., Chen, B., Lin, L., Wang, X., Tam, N. F. Y., & Luan, T. (2014). Pyrene degradation accelerated by constructed consortium of bacterium and microalga: Effects of degradation products on the microalgal growth. Environmental Science and Technology, 48(23), 13917–13924.
doi: 10.1021/es503761j
Mercado, J. E. B., de Llasera, M. P. G., & García, M. M. (2023). Size exclusion chromatography protein profile of Selenastrum capricornutum culture extracts degrading benzo (a) pyrene. Polycyclic Aromatic Compounds, 43, 9193–9209.
doi: 10.1080/10406638.2022.2159987
Murugan, P. C., Sekhar, S. J., Glivin, G., Raveendran, P. S., Le, T. H. T., & Mathimani, T. (2024). Investigation on thermochemical co-gasification of rice husk and groundnut shell in open core gasifier for the generation of producer gas: An optimization by central composite design. Environmental Research, 242, 117741.
doi: 10.1016/j.envres.2023.117741
Nazari, M. T., Mazutti, J., Basso, L. G., Colla, L. M., & Brandli, L. (2021). Biofuels and their connections with the sustainable development goals: A bibliometric and systematic review. Environment, Development and Sustainability, 23(8), 11139–11156.
doi: 10.1007/s10668-020-01110-4
Othman, H. B., Pick, F. R., Hlaili, A. S., & Leboulanger, C. (2023). Effects of polycyclic aromatic hydrocarbons on marine and freshwater microalgae—A review. Journal of Hazardous Materials, 441, 129869.
doi: 10.1016/j.jhazmat.2022.129869
Pathak, B., Gupta, S., & Verma, R. (2018). Biosorption and biodegradation of polycyclic aromatic hydrocarbons (PAHs) by microalgae. In G. Crini & E. Lichtfouse (Eds.), Green adsorbents for pollutant removal: Fundamentals and design (pp. 215–247). Springer.
doi: 10.1007/978-3-319-92111-2_7
Pugliese, A., Biondi, L., Bartocci, P., & Fantozzi, F. (2020). Selenastrum capricornutum a new strain of algae for biodiesel production. Fermentation, 6(2), 46.
doi: 10.3390/fermentation6020046
Pushpakumari Kudahettige, N., Pickova, J., & Gentili, F. G. (2018). Stressing algae for biofuel production: Biomass and biochemical composition of Scenedesmus dimorphus and Selenastrum minutum grown in municipal untreated wastewater. Frontiers in Energy Research, 6, 132.
doi: 10.3389/fenrg.2018.00132
Rai, M. P., & Gupta, S. (2017). Effect of media composition and light supply on biomass, lipid content and FAME profile for quality biofuel production from Scenedesmus abundans. Energy Conversion and Management, 141, 85–92.
doi: 10.1016/j.enconman.2016.05.018
Roja, K., Sudhakar, D. R., Anto, S., & Mathimani, T. (2019). Extraction and characterization of polyhydroxyalkanoates from marine green alga and cyanobacteria. Biocatalysis and Agricultural Biotechnology, 22, 101358.
doi: 10.1016/j.bcab.2019.101358
Saldarriaga-Hernandez, S., Hernandez-Vargas, G., Iqbal, H. M., Barceló, D., & Parra-Saldívar, R. (2020). Bioremediation potential of Sargassum sp. biomass to tackle pollution in coastal ecosystems: Circular economy approach. Science of the Total Environment, 715, 136978.
doi: 10.1016/j.scitotenv.2020.136978
Sarkar, S., Manna, M. S., Bhowmick, T. K., & Gayen, K. (2020). Extraction of chlorophylls and carotenoids from dry and wet biomass of isolated Chlorella Thermophila: Optimization of process parameters and modelling by artificial neural network. Process Biochemistry, 96, 58–72.
doi: 10.1016/j.procbio.2020.05.025
Song, M., Pei, H., Hu, W., & Ma, G. (2013). Evaluation of the potential of 10 microalgal strains for biodiesel production. Bioresource Technology, 141, 245–251.
doi: 10.1016/j.biortech.2013.02.024
Subashchandrabose, S. R., Logeshwaran, P., Venkateswarlu, K., Naidu, R., & Megharaj, M. (2017). Pyrene degradation by Chlorella sp. MM3 in liquid medium and soil slurry: Possible role of dihydrolipoamide acetyltransferase in pyrene biodegradation. Algal Research, 23, 223–232.
doi: 10.1016/j.algal.2017.02.010
Tossavainen, M., Nykänen, A., Valkonen, K., Ojala, A., Kostia, S., & Romantschuk, M. (2017). Culturing of Selenastrum on diluted composting fluids; Conversion of waste to valuable algal biomass in presence of bacteria. Bioresource Technology, 238, 205–213.
doi: 10.1016/j.biortech.2017.04.013
Touliabah, H. E. S., El-Sheekh, M. M., Ismail, M. M., & El-Kassas, H. (2022). A review of microalgae-and cyanobacteria-based biodegradation of organic pollutants. Molecules, 27(3), 1141.
doi: 10.3390/molecules27031141
Tripathy, A., More, R. D., Gupta, S., Samuel, J., Singh, J., & Prasad, R. (2021). Present and future prospect of algae: A potential candidate for sustainable pollution mitigation. The Open Biotechnology Journal, 15(1), 142–156.
doi: 10.2174/1874070702115010142
Wang, P., Luo, L., Ke, L., Luan, T., & Tam, N. F. Y. (2013). Combined toxicity of polycyclic aromatic hydrocarbons and heavy metals to biochemical and antioxidant responses of free and immobilized Selenastrum capricornutum. Environmental Toxicology and Chemistry, 32(3), 673–683.
doi: 10.1002/etc.2090
Warshawsky, D., LaDow, K., & Schneider, J. (2007). Enhanced degradation of benzo [a] pyrene by Mycobacterium sp. in conjunction with green alga. Chemosphere, 69(3), 500–506.
doi: 10.1016/j.chemosphere.2007.03.031
Yee, W. (2016). Microalgae from the Selenastraceae as emerging candidates for biodiesel production: A mini review. World Journal of Microbiology and Biotechnology, 32(4), 64.
doi: 10.1007/s11274-016-2023-6
Zhu, J., Chen, W., Chen, H., Zhang, X., He, C., Rong, J., & Wang, Q. (2016). Improved productivity of neutral lipids in Chlorella sp. A2 by minimal nitrogen supply. Frontiers in Microbiology, 7, 557.
doi: 10.3389/fmicb.2016.00557

Auteurs

Krishnamurthy Mathivanan (K)

Key Laboratory of Advanced Marine Materials, Key Laboratory of Marine Environmental Corrosion and Biofouling, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, People's Republic of China. kritamathi@qdio.ac.cn.

Abdulwahed Fahad Alrefaei (AF)

Department of Zoology, College of Science, King Saud University, 11451, Riyadh, Saudi Arabia.

Loganathan Praburaman (L)

Department of Biotechnology, Mahendra Arts and Science College (Autonomous), Kalippatti, Namakkal, Tamil Nadu, 637501, India.

Rajesh Ramasamy (R)

Department of Agricultural Microbiology, Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu, 641003, India.

Prithiva Nagarajan (P)

Department of Agricultural Entomology, Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu, 641003, India.

Eerla Rakesh (E)

Department of Microbiology, Kakatiya University, Hanmankonda, Telangana, 506009, India.

Ruiyong Zhang (R)

Key Laboratory of Advanced Marine Materials, Key Laboratory of Marine Environmental Corrosion and Biofouling, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, People's Republic of China. ruiyong.zhang@qdio.ac.cn.

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