Potencial para Degradação do Fenol por Estirpes de Bradyrhizobium do Semiárido nas Formas Livre e Imobilizada
DOI:
https://doi.org/10.26848/rbgf.v17.2.p744-757Palavras-chave:
Biofilme, Biorremediação, Exopolissacarídeo, Imobilização Celular, RizóbioResumo
O descarte de águas residuárias é um grave problema de poluição ambiental, que tem refletido na busca por microrganismos que aliem a capacidade de biodegradação e ausência de patogenicidade. Por atender ambos os critérios, as bactérias simbióticas de leguminosas são agentes promissores. Essas bactérias também produzem exopolissacarídeos e biofilme, paramêtros determinantes para imobilização celular, estratégia para aumentar a eficiência na degradação de poluentes. A atualidade, importância do tema e o potencial biorremediador ainda inexplorado dessas bactérias oriundas do Semiárido Brasileiro são justificativas para o presente trabalho. Foram selecionadas sete estirpes de rizóbios do semiárido, previamente caracterizadas, autenticadas, identificadas por sequenciamento do gene 16S rRNA e mantidas na coleção de culturas do Laboratório de Microbiologia Ambiental do Departamento de Biologia da Universidade Federal do Ceará. Essas estirpes foram avaliadas quanto à capacidade de crescer em meio com fenol nas concentrações de 100 e 500 mg.L-1. Por apresentar melhor desempenho a estirpe L04 (Bradyrhizobium elkanii), foi testada quanto à hidrofobicidade, produção de exopolissacarídeos e de biofilme. A estirpe foi hidrofóbica, produziu exopolissacarídeos e biofilme, se confirmando adequada para a imobilização sobre a matriz agar-agar. Quando imobilizada, a estirpe foi 1,4 vezes mais eficiente na produção de biomassa do que na forma livre. Dessa forma, fica claro que rizobactérias do Semiárido apresentam potencial biorremediador, e que cabem mais estudos para se avaliar esse potencial in situ visando o desenvolvimento de um produto.
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Referências
Ayhan, D. K., Temiz, A., Sana, F. A., & Gümüşderelioğlu, M. 2019. Surface properties and exopolysaccharide production of surface-associated microorganisms isolated from a dairy plant. Annals of Microbiology, 69(9), 895–907. https://doi.org/10.1007/s13213-019-01482-7 DOI: https://doi.org/10.1007/s13213-019-01482-7
Barberi, A., De Souza Moreira, F. M., Florentino, L. A., & Rodrigues, M. a. M. 2004. Crescimento de Bradyrhizobium elkanii estirpe BR 29 em meios de cultivo com diferentes valores de pH inicial. Ciencia E Agrotecnologia, 28(2), 397–405. https://doi.org/10.1590/s1413-70542004000200021 DOI: https://doi.org/10.1590/S1413-70542004000200021
Barik, M. R., Das, C. P., Verma, A. K., Sahoo, S., & Sahoo, N. K. 2021. Metabolic profiling of phenol biodegradation by an indigenous Rhodococcus pyridinivorans strain PDB9T N-1 isolated from paper pulp wastewater. International Biodeterioration & Biodegradation, 158, 105168. https://doi.org/10.1016/j.ibiod.2020.105168 DOI: https://doi.org/10.1016/j.ibiod.2020.105168
Basak, B., Jeon, B., Saratale, G. D., Bhunia, B., Chatterjee, P. K., & Dey, A. 2019. Biodegradation of high concentration phenol using sugarcane bagasse immobilized Candida tropicalis PHB5 in a packed-bed column reactor. Ecotoxicology and Environmental Safety, 180, 317–325. https://doi.org/10.1016/j.ecoenv.2019.05.020 DOI: https://doi.org/10.1016/j.ecoenv.2019.05.020
Bishop, P. N., Guevara, J. C., Engelke, J. A., & Evans, H. J. 1976. Relation between Glutamine Synthetase and Nitrogenase Activities in the Symbiotic Association between Rhizobium japonicum and Glycine max. Plant Physiology, 57(4), 542–546. https://doi.org/10.1104/pp.57.4.542 DOI: https://doi.org/10.1104/pp.57.4.542
Bromfield, E. S. P., Barran, L. R., & Wheatcroft, R. A. 1995. Relative genetic structure of a population of Rhizobium meliloti isolated directly from soil and from nodules of alfalfa (Medicago sativa) and sweet clover (Melilotus alba). Molecular Ecology, 4(2), 183–188. https://doi.org/10.1111/j.1365-294x.1995.tb00207.x DOI: https://doi.org/10.1111/j.1365-294X.1995.tb00207.x
Castellane, T. C. L., Lemos, M., & De Macedo Lemos, E. G. 2014. Evaluation of the biotechnological potential of Rhizobium tropici strains for exopolysaccharide production. Carbohydrate Polymers, 111, 191–197. https://doi.org/10.1016/j.carbpol.2014.04.066 DOI: https://doi.org/10.1016/j.carbpol.2014.04.066
Castellane, T. C. L., Persona, M. R., Campanharo, J. C., & De Macedo Lemos, E. G. 2015. Production of exopolysaccharide from rhizobia with potential biotechnological and bioremediation applications. International Journal of Biological Macromolecules, 74, 515–522. https://doi.org/10.1016/j.ijbiomac.2015.01.007 DOI: https://doi.org/10.1016/j.ijbiomac.2015.01.007
Chen, W., Chang, J. S., Wu, C., & Chang, S. 2004b. Characterization of phenol and trichloroethene degradation by the rhizobium Ralstonia taiwanensis. Research in Microbiology, 155(8), 672–680. https://doi.org/10.1016/j.resmic.2004.05.004 DOI: https://doi.org/10.1016/j.resmic.2004.05.004
Chen, W., Gao, Y., Shi, G., Li, J., Fan, G., Yang, C., Wang, B., Tong, F., & Li, Y. 2023. Enhanced degradation of fomesafen by a rhizobial strain Sinorhizobium sp. W16 in symbiotic association with soybean. Applied Soil Ecology, 187, 104847. https://doi.org/10.1016/j.apsoil.2023.104847 DOI: https://doi.org/10.1016/j.apsoil.2023.104847
Chlebek, D., & Hupert-Kocurek, K. 2019. Endophytic Bacteria In The Phytodegradation Of Persistent Organic Pollutants. Postepy Mikrobiologii, 58(1), 70–79. https://doi.org/10.21307/pm-2019.58.1.070 DOI: https://doi.org/10.21307/PM-2019.58.1.070
Cieśla, J., Kopycińska, M., Łukowska, M., Bieganowski, A., & Janczarek, M. 2016. Surface Properties of Wild-Type Rhizobium leguminosarum bv. trifolii Strain 24.2 and Its Derivatives with Different Extracellular Polysaccharide Content. PLOS ONE, 11(10), e0165080. https://doi.org/10.1371/journal.pone.0165080 DOI: https://doi.org/10.1371/journal.pone.0165080
Costa, O. Y. A., Raaijmakers, J. M., Kuramae, E. E. 2018. Microbial extracellular polymeric substances: ecological function and impact on soil aggregation. Frontiers in Microbiology, Volume 9 | Article 1636. https://doi.org/10.3389/fmicb.2018.01636 DOI: https://doi.org/10.3389/fmicb.2018.01636
Das, K., Prasanna, R., & Saxena, A. K. 2017. Rhizobia: a potential biocontrol agent for soilborne fungal pathogens. Folia Microbiologica, 62(5), 425–435. https://doi.org/10.1007/s12223-017-0513-z DOI: https://doi.org/10.1007/s12223-017-0513-z
Dashti, N., Khanafer, M., El-Nemr, I., Sorkhoh,N., Ali,N., Radwan, S. 2010.The potential of oil-utilizing bacterial consortia associated with legume root nodules for cleaning oily soils. Chemosphere 74, 1354–1359. https://doi.org/10.1016/j.Chemosphere.2008.11.028 DOI: https://doi.org/10.1016/j.chemosphere.2008.11.028
De Souza Moreira, F. M., Gillis, M., Pot, B., Kersters, K., & Franco, A. A. 1993. Characterization of Rhizobia Isolated from Different Divergence Groups of Tropical Leguminosae by Comparative Polyacrylamide Gel Electrophoresis of their Total Proteins. Systematic and Applied Microbiology, 16(1), 135–146. https://doi.org/10.1016/s0723-2020(11)80258-4 DOI: https://doi.org/10.1016/S0723-2020(11)80258-4
Dixit, S., Dubey, R. C., Maheshwari, D. K., Seth, P. K., & Bajpai, V. K. 2017. Roles of quorum sensing molecules from Rhizobium etli RT1 in bacterial motility and biofilm formation. Brazilian Journal of Microbiology, 48(4), 815–821. https://doi.org/10.1016/j.bjm.2016.08.005 DOI: https://doi.org/10.1016/j.bjm.2016.08.005
El-Naggar, N. A., Moawad, M. N., & Ahmed, E. M. 2022. Toxic phenolic compounds in the Egyptian coastal waters of Alexandria: spatial distribution, source, identification, and ecological risk assessment. Water Science, 36(1), 32–40. https://doi.org/10.1080/23570008.2022.2031724 DOI: https://doi.org/10.1080/23570008.2022.2031724
Filipowicz, N., Momotko, M., Boczkaj, G., Pawlikowski, T., Wanarska, M., & Cieśliński, H. 2017. Isolation and Characterization of Phenol-Degrading Psychrotolerant Yeasts. Water Air and Soil Pollution, 228(6). https://doi.org/10.1007/s11270-017-3391-8 DOI: https://doi.org/10.1007/s11270-017-3391-8
Frassinetti, S., Setti, L., Corti, A., Farrinelli, P., Montevecchi, P., & Vallini, G. 1998. Biodegradation of dibenzothiophene by a nodulating isolate of Rhizobium meliloti. Canadian Journal of Microbiology, 44(3), 289–297. https://doi.org/10.1139/w97-155 DOI: https://doi.org/10.1139/w97-155
Ghosh, P., & Maiti, T. K. 2016. Structure of Extracellular Polysaccharides (EPS) Produced by Rhizobia and their Functions in Legume–Bacteria Symbiosis: — A Review. Achievements in the Life Sciences, 10(2), 136–143. https://doi.org/10.1016/j.als.2016.11.003 DOI: https://doi.org/10.1016/j.als.2016.11.003
Hanafi, M., & Sapawe, N. 2020. A review on the water problem associate with organic pollutants derived from phenol, methyl orange, and remazol brilliant blue dyes. Materials Today: Proceedings, 31, A141–A150. https://doi.org/10.1016/j.matpr.2021.01.258 DOI: https://doi.org/10.1016/j.matpr.2021.01.258
Hasan, S. S., & Jabeen, S. 2015. Degradation kinetics and pathway of phenol by Pseudomonas and Bacillus species. Biotechnology & Biotechnological Equipment, 29(1), 45–53. https://doi.org/10.1080/13102818.2014.991638 DOI: https://doi.org/10.1080/13102818.2014.991638
Huang, X., Shi, J., Cui, C., Yin, H., Zhang, R., Ma, X., & Zhang, X. 2016. Biodegradation of phenanthrene by Rhizobium petrolearium SL-1. Journal of Applied Microbiology, 121(6), 1616–1626. https://doi.org/10.1111/jam.13292 DOI: https://doi.org/10.1111/jam.13292
IBGE - Instituto Brasileiro de Geografia e Estatística. Disponível em: ttps://www.ibge.gov.br/geociencias/cartas-e-mapas/mapas-regionais/15974-semiarido-brasileiro. Acesso em 27 de janeiro de 2022
Jach, M. E., Sajnaga, E., & Ziaja, M. 2022. Utilization of Legume-Nodule Bacterial Symbiosis in Phytoremediation of Heavy Metal-Contaminated Soils. Biology, 11(5), 676. https://doi.org/10.3390/biology11050676 DOI: https://doi.org/10.3390/biology11050676
Júnior, P. C. S., Da Silva Almeida, J. A., Passos, S. R., De Oliveira, P. T., Rumjanek, N. G., & Xavier, G. R. 2010. Produção e comportamento reológico de exopolissacarídeos sintetizados por rizóbios isolados de guandu. Pesquisa Agropecuaria Brasileira, 45(12), 1465–1471. https://doi.org/10.1590/s0100-204x2010001200018 DOI: https://doi.org/10.1590/S0100-204X2010001200018
Kong, Z., Li, L., Xue, Y., Yang, M., & Li, Y. Y. 2019. Challenges and prospects for the anaerobic treatment of chemical-industrial organic wastewater: A review. Journal of Cleaner Production, 231, 913–927. https://doi.org/10.1016/j.jclepro.2019.05.233 DOI: https://doi.org/10.1016/j.jclepro.2019.05.233
Krasowska, A., & Sigler, K. 2014. How microorganisms use hydrophobicity and what does this mean for human needs? Frontiers in Cellular and Infection Microbiology, 4. https://doi.org/10.3389/fcimb.2014.00112 DOI: https://doi.org/10.3389/fcimb.2014.00112
Kuykendall, L. D., Saxena, B., Devine, T. E., & Udell, S. E. 1992. Genetic diversity in Bradyrhizobium japonicum Jordan 1982 and a proposal for Bradyrhizobium elkanii sp.nov. Canadian Journal of Microbiology, 38(6), 501–505. https://doi.org/10.1139/m92-082 DOI: https://doi.org/10.1139/m92-082
Leite, J., Passos, S. R., Simões-Araújo, J. L., Rumjanek, N. G., Xavier, G. R., & Zilli, J. É. 2018a. Genomic identification and characterization of the elite strains Bradyrhizobium yuanmingense BR 3267 and Bradyrhizobium pachyrhizi BR 3262 recommended for cowpea inoculation in Brazil. Brazilian Journal of Microbiology, 49(4), 703–713. https://doi.org/10.1016/j.bjm.2017.01.007
Leite, J., Passos, S. R., Simões-Araújo, J. L., Rumjanek, N. G., Xavier, G. R., & Zilli, J. É. 2018b. Genomic identification and characterization of the elite strains Bradyrhizobium yuanmingense BR 3267 and Bradyrhizobium pachyrhizi BR 3262 recommended for cowpea inoculation in Brazil. Brazilian Journal of Microbiology, 49(4), 703–713. https://doi.org/10.1016/j.bjm.2017.01.007 DOI: https://doi.org/10.1016/j.bjm.2017.01.007
Li, Y., Liang, F., Zhu, Y. F., Wang, F. P. 2013. Phytoremediation of a PCB- contaminated soil by alfalfa and tall fescue single and mixed plants cultivation. Journal of Soils and Sediments 13, 925–931. https://doi.org/10.1007/s11368-012-0618-6. DOI: https://doi.org/10.1007/s11368-012-0618-6
Li, C.-M., Wu, H.-Z., Wang, Y.-X., Zhu, S. & Wei, C.-H. 2020. Enhancement of phenol biodegradation: metabolic division of labor in co-culture of Stenotrophomonas sp. N5 and Advenella sp. B9. Journal of Hazardous Materials 400, 12214–12223. https:// doi: 10.1016/j.jhazmat.2020.123214. DOI: https://doi.org/10.1016/j.jhazmat.2020.123214
Liu, H., Cui, Y., Zhou, J., Penttinen, P., Liu, J., Zeng, L., Chen, Q., Gu, Y., Zou, L., Zhao, K., Xiang, Q., & Yu, X. 2022. Nickel mine soil is a potential source for soybean plant growth promoting and heavy metal tolerant rhizobia. PeerJ, 10, e13215. https://doi.org/10.7717/peerj.13215 DOI: https://doi.org/10.7717/peerj.13215
Liu, Y., Wang, W., Shah, S. a. A., Zanaroli, G., Xu, P., & Tang, H. 2020. Phenol biodegradation by Acinetobacter radioresistens APH1 and its application in soil bioremediation. Applied Microbiology and Biotechnology, 104(1), 427–437. https://doi.org/10.1007/s00253-019-10271-w DOI: https://doi.org/10.1007/s00253-019-10271-w
Machado, I., Chapot-Chartier, M., & Briandet, R. 2009. Surface physicochemical analysis of natural Lactococcus lactis strains reveals the existence of hydrophobic and low charged strains with altered adhesive properties. International Journal of Food Microbiology, 131(1), 2–9. https://doi.org/10.1016/j.ijfoodmicro.2008.09.006 DOI: https://doi.org/10.1016/j.ijfoodmicro.2008.09.006
Malla, M. A., Dubey, A., Yadav, S., Kumar, A., & Kumar, A. 2018. Understanding and Designing the Strategies for the Microbe-Mediated Remediation of Environmental Contaminants Using Omics Approaches. Frontiers in Microbiology, 9. https://doi.org/10.3389/fmicb.2018.01132 DOI: https://doi.org/10.3389/fmicb.2018.01132
Mahto, K. U., Vandana, Priyadarshanee, M., Samantaray, D. P., Das, S. 2022. Bacterial biofilm and extracellular polymeric substances in the treatment of environmental pollutants: Beyond the protective role in survivability. Journal of Cleaner Production 379, 134759. https://doi.org/10.1016/j.jclepro.2022.134759 DOI: https://doi.org/10.1016/j.jclepro.2022.134759
Merino, N., Aronson, H. S., Bojanova, D., Feyhl-Buska, J., Wong, M. H., Zhang, S., & Giovannelli, D. 2019. Living at the Extremes: Extremophiles and the Limits of Life in a Planetary Context. Frontiers in Microbiology, 10. https://doi.org/10.3389/fmicb.2019.00780 DOI: https://doi.org/10.3389/fmicb.2019.00780
Miljkovic, M., Marinkovic, P., Novović, K., Jovcic, B., Terzic-Vidojevic, A., & Kojic, M. 2018. AggLr, a novel aggregation factor in Lactococcus raffinolactis BGTRK10-1: its role in surface adhesion. Biofouling. https://doi.org/10.1080/08927014.2018.1481956 DOI: https://doi.org/10.1080/08927014.2018.1481956
Misra, D., Dutta, W., Jha, G., & Ray, P. 2023. Interactions and regulatory functions of phenolics in soil-plant-climate nexus. Agronomy, 13, 280. https://doi.org/10.3390/agronomy13020280 DOI: https://doi.org/10.3390/agronomy13020280
Mtibaà, R., Ezzanad, A., Aranda, E., Pozo, C., Ghariani, B., Moraga, J., Nasri, M., Cantoral, J. M., Garrido, C. J., & Mechichi, T. 2020. Biodegradation and toxicity reduction of nonylphenol, 4-tert-octylphenol and 2,4-dichlorophenol by the ascomycetous fungus Thielavia sp. HJ22: Identification of fungal metabolites and proposal of a putative pathway. Science of the Total Environment, 708, 135129. https://doi.org/10.1016/j.scitotenv.2019.135129 DOI: https://doi.org/10.1016/j.scitotenv.2019.135129
Naidu, R., Biswas, B., Willett, I. R., Cribb, J., Singh, B. K., Nathanail, C. P., Coulon, F., Semple, K. T., Jones, K. C., Barclay, A., & Aitken, R. J. 2021. Chemical pollution: A growing peril and potential catastrophic risk to humanity. Environment International, 156, 106616. https://doi.org/10.1016/j.envint.2021.106616 DOI: https://doi.org/10.1016/j.envint.2021.106616
Oleńska, E., Cowan, D. A., Kotowska, U., Wydrych, J., Polińska, W., Swiecicka, I., Thijs, S., & Vangronsveld, J. 2021. Exopolysaccharide Carbohydrate Structure and Biofilm Formation by Rhizobium leguminosarum bv. trifolii Strains Inhabiting Nodules of Trifolium repens Growing on an Old Zn–Pb–Cd-Polluted Waste Heap Area. International Journal of Molecular Sciences, 22(6), 2808. https://doi.org/10.3390/ijms22062808 DOI: https://doi.org/10.3390/ijms22062808
Panigrahy, N., Barik, M. R., & Sahoo, N. K. 2020. Kinetics of Phenol Biodegradation by an Indigenous Pseudomonas citronellolis NS1 Isolated from Coke Oven Wastewater. Journal of Hazardous, Toxic, and Radioactive Waste, 24(3). https://doi.org/10.1061/(asce)hz.2153-5515.0000502 DOI: https://doi.org/10.1061/(ASCE)HZ.2153-5515.0000502
Panigrahy, N., Priyadarshini, A., Sahoo, M. M., Verma, A. K., Daverey, A., & Sahoo, N. K. 2022. A comprehensive review on eco-toxicity and biodegradation of phenolics: Recent progress and future outlook. Environmental Technology and Innovation, 27, 102423. https://doi.org/10.1016/j.eti.2022.102423 DOI: https://doi.org/10.1016/j.eti.2022.102423
Parvanova-Mancheva, T. 2020. Phenol Biodegradation of Immobilized Bradyrhizobium japonicum Cells. Part 2. https://inis.iaea.org/search/search.aspx?orig_q=RN:53000213
Partovinia, A., & Rasekh, B. 2018. Review of the immobilized microbial cell systems for bioremediation of petroleum hydrocarbons polluted environments. Critical Reviews In Environmental Science and Technology, 48(1):1-38. https://doi.org/10.1080/10643389.2018.1439652 DOI: https://doi.org/10.1080/10643389.2018.1439652
Perez-Montano, F., Jimenez-Guerrero, I., Del Cerro, P., Baena-Ropero, I., Lopez-Baena, F. J., Ollero, F. J., Bellogın, R., Lloret, J., Espuny, R. The symbiotic biofilm of Sinorhizobium fredii SMH12, necessary for successful colonization and symbiosis of glycine max cv Osumi, is regulated by Quorum Sensing systems and inducing flavonoids via NodD1. PLoS ONE 9(8): e105901. https://doi.org/10.1371/journal.pone.0105901 DOI: https://doi.org/10.1371/journal.pone.0105901
Pinheiro, M.S.; Sousa, J.B.; Bertini, C.H.C.M.; Martins, S.C.S.; Martins, C.M, 2014. Isolation and screening of rhizobial strains native from semiarid tolerant to environmental stress. Enciclopédia Biosfera, v. 10 (18), 2071 – 2082.
Popova-Krumova, P., Beschkov, V., Vasileva, E., & Parvanova-Mancheva, T. 2022 Modeling of 1,2-Dibromoethane Biodegradation in Constant Electric Field. ChemEngineering, 6(4), 62. https://doi.org/10.3390/chemengineering6040062 DOI: https://doi.org/10.3390/chemengineering6040062
Pradeep, N. V., S, A., Navya, K., Shalini, H. N., Idris, M., & Hampannavar, U. S. 2015a. Biological removal of phenol from wastewaters: a mini review. Applied Water Science, 5(2), 105–112. https://doi.org/10.1007/s13201-014-0176-8 DOI: https://doi.org/10.1007/s13201-014-0176-8
Qiao, D., Tu, W., Zhong, L., Wang, Z. L., Zhang, B., & Jiang, A. F. 2019. Microstructure and Mechanical/Hydrophilic Features of Agar-Based Films Incorporated with Konjac Glucomannan. Polymers, 11(12), 1952. https://doi.org/10.3390/polym11121952 DOI: https://doi.org/10.3390/polym11121952
Ramírez-Bahena, M., Peix, A., Rivas, R., Camacho, M., Rodríguez-Navarro, D. N., Mateos, P. F., Martínez-Molina, E., Willems, A., & Velázquez, E. 2009. Bradyrhizobium pachyrhizi sp. nov. and Bradyrhizobium jicamae sp. nov., isolated from effective nodules of Pachyrhizus erosus. International Journal of Systematic and Evolutionary Microbiology, 59(8), 1929–1934. https://doi.org/10.1099/ijs.0.006320-0 DOI: https://doi.org/10.1099/ijs.0.006320-0
Rammo, R. N. N. 2020 Hydrophobicity and Adhesion Properties of Bacterial Growth Under Varying Temperature-Time Environment and Material Surface. Prensa MéDica Argentina. https://doi.org/10.47275/0032-745x-216 DOI: https://doi.org/10.47275/0032-745X-216
Rucká, L., Nešvera, J., & Pátek, M. 2017. Biodegradation of phenol and its derivatives by engineered bacteria: current knowledge and perspectives. World Journal of Microbiology & Biotechnology, 33(9). https://doi.org/10.1007/s11274-017-2339-x DOI: https://doi.org/10.1007/s11274-017-2339-x
Saeed, Q., Xiukang, W., Haider, F. U., Kucerik, J., Mumtaz, M. Z., Holatko, J., Naseem, M., Kintl, A., Ejaz, M., Naveed, M., Brtnicky, M., & Mustafa, A. 2021. Rhizosphere bacteria in plant growth promotion, biocontrol, and bioremediation of contaminated sites: A comprehensive
review of effects and mechanisms. International Journal of Molecular Sciences, 22, 10529. https://doi.org/10.3390/ijms221910529 DOI: https://doi.org/10.3390/ijms221910529
Said, K. A. M., Ismail, A. F., Karim, Z. A., Abdullah, M. Z., & Hafeez, A. 2021. A review of technologies for the phenolic compounds recovery and phenol removal from wastewater. Chemical Engineering Research & Design, 151, 257–289. https://doi.org/10.1016/j.psep.2021.05.015 DOI: https://doi.org/10.1016/j.psep.2021.05.015
Samadi, R., Ghalavand, Z., Nikmanesh, B., Farahani, N. N., Yasini, M., Benvidi, M. E., & Eslami, G. 2017. Investigation of Biofilm Formation Among Methicillin-Resistant Staphylococcus aureus Isolated from Children. Archives of Pediatric Infectious Diseases, 6(3). https://doi.org/10.5812/pedinfect.61635 DOI: https://doi.org/10.5812/pedinfect.61635
Santos, J. W. M. D., Da Silva, J. L., Ferreira, T. D. D. S., Dias, M. L., Fraiz, A. C. R., Escobar, I. E. C., Santos, R. C. D., De Lima, L. M., Morgante, C. V., & Fernandes-Júnior, P. I. 2017. Molecular and symbiotic characterization of peanut bradyrhizobia from the semi-arid region of Brazil. Applied Soil Ecology, 121, 177–184. https://doi.org/10.1016/j.apsoil.2017.09.033 DOI: https://doi.org/10.1016/j.apsoil.2017.09.033
Sayyed, R. Z.; Patel, P. R.; Shaikh, S. S., 2015. Plant growth promotion and root colonization by EPS producing Enterobacter sp. RZS5 under heavy metal contaminated soil. Indian Journal of Experimental Biology. 53, 116-123.
Silva, C.S.; Silva, J.M.; Oliveira, J.U.L.; Araújo, R.G.V.; Lima, J.R.B.; Guedes, E.L.F.; Santos, M.T.; Montaldo, Y.C.; Santos, T.M.C., 2019. Bioprospecting rhizobacteria associated to cacti to water stress resistance and biofilm formation. Revista Brasileira de Gestão Ambiental e Sustentabilidade, v. 6 (14),873 - 881. https://doi.org/10.21438/rbgas.061417 DOI: https://doi.org/10.21438/rbgas.061417
Silva, V.B. Micro-organismos colonizadores de nódulos de Vigna spp. cultivadas em solos de Caatinga. Areia, PB. Universidade Federal da Paraíba, Centro de Ciências Agrárias – CCA. Tese. Setembro de 2020.
Stepanović, S., Vuković, D., Holá, V., Di Bonaventura, G., Djukic, S., Cirkovic, I., & Růžička, F. 2007. Quantification of biofilm in microtiter plates: overview of testing conditions and practical recommendations for assessment of biofilm production by staphylococci. Apmis, 115(8), 891–899. https://doi.org/10.1111/j.1600-0463.2007.apm_630.x DOI: https://doi.org/10.1111/j.1600-0463.2007.apm_630.x
Suzuki, M. T., GiovannonI, S. J. Bias caused by template annealing in the amplification of mixtures of 16S rRNA genes by PCR. Applied and Environmental Microbiology, 62(2):625-630, 1996. https://doi.org/10.1128/aem.62.2.625-630.1996. DOI: https://doi.org/10.1128/aem.62.2.625-630.1996
Sudtachat, N., Ito, N., Itakura, M., Masuda, S., Eda, S., Mitsui, H., Kawaharada, Y., Minamisawa, K. 2009. Aerobic vanillate degradation and c1 compound metabolism in bradyrhizobium japonicum. Applied and Environmental Microbiology, vol. 75, no. 15 p. 5012–5017. https://doi.org/10.1128/AEM.00755-09 DOI: https://doi.org/10.1128/AEM.00755-09
Teng, Y., Shen,Y. Y., Luo,Y. M., Sun, X. H., Sun,M. M.,Fu, D. Q.,etal.2011. Influence of Rhizobium meliloti on phytoremediation of polycyclicaromatic hydrocarbons by alfalfa in an aged contaminated soil. Journal of Hazardous Materials. 186, 1271–1276. https://doi.org/10.1016/j.jhazmat.2010.11.126 DOI: https://doi.org/10.1016/j.jhazmat.2010.11.126
Terrence, H. B., Etienne, Y., Christine, M., David, J., Lyle, G. W., Charles, W. G. 2011. Identification of nitrogen incorporating bacteria in petroleum-contaminated arctic soils by using[15N] DNA-based stable isotope probing and pyrosequencing. Applied and Environmental Microbiology, 77, 4163–4171. https://doi.org/10.1128/AEM.00172-11 DOI: https://doi.org/10.1128/AEM.00172-11
Toniutti, M. A., Albicoro, F. J., Castellani, L., García, S. L. L., Fornasero, L. V., Zuber, N., Vera, L. M., Vacca, C., Cafiero, J. H., Winkler, A., Kalinowski, J., Lagares, A., Tejerizo, G. a. T., & Del Papa, M. F. 2021. Genome sequence of Bradyrhizobium yuanmingense strain P10 130, a highly efficient nitrogen-fixing bacterium that could be used for Desmodium incanum inoculation. Gene, 768, 145267. https://doi.org/10.1016/j.gene.2020.145267 DOI: https://doi.org/10.1016/j.gene.2020.145267
Ullmann’s Encyclopedia of Industrial Chemistry 2000 Wiley EBooks. https://doi.org/10.1002/14356007 DOI: https://doi.org/10.1002/14356007
Vasileva, E.(2020, September 12. the bradyrhizobium japonicum 273 strain’s ability to degrade phenol. part 1. https://www.scientific-publications.net/en/article/1002058/
Vasileva, E., Parvanova-Mancheva, T., Beschkov, V., Alexieva, Z., Gerginova, M., & Peneva, N. 2021. Effects of Constant Electric Field on Biodegradation of Phenol by Free and Immobilized Cells of Bradyrhizobium japonicum 273. Chem. Engineering, 5(4), 75. https://doi.org/10.3390/chemengineering5040075 DOI: https://doi.org/10.3390/chemengineering5040075
Vincent, J. M. A Manual for the Practical Study of Root Nodule Bacteria. Oxford, Blackwell Scientific Publications. 164p. (IBP Handbook, 15).
Wang, Z., Walker, G. R., Muir, D. C. G., & Nagatani-Yoshida, K. 2020. Toward a Global Understanding of Chemical Pollution: A First Comprehensive Analysis of National and Regional Chemical Inventories. Environmental Science & Technology, 54(5), 2575–2584. https://doi.org/10.1021/acs.est.9b06379 DOI: https://doi.org/10.1021/acs.est.9b06379
Weissengruber, L., Möller, K., Puschenreiter, M., & Friedel, J. K. 2018. Long-term soil accumulation of potentially toxic elements and selected organic pollutants through application of recycled phosphorus fertilizers for organic farming conditions. Nutrient Cycling in Agroecosystems, 110(3), 427–449. https://doi.org/10.1007/s10705-018-9907-9 DOI: https://doi.org/10.1007/s10705-018-9907-9
Williams, M. 2013. The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 15th Edition Edited by M.J.O’Neil, Royal Society of Chemistry, Cambridge, UK ISBN 9781849736701; 2708 pages. April 2013, "50 with 1-year free access to The Merck Index Online. Drug Development Research, 74(5), 339. https://doi.org/10.1002/ddr.21085
Yang, E., Liu, J., Chen, D., Wang, S., Xu, L., Ma, K., Zhang, X., Sun, L., & Wang, W. 2022. Rhizobium cremeum sp. nov., isolated from
sewage and capable of acquisition of heavy metal and aromatic compounds resistance genes. Systematic and Applied Microbiology, 45(3), 126322. https://doi.org/10.1016/j.syapm.2022.126322 DOI: https://doi.org/10.1016/j.syapm.2022.126322
Yao, Z., Kan, F. L., Wang, E. T., Wei, G., & Chen, W. 2002. Characterization of rhizobia that nodulate legume species of the genus Lespedeza and description of Bradyrhizobium yuanmingense sp. nov. International Journal of Systematic and Evolutionary Microbiology. https://doi.org/10.1099/00207713-52-6-2219 DOI: https://doi.org/10.1099/ijs.0.01408-0
Zhou, M., Zhang, J., & Sun, C. 2017. Occurrence, Ecological and Human Health Risks, and Seasonal Variations of Phenolic Compounds in Surface Water and Sediment of a Potential Polluted River Basin in China. International Journal of Environmental Research and Public Health, 14(10), 1140. https://doi.org/10.3390/ijerph14101140 DOI: https://doi.org/10.3390/ijerph14101140
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