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NAP enzyme recruitment in simultaneous bioremediation and nanoparticles synthesis

The periplasmic nitrate reductase enzyme (NAP) has become attractive catalyst, whose exploitation has emerged as one of the indispensable strategies toward environmentally benign applications. To achieve them efficiently and overcome the sensitivity of NAP in harsh environmental circumstances, the i...

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Detalles Bibliográficos
Autores principales: Eltarahony, Marwa, Zaki, Sahar, Kheiralla, Zeinab, Abd-El-haleem, Desouky
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989592/
https://www.ncbi.nlm.nih.gov/pubmed/29876306
http://dx.doi.org/10.1016/j.btre.2018.e00257
Descripción
Sumario:The periplasmic nitrate reductase enzyme (NAP) has become attractive catalyst, whose exploitation has emerged as one of the indispensable strategies toward environmentally benign applications. To achieve them efficiently and overcome the sensitivity of NAP in harsh environmental circumstances, the immobilization for denitrifying bacteria and NAP enzyme for simultaneous bioremediation and bionanoparticles synthesis was studied. NAP catalyzed NO(3)(−) reduction at V(max) of 0.811 μM/min and K(m) of 14.02 mM. Concurrently, the immobilized MMT cells completely removed NO(3)- upon 192 h with AgNPs synthesis ranging from 23.26 to 58.14 nm as indicated by SEM. Wherase, immobilized NAP exhibited lower efficiency with 28.6% of NO(3)(−) elimination within 288 h and large aggregated AgNPs ranging from 94.44 nm to 172.22 nm. To the best of author knowledge, the immobilization for denitrifying bacteria and NAP enzyme for simultaneous bioremediation and bionanoparticles synthesis was not studied before.