Copper ions binding regulation for the high-efficiency biodegradation of ciprofloxacin and tetracycline-HCl by low-cost permeabilized-cells
Bioresource Technology, ISSN: 0960-8524, Vol: 344, Issue: Pt B, Page: 126297
2022
- 19Citations
- 2Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations19
- Citation Indexes19
- 19
- CrossRef8
- Captures2
- Readers2
Article Description
Cu 2+ plays a decisive role for the bio-oxidation in the active center of laccase. In the fermentation-purified process, the loss of Cu 2+ reduces the activity and the high cost limits the application of laccase. In this study, a fermentation-permeabilization combined process were developed which based on the regulation of Cu 2+ binding time to produce the permeabilized-cells containing laccase, in which Cu 2+ can enter the cells freely to greatly improve the laccase activity and reduce the immobilization cost by about 19 times. So, the permeabilized-cells is suitable for biodegradation of antibiotic pollution in the environment, which was applied for the biodegradation of ciprofloxacin (CIP) and tetracycline-HCl (TCH) and the degradation efficiency reached 95.42% and 98.73%, respectively, with low ecotoxicity of the degradation products. Finally, the degradation mechanism was analyzed theoretically by molecular docking. Therefore, this study provided a low-cost, eco-friendly, and widely applicable method for organic pollutants removal.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0960852421016394; http://dx.doi.org/10.1016/j.biortech.2021.126297; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85119181848&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34748981; https://linkinghub.elsevier.com/retrieve/pii/S0960852421016394; https://dx.doi.org/10.1016/j.biortech.2021.126297
Elsevier BV
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