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KB4 细胞固定化对其降解能力和对扑热息痛耐受性的影响。

Effect of KB4 Cells' Immobilisation on Their Degradation Potential and Tolerance towards Paracetamol.

机构信息

Institute of Biology, Biotechnology and Environmental Protection, Faculty of Natural Science, University of Silesia in Katowice, Jagiellonska 28, 40-032 Katowice, Poland.

出版信息

Molecules. 2021 Feb 4;26(4):820. doi: 10.3390/molecules26040820.

Abstract

KB4 is capable of degrading paracetamol, but high concentrations of this drug may cause an accumulation of toxic metabolites. It is known that immobilisation can have a protective effect on bacterial cells; therefore, the toxicity and degradation rate of paracetamol by the immobilised strain KB4 were assessed. Strain KB4 was immobilised on a plant sponge. A toxicity assessment was performed by measuring the concentration of ATP using the colony-forming unit (CFU) method. The kinetic parameters of paracetamol degradation were estimated using the Hill equation. Toxicity analysis showed a protective effect of the carrier at low concentrations of paracetamol. Moreover, a pronounced phenomenon of hormesis was observed in the immobilised systems. The obtained kinetic parameters and the course of the kinetic curves clearly indicate a decrease in the degradation activity of cells after their immobilisation. There was a delay in degradation in the systems with free cells without glucose and immobilised cells with glucose. However, it was demonstrated that the immobilised systems can degrade at least ten succeeding cycles of 20 mg/L paracetamol degradation. The obtained results indicate that the immobilised strain may become a useful tool in the process of paracetamol degradation.

摘要

KB4 能够降解扑热息痛,但这种药物的高浓度可能会导致有毒代谢物的积累。众所周知,固定化对细菌细胞具有保护作用;因此,评估了固定化菌株 KB4 对扑热息痛的毒性和降解率。将菌株 KB4 固定在植物海绵上。通过使用集落形成单位 (CFU) 法测量 ATP 浓度来进行毒性评估。使用 Hill 方程估算扑热息痛降解的动力学参数。毒性分析表明,载体在扑热息痛低浓度下具有保护作用。此外,在固定化系统中观察到明显的激素现象。所获得的动力学参数和动力学曲线的过程清楚地表明,细胞固定化后降解活性降低。在没有葡萄糖的游离细胞系统和有葡萄糖的固定化细胞系统中,降解出现延迟。然而,已经证明固定化系统可以降解至少十个 20mg/L 扑热息痛降解的连续循环。所得结果表明,固定化菌株可能成为扑热息痛降解过程中的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d8e/7915102/9915b696ee0d/molecules-26-00820-g001.jpg

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