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二苯并噻吩脱硫细菌的原位磁分离与固定化

In situ magnetic separation and immobilization of dibenzothiophene-desulfurizing bacteria.

作者信息

Li Yu-Guang, Gao Hong-Shuai, Li Wang-Liang, Xing Jian-Min, Liu Hui-Zhou

机构信息

Key Laboratory of Green Process and Engineering, Institute of Process Engineering, Chinese Academy of Sciences, P.O. Box 353, Beijing 100190, PR China.

出版信息

Bioresour Technol. 2009 Nov;100(21):5092-6. doi: 10.1016/j.biortech.2009.05.064. Epub 2009 Jun 21.

Abstract

In situ cell separation and immobilization of bacterial cells for biodesulfurization were developed by using superparamagnetic Fe(3)O(4) nanoparticles (NPs). The Fe(3)O(4) NPs were synthesized by coprecipitation followed by modification with ammonium oleate. The surface-modified NPs were monodispersed and the particle size was about 13 nm with 50.8 emu/g saturation magnetization. After adding the magnetic fluids to the culture broth, Rhodococcus erythropolis LSSE8-1 cells were immobilized by adsorption and then separated with an externally magnetic field. The maximum amount of cell mass adsorbed was about 530 g dry cell weight/g particles to LSSE8-1 cells. Analysis showed that the nanoparticles were strongly absorbed to the surface and coated the cells. Compared to free cells, the coated cells not only had the same desulfurizing activity but could also be easily separated from fermentation broth by magnetic force. Based on the adsorption isotherms and Zeta potential analysis, it was believed that oleate-modified Fe(3)O(4) NPs adsorbed bacterial cells mainly because of the nano-size effect and hydrophobic interaction.

摘要

利用超顺磁性Fe(3)O(4)纳米颗粒(NPs)开发了用于生物脱硫的原位细胞分离和细菌细胞固定化方法。通过共沉淀法合成Fe(3)O(4) NPs,随后用油酸铵进行改性。表面改性的NPs呈单分散状态,粒径约为13 nm,饱和磁化强度为50.8 emu/g。将磁性流体添加到培养液中后,通过吸附固定红平红球菌LSSE8-1细胞,然后用外部磁场进行分离。对于LSSE8-1细胞,吸附的最大细胞质量约为530 g干细胞重量/g颗粒。分析表明,纳米颗粒强烈吸附在细胞表面并包裹细胞。与游离细胞相比,被包裹的细胞不仅具有相同的脱硫活性,还能通过磁力轻松地从发酵液中分离出来。基于吸附等温线和Zeta电位分析,认为油酸改性的Fe(3)O(4) NPs吸附细菌细胞主要是由于纳米尺寸效应和疏水相互作用。

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