Lee Jin-Young, Choy Hyon E, Lee Jin-Ho, Kim Geun-Joong
Department of Biological Sciences, College of Natural Sciences, Chonnam National University, Gwangju 500-757, Republic of Korea.
Department of Microbiology, Chonnam National University Medical School, Gwangju 500-757, Republic of Korea.
J Microbiol Biotechnol. 2015 Apr;25(4):554-8. doi: 10.4014/jmb.1408.08037.
Drug delivery systems (DDSs) incorporating bacterial minicells have been evaluated as a very powerful tool in view of biocompatibility. However, limited studies have been carried out on these systems, mainly using minicells from Salmonella sp. and Escherichia coli. Thus, we generated a new minicell-producing strain from an endotoxin-free Corynebacterium glutamicum by the inactivation of genes related to cell division. The two knockout strains, ΔparA and Δncgl1366, showed distinct abilities to produce minicells. The resulting minicells were purified via sequential antibiotic treatments and centrifugations, which resulted in reproducible yields.
鉴于生物相容性,包含细菌微细胞的药物递送系统(DDSs)已被评估为一种非常强大的工具。然而,针对这些系统的研究有限,主要使用来自沙门氏菌属和大肠杆菌的微细胞。因此,我们通过使与细胞分裂相关的基因失活,从无内毒素的谷氨酸棒杆菌中产生了一种新的微细胞生产菌株。两种基因敲除菌株ΔparA和Δncgl1366表现出不同的微细胞生产能力。通过连续的抗生素处理和离心对所得微细胞进行纯化,从而获得可重复的产量。