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Heterologous protein display on the cell surface of lactic acid bacteria mediated by the s-layer protein

机译:s层蛋白介导的乳酸菌细胞表面异源蛋白的展示

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Background Previous studies have revealed that the C-terminal region of the S-layer protein from Lactobacillus is responsible for the cell wall anchoring, which provide an approach for targeting heterologous proteins to the cell wall of lactic acid bacteria (LAB). In this study, we developed a new surface display system in lactic acid bacteria with the C-terminal region of S-layer protein SlpB of Lactobacillus crispatus K2-4-3 isolated from chicken intestine. Results Multiple sequence alignment revealed that the C-terminal region (LcsB) of Lb. crispatus K2-4-3 SlpB had a high similarity with the cell wall binding domains SA and CbsA of Lactobacillus acidophilus and Lb. crispatus. To evaluate the potential application as an anchoring protein, the green fluorescent protein (GFP) or beta-galactosidase (Gal) was fused to the N-terminus of the LcsB region, and the fused proteins were successfully produced in Escherichia coli, respectively. After mixing them with the non-genetically modified lactic acid bacteria cells, the fused GFP-LcsB and Gal-LcsB were functionally associated with the cell surface of various lactic acid bacteria tested. In addition, the binding capacity could be improved by SDS pretreatment. Moreover, both of the fused proteins could simultaneously bind to the surface of a single cell. Furthermore, when the fused DNA fragment of gfp:lcsB was inserted into the Lactococcus lactis expression vector pSec:Leiss:Nuc, the GFP could not be secreted into the medium under the control of the nisA promoter. Western blot, in-gel fluorescence assay, immunofluorescence microscopy and SDS sensitivity analysis confirmed that the GFP was successfully expressed onto the cell surface of L. lactis with the aid of the LcsB anchor. Conclusion The LcsB region can be used as a functional scaffold to target the heterologous proteins to the cell surfaces of lactic acid bacteria in vitro and in vivo, and has also the potential for biotechnological application.
机译:背景技术先前的研究表明,来自乳杆菌的S层蛋白的C端区域负责细胞壁锚定,这为将异源蛋白靶向乳酸菌(LAB)的细胞壁提供了一种方法。在这项研究中,我们开发了一种新的乳酸菌表面展示系统,该系统具有从鸡肠分离出的crispactatus crispatus K2-4-3的S层蛋白SlpB的C端区域。结果多重序列比对揭示了Lb的C末端区域(LcsB)。 crispatus K2-4-3 SlpB与嗜酸乳杆菌和Lb的细胞壁结合域S A 和CbsA具有高度相似性。脆皮。为了评估作为锚定蛋白的潜在应用,将绿色荧光蛋白(GFP)或β-半乳糖苷酶(Gal)融合到LcsB区的N端,并分别在大肠杆菌中成功生产出融合蛋白。将它们与非基因修饰的乳酸菌细胞混合后,融合的GFP-LcsB和Gal-LcsB在功能上与测试的各种乳酸菌的细胞表面相关。另外,通过SDS预处理可以提高结合能力。而且,两种融合蛋白都可以同时结合到单个细胞的表面。此外,当将gfp:lcsB的融合DNA片段插入乳酸乳球菌表达载体pSec:Leiss:Nuc中时,在nisA启动子的控制下,GFP不能分泌到培养基中。 Western印迹,凝胶内荧光测定,免疫荧光显微镜和SDS敏感性分析证实,借助LcsB锚蛋白,GFP成功地表达在乳酸乳球菌的细胞表面上。结论LcsB区域可作为功能支架,将异源蛋白体外和体内靶向到乳酸菌的细胞表面,具有生物技术应用潜力。

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