摘要
目的:纯化大肠埃希菌表达的GST-颗粒溶解素融合蛋白,并分析其体外抗菌活性。方法:将IPTG诱导处理后的细菌破碎,分离含有可溶性GST-颗粒溶解素融合蛋白的细菌裂解液,并通过GSH-琼脂糖珠亲和层析柱纯化。同时采用MTT法分析该纯化蛋白的抗菌活性。结果:GST-颗粒溶解素融合蛋白能以可溶性形式在大肠埃希菌中表达,采用亲和层析法可获得分子量为44kDa的单一蛋白条带。经抗菌活性分析,表明纯化产物对金黄色葡萄球菌和甲型溶血性链球菌具有显著抑制作用,而对伤寒沙门菌和大肠埃希菌BL21的抗菌活性不明显。结论:成功纯化GST-颗粒溶解素融合蛋白,该蛋白对革兰阳性菌具有高效抗菌活性。
Objective： To purify GST-granulysin fusion protein expressed in E. coli and identify its antibacterial activity in vitro. Methods：E. coli was sonicated after it was induced by IPTG, and GST-granulysin fusion protein was separated from the soluble extract. The fusion protein was purified by affinity chromatography with glutathione agarose. Its bactericidal activity was analysed by MTT assay. Results： Expression of GST-granulysin in E. coli was detected by SDS-page methods. After affinity chromatography, a single protein band at about molecular weight 44 kDa was obtained. The result of bactericidal activity analysis indicated that it showed potent antibacterial activity against Staphylococcus aureus and Streptococcus sanguis, but it showed weaker antibacterial activity against Salmonella enterica and E. coli BI21. Conclusions ：The GST-granulysin fusion protein was successfully purified, and it exhibits effective bactericidal activity against gram positive bacteria.
出处
《蚌埠医学院学报》
CAS
2007年第3期265-267,共3页
Journal of Bengbu Medical College
基金
安徽省自然科学基金资助项目(050430603)
安徽省教育厅自然科学研究资助项目(2006kj122zc)
