Al-Homsi Lamis, Al-Okla Souad, Abbady Abdul Q
Department of Biotechnology, Faculty of Agriculture, Damascus University, Syria.
Department of Animal Biology, Faculty of Sciences, Damascus University, Syria.
Open Microbiol J. 2015 Jul 31;9:70-80. doi: 10.2174/1874285801509010070. eCollection 2015.
Mutacin I, a bacteriocin produced by streptococcus mutans, displays an antimicrobial activity against many gram positive and some gram negative bacteria. Because of its medical importance, production of this short peptide in large scale for future applications is a significant challenge. This work described the improvement of a novel system to produce the recombinant mutacin using fusion protein technology. The short peptide was expressed directly as a fusion protein with a superfolder form of the green florescent protein (sfGFP), resulting in a high yield expression of soluble sfGFP-mutacin fusion protein (30 kDa) in the cytoplasm of E. coli. Mutacin was released from the fusion by enzymatic cleavage at the tobacco etch virus (TEV) protease recognition site and separated from the carrier sfGFP by nickel affinity and gel filtration chromatography. An additional advantage of this fusion system was tested in the generation of mutacin-specific polyclonal antibodies. Specific anti-mutacin IgGs were affinity purified, and were able to recognize the mutacin-sfGFP fusion protein or the cleaved forms of mutacin. Even though it was efficiently produced (25 mg/L) by this method, pure mutacin was devoid of antibiotic activity. Fourier transform infrared spectroscopy (FTIR) analysis revealed the absence of thioether bonds in the purified mutacin, which are critical for final structure and function of this antibiotic. Determining whether the activity of pure mutacin could be recovered by the reformation of such structures by chemical reaction needs more investigations. The development of this system will provide large quantities of mutacin for future studies and applications as broad spectrum antibacterial peptide.
变链菌素I是变形链球菌产生的一种细菌素,对许多革兰氏阳性菌和一些革兰氏阴性菌具有抗菌活性。由于其医学重要性,大规模生产这种短肽以供未来应用是一项重大挑战。这项工作描述了利用融合蛋白技术改进一种生产重组变链菌素的新系统。该短肽直接作为与绿色荧光蛋白超折叠形式(sfGFP)的融合蛋白表达,从而在大肠杆菌细胞质中高产表达可溶性sfGFP - 变链菌素融合蛋白(30 kDa)。通过在烟草蚀纹病毒(TEV)蛋白酶识别位点进行酶切从融合蛋白中释放出变链菌素,并通过镍亲和层析和凝胶过滤层析将其与载体sfGFP分离。在产生变链菌素特异性多克隆抗体方面测试了该融合系统的另一个优点。特异性抗变链菌素IgG经过亲和纯化,能够识别变链菌素 - sfGFP融合蛋白或变链菌素的切割形式。尽管通过这种方法能高效生产(25 mg/L),但纯变链菌素没有抗生素活性。傅里叶变换红外光谱(FTIR)分析表明纯化的变链菌素中不存在硫醚键,而硫醚键对这种抗生素的最终结构和功能至关重要。通过化学反应重新形成此类结构能否恢复纯变链菌素的活性还需要更多研究。该系统的开发将为未来作为广谱抗菌肽的研究和应用提供大量变链菌素。