Department of Microbiology and Immunology, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt.
Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt, Cairo 11835, Egypt.
Biomolecules. 2020 Mar 12;10(3):435. doi: 10.3390/biom10030435.
is a Gram-positive pathogen that is capable of infecting almost every organ in the human body. Alarmingly, the rapid emergence of methicillin-resistant strains (MRSA) jeopardizes the available treatment options. Herein, we propose sustainable, low-cost production of recombinant lysostaphin (rLST), which is a native bacteriocin destroying the staphylococcal cell wall through its endopeptidase activity. We combined the use of BL21(DE3)/pET15b, factorial design, and simple Ni-NTA affinity chromatography to optimize rLST production. The enzyme yield was up to 50 mg/L culture, surpassing reported systems. Our rLST demonstrated superlative biofilm combating ability by inhibiting staphylococcal biofilms formation and detachment of already formed biofilms, compared to vancomycin and linezolid. Furthermore, we aimed at developing a novel rLST topical formula targeting staphylococcal skin infections. The phase inversion composition (PIC) method fulfilled this aim with its simple preparatory steps and affordable components. LST nano-emulgel (LNEG) was able to extend active LST release up to 8 h and cure skin infections in a murine skin model. We are introducing a rapid, convenient rLST production platform with an outcome of pure, active rLST incorporated into an effective LNEG formula with scaling-up potential to satisfy the needs of both research and therapeutic purposes.
金黄色葡萄球菌是一种革兰氏阳性病原体,能够感染人体几乎所有的器官。令人震惊的是,耐甲氧西林金黄色葡萄球菌(MRSA)的迅速出现危及了现有的治疗选择。在此,我们提出了一种可持续的、低成本的重组溶葡萄球菌酶(rLST)生产方法,rLST 是一种天然的细菌素,通过其内切酶活性破坏葡萄球菌细胞壁。我们结合使用 BL21(DE3)/pET15b、析因设计和简单的 Ni-NTA 亲和层析来优化 rLST 的生产。酶的产量达到了 50mg/L 培养物,超过了已报道的系统。与万古霉素和利奈唑胺相比,我们的 rLST 通过抑制葡萄球菌生物膜的形成和已经形成的生物膜的脱落,表现出了卓越的抗生物膜能力。此外,我们旨在开发一种针对葡萄球菌皮肤感染的新型 rLST 局部配方。相转化组成(PIC)方法通过其简单的制备步骤和经济实惠的成分实现了这一目标。LST 纳米乳凝胶(LNEG)能够将活性 LST 的释放延长至 8 小时,并在小鼠皮肤模型中治愈皮肤感染。我们正在引入一种快速、方便的 rLST 生产平台,其结果是纯的、活性的 rLST 被纳入到一种有效的 LNEG 配方中,具有扩大规模的潜力,以满足研究和治疗目的的需求。