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N 端融合银结合肽可增强Dispersin B 的双重活性以用于生物膜清除。

Twofold enhanced dispersin B activity by N-terminal fusion to silver-binding peptide for biofilm eradication.

机构信息

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan.

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan.

出版信息

Int J Biol Macromol. 2018 Oct 15;118(Pt A):419-426. doi: 10.1016/j.ijbiomac.2018.06.066. Epub 2018 Jul 20.

Abstract

Dispersin B (DspB) has shown a great potential for the hydrolysis of polymeric β-1,6-N-acetyl-d-glucosamine (PNAG) to disperse the biofilms formed by various bacteria but with no killing activity. Here we have investigated whether a silver-binding peptide (AgBP) fused to DspB can induce the in situ formation of silver nanoparticles (AgNP) and conjugated to the structure of DspB so that the bacteria cells released from the dispersed biofilm will be killed by the conjugated AgNP. However, the desired conjugate could be obtained because of the silver ions itself was found to precipitate DspB. But, the fusion of AgBP2 to DspB (AgBP2-DspB) could generate at least 2 fold higher activity against soluble substrate 4-nitrophenyl N-acetyl-β-D-glucosaminide (NP-GlcNAc). By applying to a preformed Staphylococcus epidermidis biofilm, AgBP2-DspB could clear 69% of the biofilm while only 37% could be cleared by DspB as observed by fluorescent microscope. As measured by crystal violet staining, biofilm could be eradicated to the same extent by loading AgBP2-DspB activity level approximately 20 fold lower than that of DspB. The biofilm formation could be prevented on a AgBP2-DspB immobilized surface as observed by confocal laser microscope.

摘要

分散素 B(DspB)在水解聚合β-1,6-N-乙酰-d-葡萄糖胺(PNAG)以分散各种细菌形成的生物膜方面显示出巨大潜力,但没有杀菌活性。在这里,我们研究了与 DspB 融合的银结合肽(AgBP)是否可以诱导原位形成银纳米颗粒(AgNP)并与 DspB 结合,从而使从分散的生物膜中释放的细菌细胞被结合的 AgNP 杀死。然而,由于发现银离子本身会沉淀 DspB,因此无法获得所需的缀合物。但是,AgBP2 与 DspB 的融合(AgBP2-DspB)至少可以提高 2 倍对可溶性底物 4-硝基苯基 N-乙酰-β-D-葡萄糖胺(NP-GlcNAc)的活性。通过应用于预先形成的表皮葡萄球菌生物膜,AgBP2-DspB 可以清除 69%的生物膜,而 DspB 只能清除 37%,这可以通过荧光显微镜观察到。通过结晶紫染色测量,通过负载 AgBP2-DspB 活性水平比 DspB 低约 20 倍,可以达到相同程度的生物膜清除。通过共聚焦激光显微镜观察到,AgBP2-DspB 固定化表面可以阻止生物膜的形成。

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