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超声化学结合胞嘧啶在 Cu-Hbpdc 中作为一种抗奇异变形杆菌的抗菌剂,针对标准和临床株,同时靶向 rsbA 基因。

Sonochemical incorporated of cytosine in Cu-Hbpdc as an antibacterial agent against standard and clinical strains of Proteus mirabilis with rsbA gene.

机构信息

Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, IR, Iran; Student Research Committee, Yasuj University of Medical Sciences, Yasuj, Iran.

Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, IR, Iran.

出版信息

Ultrason Sonochem. 2018 Jun;44:223-230. doi: 10.1016/j.ultsonch.2018.02.031. Epub 2018 Feb 19.

Abstract

The cytosine embedded copper based metal-organic framework (Bio-MOF) was synthesized by facile one-step sonochemical method by simply mixing of 4-4, biphenyldicarboxylic, cytosine and copper nitrate (Bio-Cu-Hbpdc-Cy). The prepared bio-MOF was characterized by XRD, FTIR and FE-SEM techniques. The effect of Cu-Hbpdc-Cy on the expression of the rsbA gene was evaluated in the clinical and standard Proteus mirabilis and study of MIC of Cu-Hbpdc-Cy by microdilution against them that have the rsbA gene. According to different concentrations of MIC, MBC concentrations was cultured on blood agar culture medium. Regarding to the concentration of MIC, gene expression changes were obtained by real-time PCR. MIC for standard and clinical strains of Proteus mirabilis was 1.6 and 1.8 mg/ml, and also MBC was obtained to be 1.8 and 2.0 mg/ml, respectively. Finally, in the real time PCR method, expression of the rsbA gene in presences of bio-Cu-Hbpdc-Cy was reduced, but has no effect on the gene expression of the Housekeeping DNA Gyrase-B gene. Considering the effect of Cu-Hbpdc-Cy on the rsbA gene in Proteus mirabilis bacteria, it is possible to use of Cu-Hbpdc-Cy agent as a therapeutic supplement against this bacterium.

摘要

通过简便的一步超声化学方法,通过简单混合 4-4',联苯二甲酸、胞嘧啶和硝酸铜(Bio-Cu-Hbpdc-Cy)合成了嵌入胞嘧啶的铜基金属有机骨架(Bio-MOF)。通过 XRD、FTIR 和 FE-SEM 技术对制备的生物 MOF 进行了表征。评估了 Cu-Hbpdc-Cy 对临床和标准奇异变形杆菌 rsbA 基因表达的影响,并通过微量稀释法研究了 Cu-Hbpdc-Cy 对具有 rsbA 基因的它们的 MIC。根据 MIC 的不同浓度,在血琼脂培养基上培养 MBC 浓度。根据 MIC 的浓度,通过实时 PCR 获得基因表达变化。标准和临床奇异变形杆菌株的 MIC 分别为 1.6 和 1.8mg/ml,MBC 也分别为 1.8 和 2.0mg/ml。最后,在实时 PCR 方法中,生物-Cu-Hbpdc-Cy 存在时 rsbA 基因的表达减少,但对管家基因 Gyrase-B 基因的表达没有影响。考虑到 Cu-Hbpdc-Cy 对奇异变形杆菌 rsbA 基因的影响,Cu-Hbpdc-Cy 试剂有可能被用作治疗该细菌的补充剂。

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