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具有抗生物膜活性的含酰基转移酶聚氨酯涂层。

Acylase-containing polyurethane coatings with anti-biofilm activity.

作者信息

Grover Navdeep, Plaks Joseph G, Summers Samantha R, Chado Garrett R, Schurr Michael J, Kaar Joel L

机构信息

Department of Chemical and Biological Engineering, University of Colorado, Boulder, Colorado 80309.

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado.

出版信息

Biotechnol Bioeng. 2016 Dec;113(12):2535-2543. doi: 10.1002/bit.26019. Epub 2016 Jun 20.

Abstract

Due to the prevalence of biofilm-related infections, which are mediated by bacterial quorum sensing, there is a critical need for materials and coatings that resist biofilm formation. We have developed novel anti-biofilm coatings that disrupt quorum sensing in surface-associated bacteria via the immobilization of acylase in polyurethane films. Specifically, acylase from Aspergillus melleus was covalently immobilized in biomedical grade polyurethane coatings via multipoint covalent immobilization. Coatings containing acylase were enzymatically active and catalyzed the hydrolysis of the quorum sensing (QS) molecules N-butyryl-L-homoserine lactone (C4-LHL), N-hexanoyl-L-homoserine lactone (C6-LHL), and N-(3-oxododecanoyl)-L-homoserine lactone (3-oxo-C12-LHL). In biofilm inhibition assays, immobilization of acylase led to an approximately 60% reduction in biofilm formation by Pseudomonas aeruginosa ATCC 10145 and PAO1. Inhibition of biofilm formation was consistent with a reduction in the secretion of pyocyanin, indicating the disruption of quorum sensing as the mechanism of the coating activity. Scanning electron microscopy further showed that acylase-containing coatings contained far fewer bacterial cells than control coatings that lacked acylase. Moreover, acylase-containing coatings retained 90% activity when stored dry at 37°C for 7 days and were more stable than the free enzyme in physiological conditions, including artificial urine. Ultimately, such coatings hold considerable promise for the clinical management of catheter-related infections as well as the prevention of infections in orthopedic applications (i.e., on hip and knee prostheses) and on contact lenses. Biotechnol. Bioeng. 2016;113: 2535-2543. © 2016 Wiley Periodicals, Inc.

摘要

由于由细菌群体感应介导的生物膜相关感染普遍存在,因此迫切需要能够抵抗生物膜形成的材料和涂层。我们开发了新型抗生物膜涂层,该涂层通过在聚氨酯薄膜中固定酰基转移酶来破坏表面相关细菌中的群体感应。具体而言,来自黄曲霉的酰基转移酶通过多点共价固定共价固定在生物医学级聚氨酯涂层中。含有酰基转移酶的涂层具有酶活性,并催化群体感应(QS)分子N-丁酰基-L-高丝氨酸内酯(C4-LHL)、N-己酰基-L-高丝氨酸内酯(C6-LHL)和N-(3-氧代十二烷酰基)-L-高丝氨酸内酯(3-氧代-C12-LHL)的水解。在生物膜抑制试验中,酰基转移酶的固定导致铜绿假单胞菌ATCC 10145和PAO1形成的生物膜减少约60%。生物膜形成的抑制与绿脓菌素分泌的减少一致,表明群体感应的破坏是涂层活性的机制。扫描电子显微镜进一步显示,含酰基转移酶的涂层中的细菌细胞比不含酰基转移酶的对照涂层少得多。此外,含酰基转移酶的涂层在37°C干燥储存7天时保留了90%的活性,并且在包括人工尿液在内的生理条件下比游离酶更稳定。最终,这种涂层在导管相关感染的临床管理以及骨科应用(即髋关节和膝关节假体)和隐形眼镜上预防感染方面具有很大的前景。生物技术与生物工程。2016年;113:2535-2543。©2016威利期刊公司。

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