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双酶病毒样生物纳米反应器用于转化内分泌干扰化合物。

Bi-enzymatic virus-like bionanoreactors for the transformation of endocrine disruptor compounds.

机构信息

Departamento de Microbiología, Centro de Investigación Científica y de Educación Superior de Ensenada, Ensenada, Baja California 22860, Mexico; Departamento de Bionanotecnología, Centro de Nanociencias y Nanotecnología, Universidad Nacional Autónoma de México, Km 107 Carretera Tijuana-Ensenada, Ensenada, Baja California 22860, Mexico.

Departamento de Bionanotecnología, Centro de Nanociencias y Nanotecnología, Universidad Nacional Autónoma de México, Km 107 Carretera Tijuana-Ensenada, Ensenada, Baja California 22860, Mexico.

出版信息

Int J Biol Macromol. 2020 Mar 1;146:415-421. doi: 10.1016/j.ijbiomac.2019.12.272. Epub 2020 Jan 3.

Abstract

Endocrine disruptor compounds (EDCs) are pollutants able to alter both hormone synthesis and their regulation in animals and humans, thus, EDCs represent a risk for public health and for the environment. Cytochrome P450 enzymes (CYPs) are involved in the detoxification of a wide range of compounds, and it has been established that these enzymes produce the initial biotransformation of many EDCs. In this work, a bionanoreactor based on the encapsulation of an enhanced peroxygenase CYP21B3 inside the capsid of bacteriophage P22 virus-like particles (VLPs) was designed and characterized. VLPs were functionalized with glucose oxidase to generate in situ hydrogen peroxide necessary to activate the transformation of bisphenol A, nonylphenol, 17β-estradiol, triclosan, and resorcinol. Catalytic parameters, as well as the chemical nature of reaction products are presented. The enzymatic nanoreactors showed specific activities varying from 0.175 to 0.456 min in the transformation of these EDCs, which are equivalent to 22-77% of the activity obtained with free CYP. The capacity to transform structurally diverse compounds, easy production and glucose fueled catalytic activity make these enzymatic nanoreactors an interesting platform for enzyme delivery in the biomedical field.

摘要

内分泌干扰化合物 (EDCs) 是能够改变动物和人类激素合成及其调节的污染物,因此,EDCs 对公共健康和环境构成了威胁。细胞色素 P450 酶 (CYPs) 参与广泛化合物的解毒,并且已经确定这些酶产生许多 EDCs 的初始生物转化。在这项工作中,设计并表征了一种基于将增强型过氧化物酶 CYP21B3 封装在噬菌体 P22 病毒样颗粒 (VLPs) 衣壳内的生物纳米反应器。VLPs 用葡萄糖氧化酶进行功能化,以生成原位所需的过氧化氢,以激活双酚 A、壬基酚、17β-雌二醇、三氯生和间苯二酚的转化。介绍了催化参数以及反应产物的化学性质。这些酶纳米反应器在转化这些 EDCs 时的比活性从 0.175 到 0.456 min 不等,这相当于游离 CYP 获得的活性的 22-77%。转化结构多样的化合物的能力、易于生产和葡萄糖驱动的催化活性使这些酶纳米反应器成为生物医学领域酶传递的一个有趣平台。

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