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从[具体来源]生产和纯化包裹绿色荧光蛋白的外膜囊泡:迈向可扩展外膜囊泡技术的一步。

Production and purification of outer membrane vesicles encapsulating green fluorescent protein from : a step towards scalable OMV technologies.

作者信息

Torres-Vanegas Julian Daniel, Rincon-Tellez Nicolas, Guzmán-Sastoque Paula, Valderrama-Rincon Juan D, Cruz Juan C, Reyes Luis H

机构信息

Grupo de Diseño de Productos y Procesos (GDPP), Department of Chemical and Food Engineering, Universidad de Los Andes, Bogota, Colombia.

Department of Biological Sciences, Universidad de Los Andes, Bogota, Colombia.

出版信息

Front Bioeng Biotechnol. 2024 Nov 14;12:1436352. doi: 10.3389/fbioe.2024.1436352. eCollection 2024.

Abstract

Outer membrane vesicles (OMVs) are spherical structures that contain a small fraction of the periplasm of Gram-negative bacteria, surrounded by its outer membrane. They are naturally produced and detached from the bacterial surface, participate in diverse biological processes, and their diameter size is in the range of 10-300 nm. OMVs have gained interest in different applications, such as the development of biosensors, vaccines, protein chips, and the encapsulation of heterologous proteins and peptides expressed by these microorganisms. However, the use of OMVs in these applications is limited due to the low yields and high purification costs. In this study, we produced green fluorescent protein (GFP) encapsulated into OMVs using JC8031 transformed with pTRC99A-ssTorA-GFP to establish the production and purification route. Results showed that the motility of the strain prevents its immobilization in alginate, which hampers the purification of OMVs. To address this issue, a zeolite-based column was used to chromatographically separate the OMVs from smaller particles. Further experiments will be focused on standardizing the production and purification of OMVs at a scalable level.

摘要

外膜囊泡(OMVs)是球形结构,包含革兰氏阴性菌周质的一小部分,并被其外膜包围。它们是自然产生并从细菌表面脱落的,参与多种生物过程,其直径大小在10 - 300纳米范围内。OMVs在不同应用中受到关注,如生物传感器、疫苗、蛋白质芯片的开发,以及这些微生物表达的异源蛋白质和肽的封装。然而,由于产量低和纯化成本高,OMVs在这些应用中的使用受到限制。在本研究中,我们使用用pTRC99A - ssTorA - GFP转化的JC8031生产封装在OMVs中的绿色荧光蛋白(GFP),以建立生产和纯化路线。结果表明,该菌株的运动性阻止了其固定在藻酸盐中,这阻碍了OMVs的纯化。为了解决这个问题,使用基于沸石的柱通过色谱法从较小颗粒中分离OMVs。进一步的实验将集中在规模化水平上标准化OMVs的生产和纯化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11602331/aad63be2d603/fbioe-12-1436352-g001.jpg

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