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基于微器件的固相聚合酶链反应快速检测病原微生物。

Microdevice-based solid-phase polymerase chain reaction for rapid detection of pathogenic microorganisms.

机构信息

Department of BioNano Technology, Gachon University, Seongnam-si, Gyeonggi-do, Republic of Korea.

Library of Marine Samples, Korea Institute of Ocean Science and Technology, Geoje, Republic of Korea.

出版信息

Biotechnol Bioeng. 2018 Sep;115(9):2194-2204. doi: 10.1002/bit.26734. Epub 2018 Jun 6.

Abstract

We demonstrate the integration of DNA amplification and detection functionalities developed on a lab-on-a-chip microdevice utilizing solid-phase polymerase chain reaction (SP-PCR) for point-of-need (PON) DNA analyses. First, the polycarbonate microdevice was fabricated by thermal bonding  to contain microchambers as reservoirs for performing SP-PCR. Next, the microchambers were subsequently modified with polyethyleneimine and glutaraldehyde for immobilizing amine-modified forward primers. During SP-PCR, the immobilized forward primers and freely diffusing fluorescence-labeled reverse primers cooperated to generate target amplicons, which remained covalently attached to the microchambers for the fluorescence detection. The SP-PCR microdevice was used for the direct identifications of two widely detected foodborne pathogens, namely Salmonella spp. and Staphylococcus aureus, and an alga causing harmful algal blooms annually in South Korea, Cochlodinium polykrikoides. The SP-PCR microdevice would be versatilely applied in PON testing as a universal platform for the fast identification of foodborne pathogens and environmentally threatening biogenic targets.

摘要

我们展示了在利用固相聚合酶链反应 (SP-PCR) 进行即时 (PON) DNA 分析的芯片上实验室微器件上开发的 DNA 扩增和检测功能的集成。首先,通过热键合制造聚碳酸酯微器件,以包含微室作为执行 SP-PCR 的储液器。接下来,微室随后用聚乙烯亚胺和戊二醛进行改性,用于固定胺修饰的正向引物。在 SP-PCR 期间,固定的正向引物和自由扩散的荧光标记的反向引物协同作用生成目标扩增子,这些扩增子共价附着在微室上进行荧光检测。SP-PCR 微器件用于直接鉴定两种广泛检测到的食源性病原体,即沙门氏菌属和金黄色葡萄球菌,以及每年在韩国造成有害藻华的藻类 Cochlodinium polykrikoides。SP-PCR 微器件将作为通用平台,广泛应用于 PON 测试中,用于快速鉴定食源性病原体和环境威胁性生物靶标。

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