Institute of Bioscience and BioResources, National Research Council, Via Pietro Castellino 111, 80131 Naples, Italy.
Institute of Biostructures and Bioimaging, National Research Council, Via Pietro Castellino 111, 80131 Naples, Italy.
Int J Mol Sci. 2024 Jan 23;25(3):1392. doi: 10.3390/ijms25031392.
In recent years, the loop-mediated isothermal amplification (LAMP) technique, designed for microbial pathogen detection, has acquired fundamental importance in the biomedical field, providing rapid and precise responses. However, it still has some drawbacks, mainly due to the need for a thermostatic block, necessary to reach 63 °C, which is the BstI DNA polymerase working temperature. Here, we report the identification and characterization of the DNA polymerase I Large Fragment from (DraLF-PolI) that functions at room temperature and is resistant to various environmental stress conditions. We demonstrated that DraLF-PolI displays efficient catalytic activity over a wide range of temperatures and pH, maintains its activity even after storage under various stress conditions, including desiccation, and retains its strand-displacement activity required for isothermal amplification technology. All of these characteristics make DraLF-PolI an excellent candidate for a cutting-edge room-temperature LAMP that promises to be very useful for the rapid and simple detection of pathogens at the point of care.
近年来,环介导等温扩增(LAMP)技术作为一种用于微生物病原体检测的方法,在生物医学领域具有重要意义,它提供了快速而准确的反应。然而,它仍然存在一些缺点,主要是因为需要恒温块来达到 63°C,这是 BstI DNA 聚合酶的工作温度。在这里,我们报告了 DNA 聚合酶 I 大片段(DraLF-PolI)的鉴定和特性,该酶在室温下发挥作用,并且能够抵抗各种环境应激条件。我们证明了 DraLF-PolI 在很宽的温度和 pH 范围内具有高效的催化活性,即使在各种应激条件下储存后也能保持其活性,包括干燥,并保留了其用于等温扩增技术的链置换活性。所有这些特性使 DraLF-PolI 成为一种出色的候选酶,适用于一种新颖的室温 LAMP,有望非常有助于在护理点快速简便地检测病原体。