Department of Basic Medicine, Shangqiu Medical College, Shangqiu 476100, China.
Key Laboratory of Biomedical Analytics (Southwest University), Chongqing Science and Technology Bureau, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, China.
Molecules. 2024 Sep 8;29(17):4259. doi: 10.3390/molecules29174259.
is a Gram-positive bacterium that can cause acute infection and anthracnose, which is a serious concern for human health. Determining through its spore biomarker dipicolinic acid (DPA) is crucial, and there is a strong need for a method that is rapid, sensitive, and selective. Here, we created Eu(III)-coordination polymers (Eu-CPs) with surfaces that have abundant carboxyl and hydroxyl groups. This was achieved by using citric acid and europium nitrate hexahydrate as precursors in a straightforward one-pot hydrothermal process. These Eu-CPs were then successfully utilized for highly sensitive DPA determination. The fluorescence (FL) emission of Eu-CPs, which is typically weak due to the coordination of Eu(III) with water molecules, was significantly enhanced in the presence of DPA. This enhancement is attributed to the competitive binding between DPA's carboxyl or hydroxyl groups and water molecules. As a result, the absorbed energy of DPA, when excited by 280 nm ultraviolet light, is transferred to Eu-CPs through an antenna effect. This leads to the emission of the characteristic red fluorescence of Eu at 618 nm. A strong linear relationship was observed between the enhanced FL intensity and DPA concentration in the range of 0.5-80 μM. This relationship allowed for a limit of detection (LOD) of 15.23 nM. Furthermore, the Eu-CPs we constructed can effectively monitor the release of DPA from Bacillus subtilis spores, thereby further demonstrating the potential significance of this strategy in the monitoring and management of anthrax risk. This highlights the novelty of this approach in practical applications, provides a valuable determination technique for Bacillus anthracis, and offers insights into the development cycle of microorganisms.
是一种革兰氏阳性细菌,可引起急性感染和炭疽病,对人类健康构成严重威胁。通过其孢子生物标志物二吡啶酸(DPA)来确定炭疽杆菌至关重要,因此非常需要一种快速、灵敏和选择性的方法。在这里,我们使用柠檬酸和硝酸铕六水合物作为前体,通过简单的一锅水热法制备了表面含有丰富羧基和羟基的 Eu(III)-配位聚合物(Eu-CPs)。然后,我们成功地将这些 Eu-CPs 用于高灵敏的 DPA 测定。由于 Eu(III)与水分子的配位,Eu-CPs 的荧光(FL)发射通常较弱,但在存在 DPA 的情况下,其发射显著增强。这种增强归因于 DPA 的羧基或羟基与水分子之间的竞争结合。结果,当用 280nm 紫外光激发时,DPA 吸收的能量通过天线效应转移到 Eu-CPs 上。这导致 Eu 在 618nm 处发出特征红色荧光。在 0.5-80 μM 的范围内,观察到增强的 FL 强度与 DPA 浓度之间存在强烈的线性关系。这种关系允许检测限(LOD)为 15.23 nM。此外,我们构建的 Eu-CPs 可以有效地监测芽孢杆菌孢子中 DPA 的释放,从而进一步证明了该策略在炭疽风险监测和管理中的潜在意义。这突出了该方法在实际应用中的新颖性,为炭疽杆菌提供了有价值的测定技术,并深入了解了微生物的发育周期。