Lapierre Frédéric M, Bolz Isabel, Büchs Jochen, Huber Robert
Munich University of Applied Sciences HM, Munich, Germany.
Chair of Biochemical Engineering (AVT.BioVT), RWTH Aachen University, Aachen, Germany.
Front Bioeng Biotechnol. 2022 Sep 14;10:936759. doi: 10.3389/fbioe.2022.936759. eCollection 2022.
Quantifying urease activity is an important task for Microbial Induced Calcite Precipitation research. A new urease activity microplate assay using a fluorescent pH indicator is presented. The method is also suitable for automated measurements during microbioreactor experiments. The assay reagent consists of the green fluorescent pH-indicator fluorescein, urea and a phosphate buffer. After sample addition, the microbial urease hydrolyses urea, which results in a pH and hence fluorescence increase. The fluorescence signal can be measured with a microplate reader or with the microbioreactor system BioLector, allowing for automated urease activity measurements during cultivation experiments. In both measurement systems, the fluorescence signal slope highly correlates with the urease activity measured offline with standard methods. Automated measurement is possible, as no sample preparation such as centrifugation or adjusting of the optical density is required. The assay was developed so that the culture samples turbidity, salinity or buffer concentration does not have a negative impact on the fluorescence signal. The assay allows for straightforward, non-hazardous, parallelized, cheap and reliable measurements, making research on ureolytic bacteria for Microbial Induced Calcite Precipitation more efficient. The assay could be adapted to other enzymes, which have a strong impact on the pH value.
定量测定脲酶活性是微生物诱导碳酸钙沉淀研究中的一项重要任务。本文介绍了一种使用荧光pH指示剂的新型脲酶活性微孔板检测方法。该方法也适用于微生物反应器实验中的自动测量。检测试剂由绿色荧光pH指示剂荧光素、尿素和磷酸盐缓冲液组成。加入样品后,微生物脲酶水解尿素,导致pH值升高,进而荧光增强。荧光信号可以用微孔板读数仪或微生物反应器系统BioLector进行测量,从而在培养实验中实现脲酶活性的自动测量。在这两种测量系统中,荧光信号斜率与用标准方法离线测量的脲酶活性高度相关。由于无需离心或调节光密度等样品制备步骤,因此可以进行自动测量。该检测方法的开发使得培养样品的浊度、盐度或缓冲液浓度不会对荧光信号产生负面影响。该检测方法能够实现直接、无害、并行、廉价且可靠的测量,从而使微生物诱导碳酸钙沉淀的尿素分解菌研究更加高效。该检测方法可适用于对pH值有强烈影响的其他酶。