Julou Thomas, Desprat Nicolas, Bensimon David, Croquette Vincent
Laboratoire de Physique Statistique de l'École Normale Supérieure, UMR8550, associé au CNRS et aux Universités Paris VI et Paris VII, 24 rue Lhomond, 75005 Paris, France.
Rev Sci Instrum. 2012 Jul;83(7):074301. doi: 10.1063/1.4729796.
We propose a new and simple method for the measurement of microbial concentrations in highly diluted cultures. This method is based on an analysis of the intensity fluctuations of light scattered by microbial cells under laser illumination. Two possible measurement strategies are identified and compared using simulations and measurements of the concentration of gold nanoparticles. Based on this comparison, we show that the concentration of Escherichia coli and Saccharomyces cerevisiae cultures can be easily measured in situ across a concentration range that spans five orders of magnitude. The lowest measurable concentration is three orders of magnitude (1000×) smaller than in current optical density measurements. We show further that this method can also be used to measure the concentration of fluorescent microbial cells. In practice, this new method is well suited to monitor the dynamics of population growth at early colonization of a liquid culture medium. The dynamic data thus obtained are particularly relevant for microbial ecology studies.
我们提出了一种用于测量高度稀释培养物中微生物浓度的新颖且简单的方法。该方法基于对激光照射下微生物细胞散射光强度波动的分析。通过对金纳米颗粒浓度的模拟和测量,确定并比较了两种可能的测量策略。基于此比较,我们表明可以在跨越五个数量级的浓度范围内轻松原位测量大肠杆菌和酿酒酵母培养物的浓度。最低可测量浓度比当前光密度测量低三个数量级(1000倍)。我们进一步表明,该方法还可用于测量荧光微生物细胞的浓度。在实际应用中,这种新方法非常适合监测液体培养基早期定殖时种群生长的动态。由此获得的动态数据对于微生物生态学研究尤为重要。