Earth and Space Science Department, University of Washington, Seattle, WA 98195, United States.
J Microbiol Methods. 2011 Dec;87(3):325-9. doi: 10.1016/j.mimet.2011.09.014. Epub 2011 Oct 4.
Investigating the biochemistry, resilience and environmental interactions of bacterial endospores often requires a pure endospore biomass free of vegetative cells. Numerous endospore isolation methods, however, neglect to quantify the purity of the final endospore biomass. To ensure low vegetative cell contamination we developed a quality control technique that enables rapid quantification of endospore harvest purity. This method quantifies spore purity using bright-field and fluorescence microscopy imaging in conjunction with automated cell counting software. We applied this method to Bacillus subtilis endospore harvests isolated using a two-phase separation method that utilizes mild chemicals. The average spore purity of twenty-two harvests was 88±11% (error is 1σ) with a median value of 93%. A spearman coefficient of 0.97 correlating automated and manual bacterial counts confirms the accuracy of software generated data.
研究细菌芽孢的生物化学、抗逆性和环境相互作用通常需要获得不含营养细胞的纯芽孢生物质。然而,许多芽孢分离方法都忽略了对最终芽孢生物质纯度的定量。为了确保低营养细胞污染,我们开发了一种质量控制技术,能够快速定量芽孢收获纯度。该方法使用明场和荧光显微镜成像以及自动细胞计数软件来定量孢子纯度。我们将该方法应用于使用两相分离法分离的枯草芽孢杆菌芽孢收获物,该方法利用温和的化学物质。二十二次收获的平均芽孢纯度为 88±11%(误差为 1σ),中位数为 93%。自动和手动细菌计数的斯皮尔曼系数为 0.97,证实了软件生成数据的准确性。