作者: Y. Akselband , C. Cabral , T.P. Castor , H.M. Chikarmane , P. McGrath
DOI: 10.1016/J.JEMBE.2005.08.018
关键词:
摘要: Encapsulation of cells in agarose gel microdrops (GMDs) combined with fluorescence-activated cell sorting (FACS) has been used previously to analyze and recover specific mammalian, bacterial, yeast populations. Recently, we have developed a method enrich mixed bacterial populations for slow-growing microorganisms using the GMD Growth Assay fluorochrome staining flow cytometry. Here, demonstrate feasibility this experimental approach detect clonogenic growth individual bacteria within GMDs less than 3 h separate subpopulations based on differential rates. We show that after sorting, organisms remain viable can be propagated culture further analysis.