Stuart Rhona K, Mayali Xavier, Thelen Michael P, Pett-Ridge Jennifer, Weber Peter K
Physical and Life Sciences Division, Lawrence Livermore National Laboratory, Livermore, USA.
Bio Protoc. 2017 May 5;7(9):e2263. doi: 10.21769/BioProtoc.2263.
To advance the understanding of microbial interactions, it is becoming increasingly important to resolve the individual metabolic contributions of microorganisms in complex communities. Organisms from biofilms can be especially difficult to separate, image and analyze, and methods to address these limitations are needed. High resolution imaging secondary ion mass spectrometry (NanoSIMS) generates single cell isotopic composition measurements, and can be used to quantify incorporation and exchange of an isotopically labeled substrate among individual organisms. Here, incorporation of cyanobacterial extracellular organic matter (EOM) by members of a cyanobacterial mixed species biofilm is used as a model to illustrate this method. Incorporation of stable isotope labeled (N and C) EOM by two groups, cyanobacteria and associated heterotrophic microbes, are quantified. Methods for generating, preparing, and analyzing samples for quantifying uptake of stable isotope-labeled EOM in the biofilm are described.
为了增进对微生物相互作用的理解,解析复杂群落中微生物的个体代谢贡献变得越来越重要。生物膜中的生物体尤其难以分离、成像和分析,因此需要解决这些限制的方法。高分辨率成像二次离子质谱(NanoSIMS)可生成单细胞同位素组成测量值,并可用于量化同位素标记底物在个体生物体之间的掺入和交换。在这里,以蓝藻混合物种生物膜成员对蓝藻细胞外有机物(EOM)的掺入作为模型来说明此方法。对两组(蓝藻和相关异养微生物)对稳定同位素标记(N和C)EOM的掺入进行了量化。描述了用于生成、制备和分析生物膜中稳定同位素标记EOM摄取量定量样品的方法。