“…Our characterization of the biocathode-MCL community activity by metatranscriptomics supports previous metaproteomic and 16S rRNA amplicon characterizations of biocathode-MCL indicating that there is substantial variability in the abundance of specific bacteria, even between seemingly identical reactors inoculated on the same day with the same inoculum (10, 19). However, the major constituents that are present have been stable for over 6 years, as measured by several methods, including the use of 16S clone libraries, metagenomics, proteomics, 16S amplicon sequencing, and fluorescence in situ hybridization microscopy (9, 10, 13, 19, 20), allowing us to use the previously generated metagenome sequencing data to align the metatranscriptomics data.…”