7 ± 1.4Ψ 2.7 ± 1.4 1.1 (0.8, 1.48)& Predicted peptidase proW b2678 2.4 ± 1.1 3.3 ± 1.3 -1.6 (-1.1, -2.3) Glycine betaine transporter subunit ansP b1453 2.2 ± 1.1 2.5 ± 1.1 1.2 (0.9, 1.48) L-asparagine transporter ydhB b1659 -2.2 ± 1.1 -2.9 ±

1.2 -5.0 (-4.4, -5.7) Predicted DNA-binding transcriptional regulator yhhN b3468 -2.6 ± 1.3 -3.1 ± 1.2 -3.1 (-2.8, -3.4) Conserved inner membrane protein ygeV b2869 -2.7 ± 1.1 -3.3 ± 1.4 SRT1720 -1.6 (-1.4, -1.7) Predicted DNA-binding transcriptional regulator flhE b1878 -2.7 ± 1.2 -3.2 ± 1.2 -1.8 (-1.7, -2.0) Conserved protein yicG b3646 -3.0 ± 1.2 -4.6 ± 1.3 -3.7 (-3.3, -4.1) Conserved inner membrane protein # Fold-changes of gene expression were significantly different from 2, with one-tail t-tests performed (p < 0.05). *Sorted E. coli cells: E. coli cells treated with dispersion/homogenization and IMS cell sorting after pre-stored in RNAlater; Unsorted E. coli cells: E. coli cells continuously stored in RNAlater without any treatment. ⊕Annotations are updated according to records of E. coli K-12 MG1655 in NCBI Entrenz Gene Database. ΨMean ± geometric standard deviation from two replicate slides, with three built-in replicates in each slide; positive and negative values indicate up- and down-regulation, respectively, in dispersed and IMS sorted cells. Geometric standard deviation is 2SD, where SD is standard deviation of log2 transformation of fold-change.

&Mean of the fold change in gene expression from four replicates (ranges of fold change are given in parentheses), positive and negative values indicate up- and down- regulation, https://www.selleckchem.com/screening/ion-channel-ligand-library.html respectively, in dispersed and IMS sorted cells quantified by the method of qPCR. This study developed and evaluated Fossariinae a method that can be used to study the transcriptome of one species in mixed-species communities, including suspended cultures and biofilms. It was not surprising to find some genes with changed expression after several treatment steps, i.e., cell homogenization/dispersion, re-suspension in buffer, and IMS cell sorting. However, the number of differentially

expressed genes was very low (eight genes correspond to 0.2% of the 4,289 ORFs). We further searched in the literature whether the eight differentially expressed genes were involved in species interactions or biofilm formation, since this method was specifically developed to identify genes involved in bacterial species interactions in mixed-species communities, including in biofilm communities. None of the eight genes has been shown to be involved in bacterial species interactions. With regard to biofilm formation, only one of the eight genes, flhE, showed a potential effect on biofilm formation by LXH254 concentration Salmonella typhimurium in one study [25]. Thus, it can be concluded that transcription profiles of enriched E. coli cells were well preserved during IMS and the use of IMS to separate E.