SRX7135232 GSM4159195 SRP229728 SRS5644150 GSM4159195 RNA-Seq TRANSCRIPTOMIC cDNA Bacteria were lysed by constantly grinding in the presence of liquid nitrogen with the total RNA extracted using TRIzol reagent (Invitrogen), and finally dissolved in 50 μL RNase-free water. The total RNA quality was evaluated after ribosomal RNAs were removed. The RNA was then fragmented and used as a template for a randomly primed PCR. Strand-specific cDNA libraries were prepared by standard techniques for subsequent Illumina sequencing (Illumina HiSeq 2000) Illumina HiSeq 2000 gds 304159195 GSM4159195 GEO Accession GSM4159195 SRX7135233 GSM4159196 SRP229728 SRS5644151 GSM4159196 RNA-Seq TRANSCRIPTOMIC cDNA Bacteria were lysed by constantly grinding in the presence of liquid nitrogen with the total RNA extracted using TRIzol reagent (Invitrogen), and finally dissolved in 50 μL RNase-free water. The total RNA quality was evaluated after ribosomal RNAs were removed. The RNA was then fragmented and used as a template for a randomly primed PCR. Strand-specific cDNA libraries were prepared by standard techniques for subsequent Illumina sequencing (Illumina HiSeq 2000) Illumina HiSeq 2000 gds 304159196 GSM4159196 GEO Accession GSM4159196 SRX7135234 GSM4159197 SRP229728 SRS5644152 GSM4159197 RNA-Seq TRANSCRIPTOMIC cDNA Bacteria were lysed by constantly grinding in the presence of liquid nitrogen with the total RNA extracted using TRIzol reagent (Invitrogen), and finally dissolved in 50 μL RNase-free water. The total RNA quality was evaluated after ribosomal RNAs were removed. The RNA was then fragmented and used as a template for a randomly primed PCR. Strand-specific cDNA libraries were prepared by standard techniques for subsequent Illumina sequencing (Illumina HiSeq 2000) Illumina HiSeq 2000 gds 304159197 GSM4159197 GEO Accession GSM4159197 SRX7135235 GSM4159198 SRP229728 SRS5644153 GSM4159198 RNA-Seq TRANSCRIPTOMIC cDNA Bacteria were lysed by constantly grinding in the presence of liquid nitrogen with the total RNA extracted using TRIzol reagent (Invitrogen), and finally dissolved in 50 μL RNase-free water. The total RNA quality was evaluated after ribosomal RNAs were removed. The RNA was then fragmented and used as a template for a randomly primed PCR. Strand-specific cDNA libraries were prepared by standard techniques for subsequent Illumina sequencing (Illumina HiSeq 2000) Illumina HiSeq 2000 gds 304159198 GSM4159198 GEO Accession GSM4159198