SRX3372251 GSM2844106 SRP124494 SRS2669588 GSM2844106 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844106 GSM2844106 GEO Accession GSM2844106 SRX3372252 GSM2844107 SRP124494 SRS2669587 GSM2844107 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844107 GSM2844107 GEO Accession GSM2844107 SRX3372253 GSM2844108 SRP124494 SRS2669590 GSM2844108 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844108 GSM2844108 GEO Accession GSM2844108 SRX3372254 GSM2844109 SRP124494 SRS2669589 GSM2844109 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844109 GSM2844109 GEO Accession GSM2844109 SRX3372255 GSM2844110 SRP124494 SRS2669592 GSM2844110 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844110 GSM2844110 GEO Accession GSM2844110 SRX3372256 GSM2844111 SRP124494 SRS2669595 GSM2844111 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844111 GSM2844111 GEO Accession GSM2844111 SRX3372257 GSM2844112 SRP124494 SRS2669591 GSM2844112 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844112 GSM2844112 GEO Accession GSM2844112 SRX3372258 GSM2844113 SRP124494 SRS2669594 GSM2844113 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844113 GSM2844113 GEO Accession GSM2844113 SRX3372259 GSM2844114 SRP124494 SRS2669593 GSM2844114 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844114 GSM2844114 GEO Accession GSM2844114 SRX3372260 GSM2844115 SRP124494 SRS2669596 GSM2844115 RIP-Seq TRANSCRIPTOMIC other Bacteria were lysed and the FLAG-tagged proteins was immunoprecipitated using a monoclonal anti-FLAG antibody. The samples were treated with benzonase nuclease, calf intestine phophorylase, and polynucleotide kinase in the presence of radioactive gamma-ATP. Samples were separated with SDS-PAGE and followed by transfer to nitrocellulose membranes. Radioactively labelled RNA-protein complexes were eluted from membranes and treated with Proteinase K. RNA was purified with phenol:chloroform extraction and ethanol precipitation. Purified RNA was used as input for library preparation using the NEB Next Small RNA Library kit according to the manufacturer's instructions. NextSeq 500 gds 302844115 GSM2844115 GEO Accession GSM2844115