To decipher the role of MSMEG_5850 in the physiology of mycobacteria. was knocked out and RNA sequencing was performed. MSMEG_5850 protein was purified from the pET28a system. Electrophoretic mobility shift assay and size exclusion chromatography were used to determine the binding of MSMEG_5850 to its motif and binding stoichiometry. The effect of nutritional stress was monitored. Transcriptome analysis revealed the differential expression of 148 genes in an knockout strain. MSMEG_5850 had control over 50 genes because those genes had a binding motif upstream of their sequence. The electrophoretic mobility shift assay showed MSMEG_5850 bound to its motif as a monomer. was upregulated under nutritional stress and promoted the survival of mycobacteria. The study confirms the role of MSMEG_5850 in global transcriptional regulation.
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http://dx.doi.org/10.2217/fmb-2022-0238 | DOI Listing |
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