CtcS, a MarR family regulator, regulates chlortetracycline biosynthesis

• Published in: BMC microbiology Vol. 19; no. 1; p. 279
• Main Authors: Kong, Lingxin, Liu, Jia, Zheng, Xiaoqing, Deng, Zixin, You, Delin
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 10.12.2019; BioMed Central; BMC
• Subjects: Antibiotic resistance; Antibiotics; Binding sites; Biosynthesis; Cell differentiation; Cell growth; Chlortetracycline; Control engineering; CtcS; Daptomycin; Deoxyribonuclease; Deoxyribonucleic acid; DNA; Efflux; Engineering; Footprinting; Gene regulation; Genes; Genetic engineering; Inverted repeat; MarR family regulator; Metabolism; Metabolites; Microbial drug resistance; Nucleases; Oxytetracycline; Pathogenic microorganisms; Physiological aspects; Production management; Protein binding; Proteins; Regulatory mechanisms (biology); Resource allocation; Tetracycline family antibiotics; Tetracyclines; Transcription; Transcription (Genetics); Transcriptional regulation; MarR family regulator; CtcS; Chlortetracycline; Tetracycline family antibiotics; Transcriptional regulation
• ISSN: 1471-2180; 1471-2180
• DOI: 10.1186/s12866-019-1670-9

Chlortetracycline (CTC) is one of the commercially important tetracyclines (TCs) family product and is mainly produced by Streptomyces. CTC is still in a great demand due to its broad-spectrum activity against pathogens. Engineering transcriptional control allows the cell to allocate its valuable resources towards protein production and provides an important method for the build-up of desired metabolites. Despite extensive efforts concerning transcriptional regulation for increasing the productivities of TCs, the regulatory mechanisms of the CTC biosynthesis remain poorly understood. In this study, the possible regulatory function of CtcS, a potential member of MarR (multiple antibiotic resistance regulator) family of transcriptional regulators in S. aureofaciens F3, was demonstrated. Knockdown of ctcS altered the transcription of several biosynthesis-related genes and reduced the production of tetracycline (TC) and CTC, without obvious effect on morphological differentiation and cell growth. Especially, CtcS directly repressed the transcription of the adjacent divergent gene ctcR (which encodes a putative TC resistance efflux protein). A CtcS-binding site was identified within the promoter region of ctcR by DNase I footprinting and an inverted repeat (5'-CTTGTC-3') composed of two 6-nt half sites in the protected region was found. Moreover, both CTC and TC could attenuate the binding activity of CtcS with target DNA. ctcS regulated the production of TC and CTC in S. aureofaciens F3 and the overexpression of it could be used as a simple approach for the construction of engineering strain with higher productivity. Meanwhile, CtcS was characterized as a TC- and CTC-responsive MarR family regulator. This study provides a previously unrecognized function of CtcS and will benefit the research on the regulatory machinery of the MarR family regulators.