Lincomycin is one of the most important antibiotics in clinical practice. To further understand the regulatory mechanism on lincomycin biosynthesis, we investigated a pleiotropic transcriptional regulator AdpA in the lincomycin producer NRRL 2936. Deletion of (which generated Δ ) interrupted lincomycin biosynthesis and impaired the morphological differentiation. We also found that putative AdpA binding sites were unusually scattered in the promoters of all the 8 putative operons in the lincomycin biosynthetic gene cluster (BGC). In Δ , transcript levels of structural genes in 8 putative operons were decreased with varying degrees, and electrophoretic mobility shift assays (EMSAs) confirmed that AdpA activated the overall putative operons via directly binding to their promoter regions. Thus, we speculated that the entire lincomycin biosynthesis is under the control of AdpA. Besides, AdpA participated in lincomycin biosynthesis by binding to the promoter of which encoded a cluster sited regulator (CSR) LmbU of lincomycin biosynthesis. Results of qRT-PCR and catechol dioxygenase activity assay showed that AdpA activated the transcription of . In addition, AdpA activated the transcription of the by binding to its promoter, suggesting that AdpA indirectly participated in lincomycin biosynthesis and morphological differentiation. Uncommon but understandable, AdpA auto-activated its own transcription via binding to its own promoter region. In conclusion, we provided a molecular mechanism around the effect of AdpA on lincomycin biosynthesis in , and revealed a cascade regulation of lincomycin biosynthesis by AdpA, LmbU, and BldA.
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http://dx.doi.org/10.3389/fmicb.2019.02428 | DOI Listing |
Nat Chem
December 2024
Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan.
The biosynthesis of the lincosamide antibiotics lincomycin A and celesticetin involves the pyridoxal-5'-phosphate (PLP)-dependent enzymes LmbF and CcbF, which are responsible for bifurcation of the biosynthetic pathways. Despite recognizing the same S-glycosyl-L-cysteine structure of the substrates, LmbF catalyses thiol formation through β-elimination, whereas CcbF produces S-acetaldehyde through decarboxylation-coupled oxidative deamination. The structural basis for the diversification mechanism remains largely unexplored.
View Article and Find Full Text PDFBioresour Technol
January 2025
Henan Jinbaihe Biotechnology Co., LTD, Anyang 450000, Henan, China. Electronic address:
Int J Mol Sci
October 2024
College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
causes bovine mastitis, reduces milk quantity and quality, and is often resistant to antimicrobials. Selenomethionine (SeMet) is a form of selenium, which reduces reactive oxygen species (ROS)-mediated apoptosis and intramammary infections. However, the protective effects of SeMet on -infected bovine mammary epithelial cells (bMECs) are unclear.
View Article and Find Full Text PDFChemosphere
October 2024
University of São Paulo (USP), São Carlos Institute of Chemistry, São Carlos, SP, CEP 13560-97, Brazil. Electronic address:
Numerous studies reveal pollutants like clindamycin (CLD) in the environment, posing environmental and health risks. Conventional water treatment methods are ineffective at removing these contaminants, typically found in low concentrations. An innovative treatment approach is introduced through pre-concentration via adsorption, which is highly efficient, energy-saving, and reusable.
View Article and Find Full Text PDFBiochem Cell Biol
January 2025
Departamento de Producción Animal y Ciencia de los Alimentos, Facultad de Veterinaria, Universidad de Zaragoza, Zaragoza, Spain.
Antibiotics, specifically clindamycin (Clin), cause intestinal dysbiosis, reducing the microbiota with anti-inflammatory properties. Furthermore, Clin can induce alterations in the immune responses and oxidative stress. Lactoferrin, among other activities, participates in the maintenance of intestinal homeostasis and reduces dysbiosis induced by antibiotic treatment.
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