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The Antitumor Agent Ansamitocin P-3 Binds to Cell Division Protein FtsZ in Actinosynnema pretiosum .
- Source :
-
Biomolecules [Biomolecules] 2020 Apr 30; Vol. 10 (5). Date of Electronic Publication: 2020 Apr 30. - Publication Year :
- 2020
-
Abstract
- Ansamitocin P-3 (AP-3) is an important antitumor agent. The antitumor activity of AP-3 is a result of its affinity towards β-tubulin in eukaryotic cells. In this study, in order to improve AP-3 production, the reason for severe growth inhibition of the AP-3 producing strain Actinosynnema pretiosum WXR-24 under high concentrations of exogenous AP-3 was investigated. The cell division protein FtsZ, which is the analogue of β-tubulin in bacteria, was discovered to be the AP-3 target through structural comparison followed by a SPR biosensor assay. AP-3 was trapped into a less hydrophilic groove near the GTPase pocket on FtsZ by hydrogen bounding and hydrophobic interactions, as revealed by docking analysis. After overexpression of the APASM_5716 gene coding for FtsZ in WXR-30, the resistance to AP-3 was significantly improved. Moreover, AP-3 yield was increased from 250.66 mg/L to 327.37 mg/L. After increasing the concentration of supplemented yeast extract, the final yield of AP-3 reached 371.16 mg/L. In summary, we demonstrate that the cell division protein FtsZ is newly identified as the bacterial target of AP-3, and improving resistance is an effective strategy to enhance AP-3 production.
- Subjects :
- Antineoplastic Agents chemistry
Bacterial Proteins chemistry
Binding Sites
Cytoskeletal Proteins chemistry
Maytansine chemistry
Maytansine pharmacology
Protein Binding
Tubulin Modulators chemistry
Actinobacteria drug effects
Antineoplastic Agents pharmacology
Bacterial Proteins metabolism
Cytoskeletal Proteins metabolism
Maytansine analogs & derivatives
Tubulin Modulators pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 2218-273X
- Volume :
- 10
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Biomolecules
- Publication Type :
- Academic Journal
- Accession number :
- 32365857
- Full Text :
- https://doi.org/10.3390/biom10050699