Please use this identifier to cite or link to this item:
doi:10.22028/D291-41216
Title: | Discovery and overproduction of novel highly bioactive pamamycins through transcriptional engineering of the biosynthetic gene cluster |
Author(s): | Eckert, Nikolas Rebets, Yuriy Horbal, Lilya Zapp, Josef Herrmann, Jennifer Busche, Tobias Müller, Rolf Kalinowski, Jörn Luzhetskyy, Andriy |
Language: | English |
Title: | Microbial Cell Factories |
Volume: | 22 |
Issue: | 1 |
Publisher/Platform: | BMC |
Year of Publication: | 2023 |
Free key words: | Streptomyces Gene cluster Transcriptional refactoring Strain engineering Antibiotic |
DDC notations: | 500 Science |
Publikation type: | Journal Article |
Abstract: | Background Pamamycins are a family of highly bioactive macrodiolide polyketides produced by Streptomyces alboniger as a complex mixture of derivatives with molecular weights ranging from 579 to 705 Daltons. The large derivatives are produced as a minor fraction, which has prevented their isolation and thus studies of chemical and biological properties. Results Herein, we describe the transcriptional engineering of the pamamycin biosynthetic gene cluster (pam BGC), which resulted in the shift in production profle toward high molecular weight derivatives. The pam BGC library was constructed by inserting randomized promoter sequences in front of key biosynthetic operons. The library was expressed in Streptomyces albus strain with improved resistance to pamamycins to overcome sensitivity-related host limitations. Clones with modifed pamamycin profles were selected and the properties of engineered pam BGC were studied in detail. The production level and composition of the mixture of pamamycins was found to depend on balance in expression of the corresponding biosynthetic genes. This approach enabled the isolation of known pamamycins and the discovery of three novel derivatives with molecular weights of 663 Da and higher. One of them, homopamamycin 677A, is the largest described representative of this family of natural products with an elucidated structure. The new pamamycin 663A shows extraordinary activity (IC50 2 nM) against hepatocyte cancer cells as well as strong activity (in the one-digit micromolar range) against a range of Gram-positive pathogenic bacteria. Conclusion By employing transcriptional gene cluster refactoring, we not only enhanced the production of known pamamycins but also discovered novel derivatives exhibiting promising biological activities. This approach has the potential for broader application in various biosynthetic gene clusters, creating a sustainable supply and discovery platform for bioactive natural products. |
DOI of the first publication: | 10.1186/s12934-023-02231-x |
URL of the first publication: | https://doi.org/10.1186/s12934-023-02231-x |
Link to this record: | urn:nbn:de:bsz:291--ds-412166 hdl:20.500.11880/36967 http://dx.doi.org/10.22028/D291-41216 |
ISSN: | 1475-2859 |
Date of registration: | 27-Nov-2023 |
Description of the related object: | Supplementary Information |
Related object: | https://static-content.springer.com/esm/art%3A10.1186%2Fs12934-023-02231-x/MediaObjects/12934_2023_2231_MOESM1_ESM.pdf |
Faculty: | NT - Naturwissenschaftlich- Technische Fakultät |
Department: | NT - Pharmazie |
Professorship: | NT - Prof. Dr. Alexandra K. Kiemer NT - Prof. Dr. Andriy Luzhetskyy |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
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File | Description | Size | Format | |
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s12934-023-02231-x.pdf | 2,67 MB | Adobe PDF | View/Open |
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