Combinatorial biosynthesis yields novel hybrid argimycin P alkaloids with diverse scaffolds in Streptomyces argillaceus.


Journal

Microbial biotechnology
ISSN: 1751-7915
Titre abrégé: Microb Biotechnol
Pays: United States
ID NLM: 101316335

Informations de publication

Date de publication:
Dec 2022
Historique:
revised: 06 10 2022
received: 23 06 2022
accepted: 19 10 2022
pubmed: 9 11 2022
medline: 15 12 2022
entrez: 8 11 2022
Statut: ppublish

Résumé

Coelimycin P1 and argimycins P are two types of polyketide alkaloids produced by Streptomyces coelicolor and Streptomyces argillaceus, respectively. Their biosynthesis pathways share some early steps that render very similar aminated polyketide chains, diverging the pathways afterwards. By expressing the putative isomerase cpkE and/or the putative epoxidase/dehydrogenase cpkD from the coelimycin P1 gene cluster into S. argillaceus wild type and in argimycin mutant strains, five novel hybrid argimycins were generated. Chemical characterization of those compounds revealed that four of them show unprecedented scaffolds (quinolizidine and pyranopyridine) never found before in the argimycin family of compounds. One of these compounds (argimycin DM104) shows improved antibiotic activity. Noticeable, biosynthesis of these quinolizidine argimycins results from a hybrid pathway created by combining enzymes from two different pathways, which utilizes an aminated polyketide chain as precursor instead of lysine as it occurs for other quinolizidines.

Identifiants

pubmed: 36346129
doi: 10.1111/1751-7915.14167
pmc: PMC9733639
doi:

Substances chimiques

Plicamycin NIJ123W41V
Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2905-2916

Subventions

Organisme : Gobierno del Principado de Asturias
ID : FC-15-GRUPIN14-014
Organisme : Secretaría de Estado de Investigación, Desarrollo e Innovación
ID : BIO2014-56752-R
Organisme : Secretaría de Estado de Investigación, Desarrollo e Innovación
ID : PIM2010EEI-00752

Informations de copyright

© 2022 The Authors. Microbial Biotechnology published by Applied Microbiology International and John Wiley & Sons Ltd.

Références

Front Pharmacol. 2019 Apr 12;10:351
pubmed: 31031622
Microorganisms. 2019 May 06;7(5):
pubmed: 31064143
Curr Drug Targets. 2017 Nov 30;18(16):1825-1835
pubmed: 27440186
Nat Prod Rep. 2008 Feb;25(1):139-65
pubmed: 18250900
Front Plant Sci. 2012 Oct 26;3:239
pubmed: 23112802
Chembiochem. 2015 Nov 2;16(16):2385-91
pubmed: 26403163
Molecules. 2019 Jun 15;24(12):
pubmed: 31208056
Nucleic Acids Res. 1997 Sep 1;25(17):3389-402
pubmed: 9254694
J Asian Nat Prod Res. 2013;15(3):221-4
pubmed: 23421585
Beilstein J Org Chem. 2014 Jun 24;10:1421-32
pubmed: 24991297
J Nat Prod. 2018 Feb 23;81(2):394-399
pubmed: 29389122
Planta Med. 2016 Jun;82(9-10):857-71
pubmed: 27002401
J Nat Prod. 2014 Sep 26;77(9):2118-23
pubmed: 25215605
Chembiochem. 2015 Jul 6;16(10):1461-73
pubmed: 25892546
Org Lett. 2015 Nov 6;17(21):5344-7
pubmed: 26473429
Int J Antimicrob Agents. 2014 Nov;44(5):377-86
pubmed: 25130096
Arch Microbiol. 2007 Feb;187(2):87-99
pubmed: 17009021
Curr Opin Microbiol. 2002 Jun;5(3):274-81
pubmed: 12057681
Org Lett. 2001 Sep 20;3(19):2981-3
pubmed: 11554823
Mar Drugs. 2017 Aug 02;15(8):
pubmed: 28767052
Front Pharmacol. 2016 Sep 22;7:292
pubmed: 27713699
J Bacteriol. 1998 Sep;180(18):4929-37
pubmed: 9733697
Tetrahedron Lett. 1969 Jun;(30):2535-7
pubmed: 5801605
Microb Biotechnol. 2022 Dec;15(12):2905-2916
pubmed: 36346129
J Gen Microbiol. 1990 Aug;136(8):1447-54
pubmed: 2262785
ACS Chem Biol. 2016 Dec 16;11(12):3278-3283
pubmed: 27791349
Chem Sci. 2017 Jan 1;8(1):411-415
pubmed: 28451186
Biotechnol Adv. 2015 Sep-Oct;33(5):394-411
pubmed: 25795056
J Ind Microbiol Biotechnol. 2016 Mar;43(2-3):155-76
pubmed: 26739136
J Nat Prod. 2000 Sep;63(9):1258-60
pubmed: 11000031
Eur J Pharmacol. 2019 Sep 5;858:172472
pubmed: 31228447
Front Microbiol. 2017 Feb 10;8:194
pubmed: 28239372
Front Microbiol. 2018 Feb 16;9:252
pubmed: 29503641

Auteurs

Suhui Ye (S)

Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias (I.U.O.P.A), Universidad de Oviedo, Oviedo, Spain.
Instituto de Investigación Sanitaria de Asturias (ISPA), Oviedo, Spain.

Giovanni Ballin (G)

Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias (I.U.O.P.A), Universidad de Oviedo, Oviedo, Spain.

Ignacio Pérez-Victoria (I)

Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Armilla, Granada, Spain.

Alfredo F Braña (AF)

Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias (I.U.O.P.A), Universidad de Oviedo, Oviedo, Spain.

Jesús Martín (J)

Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Armilla, Granada, Spain.

Fernando Reyes (F)

Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Armilla, Granada, Spain.

José A Salas (JA)

Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias (I.U.O.P.A), Universidad de Oviedo, Oviedo, Spain.
Instituto de Investigación Sanitaria de Asturias (ISPA), Oviedo, Spain.

Carmen Méndez (C)

Departamento de Biología Funcional e Instituto Universitario de Oncología del Principado de Asturias (I.U.O.P.A), Universidad de Oviedo, Oviedo, Spain.
Instituto de Investigación Sanitaria de Asturias (ISPA), Oviedo, Spain.

Articles similaires

Vancomycin-associated DRESS demonstrates delay in AST abnormalities.

Ahmed Hussein, Kateri L Schoettinger, Jourdan Hydol-Smith et al.
1.00
Humans Drug Hypersensitivity Syndrome Vancomycin Female Male
Humans Arthroplasty, Replacement, Elbow Prosthesis-Related Infections Debridement Anti-Bacterial Agents
Aspergillus Hydrogen-Ion Concentration Coculture Techniques Secondary Metabolism Streptomyces rimosus
Drought Resistance Gene Expression Profiling Gene Expression Regulation, Plant Gossypium Multigene Family

Classifications MeSH