Multiplexed integrating plasmids for engineering of the erythromycin gene cluster for expression in Streptomyces spp. and combinatorial biosynthesis

• Published in: Applied and Environmental Microbiology Vol. 81; no. 24; pp. 8402 - 8413
• Main Authors: Fayed, Bahgat, Ashford, David A, Hashem, Amal M, Amin, Magdy A, El Gazayerly, Omaima N, Gregory, Matthew A, Smith, Margaret C M
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.12.2015
• Subjects: Anti-Bacterial Agents - biosynthesis; Bacteria; Bacterial Proteins - biosynthesis; Bacterial Proteins - genetics; Biosynthesis; Biotechnology; Chromatography, Liquid; Erythromycin - analogs & derivatives; Erythromycin - biosynthesis; Erythromycin - metabolism; Genetic Engineering; Genomes; Glycosylation; Mass Spectrometry; Metabolites; Microbiology; Multienzyme Complexes - metabolism; Multigene Family - genetics; Plasmids; Plasmids - genetics; Streptomyces; Streptomyces - genetics; Streptomyces - metabolism
• ISSN: 0099-2240; 1098-5336; 1098-6596
• DOI: 10.1128/AEM.02403-15

Bacteria in the genus Streptomyces and its close relatives are prolific producers of secondary metabolites with antibiotic activity. Genome sequencing of these bacteria has revealed a rich source of potentially new antibiotic pathways, whose products have never been observed. Moreover, these new pathways can provide novel genes that could be used in combinatorial biosynthesis approaches to generate unnatural analogues of existing antibiotics. We explore here the use of multiple orthologous integrating plasmid systems, based on the int/attP loci from phages TG1, SV1, and ϕBT1, to express the polyketide synthase (PKS) for erythromycin in a heterologous Streptomyces host. Streptomyces strains containing the three polyketide synthase genes eryAI, eryAII, and eryAIII expressed from three different integrated plasmids produced the aglycone intermediate, 6-deoxyerythronolide B (6-dEB). A further pair of integrating plasmids, both derived from the ϕC31 int/attP locus, were constructed carrying a gene cassette for glycosylation of the aglycone intermediates, with or without the tailoring gene, eryF, required for the synthesis of erythronolide B (EB). Liquid chromatography-mass spectrometry of the metabolites indicated the production of angolosaminyl-6-dEB and angolosaminyl-EB. The advantages of using multiplexed integrating plasmids for engineering expression and for combinatorial biosynthesis were demonstrated.