A novel reporter system for bacterial and mammalian cells based on the non-ribosomal peptide indigoidine

The biosynthesis of non-ribosomal peptides, many of which have pharmaceutical activities, is an evolutionary privilege of microorganisms. Capitalizing on the universal set of the Streptomyces lavendulae non-ribosomal peptide synthase BpsA and the Streptomyces verticillus 4′-phosphopantetheinyl trans...

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Veröffentlicht in:Metabolic engineering 2012-07, Vol.14 (4), p.325-335
Hauptverfasser: Müller, Marius, Ausländer, Simon, Ausländer, David, Kemmer, Christian, Fussenegger, Martin
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Sprache:eng
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Zusammenfassung:The biosynthesis of non-ribosomal peptides, many of which have pharmaceutical activities, is an evolutionary privilege of microorganisms. Capitalizing on the universal set of the Streptomyces lavendulae non-ribosomal peptide synthase BpsA and the Streptomyces verticillus 4′-phosphopantetheinyl transferase Svp, we have engineered Escherichia coli as well as mammalian cells, including human stem cells, to produce the blue 3,3’-bipyridyl pigment keto-indigoidine and the reduced colorless but fluorescent leuco-isoform. Detailed characterization of a tailored substrate-free chromogenic assay and FACS analysis showed that indigoidine’s blue color and fluorescence could be reliably profiled in bacteria and mammalian cells using standard multiwell-compatible detection equipment. Besides serving as an inexpensive, reliable, versatile and easy-to-assay cross-kingdom reporter system, the potential of having mammalian cells produce non-ribosomal peptides, preferably ones with biopharmaceutical activities, may provide novel treatment opportunities in future gene- and cell-based therapies. ► Engineered mammalian cells produce the non-ribosomal peptide indigoidine. ► Indigoidine is an inert blue pigment that can be extracted and quantified in a single step. ► The colorless fluorescent leuco-indigoidine is compatible with FACS analysis. ► Indigoidine is a versatile and universal reporter for bacteria and mammalian cells.
ISSN:1096-7176
1096-7184
DOI:10.1016/j.ymben.2012.04.002