A derivative of the glycopeptide A40926 produced by inactivation of the β-hydroxylase gene in Nonomuraea sp. ATCC39727

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Abstract

The actinomycete Nonomuraea sp. ATCC39727 produces the glycopeptide A40926. In the corresponding dbv cluster, ORF28 encodes a putative hydroxylase. A gene replacement mutant of ORF28 in Nonomuraea produces a small amount of an A40926-related metabolite, 16 amu smaller than the parent compound, which was identified as the desoxyderivative of A40926 lacking the β-hydroxyl group on the tyrosine moiety. This result demonstrates that ORF28 is actually involved in the formation of the β-hydroxytyrosine residue present in A40926. The formation of an altered glycopeptide and the inability to rescue A40926 production upon feeding free β-hydroxytyrosine are consistent with the possibility that, in contrast to balhimycin formation, hydroxylation occurs after tyrosine activation by the nonribosomal peptide synthetase. © 2006 Federation of European Microbiological Societies Published by Blackwell Publishing Ltd. All rights reserved.

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Stinchi, S., Carrano, L., Lazzarini, A., Feroggio, M., Grigoletto, A., Sosio, M., & Donadio, S. (2006). A derivative of the glycopeptide A40926 produced by inactivation of the β-hydroxylase gene in Nonomuraea sp. ATCC39727. FEMS Microbiology Letters, 256(2), 229–235. https://doi.org/10.1111/j.1574-6968.2006.00120.x

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