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Characterisation of Taxlllaids A-G; Natural Products from Xenorhabdus indica.

Authors :
Kronenwerth, Max
Bozhüyük, Kenan A. J.
Kahnt, Astrid S.
Steinhilber, Dieter
Gaudriault, Sophie
Kaiser, Marcel
Bode, Helge B.
Source :
Chemistry - A European Journal; Dec2014, Vol. 20 Issue 52, p17478-17487, 10p
Publication Year :
2014

Abstract

Six new lipodepsipeptides and an additional linear derivative named taxlllaids A-G ( 1- 7) have been identified in the entomopathogenic bacterium Xenorhabdus indica. The structures of the main compounds have been solved by detailed NMR spectroscopic analysis and the structures of minor derivatives were elucidated by a combination of labelling experiments and detailed MS experiments. The absolute configuration of the taxlllaids was deduced by using the advanced Marfey method and analysis of the biosynthesis gene cluster showing the presence of epimerisation domains, which was subsequently proved to be correct by solid-phase peptide synthesis of all taxlllaids. The exchange of a single amino acid in the adenylation domain was shown to be responsible for substrate promiscuity of the third A domain, resulting in the incorporation of leucine, phenylalanine or tyrosine. Bioactivity testing revealed the taxlllaids to be weakly active against Plasmodium falciparum and against a number of eukaryotic cell lines. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09476539
Volume :
20
Issue :
52
Database :
Complementary Index
Journal :
Chemistry - A European Journal
Publication Type :
Academic Journal
Accession number :
100012509
Full Text :
https://doi.org/10.1002/chem.201403979