| Literature DB >> 8076655 |
F Peypoux1, J M Bonmatin, H Labbe, I Grangemard, B C Das, M Ptak, J Wallach, G Michel.
Abstract
When Bacillus subtilis S 499 was grown on a culture medium containing L-alanine as nitrogen source, a mixture of surfactins was obtained. Suitable chromatographic conditions allowed the separation of isoforms. Among these compounds, a new variant of surfactin was isolated and its structure was established by chemical and spectrometric methods, especially by NMR spectrometry. It contains a peptide sequence which differs from that of standard surfactin by the replacement of the L-valine residue by L-alanine residue in position 4. The folding mode of [Ala4]surfactin as deduced from NMR results was compared with that of standard surfactin and the structure/properties relationship issuing from the study of this new isoform is discussed.Entities:
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Year: 1994 PMID: 8076655 DOI: 10.1111/j.1432-1033.1994.tb19998.x
Source DB: PubMed Journal: Eur J Biochem ISSN: 0014-2956