NMR structure determination of a synthetic analogue of bacillomycin Lc reveals the strategic role of l-Asn1 in the natural iturinic antibiotics-Reference-Cited by-同舟云学术

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NMR structure determination of a synthetic analogue of bacillomycin Lc reveals the strategic role of l-Asn1 in the natural iturinic antibiotics

Published:2007-08 Issue:5 Volume:67 Page:1374-1381
ISSN:1386-1425
Container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

Author:

Volpon Laurent,Tsan Pascale,Majer Zsuzsa,Vass Elemer,Hollósi Miklós,Noguéra Valérie,Lancelin Jean-Marc,Besson Françoise

Publisher

Elsevier BV

Subject

Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference37 articles.

1. Iturins, a special class of pore-forming lipopeptides: biological and physicochemical properties

2. Bacterial lipopeptides induce ion-conducting pores in planar bilayers

3. Action of antifungal peptidolipids from Bacillus subtilis on the cell membrane of Saccharomyces cerevisiae.

4. Antifungal activity upon Saccharomyces cerevisiae of iturin A, mycosubtilin, bacillomycin L and of their derivatives; Inhibition of this antifungal activity by lipid antagonists.

5. NMR structure of active and inactive forms of the sterol-dependent antifungal antibiotic bacillomycin L

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5. Iturin: cyclic lipopeptide with multifunction biological potential;Critical Reviews in Food Science and Nutrition;2021-05-13

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