A novel lipopeptide, an inhibitor of bacterial adhesion, from the thermophilic and halotolerant subsurface Bacillus licheniformis strain 603

Autor: Stanislav E. Esipov, Yuri A. Nikolaev, Sergey M Lukin, Tatiana A Rodionova, Stanislav G. Batrakov, Nina V. Shekhovtsova, Nikolai S Panikov, Vladimir I Sheichenko, N. B. Polyakov
Rok vydání: 2003
Předmět:
Zdroj: Biochimica et biophysica acta. 1634(3)
ISSN: 0006-3002
Popis: A new Bacillus licheniformis strain, 603, isolated from a mixture of drilling fluid and subsurface thermal water, has been found to produce a cyclic lipopeptide which is released into cultural medium as well as present in cells as the major lipid constituent (57% of the total cell lipids extractable with 2:1 chloroform–methanol). The quantitative ratio of the extracellular and intracellular lipopeptide has been estimated as 23:10. The metabolite represents a heptapeptide, l -Asp→ l -Leu→ l -Leu→ l -Val→ l -Val→ l -Glu→ l -Leu, N-acylated to the N-terminal amino acid, l -Asp, by a 3-hydroxy fatty acid (from 13:0 to 17:0 with n-, iso-, and anteiso-chains), the 3-OH group of which is esterified by the C-terminal amino acid, l -Leu. The chemical structure of the lipopeptide has been established by means of infrared (IR), 1H- and 13C-nuclear magnetic resonance (NMR) spectroscopy, electrospray ionisation (ESI) mass spectrometry (MS), including secondary ion mass spectrometry, along with chemical and enzymatic degradation. Although a diversity of similar metabolites synthesised by various B. licheniformis strains are presently known, such a structure has not been reported thus far. Added to the growth medium of strain 603 at the concentration of 1.6 μg/ml, the lipopeptide prevents adhesion of cells to a glass surface. Also, it exhibits a considerable growth-inhibiting activity against Corynebacterium variabilis and a much lower activity against Acinetobacter sp.
Databáze: OpenAIRE