“…Considering the molecular mass of different homologs of lichenysin (C 12 –C 16 ), these peaks were identified as protonated ions [M + H] +
m/z 1049.1; sodium adduct ions [M + Na] + with m/z of 1015.5, 1029.5, 1043.5, and 1057.6; sodium adducts [M-H + 2Na] + with m/z of 1051.5, 1065.5, and 1079.5; potassium adducts [M + K] + with m/z of 1087.5. MALDI-TOF analysis of W16 biosurfactant showed similarity with lichenysin-A, produced by B. licheniformis strains (Grangemard et al, 1999; Mikkola et al, 2000; Li et al, 2008; Zhang et al, 2014; Joshi et al, 2015). They have reported that lichenysin – A is a cyclic heptalipopeptide having a small peptide (Gln, Leu, Leu, Val, Asp, Leu, and Ile) linked to 3-hydroxy fatty acid residue with amide (Gln) and lactone (Ile) bonds forming a cyclic structure, with main fatty acids are 3-hydroxylated tri, tetra, penta, and hexadecanoic acids.…”