“…When crushed, alliin is enzymatically hydrolysed to form allicin (2-propenyl-2-propene-thiosulphinate), which is unstable and rapidly converts to volatile sulphides-, mainly 2-propenyl (allyl) derivatives (Avato et al, 2000). These organosulphur compounds, including diallyl sulphide, diallyl disulphide and diallyl trisulphide (Naganawa et al, 1996;Kim et al, 2004;Avato et al, 2000), possess antimicrobial properties due to disulphide bond, against B. cereus, Cl. botulinum, E. coli, Lb plantarum, L. monocytogenes, P. auroginosa, S. typhymurium and S. aureus (Naganawa et al, 1996;Rattanachaikunsopon & Phumkhachorn, 2008;Fujisawa et al, 2009;Pirak et al, 2012;Fratianni et al, 2016).…”