6533b86efe1ef96bd12cc886

RESEARCH PRODUCT

Antilisterial effect of citrus essential oils and their performance inedible film formulations

Ana Jiménez-belenguerEristanna PalazzoloWalter RandazzoWalter RandazzoValeria GuarrasiMaría VargasLuca SettanniÁNgela PerdonesGiancarlo MoschettiMarta MoschettiMaria Germana

subject

CitrusTECNOLOGIA DE ALIMENTOSSettore AGR/13 - Chimica AgrariaCitruOrange (colour)medicine.disease_causeMass spectrometryBiopreservationEssential oilEdible coatingChitosanchemistry.chemical_compound0404 agricultural biotechnologyBiopreservation; Citrus; Edible coating; Essential oils; GC/MS; Listeria monocytogenes; Food Science; BiotechnologyListeria monocytogenesmedicineListeria monocytogeneChromatographybiologyGC/MSMICROBIOLOGIA04 agricultural and veterinary sciencesSettore AGR/15 - Scienze E Tecnologie AlimentariAntimicrobialbiology.organism_classification040401 food scienceListeria monocytogeneschemistryEssential oilsListeriaGas chromatographyFood ScienceBiotechnologySettore AGR/16 - Microbiologia Agraria

description

[EN] The antimicrobial activity of eight essential oils (EOs) extracted from the fruit peel of Citrus genotypes (orange, mandarin and lemon) was evaluated against 76 strains of Listeria monocytogenes, previously isolated from different food matrices. EOs showing the most (EO L2 and EO L8) and least (EO O3 and EO M7) effective inhibition activities were chemically characterized by gas chromatography coupled with mass spectrometry (GC/MS) to compare their composition. EO L2 and EO L8 were chosen to determine the MIC and to evaluate the cell viability of the most sensitive strains (L. monocytogenes LM35 and LM69) after 1, 2, 4 and 6 h of exposure. The effectiveness of chitosan (CH) and methylcellulose (MC) edible films, alone and in combination with EO L2 and EO L8, was determined against LM35 and LM69 at 37 C for 0, 8 and 24 h and at 8 C for 0, 1, 3 and 7 days. In addition, the analysis of the microstructure of the films were performed by scanning electron microscope (SEM) to evidence the interactions between the polymers and EOs. Thirty-five and twenty-nine strains were clearly inhibited by EO L2 and EO L8, respectively, while the other Citrus EOs showed poor (EO M1, O4, O5, O6) or minimal (EO O3 and M7) antimicrobial activity. A total of 36 chemical volatile substances was identified by GC/MS to detect the compounds that might play an important role in the characterization of the EOs. The chemical characterization points to oxygenated monoterpenes as relevant compounds in inhibiting Listeria strains, since they have been detected in lemon EOs in concentrations four/five folds higher than orange EOs. Generally, CH- and MCbased films containing EO L2 and EO L8 showed antilisterial activities, even though, the best performances were observed in case of CH-films at 8 C, with a major reduction up to 3 log (CFU/cm2) in case of EO L2 incorporation. The microstructures observed by SEM suggested a better incorporation of the EOs in CH matrix, where a higher amount of oil droplets was distinguished. Therefore, lemon EOs incorporated into chitosan films could be an efficient tool to control Listeria monocytogenes, especially in refrigerated applied conditions.

10.1016/j.foodcont.2015.06.057http://hdl.handle.net/10447/154402