2018
DOI: 10.1007/s13197-018-3373-x
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In vitro antibacterial activity of nut by-products against foodborne pathogens and their application in fresh-cut fruit model

Abstract: Aqueous extract of nut by-products (cashewnut shell, coconut shell, and peanut hull) were studied for their physicochemical properties, antibacterial activity and food preservation potential in an artificially inoculated fresh-cut fruit (papaya) model. Physicochemical characteristics revealed the colour, odor, nearly neutral pH (6.67-6.83), high water solubility (69.18-82.63%) and total phenolic content (1130.54-2403.41 mg GAE/100 g) of the extracts. The antibacterial property of the extracts evaluated by zone… Show more

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Cited by 17 publications
(7 citation statements)
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“…H2O2, ozone, organic acids (e.g. acetic, citric, succinic, malic, tartaric, benzoic, propanoic and sorbic acids) and peroxyacetic acids used as an alternative to chlorine also have limited effects in killing microorganisms (Prakash et al, 2018). Furthermore, biopreservation methods, defined as the "use of living organisms to suppress the population density or impact of a specific pest organism, making it less abundant or less damaging than it would otherwise be" (Eilenberg et al, 2001) are preferred in order to inhibit microbial growth and increase shelf life of FCFs.…”
Section: Rojas-graü Et Al 2007mentioning
confidence: 99%
“…H2O2, ozone, organic acids (e.g. acetic, citric, succinic, malic, tartaric, benzoic, propanoic and sorbic acids) and peroxyacetic acids used as an alternative to chlorine also have limited effects in killing microorganisms (Prakash et al, 2018). Furthermore, biopreservation methods, defined as the "use of living organisms to suppress the population density or impact of a specific pest organism, making it less abundant or less damaging than it would otherwise be" (Eilenberg et al, 2001) are preferred in order to inhibit microbial growth and increase shelf life of FCFs.…”
Section: Rojas-graü Et Al 2007mentioning
confidence: 99%
“…The initial inoculum was confirmed by plating 100 µl from the appropriate dilution in triplicate before inoculating it into each sample. Inoculated FCFV were kept for 30 min in the laminar hood flow for air-dried and allowed complete microbial attachment on samples (Choi et al, 2015;Prakash et al, 2018). Therefore, the experiment conducted in 1 pathogen species × 1 produces type × 3 replicates = 3 treatment combinations.…”
Section: Preparation Of Fresh-cut Samples and Inoculummentioning
confidence: 99%
“…After drying, all portions were aseptically transferred into a light density poly-ethylene (LDPE) zip-lock bag (15 × 22 cm) to prepared RTD-FCFV (22 ± 1℃), and plastic tray covered with stretchable cling film to prepare CS-FCFV (4 ± 0.5℃). One bag or tray of 25 g samples represented an experimental replicate and triplicate was done (Akbas & Ölmez, 2007;Prakash et al, 2018;Ramli et al, 2017). Microbiological analysis and flesh color measurement were conducted periodically on an hour basis (RTD-FCFV; 0 to 4 hr) and daily basis (CS-FCFV; day 0 to 4).…”
Section: Dipping Treatment In Fcfvmentioning
confidence: 99%
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