2018
DOI: 10.1016/j.lwt.2018.03.071
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Storage stability of minced beef supplemented with chickpea legumin at 4 °C as a potential substitute for nisin

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Cited by 23 publications
(22 citation statements)
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“…So, the current material is probably more useful than both legumin and nisin. Additionally, the pH maintaining action of CFG (100 µg g −1 ) on the preserved meat seems more effective than other natural preservatives, e.g., chickpea legumin, Phaseolus vulgaris protein hydrolysates, Nigella sativa oil and clove oil, which maintained the meat pH at around 6.9 after 14 days of cold storage [20][21][22][23], against a pH of only 6.2 in the current study.…”
Section: Discussionmentioning
confidence: 56%
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“…So, the current material is probably more useful than both legumin and nisin. Additionally, the pH maintaining action of CFG (100 µg g −1 ) on the preserved meat seems more effective than other natural preservatives, e.g., chickpea legumin, Phaseolus vulgaris protein hydrolysates, Nigella sativa oil and clove oil, which maintained the meat pH at around 6.9 after 14 days of cold storage [20][21][22][23], against a pH of only 6.2 in the current study.…”
Section: Discussionmentioning
confidence: 56%
“…Based on this result, it can be extrapolated that the spoilage point can be moved to a time point farther than 15 days on the storage time scale, especially when supplemented by a high dose of CFG. Resisting the increase in pH may mean reducing the contamination by the bacteria producing the basic substances (e.g., ammonia, amines) and restricting protein degradation [20,57]. The pH-reducing effect of CFG on minced beef at 100 µg g −1 is probably equivalent to the action of legumin and nisin at a higher concentration (200 µg g −1 ), as reported in [20].…”
Section: Discussionmentioning
confidence: 84%
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“…Biochemistry, Dept., Fac., Agric., Zagazig Univ., An amount of bacteriocin from lactic acid bacteria (10 mg) was dispersed in 1ml SDS 10% with 100 µl β-mercaptoethanol for 15 min with vortexing every 5 min. The extract was centrifuged at 10,000 rpm for 10 min (Osman et al, 2018). A mixture of 20 µl extract and 20 µl of SDS-loading sample buffer (SDS 4%, βmercaptoethanol 3%, glycerol 20%, Tris HCl 50 mM pH 6.8 and bromophenol blue traces), was heated at 96°C for 3 min and 10 µl aliquot (per lane) was electrophoresed by SDS-PAGE according to (Laemmli, 1970).…”
Section: Molecular Weight Determination Of Protein By Sds Pagementioning
confidence: 99%