2012
DOI: 10.1016/j.postharvbio.2012.06.001
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Storage of fresh walnuts (Juglans regia L.) – Low temperature and phenolic compounds

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Cited by 53 publications
(59 citation statements)
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“…• values were similar to those previously showed for walnut (Juglans regia L.) kernels (Christopoulos and Tsantili, 2012), higher than for Brazil nut (Bertholletia excels) kernel and whole nut (John and Shahidi 2010), and also higher than baru nuts (Dipteryx alata Vog) with and without peels (Lemos et al, 2012).…”
Section: All These Dpphsupporting
confidence: 90%
See 1 more Smart Citation
“…• values were similar to those previously showed for walnut (Juglans regia L.) kernels (Christopoulos and Tsantili, 2012), higher than for Brazil nut (Bertholletia excels) kernel and whole nut (John and Shahidi 2010), and also higher than baru nuts (Dipteryx alata Vog) with and without peels (Lemos et al, 2012).…”
Section: All These Dpphsupporting
confidence: 90%
“…Recent studies have found walnut to contain several groups of polyphenols, mainly identified as tannins (Christopoulos andTsantili, 2012, Fukuda et al, 2003). Most of them contribute to the overall antioxidant capacity of walnut extracts with different in vitro and in vivo antioxidant estimation models (Fukuda et al, 2003, Fukuda et al, 2004.…”
Section: Introductionmentioning
confidence: 99%
“…The mixture was placed in a supersonic ice bath at 4°C under darkness for 15 min and then centrifuged at 4000 × g for 5 min. The procedure was repeated three times and the combined supernatants were used for both analyses …”
Section: Methodsmentioning
confidence: 99%
“…For FRAP evaluation, 0.1 mL of extract diluted with deionized water (1:2 v/v) was added to a screw top tube containing 3 mL of preheated (37 °C) FRAP reagent (300 mmol L −1 acetate buffer (C 2 H 3 NaO 2 ·3H 2 O, C 2 H 4 O 2 ), pH 3.6; 10 mmol L −1 TPTZ (2,4,6‐tripyridyl‐ s ‐triazine) in 40 mmol L −1 HCl; 20 mmol L −1 FeCl 3 ·6H 2 O; in 10:1:1 (v/v/v) ratio) . After incubation at 37 °C for 30 min, the absorbance was read at 593 nm versus a blank . Results were expressed as trolox (6‐hydroxy‐2,5,7,8‐tetramethylchroman‐2‐carboxylic acid) equivalents on FW basis.…”
Section: Methodsmentioning
confidence: 99%
“…In addition, 14 different phenylpropanoid biosynthesis and 8 different tyrosine metabolism genes were also found in our study. The role of phenolic compounds in plant physiology has been known for many years, including procyanidin and chlorogenic acid [29]. These compounds are mainly derived from phenylalanine via the general phenylpropanoid pathway [30][31].…”
Section: Discussionmentioning
confidence: 99%