Phenolic Composition and Antioxidant Activities of 11 Celery Cultivars

Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p‐coumaric acid, and ferulic acid, while the identified flavonoids...

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Published inJournal of food science Vol. 75; no. 1; pp. C9 - C13
Main Authors Yao, Yang, Sang, Wei, Zhou, Mengjie, Ren, Guixing
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.01.2010
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Abstract Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p‐coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin–Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1‐diphenyl‐2‐picrylhydrazyl radical (DPPH) and 2, 2′‐azino‐bis (3‐ethylbenzthiazoline‐6‐sulphonic acid) (ABTS·+) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p‐coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.
AbstractList Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p-coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin-Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH) and 2, 2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS*...) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p-coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study. (ProQuest: ... denotes formulae/symbols omitted.)
Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p‐coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin–Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1‐diphenyl‐2‐picrylhydrazyl radical (DPPH) and 2, 2′‐azino‐bis (3‐ethylbenzthiazoline‐6‐sulphonic acid) (ABTS·+) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p‐coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.
Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p-coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin-Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH) and 2, 2′-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS·⁺) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p-coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.
Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p-coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin-Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH) and 2, 2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS.(+)) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p-coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.
Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p-coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin-Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH) and 2, 2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS.(+)) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p-coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid, p-coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin-Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1-diphenyl-2-picrylhydrazyl radical (DPPH) and 2, 2'-azino-bis (3-ethylbenzthiazoline-6-sulphonic acid) (ABTS.(+)) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was p-coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.
Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major phenolic acids identified in the extracts of these celeries were caffeic acid,  p ‐coumaric acid, and ferulic acid, while the identified flavonoids were apigenin, luteolin, and kaempferol. The contents of total phenolics were measured using a Folin–Ciocalteu assay and the total antioxidant capacity was estimated by the 1, 1‐diphenyl‐2‐picrylhydrazyl radical (DPPH) and 2, 2′‐azino‐bis (3‐ethylbenzthiazoline‐6‐sulphonic acid) (ABTS· + ) methods. Apigenin was the major flavonoid in these samples and the most abundant phenolic acid was  p‐ coumaric acid. Many of the investigated cultivars had high levels of phenolics and exhibited high antioxidant capacity. Among these 11 cultivars, Shengjie celery had the highest antioxidant activity whereas Tropica had the lowest. An extremely significant positive correlation between the antioxidant activity and the contents of total flavonoids, total phenolic acids, or total phenolics was observed in this study.
Author Zhou, Mengjie
Ren, Guixing
Yao, Yang
Sang, Wei
Author_xml – sequence: 1
  givenname: Yang
  surname: Yao
  fullname: Yao, Yang
  email: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren ( renguixing@caas.net.cn).
  organization: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren (E-mail: renguixing@caas.net.cn)
– sequence: 2
  givenname: Wei
  surname: Sang
  fullname: Sang, Wei
  email: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren ( renguixing@caas.net.cn).
  organization: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren (E-mail: renguixing@caas.net.cn)
– sequence: 3
  givenname: Mengjie
  surname: Zhou
  fullname: Zhou, Mengjie
  email: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren ( renguixing@caas.net.cn).
  organization: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren (E-mail: renguixing@caas.net.cn)
– sequence: 4
  givenname: Guixing
  surname: Ren
  fullname: Ren, Guixing
  email: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren ( renguixing@caas.net.cn).
  organization: Authors Yao, Sang, and Ren are with Inst. of Crop Science, Chinese Academy of Agricultural Sciences, Nr 80 South Xueyuan Rd., Haidian District, Beijing, People's Republic of China, 100081. Author Zhou is with Dong Zhimen Middle School, Nr 2 North Shuncheng St., Dong Cheng District, Beijing, People's Republic of China, 100007. Direct inquiries to author Ren (E-mail: renguixing@caas.net.cn)
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Issue 1
Keywords Polyphenol
Vegetables
Celery
Phenolic acid
phenolic acids
Phenols
Chemical composition
Antioxidant
flavonoids
Flavonoid
antioxidant capabilities
Cultivar
Language English
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CC BY 4.0
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PublicationTitle Journal of food science
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References Yildiz L, Baskan KS, Tutem ET, Apak R. 2008. Combined HPLC-CUPRAC (cupric ion reducing antioxidant capacity) assay of parsley, celery leaves, and nettle. Talanta 77(1):304-13.
Rice-Evans CA, Miller J, Paganga G. 1997. Antioxidant properties of phenolic compounds. Trends Plant Sci 2(4):152-9.
Sikora E, Cieslik E, Leszczynska T, Filipiak-Florkiewicz A, Pisulewski PM. 2008. The antioxidant activity of selected cruciferous vegetables subjected to aquathermal processing. Food Chem 107(1):55-9.
Wojdylo A, Oszmianski J, Czemerys R. 2007. Antioxidant activity and phenolic compounds in 32 selected herbs. Food Chem 105(3):940-9.
Wu X, Beecher GR, Holden JM, Haytowitz DB, Gebhardt SE, Prior RL. 2004. Hydrophilic antioxidant capacities of common foods in the United States. J Agric Food Chem 52(12):4026-37.
Laughton MJ, Evans PJ, Moroney MA, Hoult JRS, Halliwell B. 1991. Inhibition of mammalian 5-lipoxygenase and cyclooxygenase by flavonoids and phenolic dietary additives Relationship to antioxidant activity and to iron lon-reducing ability. Pharmacol Biochem 42(9):1673-81.
Beretta G, Granata P, Ferrero M, Orioli M, Maffei FR. 2005. Standardization of antioxidant properties of honey by a combination of spectrophotometric/fluorimetric assays and chemometrics. Anal Chim Acta 533(2):185-91.
Kahknen MP, Hopia AI, Vuorela HJ, Rauha JP, Pihlaja K, Kujala TS, Heinonen M. 1999. Antioxidant activity of plant extracts containing phenolic compounds. J Agric Food Chem 47:3954-62.
Shan B, Cai YZ, Sun M, Corke H. 2005. Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. J Agric Food Chem 53(20):7749-59.
Zhou S, Fang Z, Lü Y, Chen J, Liu D, Ye X. 2009. Phenolics and antioxidant properties of bayberry (Myrica rubra Sieb. et Zucc.) pomace. Food Chem 112(2):394-9.
Fang Z, Zhang Y, Lü Y, Ma G, Chen J, Liu D, Ye X. 2009. Phenolic compounds and antioxidant capacities of bayberry juices. Food Chem 113(4):884-8.
Ovodova RG, Golovchenko VV, Popov SV, Popova GY, Paderin NM, Shashkov AS, Ovodov YS. 2009. Chemical composition and anti-inflammatory activity of pectic polysaccharide isolated from celery stalks. Food Chem 114(2):610-5.
Chen XY, Ahn DU. 1998. Antioxidant activities of six natural phenolics against lipid oxidation induced by Fe2+ or ultraviolet light. J Am Oil Chem Soc 75(12):1717-21.
Dini I, Tenore GC, Dini A. 2009. Saponins in Ipomoea batatas tubers: isolation, characterization, quantification and antioxidang properties. Food Chem 113(2):411-9.
Tapiero H, Tew KD, Nguyen BG, Mathe G. 2002. Polyphenols: do they play a role in the prevention of human pathologies. Biomed Pharmacother 56(4):200-7.
Sultana S, Ahmed S, Jahangir T, Sharma S. 2005. Inhibitory effect of celery seeds extract on chemically induced hepatocarcinogenesis: modulation of cell proliferation, metabolism and altered hepatic foci development. Cancer Lett 221(1):11-20.
Tsi D, Tan BK. 2000. The mechanism underlying the hypocholesterolaemic activity of aqueous celery extract, its butanol and aqueous fractions in genetically hypercholesterolaemic rico rats. Life Sci 66(8):755-67.
Kim DO, Lee CY. 2004. Comprehensive study on vitamin C equivalent antioxidant capacity (VCEAC) of various polyphenolics in scavenging a free radical and its structural relationship. Crit Rev Food Sci Nutr 44(4):253-73.
Misic D, Zizovic I, Stamenic M, Asanin R, Ristic M, Petrovic SD, Skala D. 2008. Antimicrobial activity of celery fruit isolates and SFE process modeling. J Biomech Engr 42(2):148-52.
Lois R. 1994. Accumulation of UV-absorbing flavonoids induced by UV-B radiation in Ambidopsis thaliana L. Planta 194(4):498-503.
Cos P, Ying L, Calomme M, Hu JP, Cimanga K, Poel B, Pieters L, Vlietinck AJ, Vanden BD. 1998. Structure-activity relationship and classification of flavonoids as inhibitors of xanthine oxidase and superoxide scavengers. J Nat Prod 61(1):71-6.
Yen GC, Chen HY. 1995. Antioxidant activity of various tea extracts in relation to their antimutagenicity. J Agric Food Chem 43(1):27-32.
Li Y, Ou-Lee TM, Raba R, Amundson RG, Last RL. 1993. Arabidopsis flavonoid mutants are hypersensitive to UV-Birradiation. Plant Cell 5(2):171-9.
Huang ZL, Wang BW, Eaves DH, Shikany JM, Pace RD. 2007. Phenolic compound profile of selected vegetables frequently consumed by African Americans in the southeast United States. Food Chem 103(3):1395-402.
Luiz M, Biasutti A, Garcia NA. 2002. Micellar effect on the scavenging of singlet molecular oxygen by hydroxybenzenes. Redox Rep 7(1):23-8.
Rice-Evans CA, Miller NJ, Bolwell PG, Bramley PM, Pridham JB. 1995. The relative antioxidant activities of plantderived polyphenolic flavonoids. Free Radic Res 22(4):375-83.
Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice- Evans C. 1999. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 26(9-10):1231-7.
Katalinic V, Milos M, Kulisic T, Jukic M. 2006. Screening of 70 medicinal plant extracts for antioxidant capacity and total phenols. Food Chem 94(4):550-7.
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References_xml – reference: Beretta G, Granata P, Ferrero M, Orioli M, Maffei FR. 2005. Standardization of antioxidant properties of honey by a combination of spectrophotometric/fluorimetric assays and chemometrics. Anal Chim Acta 533(2):185-91.
– reference: Sikora E, Cieslik E, Leszczynska T, Filipiak-Florkiewicz A, Pisulewski PM. 2008. The antioxidant activity of selected cruciferous vegetables subjected to aquathermal processing. Food Chem 107(1):55-9.
– reference: Lois R. 1994. Accumulation of UV-absorbing flavonoids induced by UV-B radiation in Ambidopsis thaliana L. Planta 194(4):498-503.
– reference: Laughton MJ, Evans PJ, Moroney MA, Hoult JRS, Halliwell B. 1991. Inhibition of mammalian 5-lipoxygenase and cyclooxygenase by flavonoids and phenolic dietary additives Relationship to antioxidant activity and to iron lon-reducing ability. Pharmacol Biochem 42(9):1673-81.
– reference: Ovodova RG, Golovchenko VV, Popov SV, Popova GY, Paderin NM, Shashkov AS, Ovodov YS. 2009. Chemical composition and anti-inflammatory activity of pectic polysaccharide isolated from celery stalks. Food Chem 114(2):610-5.
– reference: Rice-Evans CA, Miller NJ, Bolwell PG, Bramley PM, Pridham JB. 1995. The relative antioxidant activities of plantderived polyphenolic flavonoids. Free Radic Res 22(4):375-83.
– reference: Kim DO, Lee CY. 2004. Comprehensive study on vitamin C equivalent antioxidant capacity (VCEAC) of various polyphenolics in scavenging a free radical and its structural relationship. Crit Rev Food Sci Nutr 44(4):253-73.
– reference: Yen GC, Chen HY. 1995. Antioxidant activity of various tea extracts in relation to their antimutagenicity. J Agric Food Chem 43(1):27-32.
– reference: Dini I, Tenore GC, Dini A. 2009. Saponins in Ipomoea batatas tubers: isolation, characterization, quantification and antioxidang properties. Food Chem 113(2):411-9.
– reference: Kahknen MP, Hopia AI, Vuorela HJ, Rauha JP, Pihlaja K, Kujala TS, Heinonen M. 1999. Antioxidant activity of plant extracts containing phenolic compounds. J Agric Food Chem 47:3954-62.
– reference: Li Y, Ou-Lee TM, Raba R, Amundson RG, Last RL. 1993. Arabidopsis flavonoid mutants are hypersensitive to UV-Birradiation. Plant Cell 5(2):171-9.
– reference: Sultana S, Ahmed S, Jahangir T, Sharma S. 2005. Inhibitory effect of celery seeds extract on chemically induced hepatocarcinogenesis: modulation of cell proliferation, metabolism and altered hepatic foci development. Cancer Lett 221(1):11-20.
– reference: Wojdylo A, Oszmianski J, Czemerys R. 2007. Antioxidant activity and phenolic compounds in 32 selected herbs. Food Chem 105(3):940-9.
– reference: Huang ZL, Wang BW, Eaves DH, Shikany JM, Pace RD. 2007. Phenolic compound profile of selected vegetables frequently consumed by African Americans in the southeast United States. Food Chem 103(3):1395-402.
– reference: Misic D, Zizovic I, Stamenic M, Asanin R, Ristic M, Petrovic SD, Skala D. 2008. Antimicrobial activity of celery fruit isolates and SFE process modeling. J Biomech Engr 42(2):148-52.
– reference: Fang Z, Zhang Y, Lü Y, Ma G, Chen J, Liu D, Ye X. 2009. Phenolic compounds and antioxidant capacities of bayberry juices. Food Chem 113(4):884-8.
– reference: Yildiz L, Baskan KS, Tutem ET, Apak R. 2008. Combined HPLC-CUPRAC (cupric ion reducing antioxidant capacity) assay of parsley, celery leaves, and nettle. Talanta 77(1):304-13.
– reference: Cos P, Ying L, Calomme M, Hu JP, Cimanga K, Poel B, Pieters L, Vlietinck AJ, Vanden BD. 1998. Structure-activity relationship and classification of flavonoids as inhibitors of xanthine oxidase and superoxide scavengers. J Nat Prod 61(1):71-6.
– reference: Luiz M, Biasutti A, Garcia NA. 2002. Micellar effect on the scavenging of singlet molecular oxygen by hydroxybenzenes. Redox Rep 7(1):23-8.
– reference: Tapiero H, Tew KD, Nguyen BG, Mathe G. 2002. Polyphenols: do they play a role in the prevention of human pathologies. Biomed Pharmacother 56(4):200-7.
– reference: Katalinic V, Milos M, Kulisic T, Jukic M. 2006. Screening of 70 medicinal plant extracts for antioxidant capacity and total phenols. Food Chem 94(4):550-7.
– reference: Rice-Evans CA, Miller J, Paganga G. 1997. Antioxidant properties of phenolic compounds. Trends Plant Sci 2(4):152-9.
– reference: Chen XY, Ahn DU. 1998. Antioxidant activities of six natural phenolics against lipid oxidation induced by Fe2+ or ultraviolet light. J Am Oil Chem Soc 75(12):1717-21.
– reference: Zhou S, Fang Z, Lü Y, Chen J, Liu D, Ye X. 2009. Phenolics and antioxidant properties of bayberry (Myrica rubra Sieb. et Zucc.) pomace. Food Chem 112(2):394-9.
– reference: Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice- Evans C. 1999. Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 26(9-10):1231-7.
– reference: Shan B, Cai YZ, Sun M, Corke H. 2005. Antioxidant capacity of 26 spice extracts and characterization of their phenolic constituents. J Agric Food Chem 53(20):7749-59.
– reference: Wu X, Beecher GR, Holden JM, Haytowitz DB, Gebhardt SE, Prior RL. 2004. Hydrophilic antioxidant capacities of common foods in the United States. J Agric Food Chem 52(12):4026-37.
– reference: Tsi D, Tan BK. 2000. The mechanism underlying the hypocholesterolaemic activity of aqueous celery extract, its butanol and aqueous fractions in genetically hypercholesterolaemic rico rats. Life Sci 66(8):755-67.
– volume: 2
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  publication-title: Trends Plant Sci
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  article-title: Chemical composition and anti‐inflammatory activity of pectic polysaccharide isolated from celery stalks
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  publication-title: Redox Rep
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  issue: 2
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  issue: 4
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– volume: 42
  start-page: 148
  issue: 2
  year: 2008
  ident: e_1_2_6_15_1
  article-title: Antimicrobial activity of celery fruit isolates and SFE process modeling
  publication-title: J Biomech Engr
– ident: e_1_2_6_21_1
  doi: 10.1016/j.foodchem.2007.07.023
SSID ssj0002236
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Snippet Eleven cultivars of celery, belonging to 2 species, were collected and analyzed for their phenolic compound composition and antioxidant activities. Major...
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SubjectTerms analysis
antioxidant activity
antioxidant capabilities
Antioxidants
Antioxidants - analysis
apigenin
Apigenin - analysis
Apium
Apium graveolens - chemistry
Apium graveolens - growth & development
Apium graveolens var. dulce
Biological and medical sciences
Caffeic Acids
Caffeic Acids - analysis
celery
chemistry
Coumaric Acids
Coumaric Acids - analysis
Cultivars
Flavonoids
Flavonoids - analysis
food analysis
food composition
Food industries
Food science
Fruit and vegetable industries
Fundamental and applied biological sciences. Psychology
growth & development
isolation & purification
Kaempferols
Kaempferols - analysis
Luteolin
Luteolin - analysis
p-coumaric acid
phenolic acids
Phenols
Phenols - analysis
Phenols - chemistry
Phenols - isolation & purification
Phytochemicals
Vegetables
Title Phenolic Composition and Antioxidant Activities of 11 Celery Cultivars
URI https://api.istex.fr/ark:/67375/WNG-P0LN2Z7F-8/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1750-3841.2009.01392.x
https://www.ncbi.nlm.nih.gov/pubmed/20492156
https://www.proquest.com/docview/194423959
https://www.proquest.com/docview/46551294
https://www.proquest.com/docview/733559441
https://www.proquest.com/docview/743724160
Volume 75
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