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Antioxidant Constituents in Distillation Residue of Awamori Spirits

Constituents in a distillation residue of Awamori (millet spirits) and their antioxidant activity are investigated in this study. The supernatant of the distillation residue obtained by centrifugation was partitioned with n-hexane, chloroform, ethyl acetate, and n-butanol against water to afford the...

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Published in:Journal of agricultural and food chemistry 2007-01, Vol.55 (1), p.75-79
Main Authors: Takaya, Yoshiaki, Furukawa, Tadashi, Miura, Shunsuke, Akutagawa, Takashi, Hotta, Yoshihiro, Ishikawa, Naohisa, Niwa, Masatake
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cited_by cdi_FETCH-LOGICAL-a471t-e42f40c225a84f58f057f76cd1a0533474f2cd9e949961469008c691cfef385b3
cites cdi_FETCH-LOGICAL-a471t-e42f40c225a84f58f057f76cd1a0533474f2cd9e949961469008c691cfef385b3
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container_issue 1
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container_title Journal of agricultural and food chemistry
container_volume 55
creator Takaya, Yoshiaki
Furukawa, Tadashi
Miura, Shunsuke
Akutagawa, Takashi
Hotta, Yoshihiro
Ishikawa, Naohisa
Niwa, Masatake
description Constituents in a distillation residue of Awamori (millet spirits) and their antioxidant activity are investigated in this study. The supernatant of the distillation residue obtained by centrifugation was partitioned with n-hexane, chloroform, ethyl acetate, and n-butanol against water to afford the corresponding solubles. Among them, n-hexane and chloroform solubles showed higher antioxidant potency than l-ascorbic acid by the bleomycin−Fe method. In chloroform solubles, seven cyclic dipeptides were identified along with ethyl 2-pyrrolidione-5-carboxylate, tyrosol, and ethyl p-hydoroxyphenyllactate. Antioxidant activity of ethyl p-hydoroxyphenyllactate was 4.2 times that of l-ascorbic acid, whereas cyclic dipeptides showed activity 0.89−1.29 times as strong as that of l-ascorbic acid. On the other hand, scavenging effect of cyclic dipeptides against O2 -• and OH• by using electron spin resonance was also investigated. In the results, cyclo(l-Ile-l-Pro) showed significantly strong inhibitory effect against OH• (95.4% at 2.5 × 10-3 M) and cyclo(l-Phe-l-Pro), cyclo(l-Pro-l-Val), and cyclo(l-Leu-l-Pro) inhibited OH• 64.9, 54.1, and 51.0%, respectively, whereas α-tocopherol showed 37.7% inhibition, though only a few cyclic dipeptides weakly inhibited O2 -•. Keywords: Awamori; distillation residue; Aspergillus awamori; cyclic dipeptide; antioxidant; bleomycin; ESR; hydroxyl radical; superoxide
doi_str_mv 10.1021/jf062029d
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The supernatant of the distillation residue obtained by centrifugation was partitioned with n-hexane, chloroform, ethyl acetate, and n-butanol against water to afford the corresponding solubles. Among them, n-hexane and chloroform solubles showed higher antioxidant potency than l-ascorbic acid by the bleomycin−Fe method. In chloroform solubles, seven cyclic dipeptides were identified along with ethyl 2-pyrrolidione-5-carboxylate, tyrosol, and ethyl p-hydoroxyphenyllactate. Antioxidant activity of ethyl p-hydoroxyphenyllactate was 4.2 times that of l-ascorbic acid, whereas cyclic dipeptides showed activity 0.89−1.29 times as strong as that of l-ascorbic acid. On the other hand, scavenging effect of cyclic dipeptides against O2 -• and OH• by using electron spin resonance was also investigated. In the results, cyclo(l-Ile-l-Pro) showed significantly strong inhibitory effect against OH• (95.4% at 2.5 × 10-3 M) and cyclo(l-Phe-l-Pro), cyclo(l-Pro-l-Val), and cyclo(l-Leu-l-Pro) inhibited OH• 64.9, 54.1, and 51.0%, respectively, whereas α-tocopherol showed 37.7% inhibition, though only a few cyclic dipeptides weakly inhibited O2 -•. Keywords: Awamori; distillation residue; Aspergillus awamori; cyclic dipeptide; antioxidant; bleomycin; ESR; hydroxyl radical; superoxide</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf062029d</identifier><identifier>PMID: 17199316</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Alcoholic Beverages - analysis ; antioxidant activity ; antioxidants ; Antioxidants - analysis ; Aspergillus - metabolism ; Awamori ; Biological and medical sciences ; cyclic dipeptides ; cyclic peptides ; distillation ; distillation residues ; distilled spirits ; Electron Spin Resonance Spectroscopy ; Fermentation ; Food industries ; Free Radical Scavengers - analysis ; free radicals ; Fundamental and applied biological sciences. 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Agric. Food Chem</addtitle><description>Constituents in a distillation residue of Awamori (millet spirits) and their antioxidant activity are investigated in this study. The supernatant of the distillation residue obtained by centrifugation was partitioned with n-hexane, chloroform, ethyl acetate, and n-butanol against water to afford the corresponding solubles. Among them, n-hexane and chloroform solubles showed higher antioxidant potency than l-ascorbic acid by the bleomycin−Fe method. In chloroform solubles, seven cyclic dipeptides were identified along with ethyl 2-pyrrolidione-5-carboxylate, tyrosol, and ethyl p-hydoroxyphenyllactate. Antioxidant activity of ethyl p-hydoroxyphenyllactate was 4.2 times that of l-ascorbic acid, whereas cyclic dipeptides showed activity 0.89−1.29 times as strong as that of l-ascorbic acid. On the other hand, scavenging effect of cyclic dipeptides against O2 -• and OH• by using electron spin resonance was also investigated. In the results, cyclo(l-Ile-l-Pro) showed significantly strong inhibitory effect against OH• (95.4% at 2.5 × 10-3 M) and cyclo(l-Phe-l-Pro), cyclo(l-Pro-l-Val), and cyclo(l-Leu-l-Pro) inhibited OH• 64.9, 54.1, and 51.0%, respectively, whereas α-tocopherol showed 37.7% inhibition, though only a few cyclic dipeptides weakly inhibited O2 -•. Keywords: Awamori; distillation residue; Aspergillus awamori; cyclic dipeptide; antioxidant; bleomycin; ESR; hydroxyl radical; superoxide</description><subject>Alcoholic Beverages - analysis</subject><subject>antioxidant activity</subject><subject>antioxidants</subject><subject>Antioxidants - analysis</subject><subject>Aspergillus - metabolism</subject><subject>Awamori</subject><subject>Biological and medical sciences</subject><subject>cyclic dipeptides</subject><subject>cyclic peptides</subject><subject>distillation</subject><subject>distillation residues</subject><subject>distilled spirits</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Fermentation</subject><subject>Food industries</subject><subject>Free Radical Scavengers - analysis</subject><subject>free radicals</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>millets</topic><topic>Oryza</topic><topic>Solubility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takaya, Yoshiaki</creatorcontrib><creatorcontrib>Furukawa, Tadashi</creatorcontrib><creatorcontrib>Miura, Shunsuke</creatorcontrib><creatorcontrib>Akutagawa, Takashi</creatorcontrib><creatorcontrib>Hotta, Yoshihiro</creatorcontrib><creatorcontrib>Ishikawa, Naohisa</creatorcontrib><creatorcontrib>Niwa, Masatake</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takaya, Yoshiaki</au><au>Furukawa, Tadashi</au><au>Miura, Shunsuke</au><au>Akutagawa, Takashi</au><au>Hotta, Yoshihiro</au><au>Ishikawa, Naohisa</au><au>Niwa, Masatake</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant Constituents in Distillation Residue of Awamori Spirits</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2007-01-10</date><risdate>2007</risdate><volume>55</volume><issue>1</issue><spage>75</spage><epage>79</epage><pages>75-79</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Constituents in a distillation residue of Awamori (millet spirits) and their antioxidant activity are investigated in this study. The supernatant of the distillation residue obtained by centrifugation was partitioned with n-hexane, chloroform, ethyl acetate, and n-butanol against water to afford the corresponding solubles. Among them, n-hexane and chloroform solubles showed higher antioxidant potency than l-ascorbic acid by the bleomycin−Fe method. In chloroform solubles, seven cyclic dipeptides were identified along with ethyl 2-pyrrolidione-5-carboxylate, tyrosol, and ethyl p-hydoroxyphenyllactate. Antioxidant activity of ethyl p-hydoroxyphenyllactate was 4.2 times that of l-ascorbic acid, whereas cyclic dipeptides showed activity 0.89−1.29 times as strong as that of l-ascorbic acid. On the other hand, scavenging effect of cyclic dipeptides against O2 -• and OH• by using electron spin resonance was also investigated. In the results, cyclo(l-Ile-l-Pro) showed significantly strong inhibitory effect against OH• (95.4% at 2.5 × 10-3 M) and cyclo(l-Phe-l-Pro), cyclo(l-Pro-l-Val), and cyclo(l-Leu-l-Pro) inhibited OH• 64.9, 54.1, and 51.0%, respectively, whereas α-tocopherol showed 37.7% inhibition, though only a few cyclic dipeptides weakly inhibited O2 -•. Keywords: Awamori; distillation residue; Aspergillus awamori; cyclic dipeptide; antioxidant; bleomycin; ESR; hydroxyl radical; superoxide</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>17199316</pmid><doi>10.1021/jf062029d</doi><tpages>5</tpages></addata></record>
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Alcoholic Beverages - analysis
antioxidant activity
antioxidants
Antioxidants - analysis
Aspergillus - metabolism
Awamori
Biological and medical sciences
cyclic dipeptides
cyclic peptides
distillation
distillation residues
distilled spirits
Electron Spin Resonance Spectroscopy
Fermentation
Food industries
Free Radical Scavengers - analysis
free radicals
Fundamental and applied biological sciences. Psychology
millets
Oryza
Solubility
title Antioxidant Constituents in Distillation Residue of Awamori Spirits
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