Antioxidant activity of different species and varieties of turmeric (Curcuma spp): Isolation of active compounds

被引:87
作者
Akter, Jesmin [1 ,2 ]
Hossain, Md Amzad [1 ,2 ]
Takara, Kensaku [1 ,2 ]
Islam, Md Zahorul [2 ,3 ]
Hou, De-Xing [1 ,4 ]
机构
[1] Kagoshima Univ, United Grad Sch Agr Sci, Kagoshima 8900065, Japan
[2] Univ Ryukyus, Fac Agr, Nishihara, Okinawa 9030213, Japan
[3] Bangladesh Agr Univ, Fac Vet Sci, Mymensingh 2202, Bangladesh
[4] Kagoshima Univ, Fac Agr, Kagoshima 8900065, Japan
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 2019年 / 215卷
关键词
Turmeric; Ryudai gold; Antioxidant; Phenolic; Flavonoid; Active compound; CAPACITY; EXTRACTS; IDENTIFICATION; GROWTH; OXYGEN; YIELD; ASSAY;
D O I
10.1016/j.cbpc.2018.09.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are > 80 species of turmeric (Curcuma app.) and some species have multiple varieties, for example, Curcuma longa (C. longa) has 70 varieties. They could be different in their chemical properties and biological activities. Therefore, we compared antioxidant activity, total phenolic and flavonoid content of different species and varieties of turmeric namely C. longa [variety: Ryudai gold (RD) and Okinawa ukon], C. xanthorrhiza, C. aromatica, C. amada, and C. zedoaria. The antioxidant activity was determined using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging activity, oxygen radical absorbance capacity (ORAC), reducing power and 2-deoxyribose (2-DR) oxidation assay. Our results suggested that RD contained significantly higher concentrations of total phenolic (157.4 mg gallic acid equivalent/g extract) and flavonoids (1089.5 mg rutin equivalent/g extract). RD also showed significantly higher DPPH radical-scavenging activity (IC50: 26.4 mu g/mL), ORAC (14,090 mu mol Trolox equivalent/g extract), reducing power absorbance (0.33) and hydroxyl radical scavenging activity (IC50: 7.4 mu g/mL). Therefore, RD was chosen for the isolation of antioxidant compounds using silica gel column, Toyopearl HW-40F column, and high-performance liquid chromatography. Structural identification of the compounds was conducted using H-1 NMR, C-13 NMR, and liquid chromatography-tandem mass spectrometry. The purified antioxidant compounds were bisabolone-9-one (1), 4-methyllene-5-hydroxybisabola-2,10-diene-9-one (2), turmeronol B (3), 5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)-1-hepten-3-one (4), 3-hydroxy-1,7-bis(4-hydroxyphenyl)-6-hepten-1,5-dione (5), cyclobisdemethoxycurcumin (6), bisdemethoxycurcumin (7), demethoxycurcumin (8) and curcumin (9). The IC50 for DPPH radical-scavenging activity were 474, 621, 234, 29, 39, 257, 198, 47 and 18 mu M and hydroxyl radical-scavenging activity were 25.1, 24.4, 20.2, 2.1, 5.1, 17.2, 7.2, 3.3 and 1.5 mu M for compound 1, 2, 3, 4, 5, 6, 7, 8 and 9, respectively. Our findings suggested that the RD variety of C. longa, developed by the University of the Ryukyus, Okinawa, Japan, is a promising source of natural antioxidants.
引用
收藏
页码:9 / 17
页数:9
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