Condensed tannins from steamed Acacia mearnsii bark

被引:23
作者
Duan, WG
Ohara, S
Hashida, K
Makino, R
机构
[1] Forestry & Forest Prod Res Inst, Dept Forest Chem, Tsukuba, Ibaraki 3058687, Japan
[2] Guangxi Univ, Coll Chem & Chem Engn, Nanning 530004, Peoples R China
关键词
Acacia meamsii; condensed tannins; proanthocyanidin dimers; steaming of bark; stereochemistry;
D O I
10.1515/HF.2005.048
中图分类号
S7 [林业];
学科分类号
0829 [林业工程]; 0907 [林学];
摘要
The optimum steaming conditions for extraction of condensed tannins from Acacia meamsii bark were explored, after which characterization of proanthocyanidins from bark steamed under optimum conditions was carried out. The optimum conditions were as follows: steaming time, 30 min; steaming temperature, 140 degrees C; and water volume, 75 ml. The total phenolics content obtained under these conditions amounted to 25.31 %, which was much higher than the 21.70% obtained by conventional hot water extraction. Six proanthocyanidin dinners were isolated from the steamed bark. Analysis revealed them to be fisetinidol-(4 beta-8)-catechin, fisetinidol-(4 alpha-8)-catechin, robinetinidol-(4 beta-8)-catechin, robinetinidol-(4 alpha-8)-catechin, robinetinidol-(4 beta-8)-gallocatechin, and robinetinidol-(4 alpha-8)-gallocatechin. Proanthocyanidin polymers were found to consist mainly of prorobinetinidin extender units, similar to those obtained from the same bark by conventional extraction with 70% acetone aqueous solution. However, nuclear magnetic resonance and gel permeation chromatography analyses suggested that during steaming the polymers undergo condensation reactions, as well as inversion of the configuration of interflavanoid bonds.
引用
收藏
页码:289 / 294
页数:6
相关论文
共 14 条
[1]
PLANT PROANTHOCYANIDINS .6. CHIROPTICAL STUDIES .95. CIRCULAR-DICHROISM OF PROCYANIDINS [J].
BARRETT, MW ;
KLYNE, W ;
SCOPES, PM ;
FLETCHER, AC ;
PORTER, LJ ;
HASLAM, E .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1979, (10) :2375-2377
[2]
SYNTHESIS OF CONDENSED TANNINS .4. A DIRECT BIOMIMETIC APPROACH TO [4,6]-BIFLAVANOIDS AND [4,8]-BIFLAVANOIDS [J].
BOTHA, JJ ;
FERREIRA, D ;
ROUX, DG .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1981, (04) :1235-1245
[3]
CONDENSED TANNINS - DIRECT SYNTHESIS, STRUCTURE, AND ABSOLUTE-CONFIGURATION OF 4 BIFLAVANOIDS FROM BLACK WATTLE BARK (MIMOSA) EXTRACT [J].
BOTHA, JJ ;
FERREIRA, D ;
ROUX, DG .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (16) :700-702
[4]
OLIGOMERIC FLAVANOIDS .16. NOVEL PROROBINETINIDINS AND THE 1ST A-TYPE PROANTHOCYANIDIN WITH A 5-DEOXY A-RING AND A 3,4-CIS C-RING FROM THE MAIDEN INVESTIGATION OF COMMERCIAL WATTLE BARK EXTRACT [J].
CRONJE, A ;
STEYNBERG, JP ;
BRANDT, EV ;
YOUNG, DA ;
FERREIRA, D .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1993, (20) :2467-2477
[5]
Biological evaluation of proanthocyanidin dimers and related polyphenols [J].
De Bruyne, T ;
Pieters, L ;
Witvrouw, M ;
De Clercq, E ;
Vanden Berghe, D ;
Vlietinck, AJ .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (07) :954-958
[6]
Haslam E., 1987, Chemistry and Industry of Forest Products, V7, P1
[7]
TANNINS AND RELATED-COMPOUNDS .53. FLAVAN-3-OL AND PROCYANIDIN GLYCOSIDES FROM QUERCUS-MIYAGII [J].
ISHIMARU, K ;
NONAKA, G ;
NISHIOKA, I .
PHYTOCHEMISTRY, 1987, 26 (04) :1167-1170
[9]
OHARA S, 1994, MOKUZAI GAKKAISHI, V40, P1363
[10]
OHARA S, 1995, MOKUZAI GAKKAISHI, V41, P498