Microbial metabolism of methyl protodioscin by Aspergillus niger culture -: A new androstenedione producing way from steroid

被引:22
作者
He, Xiangjiu [1 ]
Liu, Bo
Wang, Guanghui
Wang, Xinluan
Su, Lina
Qu, Gexia
Yao, Xinsheng
机构
[1] Jinan Univ, Inst Trad Chinese Med & Nat Prod, Guangzhou 510632, Peoples R China
[2] Cornell Univ, Dept Food Sci, Ithaca, NY 14853 USA
[3] Univ Exeter, Dept Bioinformat, Exeter EX4 6TJ, Devon, England
[4] Shenyang Pharmaceut Univ, Dept Nat Prod Chem, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
methyl protodioscin; microbial transformation; Aspergillus niger; anticancer activities;
D O I
10.1016/j.jsbmb.2006.03.007
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
Methyl protodioscin (1), a natural furostanol biglycoside steroid, was a preclinical anticancer drug, which showed potent activity against most cell lines from leukemia and solid tumors in the National Cancer Institute's (NCI) human cancer panel. Metabolism of methyl protodioscin by Aspergillus niger was investigated. Seven metabolites were isolated and identified. Two main metabolites were pregnane glycosides and four were furostanol glycosides, together with the aglycone. It was found that steroidal saponin skeleton could be converted to pregnenolone skeleton only using microbial methods, which must have chemical procedures in the reported literatures. The proposed biosynthetic pathways of the microbial conversion products of methyl protodioscin were drawn. The found enriched the reaction types of microbial bioconversion and provided a new producing way of androstenedione from steroid. Most metabolites showed strong cytotoxic activities against HepG2, NCI-H460, HeLa, and MCF-7 cell lines. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:87 / 94
页数:8
相关论文
共 17 条
[1]   NMR-SPECTROSCOPY IN THE STRUCTURAL ELUCIDATION OF OLIGOSACCHARIDES AND GLYCOSIDES [J].
AGRAWAL, PK .
PHYTOCHEMISTRY, 1992, 31 (10) :3307-3330
[2]   C-13 NMR SPECTRAL INVESTIGATIONS .10. C-13 NMR-SPECTROSCOPY OF STEROIDAL SAPOGENINS AND STEROIDAL SAPONINS [J].
AGRAWAL, PK ;
JAIN, DC ;
GUPTA, RK ;
THAKUR, RS .
PHYTOCHEMISTRY, 1985, 24 (11) :2479-2496
[3]   Total synthesis of methyl protodioscin: A potent agent with antitumor activity [J].
Cheng, MS ;
Wang, QL ;
Tian, Q ;
Song, HY ;
Liu, YX ;
Li, Q ;
Xu, X ;
Miao, HD ;
Yao, XS ;
Yang, Z .
JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (09) :3658-3662
[4]   Two novel furostanol saponins from the rhizomes of Dioscorea panthaica Prain et Burkill and their cytotoxic activity [J].
Dong, M ;
Feng, XZ ;
Wang, BX ;
Wu, LJ ;
Ikejima, T .
TETRAHEDRON, 2001, 57 (03) :501-506
[5]   Microbial conversion of steroid compounds: recent developments [J].
Fernandes, P ;
Cruz, A ;
Angelova, B ;
Pinheiro, HM ;
Cabral, JMS .
ENZYME AND MICROBIAL TECHNOLOGY, 2003, 32 (06) :688-705
[6]   Antineoplastic agents .1. Three Spirostanol glycosides from rhizomes of Dioscorea collettii var hypoglauca [J].
Hu, K ;
Dong, AJ ;
Yao, XS ;
Kobayashi, H ;
Iwasaki, S .
PLANTA MEDICA, 1996, 62 (06) :573-575
[7]   A new pregnane glycoside from Dioscorea collettii var. hypoglauca [J].
Hu, K ;
Yao, XS ;
Dong, AJ ;
Kobayashi, H ;
Iwasaki, S ;
Jing, YK .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (02) :299-301
[8]   The cytotoxicity of methyl protodioscin against human cancer cell lines in vitro [J].
Hu, K ;
Yao, XS .
CANCER INVESTIGATION, 2003, 21 (03) :389-393
[9]  
Hu K, 2002, ANTICANCER RES, V22, P1001
[10]   STEROIDAL SAPONINS FROM THE RHIZOMES OF SMILAX-MENISPERMOIDEA [J].
JU, Y ;
JIA, ZJ .
PHYTOCHEMISTRY, 1992, 31 (04) :1349-1351