Biotransformation of 4(20),11-taxadienes by cell suspension cultures of Platycodon grandiflorum

被引:9
作者
Dai, JG
Guo, HZ
Ye, M
Zhu, WH
Zhang, DY
Hu, Q
Han, J
Zheng, JH
Guo, DA [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
[2] Chinese Acad Med Sci, Inst Mat Med, Beijing 100050, Peoples R China
[3] Peking Union Med Coll, Beijing 100050, Peoples R China
基金
美国国家科学基金会;
关键词
4(20); 11-taxadiene; biotransformation; cell suspension cultures; Platycodon grandiflorum;
D O I
10.1080/1028602031000080397
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Platycodon grandiflorum cell suspension cultures were employed to biotransform the taxane diterpenoids 2alpha,5alpha, 10beta,14beta-tetraacetoxy-4(20),11-taxadiene ( 1 ) and 9alpha-hydroxy-2alpha, 5alpha,10beta,14beta-tetraacetoxy-4(20),11-taxadiene ( 2 ). One product, 10beta-hydroxy-2alpha,5alpha,14beta-triacetoxy-4(20),11-taxadiene ( 3 ) was obtained from 1 and two products, 9alpha,10beta-dihydroxy-2alpha,5alpha,14beta-triacetoxy-4(20),11-taxadiene ( 4 ) and 10beta-hydroxy-2alpha,5alpha,9alpha,14beta-tetraacetoxy-4(20),11-taxadiene ( 5 ) were obtained from 2 incubated with Platycodon cultured cells respectively, among which 5 is characterized as a new taxoid compound. The effects of the addition stage for 1 and 2 on the biotransformation were investigated and the results revealed that: (1) the optimal addition stage for 1 was in the early logarithmic phase (6th day) of the cell growth period, in which 78% of 1 was converted and the yield for 3 reached 75%; (2) the optimal addition stage for 2 was on the mid-logarithmic phase (12th day) of the cell growth period, in which 25.3% of 2 was converted and the yields for 4 and 5 reached 18.9 and 14.5%, respectively.
引用
收藏
页码:5 / 10
页数:6
相关论文
共 13 条
[1]
The taxane diterpenoids [J].
Baloglu, E ;
Kingston, DGI .
JOURNAL OF NATURAL PRODUCTS, 1999, 62 (10) :1448-1472
[2]
Cheng KD, 1992, Patent No. [JP 249047, 249047]
[3]
CHENG KD, 1994, Patent No. 9406740
[4]
Biotransformation of 2α,5α,10β,14β-tetra-acetoxy-4(20), 11-taxadiene by Ginkgo cell suspension cultures [J].
Dai, JG ;
Guo, HZ ;
Lu, DD ;
Zhu, WH ;
Zhang, DY ;
Zheng, JH ;
Guo, D .
TETRAHEDRON LETTERS, 2001, 42 (28) :4677-4679
[5]
Microbial transformation of taxoids: Selective deacetylation and hydroxylation of 2 alpha,5 alpha,10 beta,14 beta-tetra-acetoxy-4(20),11-taxadiene by the fungus Cunninghamella echinulata [J].
Hu, SH ;
Tian, XF ;
Zhu, WH ;
Fang, QC .
TETRAHEDRON, 1996, 52 (26) :8739-8746
[6]
Biotransformation of 2 alpha,5 alpha,10 beta,14 beta-tetraacetoxy-4(20),11-taxadiene by the fungi Cunninghamella elegans and Cunninghamella echinulata [J].
Hu, SH ;
Tian, XF ;
Zhu, WH ;
Fang, QC .
JOURNAL OF NATURAL PRODUCTS, 1996, 59 (11) :1006-1009
[7]
HU SH, 1996, CHINESE CHEM LETT, V6, P543
[8]
HUANG G, 1998, ACTA PHARMACOL SINIC, V33, P576
[9]
Ojima I, 1998, CHEMTECH, V28, P31
[10]
Taxezopidines B-H, new taxoids from Japanese yew Taxus cuspidata [J].
Wang, X ;
Shigemori, H ;
Kobayashi, J .
JOURNAL OF NATURAL PRODUCTS, 1998, 61 (04) :474-479