Fungal Origins of the Bicyclo[2.2.2]diazaoctane Ring System of Prenylated Indole Alkaloids

被引:133
作者
Finefield, Jennifer M. [1 ]
Frisvad, Jens C. [2 ]
Sherman, David H. [3 ,4 ,5 ,6 ]
Williams, Robert M. [1 ,7 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
[2] Tech Univ Denmark, Dept Syst Biol, DK-2800 Lyngby, Denmark
[3] Univ Michigan, Dept Med Chem, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Microbiol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Dept Immunol, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Life Sci Inst, Ann Arbor, MI 48109 USA
[7] Univ Colorado, Ctr Canc, Aurora, CO 80045 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2012年 / 75卷 / 04期
关键词
MARINE-DERIVED FUNGUS; BIOMIMETIC TOTAL-SYNTHESIS; DIELS-ALDER CYCLIZATIONS; X-RAY-ANALYSIS; ASPERGILLUS-JAPONICUS; BREVIANAMIDE-A; PENICILLIUM-CHARLESII; ANTIPARASITIC AGENTS; (-)-VERSICOLAMIDE B; NATURAL-PRODUCTS;
D O I
10.1021/np200954v
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Over eight different families of natural products consisting of nearly 70 secondary metabolites that contain the bicyclo[2.2.2]diazaoctane ring system have been isolated from various Aspergillus, Penicillium, and Malbranchea species. Since 1968, these secondary metabolites have been the focus of numerous biogenetic, synthetic, taxonomic, and biological studies and, as such, have made a lasting impact across multiple scientific disciplines. This review covers the isolation, biosynthesis, and biological activity of these unique secondary metabolites containing the bridging bicyclo[2.2.2]diazaoctane ring system. Furthermore, the diverse fungal origin of these natural products is closely examined and, in many cases, updated to reflect the currently accepted fungal taxonomy.
引用
收藏
页码:812 / 833
页数:22
相关论文
共 133 条
[1]   Itaconic acid derivatives and diketopiperazine from the marine-derived fungus Aspergillus aculeatus CRI322-03 [J].
Antia, Bassey S. ;
Aree, Thammarat ;
Kasettrathat, Chairut ;
Wiyakrutta, Suthep ;
Ekpa, Okon D. ;
Ekpe, Udofot J. ;
Mahidol, Chulabhorn ;
Ruchirawat, Somsak ;
Kittakoop, Prasat .
PHYTOCHEMISTRY, 2011, 72 (08) :816-820
[2]  
ARAI K, 1989, CHEM PHARM BULL, V37, P3229
[3]   STUDIES IN RELATION TO BIOSYNTHESIS .46. INCORPORATION OF CYCLO-L-TRYPTOPHYL-L-PROLINE INTO BREVIANAMIDE A [J].
BALDAS, J ;
BIRCH, AJ ;
RUSSELL, RA .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1974, (01) :50-52
[4]   Novel anthelmintic metabolites from an Aspergillus species; the aspergillimides [J].
Banks, RM ;
Blanchflower, SE ;
Everett, JR ;
Manger, BR ;
Reading, C .
JOURNAL OF ANTIBIOTICS, 1997, 50 (10) :840-846
[5]   STUDIES IN RELATION TO BIOSYNTHESIS .44. STRUCTURAL ELUCIDATIONS OF BREVIANAMIDE-B, BREVIANAMIDE-C, BREVIANAMIDE-D AND BREVIANAMIDE-F [J].
BIRCH, AJ ;
RUSSELL, RA .
TETRAHEDRON, 1972, 28 (11) :2999-&
[6]   STUDIES IN RELATION TO BIOSYNTHESIS .42. STRUCTURAL ELUCIDATION AND SOME ASPECTS OF BIOSYNTHESIS OF BREVIANAMIDES-A AND BREVIANAMIDES-E [J].
BIRCH, AJ ;
WRIGHT, JJ .
TETRAHEDRON, 1970, 26 (10) :2329-&
[7]  
BIRCH AJ, 1969, J CHEM SOC CHEM COMM, P644
[8]   NEW PARAHERQUAMIDE ANTIBIOTICS WITH ANTHELMINTIC ACTIVITY [J].
BLANCHFLOWER, SE ;
BANKS, RM ;
EVERETT, JR ;
MANGER, BR ;
READING, C .
JOURNAL OF ANTIBIOTICS, 1991, 44 (05) :492-497
[9]   FURTHER NOVEL METABOLITES OF THE PARAHERQUAMIDE FAMILY [J].
BLANCHFLOWER, SE ;
BANKS, RM ;
EVERETT, JR ;
READING, C .
JOURNAL OF ANTIBIOTICS, 1993, 46 (09) :1355-1363
[10]   Reclassification of the Penicillium roqueforti group into three species on the basis of molecular genetic and biochemical profiles [J].
Boysen, M ;
Skouboe, P ;
Frisvad, J ;
Rossen, L .
MICROBIOLOGY-SGM, 1996, 142 :541-549