Utilizing the power of microbial genetics to bridge the gap between the promise and the application of marine natural products

被引:51
作者
Fortman, JL
Sherman, DH
机构
[1] Univ Minnesota, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Univ Michigan, Dept Med Chem, Inst Life Sci, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Chem, Inst Life Sci, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Microbiol & Immunol, Inst Life Sci, Ann Arbor, MI 48109 USA
关键词
biosynthesis; genomics; heterologous expression; marine natural products; secondary metabolites;
D O I
10.1002/cbic.200400428
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
Marine organisms are a rich source of secondary metabolites. They have yielded thousands of compounds with a broad range of biomedical applications. Thus for, samples required for preclinical and clinical studies have been obtained by collection from the wild, by moriculture, and by total chemical synthesis. However, for a number of complex marine metabolites, none of these options is feasible for either economic or environmental reasons. In order to proceed with the development of many of these promising therapeutic compounds, a reliable and renewable source must be found. Over the last twenty years, the study of microbial secondary metabolites has greatly advanced our understanding of how nature utilizes simple starting materials to yield complex small molecules. Much of this work has focused on polyketides and nonribosomol peptides, two classes of molecules that are prevalent in marine micro- and mocroorganisms. The lessons learned from the study of terrestrial metabolite biosynthesis are now being applied to the marine world. As techniques for cloning and heterologous expression of biosynthetic pathways continue to improve, they may provide our greatest hope for bridging the gap between the promise and application of many marine natural products.
引用
收藏
页码:960 / 978
页数:19
相关论文
共 243 条
[61]   Scaled-up synthesis of discodermolide [J].
Freemantle, M .
CHEMICAL & ENGINEERING NEWS, 2004, 82 (09) :33-35
[62]   ANTIMICROBIAL METABOLITES OF THE SPONGE RENIERA SP [J].
FRINCKE, JM ;
FAULKNER, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (01) :265-269
[63]   Antibiotic optimization via in vitro glycorandomization [J].
Fu, X ;
Albermann, C ;
Jiang, JQ ;
Liao, JC ;
Zhang, CS ;
Thorson, JS .
NATURE BIOTECHNOLOGY, 2003, 21 (12) :1467-1469
[64]  
FURUSAKI A, 1968, TETRAHEDRON LETT, P6301
[65]   X-RAY CRYSTAL-STRUCTURE OF STAUROSPORINE - NEW ALKALOID FROM A STREPTOMYCES STRAIN [J].
FURUSAKI, A ;
HASHIBA, N ;
MATSUMOTO, T ;
HIRANO, A ;
IWAI, Y ;
OMURA, S .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (18) :800-801
[66]   BIOACTIVE MARINE METABOLITES SERIES .41. THEOPEDERINS-A-E, POTENT ANTITUMOR METABOLITES FROM A MARINE SPONGE, THEONELLA SP [J].
FUSETANI, N ;
SUGAWARA, T ;
MATSUNAGA, S .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (14) :3828-3832
[67]   TERPENES IN SPONGE CELL-MEMBRANES - CELL-SEPARATION AND MEMBRANE FRACTIONATION STUDIES WITH THE TROPICAL MARINE SPONGE AMPHIMEDON-SP [J].
GARSON, MJ ;
THOMPSON, JE ;
LARSEN, RM ;
BATTERSHILL, CN ;
MURPHY, PT ;
BERGQUIST, PR .
LIPIDS, 1992, 27 (05) :378-388
[68]   A sponge/dinoflagellate association in the haplosclerid sponge Haliclona sp.:: cellular origin of cytotoxic alkaloids by Percoll density gradient fractionation [J].
Garson, MJ ;
Flowers, AE ;
Webb, RI ;
Charan, RD ;
McCaffrey, EJ .
CELL AND TISSUE RESEARCH, 1998, 293 (02) :365-373
[69]  
Gerwick WH, 2001, ALKALOIDS, V57, P75, DOI 10.1016/S0099-9598(01)57003-0
[70]   STRUCTURE OF CURACIN-A, A NOVEL ANTIMITOTIC, ANTIPROLIFERATIVE, AND BRINE SHRIMP TOXIC NATURAL PRODUCT FROM THE MARINE CYANOBACTERIUM LYNGBYA-MAJUSCULA [J].
GERWICK, WH ;
PROTEAU, PJ ;
NAGLE, DG ;
HAMEL, E ;
BLOKHIN, A ;
SLATE, DL .
JOURNAL OF ORGANIC CHEMISTRY, 1994, 59 (06) :1243-1245