Biologically Active Secondary Metabolites from the Fungi

被引:289
作者
Bills, Gerald F. [1 ]
Gloer, James B. [2 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Texas Therapeut Inst, Brown Fdn Inst Mol Med, Houston, TX 77054 USA
[2] Univ Iowa, Dept Chem, Iowa City, IA 52245 USA
关键词
BIOSYNTHETIC GENE-CLUSTER; NATURAL-PRODUCT DISCOVERY; POLYKETIDE SYNTHASE GENES; AMINO-ACID BIOSYNTHESIS; KOJIC ACID; ASPERGILLUS-NIDULANS; FUNCTIONAL-ANALYSIS; MASS-SPECTROMETRY; ENDOPHYTIC FUNGUS; MYCOPHENOLIC-ACID;
D O I
10.1128/microbiolspec.FUNK-0009-2016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Many Fungi have a well-developed secondary metabolism. The diversity of fungal species and the diversification of biosynthetic gene clusters underscores a nearly limitless potential for metabolic variation and an untapped resource for drug discovery and synthetic biology. Much of the ecological success of the filamentous fungi in colonizing the planet is owed to their ability to deploy their secondary metabolites in concert with their penetrative and absorptive mode of life. Fungal secondary metabolites exhibit biological activities that have been developed into life-saving medicines and agrochemicals. Toxic metabolites, known as mycotoxins, contaminate human and livestock food and indoor environments. Secondary metabolites are determinants of fungal diseases of humans, animals, and plants. Secondary metabolites exhibit a staggering variation in chemical structures and biological activities, yet their biosynthetic pathways share a number of key characteristics. The genes encoding cooperative steps of a biosynthetic pathway tend to be located contiguously on the chromosome in coregulated gene clusters. Advances in genome sequencing, computational tools, and analytical chemistry are enabling the rapid connection of gene clusters with their metabolic products. At least three fungal drug precursors, penicillin K and V, mycophenolic acid, and pleuromutilin, have been produced by synthetic reconstruction and expression of respective gene clusters in heterologous hosts. This review summarizes general aspects of fungal secondary metabolism and recent developments in our understanding of how and why fungi make secondary metabolites, how these molecules are produced, and how their biosynthetic genes are distributed across the Fungi. The breadth of fungal secondary metabolite diversity is highlighted by recent information on the biosynthesis of important fungus-derived metabolites that have contributed to human health and agriculture and that have negatively impacted crops, food distribution, and human environments.
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页数:32
相关论文
共 268 条
[31]  
Bills G. F., 2009, SOC IND MICROBIOL NE, V59, P133
[32]  
Bills G, 2009, MYCOL SER, V27, P257
[33]  
Bills Gerald F, 2012, Methods Mol Biol, V944, P79, DOI 10.1007/978-1-62703-122-6_5
[34]   Diversity, regulation, and evolution of the gibberellin biosynthetic pathway in fungi compared to plants and bacteria [J].
Boemke, Christiane ;
Tudzynski, Bettina .
PHYTOCHEMISTRY, 2009, 70 (15-16) :1876-1893
[35]   Mass spectrometry of natural products: current, emerging and future technologies [J].
Bouslimani, Amina ;
Sanchez, Laura M. ;
Garg, Neha ;
Dorrestein, Pieter C. .
NATURAL PRODUCT REPORTS, 2014, 31 (06) :718-729
[36]   Chemistry and Biology of Mycotoxins and Related Fungal Metabolites [J].
Braese, Stefan ;
Encinas, Arantxa ;
Keck, Julia ;
Nising, Carl F. .
CHEMICAL REVIEWS, 2009, 109 (09) :3903-3990
[37]   Three Redundant Synthetases Secure Redox-Active Pigment Production in the Basidiomycete Paxillus involutus [J].
Braesel, Jana ;
Goetze, Sebastian ;
Shah, Firoz ;
Heine, Daniel ;
Tauber, James ;
Hertweck, Christian ;
Tunlid, Anders ;
Stallforth, Pierre ;
Hoffmeister, Dirk .
CHEMISTRY & BIOLOGY, 2015, 22 (10) :1325-1334
[38]   Regulation of fungal secondary metabolism [J].
Brakhage, Axel A. .
NATURE REVIEWS MICROBIOLOGY, 2013, 11 (01) :21-32
[39]   Fungal secondary metabolites - Strategies to activate silent gene clusters [J].
Brakhage, Axel A. ;
Schroeckh, Volker .
FUNGAL GENETICS AND BIOLOGY, 2011, 48 (01) :15-22
[40]  
Brase S., 2013, Chemistry of Mycotoxins, DOI [10.1007/978-3-7091-1312-7_14, DOI 10.1007/978-3-7091-1312-7_14]