Strategies to unravel the function of orphan biosynthesis pathways: recent examples and future prospects

被引:108
作者
Gross, Harald [1 ]
机构
[1] Inst Pharmaceut Biol, D-53115 Bonn, Germany
关键词
genome mining; data mining; genomics; orphan biosynthetic gene cluster; natural products;
D O I
10.1007/s00253-007-0900-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The recent increase and availability of whole genome sequences have revised our view of the metabolic capabilities of microorganisms. From these data, a large number of orphan biosynthesis pathways have been identified by bio-informatics. Orphan biosynthetic pathways are gene clusters for which the encoded natural product is unknown. It is worthy to note that the number of orphan pathways coding for putative natural products outnumbers by far the number of currently known metabolites for a given organism. Whilst Streptomyces coelicolor was known to produce only 4 secondary metabolites, the genome analysis revealed 18 additional orphan biosynthetic pathways. It is intriguing to note that this is not a particular case because analysis of other microbial genomes originating from myxobacteria, cyanobacteria and filamentous fungi showed the presence of a comparable or even larger number of orphan pathways. The discovery of these numerous pathways represents a treasure trove, which is likely to grow exponentially in the future, uncovering many novel and possibly bio-active compounds, The few natural products that have been correlated with their orphan pathway are merely the Lip of the iceberg, whilst plenty of metabolites await discovery. The recent strategies and methods to access these promising hidden natural products are discussed in this review.
引用
收藏
页码:267 / 277
页数:11
相关论文
共 78 条
[1]  
ALARCO AM, 2006, AM ASS CANC RES 97 M
[2]  
[Anonymous], 2006, Frontiers in Marine Biotechnology
[3]   NRPS-PKS: a knowledge-based resource for analysis of NRPS/PKS megasynthases [J].
Ansari, MZ ;
Yadav, G ;
Gokhale, RS ;
Mohanty, D .
NUCLEIC ACIDS RESEARCH, 2004, 32 :W405-W413
[4]   The chalcone synthase superfamily of type III polyketide synthases [J].
Austin, MB ;
Noel, JP .
NATURAL PRODUCT REPORTS, 2003, 20 (01) :79-110
[5]   Bioinformatics in microbial biotechnology - a mini review [J].
Bansal, AK .
MICROBIAL CELL FACTORIES, 2005, 4 (1)
[6]   Isolation and identification of three new 5-alkenyl-3,3(2H)-furanones from two Streptomyces species using a genomic screening approach [J].
Banskota, AH ;
McAlpine, JB ;
Sorensen, D ;
Aouidate, M ;
Piraee, M ;
Alarco, AM ;
Omura, S ;
Shiomi, K ;
Farnet, CM ;
Zazopoulos, E .
JOURNAL OF ANTIBIOTICS, 2006, 59 (03) :168-176
[7]   Genomic analyses lead to novel secondary metabolites [J].
Banskota, Arjun H. ;
McAlpine, James B. ;
Sorensen, Dan ;
Ibrahim, Ashraf ;
Aouidate, Mustapha ;
Piraee, Mahmood ;
Alarco, Anne-Marie ;
Farnet, Chris M. ;
Zazopoulos, Emmanuel .
JOURNAL OF ANTIBIOTICS, 2006, 59 (09) :533-542
[8]   Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2) [J].
Bentley, SD ;
Chater, KF ;
Cerdeño-Tárraga, AM ;
Challis, GL ;
Thomson, NR ;
James, KD ;
Harris, DE ;
Quail, MA ;
Kieser, H ;
Harper, D ;
Bateman, A ;
Brown, S ;
Chandra, G ;
Chen, CW ;
Collins, M ;
Cronin, A ;
Fraser, A ;
Goble, A ;
Hidalgo, J ;
Hornsby, T ;
Howarth, S ;
Huang, CH ;
Kieser, T ;
Larke, L ;
Murphy, L ;
Oliver, K ;
O'Neil, S ;
Rabbinowitsch, E ;
Rajandream, MA ;
Rutherford, K ;
Rutter, S ;
Seeger, K ;
Saunders, D ;
Sharp, S ;
Squares, R ;
Squares, S ;
Taylor, K ;
Warren, T ;
Wietzorrek, A ;
Woodward, J ;
Barrell, BG ;
Parkhill, J ;
Hopwood, DA .
NATURE, 2002, 417 (6885) :141-147
[9]  
Bode HB, 2002, CHEMBIOCHEM, V3, P619, DOI 10.1002/1439-7633(20020703)3:7<619::AID-CBIC619>3.0.CO
[10]  
2-9