Bioinformatic perspectives on NRPS/PKS megasynthases: Advances and challenges

被引:55
作者
Jenke-Kodama, Holger [1 ]
Dittmann, Elke [1 ]
机构
[1] Humboldt Univ, Inst Biol, Dept Mol Ecol, D-10115 Berlin, Germany
关键词
NONRIBOSOMAL PEPTIDE SYNTHETASE; MODULAR POLYKETIDE SYNTHASES; PROTEIN-PROTEIN INTERACTIONS; BIOSYNTHESIS GENE-CLUSTER; ADENYLATION DOMAINS; MICROBIAL GENOMES; SECONDARY METABOLITES; MUTATIONAL ANALYSIS; SPECIFICITY; PREDICTION;
D O I
10.1039/b810283j
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
The increased understanding of both fundamental principles and mechanistic variations of NRPS/PKS megasynthases along with the unprecedented availability of microbial genome sequences has inspired a number of in silico studies of both enzyme families. The insights that can be extracted from these analyses go far beyond a rough classification of data and have turned bioinformatics into a frontier field of natural products research. As databases are flooded with NRPS/PKS gene sequences of microbial genomes and metagenomes, increasingly reliable structural prediction methods can help to uncover hidden treasures. Already, phylogenetic analyses have revealed that NRPS/PKS pathways should not simply be regarded as enzyme complexes, specifically evolved to produce a selected natural product. Rather, they represent a collection of genetic options, allowing biosynthetic pathways to be shuffled in a process of perpetual chemical innovation. Understanding the principles underlying domain specificities, protein-protein interactions and pathway diversification in nature can give impulses for genomic mining approaches and genetic engineering of libraries of novel peptides and polyketides. The successful translation of the knowledge obtained from bioinformatic dissection of NRPS/PKS megasynthases into new techniques for drug discovery and design remain challenges for the future.
引用
收藏
页码:874 / 883
页数:10
相关论文
共 68 条
[1]   In silico analysis of methyltransferase domains involved in biosynthesis of secondary metabolites [J].
Ansari, Mohd Zeeshan ;
Sharma, Jyoti ;
Gokhale, Rajesh S. ;
Mohanty, Debasisa .
BMC BIOINFORMATICS, 2008, 9 (1)
[2]   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
[3]   Directed mutagenesis alters the stereochemistry of catalysis by isolated ketoreductase domains from the erythromycin polyketide synthase [J].
Baerga-Ortiz, A ;
Popovic, B ;
Siskos, AP ;
O'Hare, HM ;
Spiteller, D ;
Williams, MG ;
Campillo, N ;
Spencer, JB ;
Leadlay, PF .
CHEMISTRY & BIOLOGY, 2006, 13 (03) :277-285
[4]  
Beiko Robert G., 2008, V452, P457, DOI 10.1007/978-1-60327-159-2_21
[5]   Mutational analysis of the C-domain in nonribosomal peptide synthesis [J].
Bergendahl, V ;
Linne, U ;
Marahiel, MA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (02) :620-629
[6]   The impact of bacterial genomics on natural product research [J].
Bode, HB ;
Müller, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (42) :6828-6846
[7]   The structure of docking domains in modular polyketide synthases [J].
Broadhurst, RW ;
Nietlispach, D ;
Wheatcroft, MP ;
Leadlay, PF ;
Weissman, KJ .
CHEMISTRY & BIOLOGY, 2003, 10 (08) :723-731
[8]   Accurate prediction of protein-protein interactions from sequence alignments using a Bayesian method [J].
Burger, Lukas ;
van Nimwegen, Erik .
MOLECULAR SYSTEMS BIOLOGY, 2008, 4 (1)
[9]   NORINE:: a database of nonribosomal peptides [J].
Caboche, Segolene ;
Pupin, Maude ;
Leclere, Valerie ;
Fontaine, Arnaud ;
Jacques, Philippe ;
Kucherov, Gregory .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D326-D331
[10]   Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains [J].
Challis, GL ;
Ravel, J ;
Townsend, CA .
CHEMISTRY & BIOLOGY, 2000, 7 (03) :211-224