Structure and biosynthesis of myxochromides S1-3 in Stigmatella aurantiaca:: Evidence for an iterative bacterial type I polyketide synthase and for module skipping in nonribosomal peptide biosynthesis

被引:92
作者
Wenzel, SC
Kunze, B
Höfle, G
Silakowski, B
Scharfe, M
Blöcker, H
Müller, R
机构
[1] Univ Saarland, Inst Pharmazeut Biotechnol, Saarbrucken, Germany
[2] Gesellsch Biotechnol Forschung, D-38124 Braunschweig, Germany
关键词
bacterial iterative PKS; module skipping; myxobacteria; nonribosomal peptide; polyketides; secondary metabolism;
D O I
10.1002/cbic.200400282
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 myxobacterium Stigmatella aurantiaca DW4/3-1 harbours an astonishing variety of secondary metabolic gene clusters, at least two of which were found by gene inactivation experiments to be connected to the biosynthesis of previously unknown metabolites. In this study, we elucidate the structures of myxochromides S1-3, novel cyclic pentapeptide natural products possessing unsaturated polyketide side chains, and identify the corresponding biosynthetic gene locus, mode up of six nonribosomal peptide synthetase modules. By analyzing the deduced substrate specificities of the adenylation domains, it is shown that module 4 is most probably skipped during the biosynthetic process. The polyketide synthase MchA harbours only one module and is presumably responsible for the formation of the variable complete polyketide side chains. These data indicate that MchA is responsible. for on unusual iterative polyketide chain assembly.
引用
收藏
页码:375 / 385
页数:11
相关论文
共 59 条
[1]   The calicheamicin gene cluster and its iterative type I enediyne PKS [J].
Ahlert, J ;
Shepard, E ;
Lomovskaya, N ;
Zazopoulos, E ;
Staffa, A ;
Bachmann, BO ;
Huang, KX ;
Fonstein, L ;
Czisny, A ;
Whitwam, RE ;
Farnet, CM ;
Thorson, JS .
SCIENCE, 2002, 297 (5584) :1173-1176
[2]  
[Anonymous], LIEBIGS ANN CHEM
[3]   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
[4]   6-DEOXYERYTHRONOLIDE-B SYNTHASE-2 FROM SACCHAROPOLYSPORA-ERYTHRAEA - CLONING OF THE STRUCTURAL GENE, SEQUENCE-ANALYSIS AND INFERRED DOMAIN-STRUCTURE OF THE MULTIFUNCTIONAL ENZYME [J].
BEVITT, DJ ;
CORTES, J ;
HAYDOCK, SF ;
LEADLAY, PF .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (01) :39-49
[5]   Metabolic diversity in myxobacteria:: identification of the myxalamid and the stigmatellin biosynthetic gene cluster of Stigmatella aurantiaca Sg a15 and a combined polyketide-(poly)peptide gene cluster from the epothilone producing strain Sorangium cellulosum So ce90 [J].
Beyer, S ;
Kunze, B ;
Silakowski, B ;
Müller, R .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1999, 1445 (02) :185-195
[6]   The parallel and convergent universes of polyketide synthases and nonribosomal peptide synthetases [J].
Cane, DE ;
Walsh, CT .
CHEMISTRY & BIOLOGY, 1999, 6 (12) :R319-R325
[8]   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
[9]   Structural basis for the activation of phenylalanine in the non-ribosomal biosynthesis of gramicidin S [J].
Conti, E ;
Stachelhaus, T ;
Marahiel, MA ;
Brick, P .
EMBO JOURNAL, 1997, 16 (14) :4174-4183
[10]   ORGANIZATION OF THE ENZYMATIC DOMAINS IN THE MULTIFUNCTIONAL POLYKETIDE SYNTHASE INVOLVED IN ERYTHROMYCIN FORMATION IN SACCHAROPOLYSPORA-ERYTHRAEA [J].
DONADIO, S ;
KATZ, L .
GENE, 1992, 111 (01) :51-60