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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
来源:
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.
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页码:375 / 385
页数:11
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