Bacterial type III polyketide synthases: phylogenetic analysis and potential for the production of novel secondary metabolites by heterologous expression in pseudomonads.
Average rating
Cast your vote
You can rate an item by clicking the amount of stars they wish to award to this item.
When enough users have cast their vote on this item, the average rating will also be shown.
Star rating
Your vote was cast
Thank you for your feedback
Thank you for your feedback
Authors
Gross, FrankLuniak, Nora
Perlova, Olena
Gaitatzis, Nikolaos
Jenke-Kodama, Holger
Gerth, Klaus
Gottschalk, Daniela
Dittmann, Elke
Müller, Rolf
Issue Date
2006-03-01
Metadata
Show full item recordAbstract
Type III polyketide synthases (PKS) were regarded as typical for plant secondary metabolism before they were found in microorganisms recently. Due to microbial genome sequencing efforts, more and more type III PKS are found, most of which of unknown function. In this manuscript, we report a comprehensive analysis of the phylogeny of bacterial type III PKS and report the expression of a type III PKS from the myxobacterium Sorangium cellulosum in pseudomonads. There is no precedent of a secondary metabolite that might be biosynthetically correlated to a type III PKS from any myxobacterium. Additionally, an inactivation mutant of the S. cellulosum gene shows no physiological difference compared to the wild-type strain which is why these type III PKS are assumed to be "silent" under the laboratory conditions administered. One type III PKS (SoceCHS1) was expressed in different Pseudomonas sp. after the heterologous expression in Escherichia coli failed. Cultures of recombinant Pseudomonas sp. harbouring SoceCHS1 turned red upon incubation and the diffusible pigment formed was identified as 2,5,7-trihydroxy-1,4-naphthoquinone, the autooxidation product of 1,3,6,8-tetrahydroxynaphthalene. The successful heterologous production of a secondary metabolite using a gene not expressed under administered laboratory conditions provides evidence for the usefulness of our approach to activate such secondary metabolite genes for the production of novel metabolites.Citation
Arch. Microbiol. 2006, 185(1):28-38PubMed ID
16395556Type
ArticleLanguage
enISSN
0302-8933ae974a485f413a2113503eed53cd6c53
10.1007/s00203-005-0059-3
Scopus Count
The following license files are associated with this item:
Related articles
- Evolutionary diversity of ketoacyl synthases in cellulolytic myxobacterium Sorangium.
- Authors: Li ZF, Zhao JY, Xia ZJ, Shi J, Liu H, Wu ZH, Hu W, Liu WF, Li YZ
- Issue date: 2007 Apr
- Polymorphism of the polyketide synthase gene phID in biocontrol fluorescent pseudomonads producing 2,4-diacetylphloroglucinol and comparison of PhID with plant polyketide synthases.
- Authors: Ramette A, Moënne-Loccoz Y, Défago G
- Issue date: 2001 May
- NtcA: a negative regulator of secondary metabolite biosynthesis in Sorangium cellulosum.
- Authors: Rachid S, Gerth K, Müller R
- Issue date: 2009 Mar 10
- Characterisation, genome size and genetic manipulation of the myxobacterium Sorangium cellulosum So ce56.
- Authors: Pradella S, Hans A, Spröer C, Reichenbach H, Gerth K, Beyer S
- Issue date: 2002 Dec
- Complete genome sequence of the myxobacterium Sorangium cellulosum.
- Authors: Schneiker S, Perlova O, Kaiser O, Gerth K, Alici A, Altmeyer MO, Bartels D, Bekel T, Beyer S, Bode E, Bode HB, Bolten CJ, Choudhuri JV, Doss S, Elnakady YA, Frank B, Gaigalat L, Goesmann A, Groeger C, Gross F, Jelsbak L, Jelsbak L, Kalinowski J, Kegler C, Knauber T, Konietzny S, Kopp M, Krause L, Krug D, Linke B, Mahmud T, Martinez-Arias R, McHardy AC, Merai M, Meyer F, Mormann S, Muñoz-Dorado J, Perez J, Pradella S, Rachid S, Raddatz G, Rosenau F, Rückert C, Sasse F, Scharfe M, Schuster SC, Suen G, Treuner-Lange A, Velicer GJ, Vorhölter FJ, Weissman KJ, Welch RD, Wenzel SC, Whitworth DE, Wilhelm S, Wittmann C, Blöcker H, Pühler A, Müller R
- Issue date: 2007 Nov