Thioesterases and the Premature Termination of Polyketide Chain Elongation in Rifamycin B Biosynthesis by Amycolatopsis mediterranei S699.

The Journal of Antibiotics
2000.0

Abstract

The role of two thioesterase genes in the premature release of polyketide synthase intermediates during rifamycin biosynthesis in the Amycolatopsis mediterranei S699 strain was investigated. Creation of an in-frame deletion in the rifR gene led to a 30 approximately 60% decrease in the production of both rifamycin B by the S699 strain or a series of tetra- to decaketide shunt products of polyketide chain assembly by the rifF strain. Since a similar percentage decrease was seen in both genetic backgrounds, we conclude that the RifR thioesterase 2 is not involved in premature release of the carbon chain assembly intermediates. Similarly, fusion of the Saccharopolyspora erythraea DEBS3 thioesterase I domain to the C-terminus of the RifE PKS subunit did not result in a noticeable increase in the amount of the undecaketide intermediate formed nor in the amounts of the tetra- to decaketide shunt products. Hence, premature release of the carbon chain assembly intermediates is an unusual property of the Rif PKS itself.

Knowledge Graph

Similar Paper

Thioesterases and the Premature Termination of Polyketide Chain Elongation in Rifamycin B Biosynthesis by Amycolatopsis mediterranei S699.
The Journal of Antibiotics 2000.0
Isolation of 11,12-<i>seco</i>-Rifamycin W Derivatives Reveals a Cleavage Pattern of the Rifamycin <i>Ansa</i> Chain
Organic Letters 2019.0
Characterization of type II thioesterases involved in natamycin biosynthesis in <i>Streptomyces chattanoogensis</i> L10
FEBS Letters 2014.0
The Streptomyces venezuelae pikAV gene contains a transcription unit essential for expression of enzymes involved in glycosylation of narbonolide and 10-deoxymethynolide
Gene 2001.0
Assembly and Absolute Configuration of Short‐Lived Polyketides from <i>Burkholderia thailandensis</i>
Angewandte Chemie International Edition 2012.0
Thiostrepton Maturation Involving a Deesterification−Amidation Way To Process the C-Terminally Methylated Peptide Backbone
Journal of the American Chemical Society 2011.0
Insights into Lasalocid A Ring Formation by Chemical Chain Termination In Vivo
Angewandte Chemie International Edition 2011.0
Thiazorifamycins. III. Biosynthesis of rifamycins P,Q and verde, novel metabolites from a mutant of Nocardia mediterranea.
The Journal of Antibiotics 1980.0
An amplifiable and deletable locus of Streptomyces ambofaciens RP181110 contains a very large gene homologous to polyketide synthase genes
Microbiology 1996.0
Macrolide biosynthesis. 5. Intact incorporation of a chain-elongation intermediate into nargenicin
Journal of the American Chemical Society 1988.0