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1.
J Biosci Bioeng ; 124(4): 369-375, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28533156

ABSTRACT

Streptomyces lavendulae FRI-5 produces the blue pigment indigoidine and other secondary metabolites (d-cycloserine and nucleoside antibiotics). The production of these useful compounds is controlled by a signaling cascade mediated by the γ-butyrolactone autoregulator IM-2. Previously we revealed that the far regulatory island includes the IM-2 receptor, the IM-2 biosynthetic enzyme, and several transcriptional regulators, and that it contributes to the regulation of indigoidine production in response to the signaling molecule. Here, we found that the vicinity of the far regulatory island includes the putative gene cluster for the biosynthesis of indigoidine and unidentified compounds, and demonstrated that the expression of the gene cluster is under the control of the IM-2 regulatory system. Heterologous expression of lbpA, encoding a plausible nonribosomal peptide synthetase, in the versatile model host Streptomyces avermitilis SUKA22 led to indigoidine production, which was enhanced dramatically by feeding of the indigoidine precursor l-glutamine. These results confirmed that LbpA is an indigoidine biosynthetic enzyme in the IM-2 signaling cascade.


Subject(s)
Bacterial Proteins/genetics , Peptide Synthases/genetics , Piperidones/metabolism , Signal Transduction/genetics , Streptomyces/genetics , Streptomyces/metabolism , 4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/metabolism , Bacterial Proteins/metabolism , Gene Expression Regulation, Bacterial , Glutamine/metabolism , Multigene Family/genetics , Peptide Synthases/metabolism , Streptomyces/enzymology
2.
J Biosci Bioeng ; 121(4): 372-9, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26375200

ABSTRACT

The γ-butyrolactone autoregulator signaling cascade is widely distributed among Streptomyces species as an important regulatory system of secondary metabolism. In Streptomyces lavendulae FRI-5, a γ-butyrolactone autoregulator IM-2 and the IM-2 specific receptor FarA control production of the blue pigment indigoidine together with two types of antibiotics: d-cycloserine and the nucleoside antibiotics. Here, we demonstrated by in silico analysis that farR2 (a farA homologue), which is located in a cluster of regulatory genes including farA, belongs to the family of pseudoreceptor regulator genes, and that the expression of farR2 is controlled by the IM-2/FarA regulatory system. Disruption of farR2 resulted in delayed production of indigoidine and in transcriptional derepression of the clustered far regulatory genes. Moreover, FarR2 bound to the FarA-binding sequences in the promoter regions of the regulatory genes that were downregulated by FarR2.


Subject(s)
Piperidones/metabolism , Receptors, GABA-A/metabolism , Streptomyces/metabolism , 4-Butyrolactone/analogs & derivatives , 4-Butyrolactone/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Computer Simulation , Down-Regulation , Gene Expression Regulation, Bacterial , Genes, Regulator/genetics , Multigene Family/genetics , Promoter Regions, Genetic/genetics , Receptors, GABA-A/genetics , Secondary Metabolism , Streptomyces/genetics , Transcription, Genetic/genetics
3.
Appl Microbiol Biotechnol ; 98(23): 9713-21, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25125041

ABSTRACT

The Streptomyces antibiotic regulatory protein (SARP) family regulators have been shown to control the production of secondary metabolites in many Streptomyces species as the most downstream regulators in the regulatory cascade. Streptomyces lavendulae FRI-5 produces a blue pigment (indigoidine) together with two types of antibiotics: D-cycloserine and the nucleoside antibiotics. The production of these secondary metabolites is governed by a signaling system consisting of a γ-butyrolactone, IM-2 [(2R,3R,1'R)-2-1'-hydroxybutyl-3-hydroxymethyl-γ-butanolide], and its cognate receptor, FarA. Here, we characterized two regulatory genes of the SARP family, farR3 and farR4, which are tandemly located in the proximal region of farA. farR3 is transcribed both as a monocistronic RNA and as a bicistronic farR4-farR3 mRNA, and the expression profile is tightly controlled by the IM-2/FarA system. Loss of farR3 delayed and decreased the production of indigoidine without any changes in the transcriptional profile of other far regulatory genes, indicating that FarR3 positively controls the biosynthesis of indigoidine and is positioned in the downstream region of the IM-2/FarA signaling system. Meanwhile, loss of farR4 induced the early production of IM-2 by increasing transcription of an IM-2 biosynthetic gene, farX, indicating that FarR4 negatively controls the biosynthesis of IM-2. Thus, our results suggested differential contributions of the SARP family regulators to the regulation of secondary metabolism in S. lavendulae FRI-5. This is the first report to show that an SARP family regulator is involved in the biosynthesis of a signaling molecule functioning at the most upstream region of the regulatory cascade for Streptomyces secondary metabolism.


Subject(s)
Biosynthetic Pathways/genetics , Gene Expression Regulation, Bacterial , Genes, Regulator , Piperidones/metabolism , Streptomyces/genetics , Streptomyces/metabolism , Gene Expression Profiling , Pigments, Biological/metabolism , Repressor Proteins/genetics , Repressor Proteins/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism , Transcription, Genetic
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