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Pet?í?ková K,
Chro?áková A,
Zelenka T,
Chrudimský T,
Pospíšil S,
Pet?í?ek M,
Krištůfek V,
( 2015 )
Evolution of cyclizing 5-aminolevulinate synthases in the biosynthesis of actinomycete secondary metabolites: outcomes for genetic screening techniques.
Frontiers in microbiology 6 (N/A)
PMID : 26300877 :
DOI : 10.3389/fmicb.2015.00814
PMC : PMC4525017
Abstract >>
A combined approach, comprising PCR screening and genome mining, was used to unravel the diversity and phylogeny of genes encoding 5-aminolevulinic acid synthases (ALASs, hemA gene products) in streptomycetes-related strains. In actinomycetes, these genes were believed to be directly connected with the production of secondary metabolites carrying the C5N unit, 2-amino-3-hydroxycyclopent-2-enone, with biological activities making them attractive for future use in medicine and agriculture. Unlike "classical" primary metabolism ALAS, the C5N unit-forming cyclizing ALAS (cALAS) catalyses intramolecular cyclization of nascent 5-aminolevulinate. Specific amino acid sequence changes can be traced by comparison of "classical" ALASs against cALASs. PCR screening revealed 226 hemA gene-carrying strains from 1,500 tested, with 87% putatively encoding cALAS. Phylogenetic analysis of the hemA homologs revealed strain clustering according to putative type of metabolic product, which could be used to select producers of specific C5N compound classes. Supporting information was acquired through analysis of actinomycete genomic sequence data available in GenBank and further genetic or metabolic characterization of selected strains. Comparison of 16S rRNA taxonomic identification and BOX-PCR profiles provided evidence for numerous horizontal gene transfers of biosynthetic genes or gene clusters within actinomycete populations and even from non-actinomycete organisms. Our results underline the importance of environmental and evolutionary data in the design of efficient techniques for identification of novel producers.
| Keyword | MeSH Terms |
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
5-aminolevulinate synthase
C5N unit
Streptomyces
gene evolution
genetic screening
horizontal gene transfer
secondary metabolites
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Auffret M,
Pilote A,
Proulx E,
Proulx D,
Vandenberg G,
Villemur R,
( 2011 )
Establishment of a real-time PCR method for quantification of geosmin-producing Streptomyces spp. in recirculating aquaculture systems.
Water research 45 (20)
PMID : 22060964 :
DOI : 10.1016/j.watres.2011.10.020
Abstract >>
Geosmin and 2-methylisoborneol (MIB) have been associated with off-flavour problems in fish and seafood products, generating a strong negative impact for aquaculture industries. Although most of the producers of geosmin and MIB have been identified as Streptomyces species or cyanobacteria, Streptomyces spp. are thought to be responsible for the synthesis of these compounds in indoor recirculating aquaculture systems (RAS). The detection of genes involved in the synthesis of geosmin and MIB can be a relevant indicator of the beginning of off-flavour events in RAS. Here, we report a real-time polymerase chain reaction (qPCR) protocol targeting geoA sequences that encode a germacradienol synthase involved in geosmin synthesis. New geoA-related sequences were retrieved from eleven geosmin-producing Actinomycete strains, among them two Streptomyces strains isolated from two RAS. Combined with geoA-related sequences available in gene databases, we designed primers and standards suitable for qPCR assays targeting mainly Streptomyces geoA. Using our qPCR protocol, we succeeded in measuring the level of geoA copies in sand filter and biofilters in two RAS. This study is the first to apply qPCR assays to detect and quantify the geosmin synthesis gene (geoA) in RAS. Quantification of geoA in RAS could permit the monitoring of the level of geosmin producers prior to the occurrence of geosmin production. This information will be most valuable for fish producers to manage further development of off-flavour events.
| Keyword | MeSH Terms |
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Aquaculture
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