Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/120436
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dc.creatorSalvador D.
dc.creatorChurro C.
dc.creatorValério E.
dc.date.accessioned2019-05-31T16:15:45Z-
dc.date.available2019-05-31T16:15:45Z-
dc.date.issued2016
dc.identifier.issn01677012
dc.identifier.urihttps://hdl.handle.net/10216/120436-
dc.description.abstractCyanobacteria are phytoplanktonic organisms widely occurring in freshwaters, being frequently associated with the production of toxins, namely microcystins (MCs). MCs are produced non-ribosomally by a multienzyme complex (mcy genes). It has been reported that environmental factors, such as light intensity, can influence toxin production. The aim of this study was to assess the influence of light intensity in the transcription of the mcyA gene and corresponding production of microcystins in toxic isolates of Planktothrix agardhii, where little is known, and compare them to Microcystis aeruginosa. For that purpose, cultures were exposed to three different light intensities (4, 20 and 30 μmol photons m-2 s-1) for 18 days at 20 ± 1 °C. The growth was followed daily using absorbance readings. Samples were collected at each growth stage for cell counting, microcystins quantification and RNA extraction. The level of transcripts was quantified by RT-qPCR and the relative expression determined using 16S rDNA, gltA and rpoC1 as reference genes. The most stable reference genes in M. aeruginosa were rpoC1 and gltA, whereas in P. agardhii were 16S rDNA and gltA. There was a correspondence between the growth rate and light intensity in M. aeruginosa and P. agardhii. The growth rates for both species were lower at 4 and higher at 30 μmol photons m-2 s-1. Microcystin concentration per cell was similar between light intensities in M. aeruginosa and over time, while in P. agardhii it was higher in the stationary phase at 4 μmol photons m-2 s-1. There were differences in the expression of mcyA between the two species. In M. aeruginosa, the highest levels of expression occurred at 4 μmol photons m-2 s-1 in the adaptation phase, whereas for P. agardhii it was at 4 μmol photons m-2 s-1 in the exponential growth phase. Our results indicate that the light intensities tested had distinct influences on the growth, microcystin production and mcyA expression levels, presenting considerable differences in M. aeruginosa and P. agardhii. © 2016 Elsevier
dc.description.sponsorshipThis research was partially supported by the European Regional Development Fund (ERDF) through the COMPETE – Operational Competitiveness Program – and FCT — Foundation for Science and Technology national funds through Ph.D research grant SFRH/BD65706/2009 to C. Churro and Post-Doc research grant SFRH/BPD/75922/2011 to E. Valério. The authors thank Sérgio Paulino for the assistance in the microcystins quantifications with ELISA kit and Carina Menezes for the HPLC evaluations.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofJournal of Microbiological Methods, vol. 123, p. 4-12
dc.rightsrestrictedAccess
dc.subjectDNA 16S
dc.subjectmicrocystin
dc.subjectArticle
dc.subjectbacterial gene
dc.subjectbacterial growth
dc.subjectcell counting
dc.subjectcontrolled study
dc.subjectcyanobacterium
dc.subjectgene expression
dc.subjectgenetic transcription
dc.subjectgrowth rate
dc.subjectlight exposure
dc.subjectlight intensity
dc.subjectMicrocystis aeruginosa
dc.subjectnonhuman
dc.subjectphoton
dc.subjectPlanktothrix agardhii
dc.subjectpriority journal
dc.subjectreverse transcription polymerase chain reaction
dc.subjectRNA extraction
dc.subjecttemperature
dc.subjecttoxin synthesis
dc.titleEvaluating the influence of light intensity in mcyA gene expression and microcystin production in toxic strains of Planktothrix agardhii and Microcystis aeruginosa
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoCIIMAR - Centro Interdisciplinar de Investigação Marinha e Ambiental
dc.identifier.doi10.1016/j.mimet.2016.02.002
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.mimet.2016.02.002
Appears in Collections:CIIMAR - Artigo em Revista Científica Internacional

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