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NIBIOs ansatte publiserer flere hundre vitenskapelige artikler og forskningsrapporter hvert år. Her finner du referanser og lenker til publikasjoner og andre forsknings- og formidlingsaktiviteter. Samlingen oppdateres løpende med både nytt og historisk materiale. For mer informasjon om NIBIOs publikasjoner, besøk NIBIOs bibliotek.

2012

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Sammendrag

The selective serotonin reuptake inhibitors citalopram, sertraline, paroxetine, fluvoxamine and fluoxetine have been investigated in 10 l anaerobic lab-scale digesters with continuous stirring and mesophilic conditions at 37 °C to investigate whether they would be reduced or accumulated in sewage sludge depending on whether the bacteria present were able to use the SSRIs as a carbon source or not. The total SSRI concentration had a significant reduction in concentration during the anaerobic treatment process from theoretically 0.58 mg/l to 0.21 mg/l after 17 days. However, large differences in the reduction of the different compounds were found. Paroxetine and citalopram were found to be almost completely reduced at day 24 with reductions of 85% (citalopram) and 98% (paroxetine). Reductions of 32% (fluoxetine), 53% (fluvoxamine) and 38% (sertraline) indicate that these three compounds have a higher potential for accumulation. None metabolites of these compounds were found in the samples.

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A 1149 bp genomic fragment corresponding to the 5' non-coding region of the PgD1 (Picea glauca Defensin 1) gene was cloned, characterized, and compared with all Arabidopsis thaliana defensin promoters. The cloned fragment was found to contain several motifs specific to defence or hormonal response, including a motif involved in the methyl jasmonate reponse, a fungal elicitor responsive element, and TC-rich repeat cis-acting element involved in defence and stress responsiveness. A functional analysis of the PgD1 promoter was performed using the uidA (GUS) reporter system in stably transformed Arabidopsis and white spruce plants. The PgD1 promoter was responsive to jasmonic acid (JA), to infection by fungus and to wounding. In transgenic spruce embryos, GUS staining was clearly restricted to the shoot apical meristem. In Arabidopsis, faint GUS coloration was observed in leaves and flowers and a strong blue colour was observed in guard cells and trichomes. Transgenic Arabidopsis plants expressing the PgD1::GUS construct were also infiltrated with the hemibiotrophic pathogen Pseudomonas syringae pv. tomato DC3000. It caused a suppression of defensin expression probably resulting from the antagonistic relationship between the pathogen-stimulated salicylic acid pathway and the jasmonic acid pathway. It is therefore concluded that the PgD1 promoter fragment cloned appears to contain most if not all the elements for proper PgD1 expression and that these elements are also recognized in Arabidopsis despite the phylogenetic and evolutionary differences that separates them.