Specific Gene Expression in U Shows New Alternatives for Cadaverine and Putrescine Catabolism.

Genes (Basel)

Área de Bioquímica y Biología Molecular, Departamento de Biología Molecular, Universidad de León, 24007 León, Spain.

Published: September 2023

AI Article Synopsis

  • - Strain U can utilize biogenic amines like putrescine and cadaverine, along with their breakdown products (ɣ-aminobutyrate and δ-aminovalerate), as its only carbon sources.
  • - Several gene paralogs have been identified in strain U that are responsible for catabolizing these compounds, including those encoding putrescine-pyruvate and ɣ-aminobutyrate aminotransferases.
  • - Gene expression levels vary significantly based on the carbon source; putrescine upregulates certain genes while cadaverine triggers others, highlighting distinct mechanisms for polyamine metabolism in strain U.

Article Abstract

strain U can be grown using, as sole carbon sources, the biogenic amines putrescine or cadaverine, as well as their catabolic intermediates, ɣ-aminobutyrate or δ-aminovalerate, respectively. Several paralogs for the genes that encode some of the activities involved in the catabolism of these compounds, such as a putrescine-pyruvate aminotransferase ( and genes) and a ɣ-aminobutyrate aminotransferase ( and genes) have been identified in this bacterium. When the expression pattern of these genes is analyzed by qPCR, it is drastically conditioned by supplying the carbon sources. Thus, is upregulated by putrescine, whereas seems to be exclusively induced by cadaverine. However, increases its expression in response to different polyamines or aminated catabolic derivatives from them (i.e., ɣ-aminobutyrate or δ-aminovalerate), although does not change its expression level concerning no-amine unrelated carbon sources (citrate). These results reveal differences between the mechanisms proposed for polyamine catabolism in and concerning strain U, as well as allow a deeper understanding of the enzymatic systems used by this last strain during polyamine metabolism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10606097PMC
http://dx.doi.org/10.3390/genes14101897DOI Listing

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