title: Flavin uptake and metabolism in Listeria monocytogenes and FMN riboswitches as targets for riboflavin analogs
creator: Matern, Andreas
description: The riboflavin analog roseoflavin – an antibiotic produced by the bacteria Streptomyces davawensis and Streptomyces cinnabarinus, and the key intermediate of the roseoflavin biosynthesis, 8-demthyl-8-amino riboflavin which is an antibiotic as well, are both known to have a growth inhibiting effect on the human pathogen Listeria monocytogens. The adverse effect of roseoflavin on L. monocytogenes has been proposed to be a result of its interaction with the FMN riboswitch Rli96, regulating expression of the riboflavin transporter gene lmo1945. Whether flavin analogs, such as roseoflavin and 8-demethyl-8-amino riboflavin, are assimilated by L. monocytogenes through the riboflavin transporter protein Lmo1945 has not yet been known. In addition, the conversion of flavin analogs into cofactor analogs by flavokinase/FAD synthetase enzymes from L. monocytogenes has not been investigated. The functional analysis of the effect of the cofactor analogs on the FMN riboswitch Rli96 could help to elucidate how flavin analogs affect riboflavin auxotrophic bacteria, including L. monocytogenes.   Through heterologous expression of Lmo1945 in a riboflavin transporter deficient Bacillus subtilis strain, the role of Lmo1945 in the uptake of riboflavin and roseoflavin was confirmed. Two enzymes, catalyzing the conversion of riboflavin into the cofactors flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) have been identified by sequence analysis. The bifunctional flavokinase/FAD synthetase Lmo1329 and the unique monofunctional FAD synthetase Lmo0728 were purified and kinetically characterized. Additionally, their involvement in the generation of the cofactor analogs roseoflavin mononucleotide (RoFMN), 8-demethyl-8-amino riboflavin mononucleotide (AFMN), roseoflavin adenine dinucleotide (RoFAD) and 8-demethyl-8-amino riboflavin adenine dinucleotide (AFAD) were shown in vitro. Notably, the bifunctional enzyme Lmo1329 did not convert the roseoflavin derived cofactor RoFMN into RoFAD.   In vivo reporter gene assays and in vitro transcription/translation experiments showed that the FMN riboswitch Rli96, and consequently the expression of the riboflavin transporter gene lmo1945, is negatively affected by FMN and RoFMN but not by AFMN.   With the FMN riboswitch Rli96, the riboflavin transporter Lmo1945, the bifunctional flavokinase/FAD synthetase Lmo1329 and the monofunctional FAD synthetase Lmo0728, the key mechanisms of riboflavin uptake and metabolism in L. monocytogenes were identified and characterized. Particularly, the FAD synthetase Lmo0728 is the first monofunctional FAD synthetase that has been described in bacteria.   As a second part of this thesis a novel reporter system for in vivo studies of translational riboswitches in Streptomyces species was evaluated. However, the system proved to not be suitable for the desired application, i.e. the confirmation of previously obtained in vitro data. Several attempts to adapt and optimize the system failed which turned out to be due to the complexity of the natural expression platform in streptomycetes.
date: 2016
type: Dissertation
type: info:eu-repo/semantics/doctoralThesis
type: NonPeerReviewed
format: application/pdf
identifier: https://archiv.ub.uni-heidelberg.de/volltextserverhttps://archiv.ub.uni-heidelberg.de/volltextserver/21598/1/Dissertation_Andreas_Matern.pdf
identifier: DOI:10.11588/heidok.00021598
identifier: urn:nbn:de:bsz:16-heidok-215984
identifier:   Matern, Andreas  (2016) Flavin uptake and metabolism in Listeria monocytogenes and FMN riboswitches as targets for riboflavin analogs.  [Dissertation]     
relation: https://archiv.ub.uni-heidelberg.de/volltextserver/21598/
rights: info:eu-repo/semantics/openAccess
rights: http://archiv.ub.uni-heidelberg.de/volltextserver/help/license_urhg.html
language: eng