Genetic Control of Amadori Product Degradation in Bacillus subtilis via Regulation of frlBONMD Expression by FrlR

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Published inApplied and Environmental Microbiology Vol. 77; no. 9; pp. 2839 - 2846
Main Authors Deppe, Veronika Maria, Klatte, Stephanie, Bongaerts, Johannes, Maurer, Karl-Heinz, O'Connell, Timothy, Meinhardt, Friedhelm
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.05.2011
Subjects
Amadori products
Bacillus subtilis
Bacillus subtilis - enzymology
Bacillus subtilis - genetics
Bacillus subtilis - metabolism
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Binding Sites
Biological and medical sciences
DNA, Bacterial - metabolism
Food Microbiology
Fructosamine - metabolism
Fundamental and applied biological sciences. Psychology
Gene expression
gene expression regulation
Gene Expression Regulation, Bacterial
Gene Expression Regulation, Enzymologic
Genes
Genetics
Gram-positive bacteria
intergenic DNA
Microbiology
Operon
Phosphorylation
Physiology
Protein Binding
Repressor Proteins - metabolism
Studies
Transcription, Genetic
Regulation(control)
Bacillales
Bacillus subtilis
Bacteria
Bacillaceae
Genetic determinism
Degradation product
Online AccessGet full text

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Abstract Classifications Services AEM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue Spotlights in the Current Issue AEM About AEM Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AEM RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0099-2240 Online ISSN: 1098-5336 Copyright © 2014 by the American Society for Microbiology.   For an alternate route to AEM .asm.org, visit: AEM       
AbstractList Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the frlD and frlB gene products, respectively. This study addresses the physiological importance of the frlBONMD genes (formerly yurPONML), revealing the necessity of their expression for growth on fructosamines and focusing on the complex regulation of the corresponding transcription unit. In addition to the known regulation by the global transcriptional regulator CodY, the frl genes are repressed by the convergently transcribed FrlR (formerly YurK). The latter causes repression during growth on substrates other than fructosamines. Additionally, we identified in the first intergenic region of the operon an FrlR binding site which is centrally located within a 38-bp perfect palindromic sequence. There is genetic evidence that this sequence, in combination with FrlR, contributes to the remarkable decrease in the transcription downstream of the first gene of the frl operon.
Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the frlD and frlB gene products, respectively. This study addresses the physiological importance of the frlBONMD genes (formerly yurPONML ), revealing the necessity of their expression for growth on fructosamines and focusing on the complex regulation of the corresponding transcription unit. In addition to the known regulation by the global transcriptional regulator CodY, the frl genes are repressed by the convergently transcribed FrlR (formerly YurK). The latter causes repression during growth on substrates other than fructosamines. Additionally, we identified in the first intergenic region of the operon an FrlR binding site which is centrally located within a 38-bp perfect palindromic sequence. There is genetic evidence that this sequence, in combination with FrlR, contributes to the remarkable decrease in the transcription downstream of the first gene of the frl operon.
Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the frlD and frlB gene products, respectively. This study addresses the physiological importance of the frlBONMD genes (formerly yurPONML), revealing the necessity of their expression for growth on fructosamines and focusing on the complex regulation of the corresponding transcription unit. In addition to the known regulation by the global transcriptional regulator CodY, the frl genes are repressed by the convergently transcribed FrlR (formerly YurK). The latter causes repression during growth on substrates other than fructosamines. Additionally, we identified in the first intergenic region of the operon an FrlR binding site which is centrally located within a 38-bp perfect palindromic sequence. There is genetic evidence that this sequence, in combination with FrlR, contributes to the remarkable decrease in the transcription downstream of the first gene of the frl operon. [PUBLICATION ABSTRACT]
Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the frlD and frlB gene products, respectively. This study addresses the physiological importance of the frlBONMD genes (formerly yurPONML), revealing the necessity of their expression for growth on fructosamines and focusing on the complex regulation of the corresponding transcription unit. In addition to the known regulation by the global transcriptional regulator CodY, the frl genes are repressed by the convergently transcribed FrlR (formerly YurK). The latter causes repression during growth on substrates other than fructosamines. Additionally, we identified in the first intergenic region of the operon an FrlR binding site which is centrally located within a 38-bp perfect palindromic sequence. There is genetic evidence that this sequence, in combination with FrlR, contributes to the remarkable decrease in the transcription downstream of the first gene of the frl operon.Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the frlD and frlB gene products, respectively. This study addresses the physiological importance of the frlBONMD genes (formerly yurPONML), revealing the necessity of their expression for growth on fructosamines and focusing on the complex regulation of the corresponding transcription unit. In addition to the known regulation by the global transcriptional regulator CodY, the frl genes are repressed by the convergently transcribed FrlR (formerly YurK). The latter causes repression during growth on substrates other than fructosamines. Additionally, we identified in the first intergenic region of the operon an FrlR binding site which is centrally located within a 38-bp perfect palindromic sequence. There is genetic evidence that this sequence, in combination with FrlR, contributes to the remarkable decrease in the transcription downstream of the first gene of the frl operon.
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Author Veronika Maria Deppe
Karl-Heinz Maurer
Friedhelm Meinhardt
Johannes Bongaerts
Stephanie Klatte
Timothy O'Connell
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Keywords Regulation(control)
Bacillales
Bacillus subtilis
Bacteria
Bacillaceae
Genetic determinism
Degradation product
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Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the...
Bacillus subtilis is capable of degrading fructosamines. The phosphorylation and the cleavage of the resulting fructosamine 6-phosphates is catalyzed by the...
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StartPage 2839
SubjectTerms Amadori products
Bacillus subtilis
Bacillus subtilis - enzymology
Bacillus subtilis - genetics
Bacillus subtilis - metabolism
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Binding Sites
Biological and medical sciences
DNA, Bacterial - metabolism
Food Microbiology
Fructosamine - metabolism
Fundamental and applied biological sciences. Psychology
Gene expression
gene expression regulation
Gene Expression Regulation, Bacterial
Gene Expression Regulation, Enzymologic
Genes
Genetics
Gram-positive bacteria
intergenic DNA
Microbiology
Operon
Phosphorylation
Physiology
Protein Binding
Repressor Proteins - metabolism
Studies
Transcription, Genetic
Title Genetic Control of Amadori Product Degradation in Bacillus subtilis via Regulation of frlBONMD Expression by FrlR
URI http://aem.asm.org/content/77/9/2839.abstract
https://www.ncbi.nlm.nih.gov/pubmed/21398478
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https://www.proquest.com/docview/1368579060
https://www.proquest.com/docview/863429055
https://pubmed.ncbi.nlm.nih.gov/PMC3126415
Volume 77
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