Lactose-over-Glucose Preference in Bifidobacterium longum NCC2705: glcP, Encoding a Glucose Transporter, Is Subject to Lactose Repression
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| Published in | Journal of Bacteriology Vol. 188; no. 4; pp. 1260 - 1265 |
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| AbstractList | Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until depletion of lactose. Thus, unlike many other bacteria, B. longum preferentially uses lactose rather than glucose as the primary carbon source. Glucose uptake experiments with B. longum cells showed that glucose transport was repressed in the presence of lactose. A comparative analysis of global gene expression profiling using DNA arrays led to the identification of only one gene repressed by lactose, the putative glucose transporter gene glcP. The functionality of GlcP as glucose transporter was demonstrated by heterologous complementation of a glucose transport-deficient Escherichia coli strain. Additionally, GlcP exhibited the highest substrate specificity for glucose. Primer extension and real-time PCR analyses confirmed that expression of glcP was mediated by lactose. Hence, our data demonstrate that the presence of lactose in culture medium leads to the repression of glucose transport and transcriptional down-regulation of the glucose transporter gene glcP. This may reflect the highly adapted life-style of B. longum in the gastrointestinal tract of mammals.Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until depletion of lactose. Thus, unlike many other bacteria, B. longum preferentially uses lactose rather than glucose as the primary carbon source. Glucose uptake experiments with B. longum cells showed that glucose transport was repressed in the presence of lactose. A comparative analysis of global gene expression profiling using DNA arrays led to the identification of only one gene repressed by lactose, the putative glucose transporter gene glcP. The functionality of GlcP as glucose transporter was demonstrated by heterologous complementation of a glucose transport-deficient Escherichia coli strain. Additionally, GlcP exhibited the highest substrate specificity for glucose. Primer extension and real-time PCR analyses confirmed that expression of glcP was mediated by lactose. Hence, our data demonstrate that the presence of lactose in culture medium leads to the repression of glucose transport and transcriptional down-regulation of the glucose transporter gene glcP. This may reflect the highly adapted life-style of B. longum in the gastrointestinal tract of mammals. Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until depletion of lactose. Thus, unlike many other bacteria, B. longum preferentially uses lactose rather than glucose as the primary carbon source. Glucose uptake experiments with B. longum cells showed that glucose transport was repressed in the presence of lactose. A comparative analysis of global gene expression profiling using DNA arrays led to the identification of only one gene repressed by lactose, the putative glucose transporter gene glcP . The functionality of GlcP as glucose transporter was demonstrated by heterologous complementation of a glucose transport-deficient Escherichia coli strain. Additionally, GlcP exhibited the highest substrate specificity for glucose. Primer extension and real-time PCR analyses confirmed that expression of glcP was mediated by lactose. Hence, our data demonstrate that the presence of lactose in culture medium leads to the repression of glucose transport and transcriptional down-regulation of the glucose transporter gene glcP. This may reflect the highly adapted life-style of B. longum in the gastrointestinal tract of mammals. Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until depletion of lactose. Thus, unlike many other bacteria, B. longum preferentially uses lactose rather than glucose as the primary carbon source. Glucose uptake experiments with B. longum cells showed that glucose transport was repressed in the presence of lactose. A comparative analysis of global gene expression profiling using DNA arrays led to the identification of only one gene repressed by lactose, the putative glucose transporter gene glcP. The functionality of GlcP as glucose transporter was demonstrated by heterologous complementation of a glucose transport-deficient Escherichia coli strain. Additionally, GlcP exhibited the highest substrate specificity for glucose. Primer extension and real-time PCR analyses confirmed that expression of glcP was mediated by lactose. Hence, our data demonstrate that the presence of lactose in culture medium leads to the repression of glucose transport and transcriptional down-regulation of the glucose transporter gene glcP. This may reflect the highly adapted life-style of B. longum in the gastrointestinal tract of mammals. Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until depletion of lactose. Thus, unlike many other bacteria, B. longum preferentially uses lactose rather than glucose as the primary carbon source. Glucose uptake experiments with B. longum cells showed that glucose transport was repressed in the presence of lactose. A comparative analysis of global gene expression profiling using DNA arrays led to the identification of only one gene repressed by lactose, the putative glucose transporter gene glcP. The functionality of GlcP as glucose transporter was demonstrated by heterologous complementation of a glucose transport-deficient Escherichia coli strain. Additionally, GlcP exhibited the highest substrate specificity for glucose. Primer extension and real-time PCR analyses confirmed that expression of glcP was mediated by lactose. Hence, our data demonstrate that the presence of lactose in culture medium leads to the repression of glucose transport and transcriptional down-regulation of the glucose transporter gene glcP. This may reflect the highly adapted life-style of B. longum in the gastrointestinal tract of mammals. [PUBLICATION ABSTRACT] Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue JB About JB Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JB RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0021-9193 Online ISSN: 1098-5530 Copyright © 2014 by the American Society for Microbiology. For an alternate route to JB .asm.org, visit: JB |
| Author | Enea Rezzonico Ivana Jankovic Manfred Beleut Fritz Titgemeyer Doris Jacobs Fabrizio Arigoni Stephan Parche |
| AuthorAffiliation | Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland, 1 Lehrstuhl für Mikrobiologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany 2 |
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| Author_xml | – sequence: 1 givenname: Stephan surname: Parche fullname: Parche, Stephan organization: Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland – sequence: 2 givenname: Manfred surname: Beleut fullname: Beleut, Manfred organization: Lehrstuhl für Mikrobiologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany – sequence: 3 givenname: Enea surname: Rezzonico fullname: Rezzonico, Enea organization: Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland – sequence: 4 givenname: Doris surname: Jacobs fullname: Jacobs, Doris organization: Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland – sequence: 5 givenname: Fabrizio surname: Arigoni fullname: Arigoni, Fabrizio organization: Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland – sequence: 6 givenname: Fritz surname: Titgemeyer fullname: Titgemeyer, Fritz organization: Lehrstuhl für Mikrobiologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany – sequence: 7 givenname: Ivana surname: Jankovic fullname: Jankovic, Ivana organization: Nestlé Research Center, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland |
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| Keywords | Actinomycetales Lactic acid bacteria Lactose Actinomycetaceae Microbiology Bacteria Bifidobacterium longum Actinomycetes Glucose Bacteriology Carrier protein |
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Mendeley... Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until... Analysis of culture supernatants obtained from Bifidobacterium longum NCC2705 grown on glucose and lactose revealed that glucose utilization is impaired until... |
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| SubjectTerms | Bacterial Proteins - genetics Bacteriology Base Sequence Bifidobacterium - genetics Bifidobacterium - growth & development Bifidobacterium - metabolism Bifidobacterium longum Biological and medical sciences Biological Transport Carbon sources Cells Culture Media DNA, Intergenic - genetics Down-Regulation - genetics E coli Escherichia coli Fundamental and applied biological sciences. Psychology Gastrointestinal tract Gene expression Gene Expression Regulation, Bacterial Genes, Bacterial Glucose Glucose - metabolism Glucose Transport Proteins, Facilitative - genetics Lactose - physiology Microbiology Miscellaneous Molecular Sequence Data Phosphoglucomutase - genetics Physiology and Metabolism Substrate Specificity Transcription, Genetic |
| Title | Lactose-over-Glucose Preference in Bifidobacterium longum NCC2705: glcP, Encoding a Glucose Transporter, Is Subject to Lactose Repression |
| URI | http://jb.asm.org/content/188/4/1260.abstract https://www.ncbi.nlm.nih.gov/pubmed/16452407 https://www.proquest.com/docview/227109968 https://www.proquest.com/docview/17471010 https://www.proquest.com/docview/67622875 https://pubmed.ncbi.nlm.nih.gov/PMC1367232 |
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