Isolation of lactate-utilizing butyrate-producing bacteria from human feces and in vivo administration of Anaerostipes caccae strain L2 and galacto-oligosaccharides in a rat model
Lactate-utilizing butyrate-producers were isolated from human feces and identified based on the sequences of 16S rRNA gene. Anaerostipes caccae strain L2, one of the seven human fecal isolates, was administered to rats with galacto-oligosaccharides (GOS) as bifidogenic carbohydrates for stimulating...
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creator | Sato, Tadashi Matsumoto, Kazumasa Okumura, Takekazu Yokoi, Wakae Naito, Eiichiro Yoshida, Yasuto Nomoto, Koji Ito, Masahiko Sawada, Haruji |
description | Lactate-utilizing butyrate-producers were isolated from human feces and identified based on the sequences of 16S rRNA gene. Anaerostipes caccae strain L2, one of the seven human fecal isolates, was administered to rats with galacto-oligosaccharides (GOS) as bifidogenic carbohydrates for stimulating lactate formation in the hindgut. Ingestion of GOS alone increased concentrations of cecal lactate and butyrate compared with control rats (P |
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Anaerostipes caccae strain L2, one of the seven human fecal isolates, was administered to rats with galacto-oligosaccharides (GOS) as bifidogenic carbohydrates for stimulating lactate formation in the hindgut. Ingestion of GOS alone increased concentrations of cecal lactate and butyrate compared with control rats (P<0.05). Additional administration of strain L2 on GOS tended to enhance the promoting effect of GOS on cecal butyrate formation (P=0.06) and lowered the mean value of cecal lactate concentration (P=0.32). Consequently, cecal and fecal butyrate concentrations in rats administered with both strain L2 and GOS were significantly higher than those in the control rats (P<0.01 and P<0.05, respectively). Significant changes were observed in the other fermentation acids, such as succinate, acetate, and propionate, depending on the ingestion of strain L2. Administered strain L2 was retrieved from the cecal content of a rat based on randomly amplified polymorphic DNA analysis. The results suggest that synbiotic ingestion of lactate-utilizing butyrate-producers and GOS alters the microbial fermentation and promotes the formation of beneficial fermentation acids, including butyrate, in the gut.</description><identifier>ISSN: 0168-6496</identifier><identifier>EISSN: 1574-6941</identifier><identifier>DOI: 10.1111/j.1574-6941.2008.00528.x</identifier><identifier>PMID: 18554304</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Acetic acid ; Adult ; Animals ; Bacteria - classification ; Bacteria - genetics ; Bacteria - isolation & purification ; Bacteria - metabolism ; Bifidobacteria ; butyrate ; Butyrates - metabolism ; Carbohydrates ; Cecum ; Cecum - metabolism ; Cecum - microbiology ; Colony Count, Microbial ; Deoxyribonucleic acid ; DNA ; Ecology ; Fatty Acids - metabolism ; Feces ; Feces - microbiology ; Fermentation ; Fermentation - drug effects ; Galactooligosaccharides ; galacto‐oligosaccharides ; Gene sequencing ; Hindgut ; Humans ; Ingestion ; Intestines - metabolism ; Intestines - microbiology ; lactate ; Lactic acid ; Lactic Acid - metabolism ; Male ; Microbiology ; Microorganisms ; Models, Animal ; Oligosaccharides ; Oligosaccharides - administration & dosage ; Probiotics ; Propionic acid ; Rats ; Rats, Sprague-Dawley ; RNA, Ribosomal, 16S - genetics ; Rodents ; rRNA 16S ; Specific Pathogen-Free Organisms ; Succinic Acid - metabolism</subject><ispartof>FEMS microbiology ecology, 2008-12, Vol.66 (3), p.528-536</ispartof><rights>2008 Federation of European Microbiological Societies 2008</rights><rights>2008 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved</rights><rights>2008 Federation of European Microbiological Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5608-bb13df36cf3fec0813b8b6effd61d4a1f9d65c49c99d79b01f9581b2d2e9a13b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1574-6941.2008.00528.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1574-6941.2008.00528.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18554304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sato, Tadashi</creatorcontrib><creatorcontrib>Matsumoto, Kazumasa</creatorcontrib><creatorcontrib>Okumura, Takekazu</creatorcontrib><creatorcontrib>Yokoi, Wakae</creatorcontrib><creatorcontrib>Naito, Eiichiro</creatorcontrib><creatorcontrib>Yoshida, Yasuto</creatorcontrib><creatorcontrib>Nomoto, Koji</creatorcontrib><creatorcontrib>Ito, Masahiko</creatorcontrib><creatorcontrib>Sawada, Haruji</creatorcontrib><title>Isolation of lactate-utilizing butyrate-producing bacteria from human feces and in vivo administration of Anaerostipes caccae strain L2 and galacto-oligosaccharides in a rat model</title><title>FEMS microbiology ecology</title><addtitle>FEMS Microbiol Ecol</addtitle><description>Lactate-utilizing butyrate-producers were isolated from human feces and identified based on the sequences of 16S rRNA gene. Anaerostipes caccae strain L2, one of the seven human fecal isolates, was administered to rats with galacto-oligosaccharides (GOS) as bifidogenic carbohydrates for stimulating lactate formation in the hindgut. Ingestion of GOS alone increased concentrations of cecal lactate and butyrate compared with control rats (P<0.05). Additional administration of strain L2 on GOS tended to enhance the promoting effect of GOS on cecal butyrate formation (P=0.06) and lowered the mean value of cecal lactate concentration (P=0.32). Consequently, cecal and fecal butyrate concentrations in rats administered with both strain L2 and GOS were significantly higher than those in the control rats (P<0.01 and P<0.05, respectively). Significant changes were observed in the other fermentation acids, such as succinate, acetate, and propionate, depending on the ingestion of strain L2. Administered strain L2 was retrieved from the cecal content of a rat based on randomly amplified polymorphic DNA analysis. The results suggest that synbiotic ingestion of lactate-utilizing butyrate-producers and GOS alters the microbial fermentation and promotes the formation of beneficial fermentation acids, including butyrate, in the gut.</description><subject>Acetic acid</subject><subject>Adult</subject><subject>Animals</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteria - metabolism</subject><subject>Bifidobacteria</subject><subject>butyrate</subject><subject>Butyrates - metabolism</subject><subject>Carbohydrates</subject><subject>Cecum</subject><subject>Cecum - metabolism</subject><subject>Cecum - microbiology</subject><subject>Colony Count, Microbial</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Ecology</subject><subject>Fatty Acids - metabolism</subject><subject>Feces</subject><subject>Feces - microbiology</subject><subject>Fermentation</subject><subject>Fermentation - drug effects</subject><subject>Galactooligosaccharides</subject><subject>galacto‐oligosaccharides</subject><subject>Gene sequencing</subject><subject>Hindgut</subject><subject>Humans</subject><subject>Ingestion</subject><subject>Intestines - metabolism</subject><subject>Intestines - microbiology</subject><subject>lactate</subject><subject>Lactic acid</subject><subject>Lactic Acid - metabolism</subject><subject>Male</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>Models, Animal</subject><subject>Oligosaccharides</subject><subject>Oligosaccharides - administration & dosage</subject><subject>Probiotics</subject><subject>Propionic acid</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Rodents</subject><subject>rRNA 16S</subject><subject>Specific Pathogen-Free Organisms</subject><subject>Succinic Acid - metabolism</subject><issn>0168-6496</issn><issn>1574-6941</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFksFu1DAQhi0EosvCK4AlJG5ZxnHi2hKXqmqh0iIO0LPl2M7WqyRe7KR0eS1ekMluKRII4Yutme8f2zM_IZTBiuF6u12x-rQqhKrYqgSQK4C6lKu7R2TxkHhMFsCELESlxAl5lvMWgNW8gqfkhMm6rjhUC_LjKsfOjCEONLa0M3Y0oy-mMXThexg2tJnGfZpDuxTdZA8hhHwKhrYp9vRm6s1AW299pmZwNAz0NtxGalwfhpDH9FD8bDA-xTyGHaLWWGs8nfOoWJcH7cbMD4hF7MImZiRuTAoOaUQMxUq0j853z8mT1nTZv7jfl-T68uLL-Ydi_en91fnZurC1AFk0DeOu5cK2HJ8HkvFGNsK3rRPMVYa1yonaVsoq5U5VAxioJWtKV3plEOZL8uZYF__-dfJ51H3I1nedGXycshZKCmy-_C-IIxKgsONL8voPcBunNOAndMlB1FwBn6mX99TU9N7pXQq9SXv9a2oIvDsC30Ln97_zoGd36K2eTaBnE8xXS31wh77Tlxcf8YByfpTHafcPcfGXGFWvjqrWRG02KWR9_bkExtFVggEA_wl_68j9</recordid><startdate>200812</startdate><enddate>200812</enddate><creator>Sato, Tadashi</creator><creator>Matsumoto, Kazumasa</creator><creator>Okumura, Takekazu</creator><creator>Yokoi, Wakae</creator><creator>Naito, Eiichiro</creator><creator>Yoshida, Yasuto</creator><creator>Nomoto, Koji</creator><creator>Ito, Masahiko</creator><creator>Sawada, Haruji</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><general>Oxford University Press</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>200812</creationdate><title>Isolation of lactate-utilizing butyrate-producing bacteria from human feces and in vivo administration of Anaerostipes caccae strain L2 and galacto-oligosaccharides in a rat model</title><author>Sato, Tadashi ; Matsumoto, Kazumasa ; Okumura, Takekazu ; Yokoi, Wakae ; Naito, Eiichiro ; Yoshida, Yasuto ; Nomoto, Koji ; Ito, Masahiko ; Sawada, Haruji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5608-bb13df36cf3fec0813b8b6effd61d4a1f9d65c49c99d79b01f9581b2d2e9a13b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acetic acid</topic><topic>Adult</topic><topic>Animals</topic><topic>Bacteria - classification</topic><topic>Bacteria - genetics</topic><topic>Bacteria - isolation & purification</topic><topic>Bacteria - metabolism</topic><topic>Bifidobacteria</topic><topic>butyrate</topic><topic>Butyrates - metabolism</topic><topic>Carbohydrates</topic><topic>Cecum</topic><topic>Cecum - metabolism</topic><topic>Cecum - microbiology</topic><topic>Colony Count, Microbial</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Ecology</topic><topic>Fatty Acids - metabolism</topic><topic>Feces</topic><topic>Feces - microbiology</topic><topic>Fermentation</topic><topic>Fermentation - drug effects</topic><topic>Galactooligosaccharides</topic><topic>galacto‐oligosaccharides</topic><topic>Gene sequencing</topic><topic>Hindgut</topic><topic>Humans</topic><topic>Ingestion</topic><topic>Intestines - metabolism</topic><topic>Intestines - microbiology</topic><topic>lactate</topic><topic>Lactic acid</topic><topic>Lactic Acid - metabolism</topic><topic>Male</topic><topic>Microbiology</topic><topic>Microorganisms</topic><topic>Models, Animal</topic><topic>Oligosaccharides</topic><topic>Oligosaccharides - administration & dosage</topic><topic>Probiotics</topic><topic>Propionic acid</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Rodents</topic><topic>rRNA 16S</topic><topic>Specific Pathogen-Free Organisms</topic><topic>Succinic Acid - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Tadashi</creatorcontrib><creatorcontrib>Matsumoto, Kazumasa</creatorcontrib><creatorcontrib>Okumura, Takekazu</creatorcontrib><creatorcontrib>Yokoi, Wakae</creatorcontrib><creatorcontrib>Naito, Eiichiro</creatorcontrib><creatorcontrib>Yoshida, Yasuto</creatorcontrib><creatorcontrib>Nomoto, Koji</creatorcontrib><creatorcontrib>Ito, Masahiko</creatorcontrib><creatorcontrib>Sawada, Haruji</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEMS microbiology ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Tadashi</au><au>Matsumoto, Kazumasa</au><au>Okumura, Takekazu</au><au>Yokoi, Wakae</au><au>Naito, Eiichiro</au><au>Yoshida, Yasuto</au><au>Nomoto, Koji</au><au>Ito, Masahiko</au><au>Sawada, Haruji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation of lactate-utilizing butyrate-producing bacteria from human feces and in vivo administration of Anaerostipes caccae strain L2 and galacto-oligosaccharides in a rat model</atitle><jtitle>FEMS microbiology ecology</jtitle><addtitle>FEMS Microbiol Ecol</addtitle><date>2008-12</date><risdate>2008</risdate><volume>66</volume><issue>3</issue><spage>528</spage><epage>536</epage><pages>528-536</pages><issn>0168-6496</issn><eissn>1574-6941</eissn><abstract>Lactate-utilizing butyrate-producers were isolated from human feces and identified based on the sequences of 16S rRNA gene. Anaerostipes caccae strain L2, one of the seven human fecal isolates, was administered to rats with galacto-oligosaccharides (GOS) as bifidogenic carbohydrates for stimulating lactate formation in the hindgut. Ingestion of GOS alone increased concentrations of cecal lactate and butyrate compared with control rats (P<0.05). Additional administration of strain L2 on GOS tended to enhance the promoting effect of GOS on cecal butyrate formation (P=0.06) and lowered the mean value of cecal lactate concentration (P=0.32). Consequently, cecal and fecal butyrate concentrations in rats administered with both strain L2 and GOS were significantly higher than those in the control rats (P<0.01 and P<0.05, respectively). Significant changes were observed in the other fermentation acids, such as succinate, acetate, and propionate, depending on the ingestion of strain L2. Administered strain L2 was retrieved from the cecal content of a rat based on randomly amplified polymorphic DNA analysis. The results suggest that synbiotic ingestion of lactate-utilizing butyrate-producers and GOS alters the microbial fermentation and promotes the formation of beneficial fermentation acids, including butyrate, in the gut.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>18554304</pmid><doi>10.1111/j.1574-6941.2008.00528.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetic acid Adult Animals Bacteria - classification Bacteria - genetics Bacteria - isolation & purification Bacteria - metabolism Bifidobacteria butyrate Butyrates - metabolism Carbohydrates Cecum Cecum - metabolism Cecum - microbiology Colony Count, Microbial Deoxyribonucleic acid DNA Ecology Fatty Acids - metabolism Feces Feces - microbiology Fermentation Fermentation - drug effects Galactooligosaccharides galacto‐oligosaccharides Gene sequencing Hindgut Humans Ingestion Intestines - metabolism Intestines - microbiology lactate Lactic acid Lactic Acid - metabolism Male Microbiology Microorganisms Models, Animal Oligosaccharides Oligosaccharides - administration & dosage Probiotics Propionic acid Rats Rats, Sprague-Dawley RNA, Ribosomal, 16S - genetics Rodents rRNA 16S Specific Pathogen-Free Organisms Succinic Acid - metabolism |
title | Isolation of lactate-utilizing butyrate-producing bacteria from human feces and in vivo administration of Anaerostipes caccae strain L2 and galacto-oligosaccharides in a rat model |
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