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Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing
The Lactobacillus buchneri CD034 strain, known to improve the ensiling process of green fodder and the quality of the silage itself was transcriptionally analyzed by sequencing of transcriptomes isolated under anaerobic vs. aerobic conditions. L. buchneri CD034 was first cultivated under anaerobic c...
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Published in: | PloS one 2015-07, Vol.10 (7), p.e0134149-e0134149 |
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description | The Lactobacillus buchneri CD034 strain, known to improve the ensiling process of green fodder and the quality of the silage itself was transcriptionally analyzed by sequencing of transcriptomes isolated under anaerobic vs. aerobic conditions. L. buchneri CD034 was first cultivated under anaerobic conditions and then shifted to aerobic conditions by aeration with 21% oxygen. Cultivations already showed that oxygen was consumed by L. buchneri CD034 after aeration of the culture while growth of L. buchneri CD034 was still observed. RNA sequencing data revealed that irrespective of the oxygen status of the culture, the most abundantly transcribed genes are required for basic cell functions such as protein biosynthesis, energy metabolism and lactic acid fermentation. Under aerobic conditions, 283 genes were found to be transcriptionally up-regulated while 198 genes were found to be down-regulated (p-value < 0.01). Up-regulated genes i. a. play a role in oxygen consumption via oxidation of pyruvate or lactate (pox, lctO). Additionally, genes encoding proteins required for decomposition of reactive oxygen species (ROS) such as glutathione reductase or NADH peroxidase were also found to be up-regulated. Genes related to pH homeostasis and redox potential balance were found to be down-regulated under aerobic conditions. Overall, genes required for lactic acid fermentation were hardly affected by the growth conditions applied. Genes identified to be differentially transcribed depending on the aeration status of the culture are suggested to specify the favorable performance of the strain in silage formation. |
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L. buchneri CD034 was first cultivated under anaerobic conditions and then shifted to aerobic conditions by aeration with 21% oxygen. Cultivations already showed that oxygen was consumed by L. buchneri CD034 after aeration of the culture while growth of L. buchneri CD034 was still observed. RNA sequencing data revealed that irrespective of the oxygen status of the culture, the most abundantly transcribed genes are required for basic cell functions such as protein biosynthesis, energy metabolism and lactic acid fermentation. Under aerobic conditions, 283 genes were found to be transcriptionally up-regulated while 198 genes were found to be down-regulated (p-value < 0.01). Up-regulated genes i. a. play a role in oxygen consumption via oxidation of pyruvate or lactate (pox, lctO). Additionally, genes encoding proteins required for decomposition of reactive oxygen species (ROS) such as glutathione reductase or NADH peroxidase were also found to be up-regulated. Genes related to pH homeostasis and redox potential balance were found to be down-regulated under aerobic conditions. Overall, genes required for lactic acid fermentation were hardly affected by the growth conditions applied. Genes identified to be differentially transcribed depending on the aeration status of the culture are suggested to specify the favorable performance of the strain in silage formation.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0134149</identifier><identifier>PMID: 26230316</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Aeration ; Aerobic conditions ; Anaerobic conditions ; Analysis ; Bacteria ; Biology ; Biosynthesis ; Biotechnology ; Carbohydrates ; Cell culture ; Decomposition reactions ; Down-Regulation ; Energy metabolism ; Fermentation ; Fodder ; Gene expression ; Gene sequencing ; Genes ; Genes, Bacterial ; Genomes ; Glutathione ; Glutathione reductase ; Growth conditions ; Homeostasis ; Laboratories ; Lactic acid ; Lactobacillus ; Lactobacillus - genetics ; Lactobacillus - growth & development ; Life sciences ; Metabolism ; Microorganisms ; NADH ; NADH peroxidase ; Natural resources ; Nicotinamide adenine dinucleotide ; Oxidation ; Oxygen ; Oxygen - metabolism ; Oxygen consumption ; Peroxidase ; pH effects ; Physiological aspects ; Probiotics ; Protein biosynthesis ; Protein synthesis ; Protein turnover ; Proteins ; Proteomics ; Reactive oxygen species ; Redox potential ; Ribonucleic acid ; RNA ; RNA, Bacterial - genetics ; RNA, Bacterial - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Sequence Analysis, RNA ; Silage ; Transcription ; Transcriptome ; Up-Regulation</subject><ispartof>PloS one, 2015-07, Vol.10 (7), p.e0134149-e0134149</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Eikmeyer et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Eikmeyer et al 2015 Eikmeyer et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-633a0c613efc07675c8bd96af7950d79e7495126833b9575ffe1c6f21cc6fdde3</citedby><cites>FETCH-LOGICAL-c692t-633a0c613efc07675c8bd96af7950d79e7495126833b9575ffe1c6f21cc6fdde3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1700480543/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1700480543?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26230316$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>LaPointe, Gisèle</contributor><creatorcontrib>Eikmeyer, Felix Gregor</creatorcontrib><creatorcontrib>Heinl, Stefan</creatorcontrib><creatorcontrib>Marx, Hans</creatorcontrib><creatorcontrib>Pühler, Alfred</creatorcontrib><creatorcontrib>Grabherr, Reingard</creatorcontrib><creatorcontrib>Schlüter, Andreas</creatorcontrib><title>Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The Lactobacillus buchneri CD034 strain, known to improve the ensiling process of green fodder and the quality of the silage itself was transcriptionally analyzed by sequencing of transcriptomes isolated under anaerobic vs. aerobic conditions. L. buchneri CD034 was first cultivated under anaerobic conditions and then shifted to aerobic conditions by aeration with 21% oxygen. Cultivations already showed that oxygen was consumed by L. buchneri CD034 after aeration of the culture while growth of L. buchneri CD034 was still observed. RNA sequencing data revealed that irrespective of the oxygen status of the culture, the most abundantly transcribed genes are required for basic cell functions such as protein biosynthesis, energy metabolism and lactic acid fermentation. Under aerobic conditions, 283 genes were found to be transcriptionally up-regulated while 198 genes were found to be down-regulated (p-value < 0.01). Up-regulated genes i. a. play a role in oxygen consumption via oxidation of pyruvate or lactate (pox, lctO). Additionally, genes encoding proteins required for decomposition of reactive oxygen species (ROS) such as glutathione reductase or NADH peroxidase were also found to be up-regulated. Genes related to pH homeostasis and redox potential balance were found to be down-regulated under aerobic conditions. Overall, genes required for lactic acid fermentation were hardly affected by the growth conditions applied. Genes identified to be differentially transcribed depending on the aeration status of the culture are suggested to specify the favorable performance of the strain in silage formation.</description><subject>Acids</subject><subject>Aeration</subject><subject>Aerobic conditions</subject><subject>Anaerobic conditions</subject><subject>Analysis</subject><subject>Bacteria</subject><subject>Biology</subject><subject>Biosynthesis</subject><subject>Biotechnology</subject><subject>Carbohydrates</subject><subject>Cell culture</subject><subject>Decomposition reactions</subject><subject>Down-Regulation</subject><subject>Energy metabolism</subject><subject>Fermentation</subject><subject>Fodder</subject><subject>Gene expression</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Genes, Bacterial</subject><subject>Genomes</subject><subject>Glutathione</subject><subject>Glutathione reductase</subject><subject>Growth conditions</subject><subject>Homeostasis</subject><subject>Laboratories</subject><subject>Lactic acid</subject><subject>Lactobacillus</subject><subject>Lactobacillus - 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metabolism</subject><subject>Sequence Analysis, RNA</subject><subject>Silage</subject><subject>Transcription</subject><subject>Transcriptome</subject><subject>Up-Regulation</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12LGyEUhofS0t1u-w9KKxRKe5HUjxmduSmE9CuwNJBseyuOoxPDRFN1wubf12xml6TsRRFU9Dnv0VdPlr1GcIwIQ5_WrvdWdOOts2oMEclRXj3JLlFF8IhiSJ6ezC-yFyGsISxISenz7AJTTCBB9DLbzRplo9FGimicBU6D-e2-VXa0UCFJB7NT4MYLG6Q32xiAsSCuFFiaTrQKzKyTfSdsBNdCRlcLabquD6Du5coqb8D0CyQ5qPdg8XMClupPr6w0tn2ZPdOiC-rVMF5lv759vZn-GF3Pv8-mk-uRpBWOI0qIgJIiorSEjLJClnVTUaFZVcCGVYrlVYEwLQmpq4IVWiskqcZIpr5pFLnK3h51t50LfLAscMQgzEtY5CQRsyPROLHmW282wu-5E4bfLTjfcuGjkZ3ikkja4FxRrOu8aUohGGSyZrKSBGKaJ63PQ7a-3qhGJme96M5Ez3esWfHW7XheYMSKw2E-DALeJatC5BsTpOqSw8r1d-dGZYUKTBP67h_08dsNVCvSBYzVLuWVB1E-yTFhtExyiRo_QqXWqI2R6X9pk9bPAj6eBSQmqtvYij4EPlsu_p-d_z5n35-wKyW6uAqu6w9fM5yD-RGU3oXglX4wGUF-KI97N_ihPPhQHinszekDPQTd1wP5C6-hCsA</recordid><startdate>20150731</startdate><enddate>20150731</enddate><creator>Eikmeyer, Felix Gregor</creator><creator>Heinl, Stefan</creator><creator>Marx, Hans</creator><creator>Pühler, Alfred</creator><creator>Grabherr, Reingard</creator><creator>Schlüter, Andreas</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150731</creationdate><title>Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing</title><author>Eikmeyer, Felix Gregor ; Heinl, Stefan ; Marx, Hans ; Pühler, Alfred ; Grabherr, Reingard ; Schlüter, Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-633a0c613efc07675c8bd96af7950d79e7495126833b9575ffe1c6f21cc6fdde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acids</topic><topic>Aeration</topic><topic>Aerobic conditions</topic><topic>Anaerobic conditions</topic><topic>Analysis</topic><topic>Bacteria</topic><topic>Biology</topic><topic>Biosynthesis</topic><topic>Biotechnology</topic><topic>Carbohydrates</topic><topic>Cell culture</topic><topic>Decomposition reactions</topic><topic>Down-Regulation</topic><topic>Energy metabolism</topic><topic>Fermentation</topic><topic>Fodder</topic><topic>Gene expression</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Genes, Bacterial</topic><topic>Genomes</topic><topic>Glutathione</topic><topic>Glutathione reductase</topic><topic>Growth conditions</topic><topic>Homeostasis</topic><topic>Laboratories</topic><topic>Lactic acid</topic><topic>Lactobacillus</topic><topic>Lactobacillus - 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L. buchneri CD034 was first cultivated under anaerobic conditions and then shifted to aerobic conditions by aeration with 21% oxygen. Cultivations already showed that oxygen was consumed by L. buchneri CD034 after aeration of the culture while growth of L. buchneri CD034 was still observed. RNA sequencing data revealed that irrespective of the oxygen status of the culture, the most abundantly transcribed genes are required for basic cell functions such as protein biosynthesis, energy metabolism and lactic acid fermentation. Under aerobic conditions, 283 genes were found to be transcriptionally up-regulated while 198 genes were found to be down-regulated (p-value < 0.01). Up-regulated genes i. a. play a role in oxygen consumption via oxidation of pyruvate or lactate (pox, lctO). Additionally, genes encoding proteins required for decomposition of reactive oxygen species (ROS) such as glutathione reductase or NADH peroxidase were also found to be up-regulated. Genes related to pH homeostasis and redox potential balance were found to be down-regulated under aerobic conditions. Overall, genes required for lactic acid fermentation were hardly affected by the growth conditions applied. Genes identified to be differentially transcribed depending on the aeration status of the culture are suggested to specify the favorable performance of the strain in silage formation.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26230316</pmid><doi>10.1371/journal.pone.0134149</doi><oa>free_for_read</oa></addata></record> |
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subjects | Acids Aeration Aerobic conditions Anaerobic conditions Analysis Bacteria Biology Biosynthesis Biotechnology Carbohydrates Cell culture Decomposition reactions Down-Regulation Energy metabolism Fermentation Fodder Gene expression Gene sequencing Genes Genes, Bacterial Genomes Glutathione Glutathione reductase Growth conditions Homeostasis Laboratories Lactic acid Lactobacillus Lactobacillus - genetics Lactobacillus - growth & development Life sciences Metabolism Microorganisms NADH NADH peroxidase Natural resources Nicotinamide adenine dinucleotide Oxidation Oxygen Oxygen - metabolism Oxygen consumption Peroxidase pH effects Physiological aspects Probiotics Protein biosynthesis Protein synthesis Protein turnover Proteins Proteomics Reactive oxygen species Redox potential Ribonucleic acid RNA RNA, Bacterial - genetics RNA, Bacterial - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Sequence Analysis, RNA Silage Transcription Transcriptome Up-Regulation |
title | Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing |
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