Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing

Eikmeyer FG, Heinl S, Marx H, Pühler A, Grabherr R, Schlüter A (2015)
PLoS ONE 10(7): e0134149.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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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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PLoS ONE
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10
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7
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e0134149
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Article Processing Charge funded by the Deutsche Forschungsgemeinschaft and the Open Access Publication Fund of Bielefeld University.
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Eikmeyer FG, Heinl S, Marx H, Pühler A, Grabherr R, Schlüter A. Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing. PLoS ONE. 2015;10(7): e0134149.
Eikmeyer, F. G., Heinl, S., Marx, H., Pühler, A., Grabherr, R., & Schlüter, A. (2015). Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing. PLoS ONE, 10(7), e0134149. doi:10.1371/journal.pone.0134149
Eikmeyer, F. G., Heinl, S., Marx, H., Pühler, A., Grabherr, R., and Schlüter, A. (2015). Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing. PLoS ONE 10:e0134149.
Eikmeyer, F.G., et al., 2015. Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing. PLoS ONE, 10(7): e0134149.
F.G. Eikmeyer, et al., “Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing”, PLoS ONE, vol. 10, 2015, : e0134149.
Eikmeyer, F.G., Heinl, S., Marx, H., Pühler, A., Grabherr, R., Schlüter, A.: Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing. PLoS ONE. 10, : e0134149 (2015).
Eikmeyer, Felix Gregor, Heinl, Stefan, Marx, Hans, Pühler, Alfred, Grabherr, Reingard, and Schlüter, Andreas. “Identification of Oxygen-Responsive Transcripts in the Silage Inoculant Lactobacillus buchneri CD034 by RNA Sequencing”. PLoS ONE 10.7 (2015): e0134149.
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2016-11-22T11:34:10Z

5 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Lipoteichoic acid mediates binding of a Lactobacillus S-layer protein.
Bönisch E, Oh YJ, Anzengruber J, Hager FF, López-Guzmán A, Zayni S, Hinterdorfer P, Kosma P, Messner P, Duda KA, Schäffer C., Glycobiology 28(3), 2018
PMID: 29309573
A long and abundant non-coding RNA in Lactobacillus salivarius.
Cousin FJ, Lynch DB, Chuat V, Bourin MJB, Casey PG, Dalmasso M, Harris HMB, McCann A, O'Toole PW., Microb Genom 3(9), 2017
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