2020
DOI: 10.1039/d0ra05326k
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Metabolic characterisation ofMagnetospirillum gryphiswaldenseMSR-1 using LC-MS-based metabolite profiling

Abstract: Metabolic pathways in Magnetospirillum gryphiswaldense MSR-1 are significantly altered under microaerobic (O2-limited) growth conditions enabling magnetosome formation.

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Cited by 52 publications
(28 citation statements)
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“…Extraction was then performed by four freeze/thaw cycles (flash frozen in liquid nitrogen for 1 min, thawed on ice and vortexed for 30 s). Samples were then centrifuged at 17,000 rpm at 4°C for 10 min, transferred to pre-cooled tubes and stored at -80°C until LC-MS analysis [14].…”
Section: Metabolite Extractionmentioning
confidence: 99%
See 1 more Smart Citation
“…Extraction was then performed by four freeze/thaw cycles (flash frozen in liquid nitrogen for 1 min, thawed on ice and vortexed for 30 s). Samples were then centrifuged at 17,000 rpm at 4°C for 10 min, transferred to pre-cooled tubes and stored at -80°C until LC-MS analysis [14].…”
Section: Metabolite Extractionmentioning
confidence: 99%
“…Global metabolite profiling offers a comprehensive measurement of small biomolecules produced in living cells, excreted metabolites from the cells into their microenvironment and taken up by the cells from a culture medium [13,14]. Especially, liquid chromatographymass spectrometry (LC-MS)-based metabolomics is a powerful analytical tool allowing the monitoring of alterations in cell metabolism and producing a rapid snapshot of the comprehensive physiological status of the cells.…”
Section: Introductionmentioning
confidence: 99%
“…Metabolite quantification and identification were performed by PANOMIX (Chengdu, China). Metabolites were identified using the public HMDB [ 42 ], massbank [ 43 ], LipidMaps [ 44 ], mzcloud [ 45 ], and KEGG [ 46 ] databases and the self-built database of BioNovoGene (Chengdu, Sichuan, China) ( , v1.0.0.2, accessed on 25 August 2022), with the following parameters: retention time, ppm (<30 ppm), and fragmentation model. Differentially accumulated metabolites (DAMs) were screened under the following filtering conditions: variable importance in projection (VIP) ≥ 1 and absolute log2 (fold change (FC)) ≥ 1 ( p ≤ 0.05).…”
Section: Methodsmentioning
confidence: 99%
“…The metabolites were identified by accuracy mass (< 30 ppm) and MS/MS data which were matched with HMDB (Wishart et al, 2007) (http://www.hmdb. ca), massbank (Horai et al, 2010) (http://www.massbank.jp/), LipidMaps (Sud et al, 2007) (http://www.lipidmaps.org), mzclound (Abdelrazig et al, 2020) (https://www.mzcloud.org) and KEGG (Ogata et al, 1999) (http://www.genome.jp/kegg/). The robust LOESS signal correction (QC-RLSC) (Gagnebin et al, 2017) was applied for data normalization to correct for any systematic bias.…”
Section: Metabolomic Analysismentioning
confidence: 99%