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Sökning: id:"swepub:oai:research.chalmers.se:28e08c0f-db43-42c6-aa90-632b29d952df" > Expanded metabolite...

Expanded metabolite coverage of Saccharomyces cerevisiae extract through improved chloroform/methanol extraction and tert-butyldimethylsilyl derivatization

Khoomrung, Sakda, 1978 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Martinez Ruiz, Jose Luis, 1981 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Tippmann, Stefan, 1986 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
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Jansa-Ard, Suwanee, 1980 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Buffing, Marieke, 1986 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Nicastro, Raffaele (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Nielsen, Jens B, 1962 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
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 (creator_code:org_t)
Elsevier BV, 2015
2015
Engelska.
Ingår i: Analytical Chemistry Research. - : Elsevier BV. - 2214-1812. ; 6, s. 9-16
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • We present an improved extraction and derivatization protocol for GC-MS analysis of amino/non-amino acids in Saccharomyces cerevisiae. Yeast cells were extracted with chloroform: aqueous-methanol (1:1, v/v) and the resulting non-polar and polar extracts combined and dried for derivatization. Polar and non-polar metabolites were derivatized using tert-butyldimethylsilyl (t-BDMS) dissolved in acetonitrile. Using microwave treatment of the samples, the derivatization process could be completed within 2 h (from >20 h of the conventional method), providing fully derivatized metabolites that contain multiple derivatizable organic functional groups. This results in a single derivative from one metabolite, leading to increased accuracy and precision for identification and quantification of the method. Analysis of combined fractions allowed the method to expand the coverage of detected metabolites from polar metabolites i.e. amino acids, organic acids and non-polar metabolites i.e. fatty alcohols and long-chain fatty acids which are normally non detectable. The recoveries of the extraction method was found at 88 ± 4%, RSD, N = 3 using anthranilic acid as an internal standard. The method promises to be a very useful tool in various aspects of biotechnological applications i.e. development of cell factories, metabolomics profiling, metabolite identification, 13C-labeled flux analysis or semi-quantitative analysis of metabolites in yeast samples.

Ämnesord

NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)

Nyckelord

Metabolomics
Extraction
Derivatization
Saccharomyces cerevisiae

Publikations- och innehållstyp

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