High-resolution magic angle spinning 1H NMR analysis of whole cells of Thalassiosira pseudonana (Bacillariophyceae):: Broad range analysis of metabolic composition and nutritional value

被引:1
作者
Chauton, MS [1 ]
Storseth, TR
Johnsen, G
机构
[1] Norwegian Univ Sci & Technol, Trondhjem Biol Stn, N-7491 Trondheim, Norway
[2] Sintef Fisheries & Aquaculture, N-7465 Trondheim, Norway
关键词
Thalassiosira pseudonana; chemical composition; metabolic profiling; H-1; NMR; HR MAS H-1 NMR; lipophilic extract; hydrophilic extract; whole cells;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chemical composition of the microalga Thalassiosira pseudonana Hasle & Heimdal was studied with different proton nuclear magnetic resonance (H-1 NMR) techniques, and by comparing NMR spectra from extraction samples with a spectrum from a sample of whole cells we show that high-resolution magic angle spinning (HR MAS) H-1 NMR can be used for broad range analysis of metabolic composition in microalgal whole cells. Signals from important metabolites such as polyunsaturated fatty acids (PUFAs) eicosapentaenoic (EPA) and docosahexaenoic (DHA) acids were seen in a H-1 NMR spectrum of lipophilic extract, and possibly also signals from the carotenoid fucoxanthin. In a spectrum of hydrophilic extract we assigned signals to amino acids such as glutamine (Gln) and glutamic acid (Glu), carbohydrate and ATP. These findings were compared to a spectrum of HR MAS H-1 NMR analysis of whole cells, where it was possible to find signals coincident with the different metabolites seen in spectra of the extraction samples. Since the position of resonance peaks in a NMR spectrum depends on the chemical surroundings of each atom at the time of analysis some peak shift differences between extract and whole cell sample spectra may occur, but signal shifts were not significantly different between the analyses here. In addition, application of HR MAS highly increased spectral resolution in the complex whole cell sample. We therefore suggest that HR MAS H-1 NMR analysis is a suitable analysis tool to study metabolic composition directly on whole cells of microalgae, making it possible to study a broad range of metabolites simultaneously without tedious extraction procedures.
引用
收藏
页码:533 / 542
页数:10
相关论文
共 33 条
[1]   MAGIC ANGLE SPINNING IN SOLID-STATE NMR-SPECTROSCOPY [J].
ANDREW, ER .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 1981, 299 (1452) :505-520
[2]   Solution structure of nodularin - An inhibitor of serine/threonine-specific protein phosphatases [J].
Annila, A ;
Lehtimaki, J ;
Mattila, K ;
Eriksson, JE ;
Sivonen, K ;
Rantala, TT ;
Drakenberg, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16695-16702
[3]  
[Anonymous], 1995, CAROTENOIDS
[4]   Gyroxanthin - the first allenic acetylenic carotenoid [J].
Bjornland, T ;
Fiksdahl, A ;
Skjetne, T ;
Krane, J ;
Liaaen-Jensen, S .
TETRAHEDRON, 2000, 56 (46) :9047-9056
[5]   In-situ identification of major metabolites in the red alga Gracilariopsis lemaneiformis using high-resolution magic angle spinning nuclear magnetic resonance spectroscopy [J].
Broberg, A ;
Kenne, L ;
Pedersén, M .
PLANTA, 1998, 206 (02) :300-307
[6]   Use of high-resolution magic angle spinning nuclear magnetic resonance spectroscopy for in situ studies of low-molecular-mass compounds in red algae [J].
Broberg, A ;
Kenne, L .
ANALYTICAL BIOCHEMISTRY, 2000, 284 (02) :367-374
[7]   THE AMINO-ACID AND SUGAR COMPOSITION OF 16 SPECIES OF MICROALGAE USED IN MARICULTURE [J].
BROWN, MR .
JOURNAL OF EXPERIMENTAL MARINE BIOLOGY AND ECOLOGY, 1991, 145 (01) :79-99
[8]   Effects of harvest stage and light on the biochemical composition of the diatom Thalassiosira pseudonana [J].
Brown, MR ;
Dunstan, GA ;
Norwood, SJ ;
Miller, KA .
JOURNAL OF PHYCOLOGY, 1996, 32 (01) :64-73
[9]   HR MAS 1H NMR spectroscopy analysis of marine microalgal whole cells [J].
Chauton, MS ;
Optun, OI ;
Bathen, TF ;
Volent, Z ;
Gribbestad, IS ;
Johnsen, G .
MARINE ECOLOGY PROGRESS SERIES, 2003, 256 :57-62
[10]  
Claridge T. D. W., 2008, HIGH RESOLUTION NMR