Analyzing carotenoids of snow algae by Raman microspectroscopy and high-performance liquid chromatography

0506195 - MBÚ 2020 RIV GB eng J - Článek v odborném periodiku
Osterrothova, K. - Culka, A. - Němečková, K. - Kaftan, David - Nedbalová, L. - Procházková, L. - Jehlička, J.
Analyzing carotenoids of snow algae by Raman microspectroscopy and high-performance liquid chromatography.
Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy. Roč. 212, APR 5 (2019), s. 262-271. ISSN 1386-1425. E-ISSN 1873-3557
Grant CEP: GA MŠMT(CZ) LO1416
Institucionální podpora: RVO:61388971
Klíčová slova: Snow algae * Raman spectroscopy * HPLC
Obor OECD: Analytical chemistry
Impakt faktor: 3.232, rok: 2019
Způsob publikování: Omezený přístup
https://www.sciencedirect.com/science/article/pii/S1386142519300137?via%3Dihub

We tested the potential of Raman microspectroscopy to determine carotenoid pigments - both primary (lutein, beta-carotene) and secondary (astaxanthin) carotenoids - in the different species and life-cycle stages of snow algae from the order Chlamydomonadales (Chlorophyta). We compared the performance of Raman spectrometry to a reference method of biological pigment analysis, high-performance liquid chromatography (HPLC). The three main carotenoid Raman bands of the astaxanthin-rich red cysts were located at 1520, 1156 and 1006 cm(-1). The shifts (orange aplanozygotes and green motile cells with flagella) in the position of the v(1) (C-C) Raman band of the polyenic chain is consistent with the expected changes in the ratios of the various carotenoid pigments. Flagellated green cells commonly contain lutein as a major carotenoid, together with minor amounts of beta-carotene and varying amounts of antheraxanthin, violaxanthin and neoxanthin. Aplanozygotes contain mixtures of both primary and secondary carotenoids. In most cases, the v(1)(C-C) band is an overlapping set of bands, which is due to the signal of all carotenoid pigments in the sample, and a deconvolution along with the band position shifts (mainly v(1)) could be used to characterize the mixture of carotenoids. However, the ability of Raman spectroscopy to discriminate between structurally slightly differing carotenoid pigments or several carotenoids in an admixture in an unknown biological system remains limited.
Trvalý link: http://hdl.handle.net/11104/0297484