2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
2. ENVIRONMENTAL ChEMISTRy & TEChNOLOGy 2.1. Lectures
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Chem. Listy, 102, s265–s1311 (2008) Environmental Chemistry & Technology<br />
Fig. <strong>2.</strong> hPLC chromatograms of carotenoids from the Mougeotia<br />
sp. samples: a – control sample; b – illumination with<br />
4,500 μmol m –2 s –1 ; c – recovery after illumination. Peak identities<br />
are: 1: violaxanthin, 2: antheraxanthin, 3: lutein, 4: zeaxanthin,<br />
5: 5,6-epoxy-β-carotene, 6: α-carotene, 7: β-carotene, 8: 9Z<br />
– β-carotene, 9: 15Z – β-carotene<br />
a<br />
b<br />
c<br />
s440<br />
Conclusions<br />
The obtained data reveals the way in which the carotenoid<br />
pattern is affected by high light stress in the analyzed<br />
algal strain, as well as the way this reacts during the recovery<br />
stage.<br />
They proved that the xanthophyll cycle’s regulatory<br />
mechanism is functional in Mougeotia sp. algae, leading to<br />
an almost complete interconversion of violaxanthin to antheraxanthin<br />
and zeaxanthin. However, its contribution to nonphotochemical<br />
quenching is not as significant as in higher<br />
plants; the small amounts of zeaxanthin recorded during<br />
experiments suggesting that this strain posses another dissipation<br />
mechanism(s) which operates together with xanthophyll<br />
cycle.<br />
Hence, HPLC analysis revealed a particular behavior of<br />
Mougeotia spp. algae under intense illumination: the major<br />
de-epoxidation product of violaxanthin is not zeaxanthin, but<br />
antheraxanthin. More than that, the high light stress affects<br />
the whole carotenoid biosynthesis, starting with the violaxanthin<br />
cycle’s precursor: β-carotene.<br />
This work has been supported by 2-CEx06-11-54/ 2006<br />
research grant.<br />
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