Spectroscopic Properties of Violaxanthin and Lutein Triplet States in LHCII are Independent of Carotenoid Composition
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
BB/E009743/1
Biotechnology and Biological Sciences Research Council - United Kingdom
PubMed
31599594
DOI
10.1021/acs.jpcb.9b06293
Knihovny.cz E-zdroje
- MeSH
- Arabidopsis genetika fyziologie MeSH
- chlorofyl a chemie metabolismus MeSH
- karotenoidy chemie metabolismus MeSH
- lutein chemie genetika metabolismus MeSH
- mutace MeSH
- proteiny huseníčku genetika metabolismus MeSH
- spektrální analýza metody MeSH
- světlosběrné proteinové komplexy chemie metabolismus MeSH
- vazebná místa MeSH
- xanthofyly chemie metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chlorofyl a MeSH
- karotenoidy MeSH
- lutein MeSH
- proteiny huseníčku MeSH
- světlosběrné proteinové komplexy MeSH
- violaxanthin MeSH Prohlížeč
- xanthofyly MeSH
Chlorophyll triplet excited states are byproducts of photosynthetic processes that can indirectly harm biological membranes by forming highly reactive oxygen species. A crucial photoprotective mechanism evolved by plants to counter this threat involves the triplet energy transfer from chlorophylls to carotenoid molecules, in which triplet states are not reactive. In the major light-harvesting complex of photosystem II (LHCII), the two central luteins play an important role in the mechanism, but it has been shown that carotenoid triplets are formed even when other carotenoids replace them in their binding sites. In this work, we have investigated carotenoid triplet formation in LHCII isolated from Arabidopsis thaliana npq1lut2 plants, in which violaxanthin replaces lutein. Although transient absorption spectroscopy showed altered singlet excited-state dynamics in the mutant LHCII without lutein, these antennae formed carotenoid triplets that were spectrally and dynamically identical to the wild-type protein. We conclude that lutein-binding sites in LHCII have conserved characteristics to ensure efficient triplet energy transfer to the carotenoid molecules that they accommodate, making the identity of the carotenoid trivial per se.
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