TY - JOUR
T1 - Effects of excess light energy on excitation-energy dynamics in a pennate diatom Phaeodactylum tricornutum
AU - Nagao, Ryo
AU - Ueno, Yoshifumi
AU - Yokono, Makio
AU - Shen, Jian Ren
AU - Akimoto, Seiji
N1 - Funding Information:
Acknowledgements This work was supported by the Grants-in-Aid for Scientific Research from Japan Society for the Promotion of Science JP17K07442 (to R. N.), JP17H06433 (to J.-R. S.), and JP16H06553 (to S. A.).
Funding Information:
This work was supported by the Grants-in-Aid for Scientific Research from Japan Society for the Promotion of Science JP17K07442 (to R. N.), JP17H06433 (to J.-R. S.), and JP16H06553 (to S. A.).
Publisher Copyright:
© 2019, Springer Nature B.V.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Controlling excitation energy flow is a fundamental ability of photosynthetic organisms to keep a better performance of photosynthesis. Among the organisms, diatoms have unique light-harvesting complexes, fucoxanthin chlorophyll (Chl) a/c-binding proteins. We have recently investigated light-adaptation mechanisms of a marine centric diatom, Chaetoceros gracilis, by spectroscopic techniques. However, it remains unclear how pennate diatoms regulate excitation energy under different growth light conditions. Here, we studied light-adaptation mechanisms in a marine pennate diatom Phaeodactylum tricornutum grown at 30 µmol photons m−2 s−1 and further incubated for 24 h either in the dark, or at 30 or 300 µmol photons m−2 s−1 light intensity, by time-resolved fluorescence (TRF) spectroscopy. The high-light incubated cells showed no detectable oxygen-evolving activity of photosystem II, indicating the occurrence of a severe photodamage. The photodamaged cells showed alterations of steady-state absorption and fluorescence spectra and TRF spectra compared with the dark and low-light adapted cells. In particular, excitation-energy quenching is significantly accelerated in the photodamaged cells as shown by mean lifetime analysis of the Chl fluorescence. These spectral changes by the high-light treatment may result from arrangements of pigment–protein complexes to maintain the photosynthetic performance under excess light illumination. These growth-light dependent spectral properties in P. tricornutum are largely different from those in C. gracilis, thus providing insights into the different light-adaptation mechanisms between the pennate and centric diatoms.
AB - Controlling excitation energy flow is a fundamental ability of photosynthetic organisms to keep a better performance of photosynthesis. Among the organisms, diatoms have unique light-harvesting complexes, fucoxanthin chlorophyll (Chl) a/c-binding proteins. We have recently investigated light-adaptation mechanisms of a marine centric diatom, Chaetoceros gracilis, by spectroscopic techniques. However, it remains unclear how pennate diatoms regulate excitation energy under different growth light conditions. Here, we studied light-adaptation mechanisms in a marine pennate diatom Phaeodactylum tricornutum grown at 30 µmol photons m−2 s−1 and further incubated for 24 h either in the dark, or at 30 or 300 µmol photons m−2 s−1 light intensity, by time-resolved fluorescence (TRF) spectroscopy. The high-light incubated cells showed no detectable oxygen-evolving activity of photosystem II, indicating the occurrence of a severe photodamage. The photodamaged cells showed alterations of steady-state absorption and fluorescence spectra and TRF spectra compared with the dark and low-light adapted cells. In particular, excitation-energy quenching is significantly accelerated in the photodamaged cells as shown by mean lifetime analysis of the Chl fluorescence. These spectral changes by the high-light treatment may result from arrangements of pigment–protein complexes to maintain the photosynthetic performance under excess light illumination. These growth-light dependent spectral properties in P. tricornutum are largely different from those in C. gracilis, thus providing insights into the different light-adaptation mechanisms between the pennate and centric diatoms.
KW - FCP
KW - Low-energy Chl
KW - Pennate diatom
KW - Photoinhibition
KW - Time-resolved fluorescence spectroscopy
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U2 - 10.1007/s11120-019-00639-4
DO - 10.1007/s11120-019-00639-4
M3 - Article
C2 - 30993504
AN - SCOPUS:85064536496
SN - 0166-8595
VL - 141
SP - 355
EP - 365
JO - Photosynthesis Research
JF - Photosynthesis Research
IS - 3
ER -