ライフサイエンスコーパス: peridinin

1 and/or 19'-butanoyloxy-fucoxanthin but lacks peridinin.

2 tely stereocontrolled total synthesis of (-)-peridinin.

3 es possess plastids that contain the pigment peridinin and show extreme reduction and integration wit

4 of the absorption spectra has shown that the peridinins and Chls absorb at different wavelengths in t

5 yll (Chl) a molecules, whereas HSPCP has six peridinins and two Chl a molecules.

6 lorophyll (Chl) a, whereas the HSPCP has six peridinins and two Chl a, but both have very similar pig

7 strated previously that MFPCP contains eight peridinins and two chlorophyll (Chl) a molecules, wherea

8 The MFPCP contains eight peridinins and two chlorophyll (Chl) a, whereas the HSPC

9 ows significant support for the monophyly of peridinin- and fucoxanthin-containing dinoflagellates as

10 e analyses, we postulate that the plastid of peridinin- and fucoxanthin-containing dinoflagellates or

11 n plastid trees that contain genes from both peridinin- and fucoxanthin-containing dinoflagellates.

12 rbonyl group and non-hydrogen side groups of peridinin are instrumental in achieving the respective c

13 ellate plastid contains chlorophyll c(2) and peridinin as the major carotenoid.

14 ified subunits, PsaT and PsaU, as well as 13 peridinin-Chl a/c-binding light-harvesting antenna prote

15 two intergene spacer regions of lcf and the peridinin chlorophyll protein gene, pcp; a novel 13 nt s

16 The main-form (MFPCP) and high-salt (HSPCP) peridinin-chlorophyll a proteins from the dinoflagellate

17 rae: main-form (MFPCP) and high-salt (HSPCP) peridinin-chlorophyll a-proteins.

18 Peridinin-chlorophyll-protein (PCP) is a unique light-ha

19 phyte tertiary endosymbiosis in an ancestral peridinin-containing dinoflagellate.

20 hloroplasts of Amphidinium carterae, a model peridinin-containing dinoflagellate.

21 e-Fe(II) dioxygenase (2OGD) domains found in peridinin-containing dinoflagellates; other chlorophyll

22 2 ps) pathways for energy transfer from the peridinin excited singlet states to Chl.

23 c and fucoxanthin in chromophytes, Chl c and peridinin in dinophytes, and zeaxanthin in rhodophytes.

24 overlap, and the presence of two additional peridinins in MFPCP that act as polarizable units enhanc

25 ntramolecular charge transfer (ICT) state of peridinin is an evolved state formed via excited-state b

26 Triplet excitation transfer to peridinins, mediated by electron exchange, is found to e

27 Peridinin-pigmented dinoflagellates contain secondary pl

28 adapted pathways retained from the ancestral peridinin plastid symbiosis for transcript processing in

29 ing the individual 10 K spectra of Chl a and peridinin recorded in 2-MTHF.

30 t absorption the optically allowed states of peridinins share their electronic excitation in excitoni

31 ve stereogenic allene-containing core of (-)-peridinin, the first stereocontrolled coupling of haloal

32 xcitation spectroscopy has revealed that the peridinin-to-Chl a energy transfer efficiency is high (>