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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
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
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
14 two intergene spacer regions of lcf and the peridinin chlorophyll protein gene, pcp; a novel 13 nt s
15 The main-form (MFPCP) and high-salt (HSPCP) peridinin-chlorophyll a proteins from the dinoflagellate
21 c and fucoxanthin in chromophytes, Chl c and peridinin in dinophytes, and zeaxanthin in rhodophytes.
22 overlap, and the presence of two additional peridinins in MFPCP that act as polarizable units enhanc
23 ntramolecular charge transfer (ICT) state of peridinin is an evolved state formed via excited-state b
26 adapted pathways retained from the ancestral peridinin plastid symbiosis for transcript processing in
28 t absorption the optically allowed states of peridinins share their electronic excitation in excitoni
29 ve stereogenic allene-containing core of (-)-peridinin, the first stereocontrolled coupling of haloal
30 xcitation spectroscopy has revealed that the peridinin-to-Chl a energy transfer efficiency is high (>
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