β-Carotene Probes the Energy Transfer Pathway in the Photosystem II Core Complex

2019 ◽  
Vol 10 (13) ◽  
pp. 3710-3714 ◽  
Author(s):  
Yusuke Yoneda ◽  
Yutaka Nagasawa ◽  
Yasufumi Umena ◽  
Hiroshi Miyasaka
1988 ◽  
Vol 43 (3-4) ◽  
pp. 226-230 ◽  
Author(s):  
S. S. Brody

When the sub-core complex of photosystem II, D1/D2, is irradiated at 436 or 415 nm (absorption by chlorophyll and pheophytin and β-carotene) or 540 nm (absorption primarily by pheophytin), the low temperature fluorescence spectrum has two maxima, at 685 and 674 nm. This shows the existence of at least two different fluorescent forms of chlorophyll (chlorophyll a and perhaps pheophytin a). When carotene is irradiated at 485 nm (absorption primarily by β-carotene), only fluorescence at 685 nm is observed: this indicates that carotene is transferring energy to only the long-wavelength form of chlorophyll in the D1/D2 sub-core complex. The band of carotene (at 485 nm) does not appear in the fluorescence excitation spectrum, measured at 674 nm. The position of the carotene molecule relative to each of the fluorescent forms of chlorophyll was determined from the excitation spectra of each of the fluorescence bands.


2003 ◽  
Vol 107 (25) ◽  
pp. 6214-6220 ◽  
Author(s):  
Frank L. de Weerd ◽  
Jan P. Dekker ◽  
Rienk van Grondelle

2017 ◽  
Vol 19 (23) ◽  
pp. 15356-15367 ◽  
Author(s):  
Jie Pan ◽  
Andrius Gelzinis ◽  
Vladimir Chorošajev ◽  
Mikas Vengris ◽  
S. Seckin Senlik ◽  
...  

Two-dimensional electronic spectroscopy of the photosystem II core complex reveals rapid energy transfer that can be explained through excitonic-polaron formation.


2019 ◽  
Vol 216 ◽  
pp. 94-115 ◽  
Author(s):  
Shou-Ting Hsieh ◽  
Lu Zhang ◽  
De-Wei Ye ◽  
Xuhui Huang ◽  
Yuan-Chung Cheng

Coarse-grained model for dimeric PSII core complex reveals robust light harvesting through inter-monomer energy transfer and pooling in CP47s.


2007 ◽  
Vol 93 (8) ◽  
pp. 2732-2742 ◽  
Author(s):  
N.P. Pawlowicz ◽  
M.-L. Groot ◽  
I.H.M. van Stokkum ◽  
J. Breton ◽  
R. van Grondelle

2019 ◽  
Author(s):  
Randolph Escobar ◽  
Jeffrey Johannes

<div>While carbon-heteroatom cross coupling reactions have been extensively studied, many methods are specific and</div><div>limited to a set of substrates or functional groups. Reported here is a method that allows for C-O, C-N and C-S cross coupling reactions under one general methodology. We propose that an energy transfer pathway, in which an iridium photosensitizer produces an excited nickel (II) complex, is responsible for the key reductive elimination step that couples aryl halides to 1° and 2° alcohols, anilines, thiophenols, carbamates and sulfonamides.</div>


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