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1 nonequivalent beta-carotene molecules in the photosystem II reaction center.
2 a chlorophyll-binding protein located in the photosystem II reaction center.
3 subunit can be extracted and re-bound to the photosystem II reaction center.
4 either one or two copies of each protein per photosystem II reaction center.
5 n significantly impact the properties of the photosystem II reaction center.
6 sine, distinct from tyrosine D and Z, in the photosystem II reaction center.
7 hat there are two pheophytin a molecules per photosystem II reaction center.
8 ted proteins D1 and D2 together build up the photosystem II reaction center.
9 ich contain four, two, or zero manganese per photosystem II reaction center.
10 o copies of the 33 kDa extrinsic protein per photosystem II reaction center.
11 al species of the two carotenoids present in photosystem II reaction centers.
12 n of the plastoquinone QB (acceptor side) of photosystem II reaction centers.
13 appear to assemble Mn clusters in nearly all photosystem II reaction centers.
14 d H105Y strains lacked detectable amounts of photosystem II reaction centers and hence could not evol
15 t fits the extensive time-resolved data from photosystem II reaction centers and reaction center muta
16 ic cases, the two beta-carotene molecules in photosystem II reaction centers and the two luteins in t
17 and 17 kDa extrinsic polypeptides from some photosystem II reaction centers, and also modifies the s
18 of the chloroplast encoded D2 protein of the photosystem II reaction center at a point after translat
22 follows: photosystem II membranes, 274:3.2; photosystem II reaction center complexes, 78:2.5; Synech
23 ed spinach photosystem II membranes, spinach photosystem II reaction center complexes, spinach photos
27 nly half of this protein (about 1 mol/mol of photosystem II reaction centers) is susceptible to displ
29 nic connection between the photosystem I and photosystem II reaction centers of oxygenic photosynthes
31 m I P700 chlorophyll a apoprotein A1), psbA (photosystem II reaction center protein D1), and "Form I"
32 A substrate of FtsH protease in vivo, the photosystem II reaction center protein D1, is not effici
35 investigated the electronic structure of the photosystem II reaction center (PSII RC) in relation to
36 isted electronic (vibronic) coherence in the Photosystem II Reaction Center (PSII RC) indicates that
38 which encode the D2 and CP43 subunits of the photosystem II reaction center, respectively, are regula
39 ith truncated Slr2013 forms fully functional photosystem II reaction centers that differ from wild-ty
40 its ability to grow and assemble functional photosystem II reaction centers under chloride-limiting
41 sult indicated that the amount of functional photosystem II reaction centers was compromised in the p
42 psbA gene encodes the D1 polypeptide of the photosystem II reaction center, which is synthesized at
43 Electron transfer from Q(A)(-) to Q(B) in Photosystem II reaction centers with an occupied Q(B) si
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