ライフサイエンスコーパス: photooxidize

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1 en the primary chlorophyll donor, P(700), is photooxidized.

2 oxygen-containing moieties generated within photooxidized A2E include a 5,8-monofuranoid and a cycli

3 ability of UVA light-excited kynurenines to photooxidize ASC and to form AGEs in lens proteins.

4 yl]carbodiimide hydrochloride (EDC), Mn2+ is photooxidized at a lower affinity (Kd = 25 microM) site

5 At a concentration of 200 microM, DPC is photooxidized at both a high-affinity and a low-affinity

6 From the extent of photooxidized b- and c-type hemes as well as P798+, a st

7 d two histidyl ligands, and these Mn are not photooxidized by a flash even when the ligand to the pho

8 is a redox-active chlorophyll (Chl) which is photooxidized by low-temperature (<100 K) illumination o

9 ent cations, such as Zn and Co, that are not photooxidized by PSII.

10 telomeric repeats (T(2)G(4))(4) are readily photooxidized by TOTA, the major sites of oxidation bein

11 ght, added Mn(II) or Fe(II) can no longer be photooxidized by Y(Z)(*).

12 The photooxidizing capabilities of selected Cr(III) complexe

13 nium dimer, Ru(2)D, to either photoreduce or photooxidize cytochrome c(1) within 1 micros.

14 TA) has previously been shown to bind to and photooxidize duplex DNA, leading to cleavage at G residu

15 inding site for the first Mn(II) ion that is photooxidized during the light-driven assembly of the (M

16 ves oxygen from water by the accumulation of photooxidizing equivalents at the oxygen-evolving comple

17 king effect is caused by specifically bound, photooxidized Fe [> or =Fe(III)] and is accompanied by a

18 deliver electrons to other RCs which stayed photooxidized for several seconds.

19 cies, which is a neutral radical, Z*, in the photooxidized form.

20 cies, which is a neutral radical, D*, in the photooxidized form.

21 ific site on a restriction fragment, NDI can photooxidize guanine over at least 25-38 bp in each dire

22 The yield of photooxidized heme c is 20% in a single flash.

23 The photooxidized intermediate, [Mn(3+)(HCO(3)(-))], is long

24 We photooxidized (OH oxidation) primary emissions from dies

25 lve carboxyl ligands; (c) low-affinity Mn is photooxidized (possibly by YD*, the oxidized form of the

26 Cyt c2 reduces the photooxidized primary donor D+ in 0.9 +/- 0.1 micros in

27 only approximately 30% of the RCs had their photooxidized primary donor rapidly rereduced by cyt cy.

28 spectrophotometric detection of P700(+), the photooxidized primary electron donor of photosystem I.

29 rk contrast to the cryomatrix experiments, a photooxidized product cannot be detected in liquid solut

30 verified in studies of guanine oxidation by photooxidized riboflavin and nitrosoperoxycarbonate, for

31 resh and artificially weathered (evaporated, photooxidized) samples of North Sea crude oil and residu

32 lization of acriflavin in the kinetoplast to photooxidize selectively the kinetoplast DNA is suggeste

33 - 0.05, as derived from miniSOG's ability to photooxidize the fluorescent probe anthracene dipropioni

34 (1) One Mn2+ ion binds and is photooxidized to Mn3+ at a high-affinity site, forming t

35 er is a more efficient electron donor to the photooxidized tyrosine radical, TyrZ+, than is the monon

36 ght-induced charge separation, but unable to photooxidize water, largely because of the absence of a

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