Département de Biologie, Service de Radioagronomie, Centre d'Etudes Nucléaires de Cadarache, B.P. No. 1, F-13115 Saint-Paul-lez-Durance, France.
Plant Physiol. 1985 Apr;77(4):974-7. doi: 10.1104/pp.77.4.974.
We tested a number of inhibitory monovalent anions for their primary site of action on photosystem II(PSII) in chloroplasts. We find that the inhibitory effects of F(-), HCO(2) (-), NO(2) (-), NO(3) (-), and CH(3)CO(2) (-) are all reversed by addition of a high concentration of HCO(3) (-). This class of anions competitively inhibits H(14)CO(3) (-) binding to PSII. All of those anions tested reduced H(14)CO(3) (-) binding more in the light than in the dark. We conclude that the primary inhibitory site of action of a number of monovalent anions is at the HCO(3) (-) binding site(s) on the PSII complex. The carbonic anhydrase inhibitor gold cyanide, and also azide, inhibit PSII but at a site other than the HCO(3) (-) binding site. We suggest that the unique ability of HCO(3) (-) to reverse the effects of inhibitory anions reflects its singular ability to act as a proton donor/acceptor at the anion binding site. A similar role has been proposed for non-substrate-bound HCO(3) (-) on carbonic anhydrase by Yeagle et al. (1975 Proc Natl Acad Sci USA 72: 454-458).
我们测试了一些抑制性单价阴离子在叶绿体中的光系统 II(PSII)上的主要作用部位。我们发现 F(-)、HCO(2)(-)、NO(2)(-)、NO(3)(-)和 CH(3)CO(2)(-)的抑制作用都可以通过添加高浓度的 HCO(3)(-)来逆转。这一类阴离子竞争性地抑制 H(14)CO(3)(-)与 PSII 的结合。所有测试的阴离子在光下比在暗中更能减少 H(14)CO(3)(-)的结合。我们得出结论,许多单价阴离子的主要作用部位是在 PSII 复合物上的 HCO(3)(-)结合部位。碳酸酐酶抑制剂金氰化物,以及叠氮化物,也抑制 PSII,但作用部位不在 HCO(3)(-)结合部位。我们认为,HCO(3)(-)逆转抑制性阴离子作用的独特能力反映了它在阴离子结合部位作为质子供体/受体的独特能力。Yeagle 等人(1975 年美国国家科学院院刊 72:454-458)提出,非底物结合的 HCO(3)(-)在碳酸酐酶上也具有类似的作用。