Liu Yu-Xiao, Xu Xiao-Ming, Dai Xin-Bin, Qiang Sheng
Photosynthetic Research Laboratory, Nanjing Agricultural University, Nanjing 210095, China.
J Agric Food Chem. 2007 Jun 27;55(13):5180-5. doi: 10.1021/jf0701887. Epub 2007 May 26.
The action site of Alternaria alternata Crofton-weed toxin (AAC-toxin), isolated first from Alternaria alternata (Fr.) Keissler, was investigated in Chlamydomonas reinhardtii thylakoids. The results revealed that AAC-toxin inhibited photophosphorylation in a concentration-dependent pattern. Similarly, toxin inhibited uncoupled, basal electron flow and photosystem II (PSII) electron transport as well. However, toxin did not affect photosystem I (PSI) activity or the partial reaction of electron transport from H2O to silicomolybdic acid (SiMo). Therefore, the action site of toxin was located at QB level. In addition, the toxin may behave as an energy-transfer inhibitor at high concentrations by inhibiting phosphorylating electron transport and Mg2+ATPase activity. Chlorophyll a fluorescence induction and JIP test corroborated the inhibition at QB level. Through observations of the different sensitivity of toxin on D1 mutants of C. reinhardtii, evidence further confirmed that AAC-toxin inhibited electron transport by displacing the QB on the D1 protein, and the mode of action was similar to phenol-type PSII inhibitors.
对首次从链格孢(Alternaria alternata (Fr.) Keissler)中分离得到的链格孢-胜红蓟毒素(AAC-毒素)在莱茵衣藻类囊体中的作用位点进行了研究。结果表明,AAC-毒素以浓度依赖的方式抑制光合磷酸化。同样,该毒素也抑制解偶联的基础电子流以及光系统II(PSII)的电子传递。然而,毒素并不影响光系统I(PSI)的活性或从H2O到硅钼酸(SiMo)的电子传递的部分反应。因此,毒素的作用位点位于QB水平。此外,在高浓度下,该毒素可能通过抑制磷酸化电子传递和Mg2+ATP酶活性而表现为能量传递抑制剂。叶绿素a荧光诱导和JIP测试证实了在QB水平的抑制作用。通过观察毒素对莱茵衣藻D1突变体的不同敏感性,进一步证明AAC-毒素通过取代D1蛋白上的QB来抑制电子传递,其作用模式类似于酚类PSII抑制剂。