Krol M, Ivanov AG, Jansson S, Kloppstech K, Huner NP
Department of Plant Sciences, The University of Western Ontario, London, Ontario, Canada N6A 5B7 (M.K., A.G.I., N.P.A.H.).
Plant Physiol. 1999 May;120(1):193-204. doi: 10.1104/pp.120.1.193.
Etiolated seedlings of wild type and the chlorina f2 mutant of barley (Hordeum vulgare) were exposed to greening at either 5 degrees C or 20 degrees C and continuous illumination varying from 50 to 800 &mgr;mol m-2 s-1. Exposure to either moderate temperature and high light or low temperature and moderate light inhibited chlorophyll a and b accumulation in the wild type and in the f2 mutant. Continuous illumination under these greening conditions resulted in transient accumulations of zeaxanthin, concomitant transient decreases in violaxanthin, and fluctuations in the epoxidation state of the xanthophyll pool. Photoinhibition-induced xanthophyll-cycle activity was detectable after only 3 h of greening at 20 degrees C and 250 &mgr;mol m-2 s-1. Immunoblot analyses of the accumulation of the 14-kD early light-inducible protein but not the major (Lhcb2) or minor (Lhcb5) light-harvesting polypeptides demonstrated transient kinetics similar to those observed for zeaxanthin accumulation during greening at either 5 degrees C or 20 degrees C for both the wild type and the f2 mutant. Furthermore, greening of the f2 mutant at either 5 degrees C or 20 degrees C indicated that Lhcb2 is not essential for the regulation of the xanthophyll cycle in barley. These results are consistent with the thesis that early light-inducible proteins may bind zeaxanthin as well as other xanthophylls and dissipate excess light energy to protect the developing photosynthetic apparatus from excess excitation. We discuss the role of energy balance and photosystem II excitation pressure in the regulation of the xanthophyll cycle during chloroplast biogenesis in wild-type barley and the f2 mutant.
将野生型和大麦(Hordeum vulgare)的叶绿素f2突变体的黄化幼苗置于5℃或20℃下进行绿化处理,并给予50至800 μmol m-2 s-1的连续光照。暴露于中等温度和高光或低温和中等光照下会抑制野生型和f2突变体中叶绿素a和b的积累。在这些绿化条件下的连续光照导致玉米黄质的瞬时积累,伴随着紫黄质的瞬时减少,以及叶黄素库环氧化状态的波动。在20℃和250 μmol m-2 s-1的绿化处理仅3小时后,即可检测到光抑制诱导的叶黄素循环活性。对14-kD早期光诱导蛋白积累的免疫印迹分析表明,主要(Lhcb2)或次要(Lhcb5)捕光多肽的积累没有显示出与野生型和f2突变体在5℃或20℃绿化期间玉米黄质积累相似的瞬时动力学。此外,f2突变体在5℃或20℃下的绿化表明,Lhcb2对于大麦中叶黄素循环的调节不是必需的。这些结果与早期光诱导蛋白可能结合玉米黄质以及其他叶黄素并消散过量光能以保护发育中的光合机构免受过量激发的论点一致。我们讨论了能量平衡和光系统II激发压力在野生型大麦和f2突变体叶绿体生物发生过程中叶黄素循环调节中的作用。