Hardt H, Kok B
Biochim Biophys Acta. 1976 Oct 13;449(1):125-35. doi: 10.1016/0005-2728(76)90012-8.
Treatment of isolated chloroplasts with glutaraldehyde affects their ability to photoreduce artificial electron acceptors. The remaining rate of O2 evolution approaches zero with methyl viologen, is low with ferricyanide, but nearly normal with lipophilic Photosystem II acceptors, like oxidized p-phenylenediamine and oxidized diaminodurene. Since Photosystem I donor reactions are also affected, a specific site of inhibition of electron transport to Photosystem I is indicated. At the same time, glutaraldehyde prolongs the longevity of the chloroplasts stored in dark. In control samples the half-life of Photosystem II activity varied between 5 days at 4degreesC and 1 day at 25degreesC. Glutaraldehyde treatment increased these half times approx. 3-fold. The glutaraldehyde doses required to induce inhibition and stabilization were very similar.
用戊二醛处理分离的叶绿体,会影响其光还原人工电子受体的能力。用甲基紫精时,剩余的氧气释放速率接近零;用铁氰化物时,该速率较低;但用亲脂性光系统II受体(如氧化对苯二胺和氧化二氨基杜烯)时,该速率接近正常。由于光系统I供体反应也受到影响,这表明存在一个抑制电子向光系统I传输的特定位点。同时,戊二醛可延长黑暗中储存的叶绿体的寿命。在对照样品中,光系统II活性的半衰期在4℃时为5天,在25℃时为1天。戊二醛处理使这些半衰期大约增加了3倍。诱导抑制和稳定所需的戊二醛剂量非常相似。