Appalachian Soil and Water Conservation Research Station, United States Department of Agriculture, PO Box 867, 25802, Beckley, WV, USA.
Photosynth Res. 1987 Jan;12(1):63-72. doi: 10.1007/BF00019151.
The inhibition patterns of rabbit sera (RS1 & RS2) from two different rabbits on the photosynthetic electron transport of isolated spinach thylakoids were studied. Fifty μl of RSI were required for 100% inhibition of a H2O → MV/O2 reaction, while only 10 μl of a 1:10 dilution of RS2 were needed for 100% inhibition. The RS2 serum was greatly hemolyzed. The γ-globulin fraction from purified rabbit serum (RS1) did not inhibit photosynthetic electron transport, indicating that the antibody fraction of the rabbit serum does not contain the inhibitor. It appears that the inhibitor is from the hemolyzed red blood cells. Rabbit sera added prior to chloroplast illumination caused no inhibition, while addition of rabbit sera during illumination inhibited a H2O → MV/O2 reaction within 1-3s. Aminotriazole, a catalase inhibitor, did not affect the efficacy of the rabbit sera indicating that the unknown rabbit serum inhibitor is not catalase. Various Hill reactions were employed to determine the site of inhibition. Rabbit sera inhibited the following reactions: DHQ/DCMU → MV/O2, DAD/Asc/DBMIB → MV/O2, and DCIP/Asc/DBMIB → MV/O2. Rabbit sera did not inhibit a H2O → DADox reaction indicating that inhibition is on the reducing side of PSI. However, a H2O → Fd/NADP(+) reaction was not inhibited by rabbit sera. NADP did not interfere with the ability of RS2 to inhibit a MV-mediated Mehler reaction. In simultaneously measured assays of Fd-mediated O2 and NADP(+) reductions, RS2 serum inhibited the reduction of O2 by ferredoxin without inhibiting the reduction of NADP(+). These results indicate the potential involvement of parallel (branched) electron transport of the reducing side of PSI in the reduction of oxygen.
研究了来自两只不同兔子的兔血清(RS1 和 RS2)对分离的菠菜类囊体光合电子传递的抑制模式。RS1 血清需要 50μl 才能完全抑制 H2O→MV/O2 反应,而只需 10μl 稀释 1:10 的 RS2 血清即可达到 100%的抑制。RS2 血清发生了严重的溶血。从纯化的兔血清(RS1)中提取的 γ-球蛋白部分不抑制光合电子传递,表明兔血清的抗体部分不含有抑制剂。看来抑制剂来自于溶血的红细胞。在叶绿体光照之前加入兔血清不会引起抑制,而在光照期间加入兔血清则会在 1-3 秒内抑制 H2O→MV/O2 反应。过氧化氢酶抑制剂氨基三唑不会影响兔血清的功效,表明未知的兔血清抑制剂不是过氧化氢酶。采用各种希尔反应来确定抑制的部位。兔血清抑制以下反应:DHQ/DCMU→MV/O2、DAD/Asc/DBMIB→MV/O2 和 DCIP/Asc/DBMIB→MV/O2。兔血清不能抑制 H2O→DADox 反应,表明抑制发生在 PSI 的还原侧。然而,兔血清不抑制 H2O→Fd/NADP(+)反应。NADP 不会干扰 RS2 抑制 MV 介导的 Mehler 反应的能力。在同时测量的 Fd 介导的 O2 和 NADP(+)还原测定中,RS2 血清抑制了铁氧还蛋白的 O2 还原,而不抑制 NADP(+)的还原。这些结果表明,PSI 还原侧的平行(分支)电子传递可能参与了氧的还原。