Kaiser W
Biochim Biophys Acta. 1976 Sep 13;440(3):476-82. doi: 10.1016/0005-2728(76)90035-9.
Low concentration of hydrogen peroxide strongly inhibit CO2 fixation of isolated intact chloroplasts (50% inhibition at 10(-5) M hydrogen peroxide). Addition of catalase to a suspension of intact chloroplasts stimulates CO2 fixation 2--6 fold, indicating that this process is partially inhibited by endogenous hydrogen peroxide formed in a Mehler reaction. The rate of CO2 fixation is strongly increased by addition of Calvin cycle intermediates if the catalase activity of the preparation is low. However, at high catalase activity addition of Calvin cycle intermediates remains without effect. Obviously the hydrogen peroxide formed at low catalase activity leads to a loss of Calvin cycle substrates which reduces the rate of CO2 fixation. 3-Phosphoglycerate-dependent O2-evolution is not influenced by hydrogen peroxide at a concentration (5x10(-4) M) which inhibits CO2 fixation almost completely. Therefore the inhibition site of hydrogen peroxide cannot be at the step of 3-phosphoglycerate reduction. Dark CO2 fixation of lysed chloroplasts in a hypotonic medium is not or only slightly inhibited by hydrogen peroxide (2,5x10(-4) M), if ribulose-1,5-diphosphate, ribose 5-phosphate or xylulose 5-phosphate were added as substrates. However, there is a strong inhibition of CO2 fixation by hydrogen peroxide, if fructose 6-phosphate together with triose phosphate are used as substrates. This indicates that hydrogen peroxide interrupts the Calvin cycle at the transketolase step, leading to a reduced supply of the CO2-acceptor ribulose 1,5-diphosphate.
低浓度的过氧化氢会强烈抑制分离的完整叶绿体的二氧化碳固定(在10⁻⁵ M过氧化氢时抑制50%)。向完整叶绿体悬浮液中添加过氧化氢酶可刺激二氧化碳固定2至6倍,这表明该过程部分受到梅勒反应中形成的内源性过氧化氢的抑制。如果制剂的过氧化氢酶活性较低,添加卡尔文循环中间产物会使二氧化碳固定速率大幅增加。然而,在过氧化氢酶活性较高时,添加卡尔文循环中间产物则没有效果。显然,在过氧化氢酶活性较低时形成的过氧化氢会导致卡尔文循环底物的损失,从而降低二氧化碳固定速率。浓度为5×10⁻⁴ M的过氧化氢几乎完全抑制二氧化碳固定,但不影响3 - 磷酸甘油酸依赖性的氧气释放。因此,过氧化氢的抑制位点不可能在3 - 磷酸甘油酸还原步骤。如果添加1,5 - 二磷酸核酮糖、5 - 磷酸核糖或5 - 磷酸木酮糖作为底物,在低渗介质中裂解的叶绿体的暗二氧化碳固定不受或仅轻微受2.5×10⁻⁴ M过氧化氢的抑制。然而,如果使用6 - 磷酸果糖和磷酸丙糖作为底物,过氧化氢会强烈抑制二氧化碳固定。这表明过氧化氢在转酮醇酶步骤中断卡尔文循环,导致二氧化碳受体1,5 - 二磷酸核酮糖的供应减少。