Department of Chemistry, West Virginia University, Morgantown, West Virginia 26506, USA.
J Am Chem Soc. 2010 Aug 11;132(31):10802-7. doi: 10.1021/ja102264w.
We have used a rotational-echo adiabatic-passage double-resonance (13)C{(17)O} solid-state NMR experiment to prove that the glycine produced in the oxygenase reaction of ribulose bisphosphate carboxylase-oxygenase is incorporated exclusively into protein (or protein precursors) of intact, water-stressed soybean leaves exposed to (13)CO(2) and (17)O(2). The water stress increased stomatal resistance and decreased gas exchange so that the Calvin cycle in the leaf chloroplasts was no more than 35% (13)C isotopically enriched. Labeled O(2) levels were sufficient, however, to increase the (17)O isotopic concentration of oxygenase products 20-fold over the natural-abundance level of 0.04%. The observed direct incorporation of glycine into protein shows that water stress suppresses photorespiration in soybean leaves.
我们使用旋转回波绝热通道双共振 (13)C{(17)O} 固态 NMR 实验证明,在 RuBP 羧化酶-加氧酶的加氧反应中产生的甘氨酸仅被掺入到暴露于 (13)CO(2) 和 (17)O(2) 的完整、受水分胁迫的大豆叶片的蛋白质(或蛋白质前体)中。水分胁迫增加了气孔阻力并降低了气体交换,从而使叶片叶绿体中的卡尔文循环的 13C 同位素丰度富集程度不超过 35%。然而,标记的 O(2) 水平足以使加氧酶产物的 (17)O 同位素浓度比天然丰度水平 0.04%增加 20 倍。观察到的甘氨酸直接掺入蛋白质表明,水分胁迫抑制了大豆叶片中的光呼吸。