Holbrook G P, Jordan D B, Chollet R
Department of Agricultural Biochemistry, East Campus, University of Nebraska, Lincoln, Nebraska 68583-0718.
Plant Physiol. 1985 Mar;77(3):578-83. doi: 10.1104/pp.77.3.578.
The CO(2)/O(2) specificity factor of sucrose gradient purified ribulose 1,5-bisphosphate carboxylase/oxygenase from the C(3)-C(4) intermediate plants Moricandia arvensis (79 +/- 1) and Panicum milioides (89 +/- 2) was similar to the respective values of the enzyme from the closely related C(3) species, Moricandia foetida (80 +/- 5) and Panicum laxum (86 +/- 2). Thus, the kinetic properties of this bifunctional enzyme do not explain the reduced rates of photorespiration exhibited by either of these intermediate species.Dark/light ratios for aminoacetonitrile-sensitive (14)CO(2) evolution during decarboxylation of exogenous [1-(14)C]glycine by leaf discs had values of 9.0 with M. arvensis and 11.8 with P. milioides. Equivalent ratios with M. foetida and P. laxum were 2.5 and 3.2, respectively. Similar results were obtained using [1-(14)C]glycolate as the exogenous photorespiratory substrate, with dark/light (14)CO(2) evolution ratios for the C(3)-C(4) and C(3) leaf discs averaging 6.6 and 2.0, respectively. Stimulating photosynthetic CO(2) fixation by progressively increasing photon flux density from 0 to 1900 micromoles per square meter per second caused a concomitant reduction in (14)CO(2) evolution from leaf discs of M. arvensis and P. milioides supplied with [1-(14)C]glycine. Conversely, inhibition of photosynthesis by DCMU or the Calvin cycle inhibitor dl-glyceraldehyde increased (14)CO(2) evolution in the light to rates comparable to those in the dark. The data suggest that P. milioides and M. arvensis are capable of a more efficient internal recycling of photorespiratory CO(2) via ribulose bisphosphate carboxylase/oxygenase than closely related C(3) plants, and that this may partially account for the reduced rates of apparent photorespiration by these intermediate species.
从C₃ - C₄中间型植物田基麻(79±1)和细柄黍(89±2)中经蔗糖梯度纯化得到的1,5 - 二磷酸核酮糖羧化酶/加氧酶的CO₂/O₂特异性因子,与来自近缘C₃物种臭田基麻(80±5)和疏花黍(86±2)的该酶各自的值相似。因此,这种双功能酶的动力学特性并不能解释这些中间型物种中任何一种所表现出的光呼吸速率降低的现象。叶盘对外源[1 - ¹⁴C]甘氨酸脱羧过程中对氨基乙腈敏感的¹⁴CO₂释放的暗/光比,田基麻的值为9.0,细柄黍的值为11.8。臭田基麻和疏花黍的等效比值分别为2.5和3.2。以[1 - ¹⁴C]乙醇酸作为外源光呼吸底物时也得到了类似结果,C₃ - C₄和C₃叶盘的暗/光¹⁴CO₂释放比平均分别为6.6和2.0。通过将光子通量密度从0逐步增加到1900微摩尔每平方米每秒来刺激光合CO₂固定,会导致供应[1 - ¹⁴C]甘氨酸的田基麻和细柄黍叶盘的¹⁴CO₂释放随之减少。相反,用二氯苯基二甲脲(DCMU)或卡尔文循环抑制剂dl - 甘油醛抑制光合作用,会使光下的¹⁴CO₂释放速率增加到与黑暗中相当的水平。数据表明,与近缘C₃植物相比,细柄黍和田基麻能够通过1,5 - 二磷酸核酮糖羧化酶/加氧酶更有效地进行光呼吸CO₂的内部循环,这可能部分解释了这些中间型物种明显的光呼吸速率降低的原因。