Badger M R, Bassett M, Comins H N
Department of Environmental Biology, Research School of Biological Sciences, Australian National University, P.O. Box 475, Canberra, A.C.T. 2601 Australia.
Plant Physiol. 1985 Feb;77(2):465-71. doi: 10.1104/pp.77.2.465.
A simple model based on HCO(3) (-) transport has been developed to relate photosynthesis and inorganic carbon fluxes for the marine cyanobacterium, Synechococcus sp. Nägeli (strain RRIMP N1). Predicted relationships between inorganic carbon transport, CO(2) fixation, internal carbonic anhydrase activity, and leakage of CO(2) out of the cell, allow comparisons to be made with experimentally obtained data. Measurements of inorganic carbon fluxes and internal inorganic carbon pool sizes in these cells were made by monitoring time-courses of CO(2) changes (using a mass spectrometer) during light/dark transients. At just saturating CO(2) conditions, total inorganic carbon transport did not exceed net CO(2) fixation by more than 30%. This indicates CO(2) leakage similar to that estimated for C(4) plants.For this leakage rate, the model predicts the cell would need a conductance to CO(2) of around 10(-5) centimeters per second. This is similar to estimates made for the same cells using inorganic carbon pool sizes and CO(2) efflux measurements. The model predicts that carbonic anhydrase is necessary internally to allow a sufficiently fast rate of CO(2) production to prevent a large accumulation of HCO(3) (-). Intact cells show light stimulated carbonic anhydrase activity when assayed using (18)O-labeled CO(2) techniques. This is also supported by low but detectable levels of carbonic anhydrase activity in cell extracts, sufficient to meet the requirements of the model.
基于HCO(3) (-)转运建立了一个简单模型,以关联海洋蓝细菌聚球藻属纳氏藻(菌株RRIMP N1)的光合作用和无机碳通量。无机碳转运、CO(2)固定、内部碳酸酐酶活性以及CO(2)从细胞中泄漏之间的预测关系,使得能够与实验获得的数据进行比较。通过监测光/暗转换期间CO(2)变化的时间进程(使用质谱仪),对这些细胞中的无机碳通量和内部无机碳库大小进行了测量。在刚好饱和的CO(2)条件下,总无机碳转运比净CO(2)固定高出不超过30%。这表明CO(2)泄漏情况与C(4)植物的估计情况相似。对于这种泄漏率,该模型预测细胞对CO(2)的传导率约为每秒10(-5)厘米。这与使用无机碳库大小和CO(2)外流测量对相同细胞所做的估计相似。该模型预测,内部碳酸酐酶是必需的,以允许足够快的CO(2)产生速率,防止HCO(3) (-)大量积累。当使用(18)O标记的CO(2)技术进行测定时,完整细胞显示出光刺激的碳酸酐酶活性。细胞提取物中低但可检测到的碳酸酐酶活性水平也支持了这一点,足以满足模型的要求。