Pollock Steve Vincent, Colman Brian
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA; Department of Biology, York University, 4700 Keele St., Toronto, Ontario, M3J 1P3, Canada.
Physiol Plant. 2001 Apr;111(4):527-532. doi: 10.1034/j.1399-3054.2001.1110413.x.
The effects of the carbonic anhydrase (CA) inhibitors acetazolamide (AZ) and dextran-bound sulfonamide (DBS) on HCO3--dependent O2 evolution in Chlorella saccharophila were evaluated. Addition of 4 µM AZ or 0.4 mg ml-1 DBS to photosynthesizing cells reduced the O2 evolution rate at low dissolved inorganic carbon (DIC) concentration, decreased the size of the intracellular acid-labile carbon pool, and decreased the apparent affinity of the cells for DIC. Measurement of the whole-cell affinity of cells for CO2 and HCO3- in the presence and absence of inhibitors indicated that active HCO3- transport was inhibited by AZ and DBS. The inhibition of HCO3- transport was independent of the inhibition of external and internal CA. These results suggest that the active uptake of HCO3- occurs initially by the interaction of HCO3- and a CA-like transporter.
评估了碳酸酐酶(CA)抑制剂乙酰唑胺(AZ)和葡聚糖结合磺酰胺(DBS)对嗜糖小球藻中HCO₃⁻依赖型氧气释放的影响。向进行光合作用的细胞中添加4 μM AZ或0.4 mg ml⁻¹ DBS会降低低溶解无机碳(DIC)浓度下的氧气释放速率,减小细胞内酸不稳定碳库的大小,并降低细胞对DIC的表观亲和力。在有和没有抑制剂的情况下测量细胞对CO₂和HCO₃⁻的全细胞亲和力表明,AZ和DBS抑制了活跃的HCO₃⁻转运。HCO₃⁻转运的抑制与外部和内部CA的抑制无关。这些结果表明,HCO₃⁻的主动摄取最初是通过HCO₃⁻与一种类CA转运蛋白的相互作用发生的。