Hofmann Laurie C, Koch Marguerite, de Beer Dirk
Microsensor Group, Max Planck Institute for Marine Microbiology, Bremen, Germany.
Aquatic Plant Ecology Lab, Biological Sciences Department, Florida Atlantic University, Boca Raton, Florida, United States of America.
PLoS One. 2016 Jul 26;11(7):e0159057. doi: 10.1371/journal.pone.0159057. eCollection 2016.
Presently, an incomplete mechanistic understanding of tropical reef macroalgae photosynthesis and calcification restricts predictions of how these important autotrophs will respond to global change. Therefore, we investigated the mechanistic link between inorganic carbon uptake pathways, photosynthesis and calcification in a tropical crustose coralline alga (CCA) using microsensors. We measured pH, oxygen (O2), and calcium (Ca2+) dynamics and fluxes at the thallus surface under ambient (8.1) and low (7.8) seawater pH (pHSW) and across a range of irradiances. Acetazolamide (AZ) was used to inhibit extracellular carbonic anhydrase (CAext), which mediates hydrolysis of HCO3-, and 4,4' diisothiocyanatostilbene-2,2'-disulphonate (DIDS) that blocks direct HCO3- uptake by anion exchange transport. Both inhibited photosynthesis, suggesting both diffusive uptake of CO2 via HCO3- hydrolysis to CO2 and direct HCO3- ion transport are important in this CCA. Surface pH was raised approximately 0.3 units at saturating irradiance, but less when CAext was inhibited. Surface pH was lower at pHSW 7.8 than pHSW 8.1 in the dark, but not in the light. The Ca2+ fluxes were large, complex and temporally variable, but revealed net Ca2+ uptake under all conditions. The temporal variability in Ca2+ dynamics was potentially related to localized dissolution during epithallial cell sloughing, a strategy of CCA to remove epiphytes. Simultaneous Ca2+ and pH dynamics suggest the presence of Ca2+/H+ exchange. Rapid light-induced H+ surface dynamics that continued after inhibition of photosynthesis revealed the presence of a light-mediated, but photosynthesis-independent, proton pump. Thus, the study indicates metabolic control of surface pH can occur in CCA through photosynthesis and light-inducible H+ pumps. Our results suggest that complex light-induced ion pumps play an important role in biological processes related to inorganic carbon uptake and calcification in CCA.
目前,对热带珊瑚礁大型藻类光合作用和钙化作用的机制理解尚不完整,这限制了我们预测这些重要自养生物将如何应对全球变化。因此,我们使用微传感器研究了热带壳状珊瑚藻(CCA)中无机碳吸收途径、光合作用和钙化作用之间的机制联系。我们在环境海水pH值(8.1)和低海水pH值(7.8)条件下,以及一系列光照强度下,测量了藻体表面的pH值、氧气(O2)和钙(Ca2+)的动态变化及通量。使用乙酰唑胺(AZ)抑制细胞外碳酸酐酶(CAext),该酶介导HCO3-的水解,以及4,4'-二异硫氰基芪-2,2'-二磺酸盐(DIDS),其通过阴离子交换转运阻止直接的HCO3-吸收。两者均抑制了光合作用,这表明通过HCO3-水解为CO2的CO2扩散吸收以及直接的HCO3-离子转运在这种CCA中都很重要。在饱和光照强度下,表面pH值升高了约0.3个单位,但当CAext被抑制时升高幅度较小。在黑暗中,pH值为7.8的海水条件下的表面pH值低于pH值为8.1的海水条件,但在光照条件下并非如此。Ca2+通量很大、很复杂且随时间变化,但在所有条件下均显示出净Ca2+吸收。Ca2+动态变化的时间变异性可能与上皮细胞脱落期间的局部溶解有关,这是CCA去除附生植物的一种策略。同时的Ca2+和pH动态变化表明存在Ca2+/H+交换。光合作用受抑制后仍持续的快速光诱导H+表面动态变化揭示了存在一种光介导但与光合作用无关的质子泵。因此,该研究表明CCA可通过光合作用和光诱导H+泵对表面pH值进行代谢控制。我们的结果表明,复杂的光诱导离子泵在与CCA中无机碳吸收和钙化作用相关的生物过程中起重要作用。