Su Pai-Hsiang, Lai Yen-Hsun
Agricultural Biotechnology Research Center, Academia Sinica, Taipei, Taiwan.
Biotechnology Center in Southern Taiwan, Academia Sinica, Tainan, Taiwan.
Front Plant Sci. 2017 Dec 5;8:2079. doi: 10.3389/fpls.2017.02079. eCollection 2017.
The proton gradient established by the pH difference across a biological membrane is essential for many physiological processes, including ATP synthesis and ion and metabolite transport. Currently, ionophores are used to study proton gradients, and determine their importance to biological functions of interest. Because of the lack of an easy method for monitoring the proton gradient across the inner envelope membrane of chloroplasts (ΔpH), whether the concentration of ionophores used can effectively abolish the ΔpH is not proven for most experiments. To overcome this hindrance, we tried to setup an easy method for real-time monitoring of the stromal pH in buffered, isolated chloroplasts by using fluorescent pH probes; using this method the ΔpH can be calculated by subtracting the buffer pH from the measured stromal pH. When three fluorescent dyes, BCECF-AM [2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein acetoxymethyl ester], CFDA-SE [5(6)-Carboxyfluorescein diacetate succinimidyl ester] and SNARF-1 carboxylic acid acetate succinimidyl ester were incubated with isolated chloroplasts, BCECF-AM and CFDA-SE, but not the ester-formed SNARF-1 were taken up by chloroplasts and digested with esterase to release high levels of fluorescence. According to its relatively higher pKa value (6.98, near the physiological pH of the stroma), BCECF was chosen for further development. Due to shielding of the excitation and emission lights by chloroplast pigments, the ratiometric fluorescence of BCECF was highly dependent on the concentration of chloroplasts. By using a fixed concentration of chloroplasts, a highly correlated standard curve of pH to the BCECF ratiometric fluorescence with an -square value of 0.98 was obtained, indicating the reliability of this method. Consistent with previous reports, the light-dependent formation of ΔpH can be detected ranging from 0.15 to 0.33 pH units upon illumination. The concentration of the ionophore nigericin required to collapse the ΔpH was then studied. The establishment of a non-destructive method of monitoring the stromal pH will be valuable for studying the roles of the ΔpH in chloroplast physiology.
跨生物膜的pH差异所建立的质子梯度对于许多生理过程至关重要,包括ATP合成以及离子和代谢物运输。目前,离子载体被用于研究质子梯度,并确定其对感兴趣的生物学功能的重要性。由于缺乏一种简便的方法来监测叶绿体内膜的质子梯度(ΔpH),在大多数实验中,所用离子载体的浓度是否能有效消除ΔpH尚未得到证实。为了克服这一障碍,我们尝试通过使用荧光pH探针建立一种简便的方法来实时监测缓冲的分离叶绿体中的基质pH;使用该方法,可通过从测得的基质pH中减去缓冲液pH来计算ΔpH。当将三种荧光染料,BCECF-AM [2',7'-双(2-羧乙基)-5-(和-6)-羧基荧光素乙酰氧基甲酯]、CFDA-SE [5(6)-羧基荧光素二乙酸琥珀酰亚胺酯]和SNARF-1羧酸乙酸琥珀酰亚胺酯与分离的叶绿体一起孵育时,BCECF-AM和CFDA-SE被叶绿体摄取并被酯酶消化以释放高水平的荧光,但酯形式的SNARF-1则不然。根据其相对较高的pKa值(6.98,接近基质的生理pH),选择BCECF进行进一步研究。由于叶绿体色素对激发光和发射光的屏蔽作用,BCECF的比率荧光高度依赖于叶绿体的浓度。通过使用固定浓度的叶绿体,获得了pH与BCECF比率荧光的高度相关标准曲线,R平方值为0.98,表明该方法的可靠性。与先前的报道一致,光照后可检测到ΔpH的光依赖性形成,范围为0.15至0.33个pH单位。然后研究了消除ΔpH所需的离子载体尼日利亚菌素的浓度。建立一种无损监测基质pH的方法对于研究ΔpH在叶绿体生理学中的作用将具有重要价值。