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细胞外酸化对酿酒酵母质膜ATP酶活性以及胞质和液泡pH值的影响。

Effect of extracellular acidification on the activity of plasma membrane ATPase and on the cytosolic and vacuolar pH of Saccharomyces cerevisiae.

作者信息

Carmelo V, Santos H, Sá-Correia I

机构信息

Laboratório de Engenharia Bioquímica / Centro de Engenharia Biologica e Química, Instituto Superior Técnico, Lisboa, Portugal.

出版信息

Biochim Biophys Acta. 1997 Apr 3;1325(1):63-70. doi: 10.1016/s0005-2736(96)00245-3.

Abstract

The rapid in vivo activation of Saccharomyces cerevisiae plasma membrane H+-ATPase that has been attributed to medium acidification from pH 6.5 to pH 3.5 is not caused by the low pH itself but is induced by the weak organic acid (succinic) used as the acidulant. The activation induced by 50 mM succinic acid at pH 3.5 occurred in both the presence or absence of glucose. Activation at pH 3.5 was also induced by acetic acid and it was maximal at 50 mM concentration. To investigate the role of plasma membrane ATPase activation in pH homeostasis, the internal pH (cytosolic and vacuolar) of yeast cells incubated in media at pH 6.5 or at pH 3.5, acidified either with HCl or acetic acid, were compared by using in vivo (31)P-NMR. Despite plasma membrane ATPase activation by acetic acid, the decrease in cytosolic pH caused by external acidification was much more important when the permeant acetic acid was used instead of HCl as the acidulant. The supplementation of the incubation medium at pH 3.5 with glucose led to higher cytosolic pH values, consistent with the observed in vivo activation of plasma membrane ATPase by glucose. At the external pH value of 6.5 the vacuole was maintained at a mildly acidic pH (around 6) while the cytosol was at about neutral pH; however, when cytoplasmic pH decreased due to external acidification, vacuolar pH accompanied that decrease. Vacuolar pH reached 5.4-5.5 during incubation with HCI and dropped sharply to values below 4.4 in cells incubated with acetic acid. These results indicate that the vacuole also plays a role in homeostasis of the intracellular pH.

摘要

酿酒酵母质膜H⁺-ATP酶在体内的快速激活一直被认为是由于培养基pH值从6.5酸化至3.5所致,但这并非由低pH值本身引起,而是由用作酸化剂的弱有机酸(琥珀酸)诱导的。在pH 3.5时,50 mM琥珀酸诱导的激活在有无葡萄糖的情况下均会发生。pH 3.5时的激活也可由乙酸诱导,且在50 mM浓度时达到最大值。为了研究质膜ATP酶激活在pH稳态中的作用,通过体内³¹P-NMR比较了在pH 6.5或pH 3.5的培养基中培养的酵母细胞的内部pH值(胞质和液泡),这些培养基分别用HCl或乙酸酸化。尽管乙酸可激活质膜ATP酶,但当使用可渗透的乙酸而非HCl作为酸化剂时,外部酸化引起的胞质pH值下降更为显著。在pH 3.5的培养基中添加葡萄糖会导致更高的胞质pH值,这与观察到的葡萄糖在体内激活质膜ATP酶的现象一致。在外部pH值为6.5时,液泡维持在轻度酸性pH(约6),而胞质约为中性pH;然而,当由于外部酸化导致细胞质pH值下降时,液泡pH值也随之下降。在用HCl孵育期间,液泡pH值达到5.4 - 5.5,而在用乙酸孵育的细胞中,液泡pH值急剧下降至4.4以下。这些结果表明,液泡在细胞内pH稳态中也发挥作用。

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