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卡氏棘阿米巴营养细胞和包囊细胞的31P核磁共振研究。活细胞中膦酸的观察。

31P NMR studies of vegetative and encysted cells of Acanthamoeba castellanii. Observation of phosphonic acids in live cells.

作者信息

Deslauriers R, Byrd R A, Jarrell H C, Smith I C

出版信息

Eur J Biochem. 1980 Oct;111(2):369-75. doi: 10.1111/j.1432-1033.1980.tb04950.x.

Abstract

31P NMR studies have been performed on vegetative and encysted Acanthamoeba castellanii. A prominent feature of the spectra is the presence of resonances characteristic of P-C linkages. Vegetative cells show sharp phosphonate resonances whereas encysted cells show broad phosphonate resonances and narrow phosphate resonances. Studies of model compounds using 31P NMR have shown the narrow resonances to arise from 2-aminoethylphosphonic acid; the broad components from encysted cells arise from molecules with long rotational correlation times such as aggregates of lipophosphonoglycan or phosphonoprotein. Vegetative cells also show the presence of an electronegatively beta-substituted phosphonic acid, possibly 1-hydroxy-2-aminoethylphosphonic acid, a component identified in the cell membrane lipophosphoglycan. pH titration studies of a number of phosphonic acid model compounds show a chemical shift behaviour quite distinct from that of biological phosphates. Upon acidification from pH 12, resonances shift to high field followed by return to lower field at pH 1.0. These resonances can be ambiguous as monitors of cellular pH. The pH of both vegetative and encysted cells is 6.0--6.5. Encysted cells under anaerobic conditions show no spectral changes over 24 h. Vegetative cells under similar conditions show time-dependent changes characteristic of variation in cellular pH. There appears to be little correlation between pH and the variously differentiated states (vegetative or encysted) in Acanthamoeba.

摘要

已对营养态和包囊态的卡氏棘阿米巴进行了³¹P核磁共振研究。光谱的一个显著特征是存在P-C键的特征共振。营养细胞显示出尖锐的膦酸盐共振,而包囊细胞显示出宽的膦酸盐共振和窄的磷酸盐共振。使用³¹P核磁共振对模型化合物的研究表明,窄共振来自2-氨基乙基膦酸;包囊细胞的宽成分来自具有长旋转相关时间的分子,如脂膦聚糖或膦蛋白聚集体。营养细胞还显示存在带负电的β-取代膦酸,可能是1-羟基-2-氨基乙基膦酸,这是在细胞膜脂膦聚糖中鉴定出的一种成分。对多种膦酸模型化合物的pH滴定研究表明,其化学位移行为与生物磷酸盐的化学位移行为截然不同。从pH 12酸化时,共振移向高场,然后在pH 1.0时回到低场。这些共振作为细胞pH的监测指标可能会产生歧义。营养细胞和包囊细胞的pH均为6.0 - 6.5。厌氧条件下的包囊细胞在24小时内无光谱变化。在类似条件下的营养细胞显示出细胞pH变化的时间依赖性变化。在棘阿米巴中,pH与各种分化状态(营养态或包囊态)之间似乎几乎没有相关性。

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