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光合生物纤细裸藻中的硫酸盐摄取。调节机制及其对半胱氨酸稳态的贡献。

Sulfate uptake in photosynthetic Euglena gracilis. Mechanisms of regulation and contribution to cysteine homeostasis.

作者信息

García-García Jorge Donato, Olin-Sandoval Viridiana, Saavedra Emma, Girard Lourdes, Hernández Georgina, Moreno-Sánchez Rafael

机构信息

Departamento de Bioquímica, Instituto Nacional de Cardiología, México D.F. 14080, México.

出版信息

Biochim Biophys Acta. 2012 Oct;1820(10):1567-75. doi: 10.1016/j.bbagen.2012.05.002. Epub 2012 May 18.

Abstract

BACKGROUND

Sulfate uptake was analyzed in photosynthetic Euglena gracilis grown in sulfate sufficient or sulfate deficient media, or under Cd(2+) exposure or Cys overload, to determine its regulatory mechanisms and contribution to Cys homeostasis.

RESULTS

In control and sulfate deficient or Cd(2+)-stressed cells, one high affinity and two low affinity sulfate transporters were revealed, which were partially inhibited by photophosphorylation and oxidative phosphorylation inhibitors and ionophores, as well as by chromate and molybdate; H(+) efflux also diminished in presence of sulfate. In both sulfate deficient and Cd(2+)-exposed cells, the activity of the sulfate transporters was significantly increased. However, the content of thiol-metabolites was lower in sulfate-deficient cells, and higher in Cd(2+)-exposed cells, in comparison to control cells. In cells incubated with external Cys, sulfate uptake was strongly inhibited correlating with 5-times increased intracellular Cys. Re-supply of sulfate to sulfate deficient cells increased the Cys, γ-glutamylcysteine and GSH pools, and to Cys-overloaded cells resulted in the consumption of previously accumulated Cys. In contrast, in Cd(2+) exposed cells none of the already elevated thiol-metabolites changed.

CONCLUSIONS

(i) Sulfate transport is an energy-dependent process; (ii) sulfate transporters are over-expressed under sulfate deficiency or Cd(2+) stress and their activity can be inhibited by high internal Cys; and (iii) sulfate uptake exerts homeostatic control of the Cys pool.

摘要

背景

分析了在硫酸盐充足或缺乏的培养基中生长,或在镉离子暴露或半胱氨酸过载条件下的光合纤细裸藻的硫酸盐摄取情况,以确定其调节机制及其对半胱氨酸稳态的贡献。

结果

在对照、硫酸盐缺乏或镉离子胁迫的细胞中,发现了一种高亲和力和两种低亲和力的硫酸盐转运蛋白,它们会被光合磷酸化和氧化磷酸化抑制剂、离子载体以及铬酸盐和钼酸盐部分抑制;在有硫酸盐存在时氢离子外流也会减少。在硫酸盐缺乏和镉离子暴露的细胞中,硫酸盐转运蛋白的活性均显著增加。然而,与对照细胞相比,硫酸盐缺乏的细胞中硫醇代谢物的含量较低,而镉离子暴露的细胞中含量较高。在用外部半胱氨酸孵育的细胞中,硫酸盐摄取受到强烈抑制,这与细胞内半胱氨酸增加5倍相关。向硫酸盐缺乏的细胞重新供应硫酸盐会增加半胱氨酸、γ-谷氨酰半胱氨酸和谷胱甘肽池,而向半胱氨酸过载的细胞供应则会导致先前积累的半胱氨酸被消耗。相比之下,在镉离子暴露的细胞中,已经升高的硫醇代谢物均未发生变化。

结论

(i)硫酸盐转运是一个能量依赖的过程;(ii)硫酸盐转运蛋白在硫酸盐缺乏或镉离子胁迫下会过度表达,其活性可被高浓度的细胞内半胱氨酸抑制;(iii)硫酸盐摄取对半胱氨酸池发挥稳态控制作用。

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