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集胞藻PCC 6803盐胁迫应答的蛋白质组分析

Proteome analysis of salt stress response in the cyanobacterium Synechocystis sp. strain PCC 6803.

作者信息

Fulda Sabine, Mikkat Stefan, Huang Fang, Huckauf Jana, Marin Kay, Norling Birgitta, Hagemann Martin

机构信息

Universität Rostock, Institut Biowissenschaften, Pflanzengenetik, Rostock, Germany.

出版信息

Proteomics. 2006 May;6(9):2733-45. doi: 10.1002/pmic.200500538.

Abstract

In the present study, changes in protein synthesis patterns after salt shock visualized by 35S-methionine labeling and the changed protein composition in salt-acclimated cells of the cyanobacterium Synechocystis sp. strain PCC 6803 were analyzed by a combination of 2-DE for protein separation and PMF for protein identification. As a basis for the differential analysis, a proteome map with 500 identified protein spots comprising 337 different protein species was established. Fifty-five proteins were found, which are induced by salt shock or accumulated after long-term salt acclimation. Some of the proteins are salt stress-specific, such as enzymes involved in the synthesis of the compatible solute glucosylglycerol, while most of them are involved in general stress acclimation. Particularly, heat-shock proteins and proteins acting against lesions by reactive oxygen species were found. Moreover, changes in enzymes involved in basic carbohydrate metabolism were detected. The dynamic of the proteome of salt-stressed Synechocystis cells was compared to previous data concerning transcriptome analysis revealing that 89% of the proteins induced shortly after salt shock were also found to be induced at the RNA level. However, 42% of the stably up-regulated proteins in salt-acclimated cells were not detected previously using DNA microarrays. The comparison of transcriptomic and proteomic analyses shows the significance of post-transcriptional regulatory mechanisms in acclimation of Synechocystis to high salt concentrations.

摘要

在本研究中,通过³⁵S - 甲硫氨酸标记可视化盐胁迫后蛋白质合成模式的变化,并结合二维电泳(2 - DE)进行蛋白质分离和肽质量指纹图谱(PMF)进行蛋白质鉴定,分析了集胞藻PCC 6803盐适应细胞中蛋白质组成的变化。作为差异分析的基础,建立了一个包含500个已鉴定蛋白质斑点、由337种不同蛋白质组成的蛋白质组图谱。发现有55种蛋白质是由盐胁迫诱导产生或在长期盐适应后积累的。其中一些蛋白质是盐胁迫特异性的,例如参与相容性溶质葡糖基甘油合成的酶,而大多数蛋白质则参与一般胁迫适应。特别地,发现了热休克蛋白和对抗活性氧损伤的蛋白质。此外,还检测到参与基本碳水化合物代谢的酶的变化。将盐胁迫集胞藻细胞的蛋白质组动态与先前关于转录组分析的数据进行比较,结果显示盐胁迫后不久诱导产生的蛋白质中有89%在RNA水平上也被诱导。然而,在盐适应细胞中稳定上调的蛋白质中有42%在之前使用DNA微阵列时未被检测到。转录组学和蛋白质组学分析的比较显示了转录后调控机制在集胞藻适应高盐浓度过程中的重要性。

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