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sp. PCC 6803 中 SigE 突变株的中心代谢物和光合系统的比较靶向蛋白质组学

Comparative Targeted Proteomics of the Central Metabolism and Photosystems in SigE Mutant Strains of sp. PCC 6803.

机构信息

Department of Bioinformatic Engineering, Graduate School of Information Science and Technology, Osaka University, 1-5 Yamadaoka, Suita, Osaka 565-0871, Japan.

School of Agriculture, Meiji University, 1-1-1, Higashimita, Tama, Kawasaki, Kanagawa 214-8571, Japan.

出版信息

Molecules. 2018 May 1;23(5):1051. doi: 10.3390/molecules23051051.

Abstract

A targeted proteome analysis was conducted to investigate the SigE dependent-regulation of central metabolism in sp. PCC 6803 by directly comparing the protein abundance profiles among the wild type, a deletion mutant (Δ), and a over-expression (ox) strains. Expression levels of 112 target proteins, including the central metabolism related-enzymes and the subunits of the photosystems, were determined by quantifying the tryptic peptides in the multiple reaction monitoring (MRM) mode of liquid-chromatography⁻triple quadrupole mass spectrometry (LC⁻MS/MS). Comparison with gene-expression data showed that although the abundance of Gnd protein was closely correlated with that of mRNA, there were poor correlations for GdhA/ and glycogen degradation-related genes such as GlgX/ and GlgP/ pairs. These results suggested that the regulation of protein translation and degradation played a role in regulating protein abundance. The protein abundance profile suggested that SigE overexpression reduced the proteins involved in photosynthesis and increased GdhA abundance, which is involved in the nitrogen assimilation pathway using NADPH. The results obtained in this study successfully demonstrated that targeted proteome analysis enables direct comparison of the abundance of central metabolism- and photosystem-related proteins.

摘要

进行了靶向蛋白质组分析,以通过直接比较野生型、缺失突变体(Δ)和过表达(ox)菌株之间的蛋白质丰度谱,研究 SigE 对 sp. PCC 6803 中心代谢的依赖调节。通过定量液相色谱⁻三重四极杆质谱(LC-MS/MS)的多反应监测(MRM)模式下的胰蛋白酶肽,确定了 112 种靶蛋白的表达水平,包括中心代谢相关酶和光系统的亚基。与基因表达数据的比较表明,尽管 Gnd 蛋白的丰度与 mRNA 的丰度密切相关,但 GdhA/和糖原降解相关基因(如 GlgX/和 GlgP/对)的丰度相关性较差。这些结果表明,蛋白质翻译和降解的调节在调节蛋白质丰度方面发挥了作用。蛋白质丰度谱表明 SigE 过表达减少了参与光合作用的蛋白质,并增加了 GdhA 的丰度,GdhA 参与了使用 NADPH 的氮同化途径。本研究的结果成功地证明了靶向蛋白质组分析能够直接比较中心代谢和光系统相关蛋白质的丰度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cbb/6102573/e9dd789052b1/molecules-23-01051-g001.jpg

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