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肺炎链球菌锰缺乏的铁补偿机制。

The mechanism of iron-compensation for manganese deficiency of Streptococcus pneumoniae.

机构信息

Key Laboratory of Functional Protein Research of Guangdong Higher Education Institutes, Institute of Life and Health Engineering, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.

Key Laboratory of Gene Engineering of the Ministry of Education and State Key Laboratory of Biocontrol, College of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China.

出版信息

J Proteomics. 2018 Jul 30;184:62-70. doi: 10.1016/j.jprot.2018.06.004. Epub 2018 Jun 18.

Abstract

UNLABELLED

Given their involvement in catalysis, infection, and biofilm formation, Fe and Mn are essential for bacterial survival and virulence. In this study, we found that Streptococcus pneumoniae (S. pneumoniae) could grow in the Mn-deficient medium (MDCM). Furthermore, findings showed that the Fe concentration in the bacterium increased when the Mn concentration decreased. In addition, it was noted that supplementing MDCM with Fe resulted in the recovery of bacterial growth. Quantitative proteomics using stable-isotope dimethyl labeling was performed to investigate the adaptive growth mechanism of S. pneumoniae under Mn-deficient conditions. It was found that the expression levels of 25 proteins were downregulated, whereas those of 54 proteins were upregulated in S. pneumoniae grown in MDCM. It was also noted that several of the downregulated proteins were involved in cell energy metabolism, amino acid synthesis, and reduction of oxidation products. More importantly, several ATP-binding cassette transporters related to Fe uptake, such as PiuA, PiaA, PitA, and SPD_1609, were overexpressed for increased Fe uptake from the MDCM. The results suggest that Mn deficiency disturbs multiple metabolic processes in S. pneumoniae. Furthermore, it causes a compensatory effect of Fe for Mn, which is beneficial for the survival of the bacterium in extreme environments.

SIGNIFICANCE

The relationship between manganese and iron metabolism in S. pneumoniae has not been clearly revealed. In this paper, we suggest that Mn limitation disturbs multiple metabolic processes and evidently decreases the ATP level in the bacterium. In order to survive in this extreme environment, bacteria upregulated three type of Fe ion transporters PiuABC (heme), PiaABC (ferrichrome) and PitABC (Fe) to uptake enough Fe ions to response to Mn deficiency. Therefore, this study reveals a bacterial mechanism of Fe compensation for Mn, and provides new insight for investigating the relativeness of Fe and Mn metabolism of bacteria.

摘要

未加说明

鉴于其在催化、感染和生物膜形成中的作用,铁和锰对细菌的生存和毒力至关重要。在这项研究中,我们发现肺炎链球菌(S. pneumoniae)可以在缺锰培养基(MDCM)中生长。此外,研究结果表明,当锰浓度降低时,细菌内的铁浓度增加。此外,值得注意的是,在 MDCM 中补充铁可以恢复细菌的生长。使用稳定同位素二甲基标记的定量蛋白质组学来研究肺炎链球菌在缺锰条件下的适应性生长机制。结果发现,在 MDCM 中生长的肺炎链球菌中有 25 种蛋白质的表达水平下调,而有 54 种蛋白质的表达水平上调。还注意到,下调的几种蛋白质参与细胞能量代谢、氨基酸合成和氧化产物的还原。更重要的是,几种与铁摄取相关的 ABC 转运蛋白,如 PiuA、PiaA、PitA 和 SPD_1609,过度表达以增加从 MDCM 中摄取铁。结果表明,锰缺乏会扰乱肺炎链球菌中的多种代谢过程。此外,它还会导致铁对锰的补偿效应,这有利于细菌在极端环境中的生存。

意义

肺炎链球菌中锰和铁代谢之间的关系尚不清楚。在本文中,我们认为锰限制扰乱了多种代谢过程,并明显降低了细菌中的 ATP 水平。为了在这种极端环境中生存,细菌上调了三种铁离子转运蛋白 PiuABC(血红素)、PiaABC(铁红素)和 PitABC(Fe)以摄取足够的铁离子来应对锰缺乏。因此,本研究揭示了细菌铁补偿锰的机制,为研究细菌铁和锰代谢的相关性提供了新的见解。

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