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外蛋白中的甲硫氨酸残基及其由甲硫氨酸亚砜还原酶AB进行的循环利用作为一种抗氧化策略。

Methionine Residues in Exoproteins and Their Recycling by Methionine Sulfoxide Reductase AB Serve as an Antioxidant Strategy in .

作者信息

Madeira Jean-Paul, Alpha-Bazin Béatrice M, Armengaud Jean, Duport Catherine

机构信息

Sécurité et Qualité des Produits d'Origine Végétale (SQPOV), UMR0408, Avignon Université, Institut National de la Recherche AgronomiqueAvignon, France.

Commissariat à lEnergie Atomique, Direction de la Recherche Fondamentale, Institut des Sciences du vivant Frédéric-Joliot (Joliot), Service de Pharmacologie et Immunoanalyse, Laboratoire Innovations Technologiques pour la Détection et le Diagnostic (Li2D)Bagnols-sur-Cèze, France.

出版信息

Front Microbiol. 2017 Jul 26;8:1342. doi: 10.3389/fmicb.2017.01342. eCollection 2017.

Abstract

During aerobic respiratory growth, is exposed to continuously reactive oxidant, produced by partially reduced forms of molecular oxygen, known as reactive oxygen species (ROS). The sulfur-containing amino acid, methionine (Met), is particularly susceptible to ROS. The major oxidation products, methionine sulfoxides, can be readily repaired by methionine sulfoxide reductases, which reduce methionine sulfoxides [Met(O)] back to methionine. Here, we show that methionine sulfoxide reductase AB (MsrAB) regulates the Met(O) content of both the cellular proteome and exoproteome of in a growth phase-dependent manner. Disruption of leads to metabolism changes resulting in enhanced export of Met(O) proteins at the late exponential growth phase and enhanced degradation of exoproteins. This suggests that can modulate its capacity and specificity for protein export/secretion through the growth phase-dependent expression of . Our results also show that cytoplasmic MsrAB recycles Met residues in enterotoxins, which are major virulence factors in .

摘要

在有氧呼吸生长过程中,细胞会持续暴露于由部分还原形式的分子氧产生的活性氧化剂中,这些氧化剂被称为活性氧(ROS)。含硫氨基酸甲硫氨酸(Met)对ROS尤为敏感。主要的氧化产物甲硫氨酸亚砜可通过甲硫氨酸亚砜还原酶轻易修复,该酶可将甲硫氨酸亚砜[Met(O)]还原回甲硫氨酸。在此,我们表明甲硫氨酸亚砜还原酶AB(MsrAB)以生长阶段依赖的方式调节细胞蛋白质组和外蛋白质组中的Met(O)含量。该酶的破坏会导致代谢变化,从而在指数生长后期增强Met(O)蛋白的输出,并增强外蛋白的降解。这表明该酶可通过依赖生长阶段的表达来调节其蛋白质输出/分泌的能力和特异性。我们的结果还表明,细胞质中的MsrAB可循环利用肠毒素中的甲硫氨酸残基,而肠毒素是该菌的主要毒力因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e87/5526929/be21985db229/fmicb-08-01342-g0001.jpg

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