Flint Annika, Stintzi Alain
Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Ottawa Institute of Systems Biology, Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada
J Bacteriol. 2015 Mar;197(5):1002-11. doi: 10.1128/JB.02346-14. Epub 2014 Dec 29.
Catalase enzymes detoxify H2O2 by the dismutation of H2O2 into O2 and H2O through the use of hemin cofactors. While the structure and biochemical properties of catalase enzymes have been well characterized over many decades of research, it remained unclear how catalases acquire hemin. We have previously reported that Cj1386 is essential for ensuring proper hemin content in Campylobacter jejuni catalase (KatA) (A. Flint, Y. Q. Sun, and A. Stintzi, J Bacteriol 194: 334-345, 2012). In this report, an in-depth molecular characterization of Cj1386 was performed to elucidate the mechanistic details of this association. Coimmunoprecipitation assays revealed that KatA-Cj1386 transiently interact in vivo, and UV-visible spectroscopy demonstrated that purified Cj1386 protein binds hemin. Furthermore, hemin titration experiments determined that hemin binds to Cj1386 in a 1:1 ratio with hexacoordinate hemin binding. Mutagenesis of potential hemin-coordinating residues in Cj1386 showed that tyrosine 57 was essential for hemin coordination when Cj1386 was overexpressed in Escherichia coli. The importance of tyrosine 57 in hemin trafficking in vivo was confirmed by introducing the cj1386(Y57A) allele into a C. jejuni Δcj1386 mutant background. The cj1386(Y57A) mutation resulted in increased sensitivity toward H2O2 relative to the wild type, suggesting that KatA was not functional in this strain. In support of this finding, KatA immunoprecipitated from the Δcj1386+cj1386(Y57A) mutant had significantly reduced hemin content compared to that of the cj1386(WT) background. Overall, these findings indicate that Cj1386 is involved in directly trafficking hemin to KatA and that tyrosine 57 plays a key role in this function.
过氧化氢酶通过利用血红素辅因子将过氧化氢歧化为氧气和水来解毒过氧化氢。虽然经过数十年的研究,过氧化氢酶的结构和生化特性已得到充分表征,但过氧化氢酶如何获取血红素仍不清楚。我们之前报道过,Cj1386对于确保空肠弯曲菌过氧化氢酶(KatA)中适当的血红素含量至关重要(A. Flint、Y. Q. Sun和A. Stintzi,《细菌学杂志》194:334 - 345,2012年)。在本报告中,对Cj1386进行了深入的分子表征,以阐明这种关联的机制细节。免疫共沉淀分析表明,KatA - Cj1386在体内短暂相互作用,紫外可见光谱表明纯化的Cj1386蛋白结合血红素。此外,血红素滴定实验确定血红素以1:1的比例与六配位血红素结合的方式结合到Cj1386上。对Cj1386中潜在的血红素配位残基进行诱变表明,当Cj1386在大肠杆菌中过表达时,酪氨酸57对于血红素配位至关重要。通过将cj^1386(Y57A)等位基因引入空肠弯曲菌Δcj1386突变体背景中,证实了酪氨酸57在体内血红素转运中的重要性。与野生型相比,cj1386(Y57A)突变导致对过氧化氢的敏感性增加,这表明KatA在该菌株中无功能。支持这一发现的是,与cj1386(WT)背景相比,从Δcj1386 + cj1386(Y57A)突变体中免疫沉淀的KatA的血红素含量显著降低。总体而言,这些发现表明Cj1386参与将血红素直接转运至KatA,并且酪氨酸57在该功能中起关键作用。