Rv2074 is a novel F420H2-dependent biliverdin reductase in Mycobacterium tuberculosis

被引:30
作者
Ahmed, F. Hafna [1 ]
Mohamed, A. Elaaf [1 ]
Carr, Paul D. [1 ]
Lee, Brendon M. [1 ]
Condic-Jurkic, Karmen [1 ]
O'Mara, Megan L. [1 ]
Jackson, Colin J. [1 ]
机构
[1] Australian Natl Univ, Res Sch Chem, Canberra, ACT 2601, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
F420; biliverdin reductase; biliverdin; bilirubin; Mycobacterium tuberculosis; mycobacteria; enzyme catalysis; flavin/deazaflavin oxidoreductase; IX-ALPHA REDUCTASE; DEAZAFLAVIN-DEPENDENT NITROREDUCTASE; PYRIDOXINE 5'-PHOSPHATE OXIDASE; BETA REDUCTASE; CATALYTIC MECHANISM; HUMAN MACROPHAGES; ESCHERICHIA-COLI; HEME-DEGRADATION; BILIRUBIN-IX; ANTIOXIDANT;
D O I
10.1002/pro.2975
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bilirubin is a potent antioxidant that is produced from the reduction of the heme degradation product biliverdin. In mammalian cells and Cyanobacteria, NADH/NADPH-dependent biliverdin reductases (BVRs) of the Rossmann-fold have been shown to catalyze this reaction. Here, we describe the characterization of Rv2074 from Mycobacterium tuberculosis, which belongs to a structurally and mechanistically distinct family of F420H2-dependent BVRs (F-BVRs) that are exclusively found in Actinobacteria. We have solved the crystal structure of Rv2074 bound to its cofactor, F-420, and used this alongside molecular dynamics simulations, site-directed mutagenesis and NMR spectroscopy to elucidate its catalytic mechanism. The production of bilirubin by Rv2074 could exploit the anti-oxidative properties of bilirubin and contribute to the range of immuno-evasive mechanisms that have evolved in M. tuberculosis to allow persistent infection. PDB Code:
引用
收藏
页码:1692 / 1709
页数:18
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