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1.
J Biol Inorg Chem ; 24(6): 863-877, 2019 09.
Article in English | MEDLINE | ID: mdl-31414238

ABSTRACT

Outside of the photosynthetic machinery, high-valent manganese cofactors are rare in biology. It was proposed that a recently discovered subclass of ribonucleotide reductase (RNR), class Id, is dependent on a Mn2(IV,III) cofactor for catalysis. Class I RNRs consist of a substrate-binding component (NrdA) and a metal-containing radical-generating component (NrdB). Herein we utilize a combination of EPR spectroscopy and enzyme assays to underscore the enzymatic relevance of the Mn2(IV,III) cofactor in class Id NrdB from Facklamia ignava. Once formed, the Mn2(IV,III) cofactor confers enzyme activity that correlates well with cofactor quantity. Moreover, we present the X-ray structure of the apo- and aerobically Mn-loaded forms of the homologous class Id NrdB from Leeuwenhoekiella blandensis, revealing a dimanganese centre typical of the subclass, with a tyrosine residue maintained at distance from the metal centre and a lysine residue projected towards the metals. Structural comparison of the apo- and metal-loaded forms of the protein reveals a refolding of the loop containing the conserved lysine and an unusual shift in the orientation of helices within a monomer, leading to the opening of a channel towards the metal site. Such major conformational changes have not been observed in NrdB proteins before. Finally, in vitro reconstitution experiments reveal that the high-valent manganese cofactor is not formed spontaneously from oxygen, but can be generated from at least two different reduced oxygen species, i.e. H2O2 and superoxide (O 2·- ). Considering the observed differences in the efficiency of these two activating reagents, we propose that the physiologically relevant mechanism involves superoxide.


Subject(s)
Manganese/metabolism , Ribonucleotide Reductases/metabolism , Aerococcaceae/metabolism , Crystallography, X-Ray , Electron Spin Resonance Spectroscopy , Flavobacteriaceae/metabolism , Free Radicals/metabolism , Hydrogen Peroxide/metabolism , Oxidation-Reduction , Ribonucleotide Reductases/chemistry , Ribonucleotide Reductases/genetics , Superoxides/metabolism
2.
Eur J Clin Microbiol Infect Dis ; 29(6): 727-31, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20411400

ABSTRACT

We report the exceptional case of a severe intraocular Abiotrophia defectiva infection which developed after cataract surgery. Retinal involvement as a complication of A. defectiva endophthalmitis or the combination of acute-onset endophthalmitis with infiltrative keratitis caused by this pathogen has not been described. Moreover, our report represents the first documented ocular A. defectiva infection in Germany. A. defectiva was identified using biotyping and 16S ribosomal RNA gene sequence analysis. Despite vigorous antimicrobial therapy and repeated ocular surgery, visual outcome was poor.


Subject(s)
Aerococcaceae/isolation & purification , Endophthalmitis/microbiology , Gram-Positive Bacterial Infections/diagnosis , Keratitis/microbiology , Retinitis/microbiology , Aerococcaceae/classification , Aerococcaceae/genetics , Aerococcaceae/metabolism , Aged , Bacterial Typing Techniques , Cataract Extraction/adverse effects , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Endophthalmitis/complications , Female , Germany , Gram-Positive Bacterial Infections/microbiology , Humans , Keratitis/complications , RNA, Ribosomal, 16S/genetics , Retinitis/complications , Sequence Analysis, DNA , Sequence Homology, Nucleic Acid , Surgical Wound Infection/microbiology
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