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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Functional and structural studies of the disulfide isomerase DsbC from the plant pathogen Xylella fastidiosa reveals a redox-dependent oligomeric modulation in vitro

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Author(s):
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Santos, Clelton A. [1] ; Toledo, Marcelo A. S. [1] ; Trivella, Daniela B. B. [2] ; Beloti, Lilian L. [1] ; Schneider, Dilaine R. S. [1] ; Saraiva, Antonio M. [1] ; Crucello, Aline [1] ; Azzoni, Adriano R. [1, 3] ; Souza, Alessandra A. [4] ; Aparicio, Ricardo [2] ; Souza, Anete P. [1, 5]
Total Authors: 11
Affiliation:
[1] Univ Estadual Campinas, CBMEG, BR-13083875 Campinas, SP - Brazil
[2] Univ Estadual Campinas, Inst Quim, Lab Biol Estrutural & Cristalog, BR-13083875 Campinas, SP - Brazil
[3] Univ Sao Paulo, Escola Politecn, Dept Engn Quim, BR-05508 Sao Paulo - Brazil
[4] Ctr APTA Citros Sylvio Moreira IAC, Cordeiropolis - Brazil
[5] Univ Estadual Campinas, Dept Biol Vegetal, Inst Biol, BR-13083875 Campinas, SP - Brazil
Total Affiliations: 5
Document type: Journal article
Source: FEBS Journal; v. 279, n. 20, p. 3828-3843, OCT 2012.
Web of Science Citations: 3
Abstract

Xylella fastidiosa is a Gram-negative bacterium that grows as a biofilm inside the xylem vessels of susceptible plants and causes several economically relevant crop diseases. In the present study, we report the functional and low-resolution structural characterization of the X. fastidiosa disulfide isomerase DsbC (XfDsbC). DsbC is part of the disulfide bond reduction/isomerization pathway in the bacterial periplasm and plays an important role in oxidative protein folding. In the present study, we demonstrate the presence of XfDsbC during different stages of X. fastidiosa biofilm development. XfDsbC was not detected during X. fastidiosa planktonic growth; however, after administering a sublethal copper shock, we observed an overexpression of XfDsbC that also occurred during planktonic growth. These results suggest that X. fastidiosa can use XfDsbC in vivo under oxidative stress conditions similar to those induced by copper. In addition, using dynamic light scattering and small-angle X-ray scattering, we observed that the oligomeric state of XfDsbC in vitro may be dependent on the redox environment. Under reducing conditions, XfDsbC is present as a dimer, whereas a putative tetrameric form was observed under nonreducing conditions. Taken together, our findings demonstrate the overexpression of XfDsbC during biofilm formation and provide the first structural model of a bacterial disulfide isomerase in solution. Structured digital abstract XfDsbC and XfDsbC bind by x ray scattering (View Interaction: 1, 2) XfDsbC and XfDsbC bind by molecular sieving (View interaction) XfDsbC and XfDsbC bind by comigration in non denaturing gel electrophoresis (View interaction) XfDsbC and XfDsbC bind by cross-linking study (View Interaction: 1, 2) XfDsbC and XfDsbC bind by dynamic light scattering (View Interaction: 1, 2) (AU)