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


Autoria(s): Santos, Clelton A.; Toledo, Marcelo A. S.; Trivella, Daniela B. B.; Beloti, Lilian L.; Schneider, Dilaine R. S.; Saraiva, Antonio M.; Crucello, Aline; Azzoni, Adriano R.; Souza, Alessandra A.; Aparicio, Ricardo; Souza, Anete P.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

16/08/2013

16/08/2013

2012

Resumo

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)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [Process 01/07533-7, Process 08/55690-3]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Identificador

FEBS JOURNAL, HOBOKEN, v. 279, n. 20, supl. 1, Part 3, pp. 3828-3843, OCT, 2012

1742-464X

http://www.producao.usp.br/handle/BDPI/32593

10.1111/j.1742-4658.2012.08743.x

http://dx.doi.org/10.1111/j.1742-4658.2012.08743.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

HOBOKEN

Relação

FEBS JOURNAL

Direitos

openAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #BIOFILM FORMATION #DSBC #OLIGOMERIC ASSEMBLY #SAXS #XYLELLA FASTIDIOSA #SMALL-ANGLE SCATTERING #X-RAY-SCATTERING #ESCHERICHIA-COLI DSBC #BOND FORMATION #CRYSTAL-STRUCTURE #BIOFILM FORMATION #GENE-EXPRESSION #THIOREDOXIN #PROTEINS #ISOMERIZATION #BIOCHEMISTRY & MOLECULAR BIOLOGY
Tipo

article

original article

publishedVersion