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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.)

Evidences of siderophores synthesis by Grapevine Xylella fastidiosa, causal agent of pierce's disease, through instrumental approaches

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Author(s):
Simionato, Ana Valeria C. [1, 2, 3] ; Silva-Stenico, Maria Estela [4] ; Tsai, Siu Mui [4] ; Carrilho, Emanuel [1, 3]
Total Authors: 4
Affiliation:
[1] Univ Estadual Campinas, Inst Nacl Ciencia & Tecnol Bioanalit, BR-13083970 Campinas, SP - Brazil
[2] Univ Estadual Campinas, Grp Toxicol Alimentos & Farmacos, BR-13083970 Campinas, SP - Brazil
[3] Univ Sao Paulo, Grp Bioanalit Microfabricacao & Separacoes, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP - Brazil
[4] Univ Sao Paulo, Lab Biol Celular & Mol, Ctr Energia Nucl Agr, BR-13416000 Piracicaba, SP - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Journal of the Brazilian Chemical Society; v. 21, n. 4, p. 635-641, 2010.
Web of Science Citations: 1
Abstract

Siderophore molecules from grapevine Xylella fastidiosa were investigated. Such metabolites sequester iron, an essential element, from the host, making them a potential factor of pathogenicty. In an iron-limited medium, siderophores were detected in culture plates of X. fastidiosa containing the complex Chromeazurol S (CAS). A combination of different instrumental analyses was used for siderophore(s) characterization, such as: immobilized metal affinity chromatography (IMAC), micelar electrokinetic capillary chromatography (MEKC) and electrospray-mass spectrometry (ESI-MS). The results show that grapevine X. fastidiosa produced siderophore(s), as confirmed by the CAS plate assay. The extraction of the compound(s) using IMAC with immobilized Fe3+ was important for analyte purification. The chelator was not separated by capillary zone electrophoresis, indicating the possibility of a neutral compound under the investigated pHs. MEKC runs presented a different peak (when compared to the control analysis) which represented a slightly hydrophobic compound. Mass spectrometry showed that the compound(s) may have a relative molecular mass within the expected range for siderophore molecules, such as 875, 1004 and 1092 Da. (AU)

FAPESP's process: 08/57805-2 - Institute of Bioanalytics
Grantee:Lauro Tatsuo Kubota
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 99/09177-1 - Biodiversity of endophytic microorganisms and their biotechnological potential
Grantee:Itamar Soares de Melo
Support Opportunities: BIOTA-FAPESP Program - Thematic Grants