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Specific amplification of iron receptor genes in Xylella fastidiosa strains from different hosts
Pacheco, Flávia Teresa Hansen; Silva-Stenico, Maria Estela; Etchegaray, Augusto; Gomes, José Elias; Carrilho, Emanuel; Tsai, Siu Mui.
Affiliation
  • Pacheco, Flávia Teresa Hansen; Universidade de São Paulo. Centro de Energia Nuclear na Agricultura. Laboratório de Biologia Celular e Molecular. Piracicaba. BR
  • Silva-Stenico, Maria Estela; Universidade de São Paulo. Centro de Energia Nuclear na Agricultura. Laboratório de Biologia Celular e Molecular. Piracicaba. BR
  • Etchegaray, Augusto; Universidade de São Paulo. Centro de Energia Nuclear na Agricultura. Laboratório de Biologia Celular e Molecular. Piracicaba. BR
  • Gomes, José Elias; Universidade de São Paulo. Centro de Energia Nuclear na Agricultura. Laboratório de Biologia Celular e Molecular. Piracicaba. BR
  • Carrilho, Emanuel; Universidade de São Paulo. Instituto de Química de São Carlos. Laboratório de Cromatografia. São Carlos. BR
  • Tsai, Siu Mui; Universidade de São Paulo. Centro de Energia Nuclear na Agricultura. Laboratório de Biologia Celular e Molecular. Piracicaba. BR
Genet. mol. biol ; 29(1): 137-141, 2006. tab
Article in English | LILACS | ID: lil-424750
Responsible library: BR26.1
ABSTRACT
Bacterial production of siderophores may involve specific genes related to nonribosomal peptide and polyketide biosynthesis, which have not been fully identified in the genome of Xylella fastidiosa strain 9a5c. However, a search for siderophore-related genes in strain 9a5c indicated five membrane receptors, including siderophore, ferrichrome-iron and hemin receptors. All these biomolecules are thought to be associated with iron transport and utilization. Eighty isolates obtained from citrus orchards containing trees that developed citrus variegated chlorosis (CVC) were screened for siderophore production. The results demonstrated that only 10 of the isolates did not produce siderophores. Additional strains obtained from coffee, almond, mulberry, elm, ragweed, periwinkle and grape also infected by X. fastidiosa were also shown by the chromeazurol bioassay to produce siderophores. In order to correlate siderophore production with the presence of siderophore-related genes, a polymerase chain reaction (PCR) was developed using specific primers for the catechol-type ferric enterobactin receptor (pfeA) and the hydroxamate-type ferrisiderophore receptor (fiuA) genes of strain 9a5c. The PCR results confirmed our hypothesis by demonstrating that amplification products were detected in all strains except for those isolates that did not produce siderophores.
Subject(s)
Full text: Available Collection: International databases Database: LILACS Main subject: Xylella / Peptide Biosynthesis, Nucleic Acid-Independent / Multienzyme Complexes Limits: Animals Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2006 Document type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR
Full text: Available Collection: International databases Database: LILACS Main subject: Xylella / Peptide Biosynthesis, Nucleic Acid-Independent / Multienzyme Complexes Limits: Animals Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2006 Document type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR
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