Production of polyclonal and monoclonal antibodies specific against membrane proteins of “Candidatus Phytoplasma asteris”, chrysanthemum yellows isolate (CY)) (Articolo in rivista)

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Label
  • Production of polyclonal and monoclonal antibodies specific against membrane proteins of “Candidatus Phytoplasma asteris”, chrysanthemum yellows isolate (CY)) (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Alternative label
  • Galetto, L., (1) Bosco, D., (2) Fletcher, J., Marzachì, C. (2007)
    Production of polyclonal and monoclonal antibodies specific against membrane proteins of “Candidatus Phytoplasma asteris”, chrysanthemum yellows isolate (CY))
    in Bulletin of insectology
    (literal)
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  • Galetto, L., (1) Bosco, D., (2) Fletcher, J., Marzachì, C. (literal)
Pagina inizio
  • 211 (literal)
Pagina fine
  • 212 (literal)
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  • This work was funded by MIUR under the FIRB grant RBAU014S8A (literal)
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  • 60(2) (literal)
Rivista
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  • The molecular reagents produced in this work are currently used to study the role of membrane proteins in the interaction between CY and its plant and vector hosts. (literal)
Note
  • ISI Web of Science (WOS) (literal)
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  • (1) Università degli Studi di Torino, Facoltà di Agraria, Di.Va.P.R.A., Entomologia e Zoologia Applicate all’Ambiente “Carlo Vidano”, Via L. Da Vinci 44, Grugliasco (TO) 10095, Italy. (2) Oklahoma State University, Department of Entomology & Plant Pathology, Noble Research Center, Stillwater OK 74078, U.S. (literal)
Titolo
  • Production of polyclonal and monoclonal antibodies specific against membrane proteins of “Candidatus Phytoplasma asteris”, chrysanthemum yellows isolate (CY)) (literal)
Abstract
  • Three genes encoding membrane proteins of chrysanthemum yellows phytoplasma were cloned and sequenced: secY, amp and artI encoding the protein translocase subunit SecY, the antigenic membrane protein Amp and the arginine transporter ArtI, re-spectively. Alignments of CY-specific secY sequences with the corresponding genes of other phytoplasmas confirmed the 16SrDNA-based classification, while Amp sequences resulted highly variable. Five CY partial sequences were cloned into pRSetC expression vector and two (Amp 64-224 and ArtI 131-512) were expressed as fusion antigens in E. coli for the production of CY-specific polyclonal antisera (A416 against Amp 64-224; A407 against ArtI 131-512) and monoclonal antibodies. A416 recognized, in Western blots, the full length Amp from CY-infected plants (periwinkle, daisy) and insect vectors (Euscelidius variegatus, Macrosteles quadripunctulatus). A416 also reacted to European aster yellows (EAY) and primula yellows (PY) phy-toplasmas and to Northern Italian strains of “Ca. P. asteris” from lettuce (LY163) and gladiolus (GLA), but not to American aster yellows (AAY) and clover phyllody (CPh) phytoplasmas. (literal)
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