Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/27915
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dc.contributor.authorBalali, G.-
dc.contributor.authorWhisson, D.-
dc.contributor.authorScott, E.-
dc.contributor.authorNeate, S.-
dc.date.issued1996-
dc.identifier.citationFungal Biology, 1996; 100(4):467-470-
dc.identifier.issn0953-7562-
dc.identifier.issn1469-8102-
dc.identifier.urihttp://hdl.handle.net/2440/27915-
dc.description.abstractAnastomosis group 3 (AG-3) isolates of Rhizoctonia solani that cause black scurf were recovered from diseased potatoes in Virginia and Lenswood in South Australia. A highly repeated and specific DNA fingerprinting probe, pR3718, prepared from AG-3 isolate R37, hybridized to Southem blots of all AG-3 isolates tested, but had no or very weak reactions with isolates from other anastomosis groups. Genetic variation among the isolates was observed using the fingerprinting probe. Sac I or Hind III restriction endonuclease digests of DNA prepared from 136 AG-3 isolates revealed 38 fingerprint patterns, each containing 12-19 Sac I or Hind III fragments. Because the pR3718 clone recognizes a DNA sequence with a high number of copies per genome and appears to be specific for AG-3 isolates of Rhizoctonia, it has the potential to be used as a diagnostic tool to study the epidemiology, genetic diversity and population dynamics of this important plant pathogen.-
dc.language.isoen-
dc.publisherCAMBRIDGE UNIV PRESS-
dc.source.urihttp://dx.doi.org/10.1016/s0953-7562(96)80145-6-
dc.titleDNA fingerprinting probe specific to isolates of Rhizoctonia solani AG-3-
dc.typeJournal article-
dc.identifier.doi10.1016/S0953-7562(96)80145-6-
pubs.publication-statusPublished-
dc.identifier.orcidScott, E. [0000-0001-6829-519X]-
dc.identifier.orcidNeate, S. [0000-0003-0766-198X]-
Appears in Collections:Agriculture, Food and Wine publications
Aurora harvest 2

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