Fluorescent antibody-viability staining and b-glucuronidase assay as rapid methods for monitoring Escherichia coli viability in coastal marine waters (Articolo in rivista)

Type
Label
  • Fluorescent antibody-viability staining and b-glucuronidase assay as rapid methods for monitoring Escherichia coli viability in coastal marine waters (Articolo in rivista) (literal)
Anno
  • 2006-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1080/15321810500403599 (literal)
Alternative label
  • Caruso, G., De Pasquale, F., Mancuso, M., Zampino, D., Crisafi, E. (2006)
    Fluorescent antibody-viability staining and b-glucuronidase assay as rapid methods for monitoring Escherichia coli viability in coastal marine waters
    in Journal of immunoassay & immunochemistry; Marcel Dekker, Inc., New York (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Caruso, G., De Pasquale, F., Mancuso, M., Zampino, D., Crisafi, E. (literal)
Pagina inizio
  • 1 (literal)
Pagina fine
  • 13 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • prodotto con 2 citazioni SCOPUS, 2 citazioni ISI, SJR 2011 : 0.274 - SJR 2009: 0.209, IF 2009: 0.508 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 27 (literal)
Rivista
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  • 13 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 1 (literal)
Note
  • ubMe (literal)
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
  • Google Scholar (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Institute for Coastal Marine Environment (IAMC)-CNR, Section of Messina, Messina, Italy ICTP-Catania (literal)
Titolo
  • Fluorescent antibody-viability staining and b-glucuronidase assay as rapid methods for monitoring Escherichia coli viability in coastal marine waters (literal)
Abstract
  • A faecal pollution monitoring of coastal Messina waters was performed by comparing three (microscopic, enzyme, and culture) methods. Evidence of Escherichia coli cells (29.99 to 96.79% of the total enteropathogenic serotypes) retaining their viability into the marine environment was shown. beta-Glucuronidase activity rates suggested that living cells were also metabolically active. Heavily polluted sites were detected, where improperly treated urban wastes were discharged. Significant relationships between microscopic and enzymatic data proved both methods to be suitable alternatives to the culture method for E. coli detection, improving environmental quality assessment. (literal)
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