Literature DB >> 7993085

Plant and algal interference in bacterial beta-D-galactosidase and beta-D-glucuronidase assays.

C M Davies1, S C Apte, S M Peterson, J L Stauber.   

Abstract

Several commonly occurring freshwater and marine plants and algae were screened for beta-D-galactosidase and beta-D-glucuronidase activities by using a 60-min enzyme assay based on the hydrolysis by these enzymes of 4-methylumbelliferyl-beta-D-galactoside and 4-methylumbelliferyl- beta-glucuronide, respectively. All freshwater plant extracts tested showed beta-D-galactosidase activity several at relatively high levels, and a number also showed beta-D-glucuronidase activity. A number of the macroalgae showed no activity of either enzyme, but those showing beta-D-galactosidase activity also showed beta-D-glucuronidase activity. The majority of microalgae showed some beta-D-galactosidase activity, but few showed beta-D-glucuronidase activity. Further studies, using the commercial Colilert test and the marine water formulation of Colilert, revealed that 2 of 11 of the microalgal species and several of the plant extracts tested caused positive reactions. It was concluded that several plant extracts and algae could significantly interfere with the detection of coliform bacteria and Escherichia coli with the use of rapid assays, on the basis of their production of beta-D-galactosidase and beta-D-glucuronidase, respectively. The significance of the plant and algal interferences in tests such as Colilert is dependent on the levels of enzymes released under natural conditions, the dilution which they may undergo, and the numbers of algal cells present. This also applies to interferences in rapid enzyme assays.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7993085      PMCID: PMC201922          DOI: 10.1128/aem.60.11.3959-3964.1994

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  10 in total

1.  Microalgae and cyanobacteria as a source of glycosidase inhibitors.

Authors:  R J Cannell; S J Kellam; A M Owsianka; J M Walker
Journal:  J Gen Microbiol       Date:  1987-07

2.  Role of cloned carotenoid genes expressed in Escherichia coli in protecting against inactivation by near-UV light and specific phototoxic molecules.

Authors:  R W Tuveson; R A Larson; J Kagan
Journal:  J Bacteriol       Date:  1988-10       Impact factor: 3.490

3.  Regulation of beta-glucuronidase synthesis in Escherichia coli K-12: constitutive mutants specifically derepressed for uidA expression.

Authors:  M Novel; G Novel
Journal:  J Bacteriol       Date:  1976-07       Impact factor: 3.490

4.  Induction and general properties of beta-galactosidase and beta-galactoside permease in Pseudomonas BAL-31.

Authors:  C Hidalgo; J Reyes; R Goldschmidt
Journal:  J Bacteriol       Date:  1977-02       Impact factor: 3.490

5.  Evaluation of colilert-marine water for detection of total coliforms and Escherichia coli in the marine environment.

Authors:  C J Palmer; Y L Tsai; A L Lang; L R Sangermano
Journal:  Appl Environ Microbiol       Date:  1993-03       Impact factor: 4.792

6.  Rapid detection of total and fecal coliforms in water by enzymatic hydrolysis of 4-methylumbelliferone-beta-D-galactoside.

Authors:  J D Berg; L Fiksdal
Journal:  Appl Environ Microbiol       Date:  1988-08       Impact factor: 4.792

7.  Rapid enumeration of Fecal Coliforms in water by a colorimetric beta-galactosidase assay.

Authors:  L S Warren; R E Benoit; J A Jessee
Journal:  Appl Environ Microbiol       Date:  1978-01       Impact factor: 4.792

8.  A note on starch hydrolysis and beta-glucuronidase activity among flavobacteria.

Authors:  J P Petzel; P A Hartman
Journal:  J Appl Bacteriol       Date:  1986-11

9.  New medium for the simultaneous detection of total coliforms and Escherichia coli in water.

Authors:  K P Brenner; C C Rankin; Y R Roybal; G N Stelma; P V Scarpino; A P Dufour
Journal:  Appl Environ Microbiol       Date:  1993-11       Impact factor: 4.792

10.  Rapid identification of Enterobacteriaceae. II. Use of a beta-glucuronidase detecting agar medium (PGUA agar) for the identification of E. coli in primary cultures of urine samples.

Authors:  M Kilian; P Bülow
Journal:  Acta Pathol Microbiol Scand B       Date:  1979-10
  10 in total
  5 in total

1.  Marine bacteria cause false-positive results in the Colilert-18 rapid identification test for Escherichia coli in Florida waters.

Authors:  John M Pisciotta; Damon F Rath; Paul A Stanek; D Michael Flanery; Valerie J Harwood
Journal:  Appl Environ Microbiol       Date:  2002-02       Impact factor: 4.792

2.  Genotypic and phenotypic characterization of Escherichia coli isolates from feces, hands, and soils in rural Bangladesh via the Colilert Quanti-Tray System.

Authors:  Timothy R Julian; M Aminul Islam; Amy J Pickering; Subarna Roy; Erica R Fuhrmeister; Ayse Ercumen; Angela Harris; Jason Bishai; Kellogg J Schwab
Journal:  Appl Environ Microbiol       Date:  2014-12-29       Impact factor: 4.792

3.  Enzyme characteristics of beta-D-galactosidase- and beta-D-glucuronidase-positive bacteria and their interference in rapid methods for detection of waterborne coliforms and Escherichia coli.

Authors:  I Tryland; L Fiksdal
Journal:  Appl Environ Microbiol       Date:  1998-03       Impact factor: 4.792

4.  Comparison of membrane filtration and multiple-tube fermentation by the colilert and enterolert methods for detection of waterborne coliform bacteria, Escherichia coli, and enterococci used in drinking and bathing water quality monitoring in southern sweden.

Authors:  K F Eckner
Journal:  Appl Environ Microbiol       Date:  1998-08       Impact factor: 4.792

Review 5.  Marine swimming-related illness: implications for monitoring and environmental policy.

Authors:  S E Henrickson; T Wong; P Allen; T Ford; P R Epstein
Journal:  Environ Health Perspect       Date:  2001-07       Impact factor: 9.031

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.