Abstracts - faqs.org

Abstracts

Biological sciences

Search abstracts:
Abstracts » Biological sciences

Characterization of an atrazine-degrading Pseudaminobacter sp. isolated from Canadian and French agricultural soils

Article Abstract:

Research has been conducted on the herbicide atrazine used in corn production. The isolation of bacterial strains that use this herbicide as a nitrogen source has been investigated.

Author: Zhu Hong, Topp, Edward, Nour, Sarah M., Houot, Sabine, Lewis, Melanie, Cuppels, Diane
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 2000
Canada, France, Statistical Data Included, Analysis, Bacteria, Nitrogen (Chemical element), Nitrogen, Microbiological research, Atrazine

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Characterization of S-triazine herbicide metabolism by a Nocardioides sp. isolated from agricultural soils

Article Abstract:

Researchers report a novel s-triazine hydrolase from Nocardioides sp. strains that degrades a large number of s-triazine herbicides. The enzyme converts chlorine or methylthio-substituted herbicides to their corresponding hydroxy derivatives.

Author: Zhu Hong, Topp, Edward, Nour, Sarah M., Cuppels, Diane, Mulbry, Walter M.
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 2000

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Biodegradation of the herbicide Bromoxynil (3,5-dibromo-4- hydroxybenzonitrile) by purified pentachlorophenol hydroxylase and whole cells of Flavobacterium sp. strain ATCC 39723 is accompanied by cyanogenesis

Article Abstract:

Microbial degradation of the herbicide bromoxynil produced bromide and cyanide. This happened when whole cells of Flavobacterium specie strain ATCC 39723 metabolized bromoxynil. The purified pentachlorophenol(PCP) hydroxylase from the same strain metabolized PCP by stoichiometric replacement of the hydroxyl group by chlorine atoms to produce tetrachlorohydroquinone. Theenzymatic dehalogenation of PCP and cyanogenesis in bromoxynil proceeded by using similar mechanism except that PCP hydroxylase specifically attacked the para position of halogenated phenols. Metabolism of bromoxynil by the Flavobacterium strain whole cells was accompanied by cyanogenesis but not when degraded by PCP hydroxylase. Use of the purified hydroxylase in the biodegradation of bromoxynil produced dibromohydroquinone instead of bromine and cyanide as with the use of whole cells. Dibromohydroquinone can be further metabolized to achieve complete bromoxynil mineralization.

Author: Xun, Luying, Topp, Edward, Orser, Cindy S.
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 1992
Health aspects, Physiological aspects, Environmental aspects, Microbial metabolism, Cyanides, Bromoxynil

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Research, Herbicides, Biodegradation
Similar abstracts:
  • Abstracts: Biodegradation of bis(2-chloroethyl) ether by Xanthobacter sp. strain ENV481. Toluene monooxygenase-catalyzed epoxidation of alkenes
  • Abstracts: Reduction of acid tolerance by tetracycline in Escherichia coli expressing tetA(C) is reversed by cations. Contribution of dps to acid stress tolerance and oxidative stress tolerance in Escherichia coli O157:H7
  • Abstracts: Reassessment of the prevalence of heat-stable enterotoxin (NAG-ST) among environmental Vibrio cholerae non-O1 strains isolated from Calcutta, India by using a NAG-ST DNA probe
  • Abstracts: Supply-side analysis of growth of Bacillus subtilis on glucose-citrate medium: feasible network alternatives and yield optimality
  • Abstracts: PCR-based DNA amplification and presumptive detection of Escherichia coli O157:H7 with an internal fluorogenic probe and the 5' nuclease (TaqMan) assay
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2026 Advameg, Inc.