About: Biotransformation of benzonitrile herbicides via the nitrile hydratase-amidase pathway in rhodococci     Goto   Sponge   NotDistinct   Permalink

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  • The aim of this work was to determine the ability of rhodococci to transform 3,5-dichloro-4-hydroxybenzonitrile (chloroxynil), 3,5-dibromo-4-hydroxybenzonitrile (bromoxynil), 3,5-diiodo-4-hydroxybenzonitrile (ioxynil) and 2,6-dichlorobenzonitrile (dichlobenil); to identify the products and determine their acute toxicities. Rhodococcus erythropolis A4 and Rhodococcus rhodochrous PA-34 converted benzonitrile herbicides into amides, but only the former strain was able to hydrolyze 2,6-dichlorobenzamide into 2,6-dichlorobenzoic acid, and produced also more of the carboxylic acids from the other herbicides compared to strain PA-34. Transformation of nitriles into amides decreased acute toxicities for chloroxynil and dichlobenil, but increased them for bromoxynil and ioxynil. The amides inhibited root growth in Lactuca sativa less than the nitriles but more than the acids. The conversion of the nitrile group may be the first step in the mineralization of benzonitrile herbicides but cannot be itself considered to be a detoxification.
  • The aim of this work was to determine the ability of rhodococci to transform 3,5-dichloro-4-hydroxybenzonitrile (chloroxynil), 3,5-dibromo-4-hydroxybenzonitrile (bromoxynil), 3,5-diiodo-4-hydroxybenzonitrile (ioxynil) and 2,6-dichlorobenzonitrile (dichlobenil); to identify the products and determine their acute toxicities. Rhodococcus erythropolis A4 and Rhodococcus rhodochrous PA-34 converted benzonitrile herbicides into amides, but only the former strain was able to hydrolyze 2,6-dichlorobenzamide into 2,6-dichlorobenzoic acid, and produced also more of the carboxylic acids from the other herbicides compared to strain PA-34. Transformation of nitriles into amides decreased acute toxicities for chloroxynil and dichlobenil, but increased them for bromoxynil and ioxynil. The amides inhibited root growth in Lactuca sativa less than the nitriles but more than the acids. The conversion of the nitrile group may be the first step in the mineralization of benzonitrile herbicides but cannot be itself considered to be a detoxification. (en)
Title
  • Biotransformation of benzonitrile herbicides via the nitrile hydratase-amidase pathway in rhodococci
  • Biotransformation of benzonitrile herbicides via the nitrile hydratase-amidase pathway in rhodococci (en)
skos:prefLabel
  • Biotransformation of benzonitrile herbicides via the nitrile hydratase-amidase pathway in rhodococci
  • Biotransformation of benzonitrile herbicides via the nitrile hydratase-amidase pathway in rhodococci (en)
skos:notation
  • RIV/00216208:11310/12:10125772!RIV13-GA0-11310___
http://linked.open...avai/predkladatel
http://linked.open...avai/riv/aktivita
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  • I, P(GAP504/11/0394), P(GD305/09/H008), P(OC09046), S
http://linked.open...iv/cisloPeriodika
  • 12
http://linked.open...vai/riv/dodaniDat
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  • 125200
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  • RIV/00216208:11310/12:10125772
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  • Rhodococcus rhodochrous; Rhodococcus erythropolis; benzonitrile herbicides; amidase; nitrile hydratase (en)
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http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [BA328B05AEFF]
http://linked.open...i/riv/nazevZdroje
  • Journal of Industrial Microbiology and Biotechnology
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http://linked.open...v/svazekPeriodika
  • 39
http://linked.open...iv/tvurceVysledku
  • Lovecká, Petra
  • Macková, Martina
  • Martínková, Ludmila
  • Pelantová, Helena
  • Šulc, Miroslav
  • Pátek, Miroslav
  • Bhalla, Tek Chand
  • Pasquarelli, Fabrizia
  • Pičmanová, Martina
  • Thimová, Markéta
  • Veselá, Alicja Barbara
http://linked.open...ain/vavai/riv/wos
  • 000311205800009
issn
  • 1367-5435
number of pages
http://bibframe.org/vocab/doi
  • 10.1007/s10295-012-1184-z
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  • 11310
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