Ametryne and Prometryne as Sulfur Sources for Bacteria

Author:

Cook Alasdair M.1,Hütter Ralf1

Affiliation:

1. Institute of Microbiology, Swiss Federal Institute of Technology, CH-8092 Zurich, Switzerland

Abstract

Bacteria were isolated that could utilize quantitatively the s-triazine herbicide prometryne [ N,N ′ -bis(1-methylethyl)-6-(methylthio)-1,3,5-triazine-2,4-diamine] or ametryne [ N -ethyl- N ′-(1-methylethyl)-6-(methylthio)-1,3,5-triazine- 2,4-diamine], or both, as a sole source of sulfur for growth. The success of enrichments depended on previous exposure of the soil inoculum to s-triazine herbicides. Deaminoethylametryne [4-(1-methylethyl)amino-6-(methylthio)-1,3,5-triazine-2-(1H)-one], methylsulfonic acid, and sodium sulfate could also be used as sulfur sources. Utilization of a compound was quantified as the growth yield per mole of sulfur supplied. Yields were about 6 kg of protein per mol of sulfur. The product of the desulfuration of an s-triazine was identified as the corresponding hydroxy-derivative. This is the first substantiated report of the utilization of these s-triazines as sulfur sources by bacteria.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference26 articles.

1. Determination of 17 s-triazine herbicides and derivatives by high pressure liquid chromatography;Beilstein P.;J. Agric. Food Chem.,1981

2. Cain R. B. 1977. Surfactant biodegradation in waste waters p. 283-327. In A. G. Callely C. F. Forster and D. A. Stafford (ed.) Treatment of industrial effluents. Hodder and Stoughton London.

3. Phosphorus-containing pesticide breakdown products: quantitative utilization as phosphorus sources by bacteria;Cook A. M.;Appl. Environ. Microbiol.,1978

4. Benzene from bacterial cleavage of the carbon-phosphorus bond of phenylphosphonates;Cook A. M.;Biochem. J.,1979

5. Desulfuration of dialkyl thiophosphoric acids by a pseudomonad;Cook A. M.;Appl. Environ. Microbiol.,1980

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