Toxicity and biodegradation of diamines

J Environ Sci Health B. 2002 Jan;37(1):53-64. doi: 10.1081/PFC-120002897.

Abstract

Phytotoxicity and cytotoxicity of 2,4-diaminotoluene (2,4-D), 4,4'-methylenedianiline (4,4-D), and 1,6-hexanediamine (1,6-D) were investigated by observing the germination of young radish seeds and the viability of HeLa cells, respectively. 2,4-D showed the highest, 4,4-D intermediate, and 1,6-D lowest cytotoxicity. However, the phytotoxicity decreased in the order of 4,4-D > 2,4-D > 1,6-D. Contrary to the results previously reported, in the modified Sturm test the activated sludge degraded 2,4-D and 4,4-D as well as 1,6-D without any pre-acclimation. Ochrobacterium antropi was isolated for degradation of 2,4-D and 4,4-D and Pseudomonas citronellolis for 1,6-D degradation. Thielevia sp. was isolated as 2,4-D degrading fungus and Aspergillus sp. as 4,4-D and 1,6-D degrading fungus. The fungi degraded the diamines faster than the bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aniline Compounds / metabolism
  • Aniline Compounds / toxicity
  • Aspergillus / isolation & purification
  • Aspergillus / metabolism*
  • Biodegradation, Environmental
  • Cell Survival / drug effects
  • Diamines / metabolism*
  • Diamines / toxicity*
  • Germination / drug effects
  • HeLa Cells
  • Humans
  • Ochrobactrum anthropi / isolation & purification
  • Ochrobactrum anthropi / metabolism*
  • Phenylenediamines / metabolism
  • Phenylenediamines / toxicity
  • Pseudomonas / isolation & purification
  • Pseudomonas / metabolism*
  • Raphanus / drug effects
  • Raphanus / physiology
  • Seeds / drug effects
  • Seeds / physiology
  • Toxicity Tests

Substances

  • Aniline Compounds
  • Diamines
  • Phenylenediamines
  • 4,4'-diaminodiphenylmethane
  • 2,4-diaminotoluene
  • 1,6-diaminohexane