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. 1992 Jun;58(6):1823–1831. doi: 10.1128/aem.58.6.1823-1831.1992

Biodegradation of bisphenol A and other bisphenols by a gram-negative aerobic bacterium.

J H Lobos 1, T K Leib 1, T M Su 1
PMCID: PMC195690  PMID: 1622258

Abstract

A novel bacterium designated strain MV1 was isolated from a sludge enrichment taken from the wastewater treatment plant at a plastics manufacturing facility and shown to degrade 2,2-bis(4-hydroxyphenyl)propane (4,4'-isopropylidenediphenol or bisphenol A). Strain MV1 is a gram-negative, aerobic bacillus that grows on bisphenol A as a sole source of carbon and energy. Total carbon analysis for bisphenol A degradation demonstrated that 60% of the carbon was mineralized to CO2, 20% was associated with the bacterial cells, and 20% was converted to soluble organic compounds. Metabolic intermediates detected in the culture medium during growth on bisphenol A were identified as 4-hydroxybenzoic acid, 4-hydroxyacetophenone, 2,2-bis(4-hydroxyphenyl)-1-propanol, and 2,3-bis(4-hydroxyphenyl)-1,2-propanediol. Most of the bisphenol A degraded by strain MV1 is cleaved in some way to form 4-hydroxybenzoic acid and 4-hydroxyacetophenone, which are subsequently mineralized or assimilated into cell carbon. In addition, about 20% of the bisphenol A is hydroxylated to form 2,2-bis(4-hydroxyphenyl)-1-propanol, which is slowly biotransformed to 2,3-bis(4-hydroxyphenyl)-1,2-propanediol. Cells that were grown on bisphenol A degraded a variety of bisphenol alkanes, hydroxylated benzoic acids, and hydroxylated acetophenones during resting-cell assays. Transmission electron microscopy of cells grown on bisphenol A revealed lipid storage granules and intracytoplasmic membranes.

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Selected References

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  1. Cripps R. E. The microbial metabolism of acetophenone. Metabolism of acetophenone and some chloroacetophenones by an Arthrobacter species. Biochem J. 1975 Nov;152(2):233–241. doi: 10.1042/bj1520233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Gilardi G. L., Hirschl S., Mandel M. Characteristics of yellow-pigmented nonfermentative bacilli (groups VE-1 and VE-2) encountered in clinical bacteriology. J Clin Microbiol. 1975 Apr;1(4):384–389. doi: 10.1128/jcm.1.4.384-389.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Maguire H. C., Jr Experimental photoallergic contact dermatitis to bisphenol A. Acta Derm Venereol. 1988;68(5):408–412. [PubMed] [Google Scholar]
  4. Morrissey R. E., George J. D., Price C. J., Tyl R. W., Marr M. C., Kimmel C. A. The developmental toxicity of bisphenol A in rats and mice. Fundam Appl Toxicol. 1987 May;8(4):571–582. doi: 10.1016/0272-0590(87)90142-4. [DOI] [PubMed] [Google Scholar]
  5. Nelson M. J., Montgomery S. O., Mahaffey W. R., Pritchard P. H. Biodegradation of trichloroethylene and involvement of an aromatic biodegradative pathway. Appl Environ Microbiol. 1987 May;53(5):949–954. doi: 10.1128/aem.53.5.949-954.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. REYNOLDS E. S. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. J Cell Biol. 1963 Apr;17:208–212. doi: 10.1083/jcb.17.1.208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Stanier R. Y., Palleroni N. J., Doudoroff M. The aerobic pseudomonads: a taxonomic study. J Gen Microbiol. 1966 May;43(2):159–271. doi: 10.1099/00221287-43-2-159. [DOI] [PubMed] [Google Scholar]
  8. Sutherland J. B., Crawford D. L., Pometto A. L. Catabolism of substituted benzoic acids by streptomyces species. Appl Environ Microbiol. 1981 Feb;41(2):442–448. doi: 10.1128/aem.41.2.442-448.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]

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