TY - JOUR
T1 - Triclosan susceptibility and co-metabolism - A comparison for three aerobic pollutant-degrading bacteria
AU - Kim, Young Mo
AU - Murugesan, Kumarasamy
AU - Schmidt, Stefan
AU - Bokare, Varima
AU - Jeon, Jong Rok
AU - Kim, Eun Ju
AU - Chang, Yoon Seok
PY - 2011/2
Y1 - 2011/2
N2 - The antimicrobial agent triclosan is an emerging and persistent environmental pollutant. This study evaluated the susceptibility and biodegradation potential of triclosan by three bacterial strains (Sphingomonas wittichii RW1, Burkholderia xenovorans LB400 and Sphingomonas sp. PH-07) that are able to degrade aromatic pollutants (dibenzofuran, biphenyl and diphenyl ether, respectively) with structural similarities to triclosan. These strains showed less susceptibility to triclosan when grown in complex and mineral salts media. Biodegradation experiments revealed that only strain PH-07 was able to catabolize triclosan to intermediates that included hydroxylated compounds (monohydroxy-triclosan, and dihydroxy-triclosan) and the ether bond cleavage products (4-chlorophenol and 2,4-dichlorophenol), indicating that the initial dihydroxylation occurred on both aromatic rings of triclosan. Additional growth inhibition tests demonstrated that the main intermediate, 2,4-dichlorophenol, was less toxic to strain PH-07 than was triclosan. Our results indicate that ether bond cleavage might be the primary mechanism of avoiding triclosan toxicity by this strain.
AB - The antimicrobial agent triclosan is an emerging and persistent environmental pollutant. This study evaluated the susceptibility and biodegradation potential of triclosan by three bacterial strains (Sphingomonas wittichii RW1, Burkholderia xenovorans LB400 and Sphingomonas sp. PH-07) that are able to degrade aromatic pollutants (dibenzofuran, biphenyl and diphenyl ether, respectively) with structural similarities to triclosan. These strains showed less susceptibility to triclosan when grown in complex and mineral salts media. Biodegradation experiments revealed that only strain PH-07 was able to catabolize triclosan to intermediates that included hydroxylated compounds (monohydroxy-triclosan, and dihydroxy-triclosan) and the ether bond cleavage products (4-chlorophenol and 2,4-dichlorophenol), indicating that the initial dihydroxylation occurred on both aromatic rings of triclosan. Additional growth inhibition tests demonstrated that the main intermediate, 2,4-dichlorophenol, was less toxic to strain PH-07 than was triclosan. Our results indicate that ether bond cleavage might be the primary mechanism of avoiding triclosan toxicity by this strain.
KW - Antimicrobial
KW - Biodegradation
KW - Sphingomonas sp PH-07
KW - Triclosan
UR - http://www.scopus.com/inward/record.url?scp=78650831116&partnerID=8YFLogxK
U2 - 10.1016/j.biortech.2010.10.009
DO - 10.1016/j.biortech.2010.10.009
M3 - Article
C2 - 21041079
AN - SCOPUS:78650831116
SN - 0960-8524
VL - 102
SP - 2206
EP - 2212
JO - Bioresource Technology
JF - Bioresource Technology
IS - 3
ER -