Isolation and characterization of Pseudomonas sp. strain capable of degrading diethylstilbestrol
Tóm tắt
Since diethylstilbestrol (DES) interrupts endocrine systems and generates reproductive abnormalities in both wildlife and human beings, methods to remove DES from the environments are urgently recommended. In this study, bacterial strain J51 was isolated and tested to effectively degrade DES. J51 was identified as Pseudomonas sp. based on its nucleotide sequence of 16S rRNA. The quinoprotein alcohol dehydrogenase and isocitrate lyase were identified to be involved in DES degradation by MALDI–TOF–TOF MS/MS analysis. In the presence of 40 mg/l DES, increase of the genes encoding quinoprotein alcohol dehydrogenase and isocitrate lyase in both RNA and protein levels was determined. The HPLC/MS analysis showed that DES was hydrolyzed to a major degrading metabolite DES-4-semiquinone. It was the first time to demonstrate the characteristics of DES degradation by specific bacterial strain and the higher degradation efficiency indicated the potential application of Pseudomonas sp. strain J51 in the treatment of DES-contaminated freshwater and seawater environments.
Tài liệu tham khảo
Abderrazik NB, Azmani A, R’kiek C, Song WH, O’Shea KE (2005) Iron(II)-catalyzed enhancement of ultrasonic-induced degradation of diethylstilbestrol (DES). Catal Today 101:369–373
Anthony C (2001) Pyrroloquinoline quinone (PQQ) and quinoprotein enzymes. Antioxid Redox Signal 3:757–774
Beeching JR (1989) High sequence conservation between isocitrate lyase from Escherichia coli and Ricinus communis. Protein Seq Data Anal 2:463–466
Chang YS (2008) Recent developments in microbial biotransformation and biodegradation of dioxins. J Mol Microbiol Biotechnol 15:152–171
Chen TS, Chen TC, Yeh KJ, Chao HR, Liaw ET, Hsieh CY, Chen KC, Hsieh LT, Yeh YL (2010) High estrogen concentrations in receiving river discharge from a concentrated livestock feedlot. Sci Total Environ 408:3223–3230
Colborn T, Clement C (1992) Chemically-induced alterations in sexual development: the wildlife/human connection. Advances in Modern Toxicology, volume XXI. Princeton Scientific Publishing Inc., Princeton, NJ
Colborn T, VomSaal F, Soto A (1993) Developmental effects of endocrine-disrupting chemicals in wildlife and humans. Environ Health Perspect 101:378–384
Desbrow C, Routledge EJ, Brighty GC, Sumpter JP, Waldock M (1998) Identification of estrogenic chemicals in STW effluent. 1. Chemical fractionation and in vitro biological screening. Environ Sci Technol 32:1549–1558
Dodds EC, Goldberg L, Lawson W, Robinson R (1938) Estrogenic activity of certain synthetic compounds. Nature 141:247–248
Johansem H, Moeller N (1977) Solvent deposition of grugs on excipients II: interpretation of dissolution, adsorption and absorption characteristics of drugs. Arch Pharm Chem 5:33–42
Korshin GV, Kim J, Gan L (2006) Comparative study of reactions of endocrine disruptors bisphenol A and diethylstilbestrol in electrochemical treatment and chlorination. Water Res 40:1070–1078
Lane D, Pace B, Olsen G, Stahl D, Sogin M, Pace N (1985) Rapid determination of 16S ribosomal sequences for phylogenetic analyses. Proc Natl Acad Sci 82:6955–6059
Lee HB, Liu D (2002) Degradation of 17β-estradiol and its metabolites by sewage bacteria. Water Air Soil Poll 134:353–368
Liehr JG (1991) Vitamin C reduces the incidence and severity of renal tumors induced by estradiol or diethylstilbestrol. Am J Clin Nutr 54:1256–1260
Lin YX, Peng ZG, Zhang X (2009) Ozonation of estrone, estradiol, diethylstilbestrol in waters. Desalination 249:235–240
Masuda M, Yamasaki Y, Ueno S, Inoue A (2007) Isolation of bisphenol A-tolerant/degrading Pseudomonas monteilii strain N-502. Extremophiles 11:355–362
Mclachlan JA, Arnold SF (1996) Environmental estrogens. Am Sci 84:452–461
Meyers R (1983) D.E.S., the bitter pill. Seaview/Putnam, New York. ISBN 0-399-31008-8
NIH (1984) DES task force summary report. NIH publication no. 84–1688. National Institutes of Health, Bethesda, p 68
Pandey G, Dorrian SJ, Russell RJ, Brearley C, Kotsonis S, Oakeshott JG (2010) Cloning and biochemical characterization of a novel carbendazim (methyl-1H-benzimidazol-2-ylcarbamate)-hydrolyzing esterase from the newly isolated Nocardioides sp. strain SG-4G and its potential for use in enzymatic bioremediation. Appl Environ Microbiol 76:2940–2945
Potter JD (2011) Development and the environment: clues to carcinogenesis. Cancer Epidemiol Biomarkers Prev 20:574–577
Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbzor
Singh S, Kang SH, Mulchandani A, Chen W (2008) Bioremediation: environmental clean-up through pathway engineering. Curr Opin Biotechnol 19:437–444
Solé M, Lopez de Alda MJ, Castillo M, Porte C, Ladegaard-Pedersen K, Barcelo D (2000) Estrogenicity determination in sewage treatment plants and surface waters from the Catalonian area (NE Spain). Environ Sci Technol 34:5076–5083
Syn CK, Swarup S (2000) A scalable protocol for isolation of large-sized genomic DNA within an hour from several bacteria. Anal Biochem 278:86–90
Tanaka A, Atomi H, Ueda M, Hikida M, Hishida T, Teranishi Y (1990) Peroxisomal isocitrate lyase of the n-alkane-assimilating yeast Candida tropicalis: gene analysis and characterization. J Biochem 107:262–266
You C, Wang HL, Li PX, Wu F, Deng NS (2006) UV-light inducing photodegradation of diethylstilbestrol in water. Technology of water treatment 32:46–48
Zhang WW, Sun K, Cheng S, Sun L (2008) Characterization of DegQVh, a serine protease and a protective immunogen from a pathogenic Vibrio harveyi strain. Appl Environ Microbiol 74:6254–6262
Zhang WW, Hu YH, Wang HL, Sun L (2009) Identification and characterization of a virulence-associated protease from a pathogenic Pseudomonas fluorescens strain. Vet Microbiol 139:183–188
Zhang WW, Wen YY, Niu ZL, Yin K, Xu DX, Chen LX (2012) Isolation and characterization of sulfonamide-degrading bacteria Escherichia sp. HS21 and Acinetobacter sp. HS51. World J Micob Biot 28:447–452
Zhou DN, Wu F, Deng NS (2004) Fe(III)-oxalate complexes induced photooxidation of diethylstilbestrol in water. Chemosphere 57:283–291
