Toluene dioxygenase expression correlates with trichloroethylene degradation capacity in Pseudomonas putida F1 cultures

被引:13
|
作者
Liu, Jianbo [1 ,2 ]
Amemiya, Takashi [2 ]
Chang, Qing [2 ,3 ]
Qian, Yi [1 ]
Itoh, Kiminori [4 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266061, Peoples R China
[2] Yokohama Natl Univ, Grad Sch Environm & Informat Sci, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
[3] Chongqing Technol & Business Univ, Coll Environm & Biol Engn, Chongqing 400067, Peoples R China
[4] Yokohama Natl Univ, Grad Sch Engn, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
关键词
Toluene dioxygenase; Pseudomonas putida; Trichloroethylene; Bioremediation; HOUSEKEEPING GENES; QUANTIFICATION; PHENOL; BACTERIA; BIODEGRADATION; FIELD; PCR; TCE; COMETABOLISM; OXIDATION;
D O I
10.1007/s10532-012-9544-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Trichloroethylene (TCE) is extensively used in commercial applications, despite its risk to human health via soil and groundwater contamination. The stability of TCE, which is a useful characteristic for commercial application, makes it difficult to remove it from the environment. Numerous studies have demonstrated that TCE can be effectively removed from the environment using bioremediation. Pseudomonas putida F1 is capable of degrading TCE into less hazardous byproducts via the toluene dioxygenase pathway (TOD). Unfortunately, these bioremediation systems are not self-sustaining, as the degradation capacity declines over time. Fortunately, the replacement of metabolic co-factors is sufficient in many cases to maintain effective TCE degradation. Thus, monitoring systems must be developed to predict when TCE degradation rates are likely to decline. Herein, we show evidence that tod expression levels correlate with the ability of P. putida F1 to metabolize TCE in the presence of toluene. Furthermore, the presence of toluene improves the replication of P. putida F1, even when TCE is present at high concentration. These findings may be applied to real world applications to decide when the bioremediation system requires supplementation with aromatic substrates, in order to maintain maximum TCE removal capacity.
引用
收藏
页码:683 / 691
页数:9
相关论文
共 39 条
  • [31] Unexpected Mechanism of Biodegradation and Defluorination of 2,2-Difluoro-1,3-Benzodioxole by Pseudomonas putida F1
    Bygd, Madison D.
    Aukema, Kelly G.
    Richman, Jack E.
    Wackett, Lawrence P.
    MBIO, 2021, 12 (06):
  • [32] Comparative proteomic analysis reveals mechanistic insights into Pseudomonas putida F1 growth on benzoate and citrate
    Mandalakis, Manolis
    Panikov, Nicolai
    Dai, Shujia
    Ray, Somak
    Karger, Barry L.
    AMB EXPRESS, 2013, 3 : 1 - 25
  • [33] Conjugal transfer of a TOL-like plasmid and extension of the catabolic potential of Pseudomonas putida F1
    Hallier-Soulier, S
    Ducrocq, V
    Truffaut, N
    CANADIAN JOURNAL OF MICROBIOLOGY, 1999, 45 (11) : 898 - 904
  • [34] Genome-wide analytical approaches using semi-quantitative expression proteomics for aromatic hydrocarbon metabolism in Pseudomonas putida F1
    Kasahara, Yasuhiro
    Morimoto, Hajime
    Kuwano, Masayoshi
    Kadoya, Ryo
    JOURNAL OF MICROBIOLOGICAL METHODS, 2012, 91 (03) : 434 - 442
  • [35] Conversion of indene to cis-(1S),(2R)-indandiol by mutants of Pseudomonas putida F1
    Connors, N
    Prevoznak, R
    Chartrain, M
    Reddy, J
    Singhvi, R
    Patel, Z
    Olewinski, R
    Salmon, P
    Wilson, J
    Greasham, R
    JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 1997, 18 (06): : 353 - 359
  • [36] Cloning, sequence analysis; and expression of the Pseudomonas putida 33/1 1H-3-hydroxy-4-oxoquinoline 2,4-dioxygenase gene, encoding a carbon monoxide forming dioxygenase
    Max, N
    Betz, A
    Facey, S
    Lingens, F
    Hauer, B
    Fetzner, S
    BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1999, 1431 (02): : 547 - 552
  • [37] Effect of ethanol, acetate, and phenol on toluene degradation activity and tod-lux expression in Pseudomonas putida TOD102:: Evaluation of the metabolic flux dilution model
    Lovanh, N
    Alvarez, PJJ
    BIOTECHNOLOGY AND BIOENGINEERING, 2004, 86 (07) : 801 - 808
  • [38] Periplasmic expression of Pseudomonas fluorescens peroxidase Dyp1B and site-directed mutant Dyp1B enzymes enhances polymeric lignin degradation activity in Pseudomonas putida KT2440
    Ehibhatiomhan, Austine O.
    Pour, Rahman Rahman
    Farnaud, Sebastien
    Bugg, Timothy D. H.
    Mendel-Williams, Sharon
    ENZYME AND MICROBIAL TECHNOLOGY, 2023, 162
  • [39] Pseudomonas putida CE2010 can degrade biphenyl by a mosaic pathway encoded by the tod operon and cmtE, which are identical to those of P-putida F1 except for a single base difference in the operator-promoter region of the cmt operon
    Ohta, Y
    Maeda, M
    Kudo, T
    MICROBIOLOGY-SGM, 2001, 147 : 31 - 41