TY - JOUR
T1 - Characterization of a marine-isolated mercury-resistant Pseudomonas putida strain SP1 and its potential application in marine mercury reduction
AU - Zhang, Weiwei
AU - Chen, Lingxin
AU - Liu, Dongyan
PY - 2012/2
Y1 - 2012/2
N2 - The Pseudomonas putida strain SP1 was isolated from marine environment and was found to be resistant to 280 μM HgCl 2. SP1 was also highly resistant to other metals, including CdCl 2, CoCl 2, CrCl 3, CuCl 2, PbCl 2, and ZnSO 4, and the antibiotics ampicillin (Ap), kanamycin (Kn), chloramphenicol (Cm), and tetracycline (Tc). mer operon, possessed by most mercury-resistant bacteria, and other diverse types of resistant determinants were all located on the bacterial chromosome. Cold vapor atomic absorption spectrometry and a volatilization test indicated that the isolated P. putida SP1 was able to volatilize almost 100% of the total mercury it was exposed to and could potentially be used for bioremediation in marine environments. The optimal pH for the growth of P. putida SP1 in the presence of HgCl 2 and the removal of HgCl 2 by P. putida SP1 was between 8.0 and 9.0, whereas the optimal pH for the expression of merA, the mercuric reductase enzyme in mer operon that reduces reactive Hg 2+ to volatile and relatively inert monoatomic Hg 0 vapor, was around 5.0. LD 50 of P. putida SP1 to flounder and turbot was 1.5∈×∈10 9 CFU. Biofilm developed by P. putida SP1 was 1- to 3-fold lower than biofilm developed by an aquatic pathogen Pseudomonas fluorescens TSS. The results of this study indicate that P. putida SP1 is a low virulence strain that can potentially be applied in the bioremediation of HgCl 2 contamination over a broad range of pH.
AB - The Pseudomonas putida strain SP1 was isolated from marine environment and was found to be resistant to 280 μM HgCl 2. SP1 was also highly resistant to other metals, including CdCl 2, CoCl 2, CrCl 3, CuCl 2, PbCl 2, and ZnSO 4, and the antibiotics ampicillin (Ap), kanamycin (Kn), chloramphenicol (Cm), and tetracycline (Tc). mer operon, possessed by most mercury-resistant bacteria, and other diverse types of resistant determinants were all located on the bacterial chromosome. Cold vapor atomic absorption spectrometry and a volatilization test indicated that the isolated P. putida SP1 was able to volatilize almost 100% of the total mercury it was exposed to and could potentially be used for bioremediation in marine environments. The optimal pH for the growth of P. putida SP1 in the presence of HgCl 2 and the removal of HgCl 2 by P. putida SP1 was between 8.0 and 9.0, whereas the optimal pH for the expression of merA, the mercuric reductase enzyme in mer operon that reduces reactive Hg 2+ to volatile and relatively inert monoatomic Hg 0 vapor, was around 5.0. LD 50 of P. putida SP1 to flounder and turbot was 1.5∈×∈10 9 CFU. Biofilm developed by P. putida SP1 was 1- to 3-fold lower than biofilm developed by an aquatic pathogen Pseudomonas fluorescens TSS. The results of this study indicate that P. putida SP1 is a low virulence strain that can potentially be applied in the bioremediation of HgCl 2 contamination over a broad range of pH.
KW - Bioremediation of HgCl contamination
KW - Marine environment
KW - Pseudomonas putida
KW - mer operon
UR - https://www.scopus.com/pages/publications/84856390870
U2 - 10.1007/s00253-011-3454-5
DO - 10.1007/s00253-011-3454-5
M3 - 文章
C2 - 21751007
AN - SCOPUS:84856390870
SN - 0175-7598
VL - 93
SP - 1305
EP - 1314
JO - Applied Microbiology and Biotechnology
JF - Applied Microbiology and Biotechnology
IS - 3
ER -
