4.8 Article

Expression of Arsenic Regulatory Protein in Escherichia coli for Selective Accumulation of Methylated Arsenic Species

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 5, Issue 7, Pages 2767-2772

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/am400578y

Keywords

metalloregulatoty protein; ArsR; genetically engineering; methylated arsenic; accumulation; remediation

Funding

  1. Natural Science Foundation of China [21075013, 21005011, 21235001]
  2. SRFDP program [20120042110020]
  3. Fundamental Research Funds for the Central Universities [N110605001, N110705002, N110805001]

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ArsR is a metalloregulatory protein with high selectivity and affinity toward arsenic. We hereby report the expression of ArsR in Escherichia coli by cell engineering, which significantly enhances the adsorption/accumulation capacity of methylated arsenic species. The ArsR-expressed E. coli cells (denoted as E. coli-ArsR) give rise to 5.6-fold and 3.4-fold improvements on the adsorption/accumulation capacity for monomethylarsonic acid (MMA) and dimethylarsinic acid (DMA), with respect to native E. coli cells. The uptake of MMA and DMA by the E. coli-ArsR is a fast process fitting Langmuir adsorption model. It is interesting to note that the accumulation of methylated arsenic is virtually not affected by the presence of competing heavy-metal species, at least 10 times of Cd(II) and Pb(II) are tolerated for the adsorption of 1 mg L-1 methylated arsenic. In addition, an ionic strength of up to 2 g L-1 Na+ poses no obvious effect on the sorption of 1 mg L-1 MMA and DMA. Furthermore, the accumulation of MMA and DMA is less sensitive to the variation of pH value, with respect to the blank control cells. Consequently, 82.4% of MMA and 96.3% of DMA at a concentration Of 50 mu g L-1 could be readily removed from aqueous medium by 12 g of E. coli-ArsR. This illustrates a great potential for the E. coli-ArsR for selective remediation of methylated arsenic species in waters, even in the presence of a high concentration of salts.

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