Part:BBa_K1420006

phsABC Generator

Overview and Molecular Function

The phsABC gene from Salmonella enterica serovar Typhimurium LT2 encodes thiosulfate reductase, which catalyzes the stoichiometric production of hydrogen sulfide and sulfite from thiosulfate for heavy metal removal by precipitation. The phsABC operon encodes three open reading frames (ORFs), designated phsA, phsB, and phsC. Based on sequence homology to formate dehydrogenase-N, it is predicted that thiosulfate reductase behaves in a similar fashion. The PhsA subunit is predicted to be a peripheral membrane protein active site bis(molybdopterin guanine dinucleotide) molybdenum (MGD) cofactor. PhsC is an integral membrane protein that anchors the other two subunits to the membrane, and contains the site for menaquinol oxidation and two heme cofactors located at opposite sides of the membrane. PhsB is predicted to possess four iron-sulfur centers that transfer electrons between PhsC and PhsA.

Mechanism

The reduction of thiosulfate catalyzed by thiosulfate reductase is highly endergonic and must be linked to an exergonic process in order to operate in the desired direction. The process consumes the proton motive force (PMF) as electrons are moved from the cytoplasmic side from the site of menaquinone (MK) oxidation and across the membrane by means of the hemes in the membrane subunit (PhsC) and four iron-sulfur centers in PhsB to the periplasmic side of the membrane, where thiosulfate is reduced (Figure 1).

Figure 1. Reaction catalyzed by thiosulfate reductase. The process utilizes the proton motive force of electrons moving from the cytoplasm across to the periplasmic side of the membrane where thiosulfate is reduced to a hydrogen sulfide ion and hydrogen sulfite.

phsABC Expression Modifications

phsABC was obtained through Addgene from Dr. Jay Keasling's laboratory at University of California, Berkeley. It was shown to have the highest catalytic activity in the IPTG- inducible plasmid pSB74 (Table 1). The part was used by the Yale 2010 iGEM Team (Part:BBa_K393000) (inducible by IPTG) to deposit copper sulfide in a specified geometry. We sought to both improve and characterize the part for future utilization in our filtration device. We chose to improve the phsABC biological system by adding a modified lac promoter to allow for constitutive expression rather than IPTG induction within the biological system, and thus make it more applicable in the environment (Figure 2). We also improved the characterization of their part by testing its application for biological precipitation of iron and cadmium in addition to their copper testing to add to the functionality of the part.

Table 1. phsABC catalytic activity in various plasmids in E. coli. (Table adapted from "." ²)

Figure 2. Modified constructs containing phsABC gene.

Experimental Results

In order to measure the thiosulfate reducing activity of phsABC of NaS₂O₃ to H₂S, the gene was first inserted into the pBBRBB vector with a constitutive P_lac promoter and transformed into K12 strain E. coli cells. As a control, pBBRBB::GFP was tested under the same conditions. The pBBRBB:phsABC K12 and pBBRBB::GFP K12 cells were grown in three test tubes each containing heavy metal tryptone medium as well as 3mM NaS₂O₃. A third set of test tubes were set up with the same contents except without cells as an additional negative control. After 24 hours of incubation, The exact amount of H₂S present in each of three different sets of tubes was then measured using a hydrogen sulfide assay. This consisted of adding 1x or 0.5x 30μL of Cline's Reagent (2g Diamine + 3g FeCl₃ in 50mL of 50% cool HCl) to 270μL of sample. The results were tested against known a standard curve of various Na₂S concentrations. Each sample was allowed 20 minutes for the color to develop before adding 30μL of sample into 270μL of water. The samples were then further diluted 1:10 with water before testing (Figure 3). The entire well plate was then read at 670nm with the numerical compiled results displayed in Figure 4. The bar graph shows that the sulfide concentration was considerable higher for the cultures containing pBBRBB:phsABC K12 compared to the pBBRBB::GFP K12 control cells.

A second set of experiments was also conducted with pBBRBB:phsABC K12, pBBRBB::GFP K12, and an abiotic control grown in heavy metal tryptone medium, 3mM NaS₂O₃tubes, and 2.5mM Fe(II)Cl₂. Since the phsABC gene is responsible reducing thiosulfate, NaS₂O₃ would be converted to H₂S, which will further react with Fe(II)Cl₂ to produce FeS, a black precipitate. After a 24 hour incubation period, the cell cultures appeared as displayed in Figure 5. The pBBRBB:phsABC K12 cells were the only ones seen to produce FeS, the black precipitate seen in the figure, confirming the role of the phsABC gene in reducing thiosulfate. To affirm that this reaction is also successful under non-enclosed systems, the same sets of samples were also tested on 0.2% plates containing 3mM NaS₂O₃tubes and 2.5mM Fe(II)Cl₂. The results after 24 hours of incubation were similar to the experiments conducted in test tubes (Figure 6). <p>

Figure 3. 1:10 dilution of cell samples in Cline's Reagent used for hydrogen sulfide assays. The samples in box 1 contain the Na₂S standards (left to right, 1mM, 0.5mM, 0.25mM, 0.125mM, 0.0613mM, and 0.025mM), box 3 contains pBBRBB:GFP K12 cells, while box 3 contains pBBRBB:phsABC K12 cells. Boxes 4, 5, and 6 are the same as boxes 1, 2, and 3 aside from the fact that 0.5x Cline's Reagent was used as opposed to 1x Cline's Reagent that was used in box 1, 2, and 3. Box 7 contains the abiotic sample (left) and water (right) in 1x Cline's reagent. Samples from box 7 are the same as box 8 aside from using 0.5x Cline's Reagent for the latter.

Figure 4. Hydrogen sulfide assay results for pBBRBB:phsABC K12 cells compared to controls.

Figure 5.

Figure 6.

References

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal BglII site found at 135
  Illegal BglII site found at 2197
  Illegal BamHI site found at 141
  
• 23
  COMPATIBLE WITH RFC[23]
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal NgoMIV site found at 249
  Illegal AgeI site found at 2772
  Illegal AgeI site found at 3555
  
• 1000
  COMPATIBLE WITH RFC[1000]