Development of a Genetic System forGeobacter sulfurreducens

The plasmids and bacterial strains, G. sulfurreducens (ATCC 51573) andEscherichia coli, that were used in this study are listed and described in Table 1.

Total G. sulfurreducens genomic DNA was prepared using the Genome DNA Kit (Bio 101, Inc., Carlsbad, Calif.). Primers for amplification of DNA fragments from the G. sulfurreducens chromosome were designed using sequence data obtained from The Institute for Genomic Research website at http://www.tigr.org . PCR amplification was performed using AmpliTaq DNA polymerase (Roche Molecular Systems, Branchburg, N.J.) according to the manufacturer's instructions. Plasmid DNA was purified from E. coli andG. sulfurreducens strains using the Qiagen midi- or miniplasmid purification kits (Qiagen Inc., Valencia, Calif.). DNA samples for electrotransformation were subjected to a second ethanol precipitation and 70% ethanol wash followed by resuspension in 0.5× TE buffer (0.5 mM Tris HCl [pH 8.0], 0.5 mM EDTA) in order to reduce their salt concentration and prevent arcing.

The suicide vector, pBRnif::kan, was constructed for the targeted disruption of the G. sulfurreducens nifDgene. A 1.1-kb fragment consisting of the first ∼0.9 kb of thenifD coding region and ∼0.2 kb of upstream sequence was amplified from the G. sulfurreducens chromosome using the primers prDL1 (CCCCGCTGGAGATGGAAGAGC) and prDL2 (GGCGGATCCAGCCAGGGGATGCC). In primer sequences, restriction sites are italicized and annealing nucleotides are indicated in boldface. This fragment was digested withEcoRI (cleaves 18 bp downstream of prDL1) andBamHI (cleaves prDL2) and was inserted into the corresponding sites of pBR322 (6), resulting in the intermediate construct pBRnif. A kanamycin resistance cassette was amplified from pBBR1MCS-2 (12) with the primers prDL3 (CCCGGTAACCGGATGAATGTCAGC) and prDL4 (CCCGATATCGCGGTGGAATCG). The final suicide vector, pBRnif::kan (Fig. 2B), was constructed by inserting this cassette into a unique EcoRV site within pBRnif (at position 373 of the nifDcoding sequence).

The nifD expression vector pCDSnifD was constructed in order to complement the nifD1::kanphenotype. The nifD coding sequence was amplified fromG. sulfurreducens genomic DNA with the primers prDL5 (CCCGGTACCTGACAGGAGAATAC) and prDL6 (CCCAAGCTTAAAAGCGGACTCCG) and was inserted into pCR2.1-TOPO (Invitrogen, Carlsbad, Calif.). It was subsequently excised from this plasmid with EcoRI andHindIII and was inserted into the corresponding sites of the IncQ expression vector pCD342 (10). Because the resulting vector pCDnifD conferred resistance to kanamycin, it was not suitable for carrying out complementation studies in ournifD1::kan mutants. Therefore, the kanamycin resistance cassette of pCDnifD was excised withBglII and BstBI and replaced with a streptomycin resistance cassette that had been amplified from pJRD215 (8) with the primers prDL7 (CCCAGATCTTTCTCATGTTTGACAGC) and prDL8 (CCCTTCGAATGAGATTGATGTGTTCC).

The two E. coli strains listed in Table 1 were propagated according to established methods (26).

G. sulfurreducens strains were cultured at 30°C under strict anaerobic conditions as previously described (19). Plating and incubations on solid media were performed inside an anaerobic chamber (Coy Laboratory Products Inc., Grass Lake, Mich.) containing a 7% H₂–10%CO₂–83% N₂ atmosphere heated to 30°C. G. sulfurreducens strains were propagated in two types of media (see compositions below): NBAF supplemented with 0.1% yeast extract and 1 mM cysteine (NBAFYE) and FWAFC. NBAFYE was used for general propagation and plating and for the preparation of electrocompetent cells, whereas FWAFC was used for the analysis of nitrogen fixation phenotypes. Antibiotics were added to cultures or plates as needed. During extended incubations of liquid cultures, fresh antibiotics were added every 48 h.

All media were dispensed into anaerobic pressure tubes or bottles with butyl rubber stoppers and, unless otherwise indicated, bubbled with an 80% N₂–20% CO₂ gas mixture to remove dissolved oxygen and obtain a final pH of ∼6.7.

NBAF, a modified form of the medium described by Lovley et al. (16), contains 15 mM acetate as the electron donor and 40 mM fumarate as the electron acceptor. Its composition per liter of deionized water is 0.42 g of KH₂PO₄, 0.22 g of K₂HPO₄, 0.2 g of NH₄Cl, 0.38 g of KCl, 0.36 g of NaCl, 0.04 g of CaCl₂ · 2H₂O, 0.1 g of MgSO₄ · 7H₂O, 1.8 g of NaHCO₃, 0.5 g of Na₂CO₃, 2.04 g of NaC₂H₃O₂· 3H₂O, 6.4 g of Na₂C₄H₄O₄, 0.5 ml of 0.1% resazurin, 1.0 ml of 100 mM Na₂SeO₄, 10.0 ml of a vitamin solution (17), and 10.0 ml of NB trace mineral solution. The composition of the NB trace mineral solution per liter of deionized water is 2.14 g of nitriloacetic acid, 0.1 g of MnCl₂ · 4H₂O, 0.3 g of FeSO₄ · 7H₂O, 0.17 g of CoCl₂ · 6H₂O, 0.2 g of ZnSO₄ · 7H₂O, 0.3 g of CuCl₂ · 2H₂O, 0.005 g of AlK(SO₄)₂ · 12H₂O, 0.005 g of H₃BO₃, 0.09 g of Na₂MoO₄, 0.11 g of NiSO₄ · 6H₂O, and 0.2 g of Na₂WO₄· 2H₂O.

Liquid NBAFYE medium was prepared by adding appropriate volumes of sterile anoxic stock solutions of yeast extract and cysteine to NBAF medium to achieve final concentrations of 0.1% (wt/vol) and 1 mM, respectively. If NBAFYE medium was to be used for manipulations within the anaerobic chamber, the final cysteine concentration was increased to 5 mM. Solid NBAFYE was prepared by amending NBAF medium lacking CaCl₂ and MgSO₄ with 15 g of purified agar/liter. Following sterilization, the molten medium was cooled to 50°C and appropriate volumes of anaerobic stock solutions of CaCl₂, MgSO₄, yeast extract, and cysteine were added to yield final concentrations of 0.004%, 0.01%, 0.1%, and 5 mM, respectively. If necessary, antibiotics (concentrations listed below) were also added at this time.

FWAFC is a modification of FWA-Fe(III) citrate medium (19), a freshwater minimal medium containing 20 mM acetate as the electron donor and 55.9 mM Fe(III) citrate as the electron acceptor. Its composition per liter of deionized water is 13.7 g of FeC₆O₇, 2.5 g of NaHCO₃, 0.25 g of NH₄Cl, 0.6 g of NaH₃PO₄ · H₂O, 0.1 g of KCl, 1.0 ml of 100 mM Na₂SeO₄, 10.0 ml of a vitamin solution (17), and 10.0 ml of a trace mineral solution (17).

Ammonium- and nitrogen-free FWAFC medium was prepared by sparging and overlaying ammonium-free FWAFC medium with an 80% Ar–20% CO₂ gas mixture.

Antibiotics (200 μg of kanamycin, 400 μg of streptomycin, or 10 μg of chloramphenicol per ml) were added to liquid and solid medium as needed. All antibiotic stock solutions were sterile and anoxic (sparged and overlaid with an N₂ atmosphere).

The cell density (cells/milliliter) of prestationary-phase liquid cultures was determined by staining cells with acridine orange and utilizing epifluorescence microscopy as previously described (19). The density of CFU in these cultures was determined by plating serial dilutions.

ElectrocompetentE. coli was prepared according to Sambrook et al. (26). Electrocompetent G. sulfurreducens was prepared from cultures maintained in NBAFYE medium as described below.

All manipulations were carried out on ice in an anaerobic chamber, and any buffers used were ice-cold and anoxic. Four hundred milliliters of mid-log-phase cultures (optical density at 600 nm = 0.2 to 0.35; 9 × 10⁷ to 1.8 × 10⁸ cells/ml) was harvested by centrifugation at 4°C for 8 min at 4,300 × g. The cells were washed twice with 400 ml of electroporation buffer (1 mM HEPES [pH 7.0], 1 mM MgCl₂, and 175 mM sucrose) and resuspended in the same buffer at a final concentration of ∼10¹¹ cells/ml. Because G. sulfurreducens was found to be particularly susceptible to shearing, pipetting of cell suspensions was minimized and, when necessary, performed with large-bore pipette tips. An appropriate volume of a 60% dimethyl sulfoxide (DMSO)–40% electroporation buffer solution was added to the final cell suspension to achieve a final DMSO concentration of 10%. The resulting electrocompetent cells were either electroporated immediately or stored at −70°C for future use.

All electrotransformations were performed in 0.15-cm-gap microelectroporation chambers using a Cell-Porator equipped with a Voltage Booster (Life Technologies Inc., Gaithersburg, Md.). Electrocompetent E. coli cells were transformed according to the manufacturer's instructions.

Electrocompetent G. sulfurreducens cells (25 μl), either freshly prepared or thawed on ice, were pulsed at 14.7 kV/cm for ∼6 ms (resistance = 4 kΩ; capacitance = 25 μF). Immediately following electroporation, cells were washed into the bottom of the microelectroporation chamber with 1 ml of room temperature phosphate-buffered NBAF (NBAF medium containing 50 mM potassium phosphate instead of bicarbonate). The cells were then transferred to a prewarmed anaerobic pressure tube containing 9 ml of NBAFYE. The electroporated cells were allowed to recover for 5 h at 30°C, prior to plating onto the appropriate solid growth medium.

G. sulfurreducens was electrotransformed with either pBBR1MCS-2 or pJRD215 (Table 1) and plated onto selective medium (NBAFYE containing 200 μg of kanamycin/ml). The resulting kanamycin-resistant colonies were transferred to liquid selective medium until the cultures became turbid (3 to 6 days). Selective pressure was maintained throughout this incubation by adding fresh kanamycin to the cultures every 48 h. Twenty-four hours prior to the beginning of the experiment, cultures were diluted 10-fold into fresh selective medium. At time zero, the cultures were serially diluted into nonselective medium (NBAFYE) and were then plated onto both selective and nonselective media. The remainder of the various serial dilutions was incubated at 30°C. Every 48 h, a log-phase culture was selected from among the various dilutions for analysis and the process was repeated. The total number of CFU in the various cultures was determined on nonselective medium, and the percentage of kanamycin-resistant CFU was ascertained by comparison. The number of generations between time points was determined from the total CFU/milliliter using the following formula: log (final CFU per milliliter/initial CFU per milliliter)/log₂.

Following digestion of genomic DNA with the restriction enzyme EcoRV, Southern blot analysis was performed according to Sambrook et al. (26). Probes were labeled with [α-³²P]dCTP using the Multiprime DNA labeling system (Amersham Pharmacia Biotech, Piscataway, N.J.). [α-³²P]dCTP was obtained from New England Nuclear (Boston, Mass.).

In order to be able to rapidly isolate clonal populations of G. sulfurreducens, conditions for high-efficiency plating onto solid growth medium were established. Simply solidifying the two liquid media for G. sulfurreducens, NBAF and FWAFC (see Materials and Methods), was not sufficient to achieve the rapid growth of G. sulfurreducens on plates. After considerable trial and error, it was found that supplementation of the solid form of NBAF medium with 0.1% yeast extract and a high concentration (5 mM) of the reductant cysteine yielded a solid medium, NBAFYE, on which both the growth rate and the plating efficiency of G. sulfurreducens were reproducibly high. Colonies were visible on solid NBAFYE medium after only 5 days of incubation at 30°C. In addition, when pre-stationary-phase liquid cultures with a density of (3.25 ± 0.54) × 10⁸ cells/ml were plated onto this medium, (2.85 ± 0.48) × 10⁸CFU/ml were recovered (mean ± standard deviation;n = 3), demonstrating a high plating efficiency.

The growth of G. sulfurreducens on solid medium could be inhibited by a variety of commonly used antibiotics. Growth of 10⁸ cells on solid medium could be inhibited by choramphenicol (10 μg/ml), nalidixic acid (10 μg/ml), tetracycline (10 μg/ml), kanamycin (200 μg/ml), spectinomycin (50 μg/ml), streptomycin (400 μg/ml), and ampicillin (400 μg/ml). The sensitivity of G. sulfurreducens to these antibiotics in liquid culture was similar (data not shown). These results indicated that it should be possible to select for the acquisition of multiple antibiotic resistance markers by G. sulfurreducens, a requirement for many genetic manipulations.

A protocol for the electrotransformation of G. sulfurreducens was developed by modifying existing protocols (21) to account for the unique properties of G. sulfurreducens. The preparation of electrocompetent cells typically involves extensive washing of cells derived from mid-log-phase cultures in a suitable low-ionic-strength electroporation buffer, followed by resuspension of the cells at high density (10⁹ to 10¹¹cells/ml) in this buffer (21). In order to attain sufficient G. sulfurreducens biomass at mid-log phase, it was necessary to supplement the NBAF medium routinely used to culture the organism with 0.1% (wt/vol) yeast extract. When grown on this rich medium at 30°C, G. sulfurreducens had a generation time of ∼4.5 h and reached a cell density of ∼10⁸cells/ml at mid-log phase (data not shown). The composition of the electroporation buffer was found to be critical for maintaining the viability of G. sulfurreducens throughout the washing and electrotransformation procedures. The optimal composition of the electroporation buffer was found to be 1 mM HEPES (pH 7.0), 1 mM MgCl₂, and 175 mM sucrose. The addition of MgCl₂ to the electroporation buffer was absolutely required if G. sulfurreducens was to remain viable during washing and storage. In the absence of MgCl₂, 90% of the cells lysed prior to electroporation (data not shown). MgCl₂ is thought to prevent bacterial lysis by stabilizing the outer membrane (27). The concentration of sucrose was another crucial variable in the composition of the electroporation buffer. Electrotransformed G. sulfurreducens could not tolerate large changes in osmolarity upon dilution back into nonselective growth medium. To avoid such changes in osmotic pressure, 175 mM sucrose was added to the electroporation buffer such that its osmolarity was equivalent to that of NBAFYE medium. The addition of 10% DMSO to the final cell suspension permitted storage of electrocompetent G. sulfurreducens at −70°C with little or no loss in transformation efficiency. Glycerol was not a suitable cryopreservant due to the sensitivity of G. sulfurreducens to rapid changes in osmolarity.

Electroporation parameters were optimized by transforming G. sulfurreducens with the broad-host-range IncQ plasmid pJRD215 (Table 1). Electrotransformation of G. sulfurreducenswith pJRD215 resulted in the growth of kanamycin-resistant colonies. The presence of pJRD215 in these colonies was confirmed by PCR (data not shown) and by digesting plasmid DNA purified from these colonies with restriction enzymes (Fig. 1A, lane 1). Electrotransformation was optimal when G. sulfurreducenswas pulsed at 14.7 kV/cm with a time constant of approximately 6 ms. Under these conditions, (1.98 ± 0.32) × 10⁵ transformants/μg of pJRD215 DNA were obtained. Electroporation lethality was roughly 59% ± 5.23%, and transformants constituted 1 out of (1.19 ± 0.43) × 10⁴ CFU. (Data are means ± standard errors;n = 11). These data were within the range reported for other bacteria in which gene replacement has been successful (3, 23, 24, 29).

As shown in Table 2, transformation efficiency increased to (2.96 ± 1.08) × 10⁷ transformants/μg (mean ± standard error; n = 3) when pJRD215 DNA was purified fromG. sulfurreducens. This 100-fold increase in transformation efficiency suggests that G. sulfurreducens may possess a robust restriction system.

A variety of plasmids were tested for the ability to replicate in and confer antibiotic resistance upon G. sulfurreducens (Table 2). In addition to pJRD215, two other IncQ plasmids, pJRC2 and pCD342 (Table 1), were evaluated. The plasmid pJRC2 is identical to pJRD215 except that it confers resistance to chloramphenicol. pCD342 is an expression vector containing a polylinker which is preceded by the hybrid tac-lac promoter (tac and lacUV5 promoters in tandem) and followed by the rrnB transcriptional terminator (1, 20). Electroporation of G. sulfurreducens with all three IncQ plasmids resulted in the growth of numerous antibiotic-resistant transformants (Table 2), indicating that all of these plasmids were capable of replication in G. sulfurreducens. In addition, all three of the IncQ plasmids could be purified from cultures ofG. sulfurreducens in sufficient quantity to be identified by digestion with restriction enzymes (Fig. 1A), suggesting that IncQ plasmids are stable in this organism. In fact, pJRD215 has a half-life of ∼60 generations in G. sulfurreducens in the absence of antibiotic selection (Table 2; Fig. 1B). Similarly, we were able to purify pCD342 from G. sulfurreducens (Fig. 1A, lane 3) after culturing a transformant for approximately 30 generations in the absence of antibiotic selection.

To determine whether pCD342 could serve as an expression vector for G. sulfurreducens, cells were transformed with pCD354 (10), a green fluorescent protein expression vector derived from pCD342. The green fluorescent protein was detected in the resulting transformants (Fig. 1C), indicating that pCD342 is indeed a suitable expression vector for G. sulfurreducens.

Due to their large size (≥ 10 kb) and low copy number, IncQ vectors are difficult to manipulate (8, 10). The pBBR1MCS series of broad-host-range expression vectors (12), in contrast, are fairly small (∼5.3 kb) and have a higher copy number. In addition, they contain a variety of antibiotic resistance cassettes and possess an extensive multicloning site located within thelacZ alpha peptide (12). Kanamycin-resistant transformants were isolated following electroporation of G. sulfurreducens with pBBR1MCS-2 (Table 2), indicating that this class of plasmids is capable of replication in G. sulfurreducens. However, pBBR1MCS-2 was found to be unstable inG. sulfurreducens (Fig. 1B). Despite the rigorous maintenance of selective pressure during propagation of pBBR1MCS-2 in liquid culture, only 15% of the CFU in these cultures were able to grow on solid medium containing kanamycin. Furthermore, in the absence of continued selection, kanamycin resistance was lost within 12 generations. Thus, despite the fact that pBBR1MCS vectors can replicate in G. sulfurreducens, their instability renders them unsuitable for use as expression vectors.

In addition to the two types of broad-host-range plasmids mentioned above, one plasmid with limited host specificity, pBMK7 (23), was evaluated for the ability to replicate inG. sulfurreducens. The plasmid pBMK7 is a shuttle vector that contains two replicons: the pBM1 replicon, which functions inE. coli, and the pBG1 replicon, which functions inDesulfovibrio species. Members of the genusDesulfovibrio, like those of the Geobacter genus, are obligate anaerobes belonging to the delta subdivision of theProteobacteria. However, electrotransformation of G. sulfurreducens with pBMK7 repeatedly failed to yield kanamycin-resistant transformants (Table 2). Thus, even thoughGeobacter and Desulfovibrio species are closely related, the pBG1 replicon did not appear to function in G. sulfurreducens. Furthermore, these results indicated that plasmids containing the pBG1 or pBM1 replicons acted as suicide vectors in G. sulfurreducens and could, therefore, be used to introduce mutations into its chromosome.

The next step in the development of a genetic system for G. sulfurreducens was to determine whether the function of a specific gene could be eliminated by placing a mutation in the G. sulfurreducens chromosome. A gene suspected of being involved in nitrogen fixation by G. sulfurreducens was selected as the first target, because, as noted above, it is important to conclusively demonstrate that G. sulfurreducens has the capacity to fix nitrogen. In other microorganisms, nitrogen reduction is catalyzed by the nitrogenase enzyme complex, which is encoded by the highly conserved nifH, nifD, and nifKgenes (9, 30). Because the nitrogenase complex functions specifically in the nitrogen fixation pathway, inactivation of the genes for any of its components yields a predictable and easily characterized phenotype, an inability to grow in medium lacking fixed nitrogen (9). By using the nifD genes of other organisms to probe the partial sequence of the G. sulfurreducens genome, a potential G. sulfurreducens nifHDK operon was identified. Studies were initiated to determine whether disruption of the putative nifD gene of G. sulfurreducens by the single-step gene replacement method (25) would affect the ability of G. sulfurreducens to grow in a medium devoid of fixed nitrogen.

In order to disrupt the putative G. sulfurreducens nifDgene, we constructed the suicide vector pBRnif::kan (Table 1; Fig.2B), which contained a fragment of thenifD coding sequence disrupted by a kanamycin resistance cassette. To ensure that incorporation of the disrupted nifDcoding sequence into the chromosome occurred via a double recombination event, the suicide vector was linearized with NruI andScaI prior to electroporation. The recovery period following electroporation was extended to ∼18 h to allow ample time for recombination and expression of kanamycin resistance. This procedure resulted in the growth of 2.77 × 10⁵kanamycin-resistant colonies per μg of linear DNA. Eight of these kanamycin-resistant colonies were screened for the presence of the disrupted nifD (nifD1::kan) coding sequence by PCR, and all eight were found to contain thenifD1::kan insertion mutation (data not shown). These results indicated that recombination between linear DNA fragments and the G. sulfurreducens chromosome was a highly efficient process.

As shown in Fig. 2, Southern blot analysis confirmed both the presence and placement of the kanamycin resistance cassette within the 5′ end of the nifD gene in four of the eightnifD1::kan mutants described above, strains DL2A to -D. All four of these genetically identical mutants were unable to completely reduce the available Fe(III) in FWAFC medium lacking a source of fixed nitrogen (data not shown). This result suggested that disruption of the nifD gene had resulted in the expected phenotype, an inability to grow in the absence of exogenous fixed nitrogen. One of the four mutants, DL2D, was selected for a more detailed characterization of its phenotype (Fig.3).

When strain DL2D and the wild-type strain DL1 were inoculated into FWAFC medium, they grew and reduced Fe(III) at similar rates (Fig. 3). When ammonium, the source of fixed nitrogen in the medium, was omitted, the wild-type strain exhibited a longer lag but eventually grew and reduced Fe(III) to levels comparable to those observed in ammonium-containing medium. The extended lag period most probably reflected the time required to induce the expression of nitrogen fixation genes. In contrast to the wild-type strain, the mutant strain DL2D failed to grow significantly in ammonium-free FWAFC medium and reduced only a small amount of the available Fe(III). In fact, the amount of growth and Fe(III) reduction by the mutant strain in ammonium-free medium was comparable to that in medium lacking both N₂ and ammonium.

The small amount of cell growth observed in medium devoid of both N₂ and ammonium (Fig. 3) can be attributed to the fact that residual ammonium may have been present in the washed starter cultures and that any cell lysis that occurred during washing would have resulted in the release of additional fixed nitrogen. The sustained low rate of Fe(III) reduction seen in this medium at the end of the experiment is probably due to the fact that G. sulfurreducens is still capable of reducing Fe(III) even when it is not actively growing.

In order to demonstrate that the phenotype of mutant DL2D was in fact due to disruption of thenifD gene and not to an unexpected secondary mutation or to an unanticipated effect on downstream gene expression, thenifD expression vector pCDSnifD was introduced into DL2D by electroporation. To determine if expression of thenifD gene in trans complemented thenifD1::kan phenotype, the ability of DL2D/pCDSnifD to grow in the absence of fixed nitrogen was evaluated (Fig. 4). The extent of cell growth and iron reduction by both DL2D/pCDSnifD and the wild-type strain (DL1) was similar under all three conditions tested (Fig. 4): (i) in the presence of both gaseous and fixed nitrogen, (ii) in the presence of gaseous nitrogen alone, and (iii) in the absence of both gaseous and fixed nitrogen. Thus, expression of thenifD gene in trans restored the ability of thenifD1::kan mutant DL2D to grow in the absence of exogenous fixed nitrogen. In fact, DL2D/pCDSnifD can be routinely cultured in ammonium-free FWAFC medium (data not shown).

Although antibiotics, which constitute potential sources of fixed nitrogen, could not be used to select for the maintenance of pCDSnifD and the nifD1::kan mutation over the course of this experiment, PCR screening confirmed the presence of both the nifD1::kan mutation and pCDSnifD in strain DL2D/pCDSnifD at the end of the experiment (data not shown).

The results described above confirm that G. sulfurreducenshas the ability to fix nitrogen. In addition, these results demonstrate that it is possible to complement mutations in G. sulfurreducens, a genetic technique required for properly evaluating the function of genes in this organism.

In summary, this study has demonstrated that G. sulfurreducens is a genetically tractable microorganism. It is now possible to introduce foreign DNA intoG. sulfurreducens by electroporation, to place mutations at specific locations within its chromosome, and to express proteins from extrachromosomal elements. These novel genetic techniques coupled with the availability of the sequence of the G. sulfurreducensgenome will enable the rapid study of the physiological function of multiple G. sulfurreducens genes. The finding that the physiology of G. sulfurreducens can be studied by genetic techniques is significant, because microorganisms closely related toG. sulfurreducens are prominent members of a variety of Fe(III)-reducing microbial communities (22, 28). Thus, studies on the physiology of G. sulfurreducens, using the techniques outlined here, are likely to provide insights into microbial processes occurring in the Fe(III) reduction zone of subsurface environments. Studies similar to those described here but focusing on mechanisms for the reduction of Fe(III) and contaminant metals byG. sulfurreducens are currently in progress.