A Degradation Product from Hydrolysate of Imipenem with Imis Broad-Spectrum Inhibits Metallo-β-Lactamases

3.1. General Information

General chemicals were purchased from TCI (Tokyo Chemical Industry, Tokyo, Japan) and used without further purification. All antibiotics used were purchased from Sigma-Aldrich (St. Louis, MO, USA). The real-time monitoring of imipenem and faropenem hydrolysis and inhibition evaluation of MβLs were performed using an Agilent-8453 UV-visible spectrometer (Santa Clara, CA, USA). The 1H NMR and 1H-13C COSY NMR spectra were recorded on a Bruker DRX 600 MHz spectrometer (Bruker Daltonics Inc., Billerica, MA, USA).

3.2. Preparation of Escherichia coli with ImiS

The plasmid pET26b (+) with the ImiS gene was transformed into E. coli BL21. The kanamycin resistance gene existed in the plasmid. The monoclone of E. coli with ImiS was inoculated into 5 mL of Luria-Bertani media in the presence of 25 µg/mL of kanamycin and grown with shaking (150 rpm) at 37°C until the cells reached OD₆₀₀ = 0.5 - 0.6. At that time, 100 Μm of IPTG was added for MβL induction, and cells were grown for 2 hours at 37°C with shaking (150 rpm). Cell cultures were centrifuged at 5,500 g for 10 min at 4°C, the supernatant was discarded, and the cell pellets were washed thoroughly by re-suspending them in 1 mL of buffer (50 mM Tris at pH = 7.0). They were then pelleted again by centrifugation (5,500 g for 10 min at 4°C). This process was repeated three times, and finally, the cells were re-suspended in buffer with an OD₆₀₀ of 0.10 for UV-Vis studies (17, 18).

3.3. UV-Vis Monitoring of Antibiotics Hydrolysis

Either 10 µL of imipenem (12 mM) or 10 µL of faropenem (8 mM) was titrated into the sample cell filled with 990 µL of ImiS enzyme (0.2 µM) or E. coli with ImiS with OD600 of 0.10. Then, the variation of the UV spectrum in the reaction process was monitored at room temperature. This measurement continued until the UV absorption held steady on the Agilent UV8453 UV-Vis spectrometer (17, 18).

3.4. Determination of Minimum Inhibitory Concentration

The minimum inhibitory concentration (MIC) values of the antibiotics alone and in the presence of the enzyme inhibitor against antibiotic-resistant bacteria were determined using the broth micro-dilution method (19). Single colonies of E. coli-DH10B containing plasmids pBCSK(+)-VIM-2, pBCSK(+)-NDM-1, pBCSK(+)-ImiS, or pBCSK(+)-L1, in lysogeny broth agar plates were transferred into 5 mL of Mueller-Hinton liquid medium. Strains, grown in Mueller-Hinton medium to OD600 = 0.45, were used as inocula after 84-fold dilution to 1 × 10⁵ CFU/mL in Mueller-Hinton medium. Cefazolin was dissolved in Mueller-Hinton medium to prepare 4096, 2048, 1024, 512, 256, 128, 64, 32, 16, and 8 µg/mL stock solutions, and imipenem was dissolved in Mueller-Hinton medium to prepare 256, 128, 64, 32, 16, 8, 4, 2, 1, and 0.5 µg/mL stock solutions. As an inhibitor, P1 was dissolved in Mueller-Hinton media to prepare a 160 µg/mL stock solution. The prepared solutions, with different antibiotic concentrations (50 µL), were diluted to 100 µL with a 50 µL inhibitor solution. Then, 100 µL inoculum was added sequentially into the prepared solutions to yield a quarter of the initial concentrations. The mixtures were incubated at 37°C for 16 h. The MIC results were taken as the lowest concentration that completely inhibited visible growth. Each measurement was performed in duplicate, and the average value was recorded.

3.5. Cytotoxicity Evaluation

A cytotoxicity assay was performed to evaluate the toxicity of P1 in mouse fibroblast cells (L-929). The cells were seeded into 96-well plates at a cell density of 1.0 × 10⁴ cells/well in 100 µL of culture medium and maintained for 24 h. Then, the inhibitors with various working concentrations (7.8, 15.6, 31.25, 62.5, 125, 250, and 500 µg/mL) were added to the 96-well plates and incubated for another 48 h. Three wells containing only cells were suspended in a mixture solution of 98 µL complete medium, as the control for cell viability without the inhibitor. Three wells containing only the complete medium were used as blank control. Next, the medium was removed, and 100 µL of fresh culture medium and 10 µL of MTT were added to each well. After incubation for 4 h, the trays were then vigorously shaken to solubilize the formed product, and the absorbance at a wavelength of 490 nm was read on a microplate reader and analyzed. All experiments were conducted in triplicate, and the data are expressed as mean ± standard deviation.

4.1. UV-Vis Monitoring of Antibiotics Hydrolysis

To investigate the inhibition component of carbapenem hydrolysates, initially, the hydrolysis of imipenem and faropenem was monitored by UV-Vis on an Agilent UV8453 UV-Vis spectrometer in a wavelength range of 200 - 600 nm at 25°C, as previously reported (17, 18). The enzymatic and antibiotic samples were prepared with 50 mM Tris buffer, pH = 7.0. In a standard mode, 0.2 µM enzyme solution was used as control. Besides, 10 µL of imipenem (12 mM) or faropenem (8 mM) solution was added into the sample cell filled with 990 µL of ImiS enzyme solution, and the hydrolysis of the antibiotic was monitored until the characteristic absorption of the hydrolysates of the antibiotic had no changes in UV-Vis. The collected UV-Vis spectra are shown in Figure 1. It is clear that imipenem was hydrolyzed quickly in around 50 s, and the maximum absorption of the antibiotic at 300 nm disappeared (Figure 1A). With monitoring for about 1 h, a species with maximum absorption at 310 nm appeared, and with monitoring up to about 48 h, the absorbance of the species reached its maximum.

Figure 1.

The monitored UV-Vis spectra of 120 µM imipenem (A) and 80 µM faropenem (B) hydrolyses in the presence of 0.2 µM purified ImiS. Both antibiotic and enzymatic samples were prepared with 50 mM Tris buffer, pH = 7.0.

Under the same test conditions, the UV-Vis spectra monitoring of faropenem hydrolysis with the ImiS enzyme is shown in Figure 1B. It shows that faropenem was slowly (compared to imipenem) but surely hydrolyzed, in about 5 min. The difference in the hydrolysis rate was due to the structural differences between the two carbapenems (Appendix 1 in Supplementary File). However, further monitoring, up to 36 h, showed that the absorption of faropenem hydrolysate at 300 nm had no more decreases. Also, the hydrolysate had no absorption at any other wavelengths, except for 300 nm, unlike the hydrolysate of imipenem. This suggests that the hydrolysate was ring-opened faropenem, while the hydrolysate of imipenem was not a ring-opened product.

To investigate the hydrolysate of carbapenems by ImiS inside bacterial cells, the hydrolysis of imipenem and faropenem by E. coli cells with ImiS (E. coli with ImiS) was monitored by UV-Vis (Figure 2). The concentrations of the two antibiotics (imipenen and faropenem) were 120 and 80 µM, respectively, and E. coli with ImiS with an OD₆₀₀ of 0.1 was used for the evaluation. As expected, imipenem was completely hydrolyzed in E. coli cells, corresponding to a new absorption peak at 310 nm (Figure 2A), in around 15 min, which was longer than the time (5 min) of antibiotic hydrolysis by the ImiS enzyme. This difference may be due to a certain time required for the diffusion of the substrate across the bacterial outer membrane into the periplasm where ImiS was located (20). Meanwhile, the hydrolysis of faropenem by E. coli with ImiS was also monitored (Figure 2B). It can be observed that the antibiotic initially was hydrolyzed in around 20 min, corresponding to the absorption peak at 300 nm, just like the hydrolysis with the ImiS enzyme (Figure 1B), and the absorbance at 300 nm remained stable for 20 min. The imipenem-generated product was distinct from the faropenem-generated product; therefore, the hydrolysates of imipenem with the ImiS enzyme were purified, and their inhibitory activities against MβLs were tested.

Figure 2.

The monitored UV-Vis spectra of 120 µM imipenem (A) and 80 µM faropenem (B) hydrolysis in the presence of E. coli cells (OD₆₀₀ = 0.10) expressing ImiS. Both antibiotic and Escherichia coli samples were prepared with 50 mM Tris buffer, pH = 7.0.

4.2. Inhibitory Activity Evaluation of Active Competent

To ascertain whether the ring-opened product, hydrolyzed carbapenem, was the resulting hydrolyzed and active component, we hydrolyzed imipenem with ImiS, and the resulting hydrolysate was analyzed. A saturated aqueous solution of imipenem was hydrolyzed with ImiS for 60 h at 4°C (it was observed that the solution gradually changed from colorless to yellowish-brown). Then, ImiS was removed from the solution by ultrafiltration (molecular weight cutoff at 10 KD), and the solution was lyophilized overnight to yield a brown powder. The powder was purified on an LC-2010 CHT high-pressure liquid chromatography (HPLC) equipped with a Prep C18 column (10 × 150 mm, 5 µM particle size; Waters), using a gradient running from 5% to 10% water over 20 min with a flow-rate of 1 mL/min, to give one component (P1).

To identify whether P1 was the active competent, the inhibitory activity of P1 was tested against the purified MβLs from different subclasses by UV-Vis via the determination of IC₅₀ values (inhibitory concentration causing 50% decrease in enzyme activity). It was observed that MβLs VIM-2, NDM-1, ImiS, and L1 from B1, B2, and B3 sub-classes were overexpressed and purified as previously described (21-24), respectively (see the Supporting Information). The concentration of P1 ranged from 1 to 50 µM, and the concentrations of imipenem, cefazolin, and nitrocefin (25) as substrates were 40 µM. The enzyme and the inhibitor were pre-incubated for 20 min before adding the substrate and were then monitored at 300, 265, or 390 nm, in sequence, to determine the initial velocity.

The initial reaction rates were determined in triplicate, and the average value was recorded. We tested different pre-incubation times (10 - 120 min) and did not find any difference in residual activity, concluding that P1 is a time-independent inhibitor. The results summarized in Table 1 indicate that P1 exhibited a broad-spectrum inhibition on all enzymes tested (except for ImiS using imipenem as substrate), with an IC₅₀ value in the range of 8 - 32, 13.8 - 29.3, and 14.2 - 19.2 µM, using imipenem, cefazolin, and nitrocefin as substrates, respectively, and the standard deviations of IC50 values were less than 0.17.

4.3. Structure Determination of P1

To characterize the active molecule, a sample of 10 mg P1 in 500 µL of D₂O was run through 1H and 1H-13C COSY NMR (600 MHz, Bruker), suggesting that P1 could be a mercaptoethyl-form imidamide. As shown in the Appendix 1 in Supplementary File, the single peak at 7.95 ppm is assigned to a proton of an imine, and the two triple split peaks at 3.47 and 2.76 ppm are assigned to two methylene protons. Further, the ¹H-¹³C COSY spectra showed that there are cross-peaks of hydrogen directly bonding to each carbon. Each cross-peak occurs at the point where each carbon atom intersects the chemical shift of the hydrogen on that carbon. Based on the information from the above characterizations, we proposed a hydrolysis process of imipenem by ImiS, as shown in Figure 3, in which P1 is a degradation product of the ring-opened imipenem.

Figure 3.

The proposed hydrolysis process of imipenem with ImiS.

To check whether the active molecule has sulfhydryl, P1 was tested with Ellman's reagent (26). A series of solutions of P1, with concentrations ranging from 12.5 - 100 µM, were incubated with 1 mM of Ellman's reagent for 5 min, to determine the absorbance of TNB (2-nitro-5-thiobenzoic acid) at 412 nm. It can be observed (Appendix 1 in Supplementary File) that with the increase of P1 concentration, the solution turned yellow, and the corresponding absorbance of TNB increased linearly from 0.1 to 0.69, confirming that P1 does contain a sulfhydryl, which differs from the product of imipenem hydrolysis by class D β-lactamases (Appendix 1 in Supplementary File) (15). The assays suggested that P1 exists in the mercaptan form under the above activity test conditions.

4.4. Docking Studies

To explore the binding of the imipenem hydrolysate to ImiS, we performed molecular docking of inhibitor P1 into the active sites of CphA (instead of ImiS, which has not been crystallized yet, and with which it shares 96% sequence identity), using the same procedure as reported previously (27). The possible reasonable conformations (shown in Figure 4) are the lowest-energy conformations of those clusters. The sulfur atom of P1 was bound to Zn (II) ion (2.4 Å), the nitrogen atoms of imine and secondary amine formed two hydrogen bonds with carboxylate oxygen and the amino group of Asp120 (2.4 and 2.0 Å), tightly anchoring the inhibitor in the active site, revealing why P1 exhibited a low IC₅₀ value against ImiS.

Figure 4.

The conformations of P1 docked into the active site of CphA (PDB code 2QDS). The enzyme backbone is shown as a green cartoon and selected residues are shown as sticks, colored by atom (C, green; N, blue; O, red; S, yellow). The Zn (II) ion is shown as a gray sphere. The key residues displayed and interactions between the P1 and protein residues are indicated by dashed lines.

4.5. Minimum Inhibitory Concentration Determination

Given the broad-spectrum inhibition of imipenem hydrolysate against MβLs, the antibacterial activity of P1 was investigated by determining MIC values of β-lactam antibiotics in the presence and absence of P1. Four bacterial strains, E. coli-DH10B cells harboring plasmids pBCSK(+)-VIM-2, pBCSK(+)-NDM-1, pBCSK(+)-ImiS, and pBCSK(+)-L1, were used in the assays. The antibiotics imipenem and cefazolin (except for the test with E. coli with ImiS, because ImiS exclusively hydrolyzes carbapenems) were used for the assays. The MIC data (Table 2) indicated that a dose of 40 µg/mL of the degradation product P1 restored, by 16 - 32 folds and 8 - 128 folds, the antibacterial activities of imipenem and cefazolin against drug-resistant E. coli with MβLs, respectively. Additionally, P1 exhibited the best synergistic antibacterial efficacy against E. coli with ImiS and L1, resulting in a 32-128-fold decrease in the MIC of these two antibiotics, which is consistent with its inhibitory activity on the ImiS and L1 enzymes, as shown in Table 1. This assay revealed a means for the development of MβLs inhibitors, or even antibacterial reagents, from the hydrolysates of carbapenems.

4.6. Cytotoxicity Evaluation of P1

The potential toxicity of enzymatic inhibitors is a major concern for their biomedical applications. To determine the maximum non-toxic concentrations of the product inhibitor against mammalian cells, different concentrations of P1 (7.8 - 500 µg/mL) were incubated with L929 mouse fibroblast cells, and cell viability was evaluated using the MTT reagent. The results were expressed as the percent viability of each sample, compared with that of untreated control cells (PBS, pH = 7.4). The cell viability was over 94% in the presence of P1 at a dose up to 500 µM, indicating that the product inhibitor had little influence on cell proliferation (Appendix 1 in Supplementary File).