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Conceived and designed the experiments: LE RP DGG. Performed the experiments: LE. Analyzed the data: LE TKG SLC RP DGG. Wrote the paper: LE RP DGG.
This work explores the bactericidal effect of (+)-limonene, the major constituent of citrus fruits' essential oils, against E. coli. The degree of E. coli BJ4 inactivation achieved by (+)-limonene was influenced by the pH of the treatment medium, being more bactericidal at pH 4.0 than at pH 7.0. Deletion of rpoS and exposure to a sub-lethal heat or an acid shock did not modify E. coli BJ4 resistance to (+)-limonene. However, exposure to a sub-lethal cold shock decreased its resistance to (+)-limonene. Although no sub-lethal injury was detected in the cell envelopes after exposure to (+)-limonene by the selective-plating technique, the uptake of propidium iodide by inactivated E. coli BJ4 cells pointed out these structures as important targets in the mechanism of action. Attenuated Total Reflectance Infrared Microspectroscopy (ATR-IRMS) allowed identification of altered E. coli BJ4 structures after (+)-limonene treatments as a function of the treatment pH: β-sheet proteins at pH 4.0 and phosphodiester bonds at pH 7.0. The increased sensitivity to (+)-limonene observed at pH 4.0 in an E. coli MC4100 lptD4213 mutant with an increased outer membrane permeability along with the identification of altered β-sheet proteins by ATR-IRMS indicated the importance of this structure in the mechanism of action of (+)-limonene. The study of mechanism of inactivation by (+)-limonene led to the design of a synergistic combined process with heat for the inactivation of the pathogen E. coli O157:H7 in fruit juices. These results show the potential of (+)-limonene in food preservation, either acting alone or in combination with lethal heat treatments.
The compound (+)-limonene is the major constituent of citrus fruits' essential oils (EOs) , . Because of its citrus-like flavor, (+)-limonene is employed as a flavoring agent in perfumes, creams, soaps, household cleaning products and in some food products such as fruit beverages and ice creams . In addition, (+)-limonene has been found to possess antifungal , , bacteriostatic ,  and bactericidal  properties. Therefore, its use as a food preservative has also been proposed .
Antimicrobial compounds have been successfully combined with other preservation technologies in order to achieve a synergistic effect in the inactivation of the target pathogens, following the hurdle theory proposed by Leistner and Gorris . For example, exposure of Escherichia coli or Cronobacter sakazakii to citral combined with high hydrostatic pressure (HHP), pulsed electric fields (PEF) or heat treatments, respectively, increased the inactivation degree achieved for each hurdle acting alone , , . Similarly, plenty of other compounds present in EOs were found to be effective in combination with heat in the inactivation of E. coli and Listeria monocytogenes . Combinations of (+)-limonene with heat or non-thermal technologies could likewise yield a similar synergistic effect in the inactivation of the target pathogens while preserving the organoleptic properties of the fresh food product.
The use of (+)-limonene in the design of food preservation processes requires a proper understanding of its mechanism of inactivation and of the influence of environmental factors that might affect it. (+)-Limonene belongs to the cyclic monoterpene hydrocarbon family, which are considered to accumulate in the microbial plasma membrane and thus cause a loss of membrane integrity and dissipation of the proton motive force . Previous studies on the inactivation of E. coli by other terpenes and terpenoids (such as carvacrol or citral) have demonstrated the occurrence of sub-lethal injury in the outer and cytoplasmic membranes , , pointing out the membrane disruption as a mechanism of inactivation by these compounds. However, the precise targets of terpenes and terpenoids are not yet completely understood.
Description of cellular target of antimicrobial compounds could be assisted by the use of Fourier transform-infrared (FT-IR) spectroscopy . FT-IR spectroscopy is a physico–chemical analytical technique based on measurement of vibration of a molecule excited by IR radiation at a specific wavelength range. Specially, attenuated total reflectance infrared microspectroscopy (ATR-IRMS) provides bands from all the cellular components of microorganisms (e.g. cell membrane and wall components, proteins and nucleic acids), giving spectral signatures or “fingerprints” that permit the classification of a microorganism at the strain and serovar level .
Regulation of gene expression by alternative sigma factors, which are proteins that act as transcription initiation factors through specific binding of RNA polymerase to gene promoters is key in bacterial resistance to food preservation technologies . In many Gram-negative and Gram-positive genera, sigma factors, σS (encoded by rpoS gene) and σB (encoded by sigB gene), respectively, are responsible for the transcription of specific stationary-phase genes . Besides, these sigma factors could also be responsible for cell protection under environmental stresses such as acid, cold, heat or osmotic shocks , , . Since previous work showed that the expression of RpoS contributed to the higher resistance of E. coli to the terpene aldehyde citral , a similar regulation could be expected for other chemical compounds such as (+)-limonene.
The aims of this work were: (a) to study the inactivation of Escherichia coli BJ4 by (+)-limonene, describing the effect of the pH of the treatment medium, deletion of sigma factor σS and sub-lethal shocks; (b) to study the occurrence of lethal and sub-lethal injuries caused by (+)-limonene in bacterial envelopes of E. coli BJ4 and MC4100; (c) to identify the E. coli BJ4 structures affected by (+)-limonene through ATR-IRMS spectroscopy, and (d) to determine the synergistic lethal effect obtained when combining (+)-limonene with heat and PEF treatments to inactivate E. coli O157:H7.
To accomplish these objectives we used different E. coli strains. In the first part, dedicated to describing the mechanism of inactivation by (+)-limonene the strains E. coli BJ4 and its ΔrpoS mutant  were used to study the influence of this alternative sigma factor in the bacterial resistance to (+)-limonene, and E. coli K-12 MC4100 and its ΔlptD4213 mutant  to study the role of the outer membrane in this resistance. In the second part, dedicated to demonstrating that knowledge of the mechanism of inactivation by (+)-limonene may have an applied interest to develop food preservation combined processes. Thus, we evaluated the efficacy of a combined process using (+)-limonene to inactivate the foodborne bacterium E. coli O157:H7 in fruit juices in which this pathogen uses to cause food safety problems.
The strains used were Escherichia coli BJ4 and its ΔrpoS null mutant BJ4L1 , E. coli K-12 MC4100 and its ΔlptD4213 mutant  and E. coli O157:H7 VTEC - (Phage type 34) . The cultures were maintained in cryovials at -80 °C prior to use. Broth subcultures were prepared by inoculating one single colony from a plate, a test tube containing 5 mL of sterile tryptic soy broth (Biolife, Milan, Italy) with 0.6% yeast extract added (Biolife) (TSBYE). After inoculation, the tubes were incubated overnight at 37 °C. With these subcultures, 250 mL Erlenmeyer flasks containing 50 mL of TSBYE were inoculated to a final concentration of 104 CFU/mL. These flasks were incubated with agitation (130 rpm; Selecta, mod. Rotabit, Barcelona, Spain) at 37° C until the stationary growth phase was reached.
(+)-Limonene (97% purum) was purchased from Sigma-Aldrich (Sigma-Aldrich Chemie, Steinheim, Germany). This compound is practically immiscible in water, so a vigorous shaking method was used to prepare suspensions. (+)-Limonene was added at a final concentration of 200 µL/L to tubes containing 10 mL of citrate-phosphate buffer of pH 4.0 (23.85 g/L) and 7.0 (27.09 g/L). Before treatments, bacterial cultures were centrifuged at 6,000•g for 5 min and resuspended in the same buffer that of each treatment. Microorganisms were added at a final concentration of 3·107 CFU/mL and maintained under constant agitation (130 rpm) at 20 °C. Samples were taken at regular intervals, and survivors were enumerated. According to previous studies , , treatment time and temperature; and initial concentrations of (+)-limonene and bacteria were chosen to detect 5 log10 cycles of cell inactivation (i.e. from 3·107 to 3·102 CFU/mL). Minimal inhibitory concentration (MIC) of (+)-limonene determined using the tube dilution method  for E. coli BJ4 and O157:H7 was 5 µL/mL (data not shown).
Previous experiments showed that native E. coli was insensitive to incubation in citrate–phosphate buffer at pH 7.0 or pH 4.0 for 24 h at 20 °C.
One 1-mL aliquot of bacterial suspensions was centrifuged at 10,000•g for 5 min and resuspended in 1 mL of TSBYE at 45°C or 0°C (sub-lethal heat and cold shocks, respectively) or in TSBYE acidified to pH 4.5 with HCl at 20 °C (sub-lethal acid shock). Sub-lethal heat shock was performed by immersing the bacterial suspensions in a thermostatic water bath (Bunsen, mod. BTG, Madrid, Spain) and holding at 45 °C for 2 h. Suspensions were kept on ice for 4.5 h (sub-lethal cold shock) or at 20°C (sub-lethal acid shock) for 1 h. Microbial resistance to (+)-limonene was assessed as explained above. These conditions were chosen from previous published work , .
Permanent cell permeabilization of E. coli BJ4 was evaluated after the treatment with 200 µL/L of (+)-limonene (initial cell concentration: 3·107 CFU/mL) for different treatment times (10 min, 25 min, 1 h, 6 h, 24 h) at pH 4.0 and 7.0 at 20° C. Cells were centrifuged, supernatant was removed, and propidium iodide (PI) (Sigma – Aldrich, Madrid, Spain) was added to a final concentration of 0.08 mmol/L . Cell suspensions were incubated for 15 min at 20° C, centrifuged at 10,000·g for 5 min, and washed three times until no extracellular PI remained in the buffer. Cell permeabilization was analyzed using a fluorescence microscope (Nikon, Mod. L-Kc, Nippon Kogaku KK, Japan).
An aliquot of cell suspensions was centrifuged at 6,000·g for 10 min at 4° C. Pellets were washed three times with 1 mL of 0.9% NaCl and centrifuged at 6,000·g for 10 min. Pellets were placed onto grids of hydrophobic membrane (HGM; ISO-GRID, Neogen Corporation, Lansing, MI, USA) and dried out under laminar flow at room temperature for 1 h. Samples were analyzed by IR equipment (Illuminate IR, Smiths detection, The Genesis Centre Science Park South Birchwood Warrington, United Kingdom) interfaced with mercury-cadmium-telluride photoconductive detector and equipped with a microscope with a motorized x-y stage, 20x and 50x objectives, and slide-on attenuated total reflection (ATR) diamond objective (Smiths detection, United Kingdom). The hydrophobic membranes were placed on the stage of the microscope and a specific position of the microbial pellet was selected with the assistance of the microscope and live camera (Leica OM 2,500, Module FT-IR, Renishaw plc, New Mills, Wotton-under-Edge, Gloucestershire, United Kingdom). The microscope was software-controlled using Wire 3.2 version software (Renishaw plc, United Kingdom). Spectra were collected from 4,000 to 800 cm−1 with a resolution of 4 cm−1. The spectrum of each sample was obtained by taking the average of 128 scans. Spectra were displayed in terms of absorbance obtained by rationing the single beam spectrum against that of the air background. The spectrometer was completely software controlled by synchronize IR basic version 1.1 software (SensIR Technologies, Smiths detection, United Kingdom). Pirouette® multivariate analysis software (version 4.0, InfoMetrix, Inc., Woodville, WA) was used to analyze the raw spectra of bacterial cells. The IR spectral data were mean-centred, transformed to their second derivative using a 15-point Savitzky-Golay polynomial filter, and vector-length normalized; sample residuals and Mahalanobis distance were used to determine outliers , . Soft independent modeling of class analogy (SIMCA) was used to build a predictive model based on the construction of separate principal component analysis (PCA) models for each class. SIMCA class models were interpreted based on class projections, misclassifications and discriminating power. Class projections were visible through three-dimensional graphics of clustered samples. Probability clouds (95%) are built around the clusters based on PCA scores, allowing SIMCA to be used as a predictive modeling system. Total misclassifications were analyzed and interpreted for the input data. Variable importance, also known as discriminating power, was used to define the variables (wavenumbers) that have a predominant effect on bacterial classification, minimizing the difference between samples within a cluster, and maximizing differences between samples from different clusters. SIMCA analysis assesses itself by predicting each sample included in the training set comparing that prediction to its assigned class; this assessment is referred to as misclassifications. Zero misclassifications typify a model in which all samples were correctly predicted to the pre-assigned class. Compared samples were E. coli BJ4 (initial concentration: 3·107 CFU/mL) after being incubated for 24 h at 20° C in absence or presence of 200 µL/L of (+)-limonene in citrate-phosphate buffer of pH 4.0 or 7.0.
E. coli BJ4 at an initial concentration of 3·107 CFU/mL were treated for 20 min with 200 µL/L of (+)-limonene in citrate – phosphate buffer of pH 4.0 so that 1 log10 cycle of inactivation was reached. At this moment, cells were centrifuged and resuspended in TSBYE without (+)-limonene. Non-treated cells were also centrifuged, resuspended in TSBYE without (+)-limonene and adjusted at the same final concentration of live cells (3·106 CFU/mL). Optical absorbance was measured at 590 nm during growth for 14 h of both samples at 37 °C with a spectrophotometer (GENios, Tecan, Austria).
Tubes containing 5 mL of apple juice or orange juice in absence or presence of (+)-limonene added to a final concentration of 200 µL/L were placed in a shaking thermostatic bath at 54 °C (Bunsen, mod. BTG, Madrid, Spain). Before treatments, bacterial suspensions of E. coli O157:H7 were centrifuged at 10,000·g for 5 min and resuspended in apple or orange juice. Once the treatment temperature was reached, the microbial suspension was added to a final concentration of 3·107 CFU/mL. Samples were taken after 10 min and survivors were enumerated. These treatment conditions were chosen to make these data comparable with previously published data obtained under the same conditions , , , .
PEF treatments were carried out in an equipment that delivered an exponential-decay pulse previously described by García et al. , provided with a parallel-electrode treatment chamber with a distance of 0.25 cm between electrodes and an area of 2.01 cm2. Before treatments, bacterial suspensions of E. coli O157:H7 were centrifuged at 10,000·g for 5 min and resuspended in shelf-stable apple juice (pH 3.6) or orange juice (pH 3.8) (Don Simón, Murcia, Spain). Bacterial cultures were added to tubes containing 5 mL of each of these media with or without 200 µL/L of (+)-limonene, and 0.5 mL of these suspensions were placed into the treatment chamber with a sterile syringe. Exponential waveform pulses at an electrical field strength of 30 kV/cm and a pulse repetition rate of 1 Hz were used in this study. Experiments started at room temperature and after the application of 25 pulses the temperature of the samples was below 35° C. After treatment, samples were taken and survivors were evaluated.
After treatments, samples were adequately diluted in 0.1% w/v Peptone Water (Biolife), containing 1% v/v Tween 80 (Biolife) as a neutralizer. 0.1 ml aliquots from the neutralized samples were pour-plated onto Tryptic Soy Agar with 0.6% Yeast Extract added (TSAYE) as non-selective medium. Plates were incubated at 37°C for 24 h. Previous experiments showed that longer incubation times did not influence the survival counts. In order to determine bacterial cell injury, treated samples were also plated onto selective media: TSAYE with 4% (E. coli BJ4 and MC4100) or 3% (E. coli BJ4L1, O157:H7 and MC4100 ΔlptD4213) sodium chloride (Sigma-Aldrich, Madrid, Spain) added (TSAYE-SC) to evaluate cytoplasmic membrane damage; and onto TSAYE with 0.35% (E. coli O157:H7) or 0.2% (E. coli BJ4 and BJ4L1) bile salts (Biolife) added (TSAYE-BS) to evaluate outer membrane damage. These levels of sodium chloride and bile salts were determined as the maximum non-inhibitory concentrations for native cells. Plates containing selective media were incubated for 48 h at 37°C. Previous experiments showed that longer incubation times did not influence survival counts.
After incubation of plates, colonies were counted with an improved image analyzer automatic counter (Protos; Analytical Measuring Systems, Cambridge, United Kingdom) as described by Condón et al. . The extent of sub-lethal injury was expressed as the difference between the log10 count (CFU) on non-selective medium (TSAYE) and the log10 count on selective media (TSAYE-SC and TSAYE-BS) after treatments. According to this representation, “2 log10 cycles of injured cells” means a 2-log10 difference in the count on selective and non-selective media or that 99% of survivors were sub-lethally injured.
Experiments were carried out in triplicate on different working days. Inactivation was expressed in terms of the extent of reduction in log10 counts after every treatment. The error bars in the figures indicate the mean ± standard error from the data obtained from at least three independent experiments. Analyses of variance (p=0.05) were performed using SPSS software (SPSS, Chicago, IL, USA).
To characterize the growth kinetics, the absorbance values were fit using nonlinear regression with the Gompertz model , which in this case can be described by the equation:
where A(t) is the absorbance value in time t, C is the absorbance value in the stationary phase, B is the relative growth rate in point M, and M is the time in which the cells reach their maximum growth rate. The lag phase duration was calculated as .
The antimicrobial activity of 200 µL/L of (+)-limonene on the survival of 3·107 CFU/ml of E. coli BJ4 and its rpoS mutant BJ4L1 was tested at pH 4.0 and 7.0 for 10 min, 6 h and 24 h (Figure 1). Both E. coli strains were less resistant at pH 4.0 than at pH 7.0: after 24 h of treatment less than 2 log10 cycles of the initial populations were inactivated at pH 7.0 (Figure 1B), while a treatment of 6 h at pH 4.0 was able to inactivate more than 3 log10 cycles of both strains, and about 5 log10 cycles of inactivation were achieved after 24 h of storage (Figure 1A).
Regarding the comparison between the wild and the mutant strain, both wild type and rpoS mutants showed a similar (+)-limonene resistance for all the treatments assayed (p>0.05).
Development of cross-resistance to (+)-limonene as a consequence of sub-lethal shocks was studied. On the one hand, exposure to a previous sub-lethal heat or acid shock did not affect the final inactivation reached by (+)-limonene in E. coli, since no statistically significant differences were found when compared to the control treatment (p>0.05). On the other hand, exposure to a sub-lethal cold shock significantly decreased (p<0.05) the resistance of both strains to (+)-limonene (Table 1).
Bacterial counts were not modified (p>0.05) by incubation in citrate–phosphate buffer at pH 7.0 or pH 4.0 without (+)-limonene for 24 h at 20 °C (data not shown).
The enumeration of the survivors on the selective medium TSAYE-SC (with sodium chloride) and TSAYE-BS (with bile salts) (Figure 2) revealed that storage for 6 h with 200 µL/L of (+)-limonene caused sub-lethal damages neither to the cytoplasmic nor to the outer membrane of E. coli BJ4, since the levels of inactivation in these media were similar to those detected in TSAYE for each pH (p>0.05, Fig. 1). The same conclusion was drawn from the survival counts after 10 min and 24 h of treatment (data not shown).
Bacterial counts in selective or non-selective media were not modified (p>0.05) by incubation in citrate–phosphate buffer at pH 7.0 or pH 4.0 without (+)-limonene for 24 h at 20 °C (data not shown).
Moreover, we evaluated the growth of treated and non-treated cells after exposure/non-exposure to (+)-limonene. Since exponential phase started after 2 h post-inoculation in both populations (2.19±0.19 h) no lag phase delay was detected in treated cells (p>0.05) (data not shown).
Permanent membrane permeabilization of E. coli BJ4 was demonstrated by the uptake of the fluorescent probe PI. As can be seen in Figure 3, a direct correlation (R2=0.96) was found between the percentage of inactivated cells and the percentage of permeabilized cells after adding 200 µL/L of (+)-limonene for different treatment times. Furthermore, as seen with cell inactivation, the percentage of permeabilized cells after 10 min of exposure to (+)-limonene was influenced by pH: after 1 h, E. coli showed maximum cell permeabilization (>90%) at pH 4.0, corresponding to more than 2 log10 cycles of cell inactivation, while at pH 7.0 only about 50% of cells were permeabilized and inactivated. After incubation in the presence of (+)-limonene for 24 h, maximum cell permeabilization (>90%) was observed at both pHs.
No membrane permeabilization (p>0.05) was detected after incubation in citrate–phosphate buffer at pH 7.0 or pH 4.0 without (+)-limonene for 24 h at 20 °C (data not shown).
Typical spectra of E. coli BJ4 with the presence or absence of (+)-limonene at pH 4.0 and 7.0 are shown in Figures 4A and 4D, respectively. Class projections illustrate the ability of SIMCA to differentiate IR data based on the first 3 principal components. Since the range of 4000 to 2000 cm−1 was not significant to describe the biochemical differences among our samples Figures 4B, 4C, 4E and 4F only includes data obtained from the range 1,900–800 cm−1. Our classification models obtained from derivatized infrared spectra (1900–800 cm−1) of E. coli BJ4 cells (Figures 4B and 4E) allowed for the tight clustering and clear differentiation of E. coli BJ4 samples according to the presence or absence of (+)-limonene for each pH. Discriminating power of SIMCA is a measure of variable importance in infrared frequency and contributes to the development of the classification model . Figures 4C and 4F show the wavenumbers that had a predominant effect on discrimination of (+)-limonene-treated and untreated cells at pH 4.0 and 7.0, respectively. As can be seen, the discriminating power of non-treated and (+)-limonene treated samples at pH 4.0 (Figure 4C) showed two spectral bands at 1,624 and 1,395 cm−1, corresponding to changes in the amide I absorption band of β-sheet proteins , ; and in the symmetric stretching of COO- groups in amino acids and/or fatty acids , , . At pH 7.0 (Figure 4F), comparison of (+)-limonene treated and non-treated cells showed that the major discriminating bands were those located at 1,083, 1,250 and 992 cm−1, corresponding to the symmetric and asymmetric stretching of P=O groups in phosphodiester bonds and ring vibrations of carbohydrates , , . ATR-IRMS spectra of (+)-limonene treated E. coli O157:H7 allowed us obtaining similar conclusions (data not shown).
For this study we used an E. coli MC4100 ΔlptD4213 strain. This mutation disrupts the outer membrane permeability barrier, making E. coli sensitive to antimicrobial compounds that are not normally effective against Gram-negative bacteria .
The lptD4213 mutant was less resistant to (+)-limonene at pH 4.0 than its wild type strain (Figure 5A). For example, after 30 min more than 5 log10 cycles (>99.999%) of the initial lptD4213 population were dead, whereas less than 2.5 log10 cycles (99.7%) of the wild strain population were inactivated. Surviving counts in Figure 5A indicate that (+)-limonene did not induce sub-lethal injuries in the cytoplasmic membrane of the wild type strain MC4100. However, a high proportion (>2.5 log10 cycles or 99.7% of survivors) of lptD4213 cells had sub-lethal damages in their cytoplasmic membrane after (+)-limonene treatment at pH 4.0. On the contrary, the lptD4213 mutants treated by (+)-limonene at pH 7.0 showed the same resistance as wild type cells and sub-lethal injuries in the cytoplasmic membrane were not detected (Figure 5B).
Bacterial counts in selective or non-selective media were not modified (p>0.05) by incubation in citrate–phosphate buffer at pH 7.0 or pH 4.0 without (+)-limonene for 60 min at 20 °C (data not shown).
To study a combined process of (+)-limonene with a lethal heat treatment, a pathogenic E. coli serotype, E. coli O157:H7, and acid fruit juices as treatment medium were chosen. Preliminary results showed that E. coli O157:H7 (+)-limonene resistance at 20°C was similar (data not shown).
Figure 6A shows the inactivation of E. coli O157:H7 by a lethal heat treatment (54°C for 10 min) alone or in combination with 200 µL/L of (+)-limonene in apple or orange juice. A lethal heat treatment alone inactivated 0.5 log10 cycles of the initial population of E. coli O157:H7; and caused sub-lethal damages in the cytoplasmic membrane in about 2 and 0.5 log10 cycles of survivors (as seen by the difference in log10 counts between recovery in TSAYE and TSAYE with sodium chloride) when cells were treated in apple and orange juice, respectively. Moreover, 4.5 and 2 log10 cycles of survivors showed sub-lethal damages in their outer membrane (as seen by the difference in log10 counts between recovery in TSAYE and TSAYE with bile salts) after lethal heat treatments in apple or orange juice, respectively.
The combined process of lethal heat and (+)-limonene in both juices caused the inactivation of more than 4 extra log10 cycles as compared with application of separate treatments. Hence, this combination in juices resulted in a synergistic effect on the final inactivation. A synergistic effect between (+)-limonene and lethal heat treatments under the same treatment conditions was also observed in citrate-phosphate buffer at pH 7.0. As observed at pH 4.0, simultaneous application of both treatments at pH 7.0 allowed the inactivation of more than 4 extra log10 cycles (data not shown).
Bacterial counts in selective or non-selective media were not modified (p>0.05) by incubation in apple or orange juice without (+)-limonene for 60 min at 20 °C (data not shown).
Figure 6B shows the inactivation of E. coli O157:H7 by a mild PEF treatment (25 pulses at 30 kV/cm) alone or in combination with 200 µL/L of (+)-limonene in apple or orange juice.
On the one hand, a separate treatment of 200 µL/L (+)-limonene at 20°C against 3·107 CFU/mL of E. coli O157:H7 when suspended in these juices for 10 min inactivated less than 0.5 log10 cycles of the initial population (data not shown). On the other hand, a separate PEF treatment in absence of (+)-limonene inactivated less than 0.5 log10 cycles of the initial E. coli O157:H7 population, and caused sub-lethal injury in the outer membrane in less than 1 log10 cycle of surviving cells.
The final level of inactivation resulting from the combined process (PEF with (+)-limonene) was additive, i.e. was equal to the sum of the levels of inactivation of both treatments applied separately, not observing any extra inactivation because of the simultaneous application of a lethal heat treatment in presence of (+)-limonene.
Bacterial counts in selective or non-selective media were not modified (p>0.05) by incubation in apple or orange juice without (+)-limonene for 60 min at 20 °C (data not shown).
Previous research on the antibacterial activity of (+)-limonene has been mostly focused on its bacteriostatic activity , , but little is known about its activity as a bactericidal agent in food preservation. In this respect, an important aspect to consider is the pH of the treatment medium (or the food matrix), since the final inactivation achieved by (+)-limonene was considerably higher in acid conditions (Figure 1). It is generally considered that the bacterial resistance to essential oils (EO) and their components decreases with lowering pH values because of the increase in EO hydrophobicity at low pH. As a consequence, there is an easier EO dissolution in the lipids of the cell membrane .
Our research was divided into two well-differentiated parts. The first part is focused on the study of mechanism of bacterial inactivation by (+)-limonene for which two wild-type and mutant strains (BJ4 and its rpoS mutant, and MC4100 and its lptD4213 mutant) were used. The second part of our study is dedicated to a practical application in fruit juices of the knowledge obtained in the first part in order to demonstrate the key role of the outer membrane in microbial protection against (+)-limonene. For this objective, E. coli O157:H7 was used owing to its importance in food safety of fruit juices.
The expression of RpoS has been reported to cause physiological and morphological modifications that increase microbial resistance to various stresses . Since deletion of rpoS did not decrease E. coli BJ4 resistance to (+)-limonene (Figure 1), probably the expression of σS-controlled genes under stationary-phase conditions, such as dps (a stress response DNA-binding protein) or uspB (universal stress protein B) , ,  did not play a role in cell resistance to (+)-limonene. This finding would suggest different mechanisms of inactivation and microbial resistance for (+)-limonene in relation to other antimicrobial compounds such as citral  and food preservation technologies .
The application of a sub-lethal heat, cold or acid shock has been demonstrated to induce cross resistance to multiple stresses (see review ) in E. coli. In this study, we have shown that a previous sub-lethal heat or acid shock did not influence subsequent E. coli BJ4 resistance to (+)-limonene (Table 1). Interestingly, rpoS deletion did not modify (+)-limonene resistance of sub-lethally heat- and acid-shocked cells. However, a previous sub-lethal cold-shock decreased the resistance of both wild type and rpoS mutant cells to (+)-limonene (Table 1). Exposure to cold temperatures leads to a decrease in the membrane fluidity which triggers an increase in the ratio of unsaturated fatty acids , , that could be responsible of the decreased resistance to (+)-limonene (Table 1).
The occurrence of sub-lethal injuries after food preservation treatments can be evaluated using different techniques, such as different survival counts obtained between plating treated cells in non-selective and selective media , and delay in lag phase before starting growth in treated with regards non-treated cells , . At the conditions assayed in this study no sub-lethal damage in the cell envelopes was detected after exposure of E. coli BJ4 to (+)-limonene by the selective media plating technique (Figure 2). Furthermore, the same duration of lag phase was observed for treated and untreated E. coli BJ4 cells, suggesting that neither the cell envelopes nor other cell structures were sub-lethally injured. Therefore, the action of (+)-limonene could be catalogued under the “quantal” effect, a response which can be expressed in binary terms: it is either present or absent (“all or nothing”)  in which bacteria are either killed or intact after the treatment. Occurrence of sub-lethal damage in E. coli BJ4 cell envelopes by other EO compounds, such as citral or carvacrol , , would suggest a different mechanism of inactivation between these compounds and (+)-limonene.
Food preservation technologies, such as heat, pulsed electric fields (PEF), high hydrostatic pressure (HHP) and essential oils (EOs) normally target cell envelopes , , . Thus, we evaluated membrane permeabilization in E. coli BJ4 using propidium iodide. A direct correlation between the percentage of cell inactivation and the percentage of membrane permeabilization was obtained (Figure 3). The simultaneous occurrence of both phenomena identifies the cell envelopes as an important target in the mechanism of E. coli BJ4 inactivation by (+)-limonene.
To further study the damages caused by (+)-limonene, we included an analysis by ATR-IRMS. We used this technique that evaluates the biochemical composition of the bacterial cell constituents , such as water, proteins, nucleic acids, fatty acids and polysaccharides, to describe the changes caused by (+)-limonene. ATR-IRMS results allowed selecting two major discriminating bands at both pH 4.0 (Figure 4C) and pH 7.0 (Figure 4F) as the main responsible for the differences between untreated and (+)-limonene-treated E. coli BJ4 cells. At pH 4.0, the 1,624 cm−1 band corresponding to the amide I absorption band of β-sheet proteins , ; and the band at 1,395 cm−1 reflecting the symmetric stretching of COO- groups in amino acids and/or fatty acids , , . Since β-barrel membrane proteins occur in the outer membranes of Gram-negative bacteria , the main contribution to the discrimination between untreated and (+)-limonene-treated cells at pH 4.0 could come from affected outer membrane proteins that form membrane-spanning β-barrels. However, at pH 7.0, the discriminating bands for (+)-limonene treatments were found at 1,083, 1,250 and 992 cm−1, corresponding to the symmetric (1,083 cm−1) and asymmetric (1,250 cm−1) stretching of P=O groups in phosphodiester bonds and ring vibrations of carbohydrates (992 cm−1) , , . Phosphodiester bonds are present in phospholipids of the cytoplasmic membrane and of the inner leaflet of the outer membrane , while carbohydrates are found in the lipopolysaccharide (LPS) fraction of the cell wall . In consequence, (+)-limonene would target phospholipids and LPS cell fraction at pH 7.0, and the protein fraction at pH 4.0 in E. coli BJ4.
It should be noted that these conclusions related to the mechanism of bacterial inactivation by (+)-limonene were drawn from experiments using the Gram-negative strains E. coli BJ4 and its ΔrpoS mutant. Further experiments using different microorganisms are needed to extrapolate these conclusions to other Gram-negative strains.
Once we confirmed the role of cell envelopes in the (+)-limonene antimicrobial activity, we used the mutant strain ΔlptD4213 (formerly known as Δimp4213) to evaluate the role of outer membrane in the mechanism of inactivation by (+)-limonene (Figure 5). LptD is an essential β-barrel protein of the outer membrane  which is implicated in lipopolysaccharide (LPS) assembly . Depletion of this protein results in increased outer membrane permeability to lipophilic compounds, such as novobiocin or rifampin . In effect, at pH 4.0 lptD4213 mutants showed a decreased (+)-limonene resistance, and occurrence of sub-lethal damage in the cytoplasmic membrane was demonstrated after (+)-limonene treatments. This finding, together with ATR-IRMS observations, could indicate that, at pH 4.0, (+)-limonene should damage the outer membrane in order to gain access to the periplasmic space and cytoplasmic membrane and inactivate the bacterial cell. Once outer membrane permeability to (+)-limonene is increased, there would be an enhanced interaction of (+)-limonene molecules at pH 4.0 with the components in the cytoplasmic membrane. However, the bactericidal action of (+)-limonene at pH 7.0 was not enhanced by higher outer membrane permeability in lptD4213 mutants, indicating that facilitation of (+)-limonene access to the periplasmic space and cytoplasmic membrane would not be required at pH 7.0. Furthermore, results shown by ATR-IRMS would indicate that LPS damage was related to mechanism of inactivation by (+)-limonene at pH 7.0. Therefore, mechanism of E. coli BJ4 and MC4100 inactivation by (+)-limonene was different as a function of the pH of the treatment medium. In spite of differences between E. coli BJ4 and MC4100, (+)-limonene resistance shown by both strains was similar (Figures 1 and and5).5). However, further research using other microorganisms is needed in order to increase the knowledge on the mechanism of bacterial inactivation by (+)-limonene and to use this compound in practical applications.
From the study of the mechanism of inactivation by (+)-limonene in E. coli BJ4 and MC4100 we could expect that application of a food preservation technology causing sub-lethal damages in outer membrane would increase the lethal effect induced by (+)-limonene, leading to an advantageous combined process. In order to prove this hypothesis and to provide a practical application of this knowledge we studied the effect of (+)-limonene in a combined process with heat or PEF in E. coli O157:H7 because of the presence of an outer membrane in this pathogenic serotype and its importance in food safety of fruit juices , . We determined that combinations of a lethal heat treatment that damaged outer membrane with (+)-limonene also achieved a synergistic effect to inactivate E. coli O157:H7 in juice. Thus, a facilitated access of (+)-limonene to the periplasmic space and cytoplasmic membrane would cause the inactivation of these sub-lethally damaged cells (Fig. 6A). On the contrary, since PEF did not cause sub-lethal damage to the outer membrane of E. coli O157:H7 the combination of (+)-limonene and PEF did not yield any extra inactivation when compared to the inactivation by PEF alone at the assayed conditions (Figure 6B). Since E. coli O157:H7 is a virulent strain whose genome has a significant number of differences from other E. coli strains, such as the presence of more than 1,300 new genes , , transfer of the knowledge on mechanism of microbial inactivation by (+)-limonene from E. coli BJ4 and MC4100 to E. coli O157:H7 would require further studies on the influence of the factors investigated in this research.
Although preliminary results indicate that (+)-limonene concentrations used in this study were accepted by consumers, sensory analysis of apple juice with (+)-limonene should be performed to evaluate commercial viability. Previous work with citral and PEF in E. coli BJ4 reached a similar conclusion , as well as combined processes between PEF and different antimicrobials against E. coli O157:H7 in apple and orange juices .
The study of the mechanism of bacterial inactivation by (+)-limonene showed that the lethality of this compound was higher at pH 4.0 than at neutral pH. Contrary to other food preservation treatments, deletion of rpoS did not modify E. coli BJ4 resistance to (+)-limonene. Furthermore, a previous sub-lethal heat or acid shock did not change E. coli BJ4 resistance to (+)-limonene, independently of rpoS deletion. However, a previous sub-lethal cold shock decreased the resistance of wild-type E. coli BJ4 and even more the resistance of rpoS mutant to (+)-limonene. Assessment of E. coli BJ4 permeabilization with propidium iodide showed that this phenomenon occurred simultaneously with bacterial inactivation, identifying the cell envelopes as important (+)-limonene targets. In contrast to other essential oils compounds, (+)-limonene did not cause sub-lethal injuries in any E. coli BJ4 structure, cataloguing its lethal action under the “quantal” effect (“all or nothing”). Different resistance pattern of lptD4213 mutants and ATR-IRMS results showed the importance of outer membrane in the mechanism of inactivation by (+)-limonene at pH 4.0. At pH 7.0, increased outer membrane permeability did not lead to a decreased (+)-limonene resistance and ATR-IRMS spectra demonstrated the importance of LPS in the mechanism of E. coli BJ4 inactivation at this pH. Considering the orange-like flavor of (+)-limonene and its consideration as a GRAS (Generally Recognized As Safe) substance , , we propose the simultaneous application of (+)-limonene with other preservation technologies that damage outer membrane, such as heat treatments, in order to design combined food preservation processes with a synergistic lethal effect, as demonstrated for E. coli O157:H7 in this study. Although bacterial resistance of the studied E. coli strains was similar, further research is needed in order to increase the knowledge on the mechanism of inactivation by (+)-limonene in other bacteria and to use this compound in practical applications.
This study was financially supported by the Comisón Interministerial de Ciencia y Tecnolog?a (CICYT) (Projects AGL2009-11660 and AGL2012-32165), Gobierno de Aragón, European Social Fund and Departament Quimica of Universitat Rovira i Virgili. Spanish Ministerio de Ciencia e Innovación provided LE with a grant to carry out this investigation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.