Introduction

Brazil is one of the main meat producers and exporters in the world [1, 2]. Of the different meat products, fresh sausages are among the most commonly consumed processed meat products in the world [3, 4]. Lactic acid bacteria (LAB) are the main bacterial group associated with the spoilage of meat and meat products, especially in vacuum-packed products like Tuscan sausage [5,6,7]. The growth of LAB is favored by the combination of microaerophilic conditions in the presence of salt (NaCl), sodium nitrite (NaNO2), sodium nitrate (NaNO3), and the high water activity found in such products [8]. These products are usually stored at 4 °C before consumption and antimicrobial or antioxidant preservatives are employed to extend their shelf lives [9].

The shelf life of fresh sausages is not easily estimated because the deterioration of these products is a complex process which may result in the change of different sensory quality attributes (color, odor, flavor, and taste) [9]. The most important factor influencing these changes is the microbial growth [10]. As a result, the amount of natural LAB can be used to evaluate the shelf life of not only fresh sausages but also of vacuum-packed meat products in general [11]. The acceptable quality limits of LAB counts found in the literature for cooked meat products range from 6 to 8 log CFU/g [12,13,14]. One of the main techniques used to extend the shelf life of fresh sausages involves the use of chemical preservatives, such as lactate and acetate [12, 15]. Chemical or commercial synthetic preservatives are therefore widely employed in these products [16].

The use of natural antimicrobial components as preservative agents has increased due to the consumer demand for more natural food products [17, 18]. In this context, essential oils (EOs) are complex, natural, and volatile compounds. They can be found in aromatic plants as secondary metabolites and have a natural and inherently strong odor. EOs are made up of 20 to 60 components, and usually two or three major components in relatively high concentrations are responsible for the bioactivity [19]. Oregano essential oil (Origanum vulgare) (OEO) and rosemary essential oil (Rosmarinus officinalis) (REO) are known for their antimicrobial activity and are commonly used to extend the shelf life of many food products [20, 21]. Many studies have shown that the antimicrobial activity of a given essential oil can be ascribed to its main components and to the interaction between them [22]. Regarding meat products, OEO has been added to beef fillets [23], minced meat [24], chicken meat [25], fish meat [26], and ham [11]. Meanwhile, rosemary essential oil (REO) has been added to pork sausages [3], minced meat [27], and poultry fillets [28]. Despite the large amount of studies on the influence of essential oils on different meat products, there are not many studies that quantify the extension of the shelf life in terms of the concentration of EO added to each product.

The purpose of this study was to assess the impacts of different concentrations of essential oils of oregano and rosemary in the shelf life and some physicochemical parameters of vacuum-packed refrigerated Tuscan sausage.

Materials and methods

Extraction and characterization of the essential oils

Dehydrated oregano and rosemary leaves were purchased in the local commerce of the city of Chapecó, Brazil. The essential oils were extracted through steam distillation [29]. The samples were stored in amber glass flasks at 5.0 ± 1.0 °C.

To characterize the essential oils, gas chromatography/mass spectrometry analyses were conducted in a gas chromatograph (Agilent Technologies, Santa Clara, CA, USA) coupled to a mass spectrometer (Agilent) using a capillary column HP-5MS (30 m × 0.25 mm × 0.25 μm composed of 5% phenylmethylpolysiloxane, J & W Scientific Inc., Folsom, CA, USA). The following temperature program was employed: 60 °C for 1 min, increased to 240 °C at 3 °C/min. Electron impact ionization at 70 eV with scan mass range of 45–400 m/z was used. Helium was used as carrier gas at 1 mL/min and the split mode at a ratio 1:20. Compounds were identified using digital libraries (NIST14). The percentage of each individual compound in relation to the total amount of detected substances was evaluated by the peak area gas chromatography (GC) normalization method. Analyses were conducted in triplicate.

Preparation, packaging, and storage of Tuscan sausage

The Tuscan sausage was prepared according to Brazilian legislation [30]. Forty-three kilograms of deboned pork and 13 kg of fat were obtained from retail sale, Santa Maria, RS, Brazil, grinded (8-mm diameter, Jamar PJ22 Grinder, Jamar Ltda., São Paulo, SP, Brazil) and mixed (Jamar MJI 35, Jamar) with other ingredients (Table 1). The mixture was homogenized for 5 min at 7 °C to a paste, cured for 30 min, and divided into nine batches (6.5 kg each). One batch was considered as control, and the other eight batches were added with OEO and REO at 0.05 wt%, 0.1 wt%, 0.2 wt%, and 0.4 wt%. Details of composition of each treatment are presented in Table 1.

Table 1 Components (g/100 g) used in the formulation of the Tuscan sausage for each treatment adopted
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The meat pastes were embedded in natural casings immersed in a 1% acetic acid solution for 15 min for hydration. The sausages were packed in vacuum-sealed polyethylene bags (Selovac 200B, São Paulo, SP, Brazil) and stored at 4.0 ± 0.5 °C for 56 days.

pH measurements and water activity

pH was measured at 0, 2, 4, 6, 8, 10, 12, 14, 20, 26, 32, 38, 44, 50, and 56 days of storage. The measurements were performed with a pH meter (MPA-210, TECNOPON, Piracicaba, SP, Brazil) using 10 g of sample mixed with 100 mL of distilled water. The water activity (aw) of the sausage was measured only at the beginning of storage with a water activity meter (Aqualab Series 4TEV, Decagon Devices Inc., Pullman, WA, USA). All the measurements were conducted in triplicate.

Color measurements

The International Commission on Illumination (CIE) color parameters reported as lightness (L*), redness (a*), and yellowness (b*) were recorded for all of the treatments and the control. Measurements were determined with a spectrophotometer (Konica Minolta CM-700D, Osaka, Japan) after 0, 7, 14, 21, 28, 35, 42, 49, and 56 days of storage. Readings were performed using diffuse illumination, with D65 as illuminant, 8° geometry, and 8-mm port size, specular component excluded. The parameters Chroma (C*) and Hue angle (h°) were calculated according to Eqs. (1) and (2), respectively:

$$ {C}^{\ast }=\sqrt{a^{\ast 2}+{b}^{\ast 2}} $$
(1)
$$ h{}^{\circ}= arctg\left(\frac{b^{\ast }}{a^{\ast }}\right) $$
(2)

LAB enumeration

LAB populations were estimated at 0, 2, 4, 6, 8, 10, 12, 14, 20, 26, 32, 38, 44, 50, and 56 days of storage, when 25-g aliquots was obtained from each treatment and batch, transferred to sterile plastic bags, and added to 225 mL of peptone water (0.1%, w/v, Merck, Darmstadt, Hessen, Germany). The mixtures were homogenized, tenfold diluted with peptone water (0.1%, w/v, Merck), and pour plated in duplicate in de Mann, Rogosa, and Sharpe (MRS, Liofilchem, Kasvi, Roseto, Italy) agar; the plates were overlaid with MRS agar (Liofilchelm, 30 mL per plate) and incubated at 37 °C for 48 h, when the formed colonies were enumerated and the results expressed in colony-forming unities per gram (CFU/g).

Kinetics of pH changes

An adapted version of the three-phase linear model (BUC) [31]was used to describe kinetics of pH changes for each treatment. Equation (3) shows the mathematical expression corresponding to the model:

$$ \mathrm{pH}(t)={\mathrm{pH}}_0,\kern0.5em \mathrm{if}\kern0.5em t<\lambda $$
$$ \mathrm{pH}(t)={\mathrm{pH}}_0-\nu \left(t-\lambda \right),\kern0.5em \mathrm{if}\kern0.5em \lambda \le t<{t}_{\mathrm{max}} $$
(3)
$$ \mathrm{pH}(t)={\mathrm{pH}}_{\mathrm{min}},\kern0.5em \mathrm{if}\kern0.5em t\ge {t}_{\mathrm{max}} $$

where pH(t) corresponds to the pH of the sample t days after storage, pH0 stands for the initial pH, λ represents a lag before pH starts to drop during storage, ν is a rate of decrease in pH, pHmin corresponds to an asymptotic value of pH, and tmax represents the time at which pH reaches this asymptotic limit.

Shelf life modeling

The experimental growth data of the natural LAB microbiota were expressed as log CFU/g. A version of the Baranyi-Roberts growth model (BAR) [32] without lag was fitted to the experimental data to evaluate the following kinetic growth parameters: maximum specific growth rate, initial logarithmic count, and final logarithmic count. Two maximum LAB limits were considered to establish the shelf life: 6 and 7 log (CFU/g). According to the literature, LAB cause sensory changes, color changes, slime formation, gas formation, and unpleasant odors in the product above these limits, which make its consumption unfeasible [33]. Non-linear regression was performed through the nlsMicrobio and minpack.lm packages from the open-source software R v. 3.5.0 [34]. The parameterized version of the BAR growth model (without lag) used in this study is given in Eq. (4) and the net logarithmic increase after the treatment is given in Eq. (5).

$$ \mathrm{logN}(t)=\log\ \left({N}_{\mathrm{max}}\right)-\log\ \left(1+\left({10}^{\log \left({N}_{\mathrm{max}}\right)-\log \left({N}_0\right)}-1\right){e}^{-{\mu}_{\mathrm{max}}t}\right) $$
(4)
$$ A=\log \left({N}_{\mathrm{max}}\right)-\log \left({N}_0\right) $$
(5)

where N(t) stands for the bacterial population (CFU/g) after t days of the start of the experiment, Nmax stands for the final bacterial population (CFU/g), N0 represents the initial bacterial population (CFU/g), μmax represents the maximum specific growth rate (days−1), and A is the net logarithmic growth increase (log(CFU/g)).

The estimated shelf life values were modeled through a modified version of the well-known Weibull function [35], as shown in Eq. (6).

$$ \frac{1}{t_{\mathrm{SL}}}=\frac{1}{t_{\mathrm{SL}0}}-b{\left[\mathrm{EO}\right]}^c $$
(6)

where tSL (days) is the shelf life of the sample after the addition of the essential oil, tSL0 (days) corresponds to the shelf life of the Tuscan sausage without the addition of the essential oil, [EO] represents the concentration of essential oil, b (days) and c are empirical parameters. If the value of parameter c is higher than 1, the curve is concave. If c < 1, the curve is convex and if c = 1, the curve corresponds to a straight line.

The dependence of the maximum specific growth rate of the LAB on the essential oil concentration was described for a first-order kinetics model given in Eq. (7):

$$ {\upmu}_{\mathrm{max}}={\upmu}_{\max, 0}{e}^{-k\left[ EO\right]} $$
(7)

where μmax, 0 represents the maximum specific growth rate of the LAB for the samples without EO addition (days−1) and k is a rate constant. In Eq. (7), it can be seen that the fractional decrease of μmax after the addition of 0.1 wt% of EO is given by (1 − e−0.1k).

Statistical analysis

The fitting capability of the BAR growth model to describe the experimental data measured in the present study was evaluated through the following statistical indices: root mean square error (RMSE), mean absolute error (MAE), second-order Akaike information criterion (AICC), Bayesian information criterion (BIC), bias factor (BF), and accuracy factor (AF). Equations (8) to (13) provide the respective mathematical expressions.

$$ \mathrm{RMSE}=\sqrt{\frac{\sum {\left({y}_i-{\hat{y}}_i\right)}^2}{n-p}} $$
(8)
$$ \mathrm{MAE}=\frac{1}{n}\sum \left|{\hat{y}}_i-{y}_i\right| $$
(9)
$$ {\mathrm{AIC}}_{\mathrm{C}}=-2\log \left(\mathrm{Lp}\right)+2\left[\left(p+1\right)+1\right]+\frac{2p\left(p+1\right)}{n-p-1} $$
(10)
$$ \mathrm{BIC}=-2\log \left(\mathrm{Lp}\right)+\left[\ \left(p+1\right)+1\right]\ \log (n) $$
(11)
$$ \mathrm{BF}={10}^{\left(\sum \frac{\log \left(\frac{{\hat{y}}_i}{y_i}\right)}{n}\right)} $$
(12)
$$ \mathrm{AF}={10}^{\left(\sum \frac{\left|\log \left(\frac{{\hat{y}}_i}{y_i}\right)\right|}{n}\right)} $$
(13)

In Eqs. (8) to (13), the symbol \( {\hat{y}}_i \) corresponds to the ith prediction, yi represents the ith observation, Lp stands for the likelihood function, p is the number of parameters of the model, and n is the number of experimental observations.

Results and discussion

Essential oils composition

Table 2 shows the composition of OEO and REO evaluated through GC analysis: 52 components were identified in the volatile fraction of OEO and 40 components in the volatile fraction of REO. The analysis of the chemical composition of the EOs is of paramount importance due to the large variation in the composition depending on a number of factors, such as geographical region, part of the plant, and environmental conditions [36, 37].

Table 2 Chemical composition of the OEO and of the REO evaluated through GC analysis
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The main components identified in OEO were γ-terpinene (46.3%), terpinolene (21.2%), p-cymene (15.7%), and β-caryophyllene (7.7%). Other authors have obtained equivalent results with a slightly different proportion of the main components [38, 39]. Meanwhile, the main components observed in REO were 1,8-cineole (33.9%), camphor (17.6%), α-pinene (15.4%), borneol (6.9%), and camphene (5.4%), corresponding to the composition observed in other studies conducted with the same plant [40, 41].

Initial characterization of the product

The following experimental results were obtained for the pH and water activity of the fresh sausage prior to all the treatments: pH = 6.14± 0.04 and aw = 0.966±0.001. The results are expressed as mean values±standard error. The low standard errors observed in the results show that the samples were very similar in composition. The pH of a fresh sausage is directly related to its color and flavor. Thus, it can be considered as another useful index to evaluate the sausage quality. In general, the pH of Tuscan sausage ranges between 5.90 and 6.20 [42, 43].

Kinetics of change of physical-chemical parameters

The pH of a given meat product is an important parameter that influences its characteristics because it affects many quality attributes, such as color, texture, water retention capacity, flavor, and microbial stability [44]. Figure 1 presents the curves obtained after the fit of Eq. (3) to the experimental data. The values of the fitted parameters can be seen in Table 3, that shows that the estimated results for the rate of decrease of pH (given by the parameter ν) were lower for the samples treated with a higher concentration (0.4 wt%) of EO, indicating that these treatments stabilized the pH of the sausages for a longer amount of time in relation to the other treatments. However, the asymptotic value of the pH (given by the parameter pHmin) obtained with this concentration of EO was not significantly lower in relation to the other treatments. This result shows that this treatment diminishes the rate of decrease of the pH, but it does not affect the final pH. In general, it is possible to visualize that the addition of the essential oils slows the decrease of the pH of the Tuscan sausage during storage for all treatments. However, it does not affect the asymptotic pH of the samples. The same behavior was observed after the addition of OEO to black wildebeest meat [45]. This result is associated with the stationary phase of microbial growth. Since the LAB are the main responsible for the pH change, if the number of viable cells remains constant, the pH does not change as well [33]. It was also observed that the lag before the drop in pH of the sausages was longer in the samples treated with REO when compared with the samples treated with OEO.

Fig. 1
figure 1

Kinetic profile of the pH of the treatments during storage

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Table 3 Fitted parameters (± 95% CI) and RMSE obtained after the fitting of the three-phase linear model (BUC) to the experimental data of pH obtained with each treatment
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Results obtained for the kinetics of the color parameter changes are shown in Figs. 2 and 3 for the samples treated with OEO and REO, respectively. Both Figs. 2 and 3 only present values obtained until day 49 because results observed for color parameters after this period are no longer consistent due to spoilage of the sausage. It can be seen that the lightness increased in the first 14 days of storage for all of the samples, including the control, after which it decreased. A detailed analysis of values obtained for lightness must be considered cautiously, since some studies reported an increase in this parameter in minced beef treated with OEO after storage [46] and others described a decrease in the lightness over time [47]. The values of b* and C* decreased during storage, suggesting a browning of both the treated and untreated samples [46, 48]. By the end of storage, no difference was observed in the color parameters of the control and the samples with EO.

Fig. 2
figure 2

Kinetics of change in the color parameters for the different samples treated with OEO

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Fig. 3
figure 3

Kinetics of change in the color parameters for the different samples treated with REO

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Regarding the difference in the results obtained with samples treated with OEO and REO, the values of L* were generally higher for the samples treated with OEO in relation to REO. When lower doses of EO (0.05 wt% and 0.1 wt%) were added to the sausages, the values for the remaining parameters were equivalent in both EOs. However, after the addition of higher doses of EO (0.2 wt% and 0.4 wt%) the values were higher for OEO than for REO.

LAB consist in a substantial part of the natural microbiota of meat products. However, the formation of slimes and off-flavors as a result of their metabolic activity can make the consumption of the product inappropriate [13]. In the current study, two different LAB concentrations were adopted as microbiological limits for the sensory and microbiological quality of fresh sausages: 6 log (CFU/g) and 7 log (CFU/g). The period of time (in days) before the LAB concentration reached these limits was therefore adopted in the current study as the microbiological shelf life of the Tuscan sausage. After the fit of the BAR growth model to the LAB data, the microbiological shelf life of the Tuscan sausage was estimated with Eq. (4). Figure 4a presents the results obtained for the LAB concentration for OEO and Fig. 4b shows the results obtained for REO.

Fig. 4
figure 4

Experimental data and fitted growth curves of LAB in Tuscan sausage stored at 4.0 ± 0.5 °C added with different concentrations of oregano essential oil (OEO) (a) and rosemary essential oil (REO) (b)

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The initial logarithmic count of the LAB for the different treatments ranged between 2.46 log (CFU/g) and 3.13 log (CFU/g). As can be seen in Fig. 4, no sharp lag phase was observed for any of the treatments used in this study. Since the LAB are part of the natural microbiota of the sausage, it is probable that the bacteria were previously adapted to the environment when the study was carried out. In addition, the net logarithmic bacterial increase given by the difference between the final and the initial bacterial load (parameter A) was not affected by the different treatments in relation to the control sample. Similarly, for the same reason, it was not observed a lag phase for LAB in vacuum-packed cooked meat emulsions at the storage temperatures of 0 °C, 8 °C, and 15 °C [49].

Figure 4 also shows that all treatments extended the shelf life of the Tuscan sausage in relation to the control. It can also be observed that the higher the concentration of EO added to the product, the longer the extension of the shelf life. A comparison of the results obtained for the different oils reveals that the shelf life estimated with REO was higher in relation to OEO when lower concentrations of EO (0.05 wt% and 0.1 wt%) were added to the sausage. On the other hand, when higher concentrations of oil (0.2 wt% and 0.4 wt%) were added to the sausage, the shelf life obtained with OEO was greater than with REO (Table 4).

Table 4 Growth parameters (± 95% CI) estimated by fitting of the BAR growth model to the experimental data obtained with the different treatments in Tuscan sausage at 4.0 ± 0.5 °C
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Table 4 summarizes the results obtained after the fit of the BAR growth model to the experimental data. As can be seen, the LAB population of the control sample reached the level of 6 log (CFU/g) after 20.35 days of storage and the level of 7 log (CFU/g) after 28.35 days of storage. Moreover, after this period of storage (20.35 and 28.35 days), the addition of 0.4 wt% of OEO and 0.4 wt% of REO resulted in a difference of approximately 1.5 log (CFU/g) in the LAB population in relation to the control (Fig. 4). This concentration of OEO extended the shelf life of the Tuscan sausage to 34.38 and 47.84 days, according to the first (7 log CFU/g of LAB) or second criterion (6 log CFU/g of LAB), respectively. In general, adding OEO will increase the shelf life of meat products. For instance, after the addition of 0.1 wt% of OEO in red porgy meat, a shelf life extension of 11 to 16 days was obtained in relation to the control treatment [27]. Regarding the REO, the shelf life extension was of 28.66 and 39.55 days for the first and second criteria, respectively. Even though the shelf life increased with the amount of oil added to the sausages, the application of lower concentrations (0.05 wt% and 0.1 wt%) of OEO or REO can be useful for practical applications. Actually, these doses do not significantly affect the sensory properties of different meat products [50, 51].

In general, a better fit was obtained when REO was added to the sausage instead of OEO. The addition of different concentrations of OEO and REO significantly affected the parameters μmax and tSL, as can be seen in Table 4. The maximum specific growth rate estimated for the non-treated sample was 0.316 days−1. A similar value for this parameter was obtained for untreated minced pork meat stored under modified atmosphere packaging at 5 °C [52]. The results obtained for the samples treated with 0.05 wt%, 0.1 wt%, 0.2 wt%, and 0.4 wt% of OEO were 0.332, 0.307, 0.248, and 0.205 days−1, respectively. On the other hand, the values of μmax obtained for the samples treated with 0.05 wt%, 0.1 wt%, 0.2 wt%, and 0.4 wt% of REO were 0.285, 0.296, 0.248, and 0.248 days−1, respectively. One could therefore conclude that although the maximum bacterial level observed after the treatment does not depend on the oil concentration (see results for log (Nmax) in Table 4), the LAB grew slower when lower concentrations of REO were added to the Tuscan sausage in relation to lower concentrations of OEO. The same analysis shows that their growth was slower when higher doses of OEO were added to the Tuscan sausage in relation to the same doses of REO.

According to the literature, the antimicrobial activity of OEO is related to the compounds γ-terpinene and p-cymene [53] and the antimicrobial activity of REO can be ascribed to the terpene derivatives and the 1,8-cineole naturally occurring in the essential oil [54, 55]. As a matter of fact, due to the lipophilic nature of the compounds present in the oils, they promote a rupture of the bacterial cell membrane and affect the cell’s vital functions. Both OEO and REO have been successfully applied to extend the shelf life of different meat products [56, 57]. The addition of OEO and REO to vacuum-packed fresh Bologna sausage stored during 24 days at 4 °C was also shown to reduce the LAB count [51, 52].

Table 5 exhibits the statistical indices (RMSE, MAE, AICC, BIC, BF, and AF) obtained after the fit of the BAR model to the experimental data. In general, RMSE and MAE are employed to measure model performance because they summarize the mean difference in the same units of the experimental data. The RMSE values obtained for all the studied treatments were lower than 0.274, suggesting a good fit of the BAR model to the experimental data. These results are of the same magnitude as those obtained with other studies that evaluated the natural microbiota of meat products, in which the RMSE ranged between 0.409 and 1.330 [58,59,60]. The bias and accuracy factors are commonly used statistical indexes in the field of predictive microbiology. A perfect agreement between observation and prediction results in bias and accuracy factors of 1. In the current study, the BF and AF values obtained for the different treatments ranged between 1.003–1.022 and 1.124–1.337, respectively, indicating that the model can describe the experimental data accurately.

Table 5 Statistical indices obtained by the BAR growth model to the experimental data obtained with the different treatments in Tuscan sausage at 4.0 ± 0.5 °C
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After the fit of Eq. (6) to the estimated values of the shelf life for all treatments, the following empirical expressions were obtained to describe the microbiological shelf life as a function of the oil concentration when the natural LAB microbiota assumed as microbiological limit is equal to 7 log (CFU/g). These equations can provide useful insights concerning the amount of oil that can be added to the sausage in order to increase its shelf life.

$$ \frac{1}{t_{\mathrm{SLO}}}=\frac{1}{27.943}-0.031{\left[\mathrm{OEO}\right]}^{0.758} $$
(14)
$$ \frac{1}{t_{\mathrm{SLR}}}=\frac{1}{28.327}-0.015{\left[\mathrm{REO}\right]}^{0.398} $$
(15)

where tSLO and tSLR represent the microbiological shelf life of the Tuscan sausage treated with oregano and rosemary, respectively, [OEO] and [REO] correspond to the concentrations (wt%) of OEO and REO, respectively.

Equations (16) and (17) provide the empirical expressions corresponding to a microbiological limit of 6 log (CFU/g).

$$ \frac{1}{t_{\mathrm{SLO}}}=\frac{1}{20.030}-0.046{\left[\mathrm{OEO}\right]}^{0.806} $$
(16)
$$ \frac{1}{t_{\mathrm{SLR}}}=\frac{1}{20.337}-0.020{\left[\mathrm{REO}\right]}^{0.368} $$
(17)

Figures 5 and 6 present the curves obtained after the fit of the modified Weibull model to the data of the shelf life. Because parameter c is less than one for all the curves (see Eqs. (14) to (17)), it can be concluded that all of them are convex in shape. Figures 5 and 6 show that when a lower concentration of EO is added to the sausages, a small amount of REO leads to a larger increase in the shelf life in relation to the OEO. However, when higher doses of EO are added to the Tuscan sausage, the increase of the shelf life becomes less pronounced, as can be seen in the asymptotic behavior of the curves. The predictions obtained were accurate, as can be easily observed in Table 6.

Fig. 5
figure 5

Microbiological shelf life of Tuscan sausage as a function of EO concentration obtained for the treatments considering as the microbiological limit a concentration of LAB equal to 7 log CFU/g. Dark shadow represents 95% CI and light shadow represents 95% prediction interval

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Fig. 6
figure 6

Microbiological shelf life of Tuscan sausage as a function of EO concentration obtained for the treatments considering as the microbiological limit a concentration of LAB equal to 6 log CFU/g. Dark shadow represents 95% CI and light shadow represents 95% prediction interval

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Table 6 Statistical indices obtained after fit of Eq. 3 to the estimated values of the shelf life according to the different criteria adopted as microbiological limits
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Figure 7 shows the fit of the first-order kinetics model, given in Eq. (7), to the data of the maximum specific growth rate as a function of the concentration of essential oil. Table 7 shows the results obtained for the fitted parameters. Table 7 reveals that as the amount of EO added to the sausages increases, there is a larger decrease in the growth of the native LAB in the sausages. According to the values of the parameter k, on average, the addition of 0.1 wt% of OEO slows LAB growth at about 11.5% and the addition of REO slows LAB growth at about 6.0%. This result does not consider if smaller or higher doses of EO were added; it takes into account the overall behavior of the data.

Fig. 7
figure 7

Maximum specific growth rate as a function of EO concentration. Dark shadow represents 95% CI and light shadow represents 95% prediction interval

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Table 7 Fitted parameters (± 95% CI) and RMSE obtained after the fitting of the first-order kinetics model to the estimated data of maximum specific growth rate
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Conclusions

This work explored the potential of the addition of the essential oils from oregano and rosemary to extend the microbiological shelf life of vacuum-packed Tuscan sausage. Both rosemary and oregano oils are alternatives to conventional preservatives and resulted in a larger increase in the shelf life in relation to the control. The advantages derived from the use of oregano and rosemary essential oils make them promising alternatives for the preservation of Tuscan sausage due to their effectiveness in slowing the growth of lactic acid bacteria, which are the main culprits for the spoilage of many meat products, in addition to reducing the reliance on chemical and synthetic additives commonly used in these products.