Thermophilic Hydrocarbon-Utilizing Bacilli from Marine Shallow Hydrothermal Vents as Producers of Biosurfactants

: The exploitation of thermophilic hydrocarbon-utilizing bacilli could provide novel environmentally friendly surfactants. In this work, 80 thermophilic bacilli isolated from shallow hydrothermal vents of the Eolian Islands (Italy) were screened for their ability to utilize hydrocarbons and produce biosurfactants (BSs). Among them, 15 strains grew with kerosene or gasoline (2% v / v ) as the only carbon and energy source, and most of them were positive to the methylene blue agar as prescreening assay for BSs production and displayed emulsifying activity. The cell-free supernatants (CFSs) from two selected strains, Bacillus licheniformis B3-15 and Bacillus horneckiae SBP3, were both surface active and able to emulsify different hydrocarbons and vegetable oils. BSs from B3-15 (910 mg L − 1 ) and SBP3 (950 mg L − 1 ) were chemically different surfactin-like lipopeptides, with speciﬁc mineral-, castor-and crude oil removal ability from the cotton matrix. CFSs from the 15 thermophilic strains, which harbor both lipolytic and surfactant abilities, could be suitable for industrial-based applications and environmental issues, such as oil recovery and removal from polluted areas or surfaces, (e.g., oil pipelines, bilge tankers, or industrial silos), whereas the crude BSs, as high-value compounds, may be used in different ﬁelds of application, as detergent, cosmeceutical, and pharmaceutical industries.


Introduction
Hydrophobic compounds, such as hydrocarbons, possess low water solubility, thus, microorganisms are able to increase the bioavailability of these compounds, as potential carbon and energy source, by producing surface-active molecules (SAMs) [1]. The role of bacterial SAMs for growth on hydrocarbons as a carbon source has been previously described by Rosenberg [2]. Compared with industrially synthesized surfactants, bacterial SAMs possess better emulsification, detergency, and dispersion properties, and arise a great interest in different fields of application, including bioremediation, biodegradation, and oil recovery, and pharmaceutical, food, cosmeceutical, and cleaner industries [3][4][5][6]. Based on their molecular weight, bacterial SAMs can be distinguished into two classes. Compounds that have low molecular weights and efficiently reduce surface and interfacial tension are called biosurfactants (BSs) and include lipopeptides, (e.g., surfactin, iturin, and fengycin), glycolipids, (e.g., rhamnolipids, trehalose lipids, and sophorolipids) and phospholipids, (e.g., phosphatidylethanolamine) [7,8]. On the other hand, bioemulsifiers are higher in Messina, Italy. All strains were previously isolated from hydrothermal fluid and sediment samples collected from the vents of Eolian Islands (Italy) [17,20] (Table 1). All strains are routinely grown on Marine Agar 2216 (MA, Difco Laboratories, Detroit, MI, USA) and frozen at −80 • C in 40% (v/v) glycerol for long-term storage.

Petroleum Hydrocarbons Utilization
To screen the ability of the strains to grow in the presence of a hydrocarbon as unique source of carbon and energy, a basic mineral natural seawater medium (NSW), consisting of (g L −1 ) NH 4 NO 3 1.0, K 2 HPO 4 0.2, Fe-citrate 0.02 dissolved in 800 mL of seawater and 200 mL of distilled water, was utilized. The pH was adjusted to 8 with 1N NaOH and the medium was sterilized by autoclaving at 121 • C for 20 min. Kerosene (Petroleum Ether 190-250 • C, Panreac) or gasoline (from Q8 petrol station) maintained at 60 • C in a thermal bath, were sterilized separately by filtration through membrane 0.45 µm and added to the medium (2% v/v) [28]. Strains were inoculated (OD 600 nm = 0.1 equivalent to 1.5 × 10 8 bacteria mL −1 ) at each optimal temperature for at least 7 days. The bacterial growth was spectrophotometrically evaluated (Ultraspec 3000; Amersham Pharmacia Biotech, Freiburg, Germany). Based on the correspondence between absorbance and bacteria density, absorbance values (OD600nm) ≥ 0.5 were indicative for "high growth", those ranging from 0.2 to 0.5 for "low growth", and ≤0.2 for "no growth. Each experiment was performed in triplicate.

Screening for Biosurfactant/Bioemulsifier Production
The methylene blue agar (BM) assay, as a semi-quantitative assay for the detection of extracellular anionic surfactants, was used according to Siegmund and Wagner [30]. Methylene blue was added to agarized NSW at final concentration of 0.2 mg mL −1 . Strains were inoculated in three replicates and after incubation for 48 h at 45 • C, the formation of a dark blue halo around each colony was considered positive for surfactant production.
The emulsifying activity of CFSs from aerobically grown bacteria in NSW plus kerosene (2% v/v) (NSW + KER), was evaluated as reported by Cooper and Goldenberg [31], with some modifications. To obtain the CFSs, three replicates of each culture were centrifuged at 3800× g for 20 min at 4 • C. An aliquot of each CFS (2 mL) was mixed with an equal volume of kerosene in a glass tube (10 cm high and 1 cm in diameter) and vortexed at high speed for 2 min. The uncultured medium was used as negative control and Triton X-100 (Sigma-Aldrich, Milan, Italy) was used as positive control. The emulsifying index (E 24 ) was calculated after 24 h of mixing with kerosene as the ratio between the height of the emulsion layer and the total height, multiplied by 100, and normalized by dividing the E 24 values by the respective absorbances (OD 600 nm ).

CFSs Surface-Active Properties
To test the surface-active properties, the oil drop-collapse assay and the reduction of the surface tension (ST) were evaluated at 25 • C. The oil drop-collapse assay was carried out on a polystyrene lid of a 96-microwell plate (Biolog, Harward, CA, USA). Briefly, 100 µL of each CFS were spotted on the lid, then 5 µL of crude oil were added to the surface of each CFS. Biosurfactant-producing culture gave flat drops.
The reduction of the ST was measured (in triplicate) using the digital Wilhelmy platetype tensiometer K10T (Krüss, Hamburg, Germany) [32]. The ST (STi and STf as initial and final value, at the beginning and at the end of the incubation time, respectively), was evaluated.

CFSs Emulsifying Properties
To evaluate the ability to emulsify different hydrocarbons and vegetable oils, 2 mL of each CFS were mixed with an equal volume of chloroform, ethyl acetate, decane, gasoline, hexadecane, castor oil, olive oil, kerosene, or mineral oil. Each mixture was vortexed vigorously and left to stand for 24 h, and E 24 was determined as described above. Uninoculated sterile media were used as negative controls.

BSs Extraction and Characterization by ATR-FTIR
To extract the BSs from each CFS, acid precipitation method was utilized [33]. Each CFS was acidified at pH 2.0 using 2N HCl and kept overnight. BSs were dissolved into a chloroform-methanol mixture (2:1 v/v), and the organic layer, containing BSs, was separated using a rotary evaporation process (Rotavapor ® R-300, BUCHI Italia S.r.l, Cornaredo, Italy), and finally weighed.
The dried BSs were analyzed in triplicate by the attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. ATR-FTIR Vertex 70 V spectrometer (Bruker Optics GmbH & Co. KG, Ettlingen, Germany) using Platinum diamond ATR was employed to collect spectra in the 4000 to 1000 cm −1 wavenumber range. The analysis of IR spectra was carried out by using the OMNIC software (Origin Lab Co., Northampton, MA, USA).

Oil Removal Test
The ability of BSs to remove different oils (mineral, crude, and castor) from a cotton cloth matrix was investigated according to Tripathi et al. [34]. Each piece of dry cotton cloth (2 cm × 2 cm) was soaked in one of the selected oils (300 µL). Each cloth was dried overnight at 60 • C and then weighed. Then, each oil-loaded cloth was washed with an aqueous solution of the selected BSs (1 g L −1 , w/v) or in tap water as negative control, followed by stirring at 30 • C for 1 h. The cotton cloths were rinsed in water (100 mL each) and dried at 60 • C overnight. The weight difference before and after the treatment with each biosurfactant was measured, and the oil-removal percentage was calculated as reported by Chen et al. [35].

Statistical Analysis
The experiments were carried out in triplicate and data are expressed as averages and standard deviations or relative errors (where specified). To compare different experimental groups, data were analyzed by two-way ANOVA and the Tukey's test was used for post hoc analysis (GraphPad Software Inc., La Jolla, CA, USA). All statistical values were considered significant at p < 0.05.

Petroleum Hydrocarbons Utilization
The ability of the tested strains to grow using kerosene or gasoline as a unique carbon source is reported in Figure 1.
In the presence of kerosene, 15 strains (18.75%) grew well, and 47 strains (58.75%) showed low growth. Only 10 strains (12.50%) showed high growth with gasoline, and 35 (43.75%) exhibited low growth ( Figure 1). Strains showing high growth levels in the presence of kerosene (15) and gasoline (10) were selected for further investigation. The selected thermophilic bacilli, their growth characteristics, utilization of kerosene or gasoline (2% v/v) as only carbon sources, and lipase production are reported in Table 2. The full list of 80 tested strains is reported in Table S1. In the presence of kerosene, 15 strains (18.75%) grew well, and 47 strains (58.75%) showed low growth. Only 10 strains (12.50%) showed high growth with gasoline, and 35 (43.75%) exhibited low growth ( Figure 1). Strains showing high growth levels in the presence of kerosene (15) and gasoline (10) were selected for further investigation. The selected thermophilic bacilli, their growth characteristics, utilization of kerosene or gasoline (2% v/v) as only carbon sources, and lipase production are reported in Table 2. The full list of 80 tested strains is reported in Table S1. Table 2. Thermophilic bacilli isolated from hydrothermal vents of Eolian Islands, optimal characteristics for growth, utilization of kerosene (Ker) or gasoline (Gasol) (2% v/v) as only carbon sources, and enzymatic production on selected substrates.

Screening for Biosurfactants/Bioemulsifiers Production
The presence of biosurfactants/bioemulsifiers, as detected by the BM assay of the 15 selected hydrocarbon-utilizing strains grown in NSW + KER (2% v/v) after 48 h of incubation and the emulsifying activity (E 24 ) of CFS thereof are reported in Table 3. Table 3. Screening of biosurfactants/bioemulsifiers production of 15 selected hydrocarbon-utilizing bacilli on methylene blue agar plates (BM) and emulsifying index (E 24 ) of their cell-free supernatants in NSW + KER (1:1 v/v), in comparison with the industrially synthesized surfactant Triton X-100. Sterile NSW + KER was used as negative control. (+) presence of halo in BM. Data are expressed as averages and standard deviations (n = 3). [24]; c [17,36].
Most of the hydrocarbon-utilizing bacilli (13/15) were positive for biosurfactants/ bioemulsifiers production according to the BM test. CFSs from the majority of them (10/15) showed an E 24 ≥ 40%, with the highest values observed for strains B3-15 (51%) and SBP3 (55%). Based on the results obtained from the prescreening tests, Bacillus licheniformis B3-15 and B. horneckiae SBP3 were selected for further optimization of biosurfactant production.

Biosurfactant Production
The growth of B3-15 and SBP3 strains and the emulsifying activity of their CFSs were evaluated in different nutritional conditions (nitrogen sources), and saccharose or glycerol (3%) as carbon sources, after incubation for 48 h under optimal conditions (temperature 45 ± 1 • C and pH 8) (Figure 2). B3-15 and SBP3 grew in all the tested culture media (Figure 2a and Table S2), and their growth was the highest in MB + SAC (OD 600 nm = 1.4 and 2.1, respectively), (groups d and e, respectively), followed by MB or MB + GLY (groups c and d, respectively), and it was double compared to NSW + KER (OD 600 nm = 0.7 for both strains) (group a). The lowest growth of both tested strains were observed in SWY + GLY and SWY + SAC (OD 600 nm ≤ 0.4) (groups b) (Figure 2a).
Lower emulsifying activities were observed in the CFSs of B3-15 and SBP3 in the SWY medium (Figure 2b and Table S2). The SWY was the only medium that resulted in significant differences in E 24 between the two CFSs irrespective of the carbon source used (groups b and c). E 24 values were higher only for MB + SAC (group d) compared to NSW + KER and MB + GLY or MB, indicating that the emulsifying activity is greatly influenced by the nitrogen form present in the media (yeast extract + peptone in MB or the inorganic N in NSW + KER compared to low E 24 in SWY medium containing only yeast extract). Furthermore, higher E 24 values observed in MB + SAC suggest that the increasing production of emulsifiers depends not only on the nitrogen source but rather on its combination with a specific carbon source. B3-15 and SBP3 grew in all the tested culture media (Figure 2a and Table S2), and their growth was the highest in MB + SAC (OD600 nm = 1.4 and 2.1, respectively), (groups d and e, respectively), followed by MB or MB + GLY (groups c and d, respectively), and i was double compared to NSW + KER (OD600 nm = 0.7 for both strains) (group a). The lowes growth of both tested strains were observed in SWY + GLY and SWY + SAC (OD600 nm ≤ 0.4) (groups b) (Figure 2a).
Lower emulsifying activities were observed in the CFSs of B3-15 and SBP3 in the SWY medium ( Figure 2b and Table S2). The SWY was the only medium that resulted in signif icant differences in E24 between the two CFSs irrespective of the carbon source used (groups b and c). E24 values were higher only for MB + SAC (group d) compared to NSW + KER and MB + GLY or MB, indicating that the emulsifying activity is greatly influenced by the nitrogen form present in the media (yeast extract + peptone in MB or the inorgani N in NSW + KER compared to low E24 in SWY medium containing only yeast extract) Furthermore, higher E24 values observed in MB + SAC suggest that the increasing produc tion of emulsifiers depends not only on the nitrogen source but rather on its combination with a specific carbon source.
When the emulsifying activity of CFSs was normalized for the growth values of the strains, higher values were observed for B3-15 in SWY + GLY and SBP3 in NSW + KER (Table S2), suggesting that emulsifying activity might not be directly correlated to highe growth. Among all the used culture media, we selected MB + SAC for further optimization experiments, as it was the medium in which both the highest growth (OD600 nm) and emul sifying activity were observed.
To assess the optimal conditions for recovery of the biosurfactants, the growth curve of B3-15 and SBP3 strains in MB + SAC and the E24 with kerosene of their CFSs during selected incubation times were evaluated (Figure 3). When the emulsifying activity of CFSs was normalized for the growth values of the strains, higher values were observed for B3-15 in SWY + GLY and SBP3 in NSW + KER (Table S2), suggesting that emulsifying activity might not be directly correlated to higher growth. Among all the used culture media, we selected MB + SAC for further optimization experiments, as it was the medium in which both the highest growth (OD 600 nm ) and emulsifying activity were observed.
To assess the optimal conditions for recovery of the biosurfactants, the growth curves of B3-15 and SBP3 strains in MB + SAC and the E 24 with kerosene of their CFSs during selected incubation times were evaluated ( Figure 3). SBP3 strain grew better than B3-15, reaching the maximal growth (OD600 nm = 2.1) after 20 h of incubation (Figure 3a). The E24 increased during the selected incubation period and reached the maximum value after 48 h when both CFSs exhibited similar emulsifying activity (Figure 3b). These results indicated that the selected nutritional conditions are responsible for fast cell growth, resulting in the production of a great abundance of cells which, once they entered the stationary phase, produced a lot of BSs. SBP3 strain grew better than B3-15, reaching the maximal growth (OD 600 nm = 2.1) after 20 h of incubation (Figure 3a). The E 24 increased during the selected incubation period and reached the maximum value after 48 h when both CFSs exhibited similar emulsifying activity (Figure 3b). These results indicated that the selected nutritional conditions are responsible for fast cell growth, resulting in the production of a great abundance of cells which, once they entered the stationary phase, produced a lot of BSs.

CFSs Biosurfactant Activities
The CFSs (MB + SAC) from SBP3 and B3-15 strains were positive for the oil dropcollapse assay, leading to the expansion of the water droplet, by reducing the interfacial tension ( Table 4). The ST reduction values are expressed as the difference between the ST value at the beginning and at the end of the incubation period for all isolates. ST was reduced in the presence of both CFSs from B3-15 and SBP3, with the highest reduction for the SBP3 strain (Table 4). Table 4. Surface activities of (CFSs (MB + SAC) from B3-15 and SBP3 strains, using the oil dropcollapse and ST assays. Data are expressed as averages and standard deviations (n = 3). * Significantly different (p < 0.05); ** (p < 0.01).

BSs Extraction and Characterization by ATR-FTIR
After acid precipitation from CFSs MB + SAC of B3-15 and SBP3 strains, the crude BSs yields were 910 ± 15.23 and 950 ± 16.17 mg L −1 , respectively. ATR-FTIR analysis was used to determine the structural features of these crude biosurfactants. The peak wavenumbers were assigned as reported in Table 5. Phosphate groups [41] 1035-1030 Stretching vibrations of the C-O group in esters [42] The FTIR characterization of crude biosurfactants from B. licheniformis B3-15 and B. horneckiae SBP3 is reported in Figure 5. In the FTIR spectra of BSs from the two strains, the peaks observed at 3301 cm −1 were assigned to CH and OH groups of Amide A. The peaks observed at 2944 and 2927 cm −1 were attributed to the aliphatic (-CH3 and -CH2) stretching vibrations of lipids, indicating the presence of alkyl chains ( Figure 5). The peaks at 1641 and 1636 cm −1 were attributed to Amide I, indicating a peptide structure of BSs. According to other studies [43][44][45], the characteristic stretching frequency of amides in the region 3300-3250 cm −1 (Amide A) and In the FTIR spectra of BSs from the two strains, the peaks observed at 3301 cm −1 were assigned to CH and OH groups of Amide A. The peaks observed at 2944 and 2927 cm −1 were attributed to the aliphatic (-CH 3 and -CH 2 ) stretching vibrations of lipids, indicating the presence of alkyl chains ( Figure 5). The peaks at 1641 and 1636 cm −1 were attributed to Amide I, indicating a peptide structure of BSs. According to other studies [43][44][45], the characteristic stretching frequency of amides in the region 3300-3250 cm −1 (Amide A) and 1650-1500 cm −1 (Amide I) is specific for surfactin-like lipopeptides of biosurfactant. Moreover, the shifts on the peaks attributed to lipids and peptides suggested that the two lipopeptides possessed different structures.

Oil Removal Test
The oil removal ability of BSs from B3-15 and SBP3 strains is shown in Table 6. Table 6. The removal rate (%) of mineral, crude, and castor oil from cotton sections by BS solution (1 g L −1 ) obtained from B3-15 and SBP3 strains. Data are expressed as averages and standard deviations (n = 3). The removal was negligible with tap water in control tests, conversely positive effects were observed in the cotton section in the presence of both BSs, although with different levels (from 32 to 80%). When BS B3-15 (1 g L −1 ) was dispersed in tap water, the castor oil removal rate was the highest (70%) and about two-fold higher than BS SBP3, followed by mineral oil (53%) and crude oil (45%). Differently, the aqueous mixture with BS SBP3 showed the highest removal rate of crude oil (80%), about two-fold higher than BS B3-15, followed by mineral oil (48%) and castor oil (32%).

Discussion
Biosurfactants and bio-emulsifiers are gaining increasing attention in several fields of applications, such as bioremediation, pharmaceutics, and cosmeceuticals because they are eco-friendly alternatives to their industrially made counterparts.
In this study, 80 thermophilic bacilli isolated from shallow hydrothermal vents of the Eolian Islands were screened for their ability to utilize kerosene or gasoline as the only carbon source. Among them, 15 bacilli showed high growth in a mineral medium supplemented with kerosene or gasoline (2%, v/v) at 45 • C for 48 h. This prompted us to verify the surfactant production capability of these bacteria. Biosurfactants, by reducing the ST of oil droplets, make them easier for bacterial uptake [44]. Although the relationship between the production of lipases and biosurfactants has not been established yet [45], the synthesis of lipases and biosurfactants by microorganisms may occur in the metabolization of oil substrates [46].
The thermophilic bacilli utilizing hydrocarbons were able to hydrolyze Tween 20 and Tween 80, produced esterase (C4) and/or esterase lipase (C8), and interestingly, only eight strains also produced lipase (C14). Many studies reported that the lipases are produced by hydrocarbon-utilizing Bacillus, Geobacillus, and Pseudomonas species [47][48][49][50][51]. Such hydrolytic enzymes play a role in the utilization and/or degradation of hydrocarbons, since they are induced when the intracellular content of alkane catabolism intermediates, such as alkanols, long-chain, and short-chain fatty acids, increases [52]. Furthermore, thermostable lipases are among the most interesting enzymes in the food and pharmaceutical field and are promising tools as potential biocatalysts in biodiesel production and other biotechnology applications [53]. Since most of the thermophilic hydrocarbon-utilizing strains displayed both lipolytic and good emulsifying activity (E 24 ≥ 40%), their CFSs could be used, without any further extraction procedure, as detergent agents, such as surface cleaning agents for oil pipelines, bilge tanker or industrial silos.
BSs production from B3-15 and SBP3 (DSM 103062) strains, displaying the highest E 24 values in the presence of kerosene, was then investigated under different nutritional conditions. It has been reported that the choice of nitrogen sources, as an inorganic or organic nutrient, and carbon sources could have a major influence on the yield of BSs [54,55]. CFSs of B3-15 and SBP3, from the medium containing organic nitrogen (peptone in MB) and saccharose, showed the highest E 24 values, then it can be concluded that the selected nutritional conditions allowed the production of a lot of BSs, as proven by the oil dropcollapse assay and the reduction in ST, with SBP3 being the most efficient in reducing ST.
After optimization of BSs production and acid extraction, the highest yield of crude BSs was 910 mg L −1 from B3-15 and 950 mg L −1 from SBP3 strains, after incubation at 45 • C for 48 h. It is well known that bacilli are able to produce a variety of exoproducts depending on the culture conditions and the extraction procedures. Using an equal volume of cold ethanol, EPSs were previously extracted from CFSs of several Eolian bacilli, including B. licheniformis B3-15 [13], B. licheniformis T14 [25], G. thermodenitrificans B3-72 [24] and SBP3 strain [17,36], with different yields (165, 70, 70 and 70 mg L −1 , respectively). As also reported for several bacterial EPSs [64,65], the EPS-T14 was able to emulsify two immiscible liquids, but possessed low surface activity, characteristics that were related to its antiadhesive properties against the bacterial adhesion and biofilm formation [25].
The ATR-FTIR spectra of BSs showed signals attributed to Amide A, Amide I, and aliphatic stretching vibrations of lipids, specific for surfactin-like lipopeptides [43][44][45][66][67][68]. Although similar, the spectra of BSs slightly differed from each other in the peaks attributed to Amide A and lipids.
A wide range of lipopeptides with surfactant activity have been described from marine bacilli, such as pumilacidin from B. pumilus and B. stratosphericus [69,70], surfactin and lichenysin from B. licheniformis NIOT-06 [71], fengycins from B. circulans [72], iturins from B. megaterium and Bacillus sp. KCB14S006 [73,74], and surfactin and bacillomycin F from B. siamensis [75]. When compared with other marine thermophilic and halophilic bacilli the yield of crude BSs from B3-15 and SBP3 was higher than that produced by both B. licheniformis BAS50 (160 mg L −1 ) and B. licheniformis BNP29 (90 mg L −1 ), obtained in the aerobic, carbohydrate-based medium [76]. However, the yields of these surfactants greatly depended on the cultivation conditions, since the anaerobic surfactant production was three-five times lower than that of aerobic cultures [76].
The oil-removal test indicated that BS B3-15 (1 g L −1 ) efficiently removed castor oil (70.0%), whereas the BS SBP3 was more effective in removing crude oil (80.0%) from a cotton matrix, and the different activity may be ascribable to the observed differences in the chemical structure of the two lipopeptides. As previously reported, the difference in the efficacy of BSs from several bacterial strains to remove oil from the cotton matrix can be explained on the basis of their chemical properties, specifically in the distribution of polar head groups, leading to their classification as anionic, cationic and non-ionic surfactants [77]. Compared to physical methods and/or chemical products, BSs from B3-15 and SBP3 could be used for the removal of hydrocarbons from contaminated soil and cotton cloth, properties that have not been adequately explored until now [78,79].
Actually, BSs receive a great interest for oil recovery and remediation purposes, detergent products such as household, personal care products, and industrial detergents, and other possible medical applications, such as antimicrobial and antiadhesive agents. Further studies will be performed on our BSs to evaluate agro-industrial waste and by-products, such as crude glycerol from biodiesel production, and exhausted vegetable oils such as feedstocks for large-scale BSs production.

Conclusions
Thermophilic hydrocarbon utilizing bacilli from shallow hydrothermal vents of the Eolian Islands represents a valuable source of biomolecules that could be suitable for several industrial applications. CFSs of the 15 strains, able to grow with kerosene or gasoline, which harbor both lipolytic and emulsifying activity, could be used as green detergents, as well as in bioremediation. Two selected strains, B. licheniformis B3-15 and B. horneckiae SBP3 (DSM 103062), have been investigated for their ability to produce BSs. Data indicated that BSs production is dependent on nutritional factors and that the copresence of peptone and saccharose gave the best results in terms of E 24 values. Their CFSs exhibited significant potential in emulsifying both hydrocarbons and vegetable oils, suggesting a potential use in bioremediation and for cleaning petrol contaminated surfaces, such as oil pipelines, bilge tankers, or industrial silos, or as cleaning solutions in the food industry. As determined by ATR-FTIR, extracted BSs were two chemically distinct lipopeptides that can be considered for high-value biotechnological applications, such as the cosmeceutical and pharmaceutical industries.
In conclusion, CFSs from B. licheniformis B3-15 and B. horneckiae SBP3 (DSM 103062) can be employed without further chemical treatments, and BSs could be considered green detergents, as their production does not release any toxic byproducts and, differently from industrially made surfactants, does not require the use of petrochemicals.