PHB Produced by Bacteria Present in the Argan Field Soil: A New Perspective for the Synthesis of the Bio-Based Polymer

: Bio-based plastics, i.e., non-synthetic polymers produced from renewable resources are gaining special attention as a feasible solution to the environmental issues caused by concerns re-garding the impact of waste plastics. Furthermore, such materials can also represent an alternative to petroleum-derived polymers, due to the scarcity of this raw material in the near future. In the polyhydroxyalkanoates (PHA) family, polyhydroxybutyrate (PHB) was the first to be synthesized and characterized. PHB soon gained great attention from industrial and academic researchers since it can be synthesized from a wide variety of available carbon sources, such as agro-industrial and domestic wastes. The aim of this original research has been the identification of the presence of PHB synthetizing bacteria in some soils in a Moroccan region and the production of the bio-based PHB. In particular, the soils of the argan fields in Taroudant were considered. Taroudant is a southwestern region of Morocco where the argan oil tree Argania spinosa is an endemic and preserved species. Starting from rhizospheric soil samples of an argan crop area, we isolated heat-resistant bacteria and obtained pure cultures from it. These bacteria present intracellular endospores stained by the Schaeffer-Fulton method. The presence of intracellular endospores is a very important starting point to verify the effective production of PHB as a compartmentalized material. Further analyses are currently ongoing to try to extract and characterize PHB granules.


Introduction
The increasing worldwide consumption of coal, oil, and natural gases is inducing a rise in these fossil prices, and an increase in carbon dioxide emissions that cause the world's climate change. In addition, in the following decades, because of the continued need for fossil fuels, petroleum resources will be depleted in a short time. It is necessary, therefore, to reduce and replace these non-renewable resources with alternative "green" resources for the sustainable development of the next generations. As an example, biomass represents an energetic resource to solve economic, political, and environmental issues [1].
Biomass means non-fossilized and biodegradable organic material originating from plants, animals, and microorganisms. Biomass is considered a renewable resource as long as its exploitation rate does not exceed its replenishment by natural processes; it can, therefore, be conveniently used to synthesize bio-based polymers [1].  Among bio-based polymers, polyhydroxyalkanoates (PHA) are a group of polyesters synthesized by prokaryotic Gram-positive and Gram-negative enterobacteria [2,3], cyanobacteria [4,5], and archaea organisms living in extreme environmental conditions [6,7]. PHAs are thermoplastic, biodegradable, biocompatible, and non-toxic bio-based polymers. They have a high degree of polymerization, are highly crystalline and isotactic, possess optical properties, and are insoluble in water.
Microbial-derived polymers belonging to the PHA family are entirely synthesized by bacteria; at the same time, they can be completely bio-degraded by living organisms, which means that they can undergo a decomposition process that leads to small compounds, such as methane, carbon dioxide, and water, due to the microorganism's activity in particular composting conditions. The microbial species that are able to synthesize PHA acts in the presence of a renewable feedstock of pentoses, hexoses, starch, cellulose, sucrose, lactose, CO2, and CH4 under unfavorable growth conditions due to unbalanced nutrient availability. Generally, these conditions include a sufficient carbon source and a reduced number of other substrates such as nitrogen, phosphate, and oxygen. During starvation periods, in the absence of external sugars, the PHA producers can use the carbon source stored in the granules to provide the cell with the necessary amount of energy to survive in this uncomfortable condition, particularly for osmoregulation, motility, and metabolic pathways [8].
The Poly-3-hydroxybutyrate (PHB) is the most studied and characterized member of the PHA family. It is a thermoplastic homo-polyester consisting of hydroxybutyrate monomers which give the polymer 80% crystallinity. PHB has an extremely regular structure: it is almost completely isotactic (like synthetic polypropylene), with the chains forming helical structures. The chains are able to closely pack to form crystals, obtaining a stiff polymer [9].
The processing of PHB is usually carried out by extrusion in melt state for the production of polymeric films or other items [10]. PHB displays a melting temperature of 175-180 °C and thermal degradation temperature around 240 °C, which means a narrow temperature window for the processability of this material, therefore, making it difficult to process [11]. Furthermore, unfavorable conditions during processing, e.g., too high levels of humidity/temperature and/or too long permanence in the machine, can cause polymer degradation, corresponding to lower performance of the final products.
To overcome problems during processing, the bacterial production process can be modified to produce co-polymerized PHB. The crystallization of PHB can be interrupted by adding different building blocks, such as 4-hydroxybutyrate (4-HB), 3-hydroxyvalerate (3-HV) [10], or 3-hydroxyhexanoate (3-HH) [11]. Co-polymerization lowers the melting temperature down as far as 75 °C, thus facilitating the processing and production of PHB; as a consequence, the degree of the crystalline phase is reduced, depending on the percentage of PHB in the co-polymer.
The tensile strength of PHB is close to that measured on isotactic polypropylene (iPP); on the other hand, its elongation at break is significantly lower (6%) compared to that of iPP, being about 400%. This means that PHB is much more brittle compared to iPP. To overcome this weakness, PHB can be also blended with different synthetic and bio-based (such as starch, lignin-derivate) polymers with a similar melting temperature range or modified upon the addition of fillers or additives: in this way it is possible to improve the characteristics of PHB with the aim of widening its field of applications, possibly reducing also the costs of the final products [9].
The high costs of carbon substrates can limit the production of PHB on a large scale. To overcome this problem, alternative substrates rich in carbohydrates are proposed, like biomass from green spaces, wastes, secondary products of industrial processes, such as glycerol, sugarcane bagasse, and lignocellulose from agricultural and forestry residues [12].
In the last years, it is becoming interesting to study the possibility of blending PHB with industrial biowastes for two reasons: first, because the disposal of industrial bioproducts is an environmental issue, and second because it has been reported that this blending process can improve the mechanical properties of the natural polymer by creating a matrix with multiple applications [13].
The high costs of carbon substrates represent also an ethical problem for PHB production, particularly in those regions where the nutritional situation is a difficult issue to be solved. With the biotechnology techniques, it is possible to synthesize PHB from cheap renewable resources such as agricultural and industrial wastes [8,14,15], representing promising alternatives to produce PHB at competitive costs, without causing ethical conflicts [16].
The aim of this work was to isolate, for the first time, PHB synthesizing bacteria from the argan field soil and to identify the presence of the bio-based polymer granules by adopting the Schaeffer-Fulton endospore staining methods. The intracellular granules accumulation was first examined by adopting Malachite Green. Afterward, a second identification test was implemented by adopting the variation of the Schaeffer-Fulton staining, where the Malachite Green dye was replaced by a Methylene Blue solution. The presence of endospores was observed by the compound light microscope using oil immersion. This experimental work represents the first step of the synthesis of PHB bio-based polymer starting from argan wastes, resulting from the fruits and the pressing process for the argan oil extraction.

Samples Collection
The soil samples for the isolation of the PHB producing bacteria were collected from rhizospheric soil in the agricultural crops of argan oil (Argania spinosa) in Taroudant, a southwestern region of Morocco where the argan tree is endemic. All samples were collected from six different locations of the same area of the argan crop to screen the physical characteristics that best suit the PHB producing bacteria growth. The physical characteristics of the soil were the presence compared to the absence of water, the presence of domestic pollutants in the urban location compared to the absence of pollution in the rural area, and the proximity to either dead trees or healthy trees. Soil samples were collected in sterile conditions by using ethanol 70%, preserved into sterile vials, and stored at 22 °C temperature for 48 h. Afterward, all samples were stored at 4 °C for 3 weeks for the bacterial isolation.

Pretreatment: Isolation of Microorganisms
One gram of each soil sample was dispersed in 10mL of sterile water. These samples were homogenized at 200 rpm for 3 h to ensure homogeneity of bacterial organisms in a culture, and after heated at 80 °C for 10 min to isolate endospore-forming bacteria. All samples were serially diluted to 10-8 using sterile water and plated by spreading 100 µL of the dilutions −5, −6, −7, −8 on sterile nutrient agar plates, composed as follows: Peptone 5 g/L, Yeast extract 3 g/L, Sodium chloride 5 g/L, Glucose 1 g/L, Agar 18 g/L, in 1L of distilled water, at pH 7.0. Thereafter the plates were incubated at 30 °C for 48 h. All grown bacteria were isolated on modified agar plates consisting of: Beef extract (0.3%), Peptone (0.5%), Sodium Chloride (0.8%), Glucose (1%), and Agar (1.5%) [17].

Schaeffer-Fulton Endospore Staining Using Malachite Green and Safranin
The detection for PHB-producing bacteria was performed by using the Schaeffer-Fulton method for staining endospores. The staining was prepared by dissolving 0.5 g of Malachite Green in 100 mL of distilled water. The Safranin counterstain was prepared by dissolving 2.5 g of Safranin powder in 100 mL of 95% ethanol. After fixing the microorganisms on the glass slide, the specimen was covered with a square of blotting paper and saturated with Malachite Green stain solution for 5 min by steaming over boiling water and adding more dye when it dried off. After washing the slide with distilled water, the specimens were counterstained with safranin for 30 s, and once again washed with distilled water. The slides were examined under oil immersion at 1000× for the presence of endospores. The vegetative cells appear red to pink, while the endospores are bright green [18].

Schaeffer-Fulton Endospore Staining Using Methylene Blue Solutions
The newly alternative Schaeffer-Fulton endospore staining using Methylene Blue solutions was implemented to confirm the presence of endospores already identified in the staining with Malachite Green. In this proposed study, the alternative staining method resulted in coloring endospores of the species Bacillus subtilis and Clostridium tetani. A solution of Methylene Blue stain 0.5% at pH 12 was prepared by diluting 0.1 g of the dye with 20 mL of a buffer solution at pH 12. A bacterial smear of the positive endospore producing bacteria, already identified using Malachite Green staining, was prepared and fixed over low heat. The Methylene Blue stain 0.5% at pH 12 was added to the specimens and heated over a steam bath for 5 min. Afterward, the slide was washed with distilled water and counterstained with Safranin for 30 s. Before proceeding with the microscopic observations, the slides were again washed with distilled water to remove the counterstaining dye. According to this work, the warming process allows the Methylene Blue solution to penetrate the endospores' wall, and the alkaline pH of the staining solution allows the dye to penetrate the alkaline bacterial cytosol [19].

Results and Discussion
In this work, we investigated the potential presence of microorganisms able to synthesize the biopolymer PHB from Argania spinosa crop soil in a unique environmental area of Morocco where this species is endemic and preserved.

Isolation and Screening of PHB Producing Bacteria
Six soil samples were collected from the agricultural crops of argan oil (Argania spinosa) in Taroudant, a southwestern region of Morocco. Four thermo-resistant bacterial species were isolated from all six soil samples. Only one different bacterial species, represented in Figure 1a,b, was isolated from a location in proximity of an urban area where wastewater and garbage contaminate the argan field. Recent works indicated the presence of six different bacterial strains of PHB producers isolated from sewage samples. Among all the isolated species, one Strain 11 produced 45.9% of PHB by using glucose as the sole carbon source [20]. From this perspective, this work aimed to isolate new bacterial strains able to synthesize the biopolymer PHB, to subsequently optimize the synthesis, modification, and biodegradation processes of the polymer by using the argan waste biomass. Morphological analysis of the pure isolated colonies of the PHB-producing bacteria described the whole colony appearance as irregular to flat, with undulate margins of a white, opaque color, and a rough surface. Similar morphological characteristics were discussed by Kaliwal and colleagues. Of all the six PHB-producing strains isolated from fodder field soil, the researchers identified a strain called BBKGBS6, classified as a member of the genus Bacillus, that showed similar morphological characteristics and was able to accumulate 60% of intracellular PHB [21].

Identification of PHB-Producing Bacteria by Schaeffer-Fulton Endospore Staining
For rapid detection of PHB-producing bacteria, the Schaeffer-Fulton staining method was used. The pure colonies isolated from the modified agar medium were stained with Malachite Green, a preliminary screening agent for lipophilic molecules. Under microscopic observations at 100X on oil immersion, the bacterial endospores showed a green coloration as reported in Figure 2a. This positive result is explained by the activity of the lipophilic endospore membranes that allow the Malachite Green to cross the membrane and to retain the green coloration [19] (Ruth, 2009).
The endospore was also stained using a variation of Methylene Blue, which was used as a coloring alternative to Malachite Green in staining the bacterial species Bacillus subtilis and Clostridium tetani by Okatari et al. In this recent work, the endospore staining properties of Methylene Blue were investigated using differently concentrated solutions of the dye at different pH levels. Their work demonstrated that the species Bacillus subtilis are well stained at an optimal stain concentration of 0.5% and pH 12, while in staining the species Clostridium tetani, the optimal concentration was 0.5% at pH 11 [19]. In following this alternative, this study adopted confirmatory staining that was performed by using the Schaeffer-Fulton staining method where the conventional Malachite Green dye was substituted by an alcoholic solution of Methylene Blue 0.5% at pH 12. The pH and concentration parameters selected for this work correspond to the optimal staining conditions of the bacterial species Bacillus subtilis since the morphological analysis previously conducted may suggest that the species isolated belongs to the genus Bacillus. After staining with Methylene Blue 0.5% at pH 12, the specimens were counter-stained with Safranin. The colored specimens were observed under the compound light microscope at 1000× in oil immersion. Figure 2b shows how the bacterial endospores retained the blue color of the Methylene dye, which passed through the endospore membranes and colored the internal granules.

Conclusions
Top and rhizospheric soil samples collected from agricultural crops, industrial contaminated fields, and uncultivated fields have been selected as favorable environmental areas for the PHB producing bacteria growth. Notably, olive oil, vegetable oil, and sunflower oil crops have been identified as good reservoirs for the isolation of PHB synthesizers as well as for the optimization of the polymer synthesis and modification by using the corresponding biomass waste material like oil wastewater and natural solid wastes.
In this work, the soil samples were collected from the argan field in the southwestern region of Morocco, where the Argania spinosa species is endemic and preserved. Among all the soil samples collected, five different bacterial thermo-resistant specimens were isolated and tested for the identification of intracellular endospores. Only one bacterial species was identified as positive. This selected species was isolated from an area of the argan field exposed to human contaminations, such as wastewater and solid wastes. The positivity of this work was confirmed by the Schaeffer-Fulton staining methods for the identification of endospore producing bacteria. The conventional method of using Malachite Green evidenced the presence of intracellular material that retained the green dye in contrast with the red color of the vegetative compartments that retained the Safranine. Furthermore, the variation method that used the Methylene Blue stain instead of Malachite Green confirmed the presence of intracellular compartments colored in blue because they retained the first colorant, while, also in this method, the rest of the bacterial cell appeared in red. After this first identification, further biochemical and biomolecular analysis is necessary to identify the bacterial species isolated. Moreover, further research is necessary to understand the role of the microorganism in the synthesis of the PHB and how the argan waste products can be valuable for the PHB synthesis, blending, and biodegradation.

Conflicts of Interest
The authors declare that they have no conflict of interest.