key: cord-0756536-010qt9qu authors: Bjerk, Thiago R.; Severino, Patricia; Jain, Sona; Marques, Conrado; Silva, Amélia M.; Pashirova, Tatiana; Souto, Eliana B. title: Biosurfactants: Properties and Applications in Drug Delivery, Biotechnology and Ecotoxicology date: 2021-08-13 journal: Bioengineering (Basel) DOI: 10.3390/bioengineering8080115 sha: 655ad5ee49eb9866e00fd502e84c140e9cd90271 doc_id: 756536 cord_uid: 010qt9qu Surfactants are amphiphilic compounds having hydrophilic and hydrophobic moieties in their structure. They can be of synthetic or of microbial origin, obtained respectively from chemical synthesis or from microorganisms’ activity. A new generation of ecofriendly surfactant molecules or biobased surfactants is increasingly growing, attributed to their versatility of applications. Surfactants can be used as drug delivery systems for a range of molecules given their capacity to create micelles which can promote the encapsulation of bioactives of pharmaceutical interest; besides, these assemblies can also show antimicrobial properties. The advantages of biosurfactants include their high biodegradability profile, low risk of toxicity, production from renewable sources, functionality under extreme pH and temperature conditions, and long-term physicochemical stability. The application potential of these types of polymers is related to their properties enabling them to be processed by emulsification, separation, solubilization, surface (interfacial) tension, and adsorption for the production of a range of drug delivery systems. Biosurfactants have been employed as a drug delivery system to improve the bioavailability of a good number of drugs that exhibit low aqueous solubility. The great potential of these molecules is related to their auto assembly and emulsification capacity. Biosurfactants produced from bacteria are of particular interest due to their antibacterial, antifungal, and antiviral properties with therapeutic and biomedical potential. In this review, we discuss recent advances and perspectives of biosurfactants with antimicrobial properties and how they can be used as structures to develop semisolid hydrogels for drug delivery, in environmental bioremediation, in biotechnology for the reduction of production costs and also their ecotoxicological impact as pesticide alternative. Surfactants are an important class of chemical compounds widely used in various sectors of modern industry [1] [2] [3] . The world market is projected to reach USD 52.4 billion bioremediation industries [16] . It has been reported that sophorolipid has the capacity to form amphotericin B-loaded niosomal formulation with unique structural characteristics and physicochemical properties, as well as biofilm-breaking functionality and activity [17] . Lipopeptides (LPs) are composed of lipid portions linked to a peptide chain and are also reported to have biological activities, including antimicrobial properties. The most characterized LPs are daptomycin [18] and polymyxin B [19] [20] [21] , lipopeptides microbially derived from antibiotics that have been used in the development of drug delivery systems. Surfactin (SUR), iturin, and fengicin are also among the most well-known LPs and have many potential applications. They accumulate at interfaces showing different polarities, especially oil/water and air/water, and they act as wetting agents on solid surfaces (water/solid). This dynamic process is based on the ability of biosurfactants to reduce surface tension through the placement of their amphiphilic parts in specific areas of the membrane or surface in between the phases. The antimicrobial mechanism is assumed to be LPs polymerization to form transmembrane channels in cells. The antimicrobial activity of biosurfactants is generally quite sensitive to any significant structural change. Chemical synthesis taking into account structure-activity relationships will allow the development of new amphiphiles with improved pharmacological properties, bioavailability, and consequent biodegradability [10, 22] . This review summarizes the recent advances and perspectives of biosurfactants, their production from different sources, their physicochemical characterization, and their application as antimicrobial agents, in environmental bioremediation, in pharmaceutics as drug delivery systems, in biotechnology, in the reduction of production costs, and also their ecotoxicological impact. Biosurfactants can be obtained from microorganisms' activity (such as from Pseudomonas and Bacillus), through enzyme-substrate reactions and fermentation processes, as well as being synthesized extracellularly using biocatalyst enzymes. Both the hydrophobic portion and the hydrophilic portion of the biosurfactants can be synthesized in two independent pathways: both the portions can be substrate-dependent, or one can be synthesized de novo while the other is induced by the substrate [23] . Glycolipids are the most common type of biosurfactants. Some of the common glycolipid biosurfactants such as rhamnolipids, trehalolipids, sophorolipids, and mannosylerythritol lipids (MELs) contain mono and disaccharides combined with long-chain aliphatic acids or hydroxy-aliphatic acids [24] . Rhamnolipids are one of the most important glycolipids and are known for their excellent physicochemical properties [23, 24] . Rhamnolipids are mainly produced by Pseudomonas and Burkholderia species. The first step in the production of rhamnolipids includes synthesis of the sugar part containing rhamnose from D-glucose, and the hydrophobic acid part from fatty acids [25] . The enzymes necessary for this first step are usually found in most bacteria, but the specific enzymes needed for the biosynthesis of the rhamnolipids are found almost exclusively in P. aeruginosa and Burkholderia species. Five different enzymes, RhlA, RhlB, RhlC, RhlG, and RhlI, have been reported to be associated with the production of rhamnolipids in P. aeruginosa [26] . Microbial fermentation can result in different kinds of rhamnolipids. Mono-rhamnolipids and di-rhamnolipids differ in the number of rhamnose groups present in the molecular structure. Rhamnolipids also differ with respect to chain length, degree of branching, and degree of unsaturation in the fatty acid chains, all dependent on the environmental and growth conditions [27] . About 60 different rhamnolipid congeners and homologues have been reported [28] , using a combination of Pseudomonas and other bacterial species. Many Burkholderia species have been shown to produce longer alkyl chain rhamnolipids compared to those produced by P. aeruginosa [29] . Different substrates, such as alkenes, citrates, glucose, fructose, and olive oil, have also been employed for producing biosurfactants with different properties [27] . A number of studies have been carried out to disclose the best way to produce rhamnolipids, both in terms of safety and cost effectiveness. Engineering P. aeruginosa to reduce its pathogenicity is one such way, while another approach involves the expression of the key genes responsible for rhamnolipid production in non-pathogenic strains [30] . The cost of producing rhamnolipids can be reduced by selecting suitable substrates, such as vegetable oils, and optimizing the fermentation process [31] . Sophorolipids can be produced by several non-pathogenic yeast species, genus Candida being the most common, and C. bombicola and C. apicola (containing enzymes necessary for the terminal oxidation of alkanes to generate fatty acids) are the most used species [32] . Sophorolipids can be found in two different forms, the lactonic and the acidic form. Like rhamnolipids, the cost of production of sophorolipids (compared to chemically synthesized surfactants) is very high, which limits their industrial production [33] . Use of oil byproducts or food waste has been suggested as an alternative to reduce the production costs [34] . The biosynthesis of surfactin occurs through a non-ribosomal mechanism catalyzed by surfactin synthetase, a protein complex comprising four enzymatic subunits, among which the subunit SrfD is crucial to initiate the synthesis [35] . Other lipopeptide biosurfactants, such as iturin, lichenysin, and arthrofactin, are also produced by similar synthase complexes [36] . Bacillus subtilis is the main bacteria utilized for surfactin production. Genetic engineering of the wild-type strain to improve the low yield has been reported. Wu et al. (2019) modified 53 different genes in B. subtilis to reach a yield of around 42% of the theoretical yield [37] . Apart from normal fermentation, surfactin can also be produced through solid state fermentation (SSF), a process in which microorganisms grow on or inside solid substrates or supports, in the absence of free water. Lipopeptide biosurfactants have also been reported to be produced by Pseudomonas aeruginosa using renewable resources, such as lubricating oil and peanut oil [38] . Bio-emulsifiers (BE) are high-molecular-weight compounds produced by bacteria, yeast, and fungi. They are synthesized as complex mixtures of heteropolysaccharides, lipopolysaccharides, lipoproteins, and proteins which can be adhered to the cell surface or released [39] . Bio-emulsifiers show a wide variety of physicochemical properties granted by different microbes that produce them [23] . Acinetobacter spp. is among the earliest known members producing BEs. Emulsan and Alasan are the best examples of the commercially used bio-emulsifiers produced by Acinetobacter spp [40] . Emulsan is a lipoheteropolysaccharide polymer containing D-galactose-amine produced during the stationary phase. Maximum concentration is obtained when culture media containing 12 carbon-based fatty acids are used as the carbon source. Emulsan production is possible with fermentation methods such as batch, chemo-stat, immobilized cell system, and self-cycling fermentation. Other bio-emulsifiers such as mannoprotein have been reported to be produced within the cellular wall of Saccharomyces spp. and Kluyveromyces marxianus and are released from the cell wall of yeast using pressurized heat treatments [41] . Microorganisms are able to produce a wide variety of similar biosurfactants, but with a different bioactivity. In addition to their source, the physicochemical characteristics of these biosurfactants are influenced by production and purification processes. Understanding of these characteristics is important for the correct indication of their industrial application [23] . This section elucidates some important properties of biosurfactants, instrumental for their use as emulsifiers. An important feature of a bio-emulsifier is its ability to reduce surface and interfacial tension. This is an essential function of amphiphilic molecules for the formation of kinetically stabilized emulsions. These molecules adsorb on interfaces (air/liquid, liquid/liquid, solid/liquid), replacing water or oil molecules along the interface and reducing intermolecular forces between solvent molecules and surface or interfacial tension [23, 24] . Compared to chemical surfactants, biosurfactants were able to decrease the interfacial tension more efficiently [42] . Surfactin is one of the most active surface biosurfactants. Surfactin displays an expressive surface activity from 72 mN/m to 27 ± 2 mN/m [43] and interfacial tension to 3.79 ± 0.27 mN/m and 0.32 ± 0.02 mN/m under harsh physical and chemical conditions [44] . A lipopeptide biosurfactin called arthrofactin produced by Arthrobacter sp. strain MIS38 [45] and biosurfactant produced by Candida lipolytica UCP 0988 [46] showed low surface activity. Such unique surface properties are associated with the more complex chemical structure of biosurfactants. Unlike synthetic surfactants, they do not have a clear distribution of polarity, and also contain branched or ring structures [47] . Lipopeptide surfactin is capable of forming spherical structures to facilitate close packing at interfaces and the formation of structures with a low aggregation number [48] . Unusual surface properties of saponins have been observed. Their behavior was explained by a dense molecular packing at the interface of phases and a strong hydrogen bond between saccharide groups in the interfacial layer [49] . The very compact surface layers formed are denser than those observed in most common amphiphiles. The aforementioned properties of biosurfactants determine their binding mechanisms to biomolecules and cell membranes. A more detailed comparison of properties, namely, surface activity and critical micellization concentration (CMC) values, is presented in the review [50] . In some cases, low CMC values and surface activity can be associated with the presence of impurities in surfactant compositions. Micellization is a balancing process, resulting in thermodynamically stable nanostructures. Surfactants spontaneously form micelles in aqueous solvents at concentrations above the CMC [51] . Figure 1 shows the relationship between surfactant concentration and surface tension. After reaching the CMC, the surfactant monomers are grouped in micelles [52] . Biosurfactants have a tendency to spontaneously self-assemble through hydrophobic effect and weak Van der Waals interactions. The effectiveness of the biosurfactant is defined by its ability to reduce surface tension. The surface tension of the water is 72 mN/m; a good biosurfactant can reduce this value to 30 mN/m [53] . The size or shape of the micelle depends on changes in the concentration of biosurfactant, temperature, pH, pressure, and salts, among others. The repulsive forces of the head groups restrict the amount of associated biosurfactants in the formation of micelles [23] . Increasing the surfactant concentration above the CMC value favors the formation of a greater number of micelles. The formation of micelles with a low aggregation number is characteristic of both rhamnolipids and surfactin. Then, they can be reorganized into bubble structures [54] . While temperature was shown to barely affect surface activity of surfactants, rhamnolipids were transformed into vesicles upon the increase of temperature and decrease of pH [55] . Micelle formation of biosurfactants depends both on the structure of the hydrocarbon chain and on the peptide sequence. The hydrogen bonds between the head groups of biosurfactants lead to the formation of supramolecular structures with different morphologies [56] . The architecture of nanostructures formed by biosurfactants can be nanotubes, spiral, twisted cylindrical nanofibers, and others [57] . Bioengineering 2021, 8, 115 6 of 18 structure of the hydrocarbon chain and on the peptide sequence. The hydrogen bonds between the head groups of biosurfactants lead to the formation of supramolecular structures with different morphologies [56] . The architecture of nanostructures formed by biosurfactants can be nanotubes, spiral, twisted cylindrical nanofibers, and others [57] . Amphiphiles self-assembled in aqueous solutions can solubilize hydrophobic compounds (oil, for example), which preferentially reside in the hydrophobic domains of the amphiphilic nanostructure. The solubility of hydrophobic organic compounds in the presence of biosurfactant depends on the concentration, pH, and the incorporation of additives and salts (electrolytes) that can change the size of micelles [58] . Rhamnolipids can increase the solubilization of hydrophobic compounds by increasing the hydrophobicity of amphiphilic molecule. Biosurfactant molecules have a tendency to form vesicles and micelles with increasing pH, which limits the solubilization of other molecules. The properties of biosurfactants are specific to the substrate, solubilizing or emulsifying different hydrocarbons at different rates [59] . Biosurfactants are more effective solubilizing agents than synthetic surfactants [60] . For example, a biosurfactant obtained from Rhodococcus erythropolis HX-2 exhibited a higher solubilization for petroleum and polycyclic aromatic hydrocarbons than synthetic surfactants sodium dodecyl sulfate (SDS), polysorbate (Tween 80), Triton X-100, and rhamnolipid [61] . It is interesting to note that rhamnolipids can solubilize n-alkanes not only at concentrations above CMC [62] , but also below CMC [63] . Their solubilization efficiency of n-alkanes is 3-4 order higher below CMC [64] . A synergistic improvement in solubility of polycyclic aromatic hydrocarbons was observed in the case of interaction between two biosurfactants (rhamnolipid and sophorolipid) compared to one glycolipid [65] . Emulsions are kinetically stabilized systems, but without balance. Its structure, stability, and appearance depend on the composition of the liquid phases (oil and water) and of emulsifier (chemical structure and physicochemical properties) and the conditions of the preparation (temperature and pressure) and the process (input energy, mixing time, and the kind of equipment) [66] . The emulsion can be broken down by several mechanisms, including skimming, flocculation coagulation (aggregation of the emulsion droplets), Ostwald maturation, and coalescence. Creaming may happen, caused by the difference in densities between oil and water phases, where the emulsion droplets mi- Amphiphiles self-assembled in aqueous solutions can solubilize hydrophobic compounds (oil, for example), which preferentially reside in the hydrophobic domains of the amphiphilic nanostructure. The solubility of hydrophobic organic compounds in the presence of biosurfactant depends on the concentration, pH, and the incorporation of additives and salts (electrolytes) that can change the size of micelles [58] . Rhamnolipids can increase the solubilization of hydrophobic compounds by increasing the hydrophobicity of amphiphilic molecule. Biosurfactant molecules have a tendency to form vesicles and micelles with increasing pH, which limits the solubilization of other molecules. The properties of biosurfactants are specific to the substrate, solubilizing or emulsifying different hydrocarbons at different rates [59] . Biosurfactants are more effective solubilizing agents than synthetic surfactants [60] . For example, a biosurfactant obtained from Rhodococcus erythropolis HX-2 exhibited a higher solubilization for petroleum and polycyclic aromatic hydrocarbons than synthetic surfactants sodium dodecyl sulfate (SDS), polysorbate (Tween 80), Triton X-100, and rhamnolipid [61] . It is interesting to note that rhamnolipids can solubilize n-alkanes not only at concentrations above CMC [62] , but also below CMC [63] . Their solubilization efficiency of n-alkanes is 3-4 order higher below CMC [64] . A synergistic improvement in solubility of polycyclic aromatic hydrocarbons was observed in the case of interaction between two biosurfactants (rhamnolipid and sophorolipid) compared to one glycolipid [65] . Emulsions are kinetically stabilized systems, but without balance. Its structure, stability, and appearance depend on the composition of the liquid phases (oil and water) and of emulsifier (chemical structure and physicochemical properties) and the conditions of the preparation (temperature and pressure) and the process (input energy, mixing time, and the kind of equipment) [66] . The emulsion can be broken down by several mechanisms, including skimming, flocculation coagulation (aggregation of the emulsion droplets), Ostwald maturation, and coalescence. Creaming may happen, caused by the difference in densities between oil and water phases, where the emulsion droplets migrate as a function of the gravitational field, resulting in phase separation [23] . The natural emulsifier must be rapidly adsorbed on the surface of oil droplets, and thus, rapidly reduces the interfacial tension to facilitate droplet breakdown and formation of small droplets [67] . The well-known biosurfactant used as an emulsifier in the food industry is from quillaja saponin extract. The emulsifying activity of the cyclic lipopeptide pseudofactin II produced by P. fluorescens BD5 is better than synthetic surfactants Tween 20 and Triton X-100. Pseudofactin II more effectively emulsified aromatic and aliphatic hydrocarbons and some vegetable oils [68] . Rhamnolipids have a greater effect on emulsion droplet size reduction than lecithin and monoglycerides and ensure the thermal stability of emulsion [69] . Biosurfactants can have several applications, such as in bioremediation and in food, cosmetics, pharmaceutical, biomedicine, and nanotechnology industries. This may have advantages over their synthetic equivalents as the former are environmentally friendly. Due to their biodegradability and low toxicity, the use of biosurfactants has increased, for example, in the area of biotechnology. One of the most promising areas of application of biosurfactants is in the degradation of hydrocarbons in contaminated water and soil. They can also have a significant impact on the pharmaceutical sector as drug delivery systems [70, 71] . According to the work of Marchant et al. [72] and Chakraborty et al. [73] , microorganisms use a set of carbon and energy sources for growth. The combination of carbon sources with insoluble substrates favors the diffusion of the intracellular medium and the production of different substances. Moreover, depending on the nature of the carbon source in the culture medium, the synthesis of biosurfactants can be directed to one of the several metabolic pathways involved in this process [74] . In this sense, microorganisms such as bacteria, yeasts, and some filamentous fungi are capable of producing biosurfactants with different molecular structures and surface activities [75, 76] . Table 1 shows some of the different residues that have already been used for the production of biosurfactants. Thus, it is possible to observe that several renewable sources and agro-industrial residues containing an excellent source of carbohydrates and lipids can be used as rich sources of carbon and nitrogen for the growth of microorganisms to obtain biosurfactants, in addition to contributing directly to the reduction of the environmental impact caused by these residues [77] . Some examples of residues used for the production of biosurfactants include whey and cheese, animal fat, molasses, glycerol, macerated liquor, residues from the production of olive oil and other extracted vegetable oils, wastewater from cassava processing, and potato, among others [42, 78] . Biosurfactants comprise a group of amphipathic molecules with different chemical structures, which are produced by several microorganisms [79] . Besides, these substances, generated mainly from secondary metabolites, play fundamental roles in the survival of their producing microorganisms, contributing in turn to the transport of nutrients and the interactions between the microorganism and the host, as well as acting as biocides [80] . Due to their recognized potential and biological nature, biosurfactants have been the target of numerous researches on their probable therapeutic applications [78, 81, 82] . As they are of microbial origin and demonstrate a series of interesting characteristics such as low toxicity, pH tolerance, temperature, ionic strength, biodegradability, antimicrobial activity, and emulsifying and demulsifying capacity, these polymers become of great interest in applications in food, cosmetics, and advanced bioremediation processes, including in drug delivery [83] . These agents have several properties suitable for the food industry as emulsifiers in the processing of raw materials, indispensable for food products that require stability content, a characteristic sensory pattern, and longer shelf life, being applied from products derived from meat, milk, and their derivatives. Given their antimicrobial and anti-adhesive properties, these biosurfactants directly contribute to reducing contamination of processed foods [92] . Biosupplements are generally classified as low molecular weight such as glycolipids and lipopeptides and high-molecular-weight biosurfactants which are polysaccharides, proteins, lipoproteins, etc. Generally, low-molecular-weight biosurfactants demonstrate significant active properties due to their relatively simpler structures [93, 94] ; thus, as shown in Table 2 , rhamnolipids (glycolipids) and surfactin (lipopeptide) are among the most studied biosurfactants. The study by Elshikh et al. [95] demonstrated that the effect of biosurfactants associated with antibiotics as antimicrobial agents presents interesting results. According to the researchers, the combination of nisin and rhamnolipids inhibited thermophilic spores and increased the shelf life of dairy products, while the use of natamycin with rhamnolipid also promoted increased durability of the products, inhibiting the growth of yeasts in industrialized foods. These three associated substances (nisin, natamycin, and rhamnolipids) were also evaluated in some types of cheese and it was observed that there was inhibition of the growth of bacteria and yeasts in these products as well as prolonged shelf life. These results demonstrate that rhamnolipids have anionic characters mainly due to their carboxylate groups, which, in solution, these groups tend to organize on the cell surface lipid membranes, thus increasing the negative charges and promoting the electrostatic interaction between nisin and anionic membrane, which can result in synergistic effect [96] . Biosurfactants are promising for environmental bioremediation activities, which include cleaning up oil spills, removing heavy metal contaminants, and treating wastewater. Microorganisms are able to metabolize oil-related compounds, allowing the elimination of hydrophobic pollutants [107] . A critical factor in the biodegradation process is the increase in hydrophobicity on the microbial cell surface caused by biosurfactants. In the biodegradation process, microorganisms use pollutants as carbon and energy sources. These break the hydrocarbon chain, which leads to an immediate loss of amphiphilicity. Finally, the pollutants are transformed into CO 2 , water and minerals [23] . Biosurfactants can improve the hydrocarbon bioremediation, increasing the bioavailability of the substrate for microorganisms or interacting with the cell surface to increase its hydrophobicity, thus allowing an easier association between the hydrophobic substrates themselves and the bacterial cells [99, 102] . Several studies have reported the application of microbial surfactants in the process of bioremediation of contaminated soil and wastewater. In the work developed by Patowary et al. (2018) [108] , the authors describe the use of rhamnolipid obtained by Pseudomonas aeruginosa SR17 for bioremediation of soil contaminated by oil. The degradation of total petroleum hydrocarbon (TPH) in soil containing 6800 ppm and 8500 ppm TPH was evaluated. The efficiency of the rhamnolipid biosurfactant was compared with the synthetic surfactant sodium dodecyl sulfate (SDS). The soil treated with rhamnolipid showed degradation efficiency of 86.1% and 80.5%; by using synthetic surfactant, this value dropped to 70.8% and 68.1%. Sun et al. (2019) [109] reported the application of biosurfactant glycolipid produced by the strain of Pseudomonas aeruginosa S5 isolated from coking effluent for in situ remediation. The inoculation of the strain in the coke wastewater promoted the biodegradation of polycyclic aromatic hydrocarbons, reducing 44% in 15 days in the sludge. Zhou et al. (2020) [110] evaluated the effects of the addition of the lipopeptide produced by Acinetobacter sp. isolated from hydraulic fracturing flowback and produced (HF-FPW). The authors observed that inoculation of the bacterial strain in HF-FPW increased the activity and growth of Pseudomonas sp. and Rhizobium sp., known for their hydrocarbon degradation capacity, achieving a reduction of 94% and 77% for n-alkanes and polycyclic aromatic hydrocarbons in 7 days. Recently, Swati et al. (2020) [111] showed that the biosurfactant produced by the strain Pseudomonas sp. ISTPY2, isolated from the Ghazipur landfill, has a degradation efficiency of pyrene present in high concentration in the soil microcosm, reaching a removal efficiency of 94% in 10 days. Tang et al. (2018) [112] evaluated the application of rhamnolipid, saponin, and sophorolipid biosurfactants to increase the removal of heavy metals Cu, Zn, Cr, Pb, Ni, Mn, Fe, and Hg from the sludge through electrokinetic treatment. The results showed that three biosurfactants can effectively increase the removal of heavy metals from the sludge, showing chelating and binding capacity under acidic conditions. Recently, Sun et al. (2021) [113] evaluated the application of biosurfactant produced by Pseudomonas sp. CQ2 isolated from the Chongqing oilfield (China) for bioremediation of heavy metals in contaminated soil. Removal efficiency of 78.7, 65.7, and 56.9% was obtained for Cd, Cu, and Pb, respectively, values higher than those obtained using chemical surfactants. Biosurfactants can assume an immense variety of functions in the pharmaceutical industry, since they have antimicrobial, anti-adhesive, antiviral, anticancer, spermicidal, hemolytic, anti-inflammatory, and immunomodulatory activities [24, [114] [115] [116] [117] [118] [119] . Antimicrobial application is one of the most desired uses described in pharmaceutical literature. Surfactin has several interesting properties, including antimicrobial, antiviral, antitumor, hypocholesterolemic, anti-adhesive, insecticide, apoptotic, and hemolytic action. Among other functions, surfactin inhibits the fibrin clotting process and has antitumor activity against Ehrlich's ascites carcinoma cells, inhibiting cyclic adenosine 3 , 5 -monophosphate phosphodiesterase, and antifungal activities [23, 82] . Among the studies, lipopeptide biosurfactants showed in vitro antimicrobial, antibiofilm, and cytotoxic effects. The biosurfactant was produced by Acinetobacter junii (AjL), exhibiting inhibition against Candida utilis and becoming a potential new drug [120] . In this way, Fernandes et al. [121] used kitchen waste oil as Wickerhamomyces anomalus CCMA 0358 substrate to produce a biosurfactant with larvicide activity, Aedes aegypti larvae. The biomolecule also assesses activity against bacterial (Bacillus cereus, Salmonella enteritidis, Staphylococcus aureus, and Escherichia coli) and fungal strains (Aspergillus, Cercospora, Colletotrichum, and Fusarium). The main advantages concern the low cost of production and ease of scale up process. Jiang et al., 2019 [122] produced biosurfactants using Lactobacillus helveticus strains showing anti-adhesive and inhibiting effects on biofilm formation and this also was observed in studies carried out by Ashitha et al. (2020) [123] using Burkholderia sp. WYAT7 strains to obtain biosurfactant with antibacterial activity against Pseudomonas aeruginosa (MTCC 2453), Escherichia coli (MTCC 1610), Salmonella paratyphi, and Bacillus subtilis strains. Moreover, biosurfactants are promising for cosmetic applications. According to recent publications, they have lower toxicity, offering dermal compatibility and moisturizing effects [124] . Ferreira et al., 2017 [125] described a demand for green cosmetics to replace petroleum derivates. The researchers developed a biosurfactant originating from Lactobacillus paracasei by oil-in-water (o/w) emulsification. These results were compared to the traditional surfactant, sodium dodecyl sulphate (SDS), used in the cosmetics industry, and they obtained similar results. No toxicity effect was observed in fibroblasts, otherwise SDS showed a strong inhibitory effect. Biosurfactants have been employed as a drug delivery system (DDS) to improve the oral bioavailability of a large number of drugs that exhibit low aqueous solubility, and this has been a major challenge in the field of pharmaceutical sciences. The great potential of these molecules concerns in auto assembly and emulsification [126] . Hereby, some strategies, such as microemulsion drug delivery systems (MDDS), have been adopted to develop delivery systems capable of improving the oral bioavailability of hydrophobic drugs. They contain lipids, surfactants, cosurfactants, and/or cosolvents, and are generally globular in shape [127] . Currently, MDDS are being formulated for use through various routes of administration, such as oral, nasal, ocular, topical, and intravenous [128] . Hydrogels incorporating antimicrobial biosurfactants have been suggested as wound healing systems against skin drug-resistant infections [129] . Hydrogels obtained from poly (vinyl alcohol) (PVA), polyethylene oxide (PEO), and poly (acrylic acid) (PAA) polymers can be used as a semisolid vehicle for topical products containing antimicrobial surfactants. Examples of commercially available products containing antimicrobial biosurfactants are the moisturizer Kanebo (Kanebo Cosmetics, Tokyo, Japan), the facial cleaner Sopholiance (Givaudan Active Beauty, Paris, France), and the body moisturizer Relipidium (BASF, Monheim, Germany) [130] . In spite of the ever-increasing demand, the commercial production of biosurfactants is still a challenge due to high raw material costs and high processing costs together with low output. Thus, one of the current research challenges includes an increase in the yield, keeping the cost of raw materials as low as possible. Several studies have aimed to optimize the biosurfactant production process by changing the variables such as carbon and nitrogen sources, amount of oxygen, temperature, and pH that influence the type and amount of biosurfactant produced by a microorganism. However, recently, many studies have focused on biosurfactant production using renewable substrates [131] , which will be the focus of this section. Various research groups around the globe have explored the use of inexpensive alternative sources (such as agroindustrial waste) to produce different biosurfactants. The use of industrial/house byproduct/waste as raw material brings down the production costs, and at the same time reduces the environmental damage by reducing their accumulation. A large variety of waste and byproducts have been described in the literature for biosurfactants production, including oil processing waste, starch waste, sugar industry waste, fruit and vegetable waste, distillery waste, and animal fat, some of which have been listed in Table 1 . Industrial starch production using crops such as corn, rice, cassava, wheat, and potato generate high amounts of wastewater, rich in starch, which can be used as a substrate for the production of biosurfactants. Fox and Bala (2000) [132] described the use of potato substrates for producing surfactants from B. subtilis and reported a surface tension of 28.3 mN/m in solid medium and a CMC of 100 mg/L, using 60 g/L of potato substrate in the cultivation media. Minucelli et al. (2017) [133] reported the use of chicken fat, sunflower oil, sugarcane molasses, sugarcane juice, sucrose, or glucose for the production of sophorolipids by C. bombicola. About 39.8 g/L of sophorolipids were produced using 75 g/L chicken fat, 77.5 g/L glucose, and 2.5 g/L yeast extract, giving a surface tension of 35 mN/m and a CMC of 65 mg/L. Similarly, Chaves-Martins and Guimarães-Martins (2018) [134] reported the use of different industrial waste (sugarcane bagasse, fish waste, crude glycerol, and petroleum sludge from storage tanks) for biosurfactant production using Corynebacterium. Efficient biosurfactant production was achieved with the use of 3% sugarcane bagasse and 3% fish residue as a carbon source with ST values of 27.8 mN/m and 33.9 mN from sugarcane bagasse and fish residue, respectively. [136] reported sophorolipid production at a cost of USD 2.54/kg, using glucose and high oleic sunflower oil. As raw materials constitute about 50% of the overall biosurfactant production (Rufino et al., 2014) , the use of cheaper agroindustrial waste and low-cost renewable substrates can substantially reduce the production costs. The use of agroindustrial waste is thus a potential approach for reducing production costs that could make biosurfactants economically viable and commercially competitive with synthetic surfactants. Every year, plantations around the world are damaged by phytopathogens, which leads to great economic loss. Currently, the most common way to combat this problem is the use of pesticides, which is a concern for environmentalists. Many biosurfactants produced by microorganisms are being studied for their potential to inhibit the growth of phytopathogens by presenting antimicrobial and antibiofilm properties [137, 138] . The plant-associated microbiome produces a structurally diverse group of compounds with hydrophilic and hydrophobic portions, which exhibit biosurfactant activity. These can be lipopeptides, glycolipids, phospholipids, polysaccharides, neutral lipids, and fatty acids [138] . These biosurfactants are an ecofriendly alternative compared to synthetic surfactants due to their lower toxicity and biodegradable properties [23] . Chittepu (2019) [139] isolated and characterized the bacterium Bacillus pseudomycoides OR 1 that produces peanut pie dump sites. The lipopeptide from B. pseudomycoides OR 1 at a concentration of 50 µg/mL demonstrated greater antibacterial activity against E. coli, K. pneumoniae, and S. aureus, respectively (Figure 2) . In a recent study, Ohadi et al. (2020) [116] evaluated in vitro antimicrobial and antibiofilm effects of the lipopeptide produced by Acinetobacter junii. The biosurfactant showed non-selective activity against Gram-positive and Gram-negative bacterial strains. It was found that the minimum inhibitory concentration values for C. albicans and C. utilis were smaller than the standard fluconazole antifungal. The authors also highlighted a reduction in the biofilm formation of Staphylococcus aureus, Proteus mirabilis, and Pseu-domonas aeruginosa by 52%, 31%, and 70%, respectively, in the concentration of 2500 µg/mL of biosurfactant. plant-associated microbiome produces a structurally diverse group of compounds with hydrophilic and hydrophobic portions, which exhibit biosurfactant activity. These can be lipopeptides, glycolipids, phospholipids, polysaccharides, neutral lipids, and fatty acids [138] . These biosurfactants are an ecofriendly alternative compared to synthetic surfactants due to their lower toxicity and biodegradable properties [23] . Chittepu (2019) [139] isolated and characterized the bacterium Bacillus pseudomycoides OR 1 that produces peanut pie dump sites. The lipopeptide from B. pseudomycoides OR 1 at a concentration of 50 μg/mL demonstrated greater antibacterial activity against E. coli, K. pneumoniae, and S. aureus, respectively ( Figure 2 ). In a recent study, Ohadi et al. (2020) [116] evaluated in vitro antimicrobial and antibiofilm effects of the lipopeptide produced by Acinetobacter junii. The biosurfactant showed non-selective activity against Gram-positive and Gram-negative bacterial strains. It was found that the minimum inhibitory concentration values for C. albicans and C. utilis were smaller than the standard fluconazole antifungal. The authors also highlighted a reduction in the biofilm formation of Staphylococcus aureus, Proteus mirabilis, and Pseudomonas aeruginosa by 52%, 31%, and 70%, respectively, in the concentration of 2500 μg/mL of biosurfactant. Ashitha et al. (2020) [140] identified the glycolipid biosurfactant produced by Burkholderia sp. WYAT7 isolated from the medicinal plant Artemisia nilagirica (Clarke) Pamp and evaluated its antibacterial and antibiofilm potential. The biosurfactant exhibited antibacterial activity against bacterial pathogens, such as P. aeruginosa (MTCC 2453), E. coli (MTCC 1610), S. paratyphi, and B. subtilis. Glycolipid at a concentration of 2 mg/mL showed 79% antibiofilm activity against S. aureus (MTCC 1430). Numerous scientific publications, reporting the especial properties of biosurfactants (e.g., antimicrobial, emulsifying, and anti-adhesive), produced either by chemical synthesis or by microorganisms' activity, suggest the potential applications of such compounds in a range of industries. New biosurfactants (glycolipids, surfactin, and high-molecular-weight biosurfactants) produced by microorganisms (bacteria, yeasts, fungi) that may contribute to the detection of different molecules in terms of structure and physicochemical characteristics, are increasingly enhancing antimicrobial aspects, precisely in the area of food and medicine safety, defense of plants and animals, as well as in the control and treatment of diseases. Their amphiphilic nature and capacity for self-assembly open perspectives in the development of new formulations with antimicrobial properties for the delivery of bioactives of pharmaceutical interest. For topical application, these drug delivery systems can be formulated in semisolid hydrogels that can be exploited against skin drug-resistant infections and for wound treatment. Several Numerous scientific publications, reporting the especial properties of biosurfactants (e.g., antimicrobial, emulsifying, and anti-adhesive), produced either by chemical synthesis or by microorganisms' activity, suggest the potential applications of such compounds in a range of industries. New biosurfactants (glycolipids, surfactin, and high-molecular-weight biosurfactants) produced by microorganisms (bacteria, yeasts, fungi) that may contribute to the detection of different molecules in terms of structure and physicochemical characteristics, are increasingly enhancing antimicrobial aspects, precisely in the area of food and medicine safety, defense of plants and animals, as well as in the control and treatment of diseases. Their amphiphilic nature and capacity for self-assembly open perspectives in the development of new formulations with antimicrobial properties for the delivery of bioactives of pharmaceutical interest. For topical application, these drug delivery systems can be formulated in semisolid hydrogels that can be exploited against skin drug-resistant infections and for wound treatment. Several other examples on the use of biosurfactants to reduce the costs of biotechnological products have been reported, such as the use of surfactants from B. subtilis to improve cultivation media. With respect to the ecotoxicological impact, due to their antimicrobial and antibiofilm properties, several biosurfactants produced from microorganisms (e.g., lipopeptides, glycolipids, phospholipids, polysaccharides, neutral lipids, and fatty acids) have found utility in inhibiting the growth of phytopathogens. It is thus expected that biosurfactants are to be considered a potential alternative with several industrial applications. Synthesis, biological evaluation and structure-activity relationships of self-assembled and solubilization properties of amphiphilic quaternary ammonium derivatives of quinuclidine Synthesis, structure-activity relationship and biological evaluation of tetracationic gemini Dabco-surfactants for transdermal liposomal formulations Cationic Surfactants: Self-Assembly Biosurfactants and anti-inflammatory activity: A potential new approach towards COVID-19 Penetration of Surfactants into Skin Effect of synthetic surfactants on the environment and the potential for substitution by biosurfactants Current perspective of sustainable surfactants based on renewable building blocks Derivation and synthesis of renewable surfactants Physiological aspects. Part 1 in a series of papers devoted to surfactants in microbiology and biotechnology Recent food applications of microbial surfactants Biosurfactant production: Emerging trends and promising strategies Glycolipid biosurfactants: Potential related biomedical and biotechnological applications Starmerella bombicola, an industrially relevant, yet fundamentally underexplored yeast Biosurfactants, natural alternatives to synthetic surfactants: Physicochemical properties and applications Rhamnolipids functionalized with basic amino acids: Synthesis, aggregation behavior, antibacterial activity and biodegradation studies Medicinal and cosmetic potentials of sophorolipids Anti-biofilm activity of a sophorolipid-amphotericin B niosomal formulation against Candida albicans Synthesis of gold nanoflowers stabilized with amphiphilic daptomycin for enhanced photothermal antitumor and antibacterial effects Double membrane based on lidocaine-coated polymyxin-alginate nanoparticles for wound healing: In vitro characterization and in vivo tissue repair Sodium alginate-cross-linked polymyxin B sulphate-loaded solid lipid nanoparticles: Antibiotic resistance tests and HaCat and NIH/3T3 cell viability studies Antimicrobial activity of polymyxin-loaded solid lipid nanoparticles (PLX-SLN): Characterization of physicochemical properties and in vitro efficacy Structure-Activity Relationships of Daptomycin Lipopeptides Surfactin, a crystalline peptidelipid surfactant produced by Bacillus subtilis: Isolation, characterization and its inhibition of fibrin clot formation Biosurfactants: Formulations, properties, and applications A stereospecific pathway diverts β-oxidation intermediates to the biosynthesis of rhamnolipid biosurfactants Production of rhamnolipids-producing enzymes of Pseudomonas in E. coli and structural characterization Contributions of biosurfactants to natural or induced bioremediation Why do microorganisms produce rhamnolipids? Rhamnolipids and PHAs: Recent reports on Pseudomonas-derived molecules of increasing industrial interest Rhamnolipids in perspective: Gene regulatory pathways, metabolic engineering, production and technological forecasting Characterisation and antimicrobial activity of biosurfactant extracts produced by Bacillus amyloliquefaciens and Pseudomonas aeruginosa isolated from a wastewater treatment plant Microbial production and application of sophorolipids Production, characterization, and properties of sophorolipids from the yeast Candida bombicola using a low-cost fermentative medium Efficient sophorolipids production using food waste Variants of lipopeptides and glycolipids produced by Bacillus amyloliquefaciens and Pseudomonas aeruginosa cultured in different carbon substrates Genetic Regulations of the Biosynthesis of Microbial Surfactants: An Overview Systematically engineering the biosynthesis of a green biosurfactant surfactin by Bacillus subtilis 168 Biosurfactant Production by Pseudomonas aeruginosa from Renewable Resources Bioemulsifiers are not biosurfactants and require different screening approaches Production, characterization, and applications of bioemulsifiers (BE) and biosurfactants (BS) produced by Acinetobacter spp.: A review Bioemulsifiers derived from microorganisms: Applications in the drug and food industry Optimization and characterization of biosurfactant production by Bacillus subtilis isolates towards microbial enhanced oil recovery applications Bacillus amyloliquefaciens TSBSO 3.8, a biosurfactant-producing strain with biotechnological potential for microbial enhanced oil recovery Biosurfactant production by Bacillus subtilis B30 and its application in enhancing oil recovery A new lipopeptide biosurfactant produced by Arthrobacter sp. strain MIS38 Characterization and properties of the biosurfactant produced by Candida lipolytica UCP 0988 A review on new aspects of lipopeptide biosurfactant: Types, production, properties and its application in the bioremediation process Aggregation of the naturally occurring lipopeptide, surfactin, at interfaces and in solution: An unusual type of surfactant? Saponin Adsorption at the Air-Water Interface-Neutron Reflectivity and Surface Tension Study Biosurfactants and surfactants interacting with membranes and proteins: Same but different? Micellization of Aqueous Cationic Surfactant Solutions at the Micellar Structure Transition Concentration-Based upon the Concept of the Pseudophase Separation Biosurfactants-A new frontier for social and environmental safety: A mini review Microbial production of surfactants and their commercial potential. Microbiol Emulsions stabilised solely by colloidal particles Comparative studies on the surface/interface properties and aggregation behavior of mono-rhamnolipid and di-rhamnolipid Rational design, properties, and applications of biosurfactants: A short review of recent advances Amino acid sequence in constitutionally isomeric tetrapeptide amphiphiles dictates architecture of one-dimensional nanostructures Theory of surfactant self-assembly: A predictive molecular thermodynamic approach Effects of rhamnolipids on microorganism characteristics and applications in composting: A review Towards more Ecofriendly Pesticides: Use of Biosurfactants Obtained from the Corn Milling Industry as Solubilizing Agent of Copper Oxychloride Enhancement of solubilization and biodegradation of petroleum by biosurfactant from Rhodococcus erythropolis HX-2 Inhibition of pathogenic bacterial biofilms on PDMS based implants by L. acidophilus derived biosurfactant Sub-CMC solubilization of n-alkanes by rhamnolipid biosurfactant: The Influence of rhamnolipid molecular structure Enhanced octadecane dispersion and biodegradation by a Pseudomonas rhamnolipid surfactant (biosurfactant) Sustainable self-assembly strategies for emerging nanomaterials Effect of surfactant phase behavior on emulsification Natural emulsifiers-Biosurfactants, phospholipids, biopolymers, and colloidal particles: Molecular and physicochemical basis of functional performance Isolation and characterization of two new lipopeptide biosurfactants produced by Pseudomonas fluorescens BD5 isolated from water from the Arctic Archipelago of Svalbard The heat stability of Rhamnolipid containing egg-protein stabilised oil-in-water emulsions Biosurfactant: A new frontier for greener technology and environmental sustainability Biosurfactants in cosmetic formulations: Trends and challenges Production of biosurfactants from nonpathogenic bacteria Biosurfactant-Based Bioremediation of Toxic Metals Multifunctional biomolecules of the 21st century Microbial biosurfactants as additives for food industries Biosurfactant production by fungi as a sustainable alternative The yeast-like fungus Aureobasidium thailandense LB01 produces a new biosurfactant using olive oil mill wastewater as an inducer Biosurfactants Produced by Marine Microorganisms with Therapeutic Applications Microbial biosurfactants: Challenges and opportunities for future exploitation Applications of a lipopeptide biosurfactant, surfactin, produced by microorganisms Inhibition of bacterial adhesion on medical devices Potential therapeutic applications of biosurfactants Role of polyphenol in sugarcane molasses as a nutrient for hexavalent chromium bioremediation using bacteria Cost effective technologies and renewable substrates for biosurfactants' production Distillery and curd whey wastes as viable alternative sources for biosurfactant production Antimicrobial Activity of a Biosurfactant Produced by Bacillus licheniformis Strain M104 Grown on Whey Biosurfactant production by Pseudomonas aeruginosa GS3 from molasses Optimization of surfactin production by bacillus subtilis isolate BS5 Glycolipid Biosurfactant Production from Waste Cooking Oils by Yeast: Review of Substrates, Producers and Products Production of sophorolipid glycolipid biosurfactants from sugarcane molasses using Starmerella bombicola NBRC 10243 Screening and production of rhamnolipids by Pseudomonas aeruginosa 47T2 NCIB 40044 from waste frying oils Application of Microbial Biosurfactants in the Food Industry The benefits of alpha-lactalbumin in early childhood. In Dairy in Human Health and Disease Across the Lifespan Microbial production of rhamnolipids: Opportunities, challenges and strategies. Microb. Cell Factories Rhamnolipids and lactonic sophorolipids: Natural antimicrobial surfactants for oral hygiene Potential applications of biosurfactant rhamnolipids in agriculture and biomedicine Fermentative production of rhamnolipid and purification by adsorption chromatography Rhamnolipid from Pseudomonas desmolyticum NCIM-2112 and its role in the degradation of Brown 3REL Microbial Bioremediation of Petroleum Hydrocarbon-Contaminated Marine Environments Antibacterial Activity of Sophorolipids Produced by Candida bombicola on Gram-positive and Gram-negative Bacteria Isolated from Salted Hides Dechlorination of chloroorganics, decolorization, and simultaneous bioremediation of Cr 6+ from real tannery effluent employing indigenous Bacillus cereus isolate Main Classes, Functional Properties and Related Potential Applications in Environmental Biotechnology Simple glycolipids of microbes: Chemistry, biological activity and metabolic engineering Microbial biosurfactants for oil spill remediation: Pitfalls and potentials Evaluation of rhamnolipid and surfactin to reduce the adhesion and remove biofilms of individual and mixed cultures of food pathogenic bacteria Characterization and interplay of bacteriocin and exopolysaccharide-mediated silver nanoparticles as an antibacterial agent Role of biosurfactants in bioremediation of oil pollution-A review Application of biosurfactant for enhancement of bioremediation process of crude oil contaminated soil A biosurfactant-producing Pseudomonas aeruginosa S5 isolated from coking wastewater and its application for bioremediation of polycyclic aromatic hydrocarbons Enhanced bioremediation of hydraulic fracturing flowback and produced water using an indigenous biosurfactant-producing bacteria Acinetobacter sp. Y2 Evaluation of a biosurfactant producing bacterial strain Pseudomonas sp. ISTPY2 for efficient pyrene degradation and landfill soil bioremediation through soil microcosm and proteomic studies Biosurfactants enhanced heavy metals removal from sludge in the electrokinetic treatment Naz, I. Optimization of biosurfactant production from Pseudomonas sp. CQ2 and its application for remediation of heavy metal contaminated soil Improvement of the shelf life of raw ground goat meat by using biosurfactants produced by lactobacilli strains as biopreservatives A Review on the Biosurfactants: Properties, Types and its Applications Self-assembling systems based on quaternized derivatives of 1,4-diazabicyclo[2.2.2]octane in nutrient broth as antimicrobial agents and carriers for hydrophobic drugs Biosurfactants: Potential applications as immunomodulator drugs Antimicrobial and anti-adhesive properties of biosurfactant produced by lactobacilli isolates, biofilm formation and aggregation ability Production, characterization and bioactivities of biosurfactants from newly isolated strictly halophilic bacteria anti-biofilm, and anti-proliferative activities of lipopeptide biosurfactant produced by Acinetobacter junii B6. Microb. Pathog. 2020 Eco-friendly biosurfactant from Wickerhamomyces anomalus CCMA 0358 as larvicidal and antimicrobial Biosurfactants of Lactobacillus helveticus for biodiversity inhibit the biofilm formation of Staphylococcus aureus and cell invasion Biocompatible 3D Printed Microneedles for Transdermal, Intradermal, and Percutaneous Applications Biosurfactant: Pharmaceutical perspective Novel cosmetic formulations containing a biosurfactant from Lactobacillus paracasei Emulsion Polymerization with a Biosurfactant Microemulsion synthesis of silver nanoparticles using biosurfactant extracted from Pseudomonas aeruginosa MKVIT3 strain and comparison of their antimicrobial and cytotoxic activities Potential Use of Microbial Surfactant in Microemulsion Drug Delivery System: A Systematic Review Algal and microbial exopolysaccharides: New insights as biosurfactants and bioemulsifiers Microbial Biosurfactants in Cosmetic and Personal Skincare Pharmaceutical Formulations Advances on research in the use of agro-industrial waste in biosurfactant production Production of surfactant from Bacillus subtilis ATCC 21332 using potato substrates Sophorolipids production by Candida bombicola ATCC 22214 and its potential application in soil bioremediation Biosurfactant production from industrial wastes with potential remove of insoluble paint Production, formulation and cost estimation of a commercial biosurfactant A process model for approximating the production costs of the fermentative synthesis of sophorolipids Biosurfactant: Production and Application Production and potential biotechnological applications of microbial surfactants: An overview Isolation and characterization of biosurfactant producing bacteria from groundnut oil cake dumping site for the control of foodborne pathogens Characterization of biosurfactant produced by the endophyte Burkholderia sp. WYAT7 and evaluation of its antibacterial and antibiofilm potentials Institutional Review Board Statement: Not applicable. Data Availability Statement: Not applicable. The authors declare no conflict of interest.