Biotechnological Approaches Applied for Marine Hydrocarbon Spills Remediation: Comparison
Please note this is a comparison between Version 1 by Behnam Asgari Lajayer and Version 3 by Jessie Wu.

Biological and physico-chemical remediation technologies can be efficient in terms of spill cleanup and microorganisms—mainly bacteria—are the main ones responsible for petroleum hydrocarbons (PHCs) degradation such as crude oil. BCurrently, biodegradation is considered as one of the most sustainable and efficient techniques for the removal of PHCs. 

  • oil spills
  • biosurfactants
  • biostimulation

1. Microorganisms Involved in the Removal of Oil Spills from Marine Surfaces

Yeasts, fungi, and bacteria have the potential to use the various HCs in crude oil and derived products. For instance, following the Deepwater Horizon disaster (20 April 2010), the bacterial community identified was prone to succession [1][2][42,43]. At first, a primary enrichment of Pseudomonads and Oceanospirillales prevailed, followed by a change in dominance to CycloclasticusMethylotrophsColwellia, and Pseudoalteromonas. Genes associated with the transportation of iron or phosphorus and nitrogen-based compounds and associated metabolisms such as nitrate reduction were transcribed [3][44]. Correspondingly, total petroleum hydrocarbon and ammonium concentrations on the surfaces of the sediment were correlated with denitrification-related genes that were highly transcribed [4][45]. The gene expression for sulfite reduction and sulfur cycling was raised when O2 levels stayed high, however, the relevant mechanism is still unclear [5][46]. Several months after the DWH (Deepwater Horizon) spill, the sediment of the wellhead area region was enriched with ChloroflexiFirmicutesMethylotrophic, and Actinobacteria [6][47]. An exploratory survey was conducted and showed that—after a decade—the microorganisms of the sediments had returned to pre-spill composition [7][10].
While aliphatic HCs can be properly biodegraded in nature, this is completely different for branched-chain and long-chain HCs [8][9][10][48,49,50]. Moreover, with increasing pH and increasing salinity, the rate of degradation decreases, and that is why aliphatic HCs are hardly degraded in crude oil under hypersaline circumstances [11][8]. Salinity not only influences the diversity and growth of microorganisms, but also has a direct effect on biodegradation, and enzymes engaged in HCs degradation undergo some changes and lose their functioning. This inhibition is reversible when the microorganisms go back to normal conditions (moderate salinity level). Knowledge about molecular mechanisms and pathways of HCs degradation at high salinity is rare and only recently there have been a few reports explaining genes, enzymes, and breakdown steps for some HCs. These investigations have clearly shown that degradation of oxygenated and non-HCs by halophilic and halotolerant bacteria occurs by pathways similar to those found in non-halophiles [12][51]. In seasons with high temperatures and evaporation, salinity tends to increase and HCs degradation rate is remarkably reduced in deep-sea water [13][52]. During recent years many investigations have been performed on PAHs bioremediation and resources (Table 1). Several bacterial enzymes with various catabolic productivity allied with PAHs degradation have been identified and various biochemical pathways for PAH degradation (Such as naphthalene, phenanthrene, anthracene, and acenaphthene) have been introduced. Furthermore, some PAH catabolic operons have been sequenced, and their regulatory mechanism for PAH degradation has been known. In the environment, microorganisms are able to degrade different types of PAHs including quinoline, benzothiophene, and benzofuran through biochemical pathways. Nonetheless, a more detailed study is required to determine what is going on in a PAH-contaminated environment. Besides, many aspects of PAHs bioremediation have remained unknown or insufficient, which demands prospective attention. There is little knowledge on the transmembrane trafficking of PAHs, genes, enzymes, and molecular mechanisms of PAHs degradation in anaerobic conditions or high salinity and acidic environments. During the last decade, many studies have focused on Fusarium species ability in metabolizing the hydrocarbon chrysene to help to identify fungal strains displaying crude oil degradation potential under saline conditions [14][15][53,54].

2. Bioremediation and Affecting Factors

The first modern bioremediation use refers to six decades ago when George Robinson recruited the microbes to consume oil spills on the coast of Santa Barbara, California [25][64]. However, this technology was not important for the removal of HCs and other hazardous compounds like potentially toxic metals until the early 1980s [25][64]. Generally, bioremediation is a process associated with microorganisms and their metabolites to remove the different contaminants from aquatic ecosystems and sediment. Particularly, indigenous microorganisms in sediment are the main players in bioremediation because they can transform organic compounds into simple inorganic compounds or into their constituent elements through a process called mineralization [26][65]. Microorganisms in the bioremediation process have the potential to eliminate, decrease and transform oil contaminants into natural compounds found in air, sediments, water, sludge, and soil. Often, bioremediation co-occurs with detoxification, when microorganisms remove or immobilize waste materials by altering mineralization, and transformation [27][66]. For microbial cell reproduction and viability, the presence of energy is necessary, which is obtained in the bioremediation process through redox reactions like respiration. In this energy supplying system, the presence of nutrients and energy sources, including electron donor and acceptor (Such as carbon dioxide, oxygen, iron (III), and sulfate) is essential [28][67]. In HCs bioremediation, the availability of a microbial strain or consortia with suitable metabolic capabilities is the most challenging. Microbial communities adapt, change genetically and selectively enrich within hours of exposure to HCs. As a result, higher biodegradation rates are achieved than in communities with no introduction of HCs contamination [29][68]. In bioremediation of HCs polluted sites, isolation of appropriate numbers of special HCs degraders from an environment is a justification for effective bioremediation. On the other hand, usually, consortia of different strains are required in the bioremediation of oil spills because it is made of a mixture of compounds, and one strain can metabolize only a limited range of HC substrates. Bioremediation relies on nutrient presence and optimal site properties that support biological functions. For example, microbial growth is affected when exposed to a high concentration of the contaminants owing to the presence of high toxins. In contrast, low concentration can block the induction of bacterial enzymes [25][64]. Additionally, an optimum availability of water (between 14% and 27% moisture) and pH (in the range of 5.5–7.8) in the environment is vital for the proliferation and growth of microbial cells [30][69]. The biodegradation efficiency, to an extent, rises with increasing temperature and decreases with reducing temperature [30][69]. Nutrient availability (e.g., through organic substrate amendments) is also needed for cell growth, division, and electron donor as a biostimulant [25][64]. Finally, contaminant bioavailability is another factor impacting the bioremediation process. Bioavailability for microbial reactions is lower for contaminants that are more sorbed to solids attached in matrices of molecules in contaminated sites, more widely diffused in macropores of soil and sediments, or are present in non-aqueous phase liquid (NAPL) form [25][64]. In the next sections, we discuss the role of environmental factors affecting the bioremediation process will be discussed.

3. Biologically Based Solutions for Ashore and Marine Pollution

In the following sub-section,  researcherswe review three common bioremediation technologies that are practical for eliminating oil spills in marine environments by microorganisms. In addition, factors and strategies for increasing the efficiency of technologies will be discussed.  Figure 1 depicts what agents are responsible for three techniques of biosurfactant, biostimulation, and bioaugmentation.
Figure 1.
 The most prevailing bioremediation techniques are used for HCs degradation.

3.1. Bioaugmentation

Generally, adding oil-degrading bacteria to the existing microbial community is called bioaugmentation [31][70]. Bioremediation activities intend to boost the degradation efficiency that is performed by adding exogenic microorganisms. Bioaugmentation is considered a “polishing-up” or “accomplishing” process to deal with the very slow initial degradation of a fresh oil spill due to the very high concentrations of the originally spilled oil and its concomitant high abundance of toxic compounds. Usually, non-native microorganisms are looking for a suitable amount of biosurfactant when they are exposed to perilous oil spills to avoid detrimental impacts due to the toxicity of the spill. The HCs non-indigenous and indigenous degrading bacteria employ intracellular enzymes that permit bacteria to transform the HCs into another food source. Usually, on a HCs-containing culture medium or at the site of a spill in bioreactors, oil-degrading microbes are concentrated, microbial agents. These agents aim to prepare the influenced region with a significant oil-degrading microbial inoculum [32][71]. Therefore, bioaugmentation helps increasing the number of HCs degraders to a point that the spilled oil is used as the principal energy source. The most prevalent used options for bioaugmentation are the introduction of genetically engineered bacteria and the addition of biodegradation relevant genes packaged in a vector to be transferred into indigenous microorganisms by conjugation, as well as the addition of a pre-adapted consortium and a pre-adapted pure bacterial strain [33][72]. Screening followed by tailoring a competent microbial community for a particular site is a prerequisite for bioaugmentation. The first screening or selection step should pay attention to the metabolic capacities of the microorganism and vital characteristics that keep the cells active and alive under undesired environmental conditions. Prior knowledge about the microbial communities inhabiting the target site is an excellent strategy to select effective communities. Sometimes in co-contaminated sites, where both organic and metal contaminations are found, the best strategy is to take advantage of multi-component systems, i.e., a creating led microbial consortium is more beneficial than single-component systems [34][73]. Additionally, using a microbial consortium is more practical compared with a pure culture because it provides the metabolic diversity and reliability needed for field applications. Table 2 indicates relevant microbial consortia in the bioaugmentation. Some researchers using selected native strains reported full degradation of diesel oil and phenanthrene; an overall decrease of about 75% of the total HCs, and a decrease of 60% of isoprenoids in 40 days [35][36][74,75]. In 2009, Li et al. [37][76] confirmed that using indigenous microbial consortia (three bacteria including Bacillus sp., Zoogloea sp., and Flavobacterium with five fungal strains including Aspergillus nigerPhanerochaeteCuuninghamella sp, Chrysosporium, Alternaria alternate, and Keissler, Penicillium chrysogenum) enhanced the degradation of PAHs in water by 41.5%. The biomass to be employed as inoculum for bioaugmentation is produced in bioreactors, and transferring of cultures to the site is often challenging. After being exposed to environmental stresses, in contrast to the optimum conditions of culturing, the introduced population starts reducing quickly. Fluctuations and shifts in some environmental factors like temperature, pH, moisture, as well as toxic pollutant levels, and depletion of nutrients influence microbial growth. Goldstein et al. argued that in natural systems, unlike their potential in cultures, inoculant usually cannot degrade organic pollutants [38][77]. Problems regarding the adaptation of the inoculated microorganisms, the rivalry between introduced and indigenous biomass, insufficiency of the substrate, and the use of other organic substrates are the most important reasons for the failure of degradation in natural systems [32][71].

3.2. Biostimulation

In many situations, environmental criteria can be altered to boost the process of biodegradation. In marine crude oil spills, it is challenging to extend the life span of populations of HCs-eating microbes, owing to the problematic use of nutrients, and several native species can be killed or weakened because of oil toxicity in the spill region [49][88]. This toxicity is an inhibitory factor for stimulating the remaining indigenous bacteria and fungi. In this situation, biostimulation—helping optimize the environmental factors—is an appropriate strategy for degrading the HCs when the indigenous microbes are retained, and toxicity concentration is decreased [49][88]. Biostimulation may be more beneficial than bioaugmentation, as it stimulates indigenous bacteria that were already more competitive. It has been reported that if microorganisms growth is stimulated in the spill area, the HCs degrading efficiency may reach 70% during 30 days of incubation [50][89].
Nutrients are vital components of an effective biostimulation of HCs, as some nutrients may become an inhibiting factor, negatively affecting the biodegradation process [49][88]. The most prevalent additives that promote bacterial growth in a community are phosphate salts and nitrate [51][90]. The main aim is to boost the metabolism of autochthonous HCs degraders through in situ addition of limiting factors, which results in a quicker rate of the HCs degradation. The application of biostimulation in HCs bioremediation has been widely reported [52][34]; however, this approach also has its limitations and challenges [53][91]. For example, in soils, the use of inorganic fertilizer is challenged by the large cost of bioremediation and the likely chance of eutrophication [54][92].

3.3. Biosurfactants

Biological active surface molecules produced by microorganisms with a huge range of applications owing to their specific characteristics, minute toxicity, and biological admissibility are called biosurfactants [55][93]. These products as additives aim to produce petrochemicals and organic chemicals that are more accessible. Biosurfactants are amphiphilic compounds and able to alter the cell surface of microorganisms and increase the hydrophobic substance surface area. Microorganisms thanks to their ability of using hydrocarbon waste as raw materials can produce biosurfactants. One of the unique properties of biosurfactants is tolerance to environmental extreme conditions like ionic strength, acidity, temperature, salt concentration, demulsifying-emulsifying ability, and anti-inflammatory potential due to surface and interface activity [56][94]. Recent investigations have reported that lichenysin biosurfactant produced by Bacillus licheniformis was hardly impacted by Ca, NaCl concentrations, or temperature (up to 50 °C) and pH (4.5–9.0) [57][95]. Additionally, lipopeptides produced by Bacillus subtilis are stable at −15 °C, and beyond autoclavable temperature (121 °C) and concentrations, greater than 15% of NaCl when stored for six months [57][95]. An ideal biosurfactant decreases the surface tension of water. For instance, biosurfactants like surfactin, rhamnolipid, and sophorolipids produced, respectively, by B. SubtilisP. aeruginosa, and Candida bombicola lower the surface tension [58][96]. Biosurfactants are productive and efficient, and their critical micelle concentration (CMC) is ten to forty times lower than that of chemical surfactants. Hence, less biosurfactant is required to decrease the surface tension [59][97]. Biosurfactants also have antioxidant, antimicrobial, and anti-inflammatory activities. For instance, recent research suggested that the polyanionic surfactant named emulsan produced by Acinetobacter calcoaceticus has indicated lethal concentration 50 (LC50) against other microbes like Photobacterium phosphoreum, which is much less than Pseudomonas rhamnolipids [60][98]. Biodegradability and environmental toxic friendly nature are two other properties of biosurfactants, as most biosurfactants are easily degradable.
Various microorganisms produce biosurfactants involved in the bioremediation of HCs. Table 3 shows economic and prevalent biosurfactants produced by different microorganisms. Rhamnolipid in two forms of mono and di-rhamnolipid is a type of biosurfactant produced by P. aeruginosa [61][99]. A correlation exists between the type of surfactant and the type of HCs that are degraded. For example, rhamnolipids produced by P. aeruginosa specifically degrade hexadecane. Many studies were done on phenanthrene degradation by chemical surfactants, and findings have proven that increased phenanthrene degradation is along with bacterial isolates producing a non-ionic surfactant [62][100]. Based on a study, HCs degradation capacity was multiplied when it was mixed with a biosurfactant, like a combination of chemical surfactant ‘FinasolOSR-5′ with biosurfactant trehalose-5, 5′-dicorynomycolates [62][100]. It has been reported that PAHs are significantly degraded by bacteria producing sophorose lipids and glycolipids in less than a month because surface-active glycolipids increase the biodegradation of 2,4-dichlorophenolindophenol (DCPIP) when supplemented with HCs sites [63][101].

3.4. Cell Immobilization Techniques for Increasing Bioremediation Efficiency

Several techniques are available for immobilization of the microbial cells to increase the bioremediation efficiency by microorganisms. A carrier allows supplying moisture and aeration, better access to nutrients, and physical support for biomass, which increases the survival of the microbes [72][110]. To increase the viability and efficiency of the microbial cells, entrapment and encapsulation are two main techniques that accelerate the biodegradation process compared to uncoated cells.
Entrapment is an irremeable immobilization strategy for capturing cells inside fibers, and has been extensively studied. The systems provide enough protection by creating barriers around the immobilized microbial cells, therefore ensuring sustainable viability of the cell when the microorganisms are surrounded by the polymer [73][111]. Synthetic polymers like photo-cross-linkable resins and polyester as well as natural polymers like gelatin, collagen, and alginates are the most significant accessible matrices for entrapment. This process is designed with microbial cells within a solid network to allow the penetration of the substrate when inhibiting the cells from scattering into the medium. Owing to moderate required conditions and easy application of alginate gel polymer, many studies have reported practical use of this polymer for entrapment [73][111]. High cost, leakage of the cells, low loading capacity for the conjugation of biocatalysts into the matrix, limitations in disseminations, and attrition of biocarriers caused by high mechanical power are the most significant demerits of this method [74][112]. Nonetheless, this method is the most prevalent technique.
Encapsulation can reduce the concentration of toxic substances, control the availability of the nutrients, decrease the cell membrane damage, and protects the microbial cells from predation and competition [74][112]. Gellan gum, polyurethane, alginate, polyvinyl alcohol gel, kappa-carrageenan, gelatin, agar, agarose, and acrylate copolymers have been the studied components for immobilization and encapsulation of the HCs-degrader bacteria [32][71]. A study conducted by Muslemy et al. [75][113] worked on one bacterial consortium encapsulation with gellan gum microbeads and showed that encapsulated cells revealed a shorter lag phase. Consequently, a higher HCs degradation rate was observed in comparison with normal form (Free cell) at equal microbial concentrations. Liu et al. (2009) investigated the ability of Sphingomonas sp. FG03 and Acinetobacter sp. XA05 strains for biodegradation of phenol in both free and encapsulated settings in marine ecosystems [76][114]. Findings showed that a mixture of two bacterial strains had better efficiency in phenol biodegradation than pure cultures, and had enhanced functions for the high concentration of phenols [76][114]. In a study, Yaohui and Mang [77][115] worked on the differences between biostimulation and bioaugmentation treatments in the bioremediation of HCs and encapsulated the microbes with peanut hull powder as a carrier and bulking agent. They reported that mass transfer rate of nutrients, oxygen, water, HCs, and nutrition for the microflora was accelerated [77][115]. Wang et al. argued that immobilization of the Mucor sp. F2 (MF) fungal consortium, Mycobacterium sp. B2 (MB) fungal consortium, and MB+MF with pyrene, respectively, increased by 159.1%, 59.9%, and 60.0% after incubation [78][116]. Dehydrogenase activity has also a considerable improvement when biocarriers are used. Keryn et al. [79][117] investigated the effectiveness of economically sustainable biocarriers (mussel shells, coir peat complex) for marine HCs remediation and reported an accelerated degradation in the immobilized forms compared with free cells.
Researchers have investigated different ways of combining biostimulation and bioaugmentation technologies for bioremediation. Researchers have assessed several combinations of consortium or single bacteria and fungi with biostimulators such as fertilizers, corn-steep-liquor, solid-waste-dates, and other materials containing N, K, and P and obtained satisfying results. The degradation efficiency reached 97% and 91% for 0.5% w/v crude oil in 4 weeks, respectively by solid-waste-dates and corn-steep-liquor as biostimulants and using single strain Pseudomonas [80][118]. The degradation efficiency is affected by the type of total petroleum HCs pollutant to be degraded as light crude oil is more degradable than heavy crude oil, and this process is faster. In a study, Arabian light crude oil (1000 ppm) was degraded within three weeks by a single strain of Alcanivorax borkumensis SK2, and the presence of biostimulators like 0.1 g/L NaNO3, 0.077 g/L KH2PO4, and 0.2 g/L NH4Cl [81][119]. Additionally, 94.4% efficiency was obtained for 10% v/v crude oil (Escravos light) in 8 weeks by Aspergillus niger and Pseudomonas aeruginosa, and the presence of K, N, P [81][119]. Another study treated water polluted with crude oil by a combination of biostimulation and bioaugmentation technologies by A. niger and P. aeruginosa. The researchers created four different conditions including (nutrient-free), A (nutrient N, P, K), B (nutrient-plus aeration), and C (nutrient-free, aeration, and agitation), and achieved efficiencies of 92.3%, 93.6%, and 94.4%, respectively, after 56 days, for total petroleum HCs degradation [82][120].
Cross-linking is another technique employing hydrogen bonds (Covalent) between microbial cells and inorganic support by agents. Chemical modification of the surface of support materials is the main element of this technique. Compared to the previous technique, cross-linking is less practical because covalent binding often cuts functional integrities in the microbial cell. However, this method has very high efficiency for the cell when the functional integrities remain without interruption. Many successes regarding this technique refer to the immobilization of yeast cells. For example, in two studies in this area, researchers reported a successful application of cross-linking in the immobilization of Saccharomyces carlsbergensis on porous silica beads [83][121] and Saccharomyces amurcea and Saccharomyces cerevisiae on zirconia ceramics [84][122].