Johnson Matthey Technol. Rev., 2020, 64, (4), 452
油田蕴藏着多种具有不同代谢能力的微生物。为研究石油储层的微生物生态学，我们采用基于分子的方法来评估土耳其迪亚巴克尔油田的采出水细菌群落成分。执行聚合酶链反应（PCR）扩增的 16S rRNA 基因片段的变性梯度凝胶电泳（DGGE）以判断采出水样的细菌群落结构，并在分离的 DGGE 带测序后鉴定出主要的群落成员。通过采出水样的 DGGE 分析得到的大部分细菌序列属于未分类细菌（50%）。在已分类细菌中识别出了变形菌门（29.2%）、厚壁菌门（8.3%）、拟杆菌门（8.3%）和放线菌门（4.2%）群。在采水样中检测出的优势菌属是假单胞菌。本研究结果首次提供了关于迪亚巴克尔油田微生物群落及其主要成分的复杂性的见解。
Bacterial Community Composition in Produced Water of Diyarbakır Oil Fields in Turkey
Bacterial communities in produced waters of south-eastern Turkey reported in detail for the first time
- Tuğçe Tüccar*
- Department of Biology, Institute of Graduate Studies in Sciences, Istanbul University, 34134, Vezneciler, Istanbul, Turkey
- Esra Ilhan-Sungur
- Department of Biology, Faculty of Science, Istanbul University, 34134, Vezneciler, Istanbul, Turkey
- Gerard Muyzer
- Department of Biotechnology, Delft University of Technology, van der Maasweg 9, 2629 HZ Delft, The Netherlands
- Microbial Systems Ecology, Department of Freshwater and Marine Microbiology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, PO Box 94240, 1090 GE, Amsterdam, The Netherlands
Oil fields harbour a wide variety of microorganisms with different metabolic capabilities. To examine the microbial ecology of petroleum reservoirs, a molecular-based approach was used to assess the composition of bacterial communities in produced water of Diyarbakır oil fields in Turkey. Denaturing gradient gel electrophoresis (DGGE) of polymerase chain reaction (PCR)-amplified 16S rRNA gene fragments was performed to characterise the bacterial community structure of produced water samples and to identify predominant community members after sequencing of separated DGGE bands. The majority of bacterial sequences retrieved from DGGE analysis of produced water samples belonged to unclassified bacteria (50%). Among the classified bacteria, Proteobacteria (29.2%), Firmicutes (8.3%), Bacteroidetes (8.3%) and Actinobacteria (4.2%) groups were identified. Pseudomonas was the dominant genus detected in the produced water samples. The results of this research provide, for the first time, insight into the complexity of microbial communities in the Diyarbakır oil reservoirs and their dominant constituents.
Although much progress has been made in the use of renewable energy in recent years, fossil fuels (especially oil and gas) still meet most of the global energy demand, and they will continue to be the dominant source of energy worldwide over the next few decades (1).
Petroleum is a naturally occurring material found in various geological formations (reservoirs) worldwide. Crude oil, the liquid part of petroleum, is primarily composed of hydrocarbons (2). However, it may also include compounds of nitrogen, sulfur, oxygen and metals (3). Because crude oil in reservoirs is found as a mixture containing varying constituents and proportions, each crude oil has its own unique properties. The most important specified properties are density and sulfur content (4). The density of crude oil is reported in terms of American Petroleum Institute (API) gravity (specific gravity). Based on the API gravity, crude oils can be classified into light, medium, heavy and extra heavy oils (3). Depending on the amount of sulfur content (elemental sulfur or sulfur compounds such as hydrogen sulfide), the crude oil is categorised as ‘sweet’ or ‘sour’. In addition to chemical composition and physical properties, crude oil typically is also identified by underground reservoir (4). Reservoir characteristics (depth, temperature, pressure and other factors) vary significantly from one location to another, even in the same geologic formation (5, 6). The fact that microbial community composition and reservoir conditions vary dramatically not only between the different geographical areas, but also among different oil fields in the same region, makes each oil reservoir ecosystem unique.
Despite the extreme environmental conditions in the oil-bearing formations (i.e. anoxic, high temperature, high salinity), many microorganisms are capable of surviving in the oil and water phases of the oil wells (7, 8). Oil fields harbour mainly facultative aerobic and strictly anaerobic microorganisms due to the low redox potential in the reservoirs (8). These ecosystems contain different types of microbial communities (such as mesophiles, thermophiles and halophiles) which adapt to the reservoir conditions (9). Bacterial and archaeal groups identified in oil fields include sulfate-reducing bacteria (10), sulfur-oxidising bacteria (11), methanogens (12), fermentative microorganisms (13), acetogens (14), nitrate reducers (15), manganese and iron reducers (16) and hydrocarbon degraders (17). Among these microbes, sulfate-reducing bacteria have attracted much attention due to their detrimental effects such as reservoir souring and biocorrosion (7). In addition, different members of the oil microbial community are involved in syntrophic interactions. Fermenting bacteria and methanogenic archaea are involved in methanogenic hydrocarbon biodegradation through their close syntrophic associations (18). This microbial process is undesirable in oil reservoirs because it causes a decrease in oil quality and value (19). Syntrophic microorganisms in oil reservoirs also play important roles in the global biogeochemical cycling of sulfur, carbon and nitrogen. For instance, sulfate-reducing bacteria and sulfur-oxidising bacteria, the key drivers in sulfur transformations, are involved in the sulfur cycle (11). Thus, knowledge of the microbial groups and microbial dynamics in oil fields enable us to obtain detailed insights into the microbial ecology of oil associated environments.
Understanding the microbial ecology of oil reservoirs is crucial to the petroleum industry because the success of oilfield operations is strongly influenced by the activity of microorganisms. Oil microbes with different metabolic capabilities have significant negative and positive impacts on the petroleum resources and the extraction processes (7). Microbial activity may lead to severe problems such as reservoir souring and microbial corrosion. Reservoir souring, which is characterised by an increase in production of H2S in the reservoir fluids, most commonly occurs when sulfidogenic microorganisms reduce sulfate to sulfide, a toxic and corrosive product (20). Undesirable accumulation of sulfide minerals in reservoirs is one of the major challenging problems in oil production because it causes plugging of reservoirs, decreasing the oil quality and value and increasing the refining costs. Moreover, exposure to H2S can be dangerous in terms of worker health and safety due to its high toxicity. Additionally, the produced H2S promotes corrosion of the metallic equipment and structures used for oil production and processing (21). Another destructive phenomenon is biocorrosion, which is defined as microbial attack on the surface of the metal infrastructure leading to disruption of the material (22). In addition to sulfate-reducing bacteria, which play a major role in biocorrosion, other corrosive microbes, such as acetogenic bacteria and methanogenic archaea, are also associated with corrosion failures (23). Biocorrosion is a great concern because it leads to loss of material, large economic losses and safety issues in the oil industry (24). In contrast, hydrocarbon-degrading bacteria may be used for environmental clean-up processes (6). Bacterial degradation of hydrocarbons was carried out by both aerobic (for example, Rhodococcus sp., Sphingomonas sp., Pseudomonas putida, Pseudomonas stutzeri, Acinetobacter sp.) and anaerobic bacteria (such as Fe(III)-reducing bacteria, sulfate-reducing bacteria) (6, 17). Furthermore, microbial products such as biopolymers and biosurfactants can be used for facilitating oil movement in a widely used technology, known as microbial enhanced oil recovery (MEOR) (1). Compared with other conventional oil recovery techniques, MEOR has advantages such as low cost, wide application, high efficiency and low environmental pollution (25). Therefore, diversity, metabolic processes and habitat conditions of microbial communities in oil reservoirs should be investigated, so that their negative effects can be decreased and their positive effects can be exploited.
This study aimed to determine the bacterial community composition and to identify the predominant community members in produced water from oil fields located in the Diyarbakır region in Turkey. To this end, we used PCR-DGGE to analyse 20 produced water samples from the Diyarbakır region. There are limited studies on produced water from the Diyarbakır region and this paper represents the only in situ study available. The results of this study provide not only new data about the microbial ecology of the Diyarbakır oil fields, but also information on the bacterial populations which may have potential roles in terms of increasing or decreasing the efficiency of industrial applications.
2. Materials and Methods
2.1 Sampling Procedure
The sampling site, the Diyarbakır region, is located at the boundary of the Anatolian plate and the Middle Eastern oil region in south-eastern Turkey. A total of 20 crude oil samples (B1, B6, B8, B14, B23, B32, B56, GK8, GS6, GS15, M3, K2, K3, K32, K35, K44, S4, S15, Y18 and Y30) consisting of an oil/water mixture were collected from the production wells of Diyarbakır oil fields (Figure 1). These wells produced oils withdrawn from the oil sandstone deposits (depths from 1600 m to 2620 m, API gravity from 24.3° to 42.3°, water content around 94%, an average pH of 7.0 and salinity from 2966 mg l−1 to 26,961 mg l−1). The samples were aseptically taken at the wellhead and put into sterile 500 ml serum bottles sealed with rubber stoppers and aluminium caps. The samples were shipped at ambient temperature. Upon arrival at the laboratory, the samples were immediately analysed. All samples were treated within 48 h after collection. Decantation was used to separate produced water from the oil/water mixture.
2.2 DNA Extraction
Bacteria in the produced water samples were collected by filtration over 0.20 μm pore size polyamide filters (Sartolon®, Sartorius AG, Germany). Genomic DNA was extracted with the UltraClean® Microbial DNA isolation kit (MO BIO Laboratories Inc, USA) according to the manufacturer’s protocol.
2.3 Polymerase Chain Reaction Amplification
Extracted DNA was used as the template for PCR amplification of partial 16S rRNA fragments. Primer pair consisting of 341F with a GC clamp and 907R was used for DGGE analysis (26). A 40-base GC clamp was used to prevent complete denaturation of the fragment during DGGE (27).
Due to the low DNA yield, a two-step PCR strategy was used. At the first step, a real-time PCR (quantitative PCR, qPCR) approach was applied to the produced water samples. The reaction mixture in a final volume of 22.5 μl contained 0.2 μl of each primer, 12.5 μl iQTM SYBR® Green Supermix (Bio-Rad Laboratories Inc, USA), 9.6 μl RNase-Free Water (Qiagen, Germany) and 0.5 μl DNA template. qPCR was performed in iCycler iQTM Real-Time PCR Detection System (Bio-Rad Laboratories Inc, USA) using the following conditions: 5 min at 95°C; 40 cycles of 95°C for 30 s, 57°C for 40 s, 72°C for 40 s and 80°C for 25 s; and a final 72°C for 10 min. In the qPCR method, after each cycle, a signal was formed. By observing the signals for each sample, PCR products could be detected. The reaction was terminated when the desired amount of product was reached. At the second step, a conventional PCR approach was applied to the qPCR products. Reaction mixture in a final volume of 25 μl contained 0.2 μl of each primer, 12.5 μl Taq PCR Master Mix (Qiagen, Germany), 9.6 μl RNase-Free Water (Qiagen, Germany) and 0.5 μl DNA template. The PCR was performed in TGradient thermocycler (Biometra, Germany) using the following conditions: 5 min at 95°C; 12 cycles of 95°C for 30 s, 57°C for 40 s and 72°C for 40 s; and a final 74°C for 30 min.
2.4 Denaturing Gradient Gel Electrophoresis
The DCodeTM system (Bio-Rad Laboratories, USA) was used for DGGE analysis. 25 μl of each PCR product (200–300 ng) were loaded onto 6% polyacrylamide gels (w/v) containing gradients of 20% to 70% denaturants (urea/formamide). The gels were run for 16 h at 100 V and 60°C in 1× Tris-acetate-EDTA buffer. After completion of electrophoresis, the gels were stained with SYBR® Gold Nucleic Acid Gel Stain (InvitrogenTM, Thermo Fisher Scientific, USA) for 20 min, visualised and photographed. Selected predominant DGGE bands were excised, eluted in 40 μl of 1× Tris buffer (pH 8) for 2 d at 4°C and re-amplified with 25 cycles as described above. Reaction mixture in a final volume of 25 μl contained 0.125 μl of primer 341F, 0.125 μl of primer 907R, 12.5 μl of Taq PCR Master Mix, 9.75 μl of ultra-pure water and 0.5 μl of template. The PCR products were quantified on a 1.5% (w/v) agarose gel and then sequenced by Macrogen Inc (Seoul, South Korea).
2.5 Comparative Sequence Analysis
The resulting sequences were first aligned and edited using CodonCode Aligner software (CodonCode Corp, USA). Then they were compared to sequences stored in the database GenBank® using the National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST®) (28, 29). All obtained partial 16S rRNA gene sequences were deposited in GenBank® database under the following accession numbers: KF720792 - KF720796, KF720798, KF720801 - KF720802, KF720804, KF720806 - KF720808, KF720810 - KF720811, KF720814, KF720818, KF720820, KF720823, KF720825 - KF720826, KF720828, KF720830 - KF720832, KF720839, KF720844, KF720852, KF720855, KF720858, KF720872, KF720877, KF720882 - KF720884, KF720886 - KF720889, KF720891, KF720893 - KF720894, KF720896 and KF720903.
3.1 Molecular Analysis of Bacterial Communities
Bacterial DNA isolation could only be achieved for 16 (B1, B8, B6, B14, B23, B32, B56, GS6, GK8, K35, K44, M3, S4, S15, Y18, Y30) of the 20 produced water samples. Because the water phase could not be separated from the oil phase for the other four produced water samples, DNA could not be extracted from these samples. The extracted DNA was used as template DNA for the amplification of 16S rRNA gene fragment. Unfortunately, direct PCR with bacterial primers did not yield a product from any of the produced water samples. For this reason, a two-step PCR was applied: the first step was a qPCR to increase the concentration of genetic material to measurable amounts (30), while the second step was a normal PCR to obtain enough material for DGGE analysis. For produced water samples, a total of 113 DGGE gel bands were analysed, but only 69 bands yielded sequences of satisfactory quality (Figure 2).
Comparative sequence analysis of the DGGE bands indicated that 50% of the bacterial sequences belonged to ‘unclassified bacteria’. Among the classified bacteria, members of the phyla Proteobacteria, Bacteroidetes, Firmicutes and Actinobacteria, and the classes Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, Sphingobacteriia, Bacilli and Actinobacteria were identified (Figure 3).
Proteobacteria was the dominant phylum, comprising 29.2% of the total sequences retrieved from the produced water samples (Figure 3). The sequences B6_19 and B14_37 shared 100% and 99% identity with uncultured bacteria (EU044497 and JF421153, respectively) (Table I). The sequence B32_3 was distantly (94%) related to a moderately thermophilic bacterium Phenylobacterium lituiforme, a member of Alphaproteobacteria (31). Within Betaproteobacteria, the sequence represented by B32_55 was identified (98%) as Aquincola sp. THE-49 (JN128637), isolated from water reservoir (published only in GenBank®). The produced water contained different members of the class Gammaproteobacteria . DGGE bands B32_4, B14_35, S4_70, GS6_2 and GK8_79 were affiliated (100%, 94%, 99%, 93%, 99%, respectively) to Pseudomonas stutzeri (Table I), a non-fluorescent denitrifying bacterium (32). The sequence from band B1_20 showed a 100% similarity to Acinetobacter sp. VKPM 2838 (Table I). The genus Acinetobacter comprises important soil organisms where they contribute to the mineralisation of aromatic compounds and they are suited to exploitation for biotechnological purposes, such as biodegradation (33). B8_30 was related (96%) to Marinobacter sp. Trimyema-2, a thermophilic strain that was isolated from the hydrothermally heated sea floor at Vulcano Island, Italy (34). Members of the genus Marinobacter were also identified in the production water retrieved from a Dutch oil field (35). The sequence from B32_2 was distantly related (93%) to Thermithiobacillus sp. ParkerM (HM173631) that is moderately thermophilic and obligately chemolithoautotrophic on reduced inorganic sulfur compounds (36). Another member of the class Gammaproteobacteria was close to the sequence of uncultured hydrocarbon seep bacterium (91% similarity) (AF154088) (Table I).
8.3% of the sequences detected among the produced water samples fell into Bacteroidetes (Figure 3). The sequence of band B6_14 was affiliated to unclassified Chitinophagaceae. It shared 99% identity with Chitinophagaceae bacterium F1 (AB535716), isolated from compost (Table I). DGGE bands B6_16, S4_67 and B8_27 were identified (92% to 99% sequence identity) as uncultured Bacteroidetes bacteria (Table I). The sequences from S4_67 and B8_27 were related to uncultured bacteria that were taught as members of biocorroding microbiota colonising on steel surfaces immerged in coastal seawater (37).
Sequences belonging to members of Firmicutes accounted for 8.3% of the bacteria in the produced water (Figure 3). DGGE band B1_23 was distantly related (89%) to Aeribacillus pallidus strain MCM B-886 (JN701188), isolated from petroleum reservoir (published only in GenBank®) (Table I). In addition, different strains of Aeribacillus pallidus (with sequence similarity values from 98% to 99.6%) were isolated previously from various geothermal sites of Turkey (38). DGGE band B6_20 was distantly related (96%) to an uncultured Firmicutes bacterium, isolated from marine sediment in Charleston, South Carolina, USA (39). B56_17 and B1_24 were affiliated (97% and 98%, respectively) to an uncultured Firmicutes bacterium (Table I), detected in produced fluid from non-water-flooded high-temperature reservoir of the Niibori oilfield, Japan (40).
The phylum Actinobacteria comprised 4.2% of the bacterial community recovered from the produced water (Figure 3). DGGE band B6_26 displayed 100% sequence similarity to Coriobacteriaceae bacterium enrichment culture clone B3113 (HQ133029) isolated from crude oil contaminated soil of Shengli oil fields, China (41). The sequence B14_39 was closely related (100% similarity) to an aerobic bacterial strain Georgenia daeguensis 2C6-43, isolated from an activated sludge sample collected from an industrial wastewater treatment plant in Daegu, South Korea (42). Although little is known about the presence of G. daeguensis in oil associated environments, it was reported that different strains of G. daeguensis were isolated from hydrocarbon contaminated soil of an industrial zone and oil-saturated soil under laboratory conditions (43–45).
In order to increase our knowledge about microbial diversity, culture-dependent and molecular-based approaches are used for describing the diversity of microbes. Molecular-based approaches such as PCR-DGGE methodology, which is a useful tool for monitoring the genetic diversity of complex microbial populations (26), provide valuable information about the microbial community structure and dynamics in nature. For these reasons, PCR-DGGE fingerprinting analysis of environmental samples was used in this study.
The choice of appropriate primers for PCR amplification is a crucial step to accurately characterise the microbial communities. In this study, primer pair (341F-GC/907R), targeting the V3-V5 region of the 16S rRNA gene fragment, was selected due to its suitability for DGGE analysis of bacterial populations in environmental samples (26). This primer pair designed by Muyzer et al. (27, 28) has been used predominantly for microbial community analysis (26).
The DNA yield obtained from produced water samples was very low. It is known that crude oil samples contain low amounts of biomass which makes DNA isolation difficult to achieve (46). In this study, the permit included taking up to 500 ml of oil/water mixture from each sampling point so that only ca. 25 ml of each produced water sample could be obtained. In this scope, the low sample volumes of produced water separated from the oil/water mixture may be a reason for the low amount of DNA. It was reported in other studies that higher sample volumes (100–4000 ml) of produced water were used for DNA isolation (35, 47–50). The low DNA yield affected the efficiency of the PCR technique and for this reason, a two-step PCR was applied to the produced water samples. Thus, a sufficient amount of PCR product for DGGE for the produced water samples could be obtained.
Bacterial communities associated with the produced waters was analysed by the PCR-DGGE approach. Although numerous bands were visible on the DGGE gel, only dominant bands could be excised and sequenced. Most of the sequences retrieved from produced water samples were related to unclassified bacteria. Different studies on oil reservoir microbiota have also shown that oil fields harbour new and still unidentified microbial species. For example, Lenchi et al. described microbial communities in production and injection waters from the Algerian oil fields. In their study, they detected that a large number of unclassified bacterial and archaeal sequences were found in the water samples (51). Furthermore, uncultured bacteria such as uncultured Sphingomonas sp. and uncultured Caenispirillum sp. clone Ppss_Ma27 were detected in our study. This result is consistent with the fact that the vast majority of microorganisms are uncultured and do not grow under laboratory conditions as stated by Lewis et al. (52). In order to isolate more microbes, an appropriate identification laboratory protocol should be followed. At this point, different strategies such as mimicking natural conditions via decreased nutrient, extended incubation times, the modification of isolating media formulations and different incubation parameters (for example, temperature) were suggested for the cultivation of microorganisms (53). For instance, pollutant degrader Sphingomonas, which seemed to be previously uncultured by nutrient-rich methods, could be isolated from crude oil contaminated soil by using an in situ method that mimics the original environment (54). In addition, culture-dependent investigation should also be supported by molecular techniques.
Based on the sequences, organisms related to known mesophilic bacteria were predominant in the produced water samples. In addition, some organisms related to thermophilic bacteria (Aeribacillus pallidus, Marinobacter sp. Trimyema-2, Phenylobacterium lituiforme and Thermithiobacillus sp.) were also identified. Bacteria having different metabolic capabilities (denitrifying, biodegrading and sulfur removing bacteria) were also detected. In addition, bacteria which may cause biocorrosion on steel surfaces were detected.
The dominant bacterial phylum was the Proteobacteria. The members of this phylum were also frequently found in many other studies on microbial diversity of oil field produced waters (55–58). Moreover, it was stated that Proteobacteria are ubiquitous in oil reservoirs over all temperature ranges (59).
In this study, among the detected genera in produced water samples that potentially contain hydrocarbon degrading bacteria were Aeribacillus, Acinetobacter, Sphingomonas, Marinobacter and Phenylobacterium. It has been known for years that the species belonging to these genera are capable of degrading hydrocarbons (6, 17, 60, 61). In addition, G. daeguensis, a hydrocarbonoclastic bacterium, was detected in produced water sample with a 100% sequence similarity. G. daeguensis has also been demonstrated as a potential microbe for bioremediation due to its hydrocarbon degradation ability (44). Further investigations are needed because our current knowledge of the metabolic capability of G. daeguensis is limited. Moreover, sulfur-oxidising Thermithiobacillus sp. was also identified in produced water sample. Sulfur-oxidising bacteria, which oxidise the sulfur compounds produced by the activity of sulfate-reducing bacteria in oil reservoirs, may play a key role in the oil industry because they can be utilised to resolve processing problems such as reservoir souring (11).
Pseudomonas was the dominant genus detected among the produced water samples. Pseudomonas stutzeri was the species identified in five produced water samples. P. stutzeri was previously isolated not only from formation water, produced from the petroleum wells in Adıyaman (62), but also oil-contaminated soils in Batman petroleum refinery, Turkey (63). These two areas are close to the Diyarbakır region from where the samples in this study were collected and these findings show that P. stutzeri is distributed widely in south-eastern Turkey. In other different geographical areas, this species was also isolated from oil-associated environments, such as oil field production water (64), oil sludge (65) and oil contaminated soil (66). However, although P. stutzeri is often isolated from oil reservoirs, the origin of P. stutzeri in oil reservoirs is a debatable issue. Because oil reservoirs have low redox potentials and contain little oxygen, anaerobic microorganisms are considered as truly indigenous to oil reservoirs (67). In this regard, it is believed that P. stutzeri, most of whose strains are aerobes, is an exogenous organism inoculated into oil reservoirs during the oil production processes. Even if strains of P. stutzeri are introduced into oil reservoirs with injected fluids, they should adapt to the physicochemical characteristics of the reservoir to survive. At this point, it has been proposed that extreme reservoir conditions may act as special factors for the evolution of P. stutzeri, thereby forming mutant strains (68). Furthermore, P. stutzeri, being found in a wide variety of habitats, is known for its diverse metabolism. Some strains of P. stutzeri are capable of denitrification, degradation of aromatic compounds and nitrogen fixation (32). These metabolic features make P. stutzeri highly attractive for biotechnological processes, such as reservoir souring control (69), microbial enhanced oil recovery (64) and bioremediation of oil-polluted environments (65).
In undisturbed oil reservoirs, microorganisms are found in different phases such as reservoir fluid containing crude oil and formation water, and rock surfaces. While planktonic microbes thrive in the water phase, sessile microbes may attach to oil or rock surfaces (59). In addition, biofilm may form on the metal surfaces of the pipes in the oil-producing wells (70). Oil microbiome studies focus mainly on the analysis of the water phase due to its easy sampling. However, it should be noted that the water phase itself contains only a minor portion of the microbes found in the oil reservoir (59). On the other hand, the sampling of sessile microbes is likely to be more challenging (70).
This study reported for the first time the bacterial community composition of produced water from Diyarbakır oil reservoirs as obtained by DGGE analysis of PCR-amplified 16S rRNA gene fragments. DGGE analysis of produced water samples demonstrated that the majority of the bacterial sequences belonged to unclassified bacteria, indicating that oil reservoirs harbour still undescribed microbial species. Among the classified bacteria, the members of Proteobacteria were more abundant. Pseudomonas was the dominant genus detected in the produced water. Although the members of Pseudomonas were known as exogenous organisms inoculated into oil reservoirs, Pseudomonas stutzeri was found in five produced water samples. Bacteria having different metabolic capabilities (denitrifying, biodegrading and sulfur removing bacteria) were also detected. It can be stated that the metabolic capacities of these bacteria make them potential candidates for utilising in biodegradation, bioremediation, the improvement of oil quality and oil recovery processes. The knowledge of the bacterial community composition in oil reservoirs of the Diyarbakır region obtained in this study will be of great interest for both scientific research and applications in the oil industry. To build on the data presented in this study, metagenomic analyses should be performed to explore the undescribed microbes.
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This work was supported by ‘Research Fund of Istanbul University’ (Project number: 28699). Tuğçe Tüccar was awarded an Erasmus LLP Scholarship. Esra Ilhan-Sungur was awarded a Post-doctoral Research Scholarship by the Scientific and Technological Research Council of Turkey (TUBITAK-BIDEB). We thank the Turkish Petroleum Corporation for permission to collect samples, and Ender Taptık and Hasan Kaya for their assistance with the sample collection. We thank Ben Abbas for his technical assistance. We acknowledge Hakan Hosgormez for his helpful comments and suggestions.
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Tuğçe Tüccar is a PhD candidate in Fundamental and Industrial Microbiology at Istanbul University, Turkey. She received her Bachelor’s degree in Biology from Middle East Technical University, Turkey, in 2009. She obtained her Master’s degree in Fundamental and Industrial Microbiology from Istanbul University, Turkey, in 2011. Her dissertation was on investigation of sulfate-reducing bacteria in petroleum samples. She was awarded an Erasmus LLP Scholarship and conducted her research work at Delft University of Technology, The Netherlands. Areas of interest are microbial ecology, microbial genetics, petroleum microbiology and microbial corrosion.
Esra Ilhan-Sungur is professor in the Biology Department at Istanbul University, Turkey, since 2018. A key focus of her research is microbiologically induced corrosion and its prevention. Further research interests lie in the area of anaerobic bacteria (especially sulfate-reducing bacteria), petroleum microbiology, microbial diversity and ecology, microbial genetics and biofilm. She was awarded a postdoctoral research scholarship by the Scientific and Technological Research Council of Turkey (TUBITAK-BIDEB) and worked as a guest researcher at Delft University of Technology.
Gerard Muyzer is Professor in Microbial Systems Ecology at the University of Amsterdam, The Netherlands. He is studying the structure, function and dynamics of microbial communities, their role in biogeochemical cycles and their application in biotechnological processes. For this he is using a systems biology approach in which he combines experimental work, the use of state-of-the-art omics techniques, and mathematical modelling. He is mainly focusing on the microbial sulfur cycle, and in particular on sulfur bacteria that are present in natural ecosystems (such as soda lakes, stratified lakes, rhizosphere of seagrasses) as well as man-made ecosystems, such as full-scale bioreactors removing toxic sulfur compounds from wastewater.