PCR-based DGGE and FISH analysis of methanogens in an anaerobic closed digester tank for treating palm oil mill effluent
Mohd Rafein Zakaria
Raha Abdul Rahim
André-Denis G. Wright
Financial support: FELDA (Federal Land Development Authority), MOSTI (Ministry of Science, Technology and Innovation, Malaysia) and JSPS (Japan Society for the Promotion of Science).
Keywords: anaerobic digestion, DGGE, FISH, methanogens, POME.
16S ribosomal RNA (rRNA)-targeted fluorescent in situ hybridization combined with polymerase chain reaction (PCR)-cloning, light microscopy using Gram stains, scanning electron microscopy and denatured gradient gel electrophoresis were used to reveal the distribution of methanogens within an anaerobic closed digester tank fed with palm oil mill effluent. For specific detection of methanogens, 16S rRNA-cloning analysis was conducted followed by restriction fragment length polymorphism (RFLP) for presumptive identification of methanogens. To cover the drawbacks of the PCR-cloning study, the organization of the microorganisms was visualized in the activated sludge sample by using fluorescent oligonucleotide probes specific to several different methanogens, and a probe for bacteria. In situ hybridization with methanogens and bacterial probes and denatured gradient gel electrophoresis within activated sludge clearly confirmed the presence of Methanosaeta sp. and Methanosarcina sp. cells. Methanosaeta concilii was found to be the dominant species in the bioreactor. These results revealed the presence of possibly new strain of Methanosaeta in the bioreactor for treating palm oil mill effluent called Methanosaeta concilii SamaliEB (Gene bank accession number: EU580025). In addition, fluorescent hybridization pictured the close association between the methanogens and bacteria and that the number of methanogens was greater than the number of bacteria.
Ardern and Lockett developed the first activated sludge system for purification of wastewater in Manchester (Moter and Göbel, 2000). However, the role of microbial consortia in this process is still not completely understood. Culture-based techniques were found to be too selective to give a comprehensive and authentic picture of the entire microbial community as it has been estimated that the majority (over 99%) of bacteria in nature cannot be cultivated by using traditional techniques (Rondon et al. 2000). As a consequence, it is very unlikely that collections of bacterial isolates are representative of in situ diversity and community structure.
Therefore, ribosomal RNA (rRNA)-based population methods have been a very useful tool to analyze such environments like bioreactors and wastewater treatment plants. Sequences that were retrieved from molecular analysis using polymerase chain reaction (PCR)-based techniques were used to create fluorescently labelled oligonucleotide probes for fluorescence in situ hybridization (FISH) investigation of microorganisms, e.g. in activated sludge (Amann et al. 1996; Schuppler et al. 1998). As this technique allows simultaneous visualization, identification, enumeration and localization of individual microbial cells, FISH is considered useful for many applications in all fields of microbiology. Members of the domain Archaea, particularly methanogens and their association with bacteria have been found by FISH in anaerobic digesters and within anaerobic sludge samples.
Denaturing gradient gel electrophoresis (DGGE) of 16s rRNA have been used for the characterization of bacterial communities in activated sludge (Watanabe et al. 1998; Watanabe et al. 1999). The rRNA clone library and DGGE method can provide direct sequence information useful for the assessment of phylogenetic groups of methanogens present. However, the reliability and reproducibility of these methods are affected by technical factors like efficiency of DNA extraction, PCR biases, and selection of clones. Also, the relative abundance of different 16s rRNA clones amplified from a mixed population depends upon genome size and the rRNA gene copy number of bacteria present, and thus are not necessarily reflective of the relative population of different taxa (Fogel et al. 1999). The combined use of FISH, DGGE and 16S rDNA-cloning methods allowed analyzing of bacterial communities more precisely. Besides, the localization of microorganisms by FISH can prove the symbiotic relationship between specific microorganisms.
Palm oil mill effluent (POME) is one of the world most polluting wastewater in Malaysia and the world. So the anaerobic treatment of POME using anaerobic digesters is of great importance both for methane gas production and clean development mechanism (CDM). Hence, an understanding of the microbial ecology of the bioreactor systems is necessary to monitor the microbial activities. A few reports have shown promising applications of bioreactors and process designs for the treatment of POME (Najafpour et al. 2005; Yacob et al. 2006). However, to our knowledge, no studies have been reported on the microbial ecology of the POME digesters especially of methanogenic archaea in Malaysia. In the breakdown process of organic residues, approximately 70% of intermediate by-products are converted to acetate which is the main precursor in methane production. Until now, the only acetate-utilizing methanogens identified in anaerobic digestors belongs to the genera Methanosarcina and Methanosaeta (Mladenovska and Ahring, 2000). Filamentous and aggregating types of Methanosaeta spp. have been commonly observed other than Methanosarcina spp. in mesophilic granules (Sekiguchi et al. 2001). It is critical to have an accurate understanding of the microbial population of the bioreactor to provide the optimum growth conditions for the dominant species which could be consequently followed by the highest possible methane production.
The aim of the present work was to determine the methanogen community structure in the anaerobic bioreactor treating POME using 16S rRNA clone library, DGGE analysis, FISH, scanning electron microscopy (SEM) and light microscopy.
Activated sludge was collected from a 500 m3 closed digester tank (CDT) for the anaerobic treatment of POME, located in Serting Hillir Palm Oil Mill, Negeri Sembilan, Malaysia. The CDT was operated under mesophilic condition (32 - 39ºC) for 120 days. The system was equipped with a closed digester tank, settling tank, pumps, and flow meters for biogas and the effluent. There were three sampling ports at the top, in the middle and at the bottom of the CDT. The sludge sample was obtained from middle sampling port. The process parameters recorded at the time of sampling are shown in Table 1.
The chemical oxygen demand (COD), volatile fatty acids (VFA), pH, alkalinity analyses were carried based on standard method (APHA, 2005). Acetate concentration was measured by high performance liquid chromatography (SPD-10A, UV-VIS Detector; LC-10 AS Liquid Chromatography Shimadzu). The temperature, biogas mass-flow and raw POME mass-flow were recorded using an integrated on-line data recording system (Endress-Hauser Ecograph system, Germany). The methane concentration in biogas was detected on-site using a methane gas analyzer (XP314A, Shin-Cosmos Electrics Co. Ltd., Japan). Influent COD ranged between 30,000 mg/L to 90,000 mg/L across this study and it was recorded 41,300 mg/L at the time of sampling on the day 80th of the operation at the steady-state condition (Table 1). The VFA concentration at the sampling time was 517 mg/L with the acetate concentration of 275 mg/L. The activated sludge samples were transported to the laboratory in sterile 50 ml falcon tubes placed in crushed ice and stored at -20ºC until use.
DNA was extracted from activated sludge following the method of Bourrain et al.(1999) and 16S rDNA was amplified using the Wright and Pimm (2003) methanogenic specific primers Met86F (5’-GCTCAGTAACACGTGG-3’) and Met1340R (5’-CGGTGTGTGCAAG GAG-3’). PCR reactions (25 µL) were set up in 0.2 mL thin-walled Eppendorf® tubes, containing 100 ng sludge DNA, 10 X Taq DNA polymerase buffer, 0.5 µL of 10 mM dNTP mix (Fermentas, Maryland, USA), 0.5 µl of 10 mM dNTPs, 2.5 µl of 25 mM MgCl2, 0.5 µl of each methanogen primer and 0.2 µl of 5 U AmpliTaq DNA polymerase (Fermentas, Maryland, USA). DNA templates from three sludge samples obtained from the bottom and middle of the bioreactor, and from the recycling tank were amplified separately for cloning. Samples were amplified using a Perkin Elmer Gene Amp system 9600. Each PCR cycle consisted of 94ºC for 40 sec, 54ºC for 50 sec, 72ºC for 90 sec. On the 35th cycle, the elongation step was increased to 10 min at 72ºC.
PCR products were purified from a 1% agarose gel using a gel extraction kit according to the manufacturer’s instructions (Qiagen, Germany). The recovered PCR fragment was cloned into pTZ57R vector (Fermentas, Maryland, USA), and transformed into Escherichia coli TOP10 competent cells (Invitrogen, Carlsbad, CA). White colonies were randomly selected from plates and recombinant plasmids identified by size selection on a 1% agarose gel prior to restriction fragment length polymorphism (RFLP) analysis.
Cloned PCR products were digested separately with HaeIII (Fermentas, Maryland, USA) in 20 µl reaction volumes containing 10 µl of PCR product, 2 µl x 10 reaction buffer and 10 units of restriction endonuclease in sterile ultrapure water. Digested PCR products were incubated for 1 hr at 37ºC and digested fragments were separated using a 10% polyacrylamide gel (w/v). The resulting bands were visualized by silver-staining and each clone was assigned to an RFLP group based upon the banding patterns. Two groups (group I and group II) were assigned.
For each RFLP type, the 16S rRNA insert of a few representative clones were sequenced. The recombinant plasmids were extracted using the Qiagen plasmid DNA extraction kit (Qiagen, Germany) according to the manufacturer's instructions. Approximately 27 nucleotides were sequenced using an ABI 3730 XL DNA Sequencer. Chromatograms were edited using Chromas software (Technelysium, Australia), while CHECK_CHIMERA software (Maidak et al. 1997) was used to scan for potential chimeric sequences. The sequences were compared to known 16S rRNA sequences in the GenBank™ database, using the basic logical alignment search tool (BLAST) to locate nearly exact matches in the GenBank database. DNA sequences were aligned using the program CLUSTAL W (Thompson et al. 1994) and further edited manually. Phylogenetic analyses were performed using the neighbor-joining (NJ) method using the MEGA ver. 3.1 (Kumar et al. 2004).
For each RFLP group, one representative clone was selected for further study. DGGE-PCR reactions were performed on sludge DNA, as well as on the extracted plasmids from representative clones. The aim was to obtain the DGGE profiles for the archaeal and methanogenic species in the POME anaerobic bioreactor. Therefore, universal DGGE methanonenic and archaeal primers were used in the amplification reactions. The universal archaeal primers PARCH340f and PARCH519r based on the E. coli 16S rRNA gene sequence and methanogenic primers 0357F and 0691R were used to amplify 179 bp and 334 bp fragments (Watanabe et al. 2004), respectively. The GC clamp, 5’-CGC CCG GGG CGC GCC CCG GGC GGG GCG GGG GCA CGG GGG-3’ as described by Chan et al. (2001), was included on the 5 end of the forward primer PARCH340f and 0357F to enable the separation of the fragments using DGGE. PCR reactions for both primer sets were performed in 50 µl reaction volumes containing 0.5 µl of Taq DNA polymerase (5 U/µl) (Fermentas, Maryland, USA), 5 µl of 10 x PCR reaction buffer, 0.5 µl of each of the primers (10 mM), 5 µl dNTPs (10 mM), 4 µl of Mgcl2 (Fermentas, Maryland, USA) and 1 µl of the extracted DNA or plasmid. The PCR amplification conditions for the primer sets were as follows: initial denaturation was performed at 94ºC for 3 min; followed by denaturation at 94ºC for 1 min; annealing at 60ºC for archaeal primers and 58ºC for methanogenic primers for 1 min; and chain elongation at 72ºC for 2 min. On the 35th cycles, the final elongation step was performed at 72ºC for 8 min. The amplified products were checked on 1% agarose gels and visualized under UV light.
DGGE (DCode System; BioRad, Hercules, CA, USA) was used to separate the 179 bp and 334 bp PCR products. The initial parameters for the denaturing gradient were optimized empirically. The optimized gradient extended from 40% to 60% and 50% to 60% of denaturant consisting of 7 M urea and 40% formamide for methanogens and archaeal PCR products, respectively. This was established in 8% acrylamide gels. Electrophoresis was performed at 100 V for 14 hrs at a constant temperature of 60ºC. The DNA was stained with cyber green and visualized under UV light.
All DGGE bands from the methanogenic profile were punched out with a sterile pasture pipette and used as a template in a re-amplification using the methanogens` primers 0357F and 0691R (Watanabe et al. 2004). The resultant PCR products were purified using the Mag Extractor-PCR and Gel Clean up-kit. (Toyobo, Japan) according to the manufacturer’s instructions and sequenced using an ABI 3730 XL DNA Sequencer at the DNA Sequencing Facility at Kyushu Institute of Technology, Japan. The sequences obtained were compared to 16S rRNA gene sequences in the National Center for Biotechnology Information (NCBI) database using the BLAST.
To directly analyze methanogens populations in an anaerobic digester sludge sample, the probe MSMX860, complementary to the 16S rRNA of some methanogens including Methanosarcina spp., Methanococcoides spp., Methanolobus spp., Methanohalophilus spp. and Methanosaeta spp. was used (Crocetti et al. 2006). To target the sludge bacteria, the 16S rRNA probe EUB338 for the domain bacteria was used (Amann et al. 1990). Oligonucleotides and their fluorescent derivatives (5 -labelled with either FITC or rhodamine) were purchased from Hokkaido System Science (Sapporo).
Cells were fixed and hybridized using the protocol reported from Amann (1995) with some modification (Sakai et al. 2004). The sludge sample was fixed in 3% paraformaldehyde/phosphate buffer saline (PBS) (PBS; 130 mM NaCl, 10 mM sodium phosphate buffer, pH 7.0) for 1-3 hrs at 4ºC, pelleted by centrifugation (3500 x g, 15 min, 4ºC) and then stored in a 1 : 1 mixture of ethanol and PBS. Fixed cell suspensions were diluted using an ethanol/PBS mixture (8 µl) and were spotted on coated glass slides (12 wells per slide, Cel-Line; Erie Scientific, Portsmouth, New Hampshire, UK), dried at 46ºC for 30 min and immersed for 3 min each in 50%, 80%, and 99% (v/v) ethanol. Cell smears were covered with 20 µl of lysozyme (50 mg/ml PBS; 37ºC, 30 min). Enzymatic digestion was terminated by thoroughly rinsing the slides with distilled water followed by air-drying at room temperature (25 ± 2ºC).
Samples in 8 µl of hybridization buffer [0.9 M NaCl, 20 mM Tris-HCl (pH 7.2), 0.01% SDS, 60-120 ng of probe, 0-30% formamide] were applied to the wells on the slides and incubated at an appropriate temperature for 2 hrs in an equilibrated humid chamber. Unbound probes were removed from the slide by rinsing with 1 ml of washing solution (20 mM Tris-HCl, 0.01% SDS, 450 mM NaCl, 5 mM EDTA). The slides were then incubated at 48ºC for 20 min in 50 ml of washing solution, rinsed briefly with distilled water, air-dried and mounted with SlowFade antifading reagent (Molecular Probes, OR, USA). Fluorescence was observed using an epifluorescence microscope (BX50; Olympus, Tokyo, Japan) and photomicrographs were taken using a chilled 3-charge-coupled device (CCD) color camera (640 x 483 pixels, C5810; Hamamatsu Photonics, Shizuoka, Japan). Fluoro-stained cells were observed and counted in duplicate wells for appropriately diluted samples and those in five randomly selected fields for each those two replications (1000-fold magnification) were recorded on a computer and counted. The concentration of fluoro-stained cells (cells/ml) was calculated as follows:
(C x D x Am)/(V x Aw x F) [Eq. 1]
Where C is the cell number observed on a monitor (cells), D is the dilution rate, Am was the monitor area calculated using an objective micrometer (0.0024 mm2), V was the sample volume spotted in the well (8.0 x 10-3 ml), Aw was the well area on the glass slide (19.6 mm2) and F was the fixation efficiency (0.82).
Activated sludge samples were collected from the anaerobic bioreactor, gram-stained and viewed under the optical microscope (Olympus BX50, Japan). Once a sludge sample was collected from the bioreactor, it was prepared for SEM as follows: washed 3 times with 0.1 M cacodylate buffer (pH 7.4) for 10 min each time and then fixed with glutaraldehyde (2.5% v/v) in 0.2 M sodium cacodylate buffer (pH 7.1) and dehydrated with graded ethanol solutions (10%, 30%, 50%, 70%, 90%, and 100% ethanol). The samples were dehydrated by the critical point drying method and coated with gold. A Leo 1455 VP scanning electron microscope (Carl-Zeiss, Germany) was used to take the micrographs.
16S rRNA was PCR amplified from the DNA extract of sludge taken from an anaerobic bioreactor. From 237 clones screened (84 from the bottom sludge library, 75 from the middle sludge library and 78 from the recycling sludge), all had a DNA insert of the correct size (1260 bp). Two different HaeIII RFLP-patterns were observed from the clone libraries and assigned as group I and II (Figure 1). Representative examples from RFLP group I and II (SamaliEB and Samali15) are shown in Figure 1. RFLP group I contained 97.1% of clones and 2.9% fell in group II. The sequences obtained in this study have been deposited in the GenBank database under accession numbers EU580025- to EU580045.
Partial DNA sequences were obtained from representative amplicons for each RFLP group. Approximately 27 clones were sequenced (20 from group I and 7 from group II) and were used to search the GenBank nucleotide database with the BLAST search tool. One representative for each RFLP group was included in the phylogenetic tree. The sequence data set contained 20 sequences, including Methanopyrus kandleri that was used as the outgroup (Figure 2).
Matches obtained for each clone sequenced had a similarity of ≥ 99% with those contained in the GenBank nucleotide database. All RFLP groups I and II clones sequenced were Methanosaeta concilii. Although the RFLP group II clones had a unique HaeIII restriction profile, partial sequencing of the clones revealed a 99% identity with M. concilii (M59146), a sequence shared by all of the samples in RFLP group I. This distribution of the same species sequence in two different RFLP groups illustrates the limitation of relying on partial DNA sequences as well as RFLP only for representing the diversity of samples contained in a library.
A total of five methanogenic bands (EBM1, EBM2, EBM3, EBM4 and EBM5) (Figure 3a) were excised from the methanogenic DGGE fingerprints, re-amplified, purified and sequenced. Yielded sequences (334 bp) were analyzed by CHECK_CHIMERA software (Maidak et al. 1997) to scan for potential chimeric sequences and three were found chimeric. The remaining two (EBM2 and EBM4) were analyzed using the BLAST program. The RFLP groups representatives (SamaliEB and Samali15) were in line with EBM2. Band EBM4 was found to be Methanosarcina. Although band EBM2 correlated with the reference clones SamaliEB and Samali15 (Methanosaeta concilii), it was also excised and sequenced to confirm the identification of the band as Methanosaeta concilii. Band EBM2 showed a 99% sequence similarity to the uncultured Methanosaeta sp. clone I2 that had been previously found in environmental samples taken from anaerobic biofilms (AB236094, NCBI database). Band EBM4 showed a 97% sequence similarity to Methanosarcina sp. 48 (EF112192, NCBI database). The methanogenic DGGE pattern showed that the band which belonged to Methanosaetaceae appeared to be denser and sharper than the one of Methanosarcina.
The double bands observed using archaeal primers; PARCH340f and PARCH519r (Figure 3b) was a result of degeneracy of the primers used (Piceno et al. 1999). The archeal PCR products using clones SamaliEB and Samali15 as DNA template did not align on the DGGE gel with the band related to SamaliEB lying lower which was due to a single nucleotide difference between the two amplicons (Figure 4). As shown in the Figure 4, one base pair G/C in SamaliEB is replaced with A/T in Samali15. As a matter of fact, DNA fragments richer in G/C are more stable and remain double-stranded until reaching higher denaturant concentrations (lower levels of the gel). Double-stranded DNA fragments migrate better in the acrylamide gel, while denatured DNA molecules become effectively larger and stop in the gel. In this study, a DNA fragment of higher G/C content stoped at a lower level of gel and by providing a narrow range of optimized gradient (50% to 60%), a subtle difference between the DNA fragments known as single nucleotide polymorphism (SNP) was detected. This confirmed the RFLP results which found clone SamaliEB to be a different strain of Methanosaeta concilii in comparison with the other clones including clone Samali15 and the gene bank database. In combination with the DGGE fingerprint using Methanogens primers, just two of the archaeal bands should represent methanogenic archaea (archaeal bands were not analyzed).
Under optimal hybridization conditions, methanogens and bacteria were specifically visualized and detected using the corresponding probes. Figure 5 and Figure 6 show representative micrographs of the fluorescent methanogenic and bacterial cells in the sludge sample double-stained with rhodamine-EUB338 and FITC-MSMX860. Solid and complex materials in digested sludge showed strong self-fluorescence that pictures taken by a chilled CCD color camera with a modified RGB color balance helped distinguish the fluorescence of FITC-probes from the self-fluorescence of the refuse materials. The self-fluorescence of refuse materials was yellowish in the fermented sample.
The presence of members of the Methanosaetaceae and Methanosarcinaceae in sludge was also in accordance with DGGE results but, the presence of Methanosarcinaceae was not detected by PCR-cloning. All aceticlastic methanogens belong to the order Methanosarcinales comprising two families, Methanosarcinaceae and Methanosaetaceae. Among six genera belonging to Methanosarcinaceae, the genus Methanosarcina can only utilize acetate as a substrate. All members of the family Methanosaetaceae are aceticlastic (Garrity and Holt, 2001). The Methanosaetaceae and Methanosarcinaceae families differ in their physiology, biokinetics, and growth environment with respect to acetate concentrations.
The family Methanosaetaceae has a high affinity for acetate accompanied with a relatively low growth rate, while the family Methanosarcinaceae has a much lower substrate affinity but with a higher growth rate. That describes why the POME anaerobic digester used in the present study was dominated by Methanosaetaceae as the acetate concentration in the sludge digester was favorable to them and acetate is the only substrate that supports the growth of Methanosaetaceae (Garrity and Holt, 2001).
The presence of members of the Methanosaetaceae in anaerobic bioreactors has been widely reported (Chan, 2001; Batstone et al. 2004; Hulshoff Pol et al. 2004). It is also generally known that the presence of Methanosaeta species leads to an improved granulation process and it results in a more stable bioreactor performance (Hulshoff Pol et al. 2004). The bioreactor used in this study was designed for continuous or intermittent mixing to maximize the contact between POME and the microbes. This differs from the upflow anaerobic sludge blanket (UASB) design in which granules are formed. However, Methanosaetaceae is assumed to form the initial nuclei followed by floc formation as well as described in Spaghetti Theory (Wiegant, 1987). Therefore, Methanosaetaceae plays an important role in floc formation in CDT and consequently higher performance of the bioreactor in terms of COD removal and methane production. However, this contrasts with the findings of Sallis and Uyanik (2003) indicating that associations between mixed bacterial populations and inert material formed the so-called nuclei at the initial stage of granule formation and the predominance of Methanosaetaceae occurred only when the granules had developed.
This methanogen is one of the main species responsible for the conversion of acetate to methane. Species within this family use acetate as their sole energy source, which is metabolized into methane and carbon dioxide. These organisms can be found in anaerobic sediments and anaerobic sludge bioreactors (Garrity and Holt, 2001). In order to maximize the efficiency of the bioreactor in terms of COD removal and methane production, optimized running operation e.g. organic loading rate (OLR) (kg COD/m3/day), pH, alkalinity is of great importance. In this study, high COD removal 93% was observed which was higher than the findings of Choorit and Wisarnwan (2007) at mesophilic conditions. This was achieved due to a higher retention time (10 days) in comparison with 7 days used in their study. However, the methane production of 1.35 L/L[reactor]/day was lower which could be attributed to a different bioreactor design (continuous stirred tank reactor (CSTR)) which enables higher application of OLR. Hence, higher methane production could be achieved.
The results of FISH counting showed that the total number of bacteria in the sludge sample was 1.4 x 105 cells/ml sludge. The major group in the treated sludge sample was the Methanosaeta sp. which a count of 2 x 108 cells/ml sludge. In contrast, the number of Methanosarcina sp. was almost 1000 times lower and was equal to that of bacteria. In other words, for each one thousand cells of Methanosaeta sp., there was just one single cell of Methanosarcina sp. present in the sludge. These results indicate that, the closed fermentation of POME led to the domination of Methanosaeta sp. in particular Methanosaeta concilii emphasizing on the importance of the substrate. The VFAs concentration of 517 mg/L showed high activity of methanogens which was reflected by high methane production (56% v/v methane of 1200 m3 biogas/day) and satisfactory COD removal of 93% (Table 1). The high number of methanogenic archaea (2 x 108 cells/ml sludge) in comparison with the bacteria cells (1.4 x 105 cells/ml sludge) might be attributed to the stage of sampling at which the highest methane production was recorded.
The finding also showed that quantitative FISH using group and species specific rRNA-targeted probes could be applied to the direct analysis of semi-solid POME sludge to provide a good estimate of the dominant species of methanogens which plays an important role in optimizing running conditions of the digester for achieving the highest COD removal and methane production. The PCR-cloning, DGGE analysis and species-specific FISH confirmed that Methanosaeta concilii was the dominant species during the fermentation of POME.
The presence of Methanosaeta sp.in the studied industrial activated sludge was corroborated by its morphology using light microscopy (Figure 7). It has been reported that Methanosaeta sp. can form filaments of 10-300 cells (Garrity and Holt, 2001). The scanning electron microscopy provided a better resolution of Methanosaeta sp. than that obtained by conventional light microscopy. Filamentous like Methanosaeta sp. was observed and found to be the dominant species in the CDT system (Figure 8a; Figure 8b). It is clearly seen that the microorganisms bend around the organic matters and thus play an important roles in flocs/aggregate formation during POME treatment. Nevertheless, the actual size of the flocs or aggregates formed during the CDT process was not monitored. Methanosaeta sp. was normally determined to be at the core of the granules formation in UASB system (Hulshoff Pol et al. 2004). A demand to be strictly anaerobic and consume solely acetate makes them to be located at the core and other archaea-like Methanosarcina sp., fermentative and facultative bacteria are placed on the outer granules layer to prevent oxygen contamination (Savant et al. 2002). Some other microbes that coexisted in the digester are shown in Figure 8c. However, Methanosaeta-like microorganisms outnumbered short rods and cocci.
In conclusion, our results indicate that filamentous acetate-utilizing methanogens detected in anaerobic bioreactor treating POME belong to the genus Methanosaeta based on the cell-morphology, and the phenotypic and phylogenetic characteristics described above. The data obtained suggest that Methanosaeta concilii is the most abundant methanogen in POME anaerobic digestion and that it plays an important role in methane production from acetate and the optimum condition for its growth should be considered when an attempt is made to treat POME anaerobically. It also revealed the presence of possibly new strain of Methanosaeta in the bioreactor for treating POME.
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