High-quality-draft genome sequence of the fermenting bacterium Anaerobium acetethylicum type strain GluBS11T (DSM 29698)
- Yogita Patil1,
- Nicolai Müller1Email author,
- Bernhard Schink1Email author,
- William B. Whitman3,
- Marcel Huntemann4,
- Alicia Clum4,
- Manoj Pillay4,
- Krishnaveni Palaniappan4,
- Neha Varghese4,
- Natalia Mikhailova4,
- Dimitrios Stamatis4,
- T. B. K. Reddy4,
- Chris Daum4,
- Nicole Shapiro4,
- Natalia Ivanova4,
- Nikos Kyrpides4,
- Tanja Woyke4 and
- Madan Junghare1, 2Email author
© The Author(s). 2017
Received: 8 October 2016
Accepted: 26 January 2017
Published: 20 February 2017
Anaerobium acetethylicum strain GluBS11T belongs to the family Lachnospiraceae within the order Clostridiales. It is a Gram-positive, non-motile and strictly anaerobic bacterium isolated from biogas slurry that was originally enriched with gluconate as carbon source (Patil, et al., Int J Syst Evol Microbiol 65:3289-3296, 2015). Here we describe the draft genome sequence of strain GluBS11T and provide a detailed insight into its physiological and metabolic features. The draft genome sequence generated 4,609,043 bp, distributed among 105 scaffolds assembled using the SPAdes genome assembler method. It comprises in total 4,132 genes, of which 4,008 were predicted to be protein coding genes, 124 RNA genes and 867 pseudogenes. The G + C content was 43.51 mol %. The annotated genome of strain GluBS11T contains putative genes coding for the pentose phosphate pathway, the Embden-Meyerhoff-Parnas pathway, the Entner-Doudoroff pathway and the tricarboxylic acid cycle. The genome revealed the presence of most of the necessary genes required for the fermentation of glucose and gluconate to acetate, ethanol, and hydrogen gas. However, a candidate gene for production of formate was not identified.
KeywordsAnaerobic Gluconate Glycerol Microcompartments Lachnospiraceae Firmicutes Gram-staining positive Embden-Meyerhoff-Parnas pathway Entner-Doudoroff pathway Ferredoxin Transporters
Strain GluBS11T (= DSM 29698) is the type strain of the newly described species Anaerobium acetethylicum . The genus Anaerobium belongs to the family Lachnospiraceae  within the class Clostridia  of the order Clostridiales  that is largely synonymous with Clostridium rRNA cluster XIVa [5, 6]. Members of the family Lachnospiraceae have been isolated from diverse habitats, but are mainly constituents of mammalian intestinal microbiota, especially from ruminants  and humans . They are strictly anaerobic and primarily non-spore forming , and ferment polysaccharides to short-chain fatty acids such as acetate and propionate as fermentation products , e.g., Eubacterium rectale ATCC 33656 T, Eubacterium ventriosum ATCC 27560 T, Coprococcus sp. and Roseburia sp. [11, 12]. The family Lachnospiraceae as currently described in the National Center for Biotechnology Information homepage comprises 41 named genera and several unclassified isolates, of which a total of 143 draft or complete genome sequences are available. Strain GluBS11T was isolated due to its ability to ferment gluconate, and the species epithet ‘acetethylicum’ refers to its main fermentation products acetate and ethanol during gluconate fermentation . Within the diverse family of Lachnospiraceae , strain GluBS11T is phylogenetically closely related to the type strains of C. herbivorans strain 54408 [94% 16S rRNA sequence similarity); , C. populeti ATCC 35295 T (93.3% similarity); , Eubacterium uniforme ATCC 35992 T (92.4% similarity), and C. polysaccharolyticum ATCC 33142 T (91.5% similarity); [15, 16]. Of these, all strains were reported to ferment sugars mainly to butyrate plus formate, acetate, ethanol or lactate, except E. uniforme , which does not produce butyrate. Similar to E. uniforme ATCC 35992 T, strain GluBS11T does not produce butyrate during the fermentation of sugars or glycerol [1, 17]. Moreover, none of the above strains except for strain GluBS11T was tested for fermentation of gluconate.
The most prominent feature of A. acetethylicum strain GluBS11T is its ability to ferment sugars (including oxidized sugar such as gluconate) and glycerol mainly to acetate, ethanol, hydrogen, and formate [1, 17]. Therefore, we selected strain GluBS11T as a candidate for studying its potential to ferment gluconate or glycerol. Moreover, most of the described bacterial glycerol fermentations lead to 1,3-propanediol  and other undesired products such as butyrate or 2,3-butanediol. In contrast to this, strain GluBS11T ferments glycerol mainly to ethanol and hydrogen gas as well as negligible amounts of acetate and formate . Here we present the summary of the taxonomic classification and the features of A. acetethylicum strain GluBS11T together with the description of the genome sequencing and annotation. Emphasis is given on understanding the central metabolism and fermentation pathways. The putative enzymes involved in the fermentation of gluconate, glucose, and glycerol were also reconstructed from the genomic data.
Classification and features
Classification and general features of Anaerobium acetethylicum strain GluBS11T according to the MIGS recommendations 
Species Anaerobium acetethylicum
Type strain: GluBS11 T (DSM 29698)
spore formation not reported
pH range; Optimum
gluconate, glucose, glycerol
Genome sequencing information
Genome project history
An Illumina 300 bp insert standard shotgun (AZHBB)
Illumina HiSeq 2500-1 TB
Gene calling method
GenBank Date of Release
September 23, 2016
Source Material Identifier
GluBS11T (= DSM 29698)
Sugar and glycerol fermenting bacterium
Growth conditions and genomic DNA preparation
A. acetethylicum strain GluBS11T was cultivated in anoxic mineral medium supplemented with 10 mM gluconate as growth substrate at 30 °C for three days until OD600nm 1.0 was reached. Genomic DNA was isolated from the cell pellet obtained from about 500 ml of grown culture using a CTAB-based method  with slight modifications . After RNase treatment, the purity and quality of the genomic DNA preparation were assessed by DNA absorption at 260 nm and size by agarose gel electrophoresis (1% w/v; Additional file 1: Figure S1). The concentration of the isolated genomic DNA was 2.4 μg μl-1 (A260/280 = 2.03 and A260/230 = 2.47). Finally, the DNA was used to amplify the 16S rRNA gene to confirm the identity of genomic DNA by comparing with the described partial 16S rRNA gene sequence (KP233894) of A. acetethylicum strain GluBS11T. The pure and high-quality genomic DNA was shipped to the DOE, JGI for genome sequencing.
Genome sequencing and assembly
The draft genome sequencing was performed at the DOE, JGI using the Illumina technology . An Illumina 300 bp insert standard shotgun library was constructed and sequenced using the Illumina HiSeq-2500 1 TB platform, which generated 11,508,336 reads totaling 1,726.3 Mbp. All details on library construction and sequencing performed at the JGI can be found on the website. All raw Illumina sequence data were filtered using BBDuk , which removes known Illumina artifacts and PhiX. Reads with more than one “N” or with quality scores (before trimming) averaging less than 8 or reads shorter than 51 bp (after trimming) were discarded. Remaining reads were mapped to masked versions of human, cat and dog references using BBMap  and discarded if the identity exceeded 95%. Sequence masking was performed with BBMask . The following steps were performed for assembly: (1) artifact filtered Illumina reads were assembled using the SPAdes genome assembler (version 3.6.2); , (2) assembly contigs were discarded if their length was <1 kbp. Parameters for the SPAdes assembly were -cov-cutoff auto -phred-offset 33 -t 8 -m 40 -careful -k 255,595 -12. The final draft assembly contained 108 contigs in 105 scaffolds, totaling 4.609 Mbp in size, and was based on 1,500.0 Mbp of Illumina data with a mapped coverage of 336.0X.
Genes were identified with Prodigal  using standard microbial genome annotation pipeline . The predicted CDSs were translated and used to search the NCBI non-redundant database, UniProt, TIGRFam, Pfam, KEGG, COG, and InterPro databases. The tRNAScanSE tool  was used to find tRNA genes, whereas rRNA genes were found by searches against models of the rRNA genes built from SILVA . Other non-coding RNAs such as the RNA components of the protein secretion complex and the RNase P were identified by searching the genome for the corresponding Rfam profiles using INFERNAL . Additional gene prediction analysis and manual functional annotation (IMG taxon ID 2675903067) were performed within the Integrated Microbial Genomes-Expert Review platform  developed by the JGI, Walnut Creek, CA, USA.
% of Total
Genome size (bp)
DNA coding (bp)
DNA G + C (bp)
Protein coding genes
Genes in internal clusters
Genes with function prediction
Genes assigned to COGs
Genes with Pfam domains
Genes with signal peptides
Genes with transmembrane helices
Number of genes associated with general COG functional categories
Translation, ribosomal structure and biogenesis
RNA processing and modification
Replication, recombination and repair
Chromatin structure and dynamics
Cell cycle control, Cell division, chromosome partitioning
Signal transduction mechanisms
Cell wall/membrane biogenesis
Intracellular trafficking and secretion
Posttranslational modification, protein turnover, chaperones
Energy production and conversion
Carbohydrate transport and metabolism
Amino acid transport and metabolism
Nucleotide transport and metabolism
Coenzyme transport and metabolism
Lipid transport and metabolism
Inorganic ion transport and metabolism
Secondary metabolites biosynthesis, transport and catabolism
General function prediction only
Not in COGs
Insights from the genome sequence
General metabolic features
The draft genome of strain GluBS11T was further examined to understand the organism’s physiology and fermentation metabolism. The draft genome encodes most of the key enzymes of the pentose phosphate pathway, Embden-Meyerhoff-Parnas pathway, Entner-Doudoroff pathway and tricarboxylic acid cycle (Additional file 2: Table S1). Thus, strain GluBS11T is very likely to use these pathways for its central metabolism and biosynthesis. Besides this, the genome also contains the genes coding for putative enzymes of anaplerotic pathways, such as oxaloacetate decarboxylase (α-subunit, Ga0116910_1001318 and β-subunit, Ga0116910_1001319), pyruvate kinase (Ga0116910_1001611), fructose-1,6-bisphosphatase (Ga0116910_1001181 and 10346), phosphoenolpyruvate carboxykinase (Ga0116910_1001300) and pyruvate carboxylase β-subunit (Ga0116910_101716). Genes for biosynthesis of amino acids and most co-factors were also present (Additional file 2: Table S1).
Although cells of strain GluBS11T are non-motile , the genome possesses genes that are predicted to encode flagellum components (Ga0116910_1001565, Ga0116910_1002133- Ga0116910_1002135, Ga0116910_100329, Ga0116910_1002133- Ga0116910_1002135) such as flagellar protein FliO/FliZ, flagellar motor switch protein FliN/FliY/FliM, flagellar FliL protein, and pilus assembly-protein (Flp/PilA), which are located in a single gene cluster (locus tag Ga0116910_100336 to Ga0116910_100363), including the chemotaxis protein (MotB/A). The draft genome also contains genes predicted to encode seven universal stress proteins of the UspA family (gene loci Ga0116910_103114, 1003225, 10025, 10028, 10027, 104111 and 100540), 2 heat-shock proteins such as GrpE (Ga0116910_10476 and 100386), one heat-inducible transcriptional repressor (Ga0116910_100387), and six cold-shock proteins of the CspA family (Ga0116910_10067, 1002200, 1001175, 1004187, 1005160 and 1002190). Also, a DNA-directed RNA polymerase with sigma-70/32 factor (ECF family) and a heat-inducible transcriptional repressor (HrcA) along with the RNA polymerase sigma factor for flagellar operon FliA were detected in the draft genome.
Clustered regularly interspaced short palindromic repeats are segments of prokaryotic DNA containing short repetitions of base sequences followed by a short segment of ‘spacer DNA’ that function as a defense system against the introduction of foreign genetic materials (e.g., phage infection, plasmid or horizontal gene transfer). CRISPRs were found in approximately 40% of all sequenced bacterial genomes . Genome analysis of strain GluBS11T suggests that the genome does not contain CRISPR regions, although the genome of the phylogenetically closely related strain C. populeti ATCC 35295 T contains two gene coding for CRISPR-associated proteins (cas9 family protein; Ga0056054_02523 and Ga0056054_00025).
Transporters enable bacteria to accumulate required nutrients and also contribute for excretion of unwanted metabolic products. They also help to maintain the osmotic balance and the cytoplasmic pH by transporting H+ and various salts. Genome analysis of strain GluBS11T identified various membrane transporters including the ABC solute transporters (ATP-dependent) that could take part in the transport of various substrates such as ions, vitamins, sugars, amino acids, and metabolites (Additional file 3: Table S2). Most of these identified transporters belong to diverse transporter families such as the amino acid/polyamine antiporter family, the drug/metabolite transporter superfamily, and the major facilitator superfamily that is used for transport of a diverse set of small solutes in response to chemiosmotic ion gradients . The draft genome sequence also contains several genes coding for proton symporters (Additional file 3: Table S2). Thus, strain GluBS11T could generate a proton gradient using FoF1-type ATP synthase in reverse direction [42, 43].
Metabolic pathways for glucose, gluconate and glycerol utilization
The genome annotation predicted the presence of four gluconate:proton symporters (Gnt family) encoded by Ga0116910_10413, Ga0116910_10069, Ga0116910_100214 and Ga0116910_10418. In a previous study, it was shown that C. acetobutylicum ATCC 824 T takes up gluconate by gluconate:proton symporters (CA_C2835);  which showed amino acid sequence identity (24 to 41%) with the four predicted genes with highest identity (Ga0116910_10418; 42%). Thus, the product of the Ga0116910_10418 gene is the most likely candidate for uptake of gluconate. Based on the genome annotation, A. acetethylicum strain GluBS11T most likely uses the Entner-Doudoroff pathway for gluconate metabolism, through which gluconate is first phosphorylated to 6-phosphogluconate by gluconokinase (EC 184.108.40.206) followed by dehydration to 2-keto-3-deoxy-phosphogluconate by 6-phosphogluconate dehydratase (EC 220.127.116.11). Alternatively, gluconate could be first dehydrated (modified Entner-Doudoroff pathway) to 2-keto-3-deoxy gluconate by gluconate dehydratase (EC 18.104.22.168) followed by phosphorylation to KDPG by 2-keto-3-deoxygluconokinase (EC 22.214.171.124). KDPG would be further converted to pyruvate and glyceraldehyde 3-phosphate by KDPG aldolase (EC 126.96.36.199). The presence of a putative gene coding for KDPG aldolase (Ga0116910_101517) indicates that gluconate is most likely metabolized via KDPG. However, no putative genes coding for the initial enzymes that could convert gluconate to KDPG (according to two ways as mentioned above) was identified in the draft genome of strain GluBS11T. However, two putative genes were annotated as dihydroxy acid dehydratase/phosphogluconate dehydratase (Ga0116910_10068 and Ga0116910_101679) that could have this activity. The predicted dihydroxy acid dehydratase (EC 188.8.131.52) is possibly involved in the biosynthesis of amino acids (valine, isoleucine, and isoleucine). A similar observation was also reported for the gluconate-fermenting C. acetobutylicum ATCC 824 T, where the gene CA_C3170 was predicted to encode a 6-phosphogluconate dehydratase and BlastP analysis indicated that it is a dihydroxy acid dehydratase primarily involved in the synthesis of amino acids [47, 48]. BlastP search of amino acid sequence analysis of genes Ga0116910_10068 and Ga0116910_101679 showed more than 80% identity with the dihydroxy acid dehydratase of C. phytofermentans ATCC 700394 T (A9KL28) and Anaerostipes caccae DSM 14662 T, respectively, and showed only 40-60% identity with gene CA_C3170 of C. acetobutylicum ATCC 824 T. Therefore, genes Ga0116910_10068 and Ga0116910_101679 most likely encode a dihydroxy acid dehydratase that is involved in amino acid synthesis rather than in KDPG formation. Based on this information, gluconate degradation via the Entner-Doudoroff pathway involving gluconate phosphorylation to 6-phosphogluconate by gluconokinase (EC 184.108.40.206) followed by dehydration to KDPG by 6-phosphogluconate dehydratase (EC 220.127.116.11) can be ruled out. Furthermore, the presence of a putative gene coding for KDPG aldolase (Ga0116910_101517) indicates that gluconate is most likely metabolized via the modified Entner-Doudoroff pathway, which would be consistent with previous studies of the anaerobic gluconate metabolism [45, 47, 49]. Even though no genes coding for the gluconate dehydratase (EC 18.104.22.168) and KDG kinase (EC 22.214.171.124) required for initial activation of gluconate to KDPG were identified in the genome of strain GluBS11T.
While gluconate is predicted to be metabolized via the modified Entner-Doudoroff pathway, glucose could be metabolized through glycolysis. For uptake of glucose, strain GluBS11T most likely uses a phosphotransferase system (PTS) which couples glucose import to its phosphorylation with phosphoenolpyruvate, yielding glucose-6-phosphate and pyruvate . Genes Ga0116910_100991 and Ga0116910_100370 are predicted to encode PTS proteins which are most likely involved in glucose transport in strain GluBS11T. Thus, genome analysis suggests that glucose is most probably metabolized through glycolysis via glucose 6-phosphate by glucose-6-phosphate isomerase (Ga0116910_1004120 and Ga0116910_10539), 6-phosphofructokinase (Ga0116910_103531, Ga0116910_100239, Ga0116910_102039 and Ga0116910_101135), and fructose-bisphosphate aldolase (Ga0116910_101128 and Ga0116910_102024) to glyceraldehyde 3-phosphate. In the glycolysis pathway, glyceraldehyde 3-phosphate is further metabolized through the lower part of glycolysis to ethanol, acetate, hydrogen, and formate. During gluconate fermentation, KDPG aldolase would then convert KDPG to glyceraldehyde-3-phosphate and pyruvate, and only glyceraldehyde-3-phosphate passes through the lower glycolysis pathway.
Previous studies with other bacteria reported that gluconate fermentation mainly yielded acetate and butyrate as fermentation products [45, 47, 49]. Although, the draft genome of strain GluBS11T contains genes predicted to code for a putative butyrate kinase (Ga0116910_101723 and Ga0116910_102110), gluconate, glucose or glycerol fermentation by strain GluBS11T does not produce butyrate [1, 17]. The pathways were easily constructed based on the genome analysis and genes for acetate metabolism, e.g., acetate kinase (Ga0116910_103636, Ga0116910_1001586 and Ga0116910_104214), ethanol metabolism, e.g., alcohol hydrogenase (Ga0116910_101528, Ga0116910_102038, Ga0116910_102215, Ga0116910_1004154 and Ga0116910_102016), and hydrogen metabolism, e.g., putative iron-only hydrogenases and subunits coding for an NADP+-reducing hydrogenase (Ga0116910_1001473, Ga0116910_1001466, Ga0116910_1001467, Ga0116910_1001468, Ga0116910_1001470, Ga0116910_100545 and Ga0116910_1001473). No candidate gene was found to code for a putative formate-producing formate dehydrogenase in the draft genome of strain GluBS11T even though formate dehydrogenase activities were detected in cell-free extracts using benzyl viologen as an artificial electron acceptor . On the other hand, genes annotated as pyruvate:formate lyase or formate C-acetyltransferase were identified in the genome (Ga0116910_1004109, Ga0116910_100860, Ga0116910_102934 and Ga0116910_102935), but no activity for a possible pyruvate:formate lyase could be detected [Patil et al., unpublished results]. This indicates that the genomic information is sometimes insufficient to predict metabolic pathways. Thus, further biochemical and proteomics studies would be needed to investigate and confirm the gluconate and glucose fermentation pathway utilized by this bacterium.
Microcompartments and fucose utilization
The genome of A. acetethylicum strain GluBS11T harbors five genes that putatively code for bacterial microcompartment shell proteins. Four of these genes are annotated as “BMC-domain-containing protein” (Ga0116910_1005148, Ga0116910_1005149, Ga0116910_1005150 and Ga0116910_1005151), and one gene is annotated as “Carboxysome shell and ethanolamine utilization microcompartment protein CcmL/EutN” (Ga0116910_1005155). Microcompartments are protein complexes that form discrete spaces within the cell, thus enabling enzyme reactions that either produce toxic intermediates or require accumulation of a certain metabolite, e.g., the ethanolamine utilization microcompartment in Salmonella typhimurium ATCC 13311 T or the carboxysomes in cyanobacteria [50, 51]. An IMG gene search for microcompartments and subsequent comparison to other genomes using the IMG Gene Ortholog Neighborhoods viewer, revealed that the microcompartment genes in A. acetethylicum strain GluBS11T are located in a putative operon that also contains genes associated with fucose utilization in Clostridium phytofermentans ATCC 700394 T . Fucose, a deoxyhexose derived from plant biomass degradation, can be fermented to propionate, propanol, mixed acids, and ethanol by C. phytofermentans ATCC 700394 T , and the responsible genes are located in two different operons in this organism . Initially, fucose is converted to fuculose-phosphate by fucose mutarotase, fucose isomerase and fucose kinase (Cphy_3153 – Cphy_3155); . Likewise, the orthologs in A. acetethylicum strain GluBS11T are located in a similar operon (L-fucose isomerase Ga0116910_100812, rhamnulokinase/L-fuculokinase Ga0116910_100813 and L-fucose mutarotase Ga0116910_100815). Fuculose-phosphate is then further degraded to lactaldehyde and dihydroxyacetone-phosphate by fuculose-phosphate aldolase (Ga0116910_102223 in A. acetethylicum strain GluBS11T, Cphy_1177 in C. phytofermentans ). Dihydroxyacetone phosphate can then be processed through glycolysis, while lactaldehyde is reduced to 1,2-propanediol with NADH. 1,2-propanediol is then disproportionated in microcompartments to propionate and propanol by 1,2-propanediol oxidoreductase (Cphy_1185, Ga0116910_1005154), 1,2-propanediol dehydratase (Cphy_1174, Ga0116910_100557 - Ga0116910_100559 in a different area of the genome), propionaldehyde dehydrogenase (Cphy_1178, Ga0116910_1005146), phosphate propanoyl transferase (Cphy_1183, Ga0116910_1005152), acetate/propionate kinase (Cphy_1327, Ga0116910_104214, Ga0116910_1001586, or Ga0116910_103636) and propanol dehydrogenase (Cphy_1179, Ga0116910_1005147). Rhamnose can be degraded in a similar way by C. phytofermentans ATCC 700394 T , and the respective genes leading to lactaldehyde and dihydroxyacetone-phosphate were also identified in the genome of A. acetethylicum strain GluBS11T (L-rhamnose mutarotase Ga0116910_10513, L-rhamnose isomerase Ga0116910_1001301, rhamnulokinase/L-fuculokinase Ga0116910_100813) . However, earlier results demonstrated that rhamnose cannot be utilized by A. acetehylicum strain GluBS11T . Even though the genes for fucose degradation are present in the genome, it is still doubtful whether this sugar can serve as a growth-supporting substrate for strain GluBS11T.
Taken together, the draft genome sequence of A. acetethylicum strain GluBS11T expands our view on the metabolic capacities of this sugars and glycerol-fermenting bacterium. The genome sequence gives us insights into the putative enzymes involved in the pathway of glucose and gluconate (including glycerol) fermentation, and provides a brief summary of the key reactions involved. Lastly, the hypotheses concerning the glucose and gluconate fermentation pathways based on genomic data are still preliminary, and additional biochemical and functional proteomic studies will be necessary for pathway confirmation and further insights.
Coding DNA sequence
Clusters of orthologous groups
Cetyl trimethyl ammonium bromide
Kyoto encyclopedia of genes and genomes
Molecular evolutionary genetics analysis
Nicotinamide adenine dinucleotide reduced
YP thanks the LGFG scholarship funding program of the University of Konstanz for providing scholarship during this research work. The authors appreciate the service of the Electron Microscopy Center of the University of Konstanz.
During this research YP was funded by a LGFG PhD scholarship. The genome sequencing was performed under the auspices of the US Department of Energy’s Office of Science, Biological and Environmental Research Program, and by the University of California, Lawrence Berkeley National Laboratory under contract No. DE-AC02-05CH11231.
YP, MJ, NM and BS initiated the project and YP performed DNA preparation. MJ and YP performed the comparative genomics, investigated the genome for general metabolic features and fermentation pathways. MJ, YP and NM drafted the manuscript that was critically reviewed and corrected by BS, NM, WW, NS and NK, respectively. MH, AC, MP, KP, NV, NM, DS, TBKR, CD, NI, and TW performed the technical work for sequencing, assembly and annotation of the genome. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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