A comparative transcriptome analysis of the novel obligate methanotroph Methylomonas sp. DH-1 reveals key differences in transcriptional responses in C1 and secondary metabolite pathways during growth on methane and methanol
Methanotrophs play an important role in biotechnological applications, with their ability to utilize single carbon (C1) feedstock such as methane and methanol to produce a range of high-value compounds. A newly isolated obligate methanotroph strain, Methylomonas sp. DH-1, became a platform strain for biotechnological applications because it has proven capable of producing chemicals, fuels, and secondary metabolites from methane and methanol. In this study, transcriptome analysis with RNA-seq was used to investigate the transcriptional change of Methylomonas sp. DH-1 on methane and methanol. This was done to improve knowledge about C1 assimilation and secondary metabolite pathways in this promising, but under-characterized, methane-bioconversion strain.
We integrated genomic and transcriptomic analysis of the newly isolated Methylomonas sp. DH-1 grown on methane and methanol. Detailed transcriptomic analysis indicated that (i) Methylomonas sp. DH-1 possesses the ribulose monophosphate (RuMP) cycle and the Embden–Meyerhof–Parnas (EMP) pathway, which can serve as main pathways for C1 assimilation, (ii) the existence and the expression of a complete serine cycle and a complete tricarboxylic acid (TCA) cycle might contribute to methane conversion and energy production, and (iii) the highly active endogenous plasmid pDH1 may code for essential metabolic processes. Comparative transcriptomic analysis on methane and methanol as a sole carbon source revealed different transcriptional responses of Methylomonas sp. DH-1, especially in C1 assimilation, secondary metabolite pathways, and oxidative stress. Especially, these results suggest a shift of central metabolism when substrate changed from methane to methanol in which formaldehyde oxidation pathway and serine cycle carried more flux to produce acetyl-coA and NADH. Meanwhile, downregulation of TCA cycle when grown on methanol may suggest a shift of its main function is to provide de novo biosynthesis, but not produce NADH.
This study provides insights into the transcriptomic profile of Methylomonas sp. DH-1 grown on major carbon sources for C1 assimilation, providing in-depth knowledge on the metabolic pathways of this strain. These observations and analyses can contribute to future metabolic engineering with the newly isolated, yet under-characterized, Methylomonas sp. DH-1 to enhance its biochemical application in relevant industries.
KeywordsMethanotroph Serine cycle RuMP cycle TCA Carotenoid biosynthesis pathway Hopanoid biosynthesis pathway RNA-seq
Coding DNA sequence
Clusters of orthologous genes
False discovery rate
Fragments per kilobase of exon per million fragments
Reactive oxygen species
Single-carbon (C1) feedstock such as methane and methanol has great potential for a number of applications and has shown flexibility when used with biocatalysts and in bioconversion processes to produce various products [1, 2]. Methane is the main component of natural (and shale) gas and biogas. Recently, expansion of the global methane market has improved accessibility, resulting in decreasing gas prices. This has made methane an attractive next-generation feedstock . Generally, chemical conversions of methane to other chemicals require a high input of energy because of the high activation energy of the C-H bond . Thus, biological conversions of methane to higher value products using methanotrophs has grown more attractive recently. As intermediates in the aerobic methane oxidation process, methanotrophs are capable of utilizing methanol as a sole carbon source and utilize a similar pathway to that for methane assimilation . Methanol is also an attractive carbon substrate because of its high production volume and low market price . A wide range of methylotrophic bacteria has been used to produce multiple chemically valuable compounds, including single-cell proteins, biopolymers, lipids, methanol, ectoine, and vitamin B12 . In addition, genetically engineered methanotrophs have served as promising and powerful production platforms to over-produce several non-native compounds such as carotenoids, lactic acid, succinic acid, 1,4-butanediol and 2,3-butanediol [7, 8, 9]. In an effort to expand on the collection of bacterial bioconversion platforms, a novel obligate methanotroph strain, Methylomonas sp. DH-1, was recently isolated from the sludge of a brewery. However, the strain had yet to be characterized for its bioconversion abilities with molecular-level experiments . Methylomonas sp. DH-1 showed highly efficient bioconversion of methane to methanol, with a titer of 1.34 g per liter. This is more efficient than the conversion rate of previously reported biocatalysts . Furthermore, the strain’s ability to tolerate high concentrations of methanol (up to 7% [v/v]) offers advantages for high-titer methanol production . Recently, Methylomonas sp. DH-1 also proved to be a novel and competent biocatalyst for the conversion of propane to acetone, with a titer of 16.62 mM under mild reaction conditions . Furthermore, Methylomonas sp. DH-1 may become a biotechnologically important biocatalyst for its ability to produce several carotenoids (unpublished report).
Development of next-generation sequencing technology enabled the sequencing of genomes of several methanotrophs, and the genomes of those methanotrophs provided essential information for the reconstruction of methane metabolism in methanotrophs [12, 13]. In addition, multi-omics studies (which integrate transcriptomics, metabolomics, proteomics, and genomics) have provided insights to assess various metabolic engineering targets for methanotrophs . Indeed, several previous studies using a multi-omics approach to analyze multiple model methanotrophs have been reported [14, 15, 16, 17, 18]. Recently, in our previous work, a complete genome sequence for Methylomonas sp. DH-1 was determined . The strain contains one 4.86 Mb chromosome and one 278 kb plasmid, pDH1 . The availability of the complete genome sequence of Methylomonas sp. DH-1 provided an essential background for revisiting a genome-based reconstruction of methane metabolism. But to date, a comprehensive transcriptome analysis of Methylomonas sp. DH-1 is still elusive, and mechanisms responsible for the methanol tolerance of Methylomonas sp. DH-1 have yet to be investigated. An RNA-sequencing approach has been used to investigate the transcriptome and has provided insights into the methane metabolism of type I [16, 17, 18] and type II [14, 15] methanotrophs. In this study, we first detail the genome-wide transcriptional responses of methane metabolism and secondary metabolite production in Methylomonas sp. DH-1 during growth on methane. We then offer a comparative transcriptomic analysis conducted with cells grown on methane and methanol. This analysis revealed differences in the transcriptional response of multiple metabolic pathways which are relevant to C1 assimilation, secondary metabolite production, and oxidative stress.
Bacterial growth conditions
Methylomonas sp. DH-1 was isolated from the activated sludge of a brewery plant based on NMS medium using enrichment culture with methane as sole carbon source as described in our previous work . Liquid pre-cultures were grown in 180 ml baffled-flask with 10 ml NMS with a supplement of 30% methane (v/v) as a sole carbon source at 30 °C and 230 rpm, sealed with a screw cap. The precultures were then inoculated in a 500 ml baffled flask sealed with a screw cap containing 50 ml of NMS and methane also was supplied to a final concentration of 30% (v/v) by gas substitution using a gas-tight syringe, and the headspace was refreshed every day. The methanol-cultured Methylomonas sp. DH-1 was cultured in the same medium containing 1% (v/v) methanol without added methane. All cultures were grown in triplicate for subsequent RNA extraction and sequencing.
Total RNA isolation and sequencing
For sequencing library preparation, 5 ml of microbial culture broths containing either methane- or methanol-grown cultures in mid-exponential phase were harvested, and total RNA was stabilized using the bacterial reagent RNAprotect (Qiagen, Hilden, Germany). Cells were lysed and total RNA was extracted using a GeneJET RNA Purification Kit (Thermo Fisher Scientific, USA), following the manufacturer’s protocol. Total RNA quality and quantity were measured using an RNA 6000 Nano kit with the Agilent Bioanalyzer (Agilent Technologies, CA, USA). Next, rRNA was removed using the Ribo-Zero rRNA removal kit for gram-negative bacteria (Epicentre, Madison, WI, USA), and the remaining RNA was used for creating the sequencing library using the TruSeq Stranded Total RNA Sample Prep Kit (Illumina, USA) according to the manufacturer’s instructions. Transcriptome sequencing was conducted using the Illumina/Hiseq-2000 RNA sequencing platform (Macrogen, Korea).
Quantification of differentially expressed genes
After evaluating the quality of the raw sequence data with FastQC (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/), further quantitative analyses were performed. Illumina sequencing (of triplicates) was aligned against the genome sequence of Methylomonas sp. DH-1 (NZ_CP014360 for the chromosome and NZ_CP014361 for the plasmid). The Bowtie tool was used with a maximum insert size of 1000 bp and with two maximum mismatches after trimming 3 bp at the 3′ ends under the default options. The sequence alignment/map (SAM) files were post-processed using SAMTools (http://samtools.sourceforge.net/), by first converting to binary alignment/map (BAM) files and then sorting and indexing those BAM files. Indexed and sorted BAM files generated from SAMTools were analyzed by Cufflinks and Cuffdiff to calculate values for fragments per kilobase of exon per million fragments (FPKM) and differential expression, respectively (with default options and a library type of dUTP RNA-seq). Genes from the Cuffdiff output showing differential expression with a log2 fold change ≥1.0 and a false discovery rate (FDR) value ≤0.01 were considered as differentially expressed genes in our study.
Clusters of orthologous groups (COGs) functional assignment and ortholog calculation
All of the CDS regions were assigned to different functional categories based on the Clusters of orthologous genes (COGs) designation . The ortholog calculation was performed using InParanoid software .
Genome-wide transcriptome profiling
Categorization of gene expression level
Description of expression level
Number of genes
Number of genes
Number of genes
Number of genes
Expression of genes involved methane oxidation of Methylomonas sp. DH-1
Pyrroloquinoline quinone (PQQ)-dependent methanol dehydrogenase (mxaFJGI) and the PQQ biosynthesis gene cluster (pqqABCDE) were identified in the Methylomonas sp. DH-1 genome. The mxaFJGI operon for methanol oxidation (encoding two subunits of methanol dehydrogenase, cytochrome, and a protein of unknown function [mxaJ]) showed relatively high expression levels. While the expression of mxaFJGI actually decreased on methanol, the fold change was less than 2 (Fig. 2, Fig. 3c, Additional file 2: Table S2). The genes downstream of the mxaFJGI operon (which are chaperones, regulators, or have Ca2+ insertion functions) showed an intermediate or low level of expression that was 14- to 55-fold lower in comparison to the first four genes in the methanol dehydrogenase (MDH) operon (Additional file 2: Table S2). The PQQ biosynthesis gene cluster (pqqABCDE) encodes an essential system that provides cofactors for methanol oxidation. The expression level of this gene cluster was high (Additional file 2: Table S2). A homolog of mxaF, known as xoxF, was found in Methylomonas sp. DH-1. This gene showed a high expression level (Fig. 3c and Additional file 2: Table S2) when grown on methane, but was much lower than the expression of mxaF. Similar to the pmo operon, the expression of xoxF was significantly downregulated (3.65-fold change) on methanol (Fig. 3c). The homolog xoxF was firstly reported as part of a regulatory complex essential for the expression of methanol dehydrogenase in Methylobacterium extorquens AM1  and currently has been identified as a predominant methanol dehydrogenase in M. buryatense 5GB1 . Thus, it is possible that a high expression level of xoxF may contribute to methanol oxidation in Methylomonas sp. DH-1. Furthermore, direct coupling mode, in which methanol oxidation supplies electrons for methane oxidation, is most suitable mode of methane oxidation in gamma-proteobacterial methanotrophic bacteria . Surprisingly, xoxF was highly downregulated during growth on methanol, similar to the pattern seen for pmo. Thus, we can postulate that xoxF may also play a role in methane oxidation in Methylomonas sp. DH-1 during growth on methane, and the exact contribution of xoxF in methane and methanol oxidation should be experimentally explored.
From the genomic analysis a group of genes in conventional type II methanotrophic metabolic pathways (such as the tetrahydromethanopterin (H4MPT) pathway and the tetrahydrofolate [H4F] pathway) were also identified in the genome of Methylomonas sp. DH-1. Previous studies have indicated that there are three possible pathways for formaldehyde oxidation, including H4MPT, H4F, and direct oxidation by formaldehyde dehydrogenase . Genes for the direct oxidation of formaldehyde by formaldehyde dehydrogenase were not found in the Methylomonas sp. DH-1 genome. However, a broad-specificity aldehyde dehydrogenase (ald) was predicted from the genomic analysis, and the transcriptome analysis showed an intermediate expression level for this aldehyde dehydrogenase (Additional file 2: Table S2). Recently, the H4F pathway has drawn attention for its assimilatory function to convert formate to methylene-H4F. This pathway also contributes to formaldehyde oxidation in M. extorquens AM1 and M. trichosporium OB3b [14, 29]. All of the genes involved in the H4F pathway in Methylomonas sp. DH-1 were expressed at an intermediate level (Additional file 2: Table S2). During growth on methanol, the expression levels of genes in the H4F pathway were slightly increased compared to growth on methane (Fig. 3d). In particular, methenyltetrahydromethanopterin cyclohydrolase (fch) showed a fold change of 2.18 (Additional file 2: Table S2). Among the three different formaldehyde oxidation processes, the H4MPT pathway serves as the key pathway in the type II model methanotroph, M. trichosporium OB3b . Formaldehyde-activating enzyme (fae), which condenses formaldehyde with tetrahydromethanopterin (H4MPT) to produce methylene-H4MPT, is the first enzyme of the formaldehyde detoxification pathway through H4MPT. Interestingly, Methylomonas sp. DH-1 has three homologs of fae at different genomic locations. The orthologs fae1 and fae3 appear to be expressed at very low and at high levels on methane-grown cultures, respectively (Additional file 2: Table S2). However, the ortholog fae2 was expressed at a very high level (10-fold higher than fae3) (Fig. 1 and Additional file 2: Table S2). The rest of the genes encoding key enzymes in the H4MPT pathway were also expressed at a high level on methane (Fig. 1 and Additional file 2: Table S2). Thus, our transcriptomic data analysis revealed that the genes in the H4MPT pathway showed high expression at the transcriptional level, indicating this pathway was likely key for formaldehyde oxidation in Methylomonas sp. DH-1. Interestingly, the expression of fae2 was upregulated on methanol compared to methane (Fig. 2, Fig. 3d), meaning formaldehyde oxidation via H4MPT was more active during growth on methanol. Most methanotrophs use a NAD-dependent formate dehydrogenase to oxidize formate to CO2 . It has been reported that most of the reducing power for methane metabolism was provided by formate oxidation to CO2 . Methylomonas sp. DH-1 has the formate dehydrogenase (fdsABGCD) gene cluster, encoding a NAD-dependent formate dehydrogenase and an additional single copy of the alpha subunit (fdhA). Most of the genes in the operon fdsABGCD were expressed at a high level, and no significantly different expression of fdsABGCD was observed at the transcription level between methane and methanol (Fig. 3d and Additional file 2: Table S2). Overall, the transcriptomic analysis illustrate that the H4MPT pathway may serve as the key pathway for formaldehyde oxidation in Methylomonas sp. DH-1, as the pathway genes were highly expressed. Similarly, activation of H4F and the H4MPT pathway in M. buryatense strain 5GB1 and M. alcaliphilum 20ZR under methane growth were also observed [17, 18].
A complete set of functional genes for formaldehyde fixation through the ribulose monophosphate (RuMP) cycle, Embden-Meyerhof Parnas (EMP) pathway, the Entner-Doudoroff (ED) pathway, and the pentose phosphate (PP) pathway was also identified in the Methylomonas sp. DH-1 genome. More interestingly, the complete gene set implementing the serine cycle without the interconnected ethylmalonyl-CoA (EMC) cycle and TCA cycle existed in the genome of Methylomonas sp. DH-1. A transcriptional analysis of these key formaldehyde assimilation pathways is described below.
Gene expression of C1 assimilation pathway under methane growth and its response to substrate shifts
In a comparison between the transcriptome profiles of methane- and methanol-grown cultures, the expression levels of most genes in the RuMP cycle did not change significantly, with these exceptions: glucose-6-phosphate dehydrogenase (gpd1), 6-phosphogluconolactonase (pgls), and ribose 5-phosphate isomerase (rpi). Upregulation of some genes in the EMP pathway, including fructose-bisphosphatase (fbp), triose-phosphate isomerase (tpi), and phosphoglycerate mutase (gpml), was observed. Transcription of pyruvate kinase was also upregulated on methanol compared to methane (Fig. 4a, b, and Additional file 3: Table S3).
Targeted transcriptomic analysis of serine and TCA cycle suggested flux shifts under methanol-grown cultures
The genomic analysis suggested that Methylomonas sp. DH-1 possesses a complete serine cycle . This is a typical C1 assimilation pathway of the type II methanotrophs, and is not a common feature in type I methanotrophs. All of the genes involved in the serine cycle were identified in the genome of Methylomonas sp. DH-1. Interestingly, but not surprisingly, those genes were expressed when grown on methane or methanol (Fig. 1, Fig. 4c, and Additional file 4: Table S4). Among them, D-glycerate dehydrogenase (dgd) and glycerate kinase (gck) were expressed at rather low expression levels; in contrast, phosphopyruvate hydratase (eno) and malate dehydrogenase (mdh) were highly expressed. It was reported that a partial serine cycle without phosphoenolpyruvate carboxylase (ppc) in M. buryatense 5G was predicted to have a minor flux during growth on methane by steady state 13C metabolic flux analysis  and in silico simulation . Conversely, the existence and expression in Methylomonas sp. DH-1 of phosphoenolpyruvate carboxylase (ppc), a key enzyme in the serine cycle that serves as a major entry point for CO2 in alpha-proteobacterial methanotrophs , may provide the capability for CO2 fixation and malate production. Notably, the expression of ppc was significantly downregulated on methanol compared to methane. There are two types of ppc involved in a serine cycle: a “non-regulated” type where enzymatic activity is not controlled by intermediates of the TCA cycle or the glycolysis pathway, and a “regulated” type where the enzymatic activity of ppc is subject to control by various metabolic effectors [30, 35]. An ortholog analysis suggests that ppc of Methylomonas sp. DH-1 belongs to the regulated group (Additional file 5: Figure S1). Transcription of ppc decreased dramatically (9.6-fold) on methanol compared to methane, possibly because ppc was subject to metabolic effectors that are better produced on methane. As noted above, the H4F pathway can function as a part of an assimilatory pathway (via serine) that converts formate to methylene H4F. In accordance with this, upregulation of the H4F pathway was observed in the transcriptome data for growth on methanol, and this in turn may have affected expression of the serine cycle (Fig. 2 and Additional file 4: Table S4). Replenishment of glyoxylate is an essential function of the serine cycle [30, 34, 36]. However, no homolog of isocitrate lyase or malate synthase in the glyoxylate shunt was found in Methylomonas sp. DH-1, similar to other obligate methanotrophs [16, 17]. In addition, an ethylmalonyl-CoA (EMC) cycle was not identified. Thus, Methylomonas sp. DH-1 appears to have a complete serine cycle for carbon conversion to acetyl-CoA and for CO2 fixation. Among the genes in the serine cycle, the key genes such as serine-glyoxylate aminotransferase (sga) and mdh was significantly upregulated, with a 2.1-fold and 1,7-fold change, respectivelly (Fig. 2). Especially, the malyl-coA lyase (mclA), which directly produce acetyl-CoA via serine cycle, has been upregulated with a 2,78-fold change on methanol-grown cells. That suggested an increase flux towards the serine cycle to contribute acetyl-CoA production during growth on methanol.
Typically, type I and type X methanotrophs differ from type II methanotrophs because the former groups possess an incomplete tricarboxylic acid (TCA) cycle and do not have 2-oxoglutarate dehydrogenase enzyme activity [33, 37, 38]. It has been suggested that the main function of the TCA cycle in methanotrophs is to provide precursors for de novo biomass synthesis, as opposed to providing reducing power to the system . However, a recent study using 13C tracer analysis demonstrated that a complete oxidative TCA cycle operates in M. buryatense . Similar to M. buryatense, our genome analysis indicate that Methylomonas sp. DH-1 encodes all of the essential genes for the TCA cycle, and these genes are expressed on both methane and methanol (Fig. 1, Fig. 4d, Additional file 4: Table S4). Most genes in the TCA cycle were expressed at a high or intermediate level under methane growth, except for fumarate hydratase (fh), which was expressed at a low level. The 2-oxoglutarate dehydrogenase complex, which plays a key role in the TCA cycle, also was expressed at a high level. In order to confirm whether Methylomonas sp. DH-1 operates a complete TCA cycle, the ability to convert 2-oxoglutarate to succinyl-CoA or succinate needed to be tested. A succinate dehydrogenase mutant was generated to confirm any 2-oxoglutarate dehydrogenase activity. Interestingly, the mutant strain showed no difference in its growth rate compared to the wild-type strain, and succinate was accumulated in the media (data not shown). This observation supports the hypothesis that Methylomonas sp. DH-1 possesses a complete oxidative TCA cycle. This finding might be useful for future metabolic engineering of the TCA cycle in Methylomonas sp. DH-1 to produce relevant products. During growth on methanol, the expression of key genes in the TCA cycle was significantly downregulated such as succinate-coA ligase (sucCD), succinate dehydrogenase (sdh) and isocitrate dehydrogenase (idh1) (Fig. 2, Additional file 4: Table S4) which suggested the decreasing flux towards TCA cycle under methanol growth.
Upregulation of carotenoid and hopanoid biosynthesis pathways under methanol growth
The carotenoid biosynthetic pathways share an upstream pathway of hopanoid biosynthesis . Hopanoids are a group of natural pentacyclic compounds derived from the basic chemical structure of hopane. Studies in a range of bacteria suggest that hopanoids play a role in regulating membrane properties through an interaction with the outer leaflet of the outer membrane. From our genomic analysis, a complete hopanoid biosynthesis pathway is predicted in Methylomonas sp. DH-1. We predict the strain should therefore convert squalene to various hopanoids (including adenosylhopane, ribosylhopane, formylhopane, bacteriohopanetetrol), aminobacteriohopanetriol, and 3-methyl ABH) by hopanoid biosynthesis, using the associated radical S-adenosylmethionine (SAM) protein (hpnH), phosphorylase (hpnG), aminotransferase (hpnO), and hopanoid C-3 methylase (hpnR). Moreover, the existence of hopanoid biosynthesis-associated transporter (hpnN) and hopanoid biosynthesis protein (hpnM) in Methylomonas sp. DH-1 might enable the trafficking of hopanoids [42, 43]. Under methane growth, most of the genes in the hopanoid biosynthesis pathway were expressed at an intermediate level, except for hpnH and hpnR, which were expressed at a high level (Fig. 5b and Additional file 7: Table S6). Interestingly, when a carbon substrate was shifted from methane to methanol, the expression of hopanoid pathway genes increased significantly between 3.4-fold and 6.4-fold (Fig. 2, Fig. 5b, and Additional file 7: Table S6). Among them, hphH showed the highest upregulation, with a 6.4-fold change. It is tempting to speculate that such changes in gene expression in hopanoid biosynthesis pathway related to the ability to tolerate a high methanol concentration in DH-1 via modification of membrane properties.
Transcriptional responses to oxidative stress during growth on methanol
High expression of endogenous plasmid genes plays a role in recombination
Endogenous plasmids are present in several methanotroph genomes [13, 19, 52]. The loss of native plasmid in M. buryatense 5G allowed the variant strain to receive small incompatibility group P (IncP) plasmids, which are broad host range vectors, via conjugation . The native plasmid in M. buryatense 5G likely carries no genes essential for growth, since curing of that plasmid did not affect the growth phenotype . Methylomonas sp. DH-1 contains an endogenous plasmid (pDH1) of 277 kb. In classifying the plasmid genes based on the clusters of orthologous groups (COGs) protein database, we found that replication, recombination, repair (category L), and transcription (category K) were overrepresented. Attempts to cure strains of this plasmid have failed (unpublished report) because it likely plays a significant role in the metabolism of DH-1. Conjugation to introduce IncP-based broad host range vectors (for expressing foreign genes) was not successful. This may have been due to the natural restriction-methylation barrier system that cleaves transforming plasmids before they can replicate in the cell. It is equally possible that incompatibility between foreign plasmid and endogenous plasmid caused stability and maintenance issues. The transcriptomic profile of Methylomonas sp. DH-1 showed that most of the genes in the pDH1 endogenous plasmid had very high or high expression levels (Table 1, Additional file 9: Table S8). Expression of the origin of replication in the plasmid (DnaC) was very high, in fact 10-fold higher than expression of the origin of replication in the main chromosome (DnaA). Although the exact copy number of the endogenous plasmid in DH-1 has not yet been quantified, the high expression of its origin of replication protein might reflect a high plasmid copy number. Thus, integrating foreign DNA cassettes into the endogenous plasmid may be an effective way to express heterologous genes in this strain. From a total of 242 protein-coding genes, 105 had significant expression changes. Among them, 46 genes and 59 genes were downregulated and upregulated in methanol-grown cultures, respectively (Additional file 9: Table S8).
In order to provide knowledge for methanotroph-based refineries, multi-omics can be used to define which metabolic pathways are active in certain conditions, and how cells response and adapt to new environments. In our previous work, the complete genome sequence of the newly isolated methanotroph Methylomonas sp. DH-1 was reported . In the present study, a comprehensive characterization of the complete transcriptome of Methylomonas sp. DH-1 was provided and analyzed for the first time by an RNA-seq approach. This study provides in-depth knowledge about the metabolic pathways of this strain and reveals key differences in the transcriptional responses for certain metabolic pathways during growth in methane and methanol.
In the well-characterized methanotrophs, pmo is expressed at the highest level for cultures grown on methane [14, 15, 16, 17]. A previous study has determined that transcripts of pmoA are very stable, with a half-life in the range of hours to days  which supported the hypothesis that the higher expression levels of pmo compared to other enzymes in the C1 oxidation pathway led to the first step of oxidizing methane is relatively slower compared to subsequent steps. During growth on methanol, the pmo operon was dramatically downregulated, likely because pmo genes are not involved in oxidizing methane. This is consistent with our previous study in which MMO activity has been dropped more than 3-fold when DH-1 growth on methanol . Methane therefore may be a key regulator for the expression of the pmo operon. Similar to that of M. trichosporium OB3b, a type II model methanotroph, the expression of pmo and smo strongly affected by selection of different substrates . The expression level of pmo and smo and their activity extremely dropped when the growth was shifted from methane to methanol .
xoxF, Ln3+ − dependent methanol dehydrogenase, has an important enzyme in methylotrophy, providing a new outlook on the distribution of methylotrophy in the bacterial community . Interestingly, xoxF showed highly expression level without presence of Ln3+ and the similar expression pattern of xoxF and pmo supported the assumption that xoxF could contribute to the methane oxidation process in Methylomonas sp. DH-1. In agreement with our hypothesis, in most recent, the structure and function of xoxF in M. buryatense 5GB1C has been reported by investigating the possibility of interaction between pMMO and XoxF . The results indicated a XoxF monomer may bind to pMMO and suggested an alternative structure of MDH-pMMO association. On the other hand, M. trichosporium OB3b showed very low expression level of xoxF1 and xoxF2 in methane and methanol . Furthermore, the expression level of xoxF1, xoxF2 as well as mxaF in M. trichosporium OB3b were decreased when grown on methanol with the presence of 10 μM copper, highlighting the differences in gene expression regulation in response to the type of carbon sources available between Methylomonas sp. DH-1 and M. trichosporium OB3b. It should be noted that while M. trichosporium OB3b exhibited the “copper-switch” to control the expression of alternative forms of methane monooxygenase, the “copper-switch” was not exist in Methylomonas sp. DH-1.
The discovery of typical type II methanotrophs metabolic pathways, such as the H4MPT pathway, H4F pathway, and complete serine cycle, in Methylomonas sp. DH-1 raised questions about the roles of these pathways in the central metabolism of this strain. From a previously published genome-scale model of M. buryatense 5GB1, a minor carbon flux is predicted via the H4MPT and H4F pathways [17, 18, 57]. However, these pathways were more active during growth on methanol, suggesting the improvement of carbon flux towards these pathway. This observation supports our hypothesis that the H4MPT and H4F pathways are mainly responsible for formaldehyde oxidation and contribute to carbon conversion via the serine cycle when grown on methanol.
A partial serine cycle without ppc has been determined in various type I methanotrophs such as M. buryatense 5GB1 and M. alcaliphilum 20ZR which contributed a minor flux during growth in methane [17, 18]. Likewise, the complete gene set implementing the serine cycle in Methylomonas sp. DH-1 should allow the minor carbon flux needed to produce acetyl-coA. In the type II methanotroph M. trichosporium OB3b, which typically uses the serine cycle as a main pathway for C1 assimilation, there are two kinds of ppc gene: ppc1 belongs to the non-regulated group and ppc2 belongs to the regulated group . The existence of two functionally identical but different regulation systems in M. trichosporium OB3b allows control of flux through phosphoenolpyruvate-oxaloacetate in response to the serine cycle, and this flux is never blocked completely . The presence of only regulated ppc in Methylomonas sp. DH-1 indicates that carbon flux through the serine cycle can be blocked in the absence of effectors. During culture on methanol, expression of ppc was strongly downregulated, possibly because metabolite effectors which activate ppc expression were absent. The growth rate of Methylomonas sp. DH-1 in methanol was significantly decreased, perhaps because carbon flux via the serine cycle may have been blocked under methanol growth. However, most of the genes in the serine cycle were upregulated in methanol, suggesting significant shifts occur in C1 assimilation pathways, from RuMP to serine cycle. Along with RuMP cycle, the serine cycle also could take the role of producing acetyl-coA. EMP is main variant of RuMP pathway which play major role for C1 assimilation to produce NADH and ATP in type I methanotrophs [16, 17, 18]. The shifts decrease flux towards EMP pathway which subsequently decrease ATP production. Instead, the available electrons from methanol oxidation, which not used for methane oxidation under methanol growth, are transferred to the electron transport chain follow by producing ATP via oxidative phosphorylation. In order to determine the detailed rearrangement of metabolic network involved methanol-grown, 13C tracer analysis and constraint-based analysis of genome-scale metabolic network studies are needed. Thus, even the exist of the complete serine cycle in Methylomonas sp. DH-1 could not be main pathway for C1 assimilation, it could contribute to the control of carbon flux when shifting carbon substrates.
One unsolved question surrounding the central metabolism of type I methanotrophs is whether the oxidative TCA cycle is complete. In the recent time, a complete oxidative TCA cycle has been demonstrated to operate in M. buryatense 5GB1, and it has showed three separate pathways for converting 2-oxoglutarate to succinyl-CoA . In another study, highly branched TCA cycle at the 2-oxoglutarate node also has been reported in M. alcaliphilum 20ZR . In this study, we also suggested Methylomonas sp. DH-1 possesses an complete oxidative TCA cycle. However, genomic analysis indicated at 2-oxoglutarate node, Methylomonas sp. DH-1 possesses 2-oxoglutarate dehydrogenase complex only but not 2-oxoglutarate ferredoxin oxidoreductase, succinate semialdehyde dehydrogenase or 2-oxoglutarate decarboxylase. Thus, the presence of highly branched TCA cycle in DH-1 remains to be elucidate. In addition, it seems that carbon flux though TCA cycle was reduced on methanol growth and the critical function of TCA under methanol growth has changed. In methanol-grown cells, TCA cycle mostly provide precursors for de novo synthesis but not reducing power such as NADH. Instead, it appears that the activation of formaldehyde oxidation in methanol growth could produce NADH.
In our previous study, the carotenoid biosynthesis pathways which derived from MEP pathway has been proposed . The dxs is the first and one of the most important rate-limiting step in the MEP pathway, and overexpression of dxs could improve the production of several downstream secondary metabolites such as isoprenoid and carotenoid [58, 59, 60, 61]. The flux shift occurred to MEP pathway via the strong upregulation of two dxs homologs (dxs1 and dxs2) led to the accumulation of carotenoids in methanol-grown cultures. Meanwhile, the extremely upregulation of hopanoid biosynthesis pathway might related to membrane modifications under methanol growth (Fig. 2). The function of hopanoids has been characterized in several organisms, including methylotrophic bacteria [62, 63]. A lack of hopanoid biosynthesis increases sensitivity against toxins and osmotic stress. During growth on single-carbon compounds, methanol is generally converted to formaldehyde in the periplasm, and the formaldehyde is then transported and utilized in the cytoplasm. Given the toxic intermediates in this process, elevated maintenance of the inner and outer membranes is necessary. The role of hopanoids in maintaining membrane robustness and membrane barrier function is likely conserved across bacterial lineages. This function is possibly mediated through an interaction with lipid A in the outer membrane of Methylobacterium extorquens DM4 . In addition, membrane function in the hopanoid-free Methylobacterium extorquens PA1 was lower . Further investigation on the function of hopanoid biosynthesis pathway in property membranes of Methylomonas sp. DH-1 is needed to solve the question if hopanoid biosynthesis pathway could enable resistance to high methanol concentrations in Methylomonas sp. DH-1. Under methanol growth, the upregulation of carotenoid biosynthesis pathway, which produced pigmented carotenoid as antioxidant, and many regulatory defense systems against oxidative stress via damage repair and protection systems have been observed. It is speculated that such changes of these gene expression were induced by methanol which might induces ROS in Methylomonas sp. DH-1. A high expression of MEP pathway genes and an accumulation of carotenoids under stress conditions also describe previously reported in Haematococcus pluvialis . That such speculation must be more rigorously confirmed by apply a system biology approach to reconstruct genome-wide of OxyR, SoxR, and SoxS regulatory networks under oxidative stress condition in methanotrophs.
In conclusion, we have presented genomic and transcriptomic analyses of an industrially promising obligate methanotroph, Methylomonas sp. DH-1. The strain was grown on methane and methanol to analyze the shift of metabolism affecting by selection of substrates (Figs. 1, 2). While some metabolic functions had been reported in previous studies, several novel functions were identified and characterized in this strain. Methylomonas sp. DH-1 possesses the active EMP pathway which main route for C1 assimilation in this strain. In addition, Methylomonas sp. DH-1 also operates a complete oxidative TCA cycle. Along with the existence complete serine cycle, these pathways may function in C1 assimilation and energy production. We also identified a flux shift of metabolism towards formaldehyde oxidation pathway, serine and TCA cycle in Methylomonas sp. DH-1 when substrate was changed from methane and methanol. Furthermore, a significant upregulation of carotenoid and hopanoid biosynthesis pathways under methanol growth might explain the resistance to high methanol concentrations observed in Methylomonas sp. DH-1. It appears that methanotrophs are very dynamic to respond to change of environmental parameters.
We appreciate Dr. Ok Kyung Lee, In Yeub Hwang, Dong Hoon Hur and Young Chan Jeon for their invaluable discussion.
This research was supported by the C1 Gas Refinery Program through the National Research Foundation of Korea (NRF), funded by the Ministry of Science and ICT (2015M3D3A1A01064882). This work was also supported by the 2018 Research Fund (1.180074.01) of UNIST (Ulsan National Institute of Science and Technology). The funding bodies themselves did not participate in the design of the study or the collection, analysis, and interpretation of data, or in writing the manuscript.
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The data generated and analyzed in this study are included in this article, its supplementary information files and on the GEO repository with accession number of GSE101494.
ADN carried out the experimental procedures, performed a complete analysis, and prepared a draft of the manuscript. DK performed the read mapping (from the RNA-seq data to the reference sequences) and the differential expression analysis, and revised the manuscript. EYL coordinated the study and finalized the manuscript. All authors read and approved the manuscript.
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