Methanopyrus kandleri: evolutionary significance
by Kiri Staiger
Introduction
Methanopyrus kandleri is a species of hyperthermophilic, halotolerant, methanogenic archaeon, originally isolated from sediments associated with undersea hydrothermal vent fields. [1] Currently the only species in its genus, M. kandleri is thought to be part of a separate lineage from all other known methanogens, possibly a lineage that diverged extremely early on, close to the time that the kingdoms of life were themselves diverging. [1] Whether or not this is the case is unclear; M. kandleri ’s exact phylogenetic placement, and its significance, have been points of controversy since the microbe’s discovery. [2, 3] Either way, both its unique lineage and its extremophilic nature set M. kandleri apart from its fellows, and it has been the subject of much study and debate.
Classification
Assigning a classification to M. kandleri has been one of the main questions that researchers have debated about the microbe since its discovery in 1991. Although several different classifications have been suggested, the version currently accepted is:
Domain: Archaea
Phylum: Euryarchaeota
Class: Methanopyri
Order: Methanopyrales
Family: Methanopyraceae
Genus: Methanopyrus
Species: kandleri
Species description
Morphology
M. kandleri presents as motile, rod-shaped cells, growing singly or in short chains of generally less than 10 individuals. Individual cells are typically between 8 and 10 microns in length and half a micron in diameter. Occasional, very short, cells, only about .8 microns in length, are also observed, although whether these micro-cells are merely stunted or an example of intentional cell differentiation (as seen in heterocyst formation in cyanobacteria) is not currently known. Motility in M. kandleri is conferred by flagellar “tufts” located at cell poles. Cells stain gram-positive; in addition to a psuedomurein inner envelope, cells possess the protein S-layer typical of archaeons. They also exhibit a slime-like layer that coats over the S-layer. It is thought that this slime layer is what allows M. kandleri to form the long, “raft-like” structures seen when the microbe is grown under shaking conditions. [1] It may also assist the microbe in adhering to surfaces. One study looking at archaeal bio-film formation found that M. kandleri was able to adhere to even the smooth glass surface of a test tube under shaking conditions, where Pyrococcus furiosus (a different, hyperthermophilic, archaeon) could not. [4] Certainly, an enhanced ability to stick to one’s environment would not go amiss in M. kandleri ’s home in the walls of underwater thermal vents.
When cultured under less active conditions, M. kandleri may form irregularly shaped colonies, about 1 mm in diameter, that exhibit the blue-green morphology typical of methanogens. [1]
Environmental Preferences
The species was originally isolated from two sites—a “black smoker” hydrothermal vent site in the Guaymas Basin in the Gulf of California, and a shallower hydrothermal vent site at Kolbensey Ridge, off of Iceland. Although the samples were uniformly anaerobic, both sites otherwise exhibit incredible variation, in temperature—between 7° in the cooler sediments and 315° C in the vent-walls themselves—and pressure. The Guaymas Basin site is under 2000 meters of seawater; the Kolbensey Ridge site is much shallower at only around 100 m. [1] M. kandleri does not occupy the entire range of this incredibly diverse environment, but it does exhibit a fairly broad tolerance range, especially in regards to temperature and salinity. The optimum temperature for M. kandleri is 98° C, but the microbe can grow at temperatures as low 84°C and as high as 110°C—ten degrees above the boiling point of water. This extreme hyperthermophilism places M. kandleri among the most heat-tolerant organisms currently known.
Salinity preference for M. kandleri is between 0.2 and 4%, with an optimal salinity of 2%. While not extreme, this does leave M. kandleri as a moderate halophile. The microbe has also been shown to tolerate extremely high levels of internal salinity; like Halobacteria , M. kandleri builds up a high proportion of negatively charged molecules in its proteins and cell structures to counteract the positively charged salts. In the case of M. kandleri, the microbe may tolerate an internal concentration of potassium salts greater than 3M. [1,3]
pH preference is near neutral, between 5.5 and 7; cells grow optimally at a pH of 6.5.
Metabolism
M. kandleri is an obligate, anaerobic, chemolithoautotroph; di-hydrogen gas and carbon dioxide are converted to methane, in a type of metabolism known as methanogenesis. This type of metabolism is found only in archaea, and plays an important role in the carbon cycle, especially in decomposition. Several different types of methanogenesis have been observed. The chemical equation below shows the reactants and involved in the variation of methanogenesis that M. kandleri utilizes.
CO2 + 4 H2 → CH4 + 2H2O
Many methanogens may also use the carbon in organic compounds such as formate or methanol as an electron acceptor, but M. kandleri seems to strictly utilize carbon dioxide in this role. Hydrogen is similarly the sole electron donor—with one exception. Under normal circumstances, the presence of sulfur will only inhibit growth of M. kandleri ; however, sulfur is just similar enough to hydrogen that, under the right circumstances, such as during an exponential growth period where cells are growing and metabolizing rapidly, M. kandleri will mistake it for hydrogen and begin to use it as an electron donor. This is not unusual, per say; many microbes do in fact utilize sulfur in this way to no ill effect. However, one of the byproducts produced by this alternate chemical reaction is hydrogen sulfide (H2S), which appears to be toxic to the microbe, causing high rates of lysis. [1]
Genome type
Methanopyrus kandleri possesses a single, circular chromosome 1,694,969 base pairs in length, containing genes coding for 39 different structural RNAs, and 1,692 different proteins. Of these proteins, only a very few are involved in gene regulation or regulation signaling pathways; fewer than one would predict, even when one takes into consideration that hyperthermophiles as a group are generally less regulated than other microbes. M. kandleri ’s genome also encodes fewer DNA binding proteins, also associated with regulatory activity, than any other known archaeon; this suggests that regulatory activity in M. kandleri is highly reduced, and response pathways may be relatively few. [3]
In addition, M. kandleri codes for an unusually high proportion of negatively charged amino acids in its proteins, which contribute to the microbe’s high proportion of negatively charged residues that, as mentioned previously, is involved in conveying high salt tolerance.
The G+C content is about 60%, which is unusually high compared to most other methanogens, which average only 33% G+C . [1]
Novel proteins and features
A number of novel proteins and other compounds have been isolated from M. kandleri , and are of interest in perhaps shedding light on both its phylogenetic status and its highly thermophilic, halophilic existence. Many hyperthermophilic proteins and enzymes have been described from M. kandleri , and some have found applications in the world of biotechnology. Some of the more interesting discoveries, in terms of either evolutionary significance or possible applications, are outlined in this section.
Novel Psuedomurien Variate
Many archaeons possess a cell wall consisting of pseudomurein. Also called pseudopeptidoglycan, pseudomurein acts much as peptidoglycan does in bacterial cell walls, forming a thick, multi-layered envelope around the cell. Ordinarily, pseudomurein is made up of N-acetylglucosamine and N-acetyltalosaminuronic acid. However, Methanopyrus kandleri substitutes L-orthinine where N-acetylglucosamine ordinarily would go.
Novel Core Lipid
A number of novel lipids have been isolated from M. kandleri. The figure at right shows the structure of one of these lipids, 2,3-di- O-phytanyl-sn-glycerophosphocholine (Fig. 2). In addition, the microbe was found to utilize a novel core lipid. This lipid, an unsaturated, ether-linked lipid identified as 2,3-di-O-geranylgeranyl-sn-glycerol, is of a type of lipids (terpenoid lipids) thought to be a ‘primitive feature’ of many microbes. The presence of this terpenoid lipid may, in combination with other evidence (as detailed later in this article), provide some evidence for the claim that M. kandleri is of an early diverging branch from the Euryarchaeota group. [12]
Novel DNA-binding proteins
Sequence analysis of the M. kandleri genome shows a relative deficiency in this microbe of the helix-turn-helix and Arc-MetJ type DNA binding proteins that are usually found in abundance across both archaeons and bacteria. Instead, M. kandleri appears to utilize (at least) 3 novel DNA binding proteins. All are relatively small molecules, with molecular weights of 7, 10, and 30 kDa. The structure of the 7 kDa binding protein has been determined to be dimeric, consisting of a larger alpha-helical protein associated with a smaller, N-terminal beta-strand. Structural properties, as well as apparent regulatory similarities, suggest that this binding protein may be a relative of the ribbon-helix-helix family of transcription factors that are involved in DNA binding and gene regulation in bacteria, notably Pseudomonas bacteria. [10]
Hetero-dimeric reverse DNA gyrase
Reverse DNA gyrases, which positively supercoil DNA when activated by ATP, have been found to be common across nearly all hyperthermophiles, both archaeons and bacteria. However, the M. kandleri DNA reverse gyrase is the first hetero-dimeric DNA reverse gyrase to be described. The protein consists of two sub-units—a larger (138 kDa) subunit that associates with ATP and hydrolyses it to release energy; and a smaller (43 kDa) sub-unit that binds covalently to DNA as the protein works to create supercoils. The presence of these two sub-units within the gyrase, as opposed to having a single unit protein, is thought to help stabilize the protein at the incredibly high temperatures M. kandleri is subject to. In addition, high temperatures appear to be required for the two sub-units to form the stable heterodimer observed. [9]
Novel and modified RNA nucleosides
M. kandleri shows an unusual and highly diverse pattern of post-transcriptional modifications to tRNA nucleosides—4 entirely novel nucleosides have been isolated from this microbe. Modifications to these nucleosides effect structure, behavior, and stability of the tRNA strands each helps to form. The high degree of modification seen in M. kandleri may have to do with the extreme nature of its environment and the high demands that environment places on its proteins in terms of maintaining stability. [11]
Questions and Controversy- Placing M. kandleri within the evolutionary tree of life
Since its discovery, the placement of M. kandleri within a broader phylogenetic context has been a highly contested avenue of research. At different times, it has been thought to be many different things—a representative of a new class within Euryarchaeota , only very distantly related to its fellow methanogens [1, 2]; alternatively, quite closely related to other methanogens [3]; or, even more alternatively, quite unrelated from just about everything, and possibly a link to finding the much lauded Last Universal Common Ancestor [5]. Which one of these M. kandleri actually is, is still up to debate.
Initial Classification
The researchers who initially isolated the microbe placed it in a separate, deeper-branching, clade from other methanogens based on the following observations:
First, the G+C content of Methanopyrus was much higher than that of other known methanogens. At 60%G+C, Methanopyrus has almost twice the G+C in its genome as other methanogens. Second, the amount of homologous DNA sequences observed between Methanopyrus and other methanogens was, in their words, “insignificant.” Third, lipid analysis of the structures of Methanopyrus revealed a very different set of core lipids than what ought to be a closely related archaeons, Methanococcus . Where Methanococcus ’ core lipids are 85% comprised of cyclic dibisphytanyl tetraethers, Methanopyrus ’ core lipid was 2,3-di-O-phytanyl-glycerol, a very different type of lipid. Fourth, Methanopyrus had a higher halo-tolerance than other Methanobacteriales species. Fifth, Methanopyrus exhibited a novel type of psuedomurein in its cell wall, a variant that substituted L-ornithine for N-acetylglucosamine, and had not been observed previously. Sixth, and perhaps most convincingly, phylogenetic analysis of the microbe’s 16s RNA sequence placed it quite distantly from all known methanogens. In fact, 16s RNA analysis placed it so very distantly from other methanogens that the researchers designated it in a new class—Class Methanopyri, which they had branching off from the Phylum Euryarchaeota significantly earlier than any other known branch. [1]
Support for a separate lineage
In the research since Methanopyrus ’ initial discovery in 1991, there has been some support for this theory. Analysis of M. kandleri ’s 16s RNA sequence suggests that, although a Euryarchaote, Methanopyrus shares a higher degree of relatedness to the chrenarchaeota group that seen in any other Euryarchaeote , which in turn suggests that M. kandleri may have diverged very early on. A 1996 study used a Jukes-Cantor distance projection to approach the problem qualitatively, looking at distances between 16s RNA sequences and regions of the 1-α elongation factor for M. kandleri and proposed relations, including methanogens. The tree generated by this projection again placed Methanopyrus at a deep branch within Euryarchaeota , existing either within or proximal to archaebacteria. [2] (See figure) A similar study using the sequences from an operon common across methanogens, coding for methyl coenzyme M reductase, also supported the conclusion that Methanopyrus stands separate from other methanogens. [6]
If this view of Methanopyrus phylogeny is correct and Methanopyrus is of a separate lineage than other methanogens, this would indicate that methanogenesis as a metabolism has arisen at least two separate times. Perhaps more importantly, because many phylogenetic analyses of Methanopyrus place it as a representative of a very deep branching group, some have looked to Methanopyrus as perhaps the most proximal known relative of the Last Universal Common Ancestor, or LUCA. Although previous efforts to locate the LUCA placed it somewhere in the bacterial realm, more recent analyses, incorporating a greater diversity of organisms, especially the previously under-represented archaeons, tell a different story. Phylogenetic distances based on tRNA sequences, which show much lower rates of horizontal transfer than protein coding genes and, as such, are more likely to generate accurate phylogenetic trees over this kind of time-frame, suggest that the LUCA falls somewhere between Euryarchaeota and Crenarchaeota —just about, in fact, where Methanopyrus kandleri seems to fit. [8] If this is the case, than M. kandleri and its genome can tell us a lot about the early divergence of life.
Support for a monophyletic view of M. kandleri and the methanogens
As with any radical claim in science, the proposal of a Methanopyrus-proximal LUCA met with immediate refutal. Opposing this view—opposing, in fact, the entire idea that Methanopyrus is of a different lineage than its fellow methanogens—we have a second set of research. One study used full DNA sequence data and the idea of COGs—Clusters of Orthologous Groups, sets of gene orthologs that are conserved across different phylogenetic groups—to construct a very different phylogeny, that grouped M. kandleri in one lineage with other methanogens. According to this work, about 73% of the proteins coded for in M. kandleri ’s genome are part of COGs shared across a broad spectrum of life; many of the remaining proteins are common across methanogens, which supports the proposal of a single methanogenic lineage. In the trees generated by this COG analysis, M. kandleri is shown as most proximal to either Methanococcus thermoautotrophicum or Methanococcus jannaschii.
The sequence data for these three species—Methanococcus thermoautotrophicum , Methanococcus jannaschii , and Methanopyrus kandleri —is somewhat ambiguous as to who exactly is most related to whom. All three share COGs that are common across methanogens. M. jannaschii and M. thermoautotrophicum share a partial duplication in a recently described operon. The placement and order of genes and operons is more similar between M. thermoautotrophicum and M. kandleri . Depending on what metric we pick, these three species arrange themselves into various relationships. But, despite this ongoing fine-tuning, this research makes a clear case for placing Methanopyrus within a single lineage with the methanogens—no longer the deepest branching member of Euryarchaeota , no longer a clue to finding the LUCA, just another methanogen. (see figure) [3]
So—what to do with Methanopyrus , in the end? Both sides of the debate seem to present compelling evidence. Whose evidence do we choose? Do we base our phylogenetic analysis off of 16s RNA? Whole genome analysis? tRNA sequences? Whatever way we do it, we seem to get a different result. At this time, it seems as if no definite conclusion has been drawn. The apparent paradox M. kandleri presents remains.
References
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[3] 2. Rivera, M.C., and Lake, J. 1996. The Phylogeny of Methanopyrus kandleri . IJSEM 46: 348-351.
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[8] 7. Zhiliang Yu, Ken Takai, Alexei Slesarev, Hong Xue and J. Tze-Fei Wong. 2009. Search for Primitive Methanopyrus Based on Genetic Distance Between Val- and Ile-tRNA Synthetases. Journal of Molecular Evolution 69: 386-394
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[10] 9. Regis Krah, Mary H. O’Dea and Martin Gellert. 1997. RECONSTITUTION OF AN ACTIVE EXTREMOZYME FROM ITS TWO RECOMBINANT SUBUNITS. The Journal of Biological Chemistry, 272, 13986-13990.
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[12] 11. Sauerwald, Anselm1; Sitaramaiah, Devarasetty2; McCloskey, James A.2,3; Söll, Dieter1; Crain, Pamela F.. 2005. N6-Acetyladenosine: A new modified nucleoside from Methanopyrus kandleri tRNA 579: 2807-2810.
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