Methylococcus capsulatus

From MicrobeWiki, the student-edited microbiology resource

A Microbial Biorealm page on the genus Methylococcus capsulatus

Classification

Higher order taxa

Kingdom: Cellular Organism

Domain: Bacteria

Phylum: Proteobacteria

Class: Gammaproteobacteria

Order: Methylococcales

Family: Methylococcaceae

Species

Genus: Methylococcus

Species: capsulatus

Description and significance

Methylococcus capsulatus is a methylotrophic “Gram-negative” bacterium with coccus shape, live in multiple habitats, however, oxygen is a necessity for such cell to survive. Methylococcus capsulatus is also a thermophilic microbe which optically live in the temperature of 45C. Genus Methylococcus is more close related to Euryarchaota than Crenarchaeota. Methylococcus capsulatus is isolated from Methanotrophic bacterium, which serves a unique biological function in earth's environment. Methanotrophic bacteria is able to generate Green House gas, Methane, as an energy source for growth (detail mechanism refer to section, cell structure and metabolism), and contributes to lower the methane level in earth's atmosphere.


Methylococcus capsulatus.jpg(9)

Genome structure

The Complete genome of M. capsulatus (Bath) Genome is consisted with 3,304,697 base pairs along with 63.6% of G,C contents. The total number of CDSs (predicted coding sequence) is 3,120 with the average size of 962 base pairs. The number of rRNA operons (16S-23S-5S) in M. capsulatus (Bath) Genome is 2, the number of tRNA genes is 46 and the number of sRNA genes is 3. 1,766 proteins of known function and role category and 109 proteins of known function but unknown role category were discovered that serves similar function to M. capsulatus (Bath).

The M. capsulatus genome contains 51 known insertion sequence elements from various families, such as 20 elements are found in IS4 family. Majority of such elements are discovered with higher intragenome similarity. This suggests the expansion of these elements, since their introduction into the M. capsulaus genome, repeated cycles of duplication and subsequent deletion, or gene conversion. Twenty elements belonging to the IS4 family of insertion sequences encode a 366-amino-acid transposase with 100% amino acid sequence conservation between copies. One copy (MCA 1197) is found within the soluble methane monooxygenase operon, and this suggesting that this element is highly mobile. Other examples of insertion also included disrupted genes encoding tRNA pseudouridine synthase and an exopolysaccharide export protein.

Cell structure and metabolism

Methanotrophs have attracted considerable interest over the past 20 years because of their potential in producing bulk chemicals and single-cell protein and for use in biotransformation. Methanotrophs are unique in that they only grow on methane, although some will also grow on methanol. Methanotrophs are also able to metabolize or co-metabolize xenobiotic compounds, including chlorinated solvents such as trichloroethylene, and hence have potential as bioremediation tools.

There are various metabolic pathways in Methylococcus capsulatus, including the methane oxidation pathway, mechanisms for carbon fixation, and nitrogen fixation, which will be discussed later in this section.

Methane oxidation pathway: Methanotrophs are unique in their possession of methane monooxygenases (MMOs), which catalyze the first step of methane oxidation. M. capsulatus is known to generate both a particulate membrane-bound form, pMMO, and a soluble form, sMMO, and these two enzymes have been well studied because their ability to perform methane oxidation.

Carbon cycle: Carbon cycle is a process of turning the atmospheric carbon dioxide produced from combustion and respiration of all aerobes into anaerobic sediments via photo-and chemoautotrophy. Later, methanogens will generate methane from such organism. With the presence of heat and pressure, petroleum, coal, and peat can also be produced.

Nitrogen fixation: M. capsulatus is able to fix atmospheric nitrogen, conferring an advantage in environments where fixed nitrogen is limiting, and the structural genes for nitrogenase,nifH, nifD, and nifK, were previously shown to be contiguous, as they are in other nitrogen fixers. This region include the genes nifE, nifN, and nifX, which are involved in synthesis of the nitrogenase iron-molybdenum cofactor; this organization has been found in Chlorobium tepidum and some nitrogen-fixing methanogenic Archaea. Two 2Fe-2S ferredoxins and genes identified as conserved hypotheticals are interspersed with the nif genes in the same orientation. The conserved hypothetical genes share the highest sequence similarity with genes from other organisms capable of nitrogen fixation, suggesting that they also have a role in this process.

Ecology

The genome sequence of Methylococcus capsulatus was found useful to study “methane-fixing symboints,” because majority of such organisms are usually discovered inside of live-animals and cannot be grown on pure culture. Inherited the characteristic of Methanotrophs, M. Capsulatus contributes to the earth's ecosystem greatly by consuming methane, a product derived from chemical process of landfills and in the guts of ruminant livestock and also by many oil and gas processing plants.In recent years, environmental scientists have shown increasing interest in methanotrophs because their use of methane as a sole source of carbon and energy could possibly be harnessed to play an important role in efforts to reduce methane emissions that are generated by biological sources.

Pathology

The research of disease cause by Methylococcus capsulatus is still in discovering.

Application to Biotechnology

Application to Biotechnology Does this organism produce any useful compounds or enzymes? What are they and how are they used? Methanotrophs produce an enzyme called methane monooxygenase (pMMO) that is not highly specific and can degrade TCE (trichloroethylene) and other compounds in addition to methane. Such enzyme are usually present in a small amount, to obtain an appropriate amount of this organism, the energy source, methane was pumped into the contaminated soils. As a necessity to perform hydrocarbon oxidation, oxygen was also pumped into soil for pMMO generation. One advantage for such process is that its reversible, hence, along with the absence of methane, methanotroph will return to its natural level.

Methylococcus capculatus is perhaps the best studied and most useful methanotroph in the present microbiology world. pMMO is a membrane bound enzyme that can be purified from Methylococcus capculatus. This enzyme, as mentioned earlier, catalyzes the chemical process of oxidizing methane to methanol in methanotrophs, however, more surprising facts was found that enzyme pMMO is a dimer with both mononuclear copper and a copper-containing cluster. The purified enzyme, pMMO has a molecular mass of nearly 200 kDa along with an α2β2γ2 polypeptide arrangement. Each 200kDa were discovered to have approximately 4.8 copper ions and 1.5 iron ions. This experiment could only be done with great amount of pMMO enzyme, therefore, tremendous quantity of methane was conserved on agar plates to cultivate such enzyme. From the use of Electron paramagnetic resonance spectroscopic parameters corressponding to 40 to 60% of the total copper are consisted of a mononuclear type 2 copper site. X-ray absorption indicate that purified pMMO is a mixture of Cu(I) and Cu(II) oxidation states. Finally, this experiment leads to a result showing the x-ray absorption fine structure data are best fit with oxygen/nitrogen ligands with a 2.57A copper to copper interaction, proving for a copper-containing cluster in enzyme pMMO.

Current Research

Arch Microbiol. 2005 Nov 26; :1-16 16311759   	

Analysing the outer membrane subproteome of Methylococcus capsulatus (Bath) using proteomics and novel biocomputing tools. Frode Berven , Odd Karlsen , Anne Straume , Kristian Flikka , J Murrell , Anne Fjellbirkeland , Johan Lillehaug , Ingvar Eidhammer , Harald Jensen High-resolution two-dimensional gel electrophoresis and mass spectrometry has been used to identify the outer membrane (OM) subproteome of the Gram-negative bacterium Methylococcus capsulatus (Bath). Twenty-eight unique polypeptide sequences were identified from protein samples enriched in OMs. Only six of these polypeptides had previously been identified. The predictions from novel bioinformatic methods predicting beta-barrel outer membrane proteins (OMPs) and OM lipoproteins were compared to proteins identified experimentally. BOMP ( http://www.bioinfo.no/tools/bomp ) predicted 43 beta-barrel OMPs (1.45%) from the 2,959 annotated open reading frames. This was a lower percentage than predicted from other Gram-negative proteomes (1.8-3%). More than half of the predicted BOMPs in M. capsulatus were annotated as (conserved) hypothetical proteins with significant similarity to very few sequences in Swiss-Prot or TrEMBL. The experimental data and the computer predictions indicated that the protein composition of the M. capsulatus OM subproteome was different from that of other Gram-negative bacteria studied in a similar manner. A new program, Lipo, was developed that can analyse entire predicted proteomes and give a list of recognised lipoproteins categorised according to their lipo-box similarity to known Gram-negative lipoproteins ( http://www.bioinfo.no/tools/lipo ). This report is the first using a proteomics and bioinformatics approach to identify the OM subproteome of an obligate methanotroph.

Reference

1.Naomi Ward,1,2 Qivind Larsen,3 James Sakwa,1 Live Bruseth,4 Hoda Khouri,1 A. Scott Durkin,1 George Dimitrov,1 Lingxia Jiang,1 David Scanlan,1 Katherine H Kang,1 Matt Lewis,1 Karen E Nelson,1 Barbara Methé,1 Martin Wu,1 John F Heidelberg,1 Ian T Paulsen,1,5 Derrick Fouts,1 Jacques Ravel,1 Hervé Tettelin,1 Qinghu Ren,1 Tim Read,1 Robert T DeBoy,1 Rekha Seshadri,1 Steven L Salzberg,1,9 Harald B Jensen,4 Nils Kåre Birkeland,3 William C Nelson,1 Robert J Dodson,1 Svenn H Grindhaug,7 Ingeborg Holt,6 Ingvar Eidhammer,7 Inge Jonasen,7 Susan Vanaken,1 Terry Utterback,1 Tamara V Feldblyum,1 Claire M Fraser,1,8 Johan R Lillehaug,4 and Jonathan A Eisen. “Genomic Insights into Methanotrophy: The Complete Genome Sequence of Methylococcus capsulatus (Bath) ” pp. 358- 418 2004 October 2nd

2.Brock, T. D Methylococcus capsulatus is a methane-oxidising bacterium that has great potential in bioremediation Vol. 5 pp.9-33. June 1st 2002. (2)

3.Raquel L. Lieberman, Deepak, Shrestha, Peter E. Doan, Brian M. Hoffman, Timothy L. Stemmler and Amy C. Rosenzweig. “Purified particulate methane monooxygenase from ”Methylococcus capsulatus (Bath) is a dimer with both mononuclear copper and a copper-containing cluster” Vol. 100 pp. 3820-3825 April 1, 2003. (3)

4.Kylie J. Walters, George T. Gassner, Stephen J, Lippard, Gerhard Wager. “Structure of the soluble methane monooxygenase regulatory protein B” Vol. 96 pp. 7877-7882, July 1999(4)

5.Ilker Uz, M. E. Rasche, T. Townsend, A.V. Ogram, A. S. Lindner. “Characterization of methanogenic and methanotrophic assemblages in landfill samples” pp. S202-S205 November 2003 (5)

6.J.B Yavitt, D.M. Downey, G.E.Lang, A.J.Sexston. “Methane consumption in Two Temperate Forest Soils” Vol. 9 pp.39-52, Jan 1990 (6)

7.Martin Bender, Ralf Conrad. “Microbial Oxidation of Methane, Ammonium and Carbon Monoxide and Turnover of Nitrous Oxide and Nitric Oxide in Soils”Vol. 27. pp97-112, 1994 (7)

8.Govorukhina, N.I., Kletsova, L.V., Tsygankov, Yu.D. Trotsenko, Yu.A., and Netrusov, A.I. "Characteristics of a new obligate methylotroph." Mikrobiologiya (1987) 56:849-854 http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=414&lvl=3&lin=f&keep=1&srchmode=1&unlock(8)

9.DOE-Public, http://www.ncbi.nlm.nih.gov/sites/entrez?db=genomeprj&cmd=Retrieve&dopt=Overview&list_uids=21 (9)

10.Moselio Schaechter, John L. Ingraham, Frederic C. Neidhardt. “Microbe” pp.207-208, 2006(10)

11.Moselio Schaechter, John L. Ingraham, Frederic C. Neidhardt. “Microbe” pp.360-362, 2006(11)

12.Moselio Schaechter, John L. Ingraham, Frederic C. Neidhardt. “Microbe” pp.469-470, 2006(12)