| Ralstonia eutropha |
| Scientific classification |
| Kingdom: |
Bacteria |
| Phylum: |
Proteobacteria |
| Class: |
Beta Proteobacteria |
| Order: |
Burkholderiales |
| Family: |
Ralstoniaceae |
| Genus: |
Ralstonia |
| Binomial name |
Ralstonia eutropha
(Davis 1969) Yabuuchi et al. 1996 |
Ralstonia eutropha is a Gram-negative soil bacterium of the Betaproteobacteria class.[1]
Contents
- 1 Taxonomy
- 2 Metabolism
- 3 Hydrogenases
- 3.1 Regulatory hydrogenase
- 3.2 Membrane-bound hydrogenase
- 3.3 Soluble hydrogenase
- 3.3.1 Soluble hydrogenase active site
- 3.3.1.1 Typical anaerobic [Ni-Fe] hydrogenases
- 3.3.1.2 R. eutropha oxygen-tolerant soluble hydrogenase
- 3.4 Applications
- 4 References
Taxonomy
R. eutropha has gone through a series of name changes. In the first half of the 20th century, many microorganisms were isolated for their ability to use hydrogen. Hydrogen-metabolizing chemolithotrophic organisms were clustered into the group Hydrogenomonas.[2] R. eutropha was originally named Hydrogenomonas eutrophus because it fell under the Hydrogenomonas classification and was “well nourished and robust”.[3] Some of the original H. eutrophus cultures isolated were by Bovell and Wilde.[4][5] After characterizing cell morphology, metabolism and GC content, the Hydrogenomonas nomenclature was disbanded because it comprised many species of microorganisms.[2] R. eutropha at this time was renamed Alcaligenes eutropha because it was a micro-organism with degenerated peritrichous flagellation.[3][6] Investigating phenotype, lipid composition, fatty acid composition and 16S rRNA analysis, A. eutropha was found to belong to the genus Ralstonia and named Ralstonia eutropha.[1] Upon further study of the Ralstonia genus, Ralstonia was found to comprise two phenotypically distinct clusters. The new genus Wautersia was created from one of these clusters which included R. eutropha. In turn R. eutropha was renamed Wautersia eutropha.[7] Looking at DNA-DNA hybridization and phenotype comparison with Cupriavidus necator, W. eutropha was found to be the same species as previously described C. necator. Because C. necator was named in 1987 far before the name change to R. eutropha and W. eutropha, the name C. necator was assigned to R. eutropha according to Rule 23a of the International Code of Nomenclature of Bacteria.[8]
Metabolism
R. eutropha is a hydrogen-oxidizing bacterium (“knallgas” bacterium) capable of growing at the interface of anaerobic and aerobic environments. It can easily adapt between heterotrophic and autotrophic lifestyles. Both organic compounds and hydrogen can be used as a source of energy[9] R. eutropha can perform aerobic or anaerobic respiration by denitrification of nitrate and/or nitrite to nitrogen gas.[10] When growing under autotrophic conditions, R. eutropha fixes carbon through the pentose phosphate pathway.[11] It is known to produce and sequester polyhydroxyalkanoate (PHA) plastics when exposed to excess amounts of sugar substrate. PHA can accumulate to levels around 90% of the cell's dry weight.[12] To better characterize the lifestyle of R. eutropha, the genomes of two strains have been sequenced.[9][13]
Hydrogenases
R. eutropha can use hydrogen gas as a source of energy when growing under autotrophic conditions. It contains three different hydrogenases that have [Ni-Fe] active sites and all perform this reaction:[14]
- H2 2H+ + 2e−
The hydrogenases of R. eutropha are like other typical [Ni-Fe] hydrogenases because they are made up of a large and a small subunit. The large subunit is where the [Ni-Fe] active site resides and the small subunit is composed of [Fe-S] clusters.[15] However, the hydrogenases of R. eutropha are different from typical [Ni-Fe] hydrogenases because they are tolerant to oxygen and are not inhibited by CO.[14] While the three hydrogenases perform the same reaction in the cell, each hydrogenase is linked to a different cellular process. The differences between the regulatory hydrogenase, membrane bound hydrogenase, and soluble hydrogeanse in R. eutropha are described below.
Regulatory hydrogenase
The first hydrogenase is a regulatory hydrogenase (RH) that signals to the cell hydrogen is present. The RH is a protein containing large and small [Ni-Fe] hydrogenase subunits attached to a histidine protein kinase subunit.[16] The hydrogen gas is oxidized at the [Ni-Fe] center in the large subunit and in turn reduces the [Fe-S] clusters in the small subunit. It is unknown whether the electrons are transferred from the [Fe-S] clusters to the protein kinase domain.[14] The histidine protein kinase activates a response regulator. The response regulator is active in the dephosphorylated form. The dephosphorylated response regulator promotes the transcription of the membrane bound hydrogenase and soluble hydrogenase.[17]
Membrane-bound hydrogenase
The membrane-bound hydrogenase (MBH) is linked to the respiratory chain through a specific cytochrome b-related protein in R. eutropha.[18] Hydrogen gas is oxidized at the [Ni-Fe] active site in the large subunit and the electrons are shuttled through the [Fe-S] clusters in the small subunit to the cytochrome b-like protein.[14] The MBH is located on the outer cytoplasmic membrane. It recovers energy for the cell by funneling electrons into the respiratory chain and by increasing the proton gradient.[18] The MBH in R. eutropha is not inhibited by CO and is tolerant to oxygen.[19]
Soluble hydrogenase
The soluble hydrogenase (SH) creates a NADH-reducing equivalence by oxidizing hydrogen gas. The SH is a heterodimer protein[20] with two subunits making up the large and small subunits of the [Ni-Fe] hydrogenase and the other two subunits comprising a protein similar to Complex I (as shown in the accompanying figure).[21] The [Ni-Fe] active site oxidized hydrogen gas which transfers electrons to a FMNa cofactor, then to [Fe-S] clusters of the small hydrogenase subunit, then to another FMNb cofactor and finally to NAD+.[14] The reducing equivalence provide a means for fixing carbon dioxide when R. eutropha is growing autotrophically.[22]
Soluble hydrogenase active site
The active site of the soluble hydrogenase (SH) of R. eutropha H16 has been extensively studied because R. eutropha H16 can be produced in large amounts, can be genetically manipulated, and can be analyzed with spectrographic techniques. However, no crystal structure is currently available for the R. eutropha H16 soluble hydrogenase in the presence of oxygen to determine the interactions of the active site with the rest of the protein.[14]
Typical anaerobic [Ni-Fe] hydrogenases
The [Ni-Fe] hydrogenase from Desulfovibrio vulgaris and D. gigas have similar protein structures to each other and represent typical [Ni-Fe] hydrogenases.[14][23][24][25] The large subunit contains the [Ni-Fe] active site buried deep in the core of the protein and the small subunit contains [Fe-S] clusters. The Ni atom is coordinated to the Desulfovibrio hydrogenase by 4 cysteine ligands. Two of these same cysteine ligands also bridge the Fe of the [Ni-Fe] active site.[23][24] The Fe atom also contains three ligands, one CO and two CN that complete the active site.[26] These additional ligands might contribute to the reactivity or help stabilize the Fe atom in the +2 oxidation state.[23] Typical [NiFe] hydrogenases like those of D. vulgaris and D. gigas are poisoned by oxygen because an oxygen atom binds strongly to the NiFe active site.[19]
R. eutropha oxygen-tolerant soluble hydrogenase
The soluble [Ni-Fe] hydrogenases in R. eutropha are unique for other organisms because it is oxygen tolerant.[27] The active site of the SH has been studied to learn why this protein is tolerant to oxygen. A major difference of the [Ni-Fe] hydrogenases of R. eutropha is it has more coordinating ligands than in typical [Ni-Fe] hydrogenases. Two cysteine ligands bridge the Ni atom and Fe atom of the active site in R. eutropha. Two modified cysteine sulfenate ligands also are predicted to coordinate the Ni atom.[22] An additional CN ligand is added to the Ni atom and removing this CN ligand makes the enzyme susceptible to oxygen. Also, the Fe has an additional CN ligand bound in addition to the two CN ligands and one CO ligand present in typical NiFe hydrogenases (see the above figure for a schematic of the active site).[28] These additional ligands are predicted to help the protein be more oxygen tolerant because it stabilizes the Ni atom in the active, +2 oxidation state.[22]
Applications
The oxygen-tolerant hydrogenases of R. eutropha have been studied for diverse purposes. R. eutropha was studied as an attractive organism to help support life in space. It can fix carbon dioxide as a carbon source, use the urea in urine as a nitrogen source and use hydrogen as an energy source to create dense cultures that could be used as a source of protein.[29][30]
Electrolysis of water is one way of creating oxygenic atmosphere in space and R. eutropha was investigated to recycle the hydrogen produced during this process.[31]
Oxygen-tolerant hydrogenases are being used to investigate biofuels. Hydrogenases from R. eutropha have been used to coat electrode surfaces to create hydrogen fuel cells tolerant to oxygen and carbon monoxide[19] and to design hydrogen-producing light complexes.[32] In addition, the hydrogenases from R. eutropha have been used to create hydrogen sensors.[33] Genetically modified R. eutropha can produce isobutanol from CO
2 that can directly substitute or blend with gasoline. The organism emits the isobutanol without having to be destroyed to obtain it.[34]
References
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