Biology:Cupriavidus necator

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Short description: Species of bacterium


Cupriavidus necator
Cupriavidus necator.jpg
Scientific classification
Domain:
Bacteria
Phylum:
Pseudomonadota
Class:
Betaproteobacteria
Order:
Burkholderiales
Family:
Burkholderiaceae
Genus:
Cupriavidus
Species:
C. necator
Binomial name
Cupriavidus necator
(Davis 1969) Yabuuchi et al. 1996
Synonyms

Ralstonia eutropha

Cupriavidus necator is a Gram-negative soil bacterium of the class Betaproteobacteria.[1]

Taxonomy

Cupriavidus necator has gone through a series of name changes. In the first half of the 20th century, many micro-organisms were isolated for their ability to use hydrogen. Hydrogen-metabolizing chemolithotrophic organisms were clustered into the group Hydrogenomonas.[2] C. necator 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] H. eutrophus was then 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 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

Cupriavidus necator 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] C. necator can perform aerobic or anaerobic respiration by denitrification of nitrate and/or nitrite to nitrogen gas.[10] When growing under autotrophic conditions, C. necator fixes carbon through the reductive 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 C. necator, the genomes of two strains have been sequenced.[9][13]

Hydrogenases

Cupriavidus necator can use hydrogen gas as a source of energy when growing under autotrophic conditions. It contains four different hydrogenases that have [Ni-Fe] active sites and all perform this reaction:[14][15]

H2 [math]\displaystyle{ \rightleftharpoons }[/math] 2H+ + 2e−

The hydrogenases of C. necator 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.[16] However, the hydrogenases of C. necator are different from typical [Ni-Fe] hydrogenases because they are tolerant to oxygen and are not inhibited by CO.[14] While the four 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, soluble hydrogenase and actinobacterial hydrogenase in C. necator 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.[17] 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.[18]

Membrane-bound hydrogenase

The membrane-bound hydrogenase (MBH) is linked to the respiratory chain through a specific cytochrome b-related protein in C. necator.[19] 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.[19] The MBH in C. necator is not inhibited by CO and is tolerant to oxygen.[20]

NAD+-reducing hydrogenase

The NAD+-reducing hydrogenase (soluble hydrogenase, SH) creates a NADH-reducing equivalence by oxidizing hydrogen gas. The SH is a heterohexameric protein[21] with two subunits making up the large and small subunits of the [Ni-Fe] hydrogenase and the other two subunits comprising a reductase module similar to the one of Complex I.[22] The [Ni-Fe] active site oxidized hydrogen gas which transfers electrons to a FMN-a cofactor, then to a [Fe-S] cluster relay of the small hydrogenase subunit and the reductase module, then to another FMN-b cofactor and finally to NAD+.[14] The reducing equivalences are then used for fixing carbon dioxide when C. necator is growing autotrophically.

The active site of the SH of C. necator H16 has been extensively studied because C. necator 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 C. necator 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 low spin +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.[20]

C. necator oxygen-tolerant SH

The SH in C. necator 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 recent study showed that oxygen tolerance as implemented in the SH is based on a continuous catalytically driven detoxification of O
2 [Ref missing].  The genes encoding this SH can be up-regulated under heterotrophic growth condition using glycerol in the growth media [28] and this enables aerobic production and purification of the same enzyme.[29]

Applications

The oxygen-tolerant hydrogenases of C. necator have been studied for diverse purposes. C. necator 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.[30][31]

Electrolysis of water is one way of creating oxygenic atmosphere in space and C. necator was investigated to recycle the hydrogen produced during this process.[32]

Oxygen-tolerant hydrogenases are being used to investigate biofuels. Hydrogenases from C. necator have been used to coat electrode surfaces to create hydrogen fuel cells tolerant to oxygen and carbon monoxide[20] and to design hydrogen-producing light complexes.[33] In addition, the hydrogenases from C. necator have been used to create hydrogen sensors.[34] Genetically modified C. necator can produce isobutanol from CO2 that can directly substitute or blend with gasoline. The organism emits the isobutanol without having to be destroyed to obtain it.[35]

Industrial uses

Researchers at UCLA have genetically modified a strain of the species C. necator (formerly known as R. eutropha H16) to produce isobutanol from CO2 feedstock using electricity produced by a solar cell. The project, funded by the U.S. Dept. of Energy, is a potential high energy-density electrofuel that could use existing infrastructure to replace oil as a transportation fuel.[36]

Chemical and biomolecular engineers at Korea Advanced Institute of Science and Technology has presented a scalable way to convert CO
2 in the air into a polyester by means of the C. necator.[37]

References

  1. ↑ 1.0 1.1 Yabuuchi et al. (1995). "Transfer of two Burkholderia and an Alcaligenes species to Ralstonia gen. nov.: proposal of Ralstonia pickettii (Ralston, Palleroni and Doudoroff 1973) comb. nov., Ralstonia solanacearum (Smith 1896) comb. nov. and Ralstonia eutropha (Davis 1969) comb. nov". Microbiol Immunol 39 (11): 897–904. doi:10.1111/j.1348-0421.1995.tb03275.x. PMID 8657018. 
  2. ↑ 2.0 2.1 Davis, D.; Doudoroff, M.; Stanier, R. (1969). "Proposal to reject the genus Hydrogenomonas: Taxonomic implications". Int J Syst Bacteriol 19 (4): 375–390. doi:10.1099/00207713-19-4-375. 
  3. ↑ 3.0 3.1 Bowien, B.; Schlegel, H. (1981). "Physiology and biochemistry of aerobic hydrogen-oxidizing bacteria". Annu. Rev. Microbiol. 35: 405–452. doi:10.1146/annurev.mi.35.100181.002201. PMID 6271040. 
  4. ↑ Repaske, R. (1981). "Nutritional Requirements forHydrogenomonas eutropha". J. Bacteriol. 83 (2): 418–422. doi:10.1128/JB.83.2.418-422.1962. PMID 14491520. 
  5. ↑ Wilde, E. (1962). "Untersuchungen über Wachstum und Speicherstoffsynthese von Hydrogenomonas eutropha". Archiv für Mikrobiologie 43 (2): 109–137. doi:10.1007/bf00406429. 
  6. ↑ Davis, D.; Stanier, R.; Doudoroff, M. (1970). "Taxonomic Studies on Some Gram Negative Polarly Flagellated "Hydrogen Bacteria" and Related Species". Arch. Mikrobiol. 70 (1): 1–13. doi:10.1007/BF00691056. PMID 4987616. 
  7. ↑ Vaneechoutte, M.; Kampfer, P.; De Baere, T.; Falsen, E.; Verschraegen, G. (2004). "Wautersia gen. nov., a novel genus accommodating the phylogenetic lineage including Ralstonia eutropha and related species, and proposal of Ralstonia [Pseudomonas] syzygii(Roberts et al. 1990) comb. nov". International Journal of Systematic and Evolutionary Microbiology 54 (Pt 2): 317–327. doi:10.1099/ijs.0.02754-0. PMID 15023939. 
  8. ↑ Vandamme, P.; Coenye, T. (2004). "Taxonomy of the genus Cupriavidus: a tale of lost and found". International Journal of Systematic and Evolutionary Microbiology 54 (6): 2285–2289. doi:10.1099/ijs.0.63247-0. PMID 15545472. 
  9. ↑ 9.0 9.1 Pohlmann, A.; Fricke, W.; Reinecke, F.; Kusian, B.; Liesegang, H.; Cramm, R.; Eitinger, T.; Ewering, C. et al. (2006). "Genome sequence of the bioplastic-producing Knallgas bacterium Ralstonia eutropha H16". Nature Biotechnology 24 (10): 1257–1262. doi:10.1038/nbt1244. PMID 16964242. 
  10. ↑ Cramm, R. (2009). "Genomic View of Energy Metabolism in Ralstonia eutropha H16". J Mol Microbiol Biotechnol 16 (1–2): 38–52. doi:10.1159/000142893. PMID 18957861. 
  11. ↑ Bowien, B.; Kusian, B. (2002). "Genetics and control of CO
    2     assimilation in the chemoautotroph Ralstonia eutropha". Arch Microbiol 178 (2): 85–93. doi:10.1007/s00203-002-0441-3. PMID 12115053.     
  12. ↑ Spiekermann, P.; Rehm, B.; Kalscheuer, R.; Baumeister, D.; Steinbuchel A. (1999). "A sensitive, viable-colony staining method using Nile red for direct screening of bacteria that accumulate polyhydroxyalkanoic acids and other lipid storage compounds". Arch Microbiol 171 (2): 73–80. doi:10.1007/s002030050681. PMID 9914303. 
  13. ↑ Lykidis, A.; Perez-Pantoja, D.; Ledger, T.; Marvomatis, K.; Anderson, I.; Ivanova, N.; Hooper, S.; Lapidus, A. et al. (2010). Ahmed, Niyaz. ed. "The Complete Multipartite Genome Sequence of Cupriavidus necator JMP134, a Versatile Pollutant Degrader". PLOS ONE 5 (3): 1–13. doi:10.1371/journal.pone.0009729. PMID 20339589. 
  14. ↑ 14.0 14.1 14.2 14.3 14.4 14.5 14.6 Burgdorf, T.; Buhrke, T.; van der Linden, E.; Jones, A.; Albracht, S.; Friedrich, B. (2005). "[NiFe]-Hydrogenases of Ralstonia eutropha H16: Modular Enzymes for Oxygen-Tolerant Biological Hydrogen Oxidation". J Mol Microbiol Biotechnol 10 (2–4): 181–196. doi:10.1159/000091564. PMID 16645314. 
  15. ↑ Schäfer, Caspar; Friedrich, Bärbel; Lenz, Oliver (1 September 2013). "Novel, Oxygen-Insensitive Group 5 [NiFe-Hydrogenase in Ralstonia eutropha"]. Applied and Environmental Microbiology 79 (17): 5137–5145. doi:10.1128/AEM.01576-13. PMID 23793632. 
  16. ↑ Schwartz, E.; Friedrich, B. (2006). "The H2-Metabolizing Prokaryotes". Prokaryotes 2: 496–563. doi:10.1007/0-387-30742-7_17. ISBN 978-0-387-25492-0. 
  17. ↑ Lenz, O.; Friedrich, B. (1998). "A novel multicomponent regulatory system mediates H2 sensing in Alcaligenes eutrophus". PNAS 95 (21): 12474–12479. doi:10.1073/pnas.95.21.12474. PMID 9770510. 
  18. ↑ Friedrich, B.; Buhrke, T.; Burgdorf, T. (2005). "A hydrogen-sensing multiprotein complexcontrols aerobic hydrogen metabolism in Ralstonia eutropha". Biochemical Society Transactions 33 (Pt 1): 97–101. doi:10.1042/BST0330097. PMID 15667276. 
  19. ↑ 19.0 19.1 Bernhard, M.; Benelli, B.; Hochkoeppler, A.; Zannoni, D.; Friedrich, B. (1997). "Functional and structural role of the cytochrome b subunit of the membrane-bound hydrogenase complex of Alcaligenes eutrophus H16". Eur. J. Biochem. 248 (1): 179–186. doi:10.1111/j.1432-1033.1997.00179.x. PMID 9310376. 
  20. ↑ 20.0 20.1 20.2 Vincent, K.; Cracknell, J.; Lenz, O.; Zebger, I.; Friedrich, B.; Armstrong, F. (2005). "Electrocatalytic hydrogen oxidation by an enzyme at high carbon monoxide or oxygen levels". PNAS 102 (47): 16951–16954. doi:10.1073/pnas.0504499102. PMID 16260746. 
  21. ↑ Schneider, K.; Schlegel, H. (1976). "Purification and properties of soluble hydrogenase from Alcaligenes eutrophus H 16". Biochimica et Biophysica Acta (BBA) - Enzymology 452 (1): 66–80. doi:10.1016/0005-2744(76)90058-9. PMID 186126. 
  22. ↑ Tran-Betcke, A.; Warnecke, U.; Bocker, C.; Zaborosch, C.; Friedrich, B. (1990). "Cloning and Nucleotide Sequences of the Genes for the Subunits of NAD-Reducing Hydrogenase of Alcaligenes eutrophus H16". Journal of Bacteriology 172 (6): 2920–2929. doi:10.1128/jb.172.6.2920-2929.1990. PMID 2188945. 
  23. ↑ 23.0 23.1 23.2 Higuchi, .; Yagi, T.; Yasuoka, N. (1997). "Unusual ligand structure in Ni–Fe active center and an additional Mg site in hydrogenase revealed by high resolution X-ray structure analysis". Structure 5 (12): 1671–1680. doi:10.1016/S0969-2126(97)00313-4. PMID 9438867. 
  24. ↑ 24.0 24.1 Volbeda, A.; Garcin, E.; Piras, C.; de Lacey, A.; Fernandez, V.; Hatchikian, C.; Frey, M.; Fontecilla-Camps, J. (1996). "Structure of the [NiFe] Hydrogenase Active Site: Evidence for Biologically Uncommon Fe Ligands". J. Am. Chem. Soc. 118 (51): 12989–12996. doi:10.1021/ja962270g. 
  25. ↑ Volbeda, A.; Charon, M.; Piras, C.; Hatchikian, C.; Frey, M.; Fontecilla-Camps, J. (1995). "Crystal structure of the nickel-iron hydrogenase from Desulfovibrio gigas". Nature 373 (6515): 580–587. doi:10.1038/373580a0. PMID 7854413. 
  26. ↑ Happe, R.; Roseboom, W.; Pierik, A.; Albracht, S. (1997). "Biological activation of hydrogen". Nature 385 (6612): 126. doi:10.1038/385126a0. PMID 8990114. 
  27. ↑ Schneider, K.; Cammack, R.; Schlegel, G.; Hall, D. (1979). "The iron-sulphur centres of soluble hydrogenase from Alcaligenes eutrophus". Biochimica et Biophysica Acta (BBA) - Protein Structure 578 (2): 445–461. doi:10.1016/0005-2795(79)90175-2. PMID 226163. 
  28. ↑ Jugder, Bat-Erdene; Chen, Zhiliang; Ping, Darren Tan Tek; Lebhar, Helene; Welch, Jeffrey; Marquis, Christopher P. (2015-03-25). "An analysis of the changes in soluble hydrogenase and global gene expression in Cupriavidus necator (Ralstonia eutropha) H16 grown in heterotrophic diauxic batch culture". Microbial Cell Factories 14 (1): 42. doi:10.1186/s12934-015-0226-4. ISSN 1475-2859. PMID 25880663. 
  29. ↑ Jugder, Bat-Erdene; Lebhar, Helene; Aguey-Zinsou, Kondo-Francois; Marquis, Christopher P. (2016). "Production and purification of a soluble hydrogenase from Ralstonia eutropha H16 for potential hydrogen fuel cell applications". MethodsX 3: 242–250. doi:10.1016/j.mex.2016.03.005. ISSN 2215-0161. PMID 27077052. 
  30. ↑ Repaske, R.; Mayer, R. (1976). "Dense Autotrophic Cultures of Alcaligenes eutrophus". Applied and Environmental Microbiology 32 (4): 592–597. doi:10.1128/AEM.32.4.592-597.1976. PMID 10840. 
  31. ↑ Ammann, E.; Reed, L. (1967). "Metabolism of nitrogen compounds by hydrogenomonas eutropha". Biochim. Biophys. Acta 141 (1): 135–143. doi:10.1016/0304-4165(67)90252-8. PMID 4963807. 
  32. ↑ Foster, J.; Litchfield, J. (1964). "A Continuous Culture Apparatus for the Microbial Utilization of Hydrogen Produced by Electrolysis of Water in Closed-Cycle Space Systems". Biotechnology and Bioengineering 6 (4): 441–456. doi:10.1002/bit.260060406. 
  33. ↑ Ihara, M.; Mishihara, H.; Yoon, K.; Lenz, O.; Friedrich, B.; Nakamoto, H.; Kojima, K.; Honoma, D. et al. (2006). "Light-driven Hydrogen Production by a Hybrid Complex of a [NiFe]-Hydrogenase and the Cyanobacterial Photosystem I". Photochemistry and Photobiology 82 (3): 676–682. doi:10.1562/2006-01-16-RA-778. PMID 16542111. 
  34. ↑ Lutz, B.; Fan, H.; Burgdorf, T.; Friedrich, B. (2005). "Hydrogen Sensing by Enzyme-Catalyzed Electrochemical Detection". Anal. Chem. 77 (15): 4969–4975. doi:10.1021/ac050313i. PMID 16053311. 
  35. ↑ "Teaching a microbe to make fuel - MIT News Office". Web.mit.edu. http://web.mit.edu/newsoffice/2012/genetically-modified-organism-can-turn-carbon-dioxide-into-fuel-0821.html. 
  36. ↑ Li, H.; Opgenorth, P. H.; Wernick, D. G.; Rogers, S.; Wu, T.-Y.; Higashide, W.; Malati, P.; Huo, Y.-X. et al. (2012). "Integrated Electromicrobial Conversion of CO
    2     to Higher Alcohols". Science 335 (6076): 1596. doi:10.1126/science.1217643. PMID 22461604.     
  37. ↑ "Using bacteria to convert CO
    2     in the air into a polyester"    . phys.org. doi:10.1073/pnas.2221438120. https://phys.org/news/2023-03-bacteria-co2-air-polyester.html.     

External links

Wikidata ☰ Q148753 entry



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