Aquifex aeolicus: Difference between revisions

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A. aeolicus was originally isolated by R. Huber and K.O. Stetter in the Aeolic Islands north of Sicily near underwater volcanic vents. A. aeolicus forms cell conglomerations consisting of up to 100 individual cells. It is motile, and possesses monopolar polytrichous flagella. Its chemotaxis system remains as yet unidentified, though because it is an obligate chemoautotroph and hyperthermophile, A. aeolicus may respond to changes in concentration of CO2, H2 or O2 and temperature (1).
A. aeolicus was originally isolated by R. Huber and K.O. Stetter in the Aeolic Islands north of Sicily near underwater volcanic vents. A. aeolicus forms cell conglomerations consisting of up to 100 individual cells. It is motile, and possesses monopolar polytrichous flagella. Its chemotaxis system remains as yet unidentified, though because it is an obligate chemoautotroph and hyperthermophile, A. aeolicus may respond to changes in concentration of CO2, H2 or O2 and temperature (1).


[[Image:{Aquifex aeolicus}|{right}|thumb|Aquifex aeolicus. © K.O. Stetter & Reinhard Rachel, University of Regensburg.]]
[[Image:{Aquifex_aeolicus_budding.jpeg}|{right}|thumb|Aquifex aeolicus. © K.O. Stetter & Reinhard Rachel, University of Regensburg.]]


==Genome structure==
==Genome structure==

Revision as of 18:17, 5 June 2007

A Microbial Biorealm page on the genus Aquifex aeolicus

Classification

Higher order taxa

ABacteria; Aquificae; Aquificae (class); Aquificales; Aquificaceae

Species

Aquifex aeolicus

NCBI: Taxonomy

Description and significance

Aquifex aeolicus is a hemolithotrophic thermophile bacterium that grows best at 95 degrees Celsius. It can be found near underwater volcanoes and is hyperthermophilic eubacterium (6). “It can grow on hydrogen, oxygen, carbon dioxide, and mineral salts” (1). It is rod-shaped, about two to six micrometers long and has a diameter of half a micrometer.

Aquifex aeolicus is a microaerophilic aerobe, and the byproduct of its respiration is water. Oxygen is the final electron acceptor of its respiration, and this “is allowed by the presence of a complex respiratory apparatus.” Aquifex pyrophilus can grow in environments with levels of oxygen as low as 7.5 ppm (1).

A. aeolicus was originally isolated by R. Huber and K.O. Stetter in the Aeolic Islands north of Sicily near underwater volcanic vents. A. aeolicus forms cell conglomerations consisting of up to 100 individual cells. It is motile, and possesses monopolar polytrichous flagella. Its chemotaxis system remains as yet unidentified, though because it is an obligate chemoautotroph and hyperthermophile, A. aeolicus may respond to changes in concentration of CO2, H2 or O2 and temperature (1).

[[Image:{Aquifex_aeolicus_budding.jpeg}|{right}|thumb|Aquifex aeolicus. © K.O. Stetter & Reinhard Rachel, University of Regensburg.]]

Genome structure

The genome of Aquifex aeolicus is about the third of the size of E. Coli’s with 1,551,335 base pairs (1). Genomic redundancy is calculated to be 4.83 (Deckert et al. 1998). It shows that 16% of its genes originated from Archea. It is one of the earliest diverging microbes in the Bacteria Domain. A. aeolicus has one DNA molecule, a circular chromosome. It has 43.47% G-C base pairing and 1778 genes, of which 97.18% (1728) code for proteins (2). “Many genes that are functionally grouped within operons in other organisms, such as the tryptophan or histidine biosynthesis pathways, are found dispersed throughout the A. aeolicus genome or appear in novel operons…A. aeolicus is extreme in that no two amino acid biosynthetic genes are found in the same operon. In contrast, genes required for electron transport, hydrogenase subunits, transport systems, ribosomal subunits, and flagella are often in functionally related operons” (1).

A single extrachromosomal element (ECE) is present in A. aeolicus. It has more redundancy than the chromosome, and sequencing shows great redundancy between the ECE and chromosome, suggesting genetic exchange between the two (1).

Cell structure and metabolism

A. aeolicus is hemolithotrophic, meaning it uses an inorganic carbon source for biosynthesis and an inorganic chemical energy source. It is autotrophic, and so it fixes CO2. It is does not form spores, is gram-negative and has a rod shape. A. aeolicus is about 2.0-6.0 micrometers in length and a diameter of 0.4-0.5 micrometers. “The enzymes this organism uses for aerobic respiration are similar to the enzymes found in other aerobic bacteria.” A. aeolicus oxidizes hydrogen gas, and the final electron acceptor is oxygen in this process. The final product of its respiration is water, Aquifex meaning “water-maker” (1). However, Aquifex can reduce and fix nitrogen and sulfur as well as hydrogen, and, in sulfur and thiosulfate metabolism, producing sulfuric acid and H2S (8). However, A. aeolicus has not been shown to grow anaerobically on nitrogen like Aquifex pyrophilus (1).

“Aquifex aeolicus is a microaerophilic, hydrogen-oxidizing, hyperthermophilic bacterium containing three [NiFe] hydrogenases...The Aquifex hydrogenases are thermostable and tolerant to oxygen. A cellular function for the three hydrogenases has been proposed. The two membrane-bound periplasmic hydrogenases may function in energy conservation, whereas the soluble cytoplasmic hydrogenase is probably involved in the CO2 fixation pathway" (7).

A. aeolicus forms cell conglomerations consisting of up to 100 individual cells. It is motile, and possesses monopolar polytrichous flagella. Its chemotaxis system remains as yet unidentified, though because it is an obligate chemoautotroph and hyperthermophile, A. aeolicus may respond to changes in concentration of CO2, H2 or O2 and temperature (1).

Ecology

Aquifex aeolicus grow in extremely hot temperatures, such as near volcanoes and hot springs. It has been isolated in hot springs in Yellowstone National Park. It grows optimally at 80 degrees Celsius, but can grow in temperatures up to 95 degrees Celsius (1). It is microaerophilic, and Aquifex needs only 7.5 ppm oxygen for respiration. A. aeolicus can grow on hydrogen, oxygen, carbon dioxide, and mineral salts. Aquifex species generally form large cell aggregates, which can be comprised of up to 100 individual cells (1).

Pathology

There is no known pathogen among different strains of Aquifex aeolicus.

Application to Biotechnology

A. aeolicus may have many applications to the biotechnological field. It is unique in its resistance to heat and oxygen. This also would make it useful for improving industrial processes. “Aquifex aeolicus is a hyper-thermophilic eubacterium, which probably diverged at the earliest period from the other bacteria on the evolution of life. Therefore, analyses of RNA modification enzymes of this bacterium may supply important information in relation to the establishment of the early protein synthesis" (6).

“A. aeolicus hydrogenases are good candidates for biotechnological uses due to their high stability against oxygen and high temperature” (7).

Current Research

A gene in Aquifex aeolicus, AAC07157, encodes for a multicopper oxidase enzyme, McoA that contributes to heat stability. Spectroscopic and biochemical characteristics identify this enzyme as a multicopper oxidase. Because of its higher specificity (in k(cat(/K(m)) for copper and iron ions than for aromatic substrates, McoA is a metallo-oxidase. The gene is located in the genome as part of a region regarded to be a determinant of copper resistance. McoA is thought to contribute to copper and iron homeostasis in A. aeolicus because it contains a methionine rich region, similar to other copper homeostasis proteins. Mutant tests for that region provide evidence for that (3).

Data indicates that ATP binding promotes a conformational change that stabilizes complexes between enhancer binding protein (EBP) and sigma54, a bacterial RNA polymerase that initiates transcription. Binding of ATP analogs stabilize the oligomeric form of ATPase and its binding to sigma54. Subsequent hydrolysis and phosphate release drive the conformational change needed to open the polymerase/promoter complex (4).

A transporter homologue, the Aquifex aeolicus leucine transporter (LeuT), was used in a study to “evaluate the applicability of a simple and computationally attractive membrane system.” This is to create a “homology model of the human serotonin transporter (hSERT) in a membrane environment and in complex with either the natural substrate 5-HT or the selective serotonin reuptake inhibitor escitalopram.” Key interactions identified in the x-ray structure and how the fluctuations in LeuT from this homology model are in good agreement with crystallographic B factors indicated that this homology model is suitable for studying the hSERT complexed with 5-HT or escitalopram. The homology model showed that only relatively small fluctuations are observed in the ligand-binding cleft for these transporter complexes. Also, ligand recognition depends on specific

References

1) Deckert G, Warren PV, Gaasterland T, Young WG, Lenox AL, Graham DE, Overbeek R, Snead MA, Keller M, Aujay M, Huber R, Feldman RA, Short JM, Olsen GJ, Swanson RV. “The complete genome of the hyperthermophilic bacterium Aquifex aeolicus.” Nature. 1998 Mar 26. p. 392(6674):353-8.

2) Aquifex aeolicus VF5 Genome Page

3) Fernandes AT, Soares CM, Pereira MM, Huber R, Grass G, Martins LO. FEBS J. 2007 Apr 19; [Epub ahead of print]

4) Chen B, Doucleff M, Wemmer DE, De Carlo S, Huang HH, Nogales E, Hoover TR, Kondrashkina E, Guo L, Nixon BT. Structure. 2007 April. p.15(4):429-440.

5) Jorgensen AM, Tagmose L, Jorgensen AM, Bogeso KP, Peters GH. ChemMedChem. 2007 Apr 13; [Epub ahead of print]

6) Takako Awai , Toru Takehara , Hiroshi Takeda , Hiroyuki Hori. Nucleic Acids Symp Ser (Oxf). 2005. p. (49):303-304 17150754

7) Guiral M, Aubert C, Giudici-Orticoni MT. Hydrogen metabolism in the hyperthermophilic bacterium Aquifex aeolicus. Biochem Soc Trans. 2005 Feb. p. 33(Pt 1):22-4.

8) Systems Biology Inc. http://www.systems-biology.org/001/kegg/aae.html.


[Sample reference] Takai, K., Sugai, A., Itoh, T., and Horikoshi, K. "Palaeococcus ferrophilus gen. nov., sp. nov., a barophilic, hyperthermophilic archaeon from a deep-sea hydrothermal vent chimney". International Journal of Systematic and Evolutionary Microbiology. 2000. Volume 50. p. 489-500.

Edited by student of Rachel Larsen and Kit Pogliano