Thermococcus celer

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Thermococcus celer
Scientific classification
Domain: Archaea
Phylum: Euryarchaeota
Class: Thermococci
Order: Thermococcales
Family: Thermococcaceae
Genus: Thermococcus
Species: T. celer
Binomial name
Thermococcus celer

Thermococcus celer is a Gram-negative, spherical shaped archaeon of the genus Thermococcus.[1] The discovery of Thermococcus celer played an important role in re-rooting the tree of life when it was discovered that T. celer was more closely related to methanogenic Archaea than to other phenotypically similar thermophilic species [1] T. celer was the first archaeon discovered to house a circularized genome.[2] Several type strains of T. celer have been identified: Vu13, ATCC 35543, and DSM 2476.[2]

Isolation[edit]

T. celer was discovered by Dr. Wolfram Zillig in 1983.[3] The organism was isolated on the beaches of Vulcano, Italy from a sulfur rich shallow volcanic crater.[3] Original samples were isolated from the depths of the marine holes and inoculated into 10 mL anaerobic tubes.[4] The tubes contained 100 mg of elemental sulfur as well as a solution of 95% N2 and 5% H2S.[4] The pH was subsequently adjusted to a range of 5-6 through the addition of CaCO3.[4] To ensure that no oxygen had permeated the sample, researchers utilized the oxygen indicator resazurin.[4] Growth was achieved by enrichment with Brock’s Sulfolobus medium, which contains elemental sulfur and yeast, both of which are required by T. celer for optimal growth.[3] Following enrichment, the samples were plated onto polyacrylamide gel and then incubated at 85° Celsius in an anaerobic environment.[4] Once colony growth had been observed, the cells were subjected to centrifugation prior to purification in a TA buffer solution (0.05 mol/1 Tris HCL, 0.022 mol/1 NH4Cl, 0.01 mol/1 β-mercaptoethanol).[4]

Taxonomy and Phylogeny[edit]

Following Sanger sequencing of the 16s rRNA, both parsimony and distance matrix analyses were performed to determine the position of T. celer on the tree of life.[1] It was discovered that T. celer is more closely related to the methanogenic archaebacteria than the thermophilic archaebacteria.[1] This discovery resulted in a re-rooting of the archaebacterial tree and subsequently placed T. celer in a clade with the methanogens based upon their close phylogenetic relationship.[1] This placement was further supported following analysis of the organizational genome structure of the both species’ rRNA genes.[1] Both Thermococcus and methanogenic archaebacteria have a tRNA spacer gene located between the 16s rRNA gene and 23s rRNA gene.[1] This spacer gene is not found in any other thermophilic archaebacteria species.[1]

T. celer is related to Pyrococcus woesei, both belonging to the order Thermococcales.[5] Both are strictly anaerobic and sulphur reducing.[5] T. celer also shares a close relationship with Thermococcus litoralis, both belonging to the same genus, however T. celer has shown to be much more sulphur dependent than T. littorals.[5]

T. celer is currently classified as a thermophilic Archaeon.[3] Since the discovery of T. celer, the term archaebacteria has been replaced with Archaea as to reflect the most current phylogenetic relationships discovered between the organisms.[6]

Characterization[edit]

Thermococcus is constructed from two Greek nouns: therme (Greek, feminine noun) meaning heat, and kokkos (Greek, masculine noun) meaning grain or seed.[3] Celer is derived from the Greek, masculine adjective meaning fast, in reference to T. celer's high growth rates.[3]

Morphology[edit]

T. celer is a Gram-negative, spherical organism of approximately 1 μm diameter.[3] Observation using electron microscopy revealed that T. celer utilizes a monopolar polytrichous flagella for movement.[3] During replication, T. celer is condensed to a diploform shape as seen by phase contrast microscopy [3]

The T. celer plasma membrane possesses large amounts of glycerol diether lipids compared to relatively small amounts of diglycerol tetraether lipids.[7] Within glycerol, diether lipids, phytanyl (C20) is the hydrocarbon component and within diglycerol tetraether lipids, biphytanyl (C40) is the hydrocarbon component.[3] The cell wall, or S-layer, of T. celer functions as protection from cell lysis as a result of changes in osmotic gradients.[3] The envelope S-layer consists of glycoprotein subunits arranged into a two-dimensional paracrystalline hexagonal structure.[3] T. celer cell envelope lacks muramic acid, indicating resistance to penicillin and vancomycin.[3]

Metabolism[edit]

T. celer is a strict anaerobe that utilizes organotrophic metabolism.[3] T. celer metabolism utilizes peptides (i.e. from yeast extract, peptone, or tryptone) and proteins (i.e. casein) as a carbon source which are oxidized to carbon dioxide via sulphur respiration.[3] T. celer is unable to use carbohydrates as a carbon source and is considered a sulphur-dependent organism as it depends upon the reduction of sulphur to hydrogen sulfide for optimal growth.[5] Though it is less efficient, T. celer is also able to utilize fermentation.[3] Unlike most prokaryotes, T. celer is able to perform respiration via the Embden–Meyerhof Pathway (glycolysis), though it uses an alternative route.[8]

Ecology[edit]

Characteristic of the hyperthermophilic species, T. celer thrives in extremely hot temperatures.[1] More specifically, T. celer is found only in sulfur rich, shallow volcanic craters of Vulcano, Italy.[3] Temperatures in this specific habitat reach up to 90 °C [3] The maximum temperature at which T. celer can grow at is 93 °C, optimum growth temperature being 88 °C.[3] T. celer grows best at a pH of 5.8, implying that it is mildly acidophilic.[3] Optimal growth is also dependent on the presence of a NaCl concentration of 40 g/L, further demonstrating the high level of adaptation T. celer has evolved for its thermal marine environment.[3]

Genomics[edit]

Construction of a physical map of T. celer Vu13 by way of restriction enzyme fragments revealed a length of 1,890 + 27 kilobases (kb).[2] The molecular ratio of guanine to cytosine bases is approximately 56.6%.[3] This value was determined by averaging both the GC-content acquired via high-performance liquid chromatography and melting point (TM) calculations.[3] T. celer is considered to be one of the slowest evolving archaeon species, indicating that the genome could be used as a model organism for those studying early genome characteristics.[2]

In 1989, T. celer was the first archaeon discovered to house a circularized genome.[2] Genome shape was determined through three separate experiments, all utilizing restriction enzymes.[2] The T. celer genome was digested with restriction enzymes Nhe, Spe, and Xba.[2] Following digestion, hybridization analyses were used to determine genome shape.[2] Probes were synthesized from cloned genes of the 16S rRNA and 23S rRNA.[2] Both Spe and Nhe produced five fragments, all of similar shape and size.[2] Digestion with Xba produced 8 fragments.[2] Using overlap patterns, the shape of the genome was determined to be circular.[2]

Application[edit]

The domain Archaea is currently split into three major groups consisting of the extreme thermophiles, the extreme halophiles, and the extreme thermophiles that are able to reduce sulfur (methanogens).[1] These three groups are not believed to have arisen independently, but instead evolving from one to another.[1]

The discovery of T. celer turned the position of the archaebacterial phylogenetic tree.[1] T. celer was discovered to share a closer phylogenetic relationship with methanogenic archaebacteria, as opposed its phenotypic analogue, extremely thermophilic archaebacteria. This discovery was made through sequence analysis of the 16S rRNA and resulted in a re-rooting of the phylogenetic tree.[1]

This discovery suggests that extreme thermophiles could be the earliest archaeon ancestor when considering their slow evolution patterns, as well as the distribution of extreme thermophiles into both their own grouping, as well as that of the methanogens.[1]

References[edit]

  1. ^ a b c d e f g h i j k l m n Achenbach-Richter, L., R. Gupta, W. Zillig, C. R. Woese. 1988. Rooting the Archaebacterial Tree: The Pivitol Role of Thermococcus celer in Archaebacterial Evolution. Syst. Appl. Microbial. 10:231-240. Print.
  2. ^ a b c d e f g h i j k l Noll, K M. 1989. “Chromosome Map of the Thermophilic Archaebacterium Thermococcus celer.” Journal of Bacteriology 171.12: 6720–6725. Print.
  3. ^ a b c d e f g h i j k l m n o p q r s t u v w Zillig, W., I. Holtz, D. Janekovic, W. Schafer, and W. D. Reiter. 1983. The Archaebacterium Thermococcus celer Represents a Novel Genus within the Thermophilic Branch of the Archaebacteria. Syst. Appl. Microbiol. 4:88-94. Print.
  4. ^ a b c d e f Zillig, W., K. O. Stetter, W. Schafer, D. Janekovic, S. Wunderl, I. Holz, and P. Palm. "Thermoproteales: Novel Order of Archaebacteria." Zentralblatt für Bakteriologie Mikrobiologie und Hygiene 2 (1981): 205-27. Print.
  5. ^ a b c d Blamey, J., M. Chiong, C. Lopez, and E. Smith. 1999. Optimization of the growth conditions of the extremely thermophilic microorganisms Thermococcus celer and Pyrococcus woesei. Journal of Microbiological methods. Vol: 38:1-2:169-175. Print.
  6. ^ Pace, N. R. 2006. Time for a change. Nature. 441: 7091: 289. Print.
  7. ^ Boone, David R., and Richard W. Castenholz. Bergey's Manual® of Systematic Bacteriology Volume One The Archaea and the Deeply Branching and Phototrophic Bacteria. Second ed. New York, NY: Springer New York, 2001. 341-344. Print.
  8. ^ Gadd, Geoffrey M. "EMP Pathway." Bacterial Physiology and Metabolism. By Byung H. Kim. New York: Cambridge, 2008. 65-67. Print.

Further reading[edit]

  • Lee, Chi-Fung; Makhatadze, George I.; Wong, Kam-Bo (2005). "Effects of Charge-to-Alanine Substitutions on the Stability of Ribosomal Protein L30e from Thermococcus celer". Biochemistry. 44 (51): 16817–16825. doi:10.1021/bi0519654. PMID 16363795. 
  • Kim, Kee Pum; Bae, Heejin; Kim, In Hye; Kwon, Suk-Tae (2011). "Cloning, expression, and PCR application of DNA polymerase from the hyperthermophilic archaeon, Thermococcus celer". Biochemistry Letters. 33 (2): 339–346. doi:10.1007/s10529-010-0434-2. 
  • Reed, Christopher J.; Lewis, Hunter; Trejo, Eric; Winston, Vern; Evilia, Caryn (14 August 2013). "Protein Adaptations in Archaeal Extremophiles". Archaea. 2013: 14. doi:10.1155/2013/373275. 
  • Wong, Kam-Bo; Bycroft, Mark; Wong, Kam-Bo (March 18, 2003). "Crystal structure of ribosomal protein L30e from the extreme thermophile Thermococcus celer: Thermal stability and RNA binding". Biochemistry. 42 (10): 2857–2365. doi:10.1021/bi027131s. 

External links[edit]