Relevant bibliographies by topics / Archaebacteria

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Archaebacteria'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 February 2023

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Journal articles on the topic "Archaebacteria"

1

Cammarano, P., O. Tiboni, and A. M. Sanangelantoni. "Phylogenetic conservation of antigenic determinants in archaebacterial elongation factors (Tu proteins)." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 2–10. http://dx.doi.org/10.1139/m89-002.

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By using affinity chromatography methods, we have purified elongation factor Tu (EF-Tu) proteins from a host of archaebacteria covering all known divisions in the archaebacterial tree except halophiles, and from such distantly related eubacteria as Thermotoga maritima and Escherichia coli. Polyclonal antibodies were raised against the Tu proteins of Sulfolobus solfataricus, Thermoproteus tenax, Thermococcus celer, Pyrococcus wosei, Archaeoglobus fulgidus, Methanococcus thermolitotrophicus, Thermoplasma acidophilum, and Thermotoga and used to probe the immunochemical relatedness of elongation factors both within and across kingdom boundaries. A selection of the results, presented here, indicates that (i) every archaebacterial EF-Tu is closer (immunochemically) to every other archaebacterial EF-Tu than to the functionally analogous proteins of eubacteria and eukaryotes, with only one possible exception concerning die recognition of eukaryotic (EF-1α) factors by Thermococcus EF-Tu antibodies, and (ii) within the archaebacteria there appears to be a correlation between EF-Tu immunochemical similarities and the phylogenetic relatedness of the organisms inferred from other (sequence) criteria. On the whole, immunochemical similarity data argue against the proposal that the archaebacterial taxon should be split and redistributed between two superkingdoms.Key words: phylogeny, archaebacteria, elongation factor Tu antibodies, eubacteria, eukaryotes.
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2

Fedorov, Oleg V., Michael G. Pyatibratov, Alla S. Kostyukova, Natalja K. Osina, and Valery Yu Tarasov. "Protofilament as a structural element of flagella of haloalkalophilic archaebacteria." Canadian Journal of Microbiology 40, no. 1 (January 1, 1994): 45–53. http://dx.doi.org/10.1139/m94-007.

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Flagella of the haloalkalophilic archaebacterium Natronobacterium magadii were purified and characterized. The diameter of the flagella was 10 nm. It was shown that the flagella consist of four major proteins with molecular weights of 105 000, 60 000, 59 000, and 45 000. With decreasing NaCl concentration, the flagella dissociated into protofilaments. The structure of dissociated flagella and individual flagellins was studied by limited proteolysis. It was found that proteolytic cleavage of flagellins in dissociated flagella into high molecular weight fragments (about 40 000) did not lead to protofilament degradation. It was shown that the most stable fragment is formed from the 60 000 molecular weight flagellin. Cleavage of this fragment led to complete disappearance of protofilaments. On the basis of the data obtained, possible principles of archaebacterial flagellar construction are discussed.Key words: flagellin, archaebacteria, protofilaments, Natronobacterium magadii.
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3

Amils, R., L. Ramírez, J. L. Sanz, I. Marín, A. G. Pisabarro, and D. Ureña. "The use of functional analysis of the ribosome as a tool to determine archaebacterial phylogeny." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 141–47. http://dx.doi.org/10.1139/m89-021.

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Forty different antibiotics with diverse kingdom and functional specificities were used to measure the functional characteristics of the archaebacterial translation apparatus. The resulting inhibitory curves, which are characteristic of the cell-free system analyzed, were transformed into quantitative values that were used to cluster the different archaebacteria analyzed. This cluster resembles the phylogenetic tree generated by 16S rRNA sequence comparisons. These results strongly suggest that functional analysis of an appropriate evolutionary clock, such as the ribosome, is of intrinsic phylogenetic value. More importantly, they indicate that the study of the nexus between genotypic and phenotypic (functional) information may shed considerable light on the evolution of the protein synthetic machinery.Key words: antibiotics, ribosomes, archaebacteria, phylogeny, functional analysis.
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4

Olsen, Gary J., and Carl R. Woese. "A brief note concerning archaebacterial phylogeny." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 119–23. http://dx.doi.org/10.1139/m89-018.

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Critical analysis of the recently proposed alternative to the normal archaebacterial tree, the new eocyte tree, shows that the latter's central topology, in which the eubacteria branch from an entirely different section of the unrooted archaebacterial tree than the eukaryotes, is consistent with an artifact. The effects of the alignment used and the particular composition of the sequence quartets analyzed to infer this tree are discussed in detail.Key words: archaebacteria, molecular phylogeny, 16S ribosomal RNA, evolution, eocyte tree.
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5

Wolters, Jörn, and Volker A. Erdmann. "The structure and evolution of archaebacterial ribosomal RNAs." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 43–51. http://dx.doi.org/10.1139/m89-007.

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A cladistic analysis of 553 5S rRNA sequences has revealed a Ur-5S rRNA, the ancestor of all present-day 5S rRNA molecules. Previously stated characteristic differences between the eubacterial and eukaryotic molecules, namely, the length base-pairing schemes of helices D, can be used as a marker for the various archaebacterial branches. One model comprises Thermococcus, Thermoplasma, methanobacteria, and halobacteria; a second comprises the Sulfolobales; and a third is represented only by the single organism Octopus Spring species 1. A relaxed selection pressure on helix E with subsequent deletions is observed in Methanobacteriales, Methanococcales, and eubacteria. The secondary structures are supported by enzymatic digestion and chemical modification studies of the 5S rRNAs. Reconstitution of eubacterial 50S ribosomal subunits with 5S rRNA from Halobacterium and Thermoplasma has revealed 100% incorporation, while eukaryotic 5S rRNAs yielded a 50% incorporation. Relevant positions of the small-subunit rRNA are selected to answer the question of the monophyly of archaebacteria. Eight positions account for monophyly, eight for an ancestry of eubacteria with halophile methanogens and eukaryotes with eocytes (paraphyly of archaebacteria), and two for an ancestry of eubacteria with eocytes. A refinement of the neighborliness method of S. Sattath and A. Tversky resulted in a monophyly of archaebacteria when all positions are treated equally and in a paraphyly when tranversions are weighted twice over transitions.Key words: archaebacteria, ribosomal RNA, evolution, cladistic analysis.
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6

Ramirez, Celia, Lawrence C. Shimmin, C. Hunter Newton, Alastair T. Matheson, and Patrick P. Dennis. "Structure and evolution of the L11, L1, L10, and L12 equivalent ribosomal proteins in eubacteria, archaebacteria, and eucaryotes." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 234–44. http://dx.doi.org/10.1139/m89-036.

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The genes corresponding to the L11, L1, L10, and L12 equivalent ribosomal proteins (L11e, L1e, L10e, and L12e) of Escherichia coli have been cloned and sequenced from two widely divergent species of archaebacteria, Halobacterium cutirubrum and Sulfolobus solfataricus, and the L10 and four different L12 genes have been cloned and sequenced from the eucaryote Saccharomyces cerevisiae. Alignments between the deduced amino acid sequences of these proteins and to other available homologous proteins of eubacteria and eucaryotes have been made. The data suggest that the archaebacteria are a distinct coherent phylogenetic group. Alignment of the proline-rich L11e proteins reveals that the N-terminal region, believed to be responsible for interaction with release factor 1, is the most highly conserved region and that there is specific conservation of most of the proline residues, which may be important in maintaining the highly elongated structure of the molecule. Although L11 is the most highly methylated protein in the E. coli ribosome, the sites of methylation are not conserved in the archaebacterial L11e proteins. The L1e proteins of eubacteria and archaebacteria show two regions of very high similarity near the center and the carboxy termini of the proteins. The L10e proteins of all kingdoms are colinear and contain approximately three fourths of an L12e protein fused to their carboxy terminus, although much of this fusion has been lost in the truncated eubacterial protein. The archaebacterial and eucaryotic L12e proteins are colinear, whereas the eubacterial protein has suffered a rearrangement through what appear to be gene fusion events. Within the L12e derived region of the L10e proteins there exists a repeated module of 26 amino acids, present in two copies in eucaryotes, three in archaebacteria, and one in eubacteria. This modular sequence is apparently also present in the L12e proteins of all kingdoms and may play a role in L12e dimerization, L10e–L12e complex formation, and the function of the L10e–L12e complex in translation.Key words: translation, ribosome.
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7

Hensel, Reinhard, Peter Zwickl, Stefan Fabry, Jutta Lang, and Peter Palm. "Sequence comparison of glyceraldehyde-3-phosphate dehydrogenases from the three urkingdoms: evolutionary implication." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 81–85. http://dx.doi.org/10.1139/m89-012.

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The primary structure of the glyceraldehyde-3-phosphate dehydrogenase from the archaebacteria shows striking deviation from the known sequences of eubacterial and eukaryotic sequences, despite unequivocal homologies in functionally important regions. Thus, the structural similarity between the eubacterial and eukaryotic enzymes is significantly higher than that between the archaebacterial enzymes and the eubacterial and eukarytic enzymes. This preferred similarity of eubacterial and eukaryotic glyceraldehyde-3-phosphate dehydrogenase structures does not correspond to the phylogenetic distances among the three urkingdoms as deduced from comparisons of ribosomal ribonucleic acid sequences. Indications will be presented that the closer relationship of the eubacterial and eukaryotic glyceraldehyde-3-phosphate dehydrogenase resulted from a gene transfer from eubacteria to eukaryotes after the segregation of the three urkingdoms.Key words: glyceraldehyde-3-phosphate dehydrogenase, archaebacteria, protein evolution.
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8

Akanni, Wasiu A., Karen Siu-Ting, Christopher J. Creevey, James O. McInerney, Mark Wilkinson, Peter G. Foster, and Davide Pisani. "Horizontal gene flow from Eubacteria to Archaebacteria and what it means for our understanding of eukaryogenesis." Philosophical Transactions of the Royal Society B: Biological Sciences 370, no. 1678 (September 26, 2015): 20140337. http://dx.doi.org/10.1098/rstb.2014.0337.

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The origin of the eukaryotic cell is considered one of the major evolutionary transitions in the history of life. Current evidence strongly supports a scenario of eukaryotic origin in which two prokaryotes, an archaebacterial host and an α -proteobacterium (the free-living ancestor of the mitochondrion), entered a stable symbiotic relationship. The establishment of this relationship was associated with a process of chimerization, whereby a large number of genes from the α-proteobacterial symbiont were transferred to the host nucleus. A general framework allowing the conceptualization of eukaryogenesis from a genomic perspective has long been lacking. Recent studies suggest that the origins of several archaebacterial phyla were coincident with massive imports of eubacterial genes. Although this does not indicate that these phyla originated through the same process that led to the origin of Eukaryota, it suggests that Archaebacteria might have had a general propensity to integrate into their genomes large amounts of eubacterial DNA. We suggest that this propensity provides a framework in which eukaryogenesis can be understood and studied in the light of archaebacterial ecology. We applied a recently developed supertree method to a genomic dataset composed of 392 eubacterial and 51 archaebacterial genera to test whether large numbers of genes flowing from Eubacteria are indeed coincident with the origin of major archaebacterial clades. In addition, we identified two potential large-scale transfers of uncertain directionality at the base of the archaebacterial tree. Our results are consistent with previous findings and seem to indicate that eubacterial gene imports (particularly from δ - Proteobacteria, Clostridia and Actinobacteria) were an important factor in archaebacterial history. Archaebacteria seem to have long relied on Eubacteria as a source of genetic diversity, and while the precise mechanism that allowed these imports is unknown, we suggest that our results support the view that processes comparable to those through which eukaryotes emerged might have been common in archaebacterial history.
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9

Zillig, Wolfram, Hans-Peter Klenk, Peter Palm, Gabriela Pühler, Felix Gropp, Roger A. Garrett, and Henrik Leffers. "The phylogenetic relations of DNA-dependent RNA polymerases of archaebacteria, eukaryotes, and eubacteria." Canadian Journal of Microbiology 35, no. 1 (January 1, 1989): 73–80. http://dx.doi.org/10.1139/m89-011.

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Unrooted phylogenetic dendrograms were calculated by two independent methods, parsimony and distance matrix analysis, from an alignment of the derived amino acid sequences of the A and C subunits of the DNA-dependent RNA polymerases of the archaebacteria Sulfolobus acidocaldarius and Halobacterium halobium with 12 corresponding sequences including a further set of archaebacterial A + C subunits, eukaryotic nuclear RNA polymerases, pol I, pol II, and pol III, eubacterial β′ and chloroplast β′ and β″ subunits. They show the archaebacteria as a coherent group in close neighborhood of and sharing a bifurcation with eukaryotic pol II and (or) pol IIIA components. The most probable trees show pol IA branching off from the tree separately at a bifurcation with the eubacterial β′ lineage. The implications of these results, especially for understanding the possibly chimeric origin of the eukaryotic nuclear genome, are discussed.Key words: transcription, evolution, taxonomy, subunits, gene organization.
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10

Fewson, Charles A. "Archaebacteria." Biochemical Education 14, no. 3 (July 1986): 103–15. http://dx.doi.org/10.1016/0307-4412(86)90167-6.

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Dissertations / Theses on the topic "Archaebacteria"

1

Stevens, A. F. "Studies on the extremely halophilic archaebacteria." Thesis, University of Leicester, 1985. http://hdl.handle.net/2381/35419.

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A variety of techniques have been employed to study the taxonomic relationships within a large number of extremely halophilic archaebacteria, including both alkaliphilic and neutrophilic isolates. These techniques include a computer-assisted analysis of whole cell and ribosomal protein patterns, after separation by one-dimensional SDS- polyacrylamide gel electrophoresis. The API-ZYM system has been applied to the extreme halophiles to produce, and then compare, the partial enzyme profiles of a large number of strains. The serotaxonomy of the major cell envelope component of the archaebacterial halophiles (a 200 KD glycoprotein) has been investigated. The cell envelope structure was further investigated by the use of scanning and transmission electron microscopes to study the cell surface topography and composition of a number of extreme halophiles, both rodshaped and coccoid is elites. A brief investigation of the plasmid DNA present in many of the isolates was carried out by preforming hybridization experiments between plasmids from different strains. Ross and Grant (1985) have suggested that the taxonomy of the extremely halophilic archaebacteria should be revised and that these organisms should be divided into two families, comprising a total of nine genera. The work reported in this thesis provides further evidence that, in general, these suggestions are valid.
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2

Galada, Ncebakazi. "Exploring diversity and ecology of nonarchaea in hydrothermal biotopes." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&amp.

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The Nanoarchaeota were proposed as the fourth archaeal sub-division in 2002, and the only fully characterized nanoarchaeon was found to exist in a symbiotic association with the crenarchaeote, Ignicoccus sp. This nanoarchaeote, named Nanoarchaeum equitans could not be detected with &ldquo
universal&rdquo
archaeal 16S PCR primers and could only be amplified using specifically designed primers. In order to identify and access a wide diversity of archaeal phylotypes a new set of &ldquo
universal&rdquo
archaeal primers A571F (5&rsquo
-GCY TAA AGS RIC CGT AGC-3&rsquo
) and UA1204R (5&rsquo
-TTM GGG GCA TRC IKA CCT-3&rsquo
) was designed, that could amplify the 16S rRNA genes of all four archaeal sub-divisions. Using these primers community DNA was amplified from Chinese and New Zealand hydrothermal systems.
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3

Lin, Xinli. "Isolation and characterization of new pterins from nonmethanogenic archaebacteria." Diss., Virginia Polytechnic Institute and State University, 1987. http://hdl.handle.net/10919/77823.

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Several new pterins have been discovered in halophilic and thermoacidophilic archaebacteria. Two of these were identified in the extreme halophiles and were thus called halopterins. One of these halopterins is produced by Halobacterium salinarium, Halobacterium halobium, and Halococcus morrhuae and is called phosphohalopterin-1. It was given this name because it was the first halopterin discovered and it has four monophosphate esters per dimeric pterin. The proposed structure of phosphohalopterin-1 is as follows. [see document for diagram of chemical structure] The other halopterin, which is produced by Halobacterium marismortui, Halobacterium volcanii, and Halobacterial strain GN-1, is called sulfohalopterin-2 because it has two sulfate esters per dimeric pterin and it was isolated and recognized after the isolation of phosphohalopterin-1. The proposed structure of sulfohalopterin-2 is as follows. [see document for diagram of chemical structure] As shown above, both pterins are dimers with an ether linkage connecting the polyol side chains. Both of the halopterins are negatively charged because of the phosphate and sulfate esters on the side chains. In addition to the halopterins, a positively charged pterin has been isolated from Sulfolobus solfataricus. This pterin is very special since no positively charged unconjugated pterin had ever been found in nature before. This pterin is named solfapterin after the species name of the bacteria from which it was obtained. The structure of this pterin is still unknown but the preliminary data indicate that it is an unconjugated pterin with a polyol containing an amine on the side chain. Another positively charged pterin which is different from solfapterin was found in Thermoplasma. All of the above pterins are different from any previously described pterins and thus represent new pterins in the archaebacterial kingdom. The discovery of these new pterins is important both to pterin biochemistry and to archaebacterial taxonomy. These discoveries also open up a new field, that is, the exploration of the function of these new pterins in norunethanogenic archaebacteria.
Ph. D.
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4

Brown, James W. "RNA polymerase binding sites and polyadenylated RNAs in archaebacteria /." The Ohio State University, 1988. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487591658174843.

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5

Giaquinto, Laura School of Biotechnology &amp Biomolecular Science UNSW. "The characterization of Csp (Cold Shock Protein) from the Antarctic archaeon, Methanogenium frigidum." Awarded by:University of New South Wales. School of Biotechnology and Biomolecular Science, 2006. http://handle.unsw.edu.au/1959.4/26148.

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Cold shock proteins (Csp) are small acidic proteins that fold into ??-barrel structures with five anti-parallel ??-strands and are involved in essential cellular processes. Upon temperature downshift the synthesis of Csp proteins is drastically increased to enable cells to restore growth in the cold. These proteins facilitate transcription and translation at low temperature by functioning as RNA chaperones. Csp proteins have been most extensively studied in Bacteria but very few Csp homologues have been identified and studied in Archaea. This is the first study examining structural, functional and biophysical properties of Csp from the Antarctic archaeon Methanogenium frigidum. The fastidious growth requirements of M. frigidum make it difficult to cultivate, therefore recombinant methods have been developed for the expression and characterization of the protein. The analysis by transverse urea gradient gel electrophoresis (TUG-GE) revealed that M. frigidum Csp folds by a reversible two-state mechanism and has a low conformational stability. The spectroscopic analysis of the protein performed by Circular Dichroism (CD) spectroscopy disclosed features typical of other homologous proteins. A possible association between Csp and RNA has been proposed according to MALDI-TOF mass spectrometry analysis. The effect of a Nterminal polyhistidine affinity tag on the biophysical properties of Csp was also examined. The biological activity of Csp was investigated by complementation of an E. coli cold sensitive mutant. These studies revealed that the M. frigidum Csp is biologically active and can function in E. coli.
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6

Morozova, Daria. "Tolerance limits and survival potential of methanogenic archaea from Siberian permafrost under extreme living conditions = Toleranzgrenzen und Überlebensstrategien von methanogenen Archaeen aus sibirischen Permafrosthabitaten unter Extrembedingungen /." Bremerhaven : Alfred-Wegener-Institut für Polar- und Meeresforschung, 2007. http://www.loc.gov/catdir/toc/fy0804/2008384365.html.

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7

Beckler, Gregory Scott. "Structure and analysis of the hisA and hisI genes of the archaebacterium Methanococcus vannielii /." The Ohio State University, 1987. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487330761219015.

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8

Munro, Stacey. "Investigation of the transcriptional response of Sulfolobus solfataricus to damaging agents." Thesis, St Andrews, 2009. http://hdl.handle.net/10023/743.

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9

Stewart, John E. B. (John Edward Bakos). "Characterization of Aspartate Transcarbamoylase in the Archaebacterium Methanococcus Jannaschii." Thesis, University of North Texas, 1996. https://digital.library.unt.edu/ark:/67531/metadc935724/.

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Asparate transcarbamoylase catalyzes the first committed step in the de novo synthesis of pyrmidine nucleotides UMP, UDP, UTP, and CTP. The archetype enzyme found in Escherichia coli (310 kDa) exhibits sigmodial substrate binding kinetics with positive control by ATP and negative control with CTP and UTP. The ATCase characterized in this study is from the extreme thermophilic Archaebacterium, Methanococcus jannaschii. The enzyme was very stable at elevated temperatures and possessed activity from 20 degrees Celsius to 90 degrees Celsius. M. Jannaschii ATCase retained 75% of its activity after incubation at 100 degrees Celsius for a period of 90 minutes. No sigmodial allosteric response to substrate for the enzyme was observed. Velocity substrate plots gave Michaelis-Menten (hyperbolic) kinetics. The Km for aspartate was 7 mM at 30 degrees Celsius and the KM for carbamoylphosphate was .125 mM. The enzyme from M. jannaschii had a broad pH response with an optimum above pH 9. Kinetic measurements were significantly affected by changes in pH and temperature. The enzyme catalyzed reaction had an energy of activation of 10,300 calories per mole. ATCase from M. jannaschii was partially purified. The enzyme was shown to have a molecular weight of 110,000 Da., with a subunit molecular weight of 37,000 Da. The enzyme was thus a trimer composed of three identical subunits. The enzyme did not possess any regulatory response and no evidence for a regulatory polypeptide was found, DNA from M. jannaschii did hybridize to probes corresponding to genes for both the catalytic and regulatory subunits from E. coli. Analysis of DNA sequences for the M. jannaschii ATCase genes showed that the gene for the catalytic subunits shares significant homology with the pyrB genes from E. coli, and maximum homology amongst known ATCase genes to pyrB from Bacillus. An unlinked gene homologous to E. coli pyrl encoding the regulatory subunit was identified, though its expression and true function remain uncharacterized.
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10

Richards, Jodi Dominique. "Helicases and DNA dependent ATPases of Sulfolobus solfataricus /." St Andrews, 2008. http://hdl.handle.net/10023/474.

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Books on the topic "Archaebacteria"

1

Morris, Kates, Kushner Donn, and Matheson A. T, eds. The Biochemistry of archaea (archaebacteria). Amsterdam: Elsevier, 1993.

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2

J, Danson Michael, Hough D. W, and Lunt George G, eds. The archaebacteria: Biochemistry and biotechnology. London: Portland Press, 1992.

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3

1920-, Kandler Otto, Zillig Wolfram, and International Workshop on Biology and Biochemistry of Archaebacteria (1985 : Munich, Germany), eds. Archaebacteria '85: Proceedings of the EMBO Workshop on Molecular Genetics of Archaebacteria and the International Workshop on Biology and Biochemistry of Archaebacteria, Munich, June 1985. Stuttgart: Fischer, 1986.

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4

Morozova, Daria. Tolerance limits and survival potential of methanogenic archaea from Siberian permafrost under extreme living conditions =: Toleranzgrenzen und Überlebensstrategien von methanogenen Archaeen aus sibirischen Permafrosthabitaten unter Extrembedingungen. Bremerhaven: Alfred-Wegener-Institut für Polar- und Meeresforschung, 2007.

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5

Kelly, R. Hyperthermophilic archaebacteria: Prospects for bioprocessing of fossil fuels. S.l: s.n, 1990.

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6

Brierley, J. A. Acidophilic thermophilic archaebacteria--Potential application for metals recovery. S.l: s.n, 1990.

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7

Barker, David. Archaea: Salt-lovers, methane-makers, thermophiles, and other archaeans. New York: Crabtree Pub., 2010.

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8

Barker, David. Archaea: Salt-lovers, methane-makers, thermophiles, and other archaeans. New York, N.Y: Crabtree Pub. Co., 2010.

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Archaea: Salt-lovers, methane-makers, thermophiles, and other archaea. New York: Crabtree Pub., 2010.

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The third domain: The untold story of archaea and the future of biotechnology. Washington, D.C: Joseph Henry Press, 2007.

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Book chapters on the topic "Archaebacteria"

1

Gooch, Jan W. "Archaebacteria." In Encyclopedic Dictionary of Polymers, 875. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13167.

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2

Stanier, Roger Y., John L. Ingraham, Mark L. Wheelis, and Page R. Painter. "The Archaebacteria." In General Microbiology, 330–43. London: Macmillan Education UK, 1986. http://dx.doi.org/10.1007/978-1-349-08754-9_14.

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Stanier, Roger Y., John L. Ingraham, Mark L. Wheelis, and Page R. Painter. "The Archaebacteria." In General Microbiology, 330–43. London: Macmillan Education UK, 1986. http://dx.doi.org/10.1007/978-1-349-15028-1_14.

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Javor, Barbara. "Halophilic Archaebacteria." In Brock/Springer Series in Contemporary Bioscience, 101–24. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74370-2_7.

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Kandler, Otto. "Archaea Archaebacteria." In Progress in Botany / Fortschritte der Botanik, 1–24. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78020-2_1.

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Grant, W. D. "Anaerobic Archaebacteria." In Recent Advances in Anaerobic Bacteriology, 245–48. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3293-7_21.

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Hori, Hiroshi, Yukio Satow, Isao Inoue, and Mitsuo Chihara. "Archaebacteria Vs Metabacteria." In Evolution of Life, 325–36. Tokyo: Springer Japan, 1991. http://dx.doi.org/10.1007/978-4-431-68302-5_20.

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8

Zillig, Wolfram, Wolf-Dieter Reiter, Peter Palm, Felix Gropp, Horst Neumann, and Michael Rettenberger. "Viruses of Archaebacteria." In The Bacteriophages, 517–58. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5424-6_12.

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Miyata, Takashi, Naoyuki Iwabe, Kei-ichi Kuma, Yu-ichi Kawanishi, Masami Hasegawa, Hirohisa Kishino, Yasuo Mukohata, Kunio Ihara, and Syozo Osawa. "Evolution of Archaebacteria: Phylogenetic Relationships Among Archaebacteria, Eubacteria, and Eukaryotes." In Evolution of Life, 337–51. Tokyo: Springer Japan, 1991. http://dx.doi.org/10.1007/978-4-431-68302-5_21.

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Duarte, J. C. "Thermophilic Archaebacteria for Biotechnology." In Recent Advances in Biotechnology, 397–404. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2468-3_22.

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Conference papers on the topic "Archaebacteria"

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Abraham, Leo T., and Esha N. Varma. "Extraction Of Methane From Gas Hydrates Using Anaerobic Archaebacteria." In Offshore Technology Conference. Offshore Technology Conference, 2007. http://dx.doi.org/10.4043/18551-ms.

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Chrencik, B. J., and T. L. Marsh. "Contributions of methanogenic Archaebacteria in community-driven anaerobic chromate reduction by Yellowstone National Park hot spring microorganisms." In MICROBES IN APPLIED RESEARCH - Current Advances and Challenges. WORLD SCIENTIFIC, 2012. http://dx.doi.org/10.1142/9789814405041_0012.

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Reports on the topic "Archaebacteria"

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Jensen, Roy A. Biochemical-Pathway Diversity in Archaebacteria. Fort Belvoir, VA: Defense Technical Information Center, August 1990. http://dx.doi.org/10.21236/ada226200.

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Clark, Douglas S. Pressure-Temperature Effects on Thermophilic Archaebacteria. Fort Belvoir, VA: Defense Technical Information Center, August 1989. http://dx.doi.org/10.21236/ada211241.

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Gupta, Ramesh. Structure and Expression of Various RNAs in the Archaebacteria. Fort Belvoir, VA: Defense Technical Information Center, September 1988. http://dx.doi.org/10.21236/ada204058.

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Gunsalus, Robert P. Genetic Analysis of Hyperthermophilic Archaebacterial Phenomena. Fort Belvoir, VA: Defense Technical Information Center, February 1994. http://dx.doi.org/10.21236/ada286106.

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Daniels, Charles J. Processing of Archaebacterial Intron-Containing tRNA Gene Transcripts. Fort Belvoir, VA: Defense Technical Information Center, July 1988. http://dx.doi.org/10.21236/ada197868.

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Russell, Alan J. Investigation of Pressure Regulation in an Archaebacterial Enzyme. Fort Belvoir, VA: Defense Technical Information Center, March 1994. http://dx.doi.org/10.21236/ada281413.

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Kelly, Robert M. Hydrogen/Sulfur Autotrophy in the Hyperthermophilic Archaebacterium Pyrodictium brockii. Fort Belvoir, VA: Defense Technical Information Center, August 1992. http://dx.doi.org/10.21236/ada254407.

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Zinder, Stephan H. The Nitrogenase in a Methanogenic Archaebacterium and Its Regulation. Fort Belvoir, VA: Defense Technical Information Center, February 1990. http://dx.doi.org/10.21236/ada218346.

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Maier, R. Hydrogen/sulfur metabolism in the hyperthermophilic archaebacterium Pyrodictium brockii. Office of Scientific and Technical Information (OSTI), March 1990. http://dx.doi.org/10.2172/6969524.

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Daniels, C. J. Structure and regulation of an archaebacterial promoter: An in vivo study. Progress report. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10169665.

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