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1.
Appl Environ Microbiol ; 85(4)2019 02 15.
Article in English | MEDLINE | ID: mdl-30504216

ABSTRACT

The discovery of hyperthermophiles has dramatically changed our understanding of the habitats in which life can thrive. However, the extreme high temperatures in which these organisms live have severely restricted the development of genetic tools. The archaeon Pyrococcus yayanosii A1 is a strictly anaerobic and piezophilic hyperthermophile that is an ideal model for studies of extreme environmental adaptation. In the present study, we identified a high hydrostatic pressure (HHP)-inducible promoter (P hhp ) that controls target gene expression under HHP. We developed an HHP-inducible toxin-antitoxin cassette (HHP-TAC) containing (i) a counterselectable marker in which a gene encoding a putative toxin (virulence-associated protein C [PF0776 {VapC}]) controlled by the HHP-inducible promoter was used in conjunction with the gene encoding antitoxin PF0775 (VapB), which was fused to a constitutive promoter (P hmtB ), and (ii) a positive marker with the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase-encoding gene from P. furiosus controlled by the constitutive promoter P gdh The HHP-TAC was constructed to realize markerless gene disruption directly in P. yayanosii A1 in rich medium. The pop-out recombination step was performed using an HHP-inducible method. As proof, the PYCH_13690 gene, which encodes a 4-α-glucanotransferase, was successfully deleted from the strain P. yayanosii A1. The results showed that the capacity for starch hydrolysis in the Δ1369 mutant decreased dramatically compared to that in the wild-type strain. The inducible toxin-antitoxin system developed in this study greatly increases the genetic tools available for use in hyperthermophiles.IMPORTANCE Genetic manipulations in hyperthermophiles have been studied for over 20 years. However, the extremely high temperatures under which these organisms grow have limited the development of genetic tools. In this study, an HHP-inducible promoter was used to control the expression of a toxin. Compared to sugar-inducible and cold-shock-inducible promoters, the HHP-inducible promoter rarely has negative effects on the overall physiology and central metabolism of microorganisms, especially piezophilic hyperthermophiles. Previous studies have used auxotrophic strains as hosts, which may interfere with studies of adaptation and metabolism. Using an inducible toxin-antitoxin (TA) system as a counterselectable marker enables the generation of a markerless gene disruption strain without the use of auxotrophic mutants and counterselection with 5-fluoroorotic acid. TA systems are widely distributed in bacteria and archaea and can be used to overcome the limitations of high growth temperatures and dramatically extend the selectivity of genetic tools in hyperthermophiles.


Subject(s)
Adaptation, Physiological/genetics , Antitoxins/genetics , Archaea/genetics , Archaeal Proteins/metabolism , Hydrostatic Pressure , Pyrococcus/genetics , Toxins, Biological/genetics , Archaea/physiology , Archaeal Proteins/genetics , Bacterial Proteins , Base Sequence , DNA, Archaeal , DNA-Binding Proteins , Gene Expression Regulation, Archaeal , Genes, Archaeal/genetics , Hot Temperature , Hydrothermal Vents , Hydroxymethylglutaryl CoA Reductases/genetics , Membrane Glycoproteins , Orotic Acid/analogs & derivatives , Promoter Regions, Genetic , Pyrococcus/physiology , Toxins, Biological/metabolism , Transformation, Genetic
2.
World J Microbiol Biotechnol ; 33(6): 112, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28470425

ABSTRACT

The study of prokaryotic life in high temperature environments viz., geothermal areas, hot, acidic geysers and undersea hydrothermal vents has revealed the existence of thermophiles (or hyperthermophiles). These microorganisms possess various stress adaptation mechanisms which enable them to bypass multiple physical and chemical barriers for survival. The discovery of radiation resistant thermophile Deinococcus geothermalis has given new insights into the field of radiation microbiology. The ability of radiation resistant thermophiles to deal with the lethal effects of ionizing radiations like DNA damage, oxidative bursts and protein damage has made them a model system for exobiology and interplanetary transmission of life. They might be an antiquity of historical transport process that brought microbial life on Earth. These radiation resistant thermophiles are resistant to desiccation as well and maintain their homeostasis by advance DNA repair mechanisms, reactive oxygen species (ROS) detoxification system and accumulation of compatible solutes. Moreover, engineered radioresistant thermophilic strains are the best candidate for bioremediation of radionuclide waste while the extremolytes produced by these organisms may have predicted therapeutic uses. So, the present article delineate a picture of radiation resistance thermophiles, their adaptive mechanisms to evade stress viz., radiation and desiccation, their present applications along with new horizons in near future.


Subject(s)
Archaea/physiology , Archaea/radiation effects , Bacteria/radiation effects , Bacterial Physiological Phenomena/radiation effects , Hot Temperature , Actinobacteria/physiology , Actinobacteria/radiation effects , Bacteria/genetics , Bacterial Physiological Phenomena/genetics , Biodegradation, Environmental , Cyanobacteria/physiology , Cyanobacteria/radiation effects , DNA Damage/radiation effects , DNA Repair , Deinococcus/genetics , Deinococcus/physiology , Deinococcus/radiation effects , Environmental Microbiology , Exobiology , Halobacterium/physiology , Halobacterium/radiation effects , Pyrococcus/physiology , Pyrococcus/radiation effects , Radiation, Ionizing , Reactive Oxygen Species/radiation effects , Respiratory Burst/radiation effects , Stress, Physiological , Sulfolobus/physiology , Sulfolobus/radiation effects , Thermococcus/physiology , Thermococcus/radiation effects
3.
BMC Struct Biol ; 14: 23, 2014 Oct 15.
Article in English | MEDLINE | ID: mdl-25315147

ABSTRACT

BACKGROUND: The identification of the mechanisms of adaptation of protein structures to extreme environmental conditions is a challenging task of structural biology. We performed molecular dynamics (MD) simulations of the Nip7 protein involved in RNA processing from the shallow-water (P. furiosus) and the deep-water (P. abyssi) marine hyperthermophylic archaea at different temperatures (300 and 373 K) and pressures (0.1, 50 and 100 MPa). The aim was to disclose similarities and differences between the deep- and shallow-sea protein models at different temperatures and pressures. RESULTS: The current results demonstrate that the 3D models of the two proteins at all the examined values of pressures and temperatures are compact, stable and similar to the known crystal structure of the P. abyssi Nip7. The structural deviations and fluctuations in the polypeptide chain during the MD simulations were the most pronounced in the loop regions, their magnitude being larger for the C-terminal domain in both proteins. A number of highly mobile segments the protein globule presumably involved in protein-protein interactions were identified. Regions of the polypeptide chain with significant difference in conformational dynamics between the deep- and shallow-water proteins were identified. CONCLUSIONS: The results of our analysis demonstrated that in the examined ranges of temperatures and pressures, increase in temperature has a stronger effect on change in the dynamic properties of the protein globule than the increase in pressure. The conformational changes of both the deep- and shallow-sea protein models under increasing temperature and pressure are non-uniform. Our current results indicate that amino acid substitutions between shallow- and deep-water proteins only slightly affect overall stability of two proteins. Rather, they may affect the interactions of the Nip7 protein with its protein or RNA partners.


Subject(s)
Archaeal Proteins/chemistry , Nuclear Proteins/chemistry , Pyrococcus/physiology , Adaptation, Physiological , Amino Acid Substitution , Archaeal Proteins/genetics , Archaeal Proteins/metabolism , Atmospheric Pressure , Crystallography, X-Ray , Models, Molecular , Molecular Dynamics Simulation , Nuclear Proteins/genetics , Nuclear Proteins/metabolism , Protein Stability , Protein Structure, Secondary , Pyrococcus/classification , Salts/metabolism , Seawater/microbiology , Temperature
4.
J Bacteriol ; 194(16): 4434-5, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22843576

ABSTRACT

Pyrococcus sp. strain ST04 is a hyperthermophilic, anaerobic, and heterotrophic archaeon isolated from a deep-sea hydrothermal sulfide chimney on the Endeavour Segment of the Juan de Fuca Ridge in the northeastern Pacific Ocean. To further understand the distinct characteristics of this archaeon at the genome level (polysaccharide utilization at high temperature and ATP generation by a Na(+) gradient), the genome of strain ST04 was completely sequenced and analyzed. Here, we present the complete genome sequence analysis results of Pyrococcus sp. ST04 and report the major findings from the genome annotation, with a focus on its saccharolytic and metabolite production potential.


Subject(s)
DNA, Archaeal/chemistry , DNA, Archaeal/genetics , Genome, Archaeal , Hydrothermal Vents/microbiology , Pyrococcus/genetics , Sequence Analysis, DNA , Adenosine Triphosphate/metabolism , Anaerobiosis , Heterotrophic Processes , Molecular Sequence Data , Pacific Ocean , Polysaccharides/metabolism , Pyrococcus/isolation & purification , Pyrococcus/physiology , Seawater/microbiology , Sodium Chloride/metabolism , Sulfides/metabolism
6.
ISME J ; 3(7): 873-6, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19295639

ABSTRACT

A novel hydrothermal site was discovered in March 2007, on the mid-Atlantic ridge during the cruise 'Serpentine'. At a depth of 4100 m, the site 'Ashadze' is the deepest vent field known so far. Smoker samples were collected with the ROV 'Victor 6000' and processed in the laboratory for the enrichment of anaerobic heterotrophic microorganisms under high-temperature and high-hydrostatic pressure conditions. Strain CH1 was successfully isolated and assigned to the genus Pyrococcus, within the Euryarchaeota lineage within the Archaea domain. This organism grows within a temperature range of 80 to 108 degrees C and a pressure range of 20 to 120 MPa, with optima for 98 degrees C and 52 MPa respectively. Pyrococcus CH1 represents the first obligate piezophilic hyperthermophilic microorganism known so far. Comparisons of growth yields obtained under high-temperature/high-pressure conditions for relative organisms isolated from various depths, showed clear relationships between depth at origin and responses to hydrostatic pressure.


Subject(s)
Hot Temperature , Hydrostatic Pressure , Pyrococcus/classification , Pyrococcus/isolation & purification , Atlantic Ocean , Cluster Analysis , DNA, Archaeal/chemistry , DNA, Archaeal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Genes, rRNA , Hot Springs , Molecular Sequence Data , Phylogeny , Pyrococcus/physiology , RNA, Archaeal/genetics , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Sequence Homology, Nucleic Acid
7.
BMC Genomics ; 10: 639, 2009 Dec 30.
Article in English | MEDLINE | ID: mdl-20042074

ABSTRACT

BACKGROUND: Prokaryotic microorganisms are able to survive and proliferate in severe environmental conditions. The increasing number of complete sequences of prokaryotic genomes has provided the basis for studying the molecular mechanisms of their adaptation at the genomic level. We apply here a computer-based approach to compare the genomes and proteomes from P. furiosus, P. horikoshii, and P. abyssi to identify features of their molecular evolution related to adaptation strategy to diverse environmental conditions. RESULTS: Phylogenetic analysis of rRNA genes from 26 Pyrococcus strains suggested that the divergence of P. furiosus, P. horikoshii and P. abyssi might have occurred from ancestral deep-sea organisms. It was demonstrated that the function of genes that have been subject to positive Darwinian selection is closely related to abiotic and biotic conditions to which archaea managed to become adapted. Divergence of the P. furiosus archaea might have been due to loss of some genes involved in cell motility or signal transduction, and/or to evolution under positive selection of the genes for translation machinery. In the course of P. horikoshii divergence, positive selection was found to operate mainly on the transcription machinery; divergence of P. abyssi was related with positive selection for the genes mainly involved in inorganic ion transport. Analysis of radical amino acid replacement rate in evolving P. furiosus, P. horikoshii and P. abyssi showed that the fixation rate was higher for radical substitutions relative to the volume of amino acid side-chain. CONCLUSIONS: The current results give due credit to the important role of hydrostatic pressure as a cause of variability in the P. furiosus, P. horikoshii and P. abyssi genomes evolving in different habitats. Nevertheless, adaptation to pressure does not appear to be the sole factor ensuring adaptation to environment. For example, at the stage of the divergence of P. horikoshii and P. abyssi, an essential evolutionary role may be assigned to changes in the trophic chain, namely, acquisition of a consumer status at a high (P. horikoshii) or low level (P. abyssi).


Subject(s)
Evolution, Molecular , Genome, Archaeal , Pyrococcus/genetics , Adaptation, Biological , Multigene Family , Phylogeny , Pressure , Proteome/genetics , Proteome/metabolism , Pyrococcus/physiology , Selection, Genetic
8.
Structure ; 15(12): 1542-54, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18073105

ABSTRACT

Transcriptional repressor FL11 from the hyperthermophilic archaeon, Pyrococcus OT3, was crystallized in its dimer form in complex with a DNA duplex, TGAAAWWWTTTCA. Chemical contacting of FL11 to the terminal 5 bps, and DNA bending by propeller twisting at WWW confirmed specificity of the interaction. Dimer-binding sites were identified in promoters of approximately 200 transcription units coding, for example, H+-ATPase and NAD(P)H dehydrogenase. In the presence of lysine, four FL11 dimers were shown to assemble into an octamer, thereby covering the fl11 promoter. In the "feast" mode, when P. OT3 grows on amino acids, the FL11 octamer will terminate transcription of fl11, as was shown in vitro, thereby derepressing transcription of many metabolic genes. In the "famine" mode in the absence of lysine, approximately 6000 FL11 dimers present per cell will arrest growth. This regulation resembles global regulation by Escherichia coli leucine-responsive regulatory protein, and hints at a prototype of transcription regulations now highly diverged.


Subject(s)
Pyrococcus/physiology , Transcription Factors/physiology , Amino Acid Sequence , Base Sequence , Crystallography, X-Ray , Models, Molecular , Molecular Sequence Data , Protein Structure, Secondary , Sequence Homology, Amino Acid , Transcription Factors/chemistry
9.
J Biol Chem ; 281(10): 6751-9, 2006 Mar 10.
Article in English | MEDLINE | ID: mdl-16407194

ABSTRACT

The exosome is a conserved eukaryotic enzymatic complex that plays an essential role in many pathways of RNA processing and degradation. Here, we describe the structural characterization of the predicted archaeal exosome in solution using small angle x-ray scattering. The structure model calculated from the small angle x-ray scattering pattern provides an indication of the existence of a disk-shaped structure, corresponding to the "RNases PH ring" complex formed by the proteins aRrp41 and aRrp42. The RNases PH ring complex corresponds to the core of the exosome, binds RNA, and has phosphorolytic and polymerization activities. Three additional molecules of the RNA-binding protein aRrp4 are attached to the core as extended and flexible arms that may direct the substrates to the active sites of the exosome. In the presence of aRrp4, the activity of the core complex is enhanced, suggesting a regulatory role for this protein. The results shown here also indicate the participation of the exosome in RNA metabolism in Archaea, as was established in Eukarya.


Subject(s)
Pyrococcus/physiology , RNA Processing, Post-Transcriptional/physiology , RNA, Archaeal/chemistry , RNA, Archaeal/physiology , Archaeal Proteins/chemistry , Archaeal Proteins/metabolism , Archaeal Proteins/physiology , Chromatography, Gel , Electrophoretic Mobility Shift Assay , Exoribonucleases/chemistry , Exoribonucleases/metabolism , Models, Molecular , Protein Binding , Pyrococcus/chemistry , Pyrococcus/enzymology , Scattering, Radiation , Solutions , X-Ray Diffraction , X-Rays
10.
J Bioenerg Biomembr ; 36(1): 5-15, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15168605

ABSTRACT

In archaea, ATP-binding cassette (ABC) transporters play a crucial role in substrate uptake, export, and osmoregulation. Archael substrate-binding-protein-dependent ABC transporters are equipped with a very high affinity for their cognate substrates which provide these organisms with the ability to efficiently scavenge substrates from their environment even when present only at low concentration. Further adaptations to the archaeal way of life are especially found in the domain organization and anchoring of the substrate-binding proteins to the membrane. Examination of the signal peptides of binding proteins of 14 archael genomes showed clear differences between euryarchaeotes and crenarchaeotes. Furthermore, a profiling and comparison of ABC transporters in the three sequenced pyrococcal strains was performed.


Subject(s)
ATP-Binding Cassette Transporters/chemistry , ATP-Binding Cassette Transporters/metabolism , Archaea/physiology , Cell Membrane/physiology , Gene Expression Regulation, Archaeal/physiology , Protein Sorting Signals/physiology , Signal Transduction/physiology , ATP-Binding Cassette Transporters/genetics , Amino Acid Sequence , Archaeal Proteins/chemistry , Archaeal Proteins/genetics , Archaeal Proteins/metabolism , Biological Transport, Active/physiology , Molecular Sequence Data , Protein Binding , Pyrococcus/physiology , Sequence Homology, Amino Acid
11.
J Mol Evol ; 59(5): 606-19, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15693617

ABSTRACT

Attempts were made to define the relationship among the three domains (eukaryotes, archaea, and eubacteria) using phylogenetic tree analyses of 16S rRNA sequences as well as of other protein sequences. Since the results are inconsistent, it is implied that the eukaryotic genome has a chimeric structure. In our previous studies, the origin of eukaryotes to be the symbiosis of archaea into eubacteria using the whole open reading frames (ORF) of many genomes was suggested. In these studies, the species participating in the symbiosis were not clarified, and the effect of gene duplication after speciation (in-paralog) was not addressed. To avoid the influence of the in-paralog, we developed a new method to calculate orthologous ORFs. Furthermore, we separated eukaryotic in-paralogs into three groups by sequence similarity to archaea, eubacteria (other than alpha-proteobacteria), and alpha-proteobacteria and treated them as individual organisms. The relationship between the three ORF groups and the functional classification was clarified by this analysis. The introduction of this new method into the phylogenetic tree analysis of 66 organisms (4 eukaryotes, 13 archaea, and 49 eubacteria) based on gene content suggests the symbiosis of pyrococcus into gamma-proteobacteria as the origin of eukaryotes.


Subject(s)
Eukaryotic Cells/cytology , Gammaproteobacteria/cytology , Gammaproteobacteria/genetics , Phylogeny , Pyrococcus/genetics , Pyrococcus/physiology , Symbiosis/physiology , Eukaryotic Cells/physiology , Gammaproteobacteria/physiology , Genome , Mosaicism , Open Reading Frames/genetics
12.
J Bacteriol ; 185(13): 3958-61, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12813090

ABSTRACT

The mechanisms by which hyperthermophilic Archaea, such as "Pyrococcus abyssi" and Pyrococcus furiosus, survive high doses of ionizing gamma irradiation are not thoroughly elucidated. Following gamma-ray irradiation at 2,500 Gy, the restoration of "P. abyssi" chromosomes took place within chromosome fragmentation. DNA synthesis in irradiated "P. abyssi" cells during the DNA repair phase was inhibited in comparison to nonirradiated control cultures, suggesting that DNA damage causes a replication block in this organism. We also found evidence for transient export of damaged DNA out of irradiated "P. abyssi" cells prior to a restart of chromosomal DNA synthesis. Our cell fractionation assays further suggest that "P. abyssi" contains a highly efficient DNA repair system which is continuously ready to repair the DNA damage caused by high temperature and/or ionizing radiation.


Subject(s)
DNA Damage , DNA Repair , Gamma Rays/adverse effects , Hot Temperature , Pyrococcus/physiology , Blotting, Western , Culture Media , DNA Replication , Pyrococcus/growth & development , Pyrococcus/radiation effects , Pyrococcus furiosus/physiology , Pyrococcus furiosus/radiation effects , Radiation, Ionizing
13.
Biochem Soc Trans ; 31(Pt 3): 677-80, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12773181

ABSTRACT

Pyrococcus woesei ( Pw ) is an archaeal organism adapted to living in conditions of elevated salt and temperature. Thermodynamic data reveal that the interaction between the TATA-box-binding protein (TBP) from this organism and DNA has an entirely different character to the same interaction in mesophilic counterparts. In the case of the Pw TBP, the affinity of its interaction with DNA increases with increasing salt concentration. The opposite effect is observed in all known mesophilic protein-DNA interactions. The halophilic behaviour can be attributed to sequestration of cations into the protein-DNA complex. By mutating residues in the Pw TBP DNA-binding site, potential sites of cation interaction can be removed. These mutations have a significant effect on the binding characteristics, and the halophilic nature of the Pw TBP-DNA interaction can be reversed, and made to resemble that of a mesophile, in just three mutations. The genes of functionally homologous proteins in organisms existing in different environments show that adaptation is most often accompanied by mutation of an existing protein. However, the importance of any individual residue to a phenotypic characteristic is usually difficult to assess amongst the multitude of changes that occur over evolutionary time. Since the halophilic nature of this protein can be attributed to only three mutations, this reveals that the important phenotype of halophilicity could be rapidly acquired in evolutionary time.


Subject(s)
DNA, Archaeal/genetics , Pyrococcus/genetics , Archaeal Proteins/metabolism , DNA, Archaeal/metabolism , Evolution, Molecular , Ions/metabolism , Mutation , Pyrococcus/physiology , TATA-Box Binding Protein/metabolism
14.
Appl Environ Microbiol ; 68(11): 5528-36, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12406746

ABSTRACT

Our understanding of the genetics of species of the best-studied hyperthermophilic archaea, Pyrococcus spp., is presently limited by the lack of suitable genetic tools, such as a stable cloning vector and the ability to select individual transformants on plates. Here we describe the development of a reliable host-vector system for the hyperthermophilic archaeon Pyrococcus abyssi. Shuttle vectors were constructed based on the endogenous plasmid pGT5 from P. abyssi strain GE5 and the bacterial vector pLitmus38. As no antibiotic resistance marker is currently available for Pyrococcus spp., we generated a selectable auxotrophic marker. Uracil auxotrophs resistant to 5-fluoorotic acid were isolated from P. abyssi strain GE9 (devoid of pGT5). Genetic analysis of these mutants revealed mutations in the pyrE and/or pyrF genes, encoding key enzymes of the pyrimidine biosynthetic pathway. Two pyrE mutants exhibiting low reversion rates were retained for complementation experiments. For that purpose, the pyrE gene, encoding orotate phosphoribosyltransferase (OPRTase) of the thermoacidophilic crenarchaeote Sulfolobus acidocaldarius, was introduced into the pGT5-based vector, giving rise to pYS2. With a polyethylene glycol-spheroplast method, we could reproducibly transform P. abyssi GE9 pyrE mutants to prototrophy, though with low frequency (10(2) to 10(3) transformants per micro g of pYS2 plasmid DNA). Transformants did grow as well as the wild type on minimal medium without uracil and showed comparable OPRTase activity. Vector pYS2 proved to be very stable and was maintained at high copy number under selective conditions in both Escherichia coli and P. abyssi.


Subject(s)
Pyrococcus/genetics , Spheroplasts/genetics , BH3 Interacting Domain Death Agonist Protein , Carrier Proteins , Genetic Markers , Genetic Vectors/genetics , Genetic Vectors/metabolism , Mutation , Plasmids/genetics , Polyethylene Glycols , Pyrococcus/physiology , Spheroplasts/physiology , Uracil/metabolism
15.
J Biol Chem ; 275(42): 32383-6, 2000 Oct 20.
Article in English | MEDLINE | ID: mdl-10940293

ABSTRACT

While most organisms grow at temperatures ranging between 20 and 50 degrees C, many archaea and a few bacteria have been found capable of withstanding temperatures close to 100 degrees C, or beyond, such as Pyrococcus or Aquifex. Here we report the results of two independent large scale unbiased approaches to identify global protein properties correlating with an extreme thermophile lifestyle. First, we performed a comparative proteome analyses using 30 complete genome sequences from the three kingdoms. A large difference between the proportions of charged versus polar (noncharged) amino acids was found to be a signature of all hyperthermophilic organisms. Second, we analyzed the water accessible surfaces of 189 protein structures belonging to mesophiles or hyperthermophiles. We found that the surfaces of hyperthermophilic proteins exhibited the shift already observed at the genomic level, i.e. a proportion of solvent accessible charged residues strongly increased at the expense of polar residues. The biophysical requirements for the presence of charged residues at the protein surface, allowing protein stabilization through ion bonds, is therefore clearly imprinted and detectable in all genome sequences available to date.


Subject(s)
Archaea/physiology , Bacterial Physiological Phenomena , Fungi/physiology , Plant Physiological Phenomena , Proteins/metabolism , Proteome/physiology , Pyrococcus/physiology , Temperature , Animals , Proteins/genetics , Proteome/genetics
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