Base de dados : MEDLINE
Pesquisa : B03.440.425.400.750 [Categoria DeCS]
Referências encontradas : 17 [refinar]
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  1 / 17 MEDLINE  
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[PMID]:27301131
[Au] Autor:Rogozin DY; Zykova VV; Tarnovskii MO
[Ti] Título:[Dynamics of Purple Sulfur Bacteria in a Meromictic Saline Lake Shunet (Khakassia, Siberia) in 2007-2013].
[So] Source:Mikrobiologiia;85(1):73-82, 2016 Jan-Feb.
[Is] ISSN:0026-3656
[Cp] País de publicação:Russia (Federation)
[La] Idioma:rus
[Ab] Resumo:According to the results of seasonal monitoring, in 2007-2013 purple sulfur bacteria morphologically similar to Thiocapsa sp. Shira_1 (AJ633676 in EMBL/GenBank) predominated in the anoxygenic phototrophic community of the water column of the meromictic Lake Shira (Khakassia, Siberia). No pronounced seasonal periodicity in the total cell number in the water column was revealed during the period of observation. In some years cell number during the period when the lake was covered with ice was reliably higher than in summer. The absence ofseasonal periodicity was probably due to the low amplitude of seasonal variations in temperature and illumination in the redox zone, resulting from its relatively deep location (12-16 m). The year-to-year dynamics was characterized by a reliable decrease of the total cell number in 2009-2010 and maxima in 2007 and 2011-2012. Canonical correlation analysis revealed that water temperature in the redox zone was the best predictor of the PSB abundance in Lake Shira. Water temperature, in turn, depended on the depth of mixing of the water column. Intense mixing in 2009-2011 was probably responsible for decreased PSB abundance in the lake. On the other hand, the absence of deep winter mixing, resulting in stable conditions in the chemocline, favored the preservation of relatively high PSB biomass. Prediction of circulation depth, which.depends mainly on the weather conditions and dynamics of the water level, is required for prediction of PSB abundance in Lake Shira. These results may be useful for paleolimnological reconstructions of the history of the lake based on the remnants of purple sulfur bacteria in bottom sediments.
[Mh] Termos MeSH primário: Lagos/microbiologia
Thiocapsa
Microbiologia da Água
[Mh] Termos MeSH secundário: Animais
Sibéria
Thiocapsa/classificação
Thiocapsa/isolamento & purificação
Thiocapsa/metabolismo
[Pt] Tipo de publicação:ENGLISH ABSTRACT; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Em] Mês de entrada:1607
[Cu] Atualização por classe:160615
[Lr] Data última revisão:
160615
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160616
[St] Status:MEDLINE


  2 / 17 MEDLINE  
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[PMID]:20447994
[Au] Autor:Schott J; Griffin BM; Schink B
[Ad] Endereço:Microbial Ecology, Department of Biology, Universität Konstanz, D-78465 Konstanz, Germany.
[Ti] Título:Anaerobic phototrophic nitrite oxidation by Thiocapsa sp. strain KS1 and Rhodopseudomonas sp. strain LQ17.
[So] Source:Microbiology;156(Pt 8):2428-37, 2010 Aug.
[Is] ISSN:1465-2080
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:In anaerobic enrichment cultures for phototrophic nitrite-oxidizing bacteria from different freshwater sites, two different cell types, i.e. non-motile cocci and motile, rod-shaped bacteria, always outnumbered all other bacteria. Most-probable-number (MPN) dilution series with samples from two freshwater sites yielded only low numbers (
[Mh] Termos MeSH primário: Nitritos/metabolismo
Processos Fototróficos
Rodopseudomonas/metabolismo
Thiocapsa/metabolismo
[Mh] Termos MeSH secundário: Anaerobiose
DNA Bacteriano/genética
Dados de Sequência Molecular
Oxirredução
Filogenia
RNA Ribossômico 16S/genética
Rodopseudomonas/genética
Rodopseudomonas/isolamento & purificação
Esgotos/microbiologia
Thiocapsa/genética
Thiocapsa/isolamento & purificação
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (DNA, Bacterial); 0 (Nitrites); 0 (RNA, Ribosomal, 16S); 0 (Sewage)
[Em] Mês de entrada:1010
[Cu] Atualização por classe:100803
[Lr] Data última revisão:
100803
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:100508
[St] Status:MEDLINE
[do] DOI:10.1099/mic.0.036004-0


  3 / 17 MEDLINE  
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[PMID]:19580162
[Au] Autor:Turova TP; Keppen OI; Kovaleva OL; Slobodova NV; Berg IA; Ivanovskii RN
[Ti] Título:[Phylogeny of the purple sulfur bacterium Thiocapsa sp. strain BBS on the basis of analysis of 16S rRNA, cbbL and nifN and description of new species Thiocapsa bogorovii sp.nov].
[So] Source:Mikrobiologiia;78(3):381-92, 2009 May-Jun.
[Is] ISSN:0026-3656
[Cp] País de publicação:Russia (Federation)
[La] Idioma:rus
[Mh] Termos MeSH primário: Filogenia
Thiocapsa/classificação
[Mh] Termos MeSH secundário: Genes Bacterianos
Nitrogenase/genética
RNA Bacteriano/genética
RNA Ribossômico 16S/genética
Ribulose-Bifosfato Carboxilase/genética
Thiocapsa/citologia
Thiocapsa/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (RNA, Bacterial); 0 (RNA, Ribosomal, 16S); EC 1.18.6.1 (Nitrogenase); EC 4.1.1.39 (Ribulose-Bisphosphate Carboxylase)
[Em] Mês de entrada:0909
[Cu] Atualização por classe:090707
[Lr] Data última revisão:
090707
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:090708
[St] Status:MEDLINE


  4 / 17 MEDLINE  
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[PMID]:18085548
[Au] Autor:Branca RM; Bodó G; Bagyinka C; Prokai L
[Ad] Endereço:Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
[Ti] Título:De novo sequencing of a 21-kDa cytochrome c4 from Thiocapsa roseopersicina by nanoelectrospray ionization ion-trap and Fourier-transform ion-cyclotron resonance mass spectrometry.
[So] Source:J Mass Spectrom;42(12):1569-82, 2007 Dec.
[Is] ISSN:1076-5174
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:We have determined the primary structure of cytochrome c(4) from Thiocapsa roseopersicina by de novo protein sequencing using the 'bottom up' approach. Three different enzymes (trypsin, endoproteinase Lys-C, and endoproteinase Glu-C) were employed to prepare four different sets of proteolytic digests. The digestion strategy was designed to permit a gradual buildup of smaller peptides into larger ones that were overlapped to yield the complete protein sequence. In this way we countered the main problem: peptides larger than about 1500 Da were difficult to sequence fully by tandem mass spectrometry. Direct infusion and online liquid chromatography were used on a linear ion trap Fourier-transform ion-cyclotron resonance hybrid instrument. The high resolving power, high mass accuracy and the availability of electron capture dissociation and collision-induced dissociation were essential to achieve full sequence coverage. The software DeNovoX complemented by manual interpretation was used to generate sequence information from tandem mass spectra. The predominantly automated nature of data acquisition and handling allowed for a relatively straightforward and fast procedure, which could compete with the mainstream alternative of nucleotide sequence determination.
[Mh] Termos MeSH primário: Grupo dos Citocromos c/química
Thiocapsa/química
[Mh] Termos MeSH secundário: Ciclotrons
Análise de Fourier
Metilação
Peso Molecular
Nanotecnologia
Oxirredução
Peptídeo Hidrolases/química
Peptídeos/análise
Peptídeos/química
Análise de Sequência de Proteína
Espectrometria de Massas por Ionização por Electrospray
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Cytochrome c Group); 0 (Peptides); 39405-42-0 (cytochrome C4); EC 3.4.- (Peptide Hydrolases)
[Em] Mês de entrada:0803
[Cu] Atualização por classe:071224
[Lr] Data última revisão:
071224
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:071219
[St] Status:MEDLINE


  5 / 17 MEDLINE  
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[PMID]:17668427
[Au] Autor:Karyakin AA; Morozov SV; Voronin OG; Zorin NA; Karyakina EE; Fateyev VN; Cosnier S
[Ad] Endereço:Chemistry Faculty of M.V. Lomonosov Moscow State University, 119992 Moscow, Russia. aak@analyt.chem.msu.ru
[Ti] Título:The limiting performance characteristics in bioelectrocatalysis of hydrogenase enzymes.
[So] Source:Angew Chem Int Ed Engl;46(38):7244-6, 2007.
[Is] ISSN:1433-7851
[Cp] País de publicação:Germany
[La] Idioma:eng
[Mh] Termos MeSH primário: Proteínas de Bactérias/química
Técnicas Biossensoriais/métodos
Hidrogenase/química
[Mh] Termos MeSH secundário: Catálise
Eletroquímica
Thiocapsa/enzimologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Bacterial Proteins); EC 1.12.7.2 (Hydrogenase)
[Em] Mês de entrada:0712
[Cu] Atualização por classe:091119
[Lr] Data última revisão:
091119
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:070802
[St] Status:MEDLINE


  6 / 17 MEDLINE  
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[PMID]:17661016
[Au] Autor:Asao M; Takaichi S; Madigan MT
[Ad] Endereço:Department of Microbiology, Southern Illinois University, Carbondale, IL 62901-6508, USA.
[Ti] Título:Thiocapsa imhoffii, sp. nov., an alkaliphilic purple sulfur bacterium of the family Chromatiaceae from Soap Lake, Washington (USA).
[So] Source:Arch Microbiol;188(6):665-75, 2007 Dec.
[Is] ISSN:0302-8933
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:An alkaliphilic purple sulfur bacterium, strain SC5, was isolated from Soap Lake, a soda lake located in east central Washington state (USA). Cells of strain SC5 were gram-negative, non-motile, and non-gas vesiculate cocci, often observed in pairs or tetrads. In the presence of sulfide, elemental sulfur was deposited internally. Liquid cultures were pink to rose red in color. Cells contained bacteriochlorophyll a and spirilloxanthin as major photosynthetic pigments. Internal photosynthetic membranes were of the vesicular type. Optimal growth of strain SC5 occurred in the absence of NaCl (range 0-4%), pH 8.5 (range pH 7.5-9.5), and 32 degrees C. Photoheterotrophic growth occurred in the presence of sulfide or thiosulfate with only a limited number of organic carbon sources. Growth factors were not required, and cells could fix N2. Dark, microaerobic growth occurred in the presence of both an organic carbon source and thiosulfate. Sulfide and thiosulfate served as electron donors for photoautotrophy, which required elevated levels of CO2. Phylogenetic analysis placed strain SC5 basal to the clade of the genus Thiocapsa in the family Chromatiaceae with a 96.7% sequence similarity to its closest relative, Thiocapsa roseopersicina strain 1711T (DSM217T). The unique assemblage of physiological and phylogenetic properties of strain SC5 defines it as a new species of the genus Thiocapsa, and we describe strain SC5 herein as Tca. imhoffii, sp. nov.
[Mh] Termos MeSH primário: Thiocapsa/classificação
[Mh] Termos MeSH secundário: Adaptação Fisiológica
Processos Autotróficos
Técnicas de Tipagem Bacteriana
Ecossistema
Concentração de Íons de Hidrogênio
Processos Fototróficos
Filogenia
RNA Ribossômico 16S/genética
Thiocapsa/genética
Thiocapsa/isolamento & purificação
Thiocapsa/fisiologia
Washington
Microbiologia da Água
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (RNA, Ribosomal, 16S)
[Em] Mês de entrada:0806
[Cu] Atualização por classe:071206
[Lr] Data última revisão:
071206
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:070731
[St] Status:MEDLINE


  7 / 17 MEDLINE  
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PubMed Central Texto completo
[PMID]:16880567
[Au] Autor:Tomcová I; Branca RM; Bodó G; Bagyinka C; Smatanová IK
[Ad] Endereço:Institute of Physical Biology, University of South Bohemia in Ceské Budejovice, Zámek 136, CZ-373 33 Nové Hrady, Czech Republic. tomcova@ufb.jcu.cz
[Ti] Título:Cross-crystallization method used for the crystallization and preliminary diffraction analysis of a novel di-haem cytochrome c4.
[So] Source:Acta Crystallogr Sect F Struct Biol Cryst Commun;62(Pt 8):820-4, 2006 Aug 01.
[Is] ISSN:1744-3091
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The newly discovered di-haem cytochrome c4 from the purple sulfur photosynthetic bacterium Thiocapsa roseopersicina is the first cytochrome c4 to be crystallized from an anaerobic organism. It was crystallized using the addition of metal-ion salts to the standard vapour-diffusion method. Coloured well shaped three-dimensional crystals with dimensions of approximately 0.6 x 0.05 x 0.02 mm grew within 3-4 d at pH 5 and diffracted to 1.72 angstroms without radiation damage. Cytochrome c4 crystallized in space group P4(1)2(1)2 as a primitive tetragonal system with unit-cell parameters a = b = 75.29, c = 37.12 angstroms, alpha = beta = gamma = 90 degrees.
[Mh] Termos MeSH primário: Grupo dos Citocromos c/química
Thiocapsa/enzimologia
[Mh] Termos MeSH secundário: Proteínas de Bactérias/química
Proteínas de Bactérias/isolamento & purificação
Cristalização
Grupo dos Citocromos c/isolamento & purificação
Difração de Raios X
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Bacterial Proteins); 0 (Cytochrome c Group); 39405-42-0 (cytochrome C4)
[Em] Mês de entrada:0609
[Cu] Atualização por classe:170219
[Lr] Data última revisão:
170219
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:060802
[St] Status:MEDLINE


  8 / 17 MEDLINE  
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[PMID]:16011763
[Au] Autor:Herbert RA; Ranchou-Peyruse A; Duran R; Guyoneaud R; Schwabe S
[Ad] Endereço:Division of Environmental and Applied Biology, Biological Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland. r.a.herbert@dundee.ac.uk
[Ti] Título:Characterization of purple sulfur bacteria from the South Andros Black Hole cave system: highlights taxonomic problems for ecological studies among the genera Allochromatium and Thiocapsa.
[So] Source:Environ Microbiol;7(8):1260-8, 2005 Aug.
[Is] ISSN:1462-2912
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:A dense 1 m thick layer of phototrophic purple sulfur bacteria is present at the pycnocline (17.8 m depth) in the meromictic South Andros Black Hole cave system (Bahamas). Two purple sulfur bacteria present in samples collected from this layer have been identified as belonging to the family Chromatiaceae. One isolate (BH-1), pink coloured, is non-motile, non-gas vacuolated, 2-3 microm in diameter and surrounded by a capsule. The other isolates (BH-2 and BH-2.4), reddish-brown coloured, are small celled (4 microm x 2 microm), motile by means of a single polar flagellum. In both isolates (BH-1 and BH-2), the intracellular photosynthetic membranes are of the vesicular type and bacteriochlorophyll a and carotenoids of the normal spirilloxanthin series are present. Both isolates grow well in the presence of sulfide and carbon dioxide in the light. During photoautotrophic growth sulfur globules are stored intracellularly as intermediate oxidation products. According to the 16S rRNA gene sequence data the isolates belong to the genera Thiocapsa and Allochromatium. However, at the species level a number of inconsistencies exist between the phenotypic and phylogenetic data, highlighting taxonomic problems within these genera. These inconsistencies may have implications for microbiologists studying the ecology of anoxygenic phototrophs. For ecologists studying the functioning of an ecosystem it may not be particularly important to know whether a specific isolate belongs to one species or another. However, if one wants to study the role of different populations within a particular functional group then the species concept is important. This study demonstrates that further work is still required on the taxonomy of purple sulfur bacteria in order that microbial ecologists are able to accurately identify a population/species isolated from hitherto undescribed aquatic ecosystems.
[Mh] Termos MeSH primário: Chromatiaceae/classificação
Água do Mar/microbiologia
Thiocapsa/classificação
[Mh] Termos MeSH secundário: Bahamas
Composição de Bases
Chromatiaceae/genética
Chromatiaceae/fisiologia
DNA Bacteriano/análise
DNA Ribossômico/análise
Genes de RNAr
Dados de Sequência Molecular
Hibridização de Ácido Nucleico
Fotossíntese
Pigmentos Biológicos/metabolismo
RNA Ribossômico 16S/genética
Thiocapsa/genética
Thiocapsa/fisiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (DNA, Bacterial); 0 (DNA, Ribosomal); 0 (Pigments, Biological); 0 (RNA, Ribosomal, 16S)
[Em] Mês de entrada:0509
[Cu] Atualização por classe:051117
[Lr] Data última revisão:
051117
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:050714
[St] Status:MEDLINE


  9 / 17 MEDLINE  
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[PMID]:15280266
[Au] Autor:Caumette P; Guyoneaud R; Imhoff JF; Süling J; Gorlenko V
[Ad] Endereço:Laboratoire d'Ecologie Moléculaire, EA 3525, IBEAS, Université de Pau et des Pays de l'Adour, BP1155, F-64013 Pau, France. pierre.caumette@univ-pau.fr
[Ti] Título:Thiocapsa marina sp. nov., a novel, okenone-containing, purple sulfur bacterium isolated from brackish coastal and marine environments.
[So] Source:Int J Syst Evol Microbiol;54(Pt 4):1031-6, 2004 Jul.
[Is] ISSN:1466-5026
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Four marine, phototrophic, purple sulfur bacteria (strains 5811T, 5812, BM-3 and BS-1) were isolated in pure culture from different brackish to marine sediments in the Mediterranean Sea, the White Sea and the Black Sea. Single cells of these strains were coccus-shaped, non-motile and did not contain gas vesicles. The colour of cell suspensions that were grown in the light was purple-red. Bacteriochlorophyll a and carotenoids of the okenone series were present as photosynthetic pigments. Photosynthetic membrane systems were of the vesicular type. Hydrogen sulfide, thiosulfate, elemental sulfur and molecular hydrogen were used as electron donors during photolithotrophic growth under anoxic conditions; carbon dioxide was utilized as the carbon source. During growth on sulfide, elemental sulfur globules were stored inside the cells. In the presence of hydrogen sulfide, several organic substances could be photoassimilated. Comparative 16S rDNA sequence analysis revealed an affiliation of these four strains to the genus Thiocapsa. Both phylogenetic analysis and the results of DNA-DNA hybridization studies revealed that these strains formed a separate cluster within the genus Thiocapsa. Thus, according to phenotypic characteristics and mainly the carotenoid composition, 16S rDNA sequence analysis and DNA-DNA hybridization data, it is proposed that these strains should be classified as a novel species, Thiocapsa marina sp. nov., with strain 5811T (=DSM 5653T=ATCC 43172T) as the type strain.
[Mh] Termos MeSH primário: Thiocapsa/classificação
[Mh] Termos MeSH secundário: Anaerobiose
Bacterioclorofila A/análise
Composição de Bases
Dióxido de Carbono/metabolismo
Carotenoides/análise
DNA Bacteriano/química
DNA Ribossômico/química
Genes de RNAr
Sedimentos Geológicos/microbiologia
Hidrogênio/metabolismo
Sulfeto de Hidrogênio/metabolismo
Dados de Sequência Molecular
Movimento
Hibridização de Ácido Nucleico
Compostos Orgânicos/metabolismo
Filogenia
Pigmentos Biológicos/biossíntese
Pigmentos Biológicos/fisiologia
RNA Ribossômico 16S/genética
Análise de Sequência de DNA
Enxofre/metabolismo
Thiocapsa/citologia
Thiocapsa/isolamento & purificação
Thiocapsa/fisiologia
Tiossulfatos/metabolismo
Microbiologia da Água
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Bacteriochlorophyll A); 0 (DNA, Bacterial); 0 (DNA, Ribosomal); 0 (Organic Chemicals); 0 (Pigments, Biological); 0 (RNA, Ribosomal, 16S); 0 (Thiosulfates); 142M471B3J (Carbon Dioxide); 36-88-4 (Carotenoids); 70FD1KFU70 (Sulfur); 7YNJ3PO35Z (Hydrogen); YY9FVM7NSN (Hydrogen Sulfide)
[Em] Mês de entrada:0502
[Cu] Atualização por classe:131121
[Lr] Data última revisão:
131121
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:040729
[St] Status:MEDLINE


  10 / 17 MEDLINE  
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Fotocópia
[PMID]:12752441
[Au] Autor:Maróti G; Fodor BD; Rákhely G; Kovács AT; Arvani S; Kovács KL
[Ad] Endereço:Institute of Biophysics, Biological Research Center, Hungarian Academy of Sciences, Hungary.
[Ti] Título:Accessory proteins functioning selectively and pleiotropically in the biosynthesis of [NiFe] hydrogenases in Thiocapsa roseopersicina.
[So] Source:Eur J Biochem;270(10):2218-27, 2003 May.
[Is] ISSN:0014-2956
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:There are at least two membrane-bound (HynSL and HupSL) and one soluble (HoxEFUYH) [NiFe] hydrogenases in Thiocapsa roseopersicina BBS, a purple sulfur photosynthetic bacterium. Genes coding for accessory proteins that participate in the biosynthesis and maturation of hydrogenases seem to be scattered along the chromosome. Transposon-based mutagenesis was used to locate the hydrogenase accessory genes. Molecular analysis of strains showing mutant phenotypes led to the identification of hupK (hoxV ), hypC1, hypC2, hypD, hypE, and hynD genes. The roles of hynD, hupK and the two hypC genes were investigated in detail. The putative HynD was found to be a hydrogenase-specific endoprotease type protein, participating in the maturation of the HynSL enzyme. HupK plays an important role in the formation of the functionally active membrane-bound [NiFe] hydrogenases, but not in the biosynthesis of the soluble enzyme. In-frame deletion mutagenesis showed that HypC proteins were not specific for the maturation of either hydrogenase enzyme. The lack of either HypC protein drastically reduced the activity of every hydrogenase. Hence both HypCs might participate in the maturation of [NiFe] hydrogenases. Homologous complementation with the appropriate genes substantiated the physiological roles of the corresponding gene products in the H2 metabolism of T. roseopersicina.
[Mh] Termos MeSH primário: Hidrogenase/química
Hidrogenase/metabolismo
Proteínas
Thiocapsa/enzimologia
[Mh] Termos MeSH secundário: Proteínas de Bactérias/genética
Southern Blotting
Membrana Celular/metabolismo
DNA/metabolismo
Elementos de DNA Transponíveis
Endopeptidases/química
Deleção de Genes
Teste de Complementação Genética
Hidrogênio/química
Modelos Genéticos
Mutagênese Sítio-Dirigida
Plasmídeos/metabolismo
Reação em Cadeia da Polimerase
Reação em Cadeia da Polimerase Via Transcriptase Reversa
Análise de Sequência de DNA
Transcrição Genética
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Bacterial Proteins); 0 (DNA Transposable Elements); 0 (HypC protein, Bacteria); 0 (HypD protein, Bacteria); 0 (Proteins); 0 (hupK protein, Rhizobium leguminosarum); 0 (hypE protein, Bacteria); 7YNJ3PO35Z (Hydrogen); 9007-49-2 (DNA); EC 1.12.- (nickel-iron hydrogenase); EC 1.12.7.2 (Hydrogenase); EC 3.4.- (Endopeptidases)
[Em] Mês de entrada:0306
[Cu] Atualização por classe:161017
[Lr] Data última revisão:
161017
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:030520
[St] Status:MEDLINE



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