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  1 / 15812 MEDLINE  
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[PMID]:29367481
[Au] Autor:Chanwattanakit J; Chavadej S
[Ad] Endereço:The Petroleum and Petrochemical College, Chulalongkorn University.
[Ti] Título:Laundry Detergency of Solid Non-Particulate Soil Using Microemulsion-Based Formulation.
[So] Source:J Oleo Sci;67(2):187-198, 2018 Feb 01.
[Is] ISSN:1347-3352
[Cp] País de publicação:Japan
[La] Idioma:eng
[Ab] Resumo:Laundry detergency of solid non-particulate soil on polyester and cotton was investigated using a microemulsion-based formulation, consisting of an anionic extended surfactant (C -4PO-SO Na) and sodium mono-and di-methyl naphthalene sulfonate (SMDNS) as the hydrophilic linker, to provide a Winsor Type III microemulsion with an ultralow interfacial tension (IFT). In this work, methyl palmitate (palmitic acid methyl ester) having a melting point around 30°C, was used as a model solid non-particulate (waxy) soil. A total surfactant concentration of 0.35 wt% of the selected formulation (4:0.65 weight ratio of C -4PO-SO Na:SMDNS) with 5.3 wt% NaCl was able to form a middle phase microemulsion at a high temperature (40°C),which provided the highest oil removal level with the lowest oil redeposition and the lowest IFT, and was much higher than that with a commercial detergent or de-ionized water. Most of the detached oil, whether in liquid or solid state, was in an unsolubilized form. Hence, the dispersion stability of the detached oil droplets or solidified oil particles that resulted from the surfactant adsorption played an important role in the oil redeposition. For an oily detergency, the lower the system IFT, the higher the oil removal whereas for a waxy (non-particulate) soil detergency, the lower the contact angle, the higher the solidified oil removal. For a liquefied oil, the detergency mechanism was roll up and emulsification with dispersion stability, while that for the waxy soil (solid oil) was the detachment by wettability with dispersion stability.
[Mh] Termos MeSH primário: Detergentes/química
Lavanderia
Palmitatos
[Mh] Termos MeSH secundário: Fibra de Algodão
Emulsões
Interações Hidrofóbicas e Hidrofílicas
Material Particulado
Poliésteres
Tensão Superficial
Tensoativos
Temperatura Ambiente
Têxteis
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Detergents); 0 (Emulsions); 0 (Palmitates); 0 (Particulate Matter); 0 (Polyesters); 0 (Surface-Active Agents); DPY8VCM98I (methyl palmitate)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180309
[Lr] Data última revisão:
180309
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180126
[St] Status:MEDLINE
[do] DOI:10.5650/jos.ess17135


  2 / 15812 MEDLINE  
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[PMID]:29220560
[Au] Autor:Jacques-Gagnon O; Lavertu V
[Ad] Endereço:Centre antipoison du Québec, CIUSSS de la Capitale-Nationale, Québec, Québec, Canada.
[Ti] Título:L'ingestion par des enfants de détergent à lessive ensaché..
[So] Source:Perspect Infirm;14(3):38-39, 2017 May-Jun.
[Is] ISSN:1708-1890
[Cp] País de publicação:Canada
[La] Idioma:fre
[Mh] Termos MeSH primário: Detergentes/envenenamento
Produtos Domésticos/envenenamento
[Mh] Termos MeSH secundário: Criança
Ingestão de Alimentos
Seres Humanos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Detergents)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180306
[Lr] Data última revisão:
180306
[Sb] Subgrupo de revista:N
[Da] Data de entrada para processamento:171209
[St] Status:MEDLINE


  3 / 15812 MEDLINE  
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[PMID]:27774620
[Au] Autor:Vendramin C; McGuckin S; Alwan F; Westwood JP; Thomas M; Scully M
[Ad] Endereço:Department of Haematology, University College London Hospital.
[Ti] Título:A single-center prospective study on the safety of plasma exchange procedures using a double-viral-inactivated and prion-reduced solvent/detergent fresh-frozen plasma as the replacement fluid in the treatment of thrombotic microangiopathy.
[So] Source:Transfusion;57(1):131-136, 2017 01.
[Is] ISSN:1537-2995
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Patients presenting with acute episodes of thrombotic microangiopathies (TMAs) require urgent access to plasma exchange (PEX). OctaplasLG, a solvent/detergent fresh-frozen plasma product that has undergone viral inactivation and prion reduction step, has been used in our institution since 2013, replacing Octaplas. STUDY DESIGN AND METHODS: We prospectively reviewed 981 PEX procedures where OctaplasLG was the replacement fluid in 90 patients admitted acutely with a TMA presentation within our institution from January 1, 2013, to December 31, 2015. We recorded citrate toxicities, plasma reactions, viral transfer, complications related to central venous catheter, and venous thrombotic events (VTEs). RESULTS: Citrate toxicities were 5.4%, plasma reactions were 2%, and all were classified as Grade 1 or 2. VTE had an incidence of 12.2%, although 50% of the episodes occurred in early remission when patients were not receiving PEX. No line insertions complications were recorded. Line-associated infections were 2.2%. Hepatitis B and C serology and human immunodeficiency virus (HIV) were checked on admission. There were four patients who may have had passive transient transfer of hepatitis B antibodies from pooled plasma. No hepatitis C or HIV viral transfer was documented after treatment and no seroconversion was detected after treatment. CONCLUSION: Our data have demonstrated that the incidence of complications during PEX is low and using OctaplasLG is comparable to the low incidence of reactions. No cases of anaphylaxis, transfusion-related acute lung injury, or fatal plasma reactions were seen. There was no evidence of viral transmission or seroconversion after treatment.
[Mh] Termos MeSH primário: Desinfecção/métodos
Troca Plasmática/métodos
Plasma
Príons
Microangiopatias Trombóticas/terapia
Inativação de Vírus
[Mh] Termos MeSH secundário: Adolescente
Adulto
Idoso
Idoso de 80 Anos ou mais
Detergentes/química
Feminino
HIV
Infecções por HIV/prevenção & controle
Hepacivirus
Hepatite B/prevenção & controle
Vírus da Hepatite B
Hepatite C/prevenção & controle
Seres Humanos
Masculino
Meia-Idade
Estudos Prospectivos
Solventes/química
[Pt] Tipo de publicação:CLINICAL TRIAL; JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Detergents); 0 (Prions); 0 (Solvents)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:180302
[Lr] Data última revisão:
180302
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161025
[St] Status:MEDLINE
[do] DOI:10.1111/trf.13877


  4 / 15812 MEDLINE  
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[PMID]:28470613
[Au] Autor:Rues RB; Gräwe A; Henrich E; Bernhard F
[Ad] Endereço:Centre for Biomolecular Magnetic Resonance, Institute for Biophysical Chemistry, Goethe-University of Frankfurt/Main, Max-von-Laue-Str. 9, 60438, Frankfurt/Main, Germany.
[Ti] Título:Membrane Protein Production in E. coli Lysates in Presence of Preassembled Nanodiscs.
[So] Source:Methods Mol Biol;1586:291-312, 2017.
[Is] ISSN:1940-6029
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Cell-free expression allows to synthesize membrane proteins in completely new formats that can relatively easily be customized for particular applications. Amphiphilic superstructures such as micelles, lipomicelles, or nanodiscs can be provided as nano-devices for the solubilization of membrane proteins. Defined empty bilayers in the form of nanodiscs offer native like environments for membrane proteins, supporting functional folding, proper oligomeric assembly as well as stability. Even very difficult and detergent-sensitive membrane proteins can be addressed by the combination of nanodisc technology with efficient cell-free expression systems as the direct co-translational insertion of nascent membrane proteins into supplied preassembled nanodiscs is possible. This chapter provides updated protocols for the synthesis of membrane proteins in presence of preassembled nanodiscs suitable for emerging applications such as screening of lipid effects on membrane protein function and the modulation of oligomeric complex formation.
[Mh] Termos MeSH primário: Sistema Livre de Células/metabolismo
Escherichia coli/genética
Bicamadas Lipídicas/química
Proteínas de Membrana/genética
Nanoestruturas/química
Biologia Sintética/métodos
[Mh] Termos MeSH secundário: Detergentes/química
Expressão Gênica
Lipídeos/química
Proteínas de Membrana/química
Proteínas de Membrana/isolamento & purificação
Dobramento de Proteína
Solubilidade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Detergents); 0 (Lipid Bilayers); 0 (Lipids); 0 (Membrane Proteins)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180220
[Lr] Data última revisão:
180220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170505
[St] Status:MEDLINE
[do] DOI:10.1007/978-1-4939-6887-9_19


  5 / 15812 MEDLINE  
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[PMID]:28470611
[Au] Autor:Love JD
[Ad] Endereço:Department of Biochemistry, Albert Einstein College of Medicine at Yeshiva University, Bronx, NY, USA. drjamesdlove@gmail.com.
[Ti] Título:Expression of Prokaryotic Integral Membrane Proteins in E. coli.
[So] Source:Methods Mol Biol;1586:265-278, 2017.
[Is] ISSN:1940-6029
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Production of prokaryotic membrane proteins for structural and functional studies in E. coli can be parallelized and miniaturized. All stages from cloning, expression, purification to detergent selection can be investigated using high-throughput techniques to rapidly and economically find tractable targets.
[Mh] Termos MeSH primário: Proteínas Arqueais/genética
Proteínas de Bactérias/genética
Clonagem Molecular/métodos
Escherichia coli/genética
Proteínas de Membrana/genética
[Mh] Termos MeSH secundário: Proteínas Arqueais/química
Proteínas Arqueais/isolamento & purificação
Bactérias/genética
Proteínas de Bactérias/química
Proteínas de Bactérias/isolamento & purificação
Detergentes/química
Expressão Gênica
Vetores Genéticos/genética
Proteínas de Membrana/química
Proteínas de Membrana/isolamento & purificação
Proteínas Recombinantes/química
Proteínas Recombinantes/genética
Proteínas Recombinantes/isolamento & purificação
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Archaeal Proteins); 0 (Bacterial Proteins); 0 (Detergents); 0 (Membrane Proteins); 0 (Recombinant Proteins)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180220
[Lr] Data última revisão:
180220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170505
[St] Status:MEDLINE
[do] DOI:10.1007/978-1-4939-6887-9_17


  6 / 15812 MEDLINE  
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[PMID]:28470605
[Au] Autor:Errasti-Murugarren E; Rodríguez-Banqueri A; Vázquez-Ibar JL
[Ad] Endereço:Institute for Research in Biomedicine (IRB Barcelona), Barcelona Institute of Science and Technology, 08028, Barcelona, Spain.
[Ti] Título:Split GFP Complementation as Reporter of Membrane Protein Expression and Stability in E. coli: A Tool to Engineer Stability in a LAT Transporter.
[So] Source:Methods Mol Biol;1586:181-195, 2017.
[Is] ISSN:1940-6029
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Obtaining enough quantity of recombinant membrane transport proteins with optimal purity and stability for structural studies is a remarkable challenge. In this chapter, we describe a protocol to engineer SteT, the amino acid transporter of Bacillus subtilis, in order to improve its heterologous expression in Escherichia coli and its stability in detergent micelles. We built a library of 70 SteT mutants, combining a random mutagenesis protocol with a split GFP assay as reporter of protein folding and membrane insertion. Mutagenesis was restricted to residues situated in the transmembrane domains. Improved versions of SteT were successfully identified after analyzing the expression yield and monodispersity in detergent micelles of the library's members.
[Mh] Termos MeSH primário: Sistemas de Transporte de Aminoácidos/genética
Bacillus subtilis/genética
Proteínas de Bactérias/genética
Clonagem Molecular/métodos
Escherichia coli/genética
Engenharia de Proteínas/métodos
[Mh] Termos MeSH secundário: Sistemas de Transporte de Aminoácidos/química
Bacillus subtilis/química
Proteínas de Bactérias/química
Detergentes/química
Proteínas de Fluorescência Verde/química
Proteínas de Fluorescência Verde/genética
Modelos Moleculares
Dobramento de Proteína
Estabilidade Proteica
Proteínas Recombinantes de Fusão/química
Proteínas Recombinantes de Fusão/genética
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Amino Acid Transport Systems); 0 (Bacterial Proteins); 0 (Detergents); 0 (Recombinant Fusion Proteins); 147336-22-9 (Green Fluorescent Proteins)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180220
[Lr] Data última revisão:
180220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170505
[St] Status:MEDLINE
[do] DOI:10.1007/978-1-4939-6887-9_11


  7 / 15812 MEDLINE  
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[PMID]:28468513
[Au] Autor:Al Ashhab A; Sweity A; Bayramoglu B; Herzberg M; Gillor O
[Ad] Endereço:a Zuckerberg Institute for Water Research, Jacob Blaustein Institutes for Desert Research , Ben-Gurion University of the Negev , Midreshet Ben Gurion , Israel.
[Ti] Título:Biofouling of reverse osmosis membranes: effects of cleaning on biofilm microbial communities, membrane performance, and adherence of extracellular polymeric substances.
[So] Source:Biofouling;33(5):397-409, 2017 05.
[Is] ISSN:1029-2454
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Laboratory-scale reverse osmosis (RO) flat-sheet systems were used with two parallel flow cells, one treated with cleaning agents and a control (ie undisturbed). The cleaning efforts increased the affinity of extracellular polymeric substances (EPS) to the RO membrane and altered the biofilm surface structure. Analysis of the membrane biofilm community composition revealed the dominance of Proteobacteria. However, within the phylum Proteobacteria, γ-Proteobacteria dominated the cleaned membrane biofilm, while ß-Proteobacteria dominated the control biofilm. The composition of the fungal phyla was also altered by cleaning, with enhancement of Ascomycota and suppression of Basidiomycota. The results suggest that repeated cleaning cycles select for microbial groups that strongly attach to the RO membrane surface by producing rigid and adhesive EPS that hampers membrane performance.
[Mh] Termos MeSH primário: Aderência Bacteriana/efeitos dos fármacos
Biofilmes/efeitos dos fármacos
Incrustação Biológica/prevenção & controle
Detergentes/farmacologia
Membranas Artificiais
Proteobactérias/efeitos dos fármacos
[Mh] Termos MeSH secundário: Ascomicetos/efeitos dos fármacos
Ascomicetos/crescimento & desenvolvimento
Ascomicetos/fisiologia
Filtração
Osmose
Polímeros/química
Proteobactérias/crescimento & desenvolvimento
Purificação da Água/métodos
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (Detergents); 0 (Membranes, Artificial); 0 (Polymers)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:180215
[Lr] Data última revisão:
180215
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170505
[St] Status:MEDLINE
[do] DOI:10.1080/08927014.2017.1318382


  8 / 15812 MEDLINE  
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[PMID]:29208467
[Au] Autor:Aduri NG; Ernst HA; Prabhala BK; Bhatt S; Boesen T; Gajhede M; Mirza O
[Ad] Endereço:Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
[Ti] Título:Human proton coupled folic acid transporter is a monodisperse oligomer in the lauryl maltose neopentyl glycol solubilized state.
[So] Source:Biochem Biophys Res Commun;495(2):1738-1743, 2018 01 08.
[Is] ISSN:1090-2104
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The human proton coupled folic acid transporter PCFT is the major import route for dietary folates. Mutations in the gene encoding PCFT cause hereditary folic acid malabsorption, which manifests itself by compromised folate absorption from the intestine and also in impaired folate transport into the central nervous system. Since its recent discovery, PCFT has been the subject of numerous biochemical studies aiming at understanding its structure and mechanism. One major focus has been its oligomeric state, with some reports supporting oligomers and others a monomer. Here, we report the overexpression and purification of recombinant PCFT. Following detergent screening, n-Dodecyl ß-D-maltoside (DDM) and lauryl maltose neopentyl glycol (LMNG) were chosen for further work as they exhibited the most optimal solubilization. We found that purified detergent solubilized PCFT was able to bind folic acid, thus indicating a functionally active protein. Size exclusion chromatography showed that PCFT in DDM was polydisperse; the LMNG preparation was clearly monodisperse but with shorter retention time than the major DDM peak. To assess the oligomeric state negative stain electron microscopy was performed which showed a particle with the size of a PCFT dimer.
[Mh] Termos MeSH primário: Transportador de Folato Acoplado a Próton/química
[Mh] Termos MeSH secundário: Animais
Detergentes
Ácido Fólico/metabolismo
Glucosídeos
Glicóis
Seres Humanos
Ligantes
Microscopia Eletrônica
Modelos Moleculares
Multimerização Proteica
Estrutura Quaternária de Proteína
Transportador de Folato Acoplado a Próton/metabolismo
Transportador de Folato Acoplado a Próton/ultraestrutura
Proteínas Recombinantes/química
Proteínas Recombinantes/metabolismo
Proteínas Recombinantes/ultraestrutura
Células Sf9
Solubilidade
Spodoptera
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Detergents); 0 (Glucosides); 0 (Glycols); 0 (Ligands); 0 (Proton-Coupled Folate Transporter); 0 (Recombinant Proteins); 0 (SLC46A1 protein, human); 69227-93-6 (dodecyl maltoside); 935E97BOY8 (Folic Acid)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180212
[Lr] Data última revisão:
180212
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171207
[St] Status:MEDLINE


  9 / 15812 MEDLINE  
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[PMID]:29381986
[Au] Autor:Yeh IJ; Liu KT
[Ad] Endereço:Department of Emergency Medicine, Kaohsiung Medical University Hospital.
[Ti] Título:ST segment elevation associated with hydrochloric acid ingestion: A case report.
[So] Source:Medicine (Baltimore);96(47):e8819, 2017 Nov.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Electrocardiography (ECG) was used to diagnose acute coronary syndrome, but many other diseases may also result in ST segment change. We report one case of ingested hydrochloric acid present with ST segment elevation in the ECG. However, subsequent coronary angiography did not reveal significant coronary occlusion. PATIENT CONCERNS: An 83-year-old female was transferred to our emergency department (ED) from the branch hospital due to ingestion of toilet bowl cleaner containing 9.5% hydrochloric acid. She complained about chest pain and 12-lead ECG showed ST segment elevation at lead II, III, and aVF. The blood examinations revealed elevation of aspartate transaminase (69 IU/L), thrombocytopenia (62,000/µL), and acidosis (pH 7.311, pCO2 27 mm Hg, HCO3 13.3 mmol/L). Creatine kinase-MB and troponin I did not elevate then. DIAGNOSES: After transferred to our ED, coronary angiography was done within 1 hour. Angiography showed 60% stenosis in the segment 7 of left anterior descending coronary artery and 30% nonsignificant stenosis in the segment 2 of right coronary artery, with no apical ballooning. No significant lesion consistent with ST segment elevation myocardial infarction was found. INTERVENTIONS: Conservative treatment was chosen. OUTCOMES: Bradycardia was followed by cardiac arrest that developed 4 hours later. Cardiopulmonary resuscitation was applied and the patient became shock status after return of spontaneous circulation. The patient was admitted to the intensive care unit and expired on next day. LESSONS: Patients of ingested hydrochloric acid present with ST segment elevation in the ECG may not indicate coronary artery disease. This ECG finding may be a poor prognostic index in such patients.
[Mh] Termos MeSH primário: Arritmias Cardíacas/induzido quimicamente
Detergentes/envenenamento
Ácido Clorídrico/envenenamento
[Mh] Termos MeSH secundário: Idoso de 80 Anos ou mais
Bradicardia/induzido quimicamente
Evolução Fatal
Feminino
Parada Cardíaca/induzido quimicamente
Seres Humanos
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Detergents); QTT17582CB (Hydrochloric Acid)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180208
[Lr] Data última revisão:
180208
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180201
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008819


  10 / 15812 MEDLINE  
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[PMID]:29364597
[Au] Autor:Solov'ev AA; Ashikhmin AA; Moskalenko AA
[Ti] Título:Formation of a Subunit Form of the Core Light-Harvesting Complex from Sulfur Purple Bacteria Ectothiorhodospira haloalkaliphila with Different Carotenoid Composition.
[So] Source:Mikrobiologiia;85(5):497-505, 2016 Sep.
[Is] ISSN:0026-3656
[Cp] País de publicação:Russia (Federation)
[La] Idioma:eng
[Ab] Resumo:B820 subunits from a purple sulfur bacterium Ectothiorhodospira. haloalkaliphila strain ATCC 51935T were obtained by treatment of Carotenoid free LH I-RC complexes of this bacterium with P--octylglu- copyranoside (ß-OG). The same complexes with 100% carotenoid content were unable to dissociate to B820 subunits, but disintegrated to monomeric bacteriochlorophyll (BChl) regardless of their carotenoid compo- sition. The degree of dissociation of the LH 1-RC complexes with an intermediate content of carotenoids (the' B820 formation) was directly dependent on the quantity of carotenoids in the samples. The resulting B820 subunits did not contain carotenoids. B820 subunits easily aggregated to form a complex with an absorption . peak at 880 nm at decreased ß-OG concentration. Analysis of the spectra of the LH I-RC complexes isolated from the cells with different'levels of carotenogenesis inhibition led to the conclusion of the heterogeneity of the samples with a predominance in them of (a) the fraction with 100% of carotenoids and (b) the fraction of carotenoid free complexes.
[Mh] Termos MeSH primário: Proteínas de Bactérias/química
Carotenoides/isolamento & purificação
Chromatiaceae/química
Ectothiorhodospiraceae/química
Complexos de Proteínas Captadores de Luz/química
Subunidades Proteicas/química
[Mh] Termos MeSH secundário: Proteínas de Bactérias/isolamento & purificação
Bacterioclorofilas/química
Bacterioclorofilas/isolamento & purificação
Carotenoides/química
Carotenoides/classificação
Chromatiaceae/metabolismo
Detergentes/química
Ectothiorhodospiraceae/metabolismo
Glucosídeos/química
Complexos de Proteínas Captadores de Luz/isolamento & purificação
Extração Líquido-Líquido/métodos
Agregados Proteicos
Subunidades Proteicas/isolamento & purificação
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Bacterial Proteins); 0 (Bacteriochlorophylls); 0 (Detergents); 0 (Glucosides); 0 (Light-Harvesting Protein Complexes); 0 (Protein Aggregates); 0 (Protein Subunits); 29836-26-8 (octyl-beta-D-glucoside); 36-88-4 (Carotenoids)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180208
[Lr] Data última revisão:
180208
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180125
[St] Status:MEDLINE



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BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde