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1.
Sci Rep ; 10(1): 15024, 2020 09 14.
Artigo em Inglês | MEDLINE | ID: mdl-32929148

RESUMO

Newly developed millennial δ13C larch tree-ring chronology from Siberia allows reconstruction of summer (July) vapor pressure deficit (VPD) changes in a temperature-limited environment. VPD increased recently, but does not yet exceed the maximum values reconstructed during the Medieval Warm Anomaly. The most humid conditions in the Siberian North were recorded in the Early Medieval Period and during the Little Ice Age. Increasing VPD under elevated air temperature affects the hydrology of these sensitive ecosystems by greater evapotranspiration rates. Further VPD increases will significantly affect Siberian forests most likely leading to drought and forest mortality even under additional access of thawed permafrost water. Adaptation strategies are needed for Siberian forest ecosystems to protect them in a warming world.

2.
Plant Cell Environ ; 38(11): 2340-52, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25916312

RESUMO

Little is known about the dynamics of concentrations and carbon isotope ratios of individual carbohydrates in leaves in response to climatic and physiological factors. Improved knowledge of the isotopic ratio in sugars will enhance our understanding of the tree ring isotope ratio and will help to decipher environmental conditions in retrospect more reliably. Carbohydrate samples from larch (Larix gmelinii) needles of two sites in the continuous permafrost zone of Siberia with differing growth conditions were analysed with the Compound-Specific Isotope Analysis (CSIA). We compared concentrations and carbon isotope values (δ(13) C) of sucrose, fructose, glucose and pinitol combined with phenological data. The results for the variability of the needle carbohydrates show high dynamics with distinct seasonal characteristics between and within the studied years with a clear link to the climatic conditions, particularly vapour pressure deficit. Compound-specific differences in δ(13) C values as a response to climate were detected. The δ(13) C of pinitol, which contributes up to 50% of total soluble carbohydrates, was almost invariant during the whole growing season. Our study provides the first in-depth characterization of compound-specific needle carbohydrate isotope variability, identifies involved mechanisms and shows the potential of such results for linking tree physiological responses to different climatic conditions.


Assuntos
Metabolismo dos Carboidratos , Larix/metabolismo , Mudança Climática , Meio Ambiente , Frutose/química , Frutose/metabolismo , Glucose/química , Glucose/metabolismo , Inositol/análogos & derivados , Inositol/química , Inositol/metabolismo , Larix/fisiologia , Sibéria , Sacarose/química , Sacarose/metabolismo
3.
Biochem Biophys Res Commun ; 445(2): 428-32, 2014 Mar 07.
Artigo em Inglês | MEDLINE | ID: mdl-24530904

RESUMO

Recombinant mutant OmpF porins from Yersinia pseudotuberculosis outer membrane were obtained using site-directed mutagenesis. Here we used four OmpF mutants where single extracellular loops L1, L4, L6, and L8 were deleted one at a time. The proteins were expressed in Escherichia coli at levels comparable to full-sized recombinant OmpF porin and isolated from the inclusion bodies. Purified trimers of the mutant porins were obtained after dialysis and consequent ion-exchange chromatography. Changes in molecular and spatial structure of the mutants obtained were studied using SDS-PAGE and optical spectroscopy (circular dichroism and intrinsic protein fluorescence). Secondary and tertiary structure of the mutant proteins was found to have some features in comparison with that of the full-sized recombinant OmpF. As shown by bilayer lipid membrane technique, the pore-forming activity of purified mutant porins was identical to OmpF porin isolated from the bacterial outer membrane. Lacking of the external loops mentioned above influenced significantly upon the antigenic structure of the porin as demonstrated using ELISA.


Assuntos
Proteínas de Bactérias/genética , Proteínas de Bactérias/imunologia , Porinas/genética , Porinas/imunologia , Yersinia pseudotuberculosis/genética , Yersinia pseudotuberculosis/imunologia , Sequência de Aminoácidos , Animais , Anticorpos Antibacterianos/imunologia , Proteínas de Bactérias/química , Proteínas de Bactérias/metabolismo , Clonagem Molecular , Imunização , Camundongos , Camundongos Endogâmicos BALB C , Mutagênese Sítio-Dirigida , Mutação , Porinas/química , Porinas/metabolismo , Estrutura Secundária de Proteína , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Deleção de Sequência , Yersinia pseudotuberculosis/química , Yersinia pseudotuberculosis/metabolismo , Infecções por Yersinia pseudotuberculosis/imunologia , Infecções por Yersinia pseudotuberculosis/microbiologia
4.
Bioorg Khim ; 38(2): 156-65, 2012.
Artigo em Russo | MEDLINE | ID: mdl-22792719

RESUMO

Yersinia pseudotuberculosis outer membrane (OM) recombinant mutant OmpF porins with deletions of the external loops L1, L6 and L8 were obtained using site-directed mutagenesis of the recombinant plasmid including ompF gene. Heterologeous expression of the mutant proteins was carried out in strain Rosetta of Escherichia coli (Novagen, USA), porins with the deletions were isolated from the inclusion bodies. Mutant proteins in oligomeric form were obtained as result of dialysis and ion-exchange chromatography. Spatial structure of the mutant proteins was demonstrated to have special features in comparison with that of the full-structured OmpF porin on the level of both secondary and tertiary structure. Lacking of the loops L1, L6 and L8 didn't affect the conductivity level of Y pseudotuberculosis porin channel as shown using bilayer lipid membrane (BLM) technique. Lacking of the loops mentioned above has a significant influence on the antigenic structure of the mutant porins as demonstrated with use of immunoblotting technique and ELISA.


Assuntos
Sequência de Aminoácidos , Expressão Gênica , Porinas , Dobramento de Proteína , Deleção de Sequência , Yersinia pseudotuberculosis , Escherichia coli/genética , Escherichia coli/metabolismo , Plasmídeos/genética , Plasmídeos/metabolismo , Porinas/biossíntese , Porinas/química , Porinas/genética , Porinas/isolamento & purificação , Estrutura Secundária de Proteína , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/isolamento & purificação
5.
Bioorg Khim ; 36(6): 779-88, 2010.
Artigo em Russo | MEDLINE | ID: mdl-21317944

RESUMO

Multiple antigenic peptides (MAPs), a sequence which include common antigenic epitopes of outer membrane porins (OM) bacteria of the genus Yersinia (Y. pseudotuberculosis, Y. enterocolitica, Y. pestis), pathogenic for humans have been synthesized. After immunization of BALB/c mice the antiserum to the peptide have been obtained. With the help of ELISA we showed that these sera interact with porins isolated from OM pathogenic Yersinia, and MAP interact with antibodies in sera from rabbits immunized with individual porins, and with antibodies in sera of patients with intestinal yersiniosis and pseudotuberculosis.


Assuntos
Antígenos de Bactérias/farmacologia , Epitopos de Linfócito B/farmacologia , Epitopos de Linfócito T/farmacologia , Peptídeos/farmacologia , Porinas/farmacologia , Yersinia/imunologia , Animais , Anticorpos Antibacterianos/imunologia , Antígenos de Bactérias/imunologia , Epitopos de Linfócito B/imunologia , Epitopos de Linfócito T/imunologia , Feminino , Humanos , Imunização , Camundongos , Camundongos Endogâmicos BALB C , Peptídeos/síntese química , Peptídeos/imunologia , Porinas/síntese química , Porinas/imunologia , Coelhos , Infecções por Yersinia pseudotuberculosis/imunologia , Infecções por Yersinia pseudotuberculosis/prevenção & controle
6.
Bull Exp Biol Med ; 148(1): 72-4, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19902101

RESUMO

We studied the capacity of outer membrane pore-forming recombinant protein from Yersinia pseudotuberculosis to initiate the development of immune response in CBA mice. Immunization with the recombinant protein induces the production of IgG antibodies with and without adjuvants. High-avidity immune serum was obtained as a result of immunization. Bactericidal activity of peritoneal macrophages from mice immunized with recombinant protein was significantly higher than that of intact mouse macrophages. The use of recombinant porin instead of native porin as the antigen in enzyme immunoassay system for the diagnosis of acute and secondary focal pseudotuberculosis does not reduce the efficiency of detection of specific antibodies in the sera of patients.


Assuntos
Proteínas da Membrana Bacteriana Externa/imunologia , Yersinia pseudotuberculosis/imunologia , Animais , Técnicas Imunoenzimáticas , Macrófagos Peritoneais/imunologia , Camundongos , Camundongos Endogâmicos CBA , Proteínas Recombinantes/imunologia
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