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3.
Mikrobiologiia ; 77(3): 303-10, 2008.
Artigo em Russo | MEDLINE | ID: mdl-18683645

RESUMO

Data on the interrelation between the pathways of the carbon source catabolism and isoprenoid biosynthesis in anaerobic and facultatively anaerobic bacteria were obtained. Two pathways of isoprenoid biosynthesis (nonmevalonate and mevalonate) were revealed in the representatives of the genus Clostridium. The non-mevalonate pathway of isoprenoid biosynthesis and the glycolytic pathway of substrate oxidation are typical of glucose-grown bacteria, whereas the pentose phosphate cycle operates in xylose-grown bacteria. The mevalonate pathway of isoprenoid biosynthesis was revealed in strain Clostridium thermosaccharolyticum DSM 571 grown in the presence of mevinolin, as well as in a number of lactic acid bacteria. Mevinolin is known to react with the lactate dehydrogenase complex, preventing reduction of pyruvate. The nonmevalonate pathway of isoprenoid biosynthesis was revealed in Bifidobacterium bifidum. The role of different metabolic pathways in isoprenoid biosynthesis is discussed.


Assuntos
Bactérias Anaeróbias/metabolismo , Glucose/metabolismo , Terpenos/metabolismo , Xilose/metabolismo , Bactérias Anaeróbias/crescimento & desenvolvimento , Carbono/metabolismo , Clostridium/metabolismo , Lactobacillus/metabolismo , Ácido Mevalônico/metabolismo , Via de Pentose Fosfato , Especificidade por Substrato
4.
Neurosci Behav Physiol ; 36(3): 307-12, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16465498

RESUMO

Arachidonic acid and prostaglandin E2 decreased the frequency of miniature endplate potentials with producing any changes in the their amplitude-time parameters. Arachidonic acid and prostaglandin E2 decreased the quantum composition of endplate currents and the amplitude of the third phase of the nerve ending response, which reflects currents though potential-dependent K+ channels. A perineural method was used to demonstrate that arachidonic acid and prostaglandin E2 suppressed the nerve ending Ca2+ current. The cyclooxygenase blocker indomethacin increased neurotransmitter secretion and decreased the third phase of the nerve ending response. The effects of arachidonic acid and prostaglandin E2 on evoked neurotransmitter release were not seen in the presence of indomethacin, while the third phase of the response continued to show a reduction. It is suggested that prostaglandin E2 mediates the effects of arachidonic acid on spontaneous and evoked neurotransmitter secretion, Ca2+ currents, and Ca2+ -dependent K+ currents. In addition, arachidonic acid and prostaglandin E2 had their own effects on potential-dependent K+ currents in nerve endings.


Assuntos
Ácido Araquidônico/fisiologia , Dinoprostona/fisiologia , Junção Neuromuscular/fisiologia , Sinapses/fisiologia , Animais , Ácido Araquidônico/farmacologia , Cálcio/fisiologia , Inibidores de Ciclo-Oxigenase/farmacologia , Dinoprostona/farmacologia , Técnicas In Vitro , Indometacina/farmacologia , Placa Motora/fisiologia , Junção Neuromuscular/efeitos dos fármacos , Canais de Potássio/fisiologia , Rana ridibunda
5.
Ross Fiziol Zh Im I M Sechenova ; 91(3): 268-76, 2005 Mar.
Artigo em Russo | MEDLINE | ID: mdl-15881878

RESUMO

Arachidonic acid and prostaglandin E2 decreased the frequency of miniature endplate currents without changing their amplitude-temporary parameters. They also reduced the evoked transmitter release and the amplitude of the 3rd phase of nerve ending response corresponding to the voltage-dependent K(+)-current. Using perineural recording, It was shown that arachidonic acid and prostaglandin E2 decreased the Ca2+ currents of nerve endings. Indometacin: inhibitor of cyclooxygenase, enhanced the evoked transmitter release and decreased the 3rd phase of nerve ending response. Indometacin prevented the effects of arachidonic acid on evoked transmitter release, whereas the effects of arachidonic acid on the 3rd phase was preserved. Prostaglandin E2 seems to mediate the effects of arachidonic acid on spontaneous and evoked transmitter release, Ca(2+)- and Ca(2+)-activated K(+)-currents. Moreover, the arachidonic acid and prostaglandin E2 exerted their own effects upon voltage-dependent potassium current of motor nerve ending.


Assuntos
Ácido Araquidônico/fisiologia , Dinoprostona/fisiologia , Junção Neuromuscular/fisiologia , Canais de Potássio de Abertura Dependente da Tensão da Membrana/fisiologia , Terminações Pré-Sinápticas/fisiologia , Acetilcolina/metabolismo , Potenciais de Ação , Animais , Ácido Araquidônico/farmacologia , Cálcio/fisiologia , Inibidores de Ciclo-Oxigenase/farmacologia , Dinoprostona/farmacologia , Eletrofisiologia , Técnicas In Vitro , Indometacina/farmacologia , Placa Motora/efeitos dos fármacos , Placa Motora/fisiologia , Músculo Esquelético/inervação , Junção Neuromuscular/efeitos dos fármacos , Canais de Potássio/fisiologia , Terminações Pré-Sinápticas/efeitos dos fármacos , Rana ridibunda
6.
Mikrobiologiia ; 74(6): 725-37, 2005.
Artigo em Russo | MEDLINE | ID: mdl-16400981

RESUMO

This paper summarizes the current knowledge of unsaturated organic acids in their role as terminal electron acceptors of anaerobic bacteria. The mechanisms and enzyme systems involved in the reduction of fumarate by Escherichia coli, Wolinella succinogenes, and some species of the genus Shewanella are considered. Particular attention is given to reduction of the double bond of the unnatural compound methacrylate by the sigma-proteobacterium Geobacter sulfurreducens Am-1. Soluble periplasmic flavocytochromes c, found in bacteria of the genera Shewanella and Geobacter, are involved in the hydration of fumarate (in Shewanella species) and methacrylate (in G. sulfurreducens Am-1). In E. coli and W. succinogenes, fumarate is reduced in cytosol by membrane-bound fumarate reductases. The prospects for research into organic acid reduction at double bonds in bacteria are discussed.


Assuntos
Bactérias Anaeróbias/metabolismo , Bactérias Anaeróbias/enzimologia , Membrana Celular , Grupo dos Citocromos c/metabolismo , Citosol/metabolismo , Transporte de Elétrons , Escherichia coli/enzimologia , Escherichia coli/metabolismo , Fumaratos/metabolismo , Geobacter/enzimologia , Geobacter/metabolismo , Oxirredução , Oxirredutases/metabolismo , Periplasma/enzimologia , Shewanella/enzimologia , Shewanella/metabolismo , Succinato Desidrogenase/metabolismo , Wolinella/enzimologia , Wolinella/metabolismo
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