Protein expression of Yersinia pestis during changes due to long-term cultivation in vivo]

The electrophoretic study of Yersinia pestis proteins made possible to find the significant modification of Yersinia pestis polypeptide specters when the bacteria were cultivated in semi-penetrable cells implanted into the guinea pigs peritoneum. The proteinogramms of the isolates from the implanted cells lacked the stained bands characteristic of Yersinia pestis cells grown in vitro and contained the new polypeptides absent from the bacteria grown on the Hottinger agar plates. The difference was found at the late stage of bacteria incubation in implanted cells and had the predominantly reversible characteristics. The protein of Yersinia pestis being changed in vivo is proposed to be the species specific fraction I.     

Functional Condition of Photosystem II in Leaves of Spring Oats during Autumnal Decrease in Temperature

Russian Journal of Plant Physiology - Dynamics of chlorophyll a fluorescence changes (including JIP test parameters) and photosynthetic pigments were studied in oat (Avena sativa L.) leaves of late...     

Photosynthetic and Respiratory Capacity of Foliose Lichen Lobaria pulmonaria throughout the Annual Cycle

Russian Journal of Plant Physiology - Lichens are unique phototrophic organisms whose physiology of stress tolerance attracts much attention. Parameters of photosynthetic and respiratory activities...     

Seasonal changes in growth and metabolic activity of underground shoots of yarrow

Growth and metabolic activity of underground shoots of a long-rhizome perennial herbaceous species yarrow (Achillea millefolium L.) were studied. The active growth of rhizomes and the formation of new meristematic zones were observed during the second half of the growing season after termination of aboveground shoot growth. In this period, underground shoots had a rather high rate of respiration (1.3 mg CO₂/(g dry wt h)), a considerable content of nonstructural carbohydrates (15% of dry weight), and the elevated activities of IAA, cytokinins, and ABA. In autumn, the rate of respiration of underground shoots decreased to 1.0 mg CO₂/(g dry wt h), soluble sugars accumulated, the ratio between unsaturated and saturated fatty acids rose as well as the ratios GA/ABA and cytokinins/ABA. Temperature optimum for the rhizome growth lay in the range of low and moderate above-zero temperatures (5–20°C), and the freezing point of water in the apices of under-ground shoots was about ?10°C. It is concluded that rhizome quiescence predominantly depends on low temperatures and is not associated with the accumulation of growth inhibitors. In the course of plant preparation to winter, morphogenetic transformations in underground shoots depend on changes in the hormonal balance directed in favor of growth hormones and relatively high respiratory activity in the apical zones of the rhizomes.     

Bud dormancy breaking affects respiration and energy balance of bilberry shoots in the initial stage of growth

Respiration and heat production in the shoots of bilberry (Vaccinium myrtillus L.) were studied at the beginning of growth after breaking bud dormancy by means of transfer of the shoots to indoor conditions (November–April) and upon natural sprouting in spring (May). The buds released from dormancy at the beginning of winter sprouted slower and showed lower respiratory activity than the buds that started growing in May. In May, cytochrome respiratory pathway in sprouting buds was 1.3 times more active than energetically ineffective alternative pathway, whereas activity of cytochrome pathway in December was 1.4 times lower as compared with the alternative. In November–December, the rate of heat evolution by the buds was 3–5 times lower than in April–May. In case of early breaking of bud dormancy, the share of respiration energy dissipated as heat was 30% on average. In the buds whose growth was induced later, the value of this parameter was twice as much. The ratio between heat evolution and respiration depended on temperature. High temperature more intensely activated heat evolution than respiration, which caused a decrease in the level of metabolic energy available for growth. In the temperature range of 5–15°C characteristic of the beginning of vegetation, the share of respiration energy dissipated as heat was 2–3 times lower than at 20–30°C, which reflects a great adaptability of V. myrtillus to climatic conditions of the region. Our data suggest that progression through a full cycle of winter dormancy is physiologically important for shoot growth. Early dormancy release brought about changes in respiration and energy balance of the shoots in the initial stage of extra-bud growth.     

Single "early" action potential cause by Ni2+ ions in true pacemaker cells of the sinoatrial ring of the dace heart

Single "early" action potentials (AP) or "early" postdepolarization (EAD) were recorded in multicellular stripes working in the regimen of true pacemaker cells located in the basis of the sinoatrial valve of the dace (Leuciscus rutilus) heart after Ni2+ (0.3 mM) were added to superfused solution on the 15 th min. The standard microelectrode technique was used. The appearance of single EAD was preceded by increase of AP spike duration almost 1.5-fold due to increase of the duration of a final repolarization phase and of diastolic depolarization. EADs appeared at different levels of repolarization from -20 to -60 mV. EAD's amplitude was lower than the AP proper. The effect is reversible. Nifedipine (2 microM) decreased by 20% the AP duration to 50% repolarization in the cells of atrial type. In case the stripes were primarily subjected to nifedipine effect and then even after a long procedure of washout, the Ni2+ (0.3 mM) did not cause EADs. The hypothesis has been tested of what is the main reason of single EAD appearance in pacemaker cells under the effect of Ni2+; it is either blocking Ca release from the cell by Ni2+, or reactivation of L-type Ca-channels' conductivity. The analysis of the data obtained leads to the conclusion that 30-50% Na-Ca-exchangers block is the basic reason of single EAD appearance in pacemaker cells.     

The KiSS-1 receptor GPR54 is essential for the development of the murine reproductive system

GPR54 is a G-protein-coupled receptor that displays a high percentage of identity in the transmembrane domains with the galanin receptors. The ligand for GPR54 has been identified as a peptide derived from the KiSS-1 gene. KiSS-1 has been shown to have anti-metastatic effects, suggesting that KiSS-1 or its receptor represents a potential therapeutic target. To further our understanding of the physiological function of this receptor, we have generated a mutant mouse line with a targeted disruption of the GPR54 receptor (GPR54 -/-). The analysis of the GPR54 mutant mice revealed developmental abnormalities of both male and female genitalia and histopathological changes in tissues which normally contain sexually dimorphic features. These data suggest a role for GPR54/KiSS-1 in normal sexual development, and indicate that study of the GPR54 mutant mice may provide valuable insights into human reproductive syndromes.     

H+-pyrophosphatase of Rhodospirillum rubrum. High yield expression in Escherichia coli and identification of the Cys residues responsible for inactivation my mersalyl

H(+)-translocating pyrophosphatase (H(+)-PPase) of the photosynthetic bacterium Rhodospirillum rubrum was expressed in Escherichia coli C43(DE3) cells. Recombinant H(+)-PPase was observed in inner membrane vesicles, where it catalyzed both PP(i) hydrolysis coupled with H(+) transport into the vesicles and PP(i) synthesis. The hydrolytic activity of H(+)-PPase in E. coli vesicles was eight times greater than that in R. rubrum chromatophores but exhibited similar sensitivity to the H(+)-PPase inhibitor, aminomethylenediphosphonate, and insensitivity to the soluble PPase inhibitor, fluoride. Using this expression system, we showed that substitution of Cys(185), Cys(222), or Cys(573) with aliphatic residues had no effect on the activity of H(+)-PPase but decreased its sensitivity to the sulfhydryl modifying reagent, mersalyl. H(+)-PPase lacking all three Cys residues was completely resistant to the effects of mersalyl. Mg(2+) and MgPP(i) protected Cys(185) and Cys(573) from modification by this agent but not Cys(222). Phylogenetic analyses of 23 nonredundant H(+)-PPase sequences led to classification into two subfamilies. One subfamily invariably contains Cys(222) and includes all known K(+)-independent H(+)-PPases, whereas the other incorporates a conserved Cys(573) but lacks Cys(222) and includes all known K(+)-dependent H(+)-PPases. These data suggest a specific link between the incidence of Cys at positions 222 and 573 and the K(+) dependence of H(+)-PPase.     

The influence of ethanol on the functional status of GABA(A) receptors

Gamma aminobutyric acid (GABA) is one of the main inhibitory neurotransmitters in the mammalian brain. Its effects are realized via GABA_A, GABA_B, and GABA_C receptors. GABA_A is the most abundant type of GABA receptors. It consists of six classes of subunits, , , , , , and . Acute and chronic exposures to ethanol are accompanied by changes in structure and function of GABA_A receptors. These changes may be a basis for altered behavior seen in alcoholism.