Chromosome aberrations caused by the effect of ultrasound in the meristematic cells ofvicia faba

In our present work the formation of chromosome aberrations has been studied in dependence on the tima interval between sonication and fixation of the primary root tips of Vicia faba. Maximum occurrence of aberrations was recorded immediately after sonication. The results of our experiments pointed to the fact that the frequency of the induced changes was independent on the sonic waves intensity within the range of 0-2—3-0 W/cm² and on ultrasond treatment duration within the range of 1—20 min. Studies of the distribution of chromosome abnormalities caused by ultrasound between the large and small chromosomes of theVicia faba meristematic cells in various time intervals showed that the frequency of the aberrations in both chromosome groups was proportional to its total metaphase lengths. Analysis of the type of aberrations observed in various time intervals after sonication indicated the simultaneous formation of chromosome and chromatide abnormalities.     

Peroxidases of different parts of the pumpkin plant (Cucurbita pepo L.)

We compared the occurrence of peroxidase isozymes in protein extract from roots, hypocotyls and cotyledons of 10 dayCucurbita pepo plants and of adult leaves of older plants by means of starch gel and polyacryl amide gel electrophoresis. We reached maximum discrimination by means of starch gel electrophoresis: 11 zones were ascertained on the cathode side and about 2 on the anode side at pH 3.1. Two zones occurred regularly:A and (the latter having a more complicated structure). ZoneD is characteristic for roots, but is it suppressed and seldom found with leaves. On the other hand zonesC ₁ andC ₂ are clearly discernible with leaves but are substantially less evident with roots. The character of anodic zoneZ is discussed later in this paper.     

The effect of the size of soil structural aggregates on the degree of nitrification

It was experimentally demonstrated that the deviation from linearity exhibited by the dependence of intensity of nitrification on the size of the specific surface of soil structural aggregates is due to deteriorated aeration in the internal space of aggregates of greater diameter. The deteriorated aeration is due to retarded diffusion of oxygen in the aggregates containing greater amounts of moisture. Aggregates isolated from rendzine which displayed a deviation from linearity when their moisture content was equal to twice their maximum hygroscopicity (largersize aggregates produced less nitrates than would correspond to a linear relationship) showed a clear linear dependence as soon as the moisture content dropped to values lower than maximum hygroscopicity.

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Влияние размеров структурных агрегатов почвы на интенсивность нитрификации II. Значение аэрации

Интенсивность нитрификации в почвенных структурных агрегатах различной величины падает с увеличением диаметра агрегатов. Если взять отношение интенсивности нитрификации к размерам специфической поверхности агрегатов (под специфической поверхностью почвенных структурных агрегатов мы понимаем отношение общей внешней поверхности агрегатов опре-деленной фракции к единице вещества), то можно установить, или что падение интенсивности нитрификации протекает равномерно с уменьшением размеров плоцади специфической поверхность агрегатов, или что интенсивность нитри-фикации в агрегатах большего диаметра падает быстрее, чем размеры специфи-ческой поверхности. В этом случае зависимостй интенсивности нитрификации от величины специфической поверхности имеет характер кривой (рис. 1). В предыдущей работе (Сайферт, 1964) нами было высказано предположение, что это явление связано с ухудшением аэрации центральной части крупных агрегатав. Ухудшение аэрации в этих агрегатах, по нашему мнению, обусловлено водяными перегородками, которые здесь почвенная влага образует в результате действия капиллярных сил. Эти перегородки замедляют диффузию кислорода из межагрегатных про-странств внутрь агрегатов. Чтобы доказать правильность нашего предположения, мы устанавливали интенсивность нитрификации в агрегатах раз-личной величины при обычно встречающемся насыщении влагой (19% веса) и при насыщении только до степени гигроскопической влаги. Результаты опытов показали, что в первом случае зависимость интенсивности нитрификации от величины специфической поверхности выражалась кривой (рис. 2), тогда как во бтором случае она имела характер прямой (рис. 4). Ввиду того, что эти результаты полностью подтверждают наше предположение, мы можем считать доказанным, что интенсивность нитрификации в агрегатах боляших диаметров понижается в связи с ухудшением аэрации.

     

Changes in the anatomical structure of the shoot apex ofSenecio vulgaris L. during ontogenis in relation to the formation of leaves and inflorescence

An investigation was made of the anatomical structure of the shoot apex ofSenecio vulgaris L. a photoperiodically neutral plant, and compared with the formation of successive leaf primordia along the axis up to the initiation of the terminal inflorescence. In the shoot apex of a germinating plant a central zone can first be distinguished from the peripheral zone which is composed of small and intensely stained cells. Later, a rib meristem appears. At the time of the initiation of the middle (the largest) leaves, the shoot apex has a distinct small central zone and a well developed peripheral zone and rib meristem. Between these zones there is a group of cells dividing in all directions, the subcentral zone. At the time of initiation of the last leaves, the central zone extends to the flanks and gradually ceases to be distinguishable. At the same time, the subcentral zone increases in size. This is caused first by cell division and later, with the initiation of the last, most reduced leaves, by enlargement of the cells. Vacuolization in the inner part of the apex and the arrangement of the superficial cells in rows parallel to the surface of the apex, is a preparatory step to the initiation of the inflorescence.     

Die Ultrastruktur der Kapillarwand in der menschlichen Placenta zur Zeit der Schwangerschaftsmitte

Zusammenfassung Die Wand der Kapillaren in der menschlichen Placenta aus der Schwangerschaftsmitte wird elektronenmikroskopisch untersucht und zu der Wand des Sinusoides der reifen Placenta in Beziehung gesetzt. Bereits zur Zeit der Schwangerschaftsmitte sind vereinzelt Sinusoide nachweisbar, doch treten sie gegenüber den Kapillaren zahlenmäßig in den Hintergrund.Die Kapillaren des Zottenbinnenraumes besitzen keine Basalmembran; sie sitzen meist, nur durch einen Spalt getrennt, einer Pericytenschicht auf. Die Pericyten haben häufig fußförmige Ausläufer, die die Basalmembran des Cytotrophoblasten erreichen. Die Kapillarendothelien sind zwar einreihig angeordnet, überlappen aber einander in ausgedehnter Weise.Im Cytoplasma der Kapillarendothelien findet man häufig eine feinfilamentäre Zeichnung, jedoch nur nach Kaliumpermanganat-Kontrastierung.Die Kapillaren der unreifen Placenta sind durch das Fehlen der Basalmembran, durch die ungewöhnliche Dicke und durch die starke Überlappung ihres Endothels für eine Gefügedilatation besonders geeignet.Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

Biomass partitioning in twoCalamagrostis villosa stands on deforested sites

Calamagrostis villosa stands occurring in areas deforested by air-pollution impact in the Moravian-Silesian Beskydy Mountains were characterized by a high dry mass of total underground biomass (3 300 g. m^?2—the slope site, 2 850 g. m^?2—the flat site). The percentage of living roots and rhizomes in total underground biomass was very high (about 70%). The total aboveground biomass was respectively, 321 g.m^?2 (the slope site) and 726 g. m^?2 (the flat site). In unstabilized habitats on steep slope, the higher plant biomass produced was allocated to a more developed root system.     

Differential regulation of expression of two platelet-derived growth factor receptor subunits by transforming growth factor-beta

The binding of three radiolabeled isoforms of platelet-derived growth factor (PDGF), 125I-PDGF-AA, 125I-PDGF-AB, and 125I-PDGF-BB, is differentially affected by exposure of quiescent 3T3 cells to transforming growth factor-beta (TGF-beta). By 24 h after exposure to TGF-beta, binding of 125I-PDGF-AA and 125I-PDGF-AB is almost completely lost, whereas binding of 125I-PDGF-BB is reduced by only 40%. The loss of PDGF-binding sites caused by TGF-beta is time- and concentration-dependent and reflects a change in the pattern of expression of receptor subunits; the number of alpha-subunits decreases, and the number of beta-subunits increases. The loss of binding sites for PDGF-AA is accompanied by a decreased mitogenic response to PDGF-AA but not to PDGF-AB or PDGF-BB. These results suggest that TGF-beta may differentially regulate the expression of PDGF-binding sites and the mitogenic responsiveness toward the three PDGF isoforms. TGF-beta did not stimulate synthesis of PDGF A-chain mRNA or PDGF-AA protein, and PDGF-AA receptors could not be restored by the presence of suramin, suggesting that the loss of binding sites may result from direct effects on receptor expression rather than autocrine down-regulation by PDGF-AA.     

Analysis by high-resolution two-dimensional electrophoresis of differentiation-dependent alterations in cytosolic protein pattern of HL-60 leukemic cells.

HL-60 leukemic cells were differentiated along the neutrophilic pathway with retinoic acid (RA) or along the monocytic pathway with 1,25-dihydroxyvitamin D3 (1,25(OH)2D3). Using a high-resolution two-dimensional electrophoresis technique and subsequent silver staining, differentiation-dependent changes in cytosolic protein pattern of HL-60 cells were analysed and were compared with the cytosolic protein pattern of human neutrophils. The amount of 64 and 50 out of a total of 632 proteins studied was increased or decreased in RA- and 1,25(OH)2D3-differentiated HL-60 cells, respectively, in comparison to undifferentiated HL-60 cells. Thirty-three of these proteins were similarly altered in RA- and 1,25(OH)2D3-differentiated HL-60 cells. Twenty-two and 25 of the proteins altered in amount in RA- or 1,25(OH)2D3-differentiated HL-60 cells versus undifferentiated HL-60 cells were similarly altered in human neutrophils in comparison to undifferentiated HL-60 cells. Seven and 10 of the proteins altered in amount in RA- or 1,25(OH)2D3-differentiated HL-60 cells had specific equivalents in neutrophil cytosol. Our results show (i) that neutrophilic and monocytic differentiation is associated with decreases and increases in amount of cytosolic proteins; (ii) that both differentiation processes share a common set of alterations; and (iii) are associated with specific alterations in protein amount.     

Expression of the E. coli nadB gene and characterization of the gene product L-aspartate oxidase

Quinolinic acid is synthesized in E. coli by the enzymes L-aspartate oxidase and quinolinate synthase A, the genes of which are named nadB and nadA. In our previous work we cloned and characterized the two genes (Flachmann, R., Kunz, N., Seifert, J., Gütlich, M., Wientjes, F.J., L?ufer, A. & Gassen, H.G. (1988) Eur. J. Biochem. 175, 221-228). Here we report on the expression of the nadB gene under control of the inducible left promoter of the bacteriophage lambda. The yield of the active gene product L-aspartate oxidase was enhanced up to 20% of the soluble cell protein. The enzyme was purified to homogeneity in a three-step procedure and the reading frame of the L-aspartate oxidase gene was confirmed by Edman degradation of five cyanogen bromide peptides. L-Aspartate oxidase shows no classical Michaelis-Menten behaviour but is subject to a substrate inactivation. The apparent Km values were different for substrate concentrations below and above 1mM and were determined to 0.5 mM and 4.1mM, respectively. The active form of the enzyme is a monomer of 60,284 Da and contains one molecule of FAD and nine cysteine residues, four of which built up two disulfide bonds. The isoelectric point of the protein was determined to be at pH 5.6. Chemical modifications of the enzyme showed that at least one tyrosine and one histidine residue are essential for enzyme activity. The coenzyme-binding domain is located in the amino-terminal part of the polypeptide chain as revealed by a sequence comparison to other dinucleotide binding enzymes. Furthermore, there is evidence for a relationship to fumarate reductase and succinate dehydrogenase of E. coli.