Changes in myocardial contractile protein ATPases in chronically adrenalectomized rats with and without glucocorticoid replacement

Studies were conducted to examine the effects of chronic adrenalectomy (Adx) and adrenalectomy plus glucocorticoid replacement therapy on rat cardiac contractile protein ATPase activities. The Ca2+-dependent Mg-ATPase activity of myofibrils isolated from rat ventricles 3 weeks postadrenalectomy (Adx) was significantly decreased at all pCa2+ concentrations (P less than 0.01), compared to sham-operated (SO) rats. Similarly, Ca2+-, K+-EDTA, and actin-activated myosin ATPase activities of Adx rat hearts were markedly decreased below that of SO rats (P less than 0.01). Dexamethasone administration to Adx rats prevented the decrease of Ca2+- and K+-ATPase activities of myosin, but not of myofibrillar Ca2+-dependent Mg-ATPase or actin-activated myosin Mg-ATPase activities. These studies suggest that glucocorticoid insufficiency induced by adrenalectomy results in altered myocardial contractile protein ATPase activity which may underlie impaired cardiac performance.     

A comparison of snRNP-associated Sm-autoantigens: human N, rat N and human B/B''.

N is a tissue-specific, Sm-epitope bearing, snRNP-associated protein found predominantly in brain. The cDNA sequence encoding human N is compared to those for rat N and human B/B'. The amino acid sequences of human and rat N are 100% conserved. Although the amino acid sequences of N and B/B' are very similar to each other, B/B' contains 50 amino acids which are not present in N. On Northern blots the cDNAs encoding N and B/B' recognize two different RNA species. A comparison of the codon usage, as specified by the open reading frames of N and B/B' as well as results from Southern blots, show that N and B/B' are derived from different genes.     

Electron microscopy of muscle phosphorylase a

Electron microscopy of negatively stained preparations of phosphorylase a (tetrameric form) from solutions with and without added protamine revealed three characteristic types of particle images. In preparations with added protamine several types of crystalline formation were observed: three types of plane monolayers, tubes and small three-dimensional crystals. The tubes have been studied by optical diffraction and filtering. In the main class of tubes the particles form $\text{26}\text{9}$ three-start helices (it may well be that narrow tubes with different parameters exist). Now and again, one can observe tubes twice as large in diameter, and tubes with two-layer walls. Analysis of the images of particles in solution and in crystalline formations showed that their structure can be characterized in terms of one model consisting of four elongated bent subunits arranged with the point-group symmetry 222 at the vertices of a tetrahedron. The structure of phosphorylase b particles, previously studied (Kiselev et al., 1971), can also be characterized satisfactorily by the same model. The difference in the structure of these two forms expresses itself in a different character of mutual aggregation of the molecules in plane layers, and in the parameters of the helical packing of the molecules in tubes.     

Generation of a membrane potential by electron transport in plasmalemma-enriched vesicles of cotton and radish

Plasmalemma-enriched vesicles were isolated from cotton roots (Gossypium hirsutum L. cv Acala San Jose 2) and from germinating radish seeds (Raphanus sativa L. cv Tondo Rosso Quarantino). When 100 millimolar ascorbate was added to the grinding medium, the addition of ferricyanide to either preparation led to an inside positive membrane potential as measured by the accumulation of thiocyanate. It is suggested that electrons from ascorbate were being transported electrogenically across the membrane to ferricyanide, resulting in an accumulation of protons within the vesicle. The redox activity of the vesicles has some similarities to that occurring in intact cells, thus providing a simpler system to study the components and effects of transmembrane electron transport.     

Studies on H-Translocating ATPases in Plants of Varying Resistance to Salinity : II. K Strongly Promotes Development of Membrane Potential in Vesicles from Cotton Roots

Mg²⁺-ATP-dependent H⁺-translocation has been studied in membrane vesicles derived from the roots of Gossypium hirsutum L. var. Acala San Jose 2. Establishment of a positive membrane potential was followed by measuring SCN⁻ accumulation; establishment of ΔpH across the vesicle membranes by measuring quinacrine fluorescence quenching. High specificity for ATP was shown, and H⁺-translocation was oligomycin stable. The pH profile for H⁺-translocation showed an optimum at 5.5. The relationship between SCN⁻ accumulation and ATP concentration was approximately Michaelian; the apparent K_m was 0.7 millimolar. K-2-(N-morpholino)ethanesulfonic acid strongly promoted ATP-dependent SCN⁻ uptake (up to 180% stimulation). The effect was not given by Na-Mes. Carbonyl cyanide p-trifluoromethoxyphenylhydrazone totally inhibited SCN⁻ accumulation, both in the presence and absence of K-2(N-morpholino)ethanesulfonic acid. Vanadate at 200 micromolar inhibited SCN⁻ uptake by about 10 to 40% in the absence of K⁺, but more strongly in its presence (about 60%). NO₃⁻ at 100 millimolar inhibited initial rate of quinacrine quenching by about 25%. The NO₃⁻ insensitive fraction was activated by K⁺; and inhibited by 200 micromolar vanadate to about 40%, provided K⁺ was present. Saline conditions during the growth of the plants had no appreciable effect on the observed characteristics of H⁺-translocation.     

Proton Fluxes as a Response to External Salinity in Wild Type and NaCl-Adapted Nicotiana Cell Lines

Addition of 100 millimolar KCl, NaCl, or Na₂SO₄ strongly promoted acidification of the medium by cells of Nicotiana tabacum/gossii in suspension culture. Acidification was greater in the case of NaCl-adapted than in that of wild type cells, and strikingly so in KCl medium when fusicoccin (FC) was present. Back-titration indicated that net proton secretion in KCl medium was increased 4-fold by FC treatment in the case of adapted cells; but was not even doubled in wild type cells. Membrane potential was higher in NaCl-adapted cells. FC treatment hyperpolarized wild, but not NaCl-adapted cells, suggesting a higher degree of coupling between H⁺ efflux and K⁺ influx in adapted cells; FC enhanced net K⁺ uptake in adapted but not in wild cells. Acidification by cells suspended in 10 millimolar KCl was highly sensitive to vanadate, but that after addition of 100 millimolar KCl or NaCl was much less sensitive. Addition of 100 millimolar NaCl to wild type cells already provided with 10 millimolar KCl briefly accelerated, then slowed down the rate of acidification. If the addition was made after acidification had already ceased, alkalization was observed, particularly in the presence of FC. The results are consistent with the operation of a Na⁺-H⁺ antiporter.     

Induced pore formation in membranes of cortex cells in excised Sorghum roots: its effect on membrane potential and nucleotide leakage

Measurements of membrane potentials were used for screening various molecules capable of inducing pore formation in cellular membranes for their ability to penetrate into excised roots of Sorghum bicolor (L.) Moench.
Poly- l -lysine (30 000 MW) and amphotericin B did not affect cortical cells even though they affected epidermal cells; the lysine polymer and the amphotericin B micelle were apparently too large to diffuse into the roots. Polymyxins and filipin depolarized the epidermal cells as well as the cells of the cortex. Depolarization of cortical cells by filipin was slower than that by polymixins.
Leakage of adenylate nucleotides was measured to obtain information concerning the size of the pores induced by polymyxins. Incubation with 200 μg/ml polymyxin B caused leakage of ATP from root segments. Leaked nucleotides were found in the medium; however, with time they were dephosphorylated, presumably by cell wall phosphatases. In situ ATP formation was observed when root segments were incubated with polymyxin, ADP, Pi, succinate and glucose, confirming that the induced pores were larger than the size of a nucleotide.     

Localization of an Amikacin 3′-Phosphotransferase in Escherichia coli

A plasmid-encoded enzyme reported by us to phosphorylate amikacin in a laboratory strain of Escherichia coli has been localized in the bacterial cell. More than 88% of this amikacin phosphotransferase (APH) activity was retained in spheroplasts formed by ethylenediaminetetraacetate-lysozyme treatment of an APH-containing E. coli transconguant known to form spheroplasts readily. By comparison, the spheroplasts retained 94% of deoxyribonucleic acid polymerase I and 98% of glutamyl-transfer ribonucleic acid synthetase, two internal markers, whereas less than 10% of the activity of a periplasmic marker, acid phosphatase, was present in spheroplasts. Treatment of whole cells of the transconjugant with chemical probes incapable of crossing the plasma membrane obliterated acid phosphatase activity, whereas the internal markers deoxyribonucleic acid polymerase I, glutamyl-transfer ribonucleic acid synthetase, and β-galactosidase were virtually unaffected after treatment for 5 min; more than 60% of the APH activity remained. As a control, similar chemical treatment of sonic extracts, in which enzymes were not protected by bacterial compartmentalization, produced more extensive reduction in the activities of all test enzymes, including APH. Spheroplasts preincubated with adenosine triphosphatase were shown by thin-layer chromatography to phosphorylate amikacin. Spheroplasts of cells grown in the presence of H₃³²PO₄ were shown to utilize internally generated adenosine 5′-triphosphate in the phosphorylation of amikacin. The absence of ³²P-phosphorylated amikacin after incubation of [γ-³²P]adenosine 5′-triphosphate with spheroplasts confirmed that exogenous adenosine 5′-triphosphate was not used in the reaction. These results suggest an internal location for APH. This conclusion has implications for the role of such enzymes in aminoglycoside resistance of gram-negative bacteria.