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  • 1
    ISSN: 1432-2048
    Keywords: Ion channel ; Potassium ion ; Planar lipid bilayer ; Plasma membrane ; Quinine ; Secale (K+ channels)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Plasma membrane was purified from roots of rye (Secale cereale L. cv. Rheidol) by aqueous-polymer two-phase partitioning and incorporated into planar bilayers of 1-palmitoyl-2-oleoyl phosphatidylethanolamine by stirring with an osmotic gradient. Since plasmamembrane vesicles were predominantly oriented with their cytoplasmic face internal, when fused to the bilayer the cytoplasmic side of channels faced the trans chamber. In asymmetrical (cis:trans) 280∶100 mM KCl, five distinct K+-selective channels were detected with mean chord-conductances (between +30 and -30 mV; volyages cis with respect to trans) of 500 pS, 194 pS, 49 pS, 21 pS and 10 pS. The frequencies of incorporation of these K+ channels into the bilayer were 48, 21, 50, 10 and 9%, in the order given (data from 159 bilayers). Only the 49 pS channel was characterized further in this paper, but the remarkable diversity of K+ channels found in this preparation is noteworthy and is the subject of further study. In symmetrical KCl solutions, the 49 pS channel exhibited non-ohmic unitary-current/voltage relationships. The chord-conductance (between +30 and-30 mV) of the channel in symmetrical 100 mM KCl was 39 pS. The unitary current was greater at positive voltages than at corresponding negative voltages and showed considerable rectification with increasing positive and negative voltages. This would represent ‘inward rectification’ in vivo. Gating of the channel was not voltage-dependent and the channel was open for approx. 80% of the time. Presumably this is not the case in vivo, but we are at present uncertain of the in vivo controls of channel gating. The distribution of channel-open times could be approximated by the sum of two negative exponential functions, yielding two open-state time constants (τo, the apparent mean lifetime of the channel-open state) of 1.0 ms and 5.7 s. The distribution of channel-closed times was best approximated by the sum of three negative exponential functions, yielding time constants (τc, the apparent mean lifetime of the channel-closed state) of 1.1 ms, 51 ms and 11 s. This indicates at least a five-state kinetic model for the activity of the channel. The selectivity of the 49 pS channel, determined from both reversal potentials under biionic conditions (100 mM KCl∶100 mM cation chloride) and from conductance measurements in symmetrical 100 mM cation chloride, was Rb+≥ K+ 〉 Cs+ 〉 Na+ 〉 Li+ 〉 tetraethylammonium (TEA+). The 49 pS channel was reversibly inhibited by quinine (1 mM) but TEA+ (10 mM), Ba2+ (3 mM), Ca2+ (1 mM), 4-aminopyridine (1 mM) and charybdotoxin (3 μM) were without effect when applied to the extracellular (cis) surface.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Planta 198 (1996), S. 39-45 
    ISSN: 1432-2048
    Keywords: Chara ; Cell wall and zinc ; Micronutrient ; Triticum ; Zinc uptake
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The mechanism of zinc influx was investigated using giant algal cells (Chara corallina Klein ex Will.esk. R.D. Wood), in which it was possible to discriminate clearly between tracer zinc bound in the cell wall and actual uptake into the cell. It was shown that despite lengthy desorption, retention of zinc in slowly exchanging zinc pools in the cell wall can invalidate tracer influx measurements. A comparative study of zinc desorption from isolated cell walls of wheat (Triticum aestivum L.) roots indicated exchange characteristics similar to that of Chara. Fractionation of Chara internodal cells taken directly from cultures showed that most of the cell-associated zinc was in the cell walls. The cytoplasmic and vacuolar zinc concentrations were 56 mmol·m−3 and 32 mmol·m−3, respectively, for cells grown in a zinc concentration of 0.1 mmol·m−3. Influx of 65Zn in Chara was linear over several hours, with rapid transfer to the vacuole, but only slow efflux. Influx occurred in a biphasic manner, which was tentatively attributed to the operation of two separate transport systems, a high-affinity system which is saturated at 0.1 mmol·m−3 and a low-affinity system which showed a linear dependence on concentration up to at least 50 mmol·m−3. Only the low-affinity system was examined in detail. Influx through this system showed a strong dependence on external pH with an optimum around 7 and was also stimulated by cytoplasmic acidification. Influx was sensitive to metabolic inhibition, but not to blockers of Ca2+ and K+ channels. Other characteristics included a slight sensitivity to Mn2+ and Fe2+ but little sensitivity to high concentrations of K+ or Na+. Influx was independent of membrane potential difference in cells voltage-clamped at − 65 to − 300 mV.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Planta 195 (1995), S. 362-368 
    ISSN: 1432-2048
    Keywords: Aluminium toxicity ; Calcium influx ; Cellwall and calcium ; Chara Lanthanum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The proposal that aluminium (Al) toxicity in plants is caused by either inhibition of Ca2+ influx or by displacement of Ca2+ from the cell wall, was examined. For this study the giant alga Chara corallina Klein ex Will. em. R.D. Wood was selected because it shows a similar sensitivity to Al as in roots of higher plants and, more importantly, it is possible to use the large single internodal cells to make accurate and unambiguous measurements of Ca2+ influx and Ca2+ binding in cell walls. Growth of Chara was inhibited by Al at concentrations comparable to those required to inhibit growth of roots, and with a similar speed of onset and pH dependence. At Al concentrations which inhibited growth, influx of calcium (Ca2+) was only slightly sensitive to Al. The maximum inhibition of Ca2+ influx at 0.1 mol·m−3 Al at pH 4.4 was less than 50%. At the same concentration, lanthanum (La3+) inhibited influx of Ca2+ by 90% but inhibition of growth was similar for both La3+ and Al. Removal of Ca2+ from the external solution did not inhibit growth for more than 8 h whereas inhibition of growth by Al was apparent after only 2.5 h. Ca2+ influx was more sensitive to Al when stimulated by addition of high concentrations of potassium (K+) or by action potentials generated by electrical stimulation. Other membrane-related activities such as sodium influx, rubidium influx and membrane potential difference and conductance, were not strongly affected by Al even at high concentrations. In isolated cell walls equilibrated in 0.5 mol·m−3 Ca2+ at pH 4.4, 0.1 mol·m−3 Al displaced more than 80% of the bound Ca2+ with a half-time of 25 min. From the poor correlation between inhibition of growth and reduction in Ca2+ influx, it was concluded that Al toxicity was not caused by limitation of the Ca2+ supply. Short-term changes in other membrane-related activities induced by Al also appeared to be too small to explain the toxicity. However the strong displacement, and probable replacement, of cell wall ca2+ by Al may be sufficient to disrupt normal cell development.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 155-156 (1993), S. 305-308 
    ISSN: 1573-5036
    Keywords: boron ; wheat ; Triticum aestivum L. ; uptake ; genotypic variation ; toxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The mechanism of boron (B) uptake in wheat was studied using two genotypes with known differences in their ability to accumulate B. Influx and efflux of B was measured in the roots of intact 21 d old plants. Roots grown in 15 μM B, when transferred to solutions containing 1mM B showed a rapid increase in B content for up to 60 min, after which no further increase was evident up to 4 h. No genotypic difference in B influx was apparent over these time periods. Roots grown in 1mM B for 7 d and then rinsed in B-free solutions quickly lost most of B that they contained within 1 hour; little further efflux was observed over the following three hours. As with the influx, no genotypic difference in B flux was evident. It is suggested that the lack of genotypic difference in the short-term B fluxes could be due to a masking effect of extracellular B bound in the cell walls of the roots.
    Type of Medium: Electronic Resource
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