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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 72 (1988), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Plasma membranes were isolated from light-grown, 14-day-old maize leaves (Zea mays L. cv. Golden Cross Bantam) using aqueous two-phase partitioning. The plasma membrane (PM) fraction contained 〈 0.3% of the total chlorophyll, 〈 0.2% of the mitochondrial marker enzyme activity, minimal contamination by endomembranes and 34% of the total PM.A calmodulin-stimulated (Ca2++ Mg2+)-ATPase was identified in the PM-enriched fraction. The Ca2++ calmodulin stimulation was dependent on Mg2+, saturated at ca 25 μM total Ca2+, had a pH maximum at 7.2 and was maximally stimulated by 600 nM bovine brain calmodulin. The stimulation was not greatly affected by the anion present and showed a divalent cation specificity of Ca2+ 〉 Sr+2 ± Mn+2 〉 Co2+± Cu2+ 〉 Ba2+. The napthalenesulfonamide W7, an antagonist of calmodulin action, completely inhibited the calmodulin stimulation at 175 μM, while the less active analogue W5 was ineffective at this concentration. La3+, an inhibitor of PM Ca2+ transport, showed a 50% inhibition of calmodulin-stimulated ATPase activity at ca 200 μM. Taken as a whole, these data demonstrate the presence of a calmodulinstimulated, (Ca2++ Mg2+)-ATPase on the cytoplasmic surface of the plasma membrane of maize leaf cells.
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 260 (1976), S. 435-436 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Cuttings from 4-d-old green seedlings of P. aureus Roxb., grown in vermiculite, were obtained by excision 7.0 cm below the apical bud. The cuttings were transferred randomly to 12-ml vials containing 6.0ml of test solution (12 cuttings per vial), and incubated in continuous light (1.35 104 erg cm2 ...
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 73 (1988), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The plasma membrane of eukaryotic cells contains endogenous, integral electron transport proteins. In the maize (Zea mays L. cv. Golden Cross Bantam) root plasma membrane, these activities include NAD(P)H-ferricyanide reductase. NAD(P)H-duroquinone reductase (1.6.5.1) and NAD(P)H-ascorbate free-radical reductase (EC 1.6.5.4). Differences in degree of stimulation upon vesicle rupture with detergent and in specificities for pyridine nucleotides suggest that these activities constitute distinct components in the membranes. Solubilization of reductase activities was examined using Triton X-100 over a wide range of retergent-to-protein ratios. The Triton-solubilized enzymes were purified using dye-ligand affinity chromatography on Cibacron blue 3G-A agarose utilizing biospecific elution with NADH. Resolution of the redox activities was accomplished upon differential elution with 0.1.1.0 and 10 mM NADH. The distinctive characteristics of the enzymes and the differential chromatographic behavior of the respective activities provided evidence for the presence of separate enzymatic redox components in maize root plasma membranes with implications for an electron transfer chain.
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  • 4
    ISSN: 1432-2048
    Keywords: Endoplasmic reticulum ; Gravitropism ; Lepidium ; Membrane fractionation ; Root (membranes)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The first step in the gravitropic reaction chain, i.e. perception, is known to occur in the statenchyma of the root cap. Because of the importance of the root tip in graviperception, a procedure has been developed to isolate root tips from garden cress (Lepidium sativum L.). The root tip fraction contains the tissues of the root cap plus the lower half of the meristem zone, but is clearly separated from the tissues of the elongation zone, the zone of gravitropic response. Membranes from the root tip and root base fractions have been centrifuged on sucrose density gradients and the marker enzyme profiles analyzed. These results show that the marker enzyme profiles for vacuoles, dictyosomes, mitochondria, and plasma membranes are similar in the root tip or root base fractions. The endoplasmic reticulum (ER) has a shoulder of cytochrome c reductase activity at a density of 1.16 g cm-3 which is distinct from the other enzyme activities and is only observed in root tip preparations. The specific enzyme activity for ER, cytochrome c reductase, was enriched in root tip membranes 1.7 fold. This latter increase is interpreted as at least in part an increased ER content in the root tip.
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  • 5
    ISSN: 1432-2048
    Keywords: Assimilate partitioning ; Beta ; Cotransport ; Plasma membrane ; Proton motive force ; Sucrose transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The mechanism of sucrose transport across the plasma membrane (PM) was investigated in membrane vesicles isolated from sugarbeet (Beta vulgaris L.) leaves. In the presence of a membrane potential (Δψ) generated as a K+-diffusion potential, negative inside, sucrose induced a rapid and transient alkalization of the medium. Alkalization was inhibited by carbonyl cyanide m-chlorophenylhydrazone, was specific for the sucrose sugar and was dependent on the sucrose concentration with a Km of approx. 1 mM. Sucrose-induced alkalization and sucrose transport were inhibited by the sulfhydryl-reactive reagent, p-chloromercuribenzene sulfonic acid, and by the histidine-reactive reagent, diethyl pyrocarbonate. Parallel analysis of sucrose uptake and alkalization indicated that the stoichiometry of sucrose uptake to proton consumed was 1∶1. These results provide clear evidence that the saturable mechanism of sucrose transport across the PM in plants is a coupled H+-sucrose symport.
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  • 6
    ISSN: 1432-2048
    Keywords: Assimilate partitioning ; Beta ; Phloem loading ; Plasma membrane ; Proton gradient ; Symport ; Sucrose transport ; Transport (sucrose)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An analysis of the molecular mechanism of sucrose transport across the plasmalemma was conducted with isolated plasma-membrane (PM) vesicles. Plasma membrane was isolated by aqueous two-phase partitioning from fully expanded sugar beet (Beta vulgaris L.) leaves. The isolated fraction was predominantly PM vesicles as determined by marker-enzyme analysis, and the vesicles were oriented right-side-out as determined by structurally linked latency of the PM enzyme, vanadate-sensitive Mg2+-ATPase. Sucrose uptake was investigated by equilibrating PM vesicles in pH 7.6 buffer and diluting them 20-fold into pH 6.0 buffer. Using this pH-jump technique, vesicles accumulated acetate in a pH-dependent, protonophore-sensitive manner, which demonstrated the presence of a pH gradient (ΔpH) across the vesicle membrane. Addition of sucrose to pH-jumped PM vesicles resulted in a pH-dependent, protonophoresensitive uptake of sucrose into the vesicles. Uptake was sucrose-specific in that a 10-fold excess of mannose, glucose, fructose, mannitol, melibiose, lactose or maltose did not inhibit sucrose accumulation. The rate of pH-dependent uptake was saturable with respect of sucrose concentration and had an apparent K m, of 0.45 mM. Sucrose uptake was stimulated approximately twofold by the addition of valinomycin and K+, which indicated an electrogenic sucrose-H+ symport. Membrane potentials (ΔΨ) were imposed across the vesicle membrane using valinomycin and K+. A membrane potential, negative inside, stimulated pH-dependent sucrose uptake while a ΔΨ, positive inside, inhibited uptake. Conditions that produce a negative ΔΨ in the absence of a pH gradient supported, although weakly, sucrose uptake. These data support an electrogenic sucrose-H+ symport as the mechanism of sucrose transport across the PM in Beta leaves.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Planta 159 (1983), S. 84-90 
    ISSN: 1432-2048
    Keywords: Endoplasmic reticulum ; Lepidium ; Membrane isolation ; Root (endoplasmic reticulum) ; Transport (calcium)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Endoplasmic reticulum membranes were isolated from roots of garden cress (Lepidium sativum L. cv Krause) using differential and discontinuous sucrose gradient centrifugation. The endoplasmic reticulum fraction was 80% rough endoplasmic reticulum oriented with the cytoplasmic surface directed outward and contaminated with 12% unidentified smooth membranes and 8% mitochondria. Marker enzyme analysis showed that the activity for endoplasmic reticulum was enriched 2.4-fold over total membrane activity while no other organelle activity showed an enrichment. All evidence indicated that the fraction was composed of highly enriched endoplasmic reticulum membranes. Ca2+ uptake activity was measured using the filter technique described by Gross and Marmé (1978). The results of these experiments showed an ATP-dependent, oxalate-stimulated Ca2+ uptake into vesicles of the endoplasmic reticulum fraction. The majority of the transport activity was microsomal since specific inhibitors of mitochondrial Ca2+ transport (ruthenium red, LaCl3 and oligomycin) inhibited the activity by only 25%. Sodium azide showed no inhibition. The transport was likely directly coupled to ATP hydrolysis since there was no inhibition with carbonylcyanidem-chlorophenylhydrazone. The transport activity was specific for ATP showing only 36% and 29% of the activity with inosine diphosphate and guanosine 5′-triphosphate, respectively. The results indicate a Ca2+ transport function located on the endoplasmic reciculum of garden cress roots.
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  • 8
    ISSN: 1432-2048
    Keywords: Beta ; Phloem loading ; Spinacia ; Sucrose-binding protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Immunocytochemical studies using antibodies raised against a 62-kDa membrane protein isolated from developing soybean (Glycine max (L.) Merr.) cotyledons were performed on leaf tissue of spinach (Spinacia oleracea L.). This 62-kDa protein was labeled by 6′-deoxy-6′-(4-azido-2-hydroxy)-benzamidosucrose (HABS), a photoaffinity sucrose analogue (K. G. Ripp et al., 1988, Plant Physiol.88, 1435–1445). Western-blot analysis of spinach plasma-membrane proteins indicated a cross-reactive polypeptide identical in molecular mass to that found in soybean. Indirect immunogold labeling of resin-embedded sections of fully expanded leaf tissue resulted in specific localization of colloidal gold on the sieve-tube plasma membrane. The label was uniform and, except for a few non-specific gold particles over the cell wall, all other cellular organelles and membrane systems were free of label. With the exception of occasional gold particles associated with the companion-cell plasma membrane, all other cell types of the leaf contained little or no label. Control sections treated with non-immune rabbit immunoglobulin-G were also essentially free of label. Immunogold labeling of young leaves, in which the phloem contained no mature sieve-tube members, were free of label for the 62-kDa protein. However, young leaf tissue in which mature or nearly mature sieve tubes could be identified, contained immunolabel associated with the sieve-tube plasma membranes. Similar results were obtained with mature leaf tissue of sugar beet (Beta vulgaris L.). The results of the immunocytochemical studies are consistent with the suggestion that the concentrating step in the phloem-loading process in this species may occur across the sieve-tube plasma membrane.
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  • 9
    Publication Date: 1994-01-01
    Print ISSN: 0006-3134
    Electronic ISSN: 1573-8264
    Topics: Biology
    Published by Springer
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  • 10
    Publication Date: 1982-11-01
    Print ISSN: 0032-0935
    Electronic ISSN: 1432-2048
    Topics: Biology
    Published by Springer
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