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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 29 (1992), S. 153-160 
    ISSN: 1573-5044
    Keywords: micropropagation ; plant tissue culture ; phytotoxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The phytotoxic effects of antibiotic treatment on micropropagated Clematis, Delphinium, Hosta, Iris and Photinia were determined by assessing multiplication and rooting rates of plants in vitro and weaning success and flowering in vivo.
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  • 2
    ISSN: 1573-5044
    Keywords: bacteria ; contamination ; pH ; plant tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The persistence of accidentally introduced bacterial contaminants inDelphinium tissue cultures can be prevented by acidification of the tissue culture medium. Using this preservation method the contamination rate ofDelphinium cultures could be reduced by more than 50%.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 30 (1992), S. 171-179 
    ISSN: 1573-5044
    Keywords: medium pH ; micropropagation ; plant tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Micropropagated Choisya, Daphne, Delphinium, Hemerocallis, Hosta, Iris and Photinia were found to adjust the pH of Murashige and Skoog's plant tissue culture medium (initial pH 5.6 or 3.5) to different values depending on the species. When plant growth and rooting rates were determined after plants had been grown on media initially adjusted or buffered to values between 2.6 and 5.7 the different plant species were also found to have distinct pH requirements for optimal growth and/or rooting rates.
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  • 4
    ISSN: 1573-4919
    Keywords: Na+/H+ antiporter ; ethylisopropylamiloride ; human check cell ; buccal epithelium ; saliva ; ionophore
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Proton-dependent, ethylisopropylamiloride (EIPA)-sensitive Na+ uptake (Na+/H+ antiporter) studies were performed to examine if saliva, and ionophores which alter cellular electrolyte balance, could influence the activity of the cheek cell Na+/H+ antiporter. Using the standard conditions of 1 mmol/1 Na+, and a 65:1 (inside:outside) proton gradient in the assay, the uniport ionophores valinomycin (K+) and gramicidin (Na+) increased EIPA-sensitive Na+ uptake by 177% (p 〈 0.01) and 227% (p 〈 0.01), respectively. The dual antiporter ionophore nigericin (K+-H+) increased EIPA-sensitive Na+ uptake by 654% (p 〈 0.01), with maximal Na+ uptake achieved by 1 min and at an ionophore concentration of 50 μmol/l, with an EC 50 value 6.4 μmol/l. Preincubation of cheek cells with saliva or the low molecular weight (MW) components of saliva (saliva activating factors, SAF) for 2 h at 37°C, also significantly stimulated EIPA-sensitive Na+ uptake. This stimulation could be mimicked by pre-incubation with 25 mmol/l KCl or K+-phosphate buffer. Pre-incubating cheek cells with SAF and the inclusion of 20 μmol/1 nigericin in the assay, produced maximum EIPA-sensitive Na+ uptake. After pre-incubation with water, 25 mmol/1 K+-phosphate or SAF, with nigericin in all assays, the initial rate of proton-gradient dependent, EIPA-sensitive Na+ uptake was saturable with respect to external Na+ with Km values of 0.9, 1.7, and 1.8 mmol/l, and V max values of 13.4, 25.8, and 31.1 nmol/mg protein/30 sec, respectively. With 20 μmol/1 nigericin in the assay, Na+ uptake was inhibited by either increasing the [K+]o in the assay, with an ID 50 of 3 mmol/l. These results indicate that nigericin can facilitate K+ i exchange for H+ o and the attending re-acidification of the cheek cell amplifies IINa+ uptake via the Na+/H+ antiporter. The degree of stimulation of proton-dependent, EIPA-sensitive Na+ uptake is therefore dependent, in part, on the intracellular K+ i.
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