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   <subfield code="a">Nitrate use by tobacco cells in response to N-stress and ammonium nutrition</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ningyan Zhang, Charles MacKown]</subfield>
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   <subfield code="a">Summary: Characterization of NO 3 − use by suspension cultured tobacco cells during a culture cycle is needed to take advantage of cell cultures for further study of the biochemical regulation of NO 3 − uptake induction and decay processes. Tobacco (Nicotiana tabacum L., cv. Ky14) cells were cultured with media containing different N sources. Cells cultured with a mixture of NO 3 − and NH 4 + (40 mM NO 3 − plus 20 mM NH 4 + , in Murashige and Skoog media) initially grew slightly faster but attained the same maximum cell culture density as those cultured with 40 mM NO 3 − only. Cells subcultured with N-free media grew at a similar rate for the first 3 d as those cells grown with N, then ceased further growth. The cessation of growth of cells subcultured with N-free media coincided with depletion of cell NO 3 − . The NO 3 − influx of cells subcultured with N-free media increased eleven-fold and those grown with N increased four- to five-fold before declining. Maximal NO 3 − influx rates occurred at the onset of the stationary growth phase for N-stressed cells, while cells grown with N reached maximums prior to the stationary phase of cell growth. Cells grown with a mixture of NO 3 − and NH 4 + had lower NO 3 − reductase (NR) activity and higher cell NO 3 − levels than those of cells grown with NO 3 − only. The NR activity of cells subcultured with N-free media peaked within 1 d after subculture before declining to a constitutive level when cell NO 3 − was depleted. The level of cell NO 3 − plays a critical role in the expression of the NO 3 − uptake and reduction processes. The transitions in the expression of NO 3 − uptake and reduction activities of tobacco cell suspension cultures should prove valuable for further study of the biochemical and molecular basis for the regulation of these processes.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Zhang</subfield>
   <subfield code="D">Ningyan</subfield>
   <subfield code="u">Department of Agronomy, University of Kentucky and USDA-ARS, 40546-0091, Lexington, KY, USA</subfield>
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   <subfield code="t">Plant Cell Reports</subfield>
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   <subfield code="g">11/9(1992-08-01), 470-475</subfield>
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