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Measuring Nitrate in Plant Cells byin VivoNMR Using Gd3+as a Shift Reagent

โœ Scribed by Yair Shachar-Hill; Philip E. Pfeffer; R.George Ratcliffe


Book ID
102597947
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
110 KB
Volume
111
Category
Article
ISSN
1064-1866

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โœฆ Synopsis


NMR investigations of nitrate in plant cells and tissues have

In fact, severe quadrupolar broadening restricts the applicahitherto been limited by the indistinguishability of the signals from tion of in vivo 35 Cl NMR to the detection of chloride in intracellular and extracellular nitrate. Gd 3/ is shown to be an compartments, such as plant cell vacuoles, with low protein effective shift reagent for 14 N and 15 N nitrate NMR signals, resolvcontent. In contrast, the 14 N and 15 N NMR signals from tissue ing the internal and external nitrate signals in plant tissues, includnitrate are fully detectable, and a shift reagent for nitrate ing cell suspensions and root material. However, time-course exwould be expected to facilitate nitrate transport studies in periments show that, while the use of Gd 3/ allows nitrate levels microorganisms and plant tissues.

to be monitored over extended periods, it also has adverse effects

Nitrate is an important source of nitrogen for many plants, on growth and nitrate uptake. Accordingly, a number of chelated and nitrate uptake and storage are important phenomena (4).

forms of gadolinium were investigated, and it is concluded that

The main techniques currently available used for studying the NMR contrast agent Gd(DTPA-BMA) is likely to be a suitable shift reagent for physiologically relevant studies of nitrate trans-these processes are 13 N and 15 N tracer methods (5, 6) (which port in roots.


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