In vivo Nitrate Reductase Activity in Leaves of Pearl Millet, Pennisetum americanum (L.) Leeke

1987 ◽  
Vol 14 (2) ◽  
pp. 125 ◽  
Author(s):  
SV Chanda ◽  
AK Joshi ◽  
PN Krishnan ◽  
YD Singh
Keyword(s):  
Nitrate Reductase ◽  
Reductase Activity ◽  
Potassium Phosphate ◽  
Limiting Factor ◽  
Growth Stages ◽  
In Vivo Assay ◽  
Rate Limiting ◽  
Nr Activity

In the in vivo assay of nitrate reductase (NR) in P. americanum leaves, addition of 1% (v/v) Triton X-100, potassium phosphate buffer (80 mM, pH 7.4) and 1.13 mM NADH to the assay medium resulted in maximum activity. With increasing concentration of NADH, saturation-type kinetics were observed. Based on this data metabolic pool concentration for NADH and apparent Km for nitrate reductase were determined. In field studies with cultivars BJ-104, J-104 and 5141-A of P. americanum, the relative limitation of NO3-, NADH and nitrate reductase in NO3- assimilation was determined. NR activity was measured by four modifications of the in vivo assay technique (with NO3-, with NADH, without NO3- and NADH and with both NO3- and NADH additions to the reaction mixture) and with one in vitro technique. For all the cultivars, NADH was the major rate-limiting factor for in vivo assay during early growth stages, while at later stages, NO3- was limiting. At no stage was NR rate-limiting. It is concluded that NR activity alone may not serve as biochemical marker for improved efficiency of utilisation of nitrogen in P. americanum.

The Determination of Nitrate Reductase Activity of Leaves to the Dominant Species in Forest Community of Northern Aspect of Changbai Mountains

2011 ◽  
Vol 183-185 ◽  
pp. 900-904
Author(s):  
Yu Wen Li ◽  
Yun Jie Wu
Keyword(s):  
Nitrate Reductase ◽  
Tree Species ◽  
Reductase Activity ◽  
Forest Community ◽  
High Yield ◽  
Changbai Mountains ◽  
Ecological Situation ◽  
Nr Activity

This paper addresses the application of improvement in vivo of traditional method for determination of nitrate reductase (NR) activity of leaves to dominant tree species in forest community of northern aspect of Changbai Mountains. It describes the NR activity of tree species related to the shade-endurance and shows that the intolerance tree species has higher NR activity. The NR of a species is also related to the ecological situation of the sites. Tree species with higher NR activities should be selected for breeding of fast growing and high yield tree species.

scholarly journals Effects of growth retarding compounds on chlorophyll accumulation and nitrate reductase activity in nitrate induced cucumber cotyledons

2015 ◽  
Vol 42 (3) ◽  
pp. 431-439 ◽  
Author(s):  
J. S. Knypl
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reductase Activity ◽  
Reductase Activity ◽  
Chlorophyll Synthesis ◽  
Growth Retardants ◽  
Chlorophyll Accumulation ◽  
High Concentrations ◽  
Amo 1618 ◽  
Nr Activity

Cotyledons were excised from 5-day old etiolated cucumber seedlings and .grown for 24 or 48 h in solutions of plant growth retardants: AMO-1618,B-Nine, CCC and phosfon D, supplemented with KNO<sub>3</sub> (10<sup>-2</sup>M) in light. Nitrate reductase (NR) activity was determined <i>in vivo</i>. CCC and Phosfon D at high concentrations had no effect on nitrate reductase activity in 24 h tests. CCC at 5xl0<sup>-2</sup> M enhanced NR activity in longer 48 h tests; Phosfon D was inhibitory in that case. AMO-1618 markedly decreased NR activity. B-Nine strikingly enhanced NR activity in KNO<sub>3</sub> induced cytoledons; the effect was positively correlated with the concentration of B-Nine. Ali the compounds inhibited chlorophyll synthesis.

Changes in Leaf Nitrate Reductase Activity In Vivo and In Vitro During Light-Dark Transitions

1999 ◽  
Vol 8 (1) ◽  
pp. 37-40 ◽  
Author(s):  
B. K. Salalkar ◽  
R. S. Shaikh ◽  
R. M. Naik ◽  
S. V. Munjal ◽  
B. B. Desai ◽  
...  
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reductase Activity ◽  
Reductase Activity ◽  
Leaf Nitrate

scholarly journals Effect of lead on nitrate reductase activity and nitrate assimilation in pea leaves

2014 ◽  
Vol 57 (4) ◽  
pp. 457-463 ◽  
Author(s):  
S. K. Sinha ◽  
H. S. Srivastava ◽  
S. N. Mishra
Keyword(s):  
Enzyme Activity ◽  
Nitrate Reductase ◽  
Nitrate Reductase Activity ◽  
Organic Nitrogen ◽  
Reductase Activity ◽  
Total Organic Nitrogen ◽  
Intact Leaf ◽  
Leaf Tissues

The effect of Pb on nitrate reductase activity, protein, total organic nitrogen and on the chlorophyll content in excised and intact leaf tissues of <em>Pisum sativum</em> was examine. Enzyme activity assayed in vitro or in vivo in the excised leaves showed marked increase at lower concentrations of Pb while being inhibited at higher concentrations. In intact leaf tissues, the enzyme activity (in vivo or in vitro) was unaffected at lower concentrations but was inhibited at higher concentrations of Pb. Chlorophyll, carotenoids (non-nitrogenous pigments), soluble protein and organic nitrogen contents remained almost unaffected at all concentrations of Pb tested. It seems that nitrate reductase has a different response towards Pb pollution in this species, which is more tolerant to heavy metal pollution, especially Pb.

scholarly journals Nitrate reductase and acid phosphatase activities as affected by inorganic phosphate in corn roots

2014 ◽  
Vol 52 (1) ◽  
pp. 77-86 ◽  
Author(s):  
Marie Kummerova ◽  
Józef Buczek
Keyword(s):  
Acid Phosphatase ◽  
Nitrate Reductase ◽  
Nutrient Solution ◽  
Inorganic Phosphate ◽  
Acid Phosphatases ◽  
Weak Effect ◽  
Corn Roots ◽  
Nr Activity

The deficieny of inorganic phosphate in nutrient solution reduces by about 50 per cent NO<sub>3</sub>- absorption in corn seedlings, it decreases both <em>in vitro</em> and in vivo nitrate reductase (NR) activity, as well the potential and actual NR level and has a very weak effect on NR induction. Acid phosphatases activities increase in corn roots when the plants are grown in nutrient solution without phosphorus. We suggest that inorganic phosphate is required mainly for maintenance of NR activity rather, than for induction <em>in vivo</em> of nitrate reductase. It is not excluded that deficiency of inorganic phosphate in root tissue may be partly supplemented as the result of enhanced acid phosphatase activity.

Inhibition of 17β-hydroxysteroid-oxidoreductase activity in purified rat Leydig cells by single injection of human choriogonadotrophin

1984 ◽  
Vol 105 (4) ◽  
pp. 571-576 ◽  
Author(s):  
Nikolaus Kühn-Velten ◽  
Wolfgang Staib
Keyword(s):  
Leydig Cells ◽  
Time Course ◽  
Marked Decrease ◽  
Single Injection ◽  
Reductase Activity ◽  
Competitive Inhibitor ◽  
Oxidoreductase Activity ◽  
Rate Limiting

Abstract. A marked decrease of progesterone conversion to androgens in vitro by purified rat testis Leydig cells is observed from 1/2 to 3 days after treatment of the rats with 100 IU human choriogonadotrophin (hCG) in vivo. The maximal inhibition results 2 days after hCG injection and is denoted by a 72% reduction of androstenedione formation and a 78% reduction of testosterone formation from 2.5 μmol progesterone · l7#x2212;1. The testosterone/androstenedione ratio (about 0.4), however, is not changed after hCG treatment, indicating that the 17-ketosteroid-reductase activity is not rate-limiting under these conditions. Nevertheless, testosterone formation from 2.5 μmol androstenedione · l−1 is reduced by 67% and androstenedione formation from 2.5 μmol testosterone · l−1 is reduced by 79% 1 and 2 days after hCG treatment. The time-course of this hCG-induced decrease in both reductase and oxidase activities of the Leydig cell 17β-hydroxysteroid-oxidoreductase parallels the decrease of androgen formation from progesterone. Kinetic analyses reveal that the Vmax of the oxidase is reduced to a significantly (P < 0.05) greater extent than the Vmax of the reductase (79 and 62%, respectively), whereas the respective Km values remain unchanged. From these results it may be concluded that either a loss, or an inactivation of the enzyme protein, or the formation of non-competitive inhibitor occur during hCG action and that hCG may affect different enzyme activities involved in testicular androgen biosynthesis in a similar way.

RELATIONS BETWEEN NITRATE REDUCTASE ACTIVITY AND NITROGEN ACCUMULATION IN SOYBEANS

1976 ◽  
Vol 56 (2) ◽  
pp. 377-384 ◽  
Author(s):  
MIR HATAM ◽  
D. J. HUME
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reduction ◽  
Nitrate Uptake ◽  
Reductase Activity ◽  
N Uptake ◽  
Nitrogen Accumulation ◽  
Total N ◽  
Total Plant ◽  
Nr Activity

An in vivo assay for nitrate reductase (NR) activity was adapted to measure total NR activity in soybean [Glycine max (L.) Merr.] plants grown for a 29-day period indoors. Disappearance of nitrate from the nutrient solution, plant nitrate and total plant nitrogen (N) also were measured. Under the conditions of this experiment, nitrate reduction estimated from NR activities agreed closely with actual nitrate reduction. The same assay was used to measure leaf NR activities of field-grown soybeans throughout the 1971 growing season. Leaf NR activities accounted for 77 and 72% of the total N uptake in plants receiving 0 and 280 kg N as NH4NO3/ha, respectively. Measurements of nitrate and ammonium losses from soil under soybeans and under adjacent bare soil at three stages of plant development suggested that in plots receiving no fertilizer N, 86% of N uptake from the soil was in the form of nitrate. The NR activity of field-grown plants agreed well with total plant N derived from soil nitrates. Results indicated that leaf NR activities were proportional to nitrate uptake and might be used to determine amounts and seasonal patterns of nitrate uptake by soybean plants.

Effects of Glufosinate on Anion Uptake in Lemna gibba G 1

1989 ◽  
Vol 44 (1-2) ◽  
pp. 33-38 ◽  
Author(s):  
Gudrun D. Trogisch ◽  
Helmut Köcher ◽  
Wolfram R. Ullrich
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reductase Activity ◽  
Nitrate Uptake ◽  
Dark Respiration ◽  
Reductase Activity ◽  
Lemna Gibba ◽  
Proton Cotransport ◽  
Chlorophyll Formation

Abstract The duckweed Lemna gibba G 1 was used as a model to study inhibitory sites with the herbicide and glutamate analogue glufosinate (PPT). Growth and chlorophyll formation were partly inhibited by 25 n-M, completely suppressed by 250 (im PPT. Photosynthesis showed partial inhibition within few hours, dark respiration ( 0 2 consumption) increased already within one hour. In the presence of 1 mM PPT in the light, the ammonium pool of Lemna increased to 600% within few hours, later to 1000%. The overall amino acid pool exhibited a slower increase to 300%, the nitrate pool only a slight increase, while total phosphate remained almost unchanged. In the dark all these effects were less pronounced than in the light. Nitrate, nitrite and phosphate uptake were partially inhibited by PPT, especially after 19 h PPT pretreatment. Nitrate reductase activity in vitro, after PPT treatment in vivo, showed an inhibition similar to that of nitrate uptake. Ammonium was not taken up but released under the same conditions. The data are explained by a combined effect of PPT, by inhibition of glutamine synthetase leading to accumulation of ammonium from photorespiration and proteolysis, by membrane depolarization and inhibition of anion/proton cotransport, by secondary uncoupling of phosphorylation, and by secondary inhibition of nitrate reductase activity.

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