The nitrate reductase Essay

It is reported that nitrate reductase is an of import enzyme of nitrogen metamorphosis. It is inducible by No3 contents Huffaker, et Al ( 1982 ) . Under drought conditions, merely vaccination with alien carbuncular mycorrhizal Fungis increased shoot and root nitrate reductase activity 188 % and 38 % severally with regard to workss neither inoculated nor treated with compost. Alguacil, et Al. ( 2006 ) . It is besides concluded that nitrate supply to the foliages from roots play a much larger regulative function in commanding nitrate reductase activity in workss. Nitrate reductase activity in corn leave was consistent with the well known fact that nitrate additions and NH4 decreases nitrate reductase active ( Dale, et al.1976. , David, et Al. 1983 )

Pace et-al ( 1990 ) The consequences demonstrate that decrease of come ining nitrate by roots every bit good as shoots was regulated by coincident photosynthesis. Although in vitro nitrate reductase activity of both tissues declined by 60 % during a 10-hour period of CO2 emphasis, the staying activity was greatly in surplus of that required to catalyse the mensural rate of 15NO3- decrease. Root respiration and soluble saccharide degrees in root tissue were besides decreased by CO2 emphasis. Jointly, the consequences indicate that nitrate consumption and decrease were regulated by the supply of energy and C skeletons required to back up these procedures, instead than by the possible enzymatic capacity to catalyse nitrate decrease, as measured by in vitro nitrate reductase activity. ( Konard, et al. , 1983 ) . Widman, et Al. ( 1993 ) besides concluded that nitrate reductase activity of workss species was reduced in nitrate deficient dirt.

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Soraya, et Al. ( 2007 ) found that cells halotolerant cyanobactarium grown in nitrate containing medium showed higher nitrate reductase activity than the cells grown in glutamine medium. Nitrate reductase degrees are besides regulated by denovo synthesis and protein debasement ( David, et al. , 1983 ) . Andrew, et Al. ( 1980 ) reported that nitrate reductase activity was higher in comparable foliages from the high than from the low nitrate reductase genotype through the grain development period. There was no correlativity between nitrate reductase activity and nitrate content of foliages. However, high nitrate reductase genotype maintained higher sum of nitrate during ulterior phase of grain development.

The NR activities were maximal in 100 % NPK followed by organically treated secret plans. This was attributed to provide of readily available nitrate from inorganic fertilisers to the workss while in organically treated secret plans, nitrate release was relatively slow. Further, in the organically treated secret plans ammonium ions are released after decomposition of organic affair and the ammonium ions so released are repressive to the NR activity ( Claussen and Lenz, 1999 ) . Thus the consequences clearly showed that all the organic manures used in the survey played a important function in increasing root and shoot biomass, chlorophyll content of rainy season harvests ( i.e. , soya bean and sorghum ) and the subsequent wheat harvest in the winter season for all the three cropping systems.

Alguacil ( 2006 ) reported that compost add-on had no important consequence on NR activity in shoots of J. oxycedrus seedlings, under either well-watered or drought-stressed conditions. The seedlings inoculated with alien AM Fungi showed the highest values of shoot NR activity in drought emphasis conditions. Compost add-on and alien AM fungi vaccination increased significantly the NR activity in roots. The H2O emphasis decreased NR activity in roots of J. oxycedrus workss grown in the dirt amended with compost.

Foyer et Al ( 1998 ) A correlativity between maximum extractible foliar nitrate reductase ( NR ) activity and the rate of CO2 assimilation was observed. The NR activation province and maximum extractible NR activity declined quickly in response to drouth. Photosynthesis and NR activity recovered quickly when alimentary solution was restored at this point. The lessening in maximum extractible NR activity was accompanied by a lessening in NR transcripts, whereas Suc phosphate synthase and phosphoenolpyruvate carboxylase messenger RNA were much less affected. The coordination of N and C metamorphosis is retained during drought conditions via transition of the activities of Suc phosphate synthase and NR commensurate with the predominating rate of photosynthesis.

Konard et-al ( 1983 ) observed that Nitrate reductase activity in foliages was consistent with the well known fact that N03- additions, and NH4+ and amide-N lessening, nitrate reductase activity. In roots, nitrate reductase activity in vitro was correlated with the rate of nitrate decrease in vivo. Inasmuch as nitrate decrease consequences in the production of OH- and stimulates the synthesis of organic anions, it was postulated that nitrate reductase activity of roots is stimulated by the released OH- or by the synthesized organic anions instead than by nitrate itself. Addtion of HCO3- to alimentary solution of maize seedlings resulted in a important addition of the nitrate reductase activity in the roots. As HCO3- , like OH- , increases pH and promotes the synthesis of organic anions, this provides circumstantial grounds that alkamne conditions and/or organic anions have a more direct impact on nitrate reductase activity than make N03- , NH4-N, and amide-N.

It is besides reported that NRA in works tissue is relative to nitrate concentration in dirt solution and its synthesis is regulated by flux instead than flick nitrate contents. ( Naqvi et al.,1996 ) .Shanker et Al ; ( 2001 ) reported that there is positive correlativity between NRA and entire organic nitrogen.Wang et Al ; ( 2004 ) concluded that Nitrate regulates nitrate reductase written text, translocation and activation in higher plants.Hageman and Flesher, ( 1960 ) reported that NR is induced by No2.Ben Zioni et al. , ( 1971 ) proposed mechanism how No3 decrease in the shoots may increase the soaking up of No3 by the roots.They suggested that after KNO3 translocation to hit from the roots, a stoichometric sum of malate is produced for the No3 decrease in the shoots.After the malate is synthesized, portion of it moves downto the roots system as K -malate, where it is oxidized, giving KHCo3, which exchanges for KNo3 in the external medium. Thus No3 decrease in shoots promotes discriminatory consumption of No3 by the roots.

NPK Concentration

Prasad and Sinha ( 2000 ) investigated that the K, Zn, Cu, Fe and Mn demand of rice and wheat could be met by the incorporation of harvest residues. Recycling of harvest residues can refill 37 % of the N remotion by rice and wheat, 18 % of P remotion by wheat and 28 % of P remotion by rice in chalky dirt. Available N, K, S, Zn, Fe, Cu, Mn, B and Mo increased when different degrees of fertilisers were applied along with FYM and harvest residues. Gondhk and Mazzar ( 2005 ) reported that mineral and organo-mineral fertiliser resulted in diminution of organic content in dirt whereas FYM increased organic C in dirt. Application of organic-mineral fertiliser increased available Zn content. Nardi et Al. ( 2004 ) investigated evaluated that 40 old ages of FYM manure application sustained entire organic C ( TOC ) in the top beds while mineral interventions entirely or assorted with FYM showed a minor consequence on the organic affair development in a corn system.

NPK content in corn foliages and grain were besides increased significantly with the application of organic and inorganic fertilisers ( Sial, et al. , 2007 ) .

Crop Residues and Soil Properties

Ranjan, et Al. ( 2007 ) reported that combined usage of NPK and FYM increased SOC, entire N, Olsen P and ammonium ethanoate extractible K by 47 % , 31 % and 73 % receptively. It besides showed the highest degrees of dirt microbic biomass C and dehydrogenase activity.The usage of organic beginnings along-with inorganic fertilisers besides improves soil physical conditions. Prasad and Sinha ( 2000 ) found that dirt collection and dirt porosity-hydraulic conduction was increased with incorporate alimentary direction. Entire porousness of dirt and H2O keeping capacity were increased with the application of both FYM and inorganic fertiliser. In 0-15 centimeter dirt bed, the entire porousness significantly increased with FYM over control ( Rehana et al. 2007 ) . Application of 5 t FYM ha-1 every twelvemonth significantly improved the dirt organic content ( Petal et al. , 2008 ) .

MATERIAL AND METHODS

Enzyme Extraction

For pull outing antioxidant enzymes, fresh foliages ( 0.5 g ) were ground utilizing a tissue bomber in 5 milliliter of 50 millimeters cooled phosphate buffer ( pH 7.8 ) placed in an ice bath. The homogenate was centrifuged at 15000 tens g for 20 min at 4 & A ; deg ; C. The supernatant was used for finding the activities of enzymes.

Superoxide dismutase: ( SOD )

The activity of SOD was determined by mensurating its ability to suppress the photoreduction of nitroblue tetrazolium ( NBT ) following the method of Giannopolitis and Ries ( 1977 ) . The reaction solution ( 3 milliliter ) contained 50 µM NBT, 1.3 µM vitamin B2, 13 millimeter methionine, 75 nanometer EDTA, 50 millimeter phosphate buffer ( pH 7.8 ) , and 20 to 50 µl of enzyme infusion. The trial tubing incorporating the reaction solution were irradiated under visible radiation ( 15 fluorescent lamps ) at 78 µmol m-2 s-1 for 15 min. The optical density of the irradiated solution at 560 nanometer was read utilizing a spectrophotometer ( IRMECO, U2020 ) . One unit of SOD activity was defined as the sum of enzyme that inhibited 50 % of NBT photoreduction.

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