scholarly journals Enlisting wild grass genes to combat nitrification in wheat farming: A nature-based solution

2021 ◽  
Vol 118 (35) ◽  
pp. e2106595118
Author(s):  
Guntur V. Subbarao ◽  
Masahiro Kishii ◽  
Adrian Bozal-Leorri ◽  
Ivan Ortiz-Monasterio ◽  
Xiang Gao ◽  
...  

Active nitrifiers and rapid nitrification are major contributing factors to nitrogen losses in global wheat production. Suppressing nitrifier activity is an effective strategy to limit N losses from agriculture. Production and release of nitrification inhibitors from plant roots is termed “biological nitrification inhibition” (BNI). Here, we report the discovery of a chromosome region that controls BNI production in “wheat grass” Leymus racemosus (Lam.) Tzvelev, located on the short arm of the “Lr#3Nsb” (Lr#n), which can be transferred to wheat as T3BL.3NsbS (denoted Lr#n-SA), where 3BS arm of chromosome 3B of wheat was replaced by 3NsbS of L. racemosus. We successfully introduced T3BL.3NsbS into the wheat cultivar “Chinese Spring” (CS-Lr#n-SA, referred to as “BNI-CS”), which resulted in the doubling of its BNI capacity. T3BL.3NsbS from BNI-CS was then transferred to several elite high-yielding hexaploid wheat cultivars, leading to near doubling of BNI production in “BNI-MUNAL” and “BNI-ROELFS.” Laboratory incubation studies with root-zone soil from field-grown BNI-MUNAL confirmed BNI trait expression, evident from suppression of soil nitrifier activity, reduced nitrification potential, and N2O emissions. Changes in N metabolism included reductions in both leaf nitrate, nitrate reductase activity, and enhanced glutamine synthetase activity, indicating a shift toward ammonium nutrition. Nitrogen uptake from soil organic matter mineralization improved under low N conditions. Biomass production, grain yields, and N uptake were significantly higher in BNI-MUNAL across N treatments. Grain protein levels and breadmaking attributes were not negatively impacted. Wide use of BNI functions in wheat breeding may combat nitrification in high N input–intensive farming but also can improve adaptation to low N input marginal areas.

2009 ◽  
Vol 9 ◽  
pp. 138-146
Author(s):  
O.O. Shahovnina ◽  
O.V. Nadkernichna ◽  
Y.O. Vorobey ◽  
V.V. Krivopisha

Use of new strain of nitrogen fixing bacteria Azospirillum sp. 77 for inoculation of spring wheat and spring triticale permitted to form an effective associative system diasotroph - plant. The bacterization promoted the reliable increase of potential nitrogenase activity in root zone of plant by 38-220 %, activated the biosynthetic processes, in particular, glutamine synthetase activity increased by 57,0-71,9 %, content of protein in leaves - by 9,7-16,3 %, top of the plants - by 11,9- 18,9 %, weight of the roots - by 7,2-7,3 %.


1979 ◽  
Vol 57 (7) ◽  
pp. 754-758 ◽  
Author(s):  
D. Barry Scott ◽  
Carlos A. Neyra

The patterns of nitrate reduction, nitrate accumulation, and glutamine synthetase activity as a function of leaf development were studied in glasshouse-grown sorghum (Sorghum vulgare L. var. Dourado) seedlings. Leaf nitrate reductase activity increased during early leaf development and reached a maximum at full leaf expansion which was followed by a decline with leaf maturation. Leaf nitrate content closely paralleled the pattern of nitrate reductase activity for each individual leaf along the canopy. Glutamine synthetase activity increased during early leaf development but then remained constant until senescence. Etiolated leaves from nitrate-grown plants had minimal levels of nitrate reductase activity which increased markedly upon illumination. Glutamine synthetase activity was already high in those leaves and increased only slightly during greening. Crude preparations of glutamine synthetase were insensitive to cyanide and both the biosynthetic and transferase assays were enhanced by cysteine. The relatively high activities of glutamine synthetase throughout leaf development and greening indicate that this enzyme does not limit the assimilation of nitrate into amino acids and plays a role in the assimilation of ammonia from sources other than NO3− reduction.


1991 ◽  
Vol 102 (2) ◽  
Author(s):  
Th�ophile Soni ◽  
Claire Wolfrom ◽  
Samia Guerroui ◽  
Nicole Raynaud ◽  
Jos�phine Poggi ◽  
...  

1987 ◽  
Vol 65 (3) ◽  
pp. 432-437 ◽  
Author(s):  
Iftikhar Ahmad ◽  
Johan A. Hellebust

Stichococcus bacillaris Naeg. (Chlorophyceae) grown on a 12 h light: 12 h dark cycle divides synchronously under photoautotrophic conditions and essentially nonsynchronously under mixotrophic conditions. Photoassimilation of carbon under photoautotrophic conditions was followed by a decline in cell carbon content during the dark period, whereas under mixotrophic conditions cell carbon increased throughout the light–dark cycle. The rates of nitrogen assimilation by cultures grown on either nitrate or ammonium declined sharply during the dark, and these declines were most pronounced under photoautotrophic conditions. Photoautotrophic cells synthesized glutamine synthetase and NADPH – glutamate dehydrogenase (GDH) exclusively in the light, whereas in mixotrophic cells about 20% of the total synthesis of these enzymes during one light–dark cycle occurred in the dark. NADH–GDH was synthesized almost continuously over the entire light–dark cycle. In the dark, both under photoautotrophic and mixotrophic conditions, the alga contained more than 50% of glutamine synthetase in an inactive form, which was reactivated in vitro in the presence of mercaptoethanol and in vivo after returning the cultures to the light. The thermal stability of glutamine synthetase activity was less in light-harvested cells than in dark-harvested cells. The inactivation of glutamine synthetase did not occur in cultures growing either heterotrophically in continuous darkness or photoautotrophically in continuous light. This enzyme appears to be under thiol control only in cells grown under alternating light–dark conditions, irrespective of whether this light regime results in synchronous cell division or not.


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