Effect of Herbicides on In Vivo Nitrate and Nitrite Reduction

Weed Science ◽  
1977 ◽  
Vol 25 (1) ◽  
pp. 18-22 ◽  
Author(s):  
R.L. Finke ◽  
R.L. Warner ◽  
T.J. Muzik
Keyword(s):  
Hordeum Vulgare ◽  
Nitrate Reductase ◽  
Nitrate Reduction ◽  
Amaranthus Retroflexus ◽  
Nitrite Reduction ◽  
Nitrite Accumulation ◽  
Inhibitory Effects ◽  
Potassium Azide ◽  
Nitrate And Nitrite

The effects of herbicides on in vivo nitrate and nitrite reduction were determined by vacuum infiltrating sections of barley (Hordeum vulgareL.) or bean (Phaseolus vulgarisL.) leaves with solutions containing nitrate and herbicides. Herbicides causing a reduction of nitrite accumulation in the dark were considered to have inhibitory effects upon nitrate reduction and those causing an accumulation of nitrite in the light were considered to inhibit nitrite reduction. Only dinoseb (2-sec-butyl-4,6-dinitrophenol) and potassium azide significantly reduced nitrate reduction in both barley and bean. All of the herbicides which inhibit photosynthesis inhibited nitrite reduction but had no significant effect on nitrate reduction in barley and bean. Nitrite reduction in an atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] resistant pigweed (Amaranthus retroflexusL.) biotype was not affected by any triazine tested. However, these triazines significantly inhibited nitrite reduction in barley, bean, and the susceptible pigweed biotype. The results suggest that the in vivo nitrate reductase technique may be a useful technique for identifying chemicals which inhibit the flow of electrons to ferredoxin, thereby inhibiting nitrite reduction in light.

Nitrate reduction and nitrogenase activity in Spirillum lipoferum

1977 ◽  
Vol 23 (3) ◽  
pp. 306-310 ◽  
Author(s):  
Carlos A. Neyra ◽  
Peter Van Berkum
Keyword(s):  
Nitrate Reduction ◽  
Time Course ◽  
Nitrogenase Activity ◽  
Reductase Activity ◽  
Nitrite Reduction ◽  
Lag Phase ◽  
Nitrite Accumulation ◽  
Assimilatory Nitrate Reduction ◽  
Nitrate And Nitrite ◽  
Anaerobic Pretreatment

Nitrate and nitrite reduction under aerobic, microaerophillic, and anaerobic conditions was demonstrated in Spirillum lipoferum (ATCC 29145). Nitrite did not accumulate during assimilatory nitrate reduction in air. The nitrite produced during dissimilatory nitrate reduction accumulated in the medium but not in the cells. On exposure of the bacteria to nitrate and anaerobiosis, a low initial rate (lag) was followed by accelerated rates of nitrite accumulation. A 3-h anaerobic pretreatment, in the absence of nitrate, did not avoid the lag phase. No nitrate reductase activity (NRA) developed in the presence of chloramphenicol. The data suggest that induction of anaerobic NRA in S. lipoferum required nitrate and protein synthesis.Anaerobic N2ase activity by S. lipoferum was greatly stimulated in the presence of nitrate. The time course of nitrate reduction was coincidental with the pattern of nitrate-stimulated N2ase activity indicating that a relationship exists between these two processes.

scholarly journals Glycerol-driven Denitratation: Process Kinetics, Microbial Ecology, and Operational Controls

2021 ◽  
Author(s):  
Matthew P. Baideme ◽  
Chenghua Long ◽  
Luke T. Plante ◽  
Jeffrey A. Starke ◽  
Michael A. Butkus ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Microbial Ecology ◽  
Nitrate Reduction ◽  
Carbon Sources ◽  
Selective Reduction ◽  
Nitrite Reduction ◽  
Nitrite Accumulation ◽  
Ammonium Oxidation ◽  
Order Of Magnitude ◽  
Nitrate And Nitrite

ABSTRACTDenitratation, the selective reduction of nitrate to nitrite, is a novel process when coupled with anaerobic ammonium oxidation (anammox) could achieve resource-efficient biological nitrogen removal of ammonium- and nitrate-laden waste streams. Using a fundamentally-based, first principles approach, this study optimized a stoichiometrically-limited, glycerol-driven denitratation process and characterized mechanisms supporting nitrite accumulation with results that aligned with expectations. Glycerol supported selective nitrate reduction to nitrite and near-complete nitrate conversion, indicating its viability in a denitratation system. Glycerol-supported specific rates of nitrate reduction (135.3 mg-N/g-VSS/h) were at least one order of magnitude greater than specific rates of nitrite reduction (14.9 mg-N/g-VSS/h), potentially resulting in transient nitrite accumulation and indicating glycerol’s superiority over other organic carbon sources in denitratation systems. pH and ORP inflection points in nitrogen transformation assays corresponded to maximum nitrite accumulation, indicating operational setpoints to prevent further nitrite reduction. Denitratation conditions supported enrichment of Thauera sp. as the dominant genus. Stoichiometric limitation of influent organic carbon, coupled with differential nitrate and nitrite reduction kinetics, optimized operational controls, and a distinctively enriched microbial ecology, was identified as causal in glycerol-driven denitratation.

Inhibition of Nitrite Reduction with Photosynthetic Inhibitors

Weed Science ◽  
1975 ◽  
Vol 23 (3) ◽  
pp. 188-190 ◽  
Author(s):  
Lowell A. Klepper
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reduction ◽  
Leaf Tissue ◽  
Nitrite Reduction ◽  
Green Leaf ◽  
Nitrate Reductase Assay ◽  
Herbicide Concentration ◽  
Photosynthetic Inhibitors

Using a modified in vivo nitrate reductase assay, all photosynthetic inhibitors tested were shown to effectively block light-dependent nitrite reduction in green leaf tissue. Nitrate reduction continued so that nitrite accumulated. Nitrite, vacuum infiltrated into leaf tissue, disappeared linearly with time when incubated in the light. Nitrite, vacuum infiltrated with a photosynthetic inhibitor, did not disappear but accumulated to even higher levels. The degree of inhibition of nitrite reduction was a function of herbicide concentration and time of incubation.

Effects of pH and alkalinity on sulfur-denitrification in a biological granular filter

1996 ◽  
Vol 34 (1-2) ◽  
pp. 355-362 ◽  
Author(s):  
Hiroaki Furumai ◽  
Hideki Tagui ◽  
Kenji Fujita
Keyword(s):  
Enrichment Culture ◽  
Nitrite Reduction ◽  
The Other ◽  
Nitrite Accumulation ◽  
Ph Dependency ◽  
Effects Of Ph ◽  
Rapid Removal ◽  
Nitrate And Nitrite ◽  
The Relationship ◽  
Biological Filters

Two laboratory-scale biological filters were operated to investigate the effects of alkalinity and pH on removal of nitrate and nitrite in sulfur denitrification filter processes. The concentration of sodium bicarbonate in the feed media was changed from 120 to 240 mg/l during about 3 months in a filter (Run A). The other filter was initially fed with 300 mg/l and then with 240 mg/l (Run B). The performance of the filter was monitored by measuring pH, nitrate, nitrite, sulfate, alkalinity, and thiosulfate. Nitrate concentration in effluent rapidly decreased to lower levels within several days for both filters after inoculation of enrichment culture of sulfur denitrifiers. However there was a large difference in removal of nitrite. When rapid removal of nitrate took place, nitrite accumulation was observed and remained while the bicarbonate concentration was 120 and 150 mg/l. On the other hand the nitrite accumulation disappeared when more bicarbonate (240 and 300 mg/l) was supplied. The experimental results indicated that the nitrite accumulation was closely related to pH condition and alkalinity level in the filter. The stable data of effluent water quality for 5 cases were collected and the relationship discussed between nitrite concentration and pH in effluents. The relationship indicated a strong pH dependency on nitrite accumulation below pH of 7.4. The pH condition around 7 is not so inhibitory to biological activity. Therefore, the pH within the biofilm would be low enough to suppress the nitrite reduction by sulfur denitrifiers, while the pH in effluent was not in the inhibitory range. It was recommended to keep the pH higher than 7.4 to prevent nitrite accumulation in the sulfur denitrification filter.

scholarly journals Biogenic Fe(II-III) Hydroxycarbonate Green Rust Enhances Nitrate Removal and Decreases Ammonium Selectivity during Heterotrophic Denitrification

Minerals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 818
Author(s):  
Georges Ona-Nguema ◽  
Delphine Guerbois ◽  
Céline Pallud ◽  
Jessica Brest ◽  
Mustapha Abdelmoula ◽  
...  
Keyword(s):  
Nitrate Reduction ◽  
Nitrate Removal ◽  
Green Rust ◽  
Nitrite Reduction ◽  
Nitrite Accumulation ◽  
Bacterial Reduction ◽  
Water Treatment Process ◽  
Nitrite Production ◽  
Ammonium Production ◽  
Biogenic Iron

Nitrification-denitrification is the most widely used nitrogen removal process in wastewater treatment. However, this process can lead to undesirable nitrite accumulation and subsequent ammonium production. Biogenic Fe(II-III) hydroxycarbonate green rust has recently emerged as a candidate to reduce nitrite without ammonium production under abiotic conditions. The present study investigated whether biogenic iron(II-III) hydroxycarbonate green rust could also reduce nitrite to gaseous nitrogen during bacterial nitrate reduction. Our results showed that biogenic iron(II-III) hydroxycarbonate green rust could efficiently decrease the selectivity of the reaction towards ammonium during heterotrophic nitrate reduction by native wastewater-denitrifying bacteria and by three different species of Shewanella: S. putrefaciens ATCC 12099, S. putrefaciens ATCC 8071 and S. oneidensis MR-1. Indeed, in the absence of biogenic hydroxycarbonate green rust, bacterial reduction of nitrate converted 11–42% of the initial nitrate into ammonium, but this value dropped to 1–28% in the presence of biogenic hydroxycarbonate green rust. Additionally, nitrite accumulation did not exceed the 2–13% in the presence of biogenic hydroxycarbonate green rust, versus 0–28% in its absence. Based on those results that enhance the extent of denitrification of about 60%, the study proposes a water treatment process that couples the bacterial nitrite production with the abiotic nitrite reduction by biogenic green rust.

scholarly journals Implications of Limited Thermophilicity of Nitrite Reduction for Control of Sulfide Production in Oil Reservoirs

2016 ◽  
Vol 82 (14) ◽  
pp. 4190-4199 ◽  
Author(s):  
Tekle Tafese Fida ◽  
Chuan Chen ◽  
Gloria Okpala ◽  
Gerrit Voordouw
Keyword(s):  
Nitrate Reduction ◽  
Nitrite Reduction ◽  
Oil Fields ◽  
Microbial Consortia ◽  
Subsequent Reduction ◽  
Content Type ◽  
Reduction Activity ◽  
Pure Cultures ◽  
Nitrate And Nitrite ◽  
Reducing Bacteria

ABSTRACTNitrate reduction to nitrite in oil fields appears to be more thermophilic than the subsequent reduction of nitrite. Concentrated microbial consortia from oil fields reduced both nitrate and nitrite at 40 and 45°C but only nitrate at and above 50°C. The abundance of thenirSgene correlated with mesophilic nitrite reduction activity.ThaueraandPseudomonaswere the dominant mesophilic nitrate-reducing bacteria (mNRB), whereasPetrobacterandGeobacilluswere the dominant thermophilic NRB (tNRB) in these consortia. The mNRBThauerasp. strain TK001, isolated in this study, reduced nitrate and nitrite at 40 and 45°C but not at 50°C, whereas the tNRBPetrobactersp. strain TK002 andGeobacillussp. strain TK003 reduced nitrate to nitrite but did not reduce nitrite further from 50 to 70°C. Testing of 12 deposited pure cultures of tNRB with 4 electron donors indicated reduction of nitrate in 40 of 48 and reduction of nitrite in only 9 of 48 incubations. Nitrate is injected into high-temperature oil fields to prevent sulfide formation (souring) by sulfate-reducing bacteria (SRB), which are strongly inhibited by nitrite. Injection of cold seawater to produce oil creates mesothermic zones. Our results suggest that preventing the temperature of these zones from dropping below 50°C will limit the reduction of nitrite, allowing more effective souring control.IMPORTANCENitrite can accumulate at temperatures of 50 to 70°C, because nitrate reduction extends to higher temperatures than the subsequent reduction of nitrite. This is important for understanding the fundamentals of thermophilicity and for the control of souring in oil fields catalyzed by SRB, which are strongly inhibited by nitrite.

scholarly journals Contribution of shoots and roots to in vivo nitrate reduction in NADH-specific nitrate reductase-deficient mutant seedlings of barley (Hordeum vulgareL.)

2004 ◽  
Vol 50 (4) ◽  
pp. 527-535 ◽  
Author(s):  
Salwa Abdel-Latif ◽  
Tahei Kawachi ◽  
Hiroyuki Fujikake ◽  
Norikuni Ohtake ◽  
Takuji Ohyama ◽  
...  
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reduction ◽  
Deficient Mutant

scholarly journals Two Nitrate/Nitrite Transporters Are Encoded within the Mobilizable Plasmid for Nitrate Respiration of Thermus thermophilus HB8

2000 ◽  
Vol 182 (8) ◽  
pp. 2179-2183 ◽  
Author(s):  
Sandra Ramírez ◽  
Renata Moreno ◽  
Olga Zafra ◽  
Pablo Castán ◽  
Cristina Vallés ◽  
...  
Keyword(s):  
Nitrate Reductase ◽  
Average Distance ◽  
Thermus Thermophilus ◽  
Major Facilitator Superfamily ◽  
Nitrate Respiration ◽  
Mobilizable Plasmid ◽  
Excretion Rates ◽  
Major Facilitator ◽  
Nitrate And Nitrite

ABSTRACT Thermus thermophilus HB8 can grow anaerobically by using a membrane-bound nitrate reductase to catalyze the reduction of nitrate as a final electron acceptor in respiration. In contrast to other denitrifiers, the nitrite produced does not continue the reduction pathway but accumulates in the growth medium after its active extrusion from the cell. We describe the presence of two genes,narK1 and narK2, downstream of the nitrate reductase-encoding gene cluster (nar) that code for two homologues to the major facilitator superfamily of transporters. The sequences of NarK1 and NarK2 are 30% identical to each other, but whereas NarK1 clusters in an average-distance tree with putative nitrate transporters, NarK2 does so with putative nitrite exporters. To analyze whether this differential clustering was actually related to functional differences, we isolated derivatives with mutations of one or both genes. Analysis revealed that single mutations had minor effects on growth by nitrate respiration, whereas a double narK1 narK2 mutation abolished this capability. Further analysis allowed us to confirm that the double mutant is completely unable to excrete nitrite, while single mutants have a limitation in the excretion rates compared with the wild type. These data allow us to propose that both proteins are implicated in the transport of nitrate and nitrite, probably acting as nitrate/nitrite antiporters. The possible differential roles of these proteins in vivo are discussed.

A composite biochemical system for bacterial nitrate and nitrite assimilation as exemplified by Paracoccus denitrificans

2011 ◽  
Vol 435 (3) ◽  
pp. 743-753 ◽  
Author(s):  
Andrew J. Gates ◽  
Victor M. Luque-Almagro ◽  
Alan D. Goddard ◽  
Stuart J. Ferguson ◽  
M. Dolores Roldán ◽  
...  
Keyword(s):  
Nitrate Reductase ◽  
Nitrogen Source ◽  
Nitrite Reductase ◽  
Paracoccus Denitrificans ◽  
Gene Clusters ◽  
Anion Exchange Chromatography ◽  
Exchange Chromatography ◽  
Nitrite Reduction ◽  
Anaerobic Growth ◽  
Nitrate And Nitrite

The denitrifying bacterium Paracoccus denitrificans can grow aerobically or anaerobically using nitrate or nitrite as the sole nitrogen source. The biochemical pathway responsible is expressed from a gene cluster comprising a nitrate/nitrite transporter (NasA), nitrite transporter (NasH), nitrite reductase (NasB), ferredoxin (NasG) and nitrate reductase (NasC). NasB and NasG are essential for growth with nitrate or nitrite as the nitrogen source. NADH serves as the electron donor for nitrate and nitrite reduction, but only NasB has a NADH-oxidizing domain. Nitrate and nitrite reductase activities show the same Km for NADH and can be separated by anion-exchange chromatography, but only fractions containing NasB retain the ability to oxidize NADH. This implies that NasG mediates electron flux from the NADH-oxidizing site in NasB to the sites of nitrate and nitrite reduction in NasC and NasB respectively. Delivery of extracellular nitrate to NasBGC is mediated by NasA, but both NasA and NasH contribute to nitrite uptake. The roles of NasA and NasC can be substituted during anaerobic growth by the biochemically distinct membrane-bound respiratory nitrate reductase (Nar), demonstrating functional overlap. nasG is highly conserved in nitrate/nitrite assimilation gene clusters, which is consistent with a key role for the NasG ferredoxin, as part of a phylogenetically widespread composite nitrate and nitrite reductase system.

Differential effects of ozone on in vivo nitrate reduction in soybean cultivars. I. Response to exogenous sugars

1978 ◽  
Vol 56 (13) ◽  
pp. 1540-1544 ◽  
Author(s):  
Albert C. Purvis
Keyword(s):  
Nitrate Reductase ◽  
Nitrate Reduction ◽  
Nitrate Reductase Activity ◽  
Reductase Activity ◽  
Foliar Injury ◽  
Glycolytic Intermediates ◽  
Glycine Max L ◽  
Growth Chambers ◽  
Visible Foliar Injury

Two cultivars of soybeans (Glycine max (L.) Merr.) differing widely in their resistance to ozone were exposed to 0.5 μl/ℓ ozone for 2 h in growth chambers. In vivo nitrate reduction was depressed by more than 50% in the primary leaves of Dare, the ozone-sensitive cultivar, but was not significantly altered in Hood, the ozone-resistant cultivar. Sucrose, up to 1.5% (w/v), added to excised seedlings of the Dare cultivar during exposure to ozone eliminated the ozone depression of in vivo nitrate reductase activity and also reduced foliar injury. Addition of two glycolytic intermediates, glyceraldehyde-3-phosphate and fructose-1,6-diphosphate, to the infiltration medium recovered some in vivo nitrate reduction in treated Dare leaves. The levels of extractable nitrate reductase and glyceraldehyde-3-phosphate dehydrogenase in the primary leaves of both cultivars were unaltered by ozone fumigations. These observations led to the conclusion that ozone depression of in vivo nitrate reduction is not due to ozone inactivation of nitrate reductase or of the enzymes coupling nitrate reduction to glycolysis, but may be caused by an inadequate supply of photosynthetic sugars. It was also noted that ozone depression of in vivo nitrate reduction only occurred with treatments which subsequently caused the development of visible foliar injury.

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