Amide Concentrations Research Articles

Characteristics and evolution of bioethanol from Manila Tamarind (Pithecellobium dulce) leaf through fermentation

<p>This study's two primary goals are to synthesize bioethanol from biowaste and examine its thermal characteristics. Bioethanol must first undergo a comprehensive assessment of its thermal characteristics in order to be approved for usage in spark-ignition engines. A multi-step procedure comprising extraction, pretreatment, enzymatic hydrolysis, and fermentation was used to manufacture the bioethanol. The raw material was put through a preliminary screening using thermogravimetric analysis to find the mass loss rate as a function of temperature before to starting this process. Remarkably, the Manila tamarind leaves exhibited the highest mass loss, up to 34%. Enzymatic cellulose conversion to fermentable sugars was a critical step in the production of cellulosic ethanol. Following hydrolysis, Saccharomyces cerevisiae was employed in the fermentation process, leading to the bioethanol synthesis phase. The Manila Tamarind leaves yielded the most, around 29% by weight, which is amazing. In order to assess the thermal properties of the extracted ethanol, a variety of parameters were carefully examined, including the viscosity, density, cetane number, and calorific value. In each of these areas, mixtures of tire oil, gasoline, and bioethanol consistently outperformed the others. Furthermore, Fourier Transform Infrared Spectrometry spectra were utilized to validate the concentrations of potential groups, including alcohol, aromatic, alkyne, amide, and carbonyl groups. Clear objectives guide the fermentation process, aiming for consistent quality, safety, and functionality in the end product.</p>

Inactivation of foodborne and other pathogenic bacteria with pyrrolidine based fatty acid amide derivatives

AbstractFoodborne pathogens are a persistent threat to food and consumer safety. To mitigate outbreaks and contamination incited by these pathogens, the development of novel preventative safety controls and biorational inactivation measures are paramount. The objectives of this research were to evaluate the efficacy of pyrrolidine‐based amide derivatives of decanoic (DEPY), lauric (LAPY), myristic (MYPY) and palmitic (PAPY) fatty acids for in‐vitro inhibition and inactivation of various Gram‐positive bacterial strains including Listeria monocytogenes (typically associated with foodborne illness), Bacillus subtilis, and Streptococcus mutans and Streptococcus sobrinus (both normally present in the oral cavity and involved with dental caries). Compared to no treatment (control), significant differences (P < 0.05) in the growth of Listeria strains were seen in‐vitro with increased inhibition at higher amide concentrations (10,000–20,000 ppm). Furthermore, in‐vitro growth inhibition of B. subtilis, S. sobrinus, and S. mutans was also observed with an effectiveness of LAPY>MYPY>PAPY>DEPY. In co‐inoculation assays, LAPY treatment significantly reduced Listeria growth from 1.55 to >5.0 Log CFU/mL when a concentration range of 5 to 250 ppm was applied. Moreover, Listeria populations on pathogen‐inoculated produce were significantly (P < 0.05) reduced from 0.51 to >3.00 Log CFU/g with greater inactivation on carrots compared to alfalfa, soybean, and pistachio. These results demonstrated the potential value of these FA amides against Gram‐positive pathogenic bacteria. Biorational applications of antibacterial FA amides on fresh produce as a postharvest intervention process offers a great potential for enhancement of food safety.

N-terminal loops at the tetramer interface of nitrile hydratase act as “hooks” determining resistance to high amide concentrations

Nitrile hydratase (NHase) has been extensively utilized in industrial acrylamide production. However, the vulnerability to high concentrations of acrylamide limits its further application. Herein, we redesigned the N-terminal loop at the tetramer interface of a thermophilic NHase from Pseudonocardia thermophila JCM3095 (PtNHase), and its catalytic activity, resistance to high acrylamide concentrations, and thermostability were improved. Amino acid residues located in the N-terminal loop of the tetramer interface that are responsible for enhancing the resistance to high acrylamide concentrations were identified via static structural analysis and molecular dynamics simulations. A variant library was used to fine-tune the tetramer interface. Variant αL6T exhibited 3.5-fold greater resistance to 50% (v/v) acrylamide, whereas its activity was 1.2-fold higher than that of the wild-type (WT) enzyme, revealing no activity-stability trade-off. Compared to the use of Escherichia coli harboring the WT enzyme, the use of E. coli harboring αL6T increased the acrylamide concentration from 398.1 g/L to 500 g/L. Crystal structure-guided analysis of αL6T and molecular dynamics simulations revealed that increased enzyme surface hydration and the introduction of positive cross-correlation into the N-terminal loop of the tetramer interface caused the two loop regions to hook to each other, thus improving the resistance to high acrylamide concentrations.

Hydrochar promoted anaerobic digestion of hydrothermal liquefaction wastewater: Focusing on the organic degradation and microbial community

Hydrothermal liquefaction wastewater (HTLWW) can be used for biogas production through anaerobic digestion (AD). Nevertheless, it generally contains refractory and toxic organics which causes low methane production. The present study showed that the methane yield and methane production rate were increased by 32–52 % and by 51–84 %, respectively, with the addition of hydrochars derived from different feedstocks including sludge, corn straw, poplar wood and Enteromorpha algae. Although hydrochars could adsorb certain amount of organics, the adsorption capacity was not related with the promotion of AD. The adsorbed organics could be neglected after AD due to the biodegradation. 3-dimensional fluorescence excitation emission matrix analysis revealed that hydrochars increased the degradation of all types of fluorescent compounds. Fourier-transform infrared spectroscopy analysis showed hydrochars significantly reduced the concentrations of aromatic, amino acids, amide I and amide II functional groups compounds in HTLWW during AD. Hydrochars also led to higher degradation of nitrogenous, aromatic and phenolic compounds as revealed by gas chromatography mass spectrometry analysis. In addition, it was shown that hydrochars resulted in low number of organic species whose concentration increased during partly degradation. Microbial analysis showed hydrochars enhanced the growth of syntrophic bacteria (e.g. Syntrophomonas and Syntrophorhabdus) which had ability to degrade an extensive range of various types of organics including aromatic and phenolic organics. Hydrochars also facilitated direct interspecies electron transfer considering the enrichment of known microbes involved in direct interspecies electron transfer (DIET) process including Geobacter and certain methanogens (Methanosaeta and Methanobacterium).

Piperine Inhibits TGF-β Signaling Pathways and Disrupts EMT-Related Events in Human Lung Adenocarcinoma Cells.

Background: Piperine, an amide extracted from the Piper spices, exhibits strong anti-tumor properties. However, its effect on the epithelial–mesenchymal transition (EMT) process has never been investigated. Herein, we evaluate the toxic effect of piperine on lung adenocarcinoma (A549), breast adenocarcinoma (MDA-MB-231) and hepatocellular carcinoma (HepG2) cell lines, as well as its ability to inhibit EMT-related events induced by TGF-β1 treatment. Methods: The cell viability was investigated by MTT assay. Protein expression was evaluated by Western blot. Gene expression was monitored by real-time PCR. Zymography assay was employed to detect metalloproteinase (MMP) activity in conditioned media. Cell motility was assessed by the wound-healing and phagokinetic gold sol assays. Results: The results revealed that piperine was cytotoxic in concentrations over 100 µM, showing IC50 values for HepG2, MDA-MB-231 and A549 cell lines of 214, 238 and 198 µM, respectively. In order to investigate whether piperine would reverse the TGF-β1 induced-EMT, the A549 cell line was pretreated with sublethal concentrations of the natural amide followed by the addition of TGF-β1. Besides disrupting EMT-related events, piperine also inhibited both ERK 1/2 and SMAD 2 phosphorylation. Conclusions: These results suggest that piperine might be further used in therapeutic strategies for metastatic cancer and EMT-related disorders.

High temperature utilization of PAM and HPAM by microbial communities enriched from oilfield produced water and activated sludge

Non-hydrolyzed polyacrylamide (PAM) and partially hydrolyzed polyacrylamide (HPAM) are commonly used polymers in various industrial applications, including in oil and gas production operations. Understanding the microbial utilization of such polymers can contribute to improved recovery processes and help to develop technologies for polymer remediation. Microbial communities enriched from oilfield produced water (PW) and activated sludge from Alberta, Canada were assessed for their ability to utilize PAM and HPAM as nitrogen and carbon sources at 50 °C. Microbial growth was determined by measuring CO2 production, and viscosity changes and amide concentrations were used to determine microbial utilization of the polymers. The highest CO2 production was observed in incubations wherein HPAM was added as a nitrogen source for sludge-derived enrichments. Our results showed that partial deamination of PAM and HPAM occurred in both PW and sludge microbial cultures after 34 days of incubation. Whereas viscosity changes were not observed in cultures when HPAM or PAM was provided as the only carbon source, sludge enrichment cultures amended with HPAM and glucose showed significant decreases in viscosity. 16S rRNA gene sequencing analysis indicated that microbial members from the family Xanthomonadaceae were enriched in both PW and sludge cultures amended with HPAM or PAM as a nitrogen source, suggesting the importance of this microbial taxon in the bio-utilization of these polymers. Overall, our results demonstrate that PAM and HPAM can serve as nitrogen sources for microbial communities under the thermophilic conditions commonly found in environments such as oil and gas reservoirs.

Amides as a model system of low molar mass algal organic matter. Influence on the adsorption of p-nitrophenol on activated carbon

In this study, the adsorption equilibrium and diffusivity parameters of p-nitrophenol were estimated for water containing different concentrations of secondary amides. Commercial powdered activated carbon was used as an adsorbent. The external mass transfer coefficient (kf), the surface diffusion coefficient (Ds) and the standard free Gibbs energy were calculated for p-nitrophenol in the presence of different secondary amide concentrations. The analysis established that there are correlations between structural parameters of amides, on the one hand, and diffusion and thermodynamic parameters for p-nitrophenol adsorption process, on the other. It was noticed that voluminous hydrophobic amides decreased the adsorption capacity of p-nitrophenol on activated carbon. On the basis of the results obtained for external mass transfer coefficients, it is assumed that amides cause the reduction of adsorption capacity of p-nitrophenol onto activated carbon by concentrating at the solid/liquid interface.

Temperature Perturbation on Hydrogen Bonding in Aqueous Solutions at Different Amide Concentrations

AbstractA series of amides with variation in the number of methyl and amine groups were used as additives of water. Perturbations of water structure by variation of temperature and concentration of urea, formamide, N‐methylformamide, and N,N‐dimethylformamide was systematically analyzed by vibrational spectroscopy. The water absorption band was critically analyzed by 2D‐correlation spectroscopy, its deconvolution and derivative spectra. Degree of perturbation of the water structure was evaluated to provide strong evidence on molecular level interactions, self‐aggregation, and modification of the network of water structure. Clusters of water‐amides were energetically optimized and consequent theoretical vibrational frequencies of C−N and C=O groups of amide were found to be consistent with experimental frequencies. The water structure underwent disruption through formation of hydrogen bond with amide; while self‐aggregated amide and hydrophobic alkyl group assisted formation of ice‐like network around them.

Construction of a subunit-fusion nitrile hydratase and discovery of an innovative metal ion transfer pattern.

Metallochaperones are metal-binding proteins designed to deliver the appropriate metal to a target protein. The metal is usually transferred between different proteins. In this study, we discovered that metal was transferred between the same subunit of a mutant nitrile hydratase (NHase). Various “activator proteins” mediate the trafficking of metal ions into NHases. We constructed fusion NHases by fusing the β- and α-subunits and/or the “activator proteins” of the NHase from Pseudomonas putida. The fusion NHases exhibited higher thermostability and tolerance to high concentrations of the product amide. The mechanism of the cobalt incorporation changed from a self-subunit swapping pattern to an apoprotein-specific molecular chaperone pattern in vivo and a metallochaperone pattern in vitro. Notably, the cobalt transfer occurred between the same α-subunit in the metallochaperone pattern. These results not only demonstrated the superiority of fusion-type NHases, but also revealed an innovative metal ion transfer pattern in metalloprotein biosynthesis.

Modelling of immobilised enzyme biocatalytic membrane reactor performance

Immobilised enzyme-catalysed conversions frequently provide specific advantages of selectivity over chemical conversions and further, facilitate continuous operation through biocatalyst retention and reuse. This study focuses on the development and modelling of an enzyme-catalysed continuous immobilised enzyme biocatalytic membrane reactor (BMR). The conversion of the amidase-catalysed lactamide to lactic acid process was used as an industrially representative system with which to evaluate the process performance of the BMR.The model was developed from unsteady state differential mass balances incorporating a second order enzyme decay. This model was validated from empirically determined conversions in dual experiments using 80 and 40mM amide substrate, 6.4 and 20.1mg immobilised amidase and a flow rate of 0.0005 and 0.0001L/min respectively.Model predictions over a range of amidase amounts and stabilities, flow rates and initial amide concentrations quantified the direction and extent of the influence of these parameters on the maximum conversions attainable, consequently identifying the critical parameter ranges defining optimal BMR performance. Although the model has been developed and validated for the prediction of BMR performance of the specific lactamide-lactic acid system, it nevertheless has broad applicability for and relevance to broad-based prediction of the performance of immobilised enzyme BMR processes in general, irrespective of the specific enzyme or substrate moieties.

Long-Spaced Polyamides: Elucidating the Gap between Polyethylene Crystallinity and Hydrogen Bonding

Aliphatic polyamides with so far inaccessibly low amide contents were prepared by acyclic diene metathesis (ADMET) copolymerization of N-(undec-10-en-1-yl)undec-10-enamide (1) and undeca-1,10-diene (2) applying different Grubbs and Hoveyda–Grubbs type olefin metathesis catalyst precursors, followed by exhaustive postpolymerization hydrogenation to yield saturated copolymers. These polyamides, containing between 1.0 and ca. 50.5 amide groups per 1000 methylene units, fill the gap between polyamides from classical polymerization approaches, like polycondensation of diamines with diacids, and linear polyethylene. With reduced amide concentrations the melting points of polyamides converge toward polyethylene, passing through a distinct melting point minimum observed around 110 °C for polyamides with ca. 35 amide groups per 1000 methylene units. The minimum goes in hand with a change in the crystal structure related to the different ratios of intersegment interactions from hydrogen bonding and nonpolar van der...

Assessment of the pharmacology and tolerability of PF‐04457845, an irreversible inhibitor of fatty acid amide hydrolase‐1, in healthy subjects

AIMS To evaluate the pharmacology and tolerability of PF-04457845, an orally available fatty acid amide hydrolase-1 (FAAH1) inhibitor, in healthy subjects. Double-blind, randomized, placebo-controlled single and multiple rising dose studies and an open-label, randomized, food effect study were conducted. Plasma and urine PF-04457845 concentrations, plasma fatty acid amide concentrations and FAAH1 activity in human leucocytes were measured. Tolerability, including effects on cognitive function, were assessed. PF-04457845 was rapidly absorbed (median t(max) 0.5-1.2 h). Exposure increased supraproportionally to dose from 0.1 to 10 mg and proportionally between 10 and 40 mg single doses. The pharmacokinetics appeared dose proportional following 14 days once daily dosing between 0.5 and 8 mg. Steady-state was achieved by day 7. Less than 0.1% of the dose was excreted in urine. Food had no effect on PF-04457845 pharmacokinetics. FAAH1 activity was almost completely inhibited (>97%) following doses of at least 0.3 mg (single dose) and 0.5 mg once daily (multiple dose) PF-04457845. Mean fatty acid amide concentrations increased (3.5- to 10-fold) to a plateau and then were maintained following PF-04457845. FAAH1 activity and fatty acid amide concentrations returned to baseline within 2 weeks following cessation of dosing at doses up to 4 mg. There was no evidence of effects of PF-04457845 on cognitive function. PF-04457845, at doses up to 40 mg single dose and 8 mg once daily for 14 days, was well tolerated. PF-04457845 was well tolerated at doses exceeding those required for maximal inhibition of FAAH1 activity and elevation of fatty acid amides.

Optical multichannel (optimul) platelet aggregometry in 96-well plates as an additional method of platelet reactivity testing

Platelet reactivity testing is important for the diagnosis of bleeding disorders, and increasingly to optimise anti-platelet therapy. Traditional light transmission aggregometry is considered the gold standard, whilst 96-well plate aggregometry, founded on similar principles, provides a higher throughput screening method. Despite the widespread use of both, methodologies and outputs vary widely between laboratories. We report a methodological approach towards providing a standardised optical detection of platelet aggregation (optimul method) based upon 96-well plate aggregometry. Individual wells of half-area 96-well plates were coated with gelatine and one of seven concentrations of arachidonic acid (AA), adenosine diphosphate (ADP), collagen, epinephrine (EPI), ristocetin, TRAP-6 amide or U46619, before being lyophilised, vacuum-sealed, foil-packed and stored at room temperature for up to 24 weeks. For platelet testing, 40 µl of platelet-rich plasma was added to each well. Platelet aggregation was determined by changes in light absorbance, release of ATP/ADP by luminescence and release of thromboxane (TX) A2 by ELISA. Some experiments were conducted in the presence of aspirin (30 µM) or prasugrel active metabolite (PAM; 3 µM). Optimul plates stored for up to 12 weeks permitted reliable detection of concentration-dependent platelet aggregation, ATP/ADP release and TXA2 production. PAM caused reductions in platelet responses to AA, ADP, collagen, EPI, TRAP-6 and U46619, whilst aspirin inhibited responses to AA, collagen and EPI. We conclude that the optimul method offers a viable, standardised approach, allowing platelet reactivity testing and could provide a broad platelet function analysis without the need for dedicated equipment.

12 Relationship between proportions of P2Y12 inhibited platelets and aggregation in vitro

Inhibition of platelet aggregation following aspirin ingestion is thought to be overcome by the presence of a small minority of uninhibited platelets. Indeed, it is often quoted that more than...

Aquatic toxicity assessment of single-walled carbon nanotubes using zebrafish embryos

Zebrafish embryos selected at the 64-cell stage were exposed to various concentrations of amide functionalized single-walled carbon nanotubes (SWCNTs) ranging from 1 to 10 μg/ml dissolved in 1% Pluronic F-68 (a cell culture grade surfactant), and the development of embryos was examined from 24 to 120 hours post fertilization (hpf). Incubation of embryos in 1% F-68 did not induce overt abnormal phenotype as compared to the wild-type; neither did it cause significant mortality during the exposure period. Generally, there was a slight developmental delay in larvae treated with SWCNTs of 5 μg/ml or above. Only larvae exposed to ≥ 5 μg/ml SWCNTs showed significantly reduced survival rates. About 50% of the embryos exposed to 5 μg/ml showed abnormal phenotypes at 24 hpf as compared to the control group. As development proceeds to 120 hpf, more embryos displayed defective morphology. A slight hatching delay was observed in embryos exposed to concentrations above 5 μg/ml. There was a general reduction of body axes, including narrowed somite and shortened yolk stalk. In addition, pigmentation in the ventral trunk area was less than that observed in control group. The body lengths of the exposed embryos were decreased significantly at 48 hpf (3.11 mm in control vs. 3.00 mm in SWCNTs-exposed embryos). However, exposure to SWCNTs did not affect the number of somites. Other features that were noticed in the SWCNTs-exposed embryos included edema and shrinkage and blebbling of the epidermal lining. Most of these observed phenotypes persisted from 48 hpf through 120 hpf. Overall, the aforementioned results indicate that soluble amide-functionalized SWCNTs are toxic to zebrafish embryos at a minimum concentration of 5 μg/ml.

Aqueous Humor Concentrations of Bimatoprost Free Acid, Bimatoprost and Travoprost Free Acid in Cataract Surgical Patients Administered Multiple Topical Ocular Doses of LUMIGAN®or TRAVATAN®

To quantify the aqueous humor (AH) concentrations of bimatoprost (amide), travoprost (isopropyl ester), and their hydrolysis products, bimatoprost free acid (BFA) and travoprost free acid (TFA), after multiple topical ocular doses of LUMIGAN and TRAVATAN, respectively, in patients awaiting cataract surgery. In 2 separate open-label, sparse-sampling trials, glaucoma patients with cataracts received LUMIGAN (bimatoprost ophthalmic solution, 0.03%) or TRAVATAN (travoprost ophthalmic solution, 0.004%) bilaterally once daily for at least 21 days prior to cataract surgery. Anterior chamber paracentesis was performed at selected times up to 5 h after the last dose and an AH sample was collected. AH samples were assayed by an independent bioanalytical laboratory using a sensitive and validated tandem LC-MS/MS method. The assay lower limits of quantitation were 0.59 nM for bimatoprost, 0.29 nM for BFA, and 0.44 nM for TFA. AH concentrations of BFA (17-phenyl-trinor PGF(2alpha)) were quantifiable in all but one sample at 0.5 h. The maximum concentration achieved (C(max)) of BFA was 30.9 + or - 16.41 nM (n =5), observed at 2 h postdose. AH concentrations of bimatoprost amide were lower than BFA at all time points, with a C(max) of 6.81 + or - 1.36 nM (n = 7) at 1 h postdose. For TFA, measurable AH concentrations were obtained at all time points with a TFA C(max) of 3.91 + or - 2.27 nM (n = 5), which was observed at 3 h after the dose (all data are mean + or - SEM). Once daily topical ocular administration of LUMIGAN or TRAVATAN for 3 weeks resulted in significant concentrations of BFA and TFA in the AH. Quantifiable levels of bimatoprost amide were also measured. Maximum concentrations of BFA (30.9 nM) and TFA (3.91 nM) in the anterior chamber are sufficient to fully activate the FP prostanoid receptors in the target cells of the ciliary muscle and trabecular meshwork. Both bimatoprost in LUMIGAN and travoprost in TRAVATAN are essentially prodrugs that are rapidly hydrolyzed to their respective free acids that induce the IOP-lowering effect observed with both drugs in vivo.

Thermochemical parameters of Ni(NO3)2 solutions in water + formamide + α-alanine mixtures at 298 K

The enthalpies of mixing of aqueous solutions of nickel(II) nitrate in water + formamide + α-alanine mixtures in the range of existing amide concentrations have been measured calorimetrically. From these data the standard enthalpies of electrolyte transfer from water into ternary mixtures have been calculated. The type and character of electrolyte transfer isotherms are discussed on the basis of the heats of transfer of individual ions that were studied earlier, as well as the contributions into these values that characterize structural changes in the solution and chemical ion-solvent interactions.

Enhancement of transdermal delivery of phenylbutazone from liposomal gel formulations through deer skin

Phenylbutazone (PBZ) is a nonsteroidal anti-inflammatory drug used in the treatment of chronic pain and arthritis. Topical and transdermal administration of PBZ would be beneficial in large animals in terms of minimizing gastro-intestinal ulcerations and other side effects, easy administration to legs and joints and minimizing the dose to reduce systemic toxicity of the drug. A topical liposomal preparation with different concentrations of a mono-substituted alkyl amide (MSA) and PBZ was formulated. The formulations were evaluated by in vitro skin-permeation kinetics through deer skin using Franz diffusion cells. By increasing drug loading from 1% to 5% w/w, the steady-state flux (microg/cm(2)/h) of PBZ was increased twofold (P < 0.001). Similarly, by increasing the MSA concentration from 0% to 4%, the steady-state flux (microg/cm(2)/h) of PBZ was increased twofold (P < 0.001). Overall, by increasing the drug load and the use of an appropriate amount of the penetration enhancer, the steady-state flux of PBZ through skin was increased fourfold (P < 0.001). MSA at both 2% and 4% w/w concentrations significantly increased the skin levels of PBZ as compared with control (P < 0.05). In conclusion, MSA served as an effective skin-penetration enhancer in the liposomal gel of PBZ for deer.

Thermodynamic Parameters of Solvation and Complexing of Copper(II) Nitrate and Nickel(II) Nitrate in Water + Acetamide Mixtures at 298.15 K

The heats of mixing of aqueous solutions of copper(II) or nickel(II) nitrate in water + acetamide (AA) mixtures in the existing range of amide concentrations have been studied. A rise in the amide concentration enhances solvation more strongly in copper(II) salt solutions. Data are analyzed with reference to previous results on the enthalpies of transfer of the salts studied in water + formamide (FA) and water + N,N-dimethylformamide (DMF) mixtures. Electronic absorbance spectra have been recorded at a fixed electrolyte concentration for all thermochemically studied systems, and a linear correlation has been found between the enthalpy of transfer of Cu(NO3)2 and the optical density of the solution. The enhanced solvation of copper(II) nitrate in aqueous acetamide is due to inner-sphere interactions between the cation and acetamide; that of nickel(II) nitrate is more due to outer-sphere interactions.

Drought-induced changes in free amino acid and ureide concentrations of nitrogen-fixing chickpea

The metabolic products of nitrogen (N) fixation in a legume can be amides or ureides. Chickpea (Cicer arientinum L.) is a cool-season legume which transports both ureides and amides from N fixation. Ureides are purine derivatives which are synthesized solely in the nodules. Drought-sensitive legumes accumulate ureides, but the regulation of these N fixation products during drought in chickpea is not yet known. The objectives of this study were (1) to measure the metabolic products of N fixation during drought and (2) to quantify the differences in N fixation among chickpea cultivars during drought by acetylene reduction activity under controlled environment conditions. Five chickpea cultivars were exposed to drought by soil dehydration. Plants were harvested at 1, 5, 10 and 15 d after drought and were analyzed for leaf and stem ureide concentrations and total N. In separate growth chamber experiments, N fixation was quantified daily. Leaf ureide and free amino acid concentrations were analyzed at 1, 5, and 15 d after drought. Drought increased ureide accumulation in drought-sensitive cultivars and decreased total N, alanine and asparagine concentrations over time. Drought-tolerant chickpea cultivars maintained ureide and amide concentrations during drought. Of the chickpea cultivars examined, Myles was the most drought tolerant and CDC Chico was the least. Further research on leaf ureides, alanine and asparagine concentrations would be valuable to determine if these metabolic products could serve as measures for screening chickpea germplasm for drought-tolerant N fixation. Key words: Ureides, N fixation, Asparagine, Acetylene reduction