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Nitric oxide synthase

Nitric oxide synthase (NOS) is a family of enzymes that catalyze the conversion of L-arginine to nitric oxide (NO) and L-citrulline, using oxygen and NADPH as cofactors, thereby producing the key signaling molecule NO involved in diverse physiological processes such as vasodilation, neurotransmission, and immune defense.^[1] In mammals, there are three principal isoforms: neuronal NOS (nNOS or NOS1), inducible NOS (iNOS or NOS2), and endothelial NOS (eNOS or NOS3), each encoded by distinct genes and exhibiting unique regulatory mechanisms and tissue distributions.^[2] The neuronal isoform (nNOS) is predominantly expressed in the central and peripheral nervous systems, where it generates low levels of NO to modulate synaptic plasticity, neurotransmitter release, and neuronal signaling, contributing to functions like learning, memory, and autonomic regulation.^[3] In contrast, endothelial NOS (eNOS) is mainly found in vascular endothelial cells and produces constitutive, low-output NO that promotes vasodilation, inhibits platelet aggregation, and prevents smooth muscle proliferation, thereby maintaining cardiovascular homeostasis.^[4] The inducible isoform (iNOS), expressed in immune cells such as macrophages upon stimulation by cytokines or microbial products, generates high levels of NO in a calcium-independent manner to mediate cytotoxicity against pathogens, regulate inflammation, and influence tumor biology, though excessive activity can contribute to tissue damage in chronic conditions.^[5] All NOS isoforms share a conserved structure consisting of an N-terminal oxygenase domain for substrate binding and catalysis, a central calmodulin-binding domain for regulation, and a C-terminal reductase domain that transfers electrons from NADPH via flavin cofactors, with dimerization essential for activity.^[6] Dysregulation of NOS expression or function has been implicated in numerous pathologies, including hypertension, neurodegeneration, sepsis, and cancer, making these enzymes important therapeutic targets.^[7]

Biochemical Properties

Chemical Reaction

Nitric oxide synthase (NOS) catalyzes the oxidation of L-arginine to L-citrulline and nitric oxide (NO), utilizing molecular oxygen (O₂) and NADPH as cosubstrates.^[8] This enzymatic process is a five-electron oxidation that requires precise coordination of electron transfer to ensure efficient NO production.^[9] The overall reaction follows a two-step mechanism. In the first step, L-arginine is hydroxylated at the N^ω-guanidino nitrogen to form N^ω-hydroxy-L-arginine (NOHA), consuming one equivalent of O₂ and 0.5 equivalents of NADPH, with the oxygenase domain activating O₂ via its heme iron center.^[9] The second step involves the oxidation of NOHA to L-citrulline and NO, incorporating another O₂ molecule and a full equivalent of NADPH, where the guanidino group of NOHA is cleaved to release NO and form the ureido group of L-citrulline.^[9] This biphasic process ensures the sequential incorporation of oxygen atoms from the two O₂ molecules into the products. The stoichiometrically balanced equation for the complete reaction is:

\text{L-arginine} + 2\, \text{O}_2 + 1.5\, \text{NADPH} + 1.5\, \text{H}^+ \rightarrow \text{L-citrulline} + \text{NO} + 1.5\, \text{NADP}^+ + 2\, \text{H}_2\text{O}

^[6] This reflects the consumption of two O₂ molecules and 1.5 NADPH per NO produced, highlighting the electron demands of the oxidation.^[6] NOS activity depends on several essential cofactors that facilitate electron transfer and substrate binding. The oxygenase domain binds heme (iron-protoporphyrin IX) as the site for O₂ activation and catalysis, while tetrahydrobiopterin (BH₄) serves as a redox-active cofactor that donates electrons to stabilize the reaction intermediates and prevent uncoupling.^[10] The reductase domain incorporates flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) for NADPH-dependent electron shuttling, and calmodulin binds to eukaryotic isoforms to link the domains and regulate activity in response to calcium signaling.^[9] Kinetic parameters underscore the enzyme's high affinity for substrates under physiological conditions. The Michaelis constant (K_m) for L-arginine ranges from approximately 2 to 10 μM across isoforms, ensuring efficient utilization even at low substrate concentrations. Similarly, the K_m for O₂ is about 8 μM for endothelial NOS, reflecting sensitivity to ambient oxygen levels.^[11] BH₄ maintains tight coupling between NADPH oxidation and NO formation; its depletion leads to uncoupling, where the enzyme produces superoxide (O₂⁻) instead of NO, diverting electrons and reducing catalytic efficiency.^[10]

Structure

Nitric oxide synthase (NOS) enzymes are homodimeric proteins with a total molecular mass of approximately 260–320 kDa, depending on the isoform, where each monomer comprises an N-terminal oxygenase domain and a C-terminal reductase domain connected by a flexible linker region.^[2] The oxygenase domain, located at the N-terminus, houses the catalytic site for nitric oxide (NO) production and includes binding sites for heme (iron protoporphyrin IX, axially ligated by a cysteine residue), L-arginine (the substrate), and tetrahydrobiopterin (BH₄, a essential cofactor).^[12] In certain isoforms, a zinc ion coordinates with cysteine residues at the dimer interface to enhance stability.^[13] The reductase domain, at the C-terminus, resembles the structure of cytochrome P450 reductase and contains flavin mononucleotide (FMN)- and flavin adenine dinucleotide (FAD)-binding subdomains, along with a site for the electron donor NADPH. Electrons flow from NADPH through FAD and FMN to the heme in the oxygenase domain, a process facilitated by conformational changes upon cofactor binding.^[14] The linker region between the domains features a calmodulin-binding motif that is crucial for inter-domain communication and electron transfer; calmodulin binding activates the enzyme by bridging the domains and enabling efficient flavin-to-heme electron shuttling. Dimerization occurs primarily through the oxygenase domains, involving an interface of intertwined β-sheets and, in some cases, the zinc tetrathiolate center formed by cysteines from each monomer.^[12] Crystal structures of NOS domains, resolved starting in the late 1990s, have elucidated these features; for example, the oxygenase domain of rat neuronal NOS (nNOS) was crystallized in complex with BH₄ and L-arginine (PDB: 1OM4), revealing the dimeric architecture and active site geometry.^[15] Similarly, structures of the human inducible NOS (iNOS) oxygenase domain (PDB: 1NSI) highlight the role of zinc in dimer stabilization.^[13] BH₄ deficiency disrupts proper electron pairing at the heme, leading to enzyme uncoupling where the reductase domain generates superoxide instead of transferring electrons for NO synthesis.^[16] Isoform-specific variations, such as an autoinhibitory insert in the FMN subdomain of nNOS, modulate domain interactions but preserve the overall homodimeric scaffold.

Mammalian Isoforms

Neuronal NOS (nNOS)

Neuronal nitric oxide synthase (nNOS), also known as NOS1, is encoded by the NOS1 gene located on human chromosome 12q24.22.^[17] The gene produces multiple splice variants through alternative splicing, with nNOSα serving as the primary full-length isoform responsible for most neuronal functions, while shorter variants such as nNOSβ and nNOSγ lack portions of the N-terminal regulatory region and exhibit altered subcellular localization and activity.^[18] A muscle-specific splice variant, nNOSμ, includes an additional 33-amino-acid insert in the spectrin-like repeat region, enhancing its association with the dystrophin complex.^[19] Structurally, nNOS exists as a ~160 kDa monomer that dimerizes via its oxygenase domain to form the active enzyme, comprising an N-terminal oxygenase domain for L-arginine and heme binding, a central calmodulin-binding site, and a C-terminal reductase domain containing FAD, FMN, and NADPH-binding motifs.^[20] The N-terminal PDZ domain facilitates protein-protein interactions, notably with postsynaptic density protein 95 (PSD-95) in neurons, anchoring nNOS to NMDA receptor complexes for localized signaling.^[21] Additionally, an autoinhibitory loop in the FMN module maintains low basal activity until relieved by calmodulin binding, ensuring tight regulation of NO production.^[22] nNOS is primarily expressed in central and peripheral neurons, where it localizes to postsynaptic densities and axonal varicosities, as well as in skeletal muscle via the nNOSμ variant associated with sarcolemmal membranes, and in testicular Leydig and germ cells to support spermatogenesis.^[21]^[23] As a constitutively expressed enzyme, nNOS activity is calcium/calmodulin-dependent, generating low basal levels of NO in the picomolar range under resting conditions to maintain tonic signaling without overwhelming cellular defenses.^[24]^[25] The enzyme was first identified in 1990 as a calmodulin-requiring activity enriched in rat brain, particularly cerebellum, marking the discovery of NO as a neuronal signaling molecule.^[26] Studies using nNOS knockout mice have revealed deficits in learning and memory, including impaired contextual fear conditioning and working memory tasks, underscoring its role in cognitive processes.^[27] In the nervous system, nNOS-derived NO promotes synaptic plasticity through retrograde signaling that enhances long-term potentiation in hippocampal and cerebellar circuits, while in the cerebellum, it mediates local vasodilation to couple neural activity with increased blood flow during sensory processing.^[28]^[29]

Inducible NOS (iNOS)

Inducible nitric oxide synthase (iNOS), also known as NOS2, is the isoform primarily responsible for high-level, sustained nitric oxide (NO) production in response to inflammatory stimuli. It is encoded by the NOS2 gene on human chromosome 17q11.2, which spans approximately 44 kb and consists of 27 exons.^[30] The enzyme exists as a homodimer with each monomer having a molecular weight of about 130 kDa, comprising an N-terminal oxygenase domain that binds heme, tetrahydrobiopterin (BH4), and L-arginine, and a C-terminal reductase domain containing FAD, FMN, and NADPH binding sites.^[6] Unlike neuronal NOS (nNOS) and endothelial NOS (eNOS), iNOS lacks autoinhibitory elements in its FMN-binding subdomain, which contributes to its constitutive activity once expressed.^[31] Expression of iNOS is tightly regulated at the transcriptional level and is inducible in various cell types, including macrophages, hepatocytes, and vascular smooth muscle cells, primarily by proinflammatory cytokines such as interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), and bacterial lipopolysaccharide (LPS).^[32] This induction involves activation of transcription factors like nuclear factor-kappa B (NF-κB) and signal transducer and activator of transcription 1 (STAT1), leading to de novo synthesis of iNOS mRNA and protein, with a delayed onset typically requiring 3-6 hours and peaking within 12-48 hours.^[33] Once induced, iNOS activity is calcium-independent due to its high-affinity binding to calmodulin, even at resting intracellular Ca2+ levels, enabling continuous electron transfer from NADPH to the heme center for NO synthesis.^[34] This results in high-output NO production, generating sustained micromolar concentrations (up to 1-5 μM in activated cells) compared to the nanomolar levels from constitutive isoforms.^[33] Structurally, iNOS forms a particularly stable dimer stabilized by intersubunit interactions at the oxygenase domain, including a zinc tetrathiolate center coordinated by cysteine residues, which is essential for maintaining enzymatic activity under inflammatory conditions.^[35] Notably, iNOS lacks the PDZ domain found in nNOS, which otherwise mediates protein-protein interactions for subcellular localization in neurons.^[3] The discovery of iNOS stemmed from studies on macrophage-mediated cytotoxicity in the late 1980s, with the first cDNA cloning achieved in 1992 from LPS- and IFN-γ-stimulated murine macrophages using monospecific antibodies against the purified enzyme.^[36] Its role in sepsis was confirmed in the 1990s through observations in animal models and human patients, where iNOS-derived NO contributes to refractory hypotension and vascular hyporeactivity during septic shock by excessive vasodilation and myocardial depression.^[37] In severe cases, this overproduction can lead to systemic hypotension, with mean arterial pressures dropping below 60 mmHg, exacerbating organ dysfunction.^[38]

Endothelial NOS (eNOS)

Endothelial nitric oxide synthase (eNOS), also known as NOS3, is encoded by the NOS3 gene located on the long arm of human chromosome 7 at position 7q36.1.^[39] This isoform was first identified in 1990 through purification and characterization of a constitutive NO-generating enzyme from bovine aortic endothelial cells.^[40] Molecular cloning in 1992 confirmed eNOS as a distinct isoform, revealing a protein sequence of 1205 amino acids with a predicted molecular mass of approximately 133 kDa as a monomer, though it functions primarily as a homodimer.^[41] Post-translational lipid modifications, including N-terminal myristoylation at glycine 2 and palmitoylation at cysteine residues 15 and 26, are essential for targeting eNOS to cellular membranes, particularly the plasma membrane and Golgi apparatus.^[42] These acylations enable eNOS localization to caveolae, where it interacts with caveolin-1 via a specific caveolin-binding motif (amino acids 339–355), leading to tonic inhibition of its activity under basal conditions.^[42] eNOS is constitutively expressed in endothelial cells lining blood vessels, as well as in platelets and cardiomyocytes, where it generates low levels of nitric oxide (NO) in a pulsatile manner synchronized with hemodynamic forces, typically in the picomolar range for localized signaling.^[43] Its enzymatic activity is calcium/calmodulin-dependent, requiring elevated intracellular Ca²⁺ to bind calmodulin and displace inhibitory factors like caveolin-1, thereby activating NO production from L-arginine.^[44] Unlike inducible isoforms, eNOS expression is generally constitutive but can be upregulated by shear stress from blood flow, which enhances transcription via shear-responsive elements in the NOS3 promoter.^[45] Genetic disruption of eNOS in mice (eNOS⁻/⁻) results in systemic hypertension, underscoring its critical role in vascular tone regulation, with systolic blood pressure elevated by approximately 20 mm Hg compared to wild-type controls.^[46] Regulation of eNOS involves multiple phosphorylation sites that modulate activity in response to vascular stimuli. For instance, phosphorylation at serine 1177 by Akt (protein kinase B) enhances electron flux through the enzyme's reductase domain, increasing NO output and decoupling it from caveolin-mediated inhibition.^[47] This site is particularly activated by agonists such as acetylcholine, which triggers Ca²⁺ influx and subsequent kinase signaling to stimulate eNOS-derived NO for endothelium-dependent vasodilation.^[48] Additionally, eNOS contributes to angiogenesis by promoting endothelial cell migration and proliferation in response to factors like vascular endothelial growth factor (VEGF), where NO acts as a downstream mediator to facilitate vessel formation.^[49] These features distinguish eNOS in vascular biology, emphasizing its integration with hemodynamic and agonist signals for precise NO signaling.

Function and Regulation

Physiological Roles

Nitric oxide (NO), produced by nitric oxide synthase (NOS), functions as a diffusible gaseous signaling molecule that readily crosses cell membranes to activate soluble guanylate cyclase (sGC) in target cells.^[50] This activation catalyzes the conversion of guanosine triphosphate (GTP) to cyclic guanosine monophosphate (cGMP), which in turn activates protein kinase G (PKG), modulating downstream physiological responses such as ion channel activity and protein phosphorylation.^[51] The NO/sGC/cGMP/PKG pathway is central to many non-adrenergic, non-cholinergic (NANC) signaling processes across tissues.^[52] In the vascular system, NO promotes vasodilation by inducing relaxation of vascular smooth muscle cells through the cGMP/PKG-mediated reduction of intracellular calcium levels and dephosphorylation of myosin light chains.^[53] This effect maintains basal vascular tone and facilitates blood flow regulation, with endothelial NOS (eNOS) primarily contributing to this constitutive activity.^[54] Additionally, NO inhibits platelet aggregation by elevating cGMP in platelets, thereby suppressing calcium mobilization and promoting vasodilation to prevent thrombus formation.^[55] In the nervous system, NO serves as a retrograde messenger in neurotransmission, particularly in the hippocampus where it facilitates long-term potentiation (LTP), a cellular correlate of learning and memory.^[56] During LTP induction, postsynaptic calcium influx activates neuronal NOS (nNOS), releasing NO that diffuses to presynaptic terminals to enhance neurotransmitter release via cGMP signaling.^[57] In immune responses, NO exerts cytotoxicity against pathogens, primarily through inducible NOS (iNOS) in macrophages, where it reacts with superoxide to form peroxynitrite (ONOO⁻), a potent oxidant that damages microbial proteins, lipids, and DNA.^[58] This mechanism contributes to antimicrobial defense during infections.^[59] Beyond these primary roles, NO regulates gastrointestinal motility by relaxing smooth muscle in the enteric nervous system, enabling peristalsis and preventing disorders like achalasia.^[60] It also mediates penile erection through corpus cavernosum smooth muscle relaxation, increasing blood inflow via the NO/cGMP pathway.^[61] Furthermore, NO modulates insulin secretion from pancreatic β-cells, where physiological levels enhance glucose-stimulated release, though high concentrations can inhibit it via cGMP-independent oxidative stress.^[62] A 2020 study in patients with major depressive episodes found lower baseline NOS activity, which increased after antidepressant treatment and predicted better treatment response, indicating a correlation between NOS activity and antidepressant responses in major depression.^[63]

Regulatory Mechanisms

The regulation of nitric oxide synthase (NOS) occurs at multiple levels, including transcriptional, post-transcriptional, post-translational, allosteric, genetic, and feedback mechanisms, ensuring precise control of nitric oxide (NO) production in response to physiological demands.^[3] At the transcriptional level, inducible NOS (iNOS, encoded by NOS2) is primarily regulated through activation of the nuclear factor kappa B (NF-κB) pathway in response to proinflammatory stimuli such as cytokines, leading to rapid induction of iNOS expression in immune cells.^[64] In contrast, endothelial NOS (eNOS, encoded by NOS3) transcription is upregulated by shear stress in vascular endothelial cells via specific shear stress response elements (SSREs) in its promoter, such as the GAGACC motif that binds NF-κB subunits p50 and p65.^[65] Post-transcriptional regulation fine-tunes NOS expression, particularly for iNOS, where AU-rich elements (AREs) in the 3'-untranslated region (3'-UTR) of NOS2 mRNA influence its stability; these elements typically promote rapid degradation but can be modulated by binding proteins to extend mRNA half-life during inflammation.^[66] Post-translational modifications provide dynamic control over NOS activity. For eNOS, phosphorylation at serine 1177 (Ser1177) by kinases such as Akt, protein kinase A (PKA), Ca²⁺/calmodulin-dependent kinase II (CaMKII), and AMP-activated protein kinase (AMPK) enhances electron transfer and NO synthesis, while phosphorylation at threonine 495 (Thr495) by protein kinase C (PKC) inhibits activity by blocking calmodulin binding. S-nitrosylation of cysteine residues in NOS isoforms modulates enzyme function, often serving as a feedback mechanism to limit NO overproduction. Additionally, the cofactor tetrahydrobiopterin (BH4) is crucial for maintaining NOS dimerization and coupled NO production; BH4 depletion leads to enzyme uncoupling, shifting output toward superoxide generation instead of NO. Allosteric regulation involves protein interactions that relieve autoinhibition. Calmodulin binding to NOS in a calcium-dependent manner (except for iNOS, which binds constitutively at low calcium levels) activates the enzyme by displacing the autoinhibitory pseudosubstrate domain in the FMN module. For eNOS, sequestration by caveolin-1 in caveolae membranes inhibits activity under basal conditions, but this is reversed by stimuli that promote calmodulin or heat shock protein 90 (Hsp90) binding to displace caveolin. Genetic variations influence NOS regulation and function. The NOS3 Glu298Asp polymorphism (rs1799983) in the coding region reduces eNOS efficiency and has been associated with increased risk of hypertension in meta-analyses of population studies.^[67] Promoter variants in NOS1, such as those affecting exon 1c or 1f usage, alter neuronal NOS (nNOS) transcriptional regulation and have been linked to variations in cognitive and emotional processing.^[68] Feedback regulation by NO itself provides negative autoregulation; NO binds to the heme iron in NOS, forming a nitrosyl-heme complex that inhibits oxygenase activity and prevents excessive NO production. Isoform-specific inducers, such as cytokines for iNOS, integrate these regulatory layers to tailor NO output to cellular contexts.^[64]

Inhibitors and Pharmacology

Types of Inhibitors

Nitric oxide synthase (NOS) inhibitors are diverse in their mechanisms and selectivity, targeting various domains of the enzyme to block nitric oxide (NO) production. Early inhibitors, such as N^G-monomethyl-L-arginine (L-NMMA), emerged in the late 1980s and were instrumental in elucidating the role of endogenous NO by competitively antagonizing NOS activity across isoforms. These compounds laid the foundation for subsequent developments in pharmacological blockade of NO biosynthesis. Substrate analogs represent a primary class of NOS inhibitors, mimicking the natural substrate L-arginine to competitively bind at the catalytic site and prevent NO formation. A prototypical example is NG-nitro-L-arginine methyl ester (L-NAME), which exhibits non-selective inhibition of neuronal NOS (nNOS), inducible NOS (iNOS), and endothelial NOS (eNOS) with high potency, typically in the micromolar range. Similarly, L-NMMA functions as a competitive inhibitor, though it shows slightly lower efficacy compared to L-NAME due to slower hydrolysis and time-dependent inactivation in some contexts. These analogs bind directly to the heme-containing oxygenase domain, blocking the transfer of electrons necessary for L-arginine oxidation. Cofactor-targeted inhibitors, particularly analogs of the essential pterin cofactor tetrahydrobiopterin (BH4), disrupt NOS function by interfering with BH4 binding and promoting enzyme uncoupling, where the enzyme produces superoxide instead of NO. For instance, 7,8-dihydroneopterin acts as a BH4 antagonist, competitively inhibiting cofactor association and thereby reducing NO output while enhancing reactive oxygen species generation. This uncompetitive mechanism highlights how BH4 analogs can indirectly modulate NOS activity, contrasting with direct substrate competition; notably, BH4 supplementation itself serves as an indirect strategy to recouple and restore proper NOS function in deficiency states. Flavoprotein inhibitors target the reductase domain of NOS, which contains flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) cofactors responsible for electron transfer from NADPH. Diphenyleneiodonium (DPI) exemplifies this class, irreversibly binding to the flavoprotein components and non-selectively inhibiting all NOS isoforms by halting electron flow to the oxygenase domain, with IC50 values around 30 nM in cellular models. Isoform-selective inhibitors have been developed to target specific NOS variants, minimizing off-target effects. For nNOS, 7-nitroindazole (7-NI) provides potent selectivity, with an IC50 of approximately 0.47 μM against nNOS while sparing iNOS and eNOS at higher concentrations. In contrast, 1400W (N-(3-(aminomethyl)benzyl)acetamidine) is highly selective for iNOS, acting as a slow, tight-binding competitive inhibitor with an IC50 of about 4 nM, and shows minimal activity against nNOS or eNOS. For eNOS, N^5-(1-iminoethyl)-L-ornithine (L-NIO) offers selectivity, functioning as an amidine-based competitive inhibitor with an IC50 of around 0.5 μM, though it can inactivate the enzyme via heme modification under certain conditions. Natural inhibitors, derived from dietary or plant sources, often exhibit milder, less selective effects on NOS. Flavonoids such as quercetin inhibit NO production primarily by suppressing iNOS induction in inflammatory contexts, with concentrations of 10-100 μM reducing nitrite formation in macrophage models. Arginine derivatives from natural origins, including modified guanidino compounds, similarly compete at the substrate site but with variable potency across isoforms. These compounds underscore the potential for isoform-specific modulation through polyphenol interference with signaling pathways upstream of NOS expression.

Clinical Applications

Dysfunction in endothelial nitric oxide synthase (eNOS) contributes to hypertension by impairing vasodilation and endothelial integrity, making eNOS enhancement a therapeutic target for cardiovascular conditions.^[69] Overactivity of neuronal nitric oxide synthase (nNOS) in neurodegenerative processes, such as excitotoxic damage during stroke, exacerbates neuronal injury through excessive nitric oxide production, prompting investigations into nNOS inhibition for neuroprotection.^[70] In inflammatory conditions like sepsis and rheumatoid arthritis, inducible nitric oxide synthase (iNOS) drives excessive nitric oxide-mediated inflammation and tissue damage, supporting the rationale for iNOS-selective inhibitors to mitigate cytokine storms and autoimmune responses.^[71]^[72] Therapeutic strategies targeting NOS isoforms include inhibitors in clinical development; for instance, the non-selective NOS inhibitor ronopterin (VAS203) reached phase III trials for traumatic brain injury in the 2010s, aiming to reduce nNOS-driven secondary brain damage, though it failed to meet primary endpoints in 2021.^[73] Selective iNOS inhibitors have been explored for rheumatoid arthritis, with preclinical evidence suggesting efficacy in reducing joint inflammation, but clinical translation remains limited due to challenges in isoform specificity.^[72] Recent updates include phase II trials of iNOS inhibitors combined with immunotherapy, such as the 2023 study of an iNOS inhibitor with alpelisib and nab-paclitaxel for chemorefractory breast cancer, to enhance antitumor immune responses by modulating the tumor microenvironment; preliminary results from 2025 indicate potential efficacy in improving outcomes for HER2-negative metaplastic breast cancer.^[74]^[75] A 2024 phase 1/2 trial of L-NMMA (an iNOS inhibitor) with taxane chemotherapy for chemoresistant triple-negative breast cancer further supports this approach.^[76] As alternatives to direct NOS modulation, nitric oxide donors and downstream enhancers like sildenafil treat erectile dysfunction by amplifying cyclic GMP signaling from endogenous nitric oxide produced by eNOS in penile tissue.^[77] Gene therapy approaches, such as NOS3 (eNOS) overexpression via viral vectors, have shown promise in preclinical models of cardiovascular disease, improving vascular function and reducing atherosclerosis in animal studies.^[78] Diagnostics leverage plasma nitrite levels as a biomarker of NOS activity, particularly reflecting endothelial dysfunction in conditions like hypertension and pulmonary arterial hypertension, where reduced nitrite correlates with impaired NO bioavailability.^[79]^[80] Post-2020 developments highlight nNOS inhibitors in preclinical pain models, demonstrating reduced neuropathic pain transmission in rodents, though human trials remain exploratory.^[81] Studies from 2021 linked iNOS upregulation to the cytokine storm in severe COVID-19, with elevated iNOS expression in lung epithelial cells contributing to hyperinflammation and suggesting potential for iNOS-targeted interventions in viral sepsis.^[82]^[83] As of 2025, emerging research explores selective iNOS inhibitors for pulmonary hypertension, showing promise in reducing right ventricular pressure in preclinical models.^[84]

Distribution Across Species

In Non-Mammalian Eukaryotes

In non-mammalian eukaryotes, nitric oxide synthase (NOS) activity exhibits significant diversity, often diverging from the canonical mammalian isoforms in structure, regulation, and function, reflecting adaptations to specific ecological and developmental needs. While true NOS enzymes with fused oxygenase and reductase domains are rare outside metazoans, NOS-like activities contribute to nitric oxide (NO) production for signaling in defense, growth, and stress responses. These systems highlight an ancient evolutionary origin for NO biosynthesis, predating the divergence of bilaterians, with sequence homologies to mammalian NOS typically around 40% in identified homologs.^[85] In plants, canonical NOS enzymes are absent, and NO is primarily generated through NOS-like pathways involving nitrate reductase (NR), which reduces nitrite to NO under hypoxic or stress conditions, alongside polyamine and hydroxylamine metabolism. For instance, in Arabidopsis thaliana, the protein formerly annotated as AtNOS1 (now redesignated AtNOA1) is a circularly permuted GTPase that indirectly modulates NO levels by influencing mitochondrial function and oxidative stress responses, rather than directly catalyzing L-arginine oxidation. Mutants lacking AtNOA1 display reduced NO production and heightened sensitivity to abiotic stresses such as drought and salt, as well as impaired pathogen defense, underscoring its role in hormonal signaling (e.g., abscisic acid-mediated stomatal closure) and developmental processes like flowering. Additionally, NR isoforms exhibit dual functionality, contributing to NO bursts during immune responses against pathogens, thereby linking nitrogen assimilation to defense signaling. NO concentrations in plants are generally lower than in mammals, often in the nanomolar range, facilitating localized signaling without widespread cytotoxicity.^[86]^[87]^[88] Fungi possess NOS homologs or activities that support morphogenesis and environmental adaptation, though these enzymes often lack the full reductase domain found in animals. In the model fungus Neurospora crassa, a ~100 kDa NOS-like protein has been implicated in hyphal growth and conidiation, where NO acts as a signaling molecule to regulate light-induced sporulation and development. Endogenous NO production in N. crassa, detectable via fluorescence probes, peaks during asexual reproduction and is sensitive to NOS inhibitors like N^G-monomethyl-L-arginine, suggesting enzymatic control akin to eukaryotic NOS. This activity promotes hyphal differentiation and stress tolerance, with NO levels modulated to influence gene expression networks for nutrient scavenging and pathogenesis. In other fungi, such as Phycomyces blakesleeanus, a calcium-independent NOS drives sporangiophore phototropism, illustrating conserved roles in sensory and developmental signaling across fungal lineages.^[89]^[90]^[91] Among invertebrate eukaryotes, NOS is more structurally conserved with mammalian forms, particularly in arthropods, where it supports neural and behavioral functions. In Drosophila melanogaster, the single NOS gene (dNOS) encodes a calcium/calmodulin-dependent enzyme homologous to neuronal NOS (nNOS), with approximately 45% sequence identity in the oxygenase domain and full retention of the reductase module. Expressed primarily in the central nervous system, dNOS generates NO for synaptic plasticity, learning, and memory consolidation, as mutants exhibit deficits in olfactory habituation and courtship behaviors. It also contributes to hypoxia responses and embryonic patterning, with NO diffusing to regulate cell proliferation and axon guidance. Compared to mammals, invertebrate NOS produces lower steady-state NO levels, emphasizing paracrine signaling over sustained vasodilation. Evolutionary analyses indicate that dNOS diverged from an ancestral bilaterian NOS prior to arthropod radiation, retaining core catalytic mechanisms while adapting to compact genomes.^[92]

In Prokaryotes

Nitric oxide synthase (NOS) in prokaryotes, often referred to as bacterial NOS (bNOS), is found in a limited number of bacterial species from specific phyla such as Firmicutes, Actinobacteria, and Deinococci, including Bacillus subtilis, Deinococcus radiodurans, and Staphylococcus aureus, representing a small portion of sequenced bacterial genomes based on genomic surveys. Unlike eukaryotic NOS, bNOS consists of a standalone oxygenase domain of approximately 45 kDa, lacking the reductase domain and calmodulin-binding linker present in mammalian isoforms. This domain binds heme and tetrahydrobiopterin (BH4) in a manner similar to eukaryotic NOS, facilitating the oxidation of L-arginine to nitric oxide (NO) and L-citrulline, but bNOS enzymes are typically monomeric or dimeric without the extensive interdomain linker. Crystal structures, such as that of B. subtilis NOS (PDB: 2FC2), reveal a conserved active site with a heme cofactor coordinated by a cysteine residue, highlighting structural adaptations for prokaryotic environments.^[93]^[94]^[95] The catalytic activity of bNOS relies on external electron donors rather than direct NADPH utilization via an internal reductase. Flavodoxin or ferredoxin, often in conjunction with NAD(P)H-dependent oxidoreductases, supply the necessary electrons for the two-step oxidation process, enabling NO production under aerobic conditions without dedicated reductase subunits. This modular electron transfer system underscores the evolutionary simplicity of bNOS compared to eukaryotic counterparts. Functions of bNOS-derived NO in prokaryotes include mediation of quorum sensing through nitrosylation of regulatory proteins, enhancement of antibiotic resistance by detoxifying reactive oxygen species generated during oxidative stress, promotion of biofilm formation for community protection, and direct cytoprotection against environmental stressors like UV radiation or hydrogen peroxide. In S. aureus, for instance, bNOS supports virulence by aiding nasal colonization and resistance to membrane-targeting antibiotics such as daptomycin, thereby contributing to pathogenesis in host environments.^[96]^[94]^[97] Homologs have also been identified in select archaea, such as the haloalkaliphilic Natronomonas pharaonis, where a bacterial-like NOS (npNOS) exhibits a similar oxygenase domain and contributes to adaptation to extreme environments.^[98] Evolutionarily, bNOS represents the oldest forms of NOS, likely emerging around 2.5 billion years ago during the Great Oxidation Event, when atmospheric oxygen levels rose and NO began serving roles in redox homeostasis. The distribution of NOS genes across distantly related bacteria suggests horizontal gene transfer as a key mechanism in their spread, allowing adaptation to oxidative niches; bNOS is considered a precursor to eukaryotic NOS, with the reductase domain acquired later through domain fusion in metazoan lineages.^[99]

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[11]
Nitric oxide and mitochondrial respiration in the heart
Oxygen is a substrate for all NO synthases with apparent. KM values of 4, 130 and 350 μM O2 for eNOS, iNOS and ... Nitric oxide synthase in porcine heart.
[12]
https://doi.org/10.1126/science.278.5337.425
[13]
https://doi.org/10.1038/6141
[14]
https://doi.org/10.1126/science.279.5359.2121
[15]
Regulation of Endothelial Nitric Oxide Synthase by ...
When BH4 is limiting, electron transfer from eNOS flavins becomes uncoupled from l-arginine oxidation, the ferrous-dioxygen complex dissociates, and superoxide ...
[16]
NOS1 Gene - Nitric Oxide Synthase 1 - GeneCards
Complete information for NOS1 gene (Protein Coding), Nitric Oxide Synthase 1, including: function, proteins, disorders, pathways, orthologs, and expression.<|separator|>
[17]
Transcription of human neuronal nitric oxide synthase mRNAs ...
The human neuronal nitric oxide synthase (NOS1) gene is subject to extensive splicing. A total of 12 NOS1 mRNA species have been identified.
[18]
Analysis of neuronal nitric oxide synthase isoform expression and ...
An nNOS splice variant form, nNOS-mu, was first reported to be specifically expressed in skeletal muscle and heart in the rat, but later also identified in rat ...Missing: central peripheral testes
[19]
Neuronal Nitric Oxide Synthase - IntechOpen
Post‐synaptic targeting of nNOS is directed by binding to PSD95 (Figure 3). nNOS–PSD95 is a typical PDZ–PDZ binding, which needs the intact tertiary structure ...
[20]
Neuronal Nitric Oxide Synthase - an overview | ScienceDirect Topics
nNOS contains a PDZ (PSD-95/discs large/ZO-1 homologous) ... Within the FMN binding domain, there is an autoinhibitory loop which controls nNOS activity.
[21]
Inducible Nitric Oxide Synthase: Regulation, Structure, and Inhibition
This review summarizes the structure, function, and regulation of iNOS, with focus on the development of iNOS inhibitors (historical and recent).
[22]
A Novel, Testis-specific mRNA Transcript Encoding an NH2-terminal ...
The downstream pro- moter of the human nNOS gene, which directs testis- specific expression of a novel NH2-terminal truncated nitric-oxide synthase, represents ...
[23]
Removal of a Putative Inhibitory Element Reduces the Calcium ...
Neuronal nitric-oxide synthase (NOS) and endothelial. NOS are constitutive NOS isoforms that are activated by binding calmodulin in response to elevated ...Missing: Ca2+ | Show results with:Ca2+
[24]
Neuronal Nitric Oxide Synthase Regulates Basal Microvascular ...
Apr 7, 2008 · Tonic NO generation by nNOS is important for regulation of basal vasomotor tone and may therefore influence blood pressure, whereas eNOS- ...
[25]
Isolation of nitric oxide synthetase, a calmodulin-requiring enzyme.
We show that nitric oxide synthetase activity requires calmodulin. Utilizing a 2',5'-ADP affinity column eluted with NADPH, we have purified nitric oxide ...
[26]
Working Memory Deficits in Neuronal Nitric Oxide Synthase ...
Here, we report that nNOS knockout (KO) mice exhibit hyperactivity and impairments in contextual fear conditioning, results consistent with previous reports.2.2. Behavioral Tests · 3.6. Nnos-Disc1 Interaction... · Fig. 4. Nnos-Disc1...
[27]
The role of nitric oxide in pre-synaptic plasticity and homeostasis
In this review we focus on the role of NO in synaptic plasticity and specifically its function as a retrograde messenger.
[28]
Nitric oxide is the predominant mediator of cerebellar hyperemia ...
Unlike in neocortex, in cerebellum the vasodilation depends almost exclusively on NO. The findings underscore the unique role of NO in the mechanisms of ...
[29]
4843 - Gene ResultNOS2 nitric oxide synthase 2 [ (human)] - NCBI
Aug 19, 2025 · NOS2 was confirmed to be expressed in both the glioma cell line and a human glioma primary culture, and overexpressed in relative derived ...
[30]
Insights into human eNOS, nNOS and iNOS structures ... - SciOpen
Nov 3, 2023 · Both Human nNOS and eNOS have auto-inhibitory elements which human iNOS lacks. Regulatory Calmodulin is shown by “CaM” near the CaM binding ...
[31]
Inducible nitric oxide synthase: An asset to neutrophils - Saini - 2019
Oct 4, 2018 · Like TNF-α, IL-1β and IFN-γ are known to induce iNOS activity in macrophages, fibroblasts, vascular smooth muscle (VSM) cells, and hepatocytes.
[32]
Inducible nitric oxide synthase (iNOS) - PubMed Central - NIH
Nitric oxide (NO) is a critical signaling molecule synthesized from L-arginine by nitric oxide synthase (NOS). The three NOS isoforms—neuronal NOS (nNOS; ...
[33]
Inducible Nitric Oxide Synthase Requires Both the Canonical ...
All three mammalian isoforms of nitric oxide synthase (NOS) must bind calmodulin (CaM) for enzymatic activity. Only NOS2 (the inducible isoform, iNOS) does ...
[34]
Subunit Interactions of Endothelial Nitric-oxide Synthase
Jan 10, 1997 · ... PDZ domain may also be involved in nNOS dimer formation. Alternatively, attachment of the PDZ domain to the nNOS oxygenase domain may alter ...<|control11|><|separator|>
[35]
Cloning and Characterization of Inducible Nitric Oxide Synthase ...
A monospecific antibody was used to clone complementary DNA that encoded two isoforms of NO synthase from immunologically activated mouse macrophages. Liquid ...
[36]
The role of nitric oxide in sepsis--an overview - PubMed
A hyperproduction of NO by the inducible form of NO synthase (iNOS) may contribute to the hypotension, cardiodepression and vascular hyporeactivity in septic ...
[37]
Effects of Nitric Oxide in Septic Shock - ATS Journals
Dec 2, 1998 · Nitric oxide (NO) is believed to play a key role in the pathogenesis of septic shock, although many aspects of NO's involvement remain poorly defined.
[38]
4846 - Gene ResultNOS3 nitric oxide synthase 3 [ (human)] - NCBI
Sep 5, 2025 · NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients. Endothelial nitric oxide ...<|control11|><|separator|>
[39]
Endothelial nitric oxide generating enzyme(s) in the bovine aorta
Endothelial nitric oxide generating enzyme(s) in the bovine aorta: subcellular location and metabolic characterization. J Pharmacol Exp Ther. 1990 Apr;253(1):20 ...Missing: synthase discovery paper
[40]
Endothelial nitric oxide synthase: molecular cloning and ... - PNAS
A full-length NO synthase cDNA clone was isolated, representing a protein of 1205 amino acids with a molecular mass of 133 kDa.
[41]
Targeting of nitric oxide synthase to endothelial cell caveolae via ...
eNOS, but not the palmitoylation mutant form of the enzyme, colocalizes with caveolin on the cell surface in transfected NIH. 3T3 cells, demonstrating that ...
[42]
Cell-Based Indicator to Visualize Picomolar Dynamics of Nitric Oxide ...
We report a novel cell-based indicator that is able to visualize picomolar dynamics of nitric oxide release from living cells.
[43]
Signal transduction of eNOS activation - PubMed
Consistent with its classification as a Ca2+/calmodulin-dependent enzyme the constitutive endothelial nitric oxide (NO) synthase (eNOS) can be activated by ...Missing: pulsatile picomolar
[44]
Nitric Oxide Synthase Expression in Endothelial Cells Exposed to ...
Expression of eNOS mRNA was increased and promoter activity was enhanced by unidirectional shear stress compared with static control. Oscillatory shear slightly ...
[45]
Elevated blood pressures in mice lacking endothelial nitric ... - PNAS
To specifically study the role of NO produced by eNOS in blood pressure regulation, we have generated mice that lack a functional endothelial nitric oxide gene ...Missing: paper | Show results with:paper
[46]
The Akt kinase signals directly to endothelial nitric oxide synthase
We foun that purified Akt phosphorylated cardiac eNOS at Ser1177, resulting in activation of eNOS. Phosphorylation at this site was stimulated by treatment of ...
[47]
Nitric oxide synthases: regulation and function - Oxford Academic
Endothelial NOS (eNOS, NOS III) is mostly expressed in endothelial cells. It keeps blood vessels dilated, controls blood pressure, and has numerous other ...Nitric Oxide Synthases... · Mechanisms Of Nitric Oxide... · Endothelial Nitric Oxide...<|control11|><|separator|>
[48]
Role of Endothelial Nitric Oxide Synthase in Endothelial Cell Migration
Bovine aortic endothelial cells (BAECs) were isolated after collagenase digestion of the intimal layer of the thoracic aorta. Cells were grown in minimal ...Missing: paper | Show results with:paper
[49]
Nitric oxide synthases: regulation and function - PubMed - NIH
Sep 1, 2011 · Its functions include synaptic plasticity in the central nervous system (CNS), central regulation of blood pressure, smooth muscle relaxation, ...
[50]
Nitric oxide signaling in health and disease - ScienceDirect.com
Aug 4, 2022 · Nitric oxide activates guanylate cyclase and increases guanosine 3′:5′-cyclic monophosphate levels in various tissue preparations. Proc. Natl ...
[51]
Cyclic GMP and PKG Signaling in Heart Failure - Frontiers
Apr 10, 2022 · cGMP/PKG signal is activated by two intrinsic pathways: nitric oxide (NO)-soluble GC and natriuretic peptide (NP)-particulate GC (pGC) pathways.
[52]
Nitric oxide and regulation of vascular tone - PubMed
Acting by this pathway, nitric oxide induces relaxation of vascular smooth muscle and inhibits platelet activation and aggregation.
[53]
Nitric Oxide-cGMP Signaling in Hypertension
Aug 24, 2020 · NO-bound sGC produces cGMP, a key regulator of vascular tone. The rise in intracellular cGMP in VSMCs triggers activation of PKG (protein kinase ...
[54]
Nitric Oxide Insufficiency, Platelet Activation, and Arterial Thrombosis
Akin to its effects in vascular smooth muscle cells, nitroglycerin also inhibits platelet aggregation by activating guanylyl cyclase, and this inhibitory action ...
[55]
On the Role of Nitric Oxide in Hippocampal Long-Term Potentiation
Nitric oxide (NO) functions in several types of synaptic plasticity, including hippocampal long-term potentiation (LTP), in which it may serve as a retrograde ...
[56]
A Requirement for the Intercellular Messenger Nitric Oxide in Long ...
These findings suggest that nitric oxide liberated from postsynaptic neurons may travel back to presynaptic terminals to cause LTP expression.
[57]
Nitric Oxide and Peroxynitrite in Health and Disease - PMC
Recent evidence indicates that most of the cytotoxicity attributed to NO is rather due to peroxynitrite, produced from the diffusion-controlled reaction between ...
[58]
Peroxynitrite generated by inducible nitric oxide synthase ... - PNAS
Blocking peroxynitrite formation with nitric oxide synthase inhibitors, superoxide dismutase mimics, or a decomposition catalyst abrogated the cytotoxicity.
[59]
Nitric Oxide: From Gastric Motility to Gastric Dysmotility - PMC
Sep 16, 2021 · It is known that nitric oxide (NO) plays a key physiological role in the control of gastrointestinal (GI) motor phenomena.
[60]
The role of nitric oxide in penile erection - PubMed
This review examines the role of NO in the penis in detail. Established and new treatments for erectile dysfunction whose effects are mediated via manipulation ...
[61]
Role of Nitric Oxide in Insulin Secretion and Glucose Metabolism
Nitric oxide (NO) contributes to carbohydrate metabolism and decreased NO bioavailability is involved in the development of type 2 diabetes mellitus (T2DM).
[62]
Pharmacological evaluation of NO/cGMP/KATP channels pathway in ...
Feb 1, 2021 · In the present study, the involvement of NO/cyclic GMP/KATP channels pathway in the antidepressant action of carbamazepine was investigated in ...Missing: major | Show results with:major<|control11|><|separator|>
[63]
https://pubmed.ncbi.nlm.nih.gov/32524920/
[64]
Shear Stress Regulates Endothelial Nitric-oxide Synthase Promoter ...
We have previously demonstrated that shear stress increases transcription of the endothelial nitric-oxide synthase (eNOS) by a pathway involving activation ...
[65]
Similar Regulation of Human Inducible Nitric-oxide Synthase ...
AU-rich elements (ARE) are well characterized cis-acting elements involved in the regulation of mRNA stability (4, 5, 6, 7). They are often located in the ...
[66]
Endothelial Nitric Oxide Synthase Gene Polymorphisms and ...
Abstract. This review examines the association of a subset of endothelial nitric oxide synthase gene (NOS3) polymorphisms (Glu298Asp, intron 4, and -786T&g.Missing: seminal | Show results with:seminal
[67]
A NOS1 variant implicated in cognitive performance influences ...
NOS1 is characterized by complex transcriptional regulation. We previously investigated whether the cognitive effects of this NOS1 variant could be ...
[68]
Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as ...
Oct 10, 2022 · Association of rare variants in the nitric oxide synthase 3 (NOS3) gene and risk of coronary artery disease and hypertension. Panel (A) is a ...Missing: preclinical | Show results with:preclinical
[69]
Role of Nitric Oxide in Neurodegeneration: Function, Regulation ...
Elevated production of higher amounts of nitric oxide (NO) takes place in numerous pathological conditions, such as neurodegenerative diseases, inflammation, ...Missing: applications sepsis
[70]
Inducible Nitric Oxide Synthase and Inflammatory Diseases
May 1, 2000 · This work focuses on the complex role of NO produced by the inducible form of nitric oxide synthase (iNOS) in inflammatory and autoimmune diseases.
[71]
[PDF] Nitric Oxide Synthase Inhibitors into the Clinic at Last
Jan 1, 2021 · Its structure has important features, including (1) an autoinhibitory loop within the FMN binding domain where CaM can be removed in the absence ...
[72]
Vasopharm's ronopterin fails in traumatic brain injury trial
Jun 4, 2021 · vasopharm has reported that its Phase III trial of ronopterin (VAS203) failed to meet the pre-specified primary goal in traumatic brain injury (TBI) patients.Missing: rheumatoid arthritis inhibitor
[73]
https://www.clinicaltrialsarena.com/news/vasopharm-ronopterin-fails-trial/
[74]
Targeting iNOS to increase efficacy of immunotherapies - PMC - NIH
In addition to PDAC, multiple studies point to that inhibiting iNOS could increase efficacy of immunotherapy of other cancers as well.Missing: 2023 | Show results with:2023<|separator|>
[75]
The Role of Nitric Oxide in Erectile Dysfunction - PubMed Central - NIH
NO promotes penile vasodilation and blood flow by diffusing across the smooth muscle membrane and activating sGC to produce cGMP, resulting in an enzymatic ...Missing: gastrointestinal motility insulin
[76]
Nitric Oxide Synthase Gene Therapy for Cardiovascular Disease
This review will discuss the rationale of NOS gene therapy in different cardiovascular disease settings and summarize the results of experimental NOS gene ...Missing: preclinical | Show results with:preclinical
[77]
Plasma nitrite/nitrate levels: a new biomarker for pulmonary arterial ...
Circulating nitrite/nitrate (NOx) levels not only reflect the level of NO synthesis but also act as a reservoir of alternative substrate for NO synthesis. NO ...
[78]
Association of plasma nitrite levels with obesity and metabolic ...
Jun 20, 2018 · Plasma nitrite is a metabolite of nitric oxide and reflects endogenous nitric oxide synthase (NOS) activity. Although plasma nitrites were ...
[79]
Effects of selective inhibition of nNOS and iNOS on neuropathic pain ...
Our study innovatively shows that nNOS may strongly modulate nociceptive transmission in rats with neuropathic pain.Missing: management clinical trials
[80]
Cytokine-Induced iNOS in A549 Alveolar Epithelial Cells - MDPI
Oct 3, 2023 · An association has been widely demonstrated in COVID-19 between the presence of the so-called cytokine storm and disease severity, with a strong ...
[81]
Inducible Nitric Oxide Synthase (iNOS): Why a Different Production ...
Mar 4, 2022 · We previously studied 35 hospitalized COVID-19 patients of the 1st wave demonstrating a cytokine storm and the exhaustion of most lymphocyte ...
[82]
Molecular evolution of nitric oxide synthases in metazoans - PubMed
Nitric oxide synthases (NOS), the enzymes responsible for the NO synthesis, are present in all eukaryotes. Three isoforms (neuronal, inducible and ...
[83]
AtNOS/AtNOA1 Is a Functional Arabidopsis thaliana cGTPase and ...
AtNOS1 was previously identified as a potential nitric-oxide synthase (NOS) in Arabidopsis thaliana, despite lack of sequence similarity to animal NOSs.
[84]
A new role for an old enzyme: Nitrate reductase-mediated ... - PNAS
In this article, we provide genetic evidence that NR-mediated NO synthesis is required for ABA-induced stomatal closure in Arabidopsis.
[85]
Nitric Oxide Synthase-Dependent Nitric Oxide Production Is ...
These findings provide direct evidence to support that disruption of NOS-dependent NO production is associated with salt tolerance in Arabidopsis.
[86]
Indications for the occurrence of nitric oxide synthases in fungi and ...
An exogenous nitic oxide donor, sodium nitroprusside, inhibited light-stimulated conidiation in N. crassa. Specific inhibitors of nitric oxide synthase, like ...
[87]
Identification and functional analysis of endogenous nitric oxide in a ...
Jul 18, 2016 · We present here our observations on production of intracellular NO and its possible roles during development of Neurospora crassa, a model filamentous fungus.
[88]
Role of Nitric Oxide Synthase in the Light-Induced ... - NIH
We suggest that a fungal NO synthase is involved in sporangiophore development and propose its participation in light signaling. Nitric oxide synthases (NOS) ...
[89]
The Drosophila nitric-oxide synthase gene (dNOS) encodes a family ...
Nov 9, 2001 · Nitric oxide (NO) is involved in organ development, synaptogenesis, and response to hypoxia in Drosophila. We cloned and analyzed the only ...
[90]
Structural and biological studies on bacterial nitric oxide synthase ...
Nitric oxide (NO) produced by bacterial nitric oxide synthase has recently been shown to protect the Gram-positive pathogens Bacillus anthracis and ...Missing: prevalence | Show results with:prevalence
[91]
[PDF] Nitric Oxide Synthases of Bacteria – and Other Unicellular Organisms
Feb 6, 2011 · Crystal structure of sanos a bacterial nitric oxide synthase oxygenase protein from staphylococcus aureus. Structure, 2002, 10, 1687-1696. [16].
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https://pubmed.ncbi.nlm.nih.gov/11526108/
[93]
An Essential Role for Bacterial Nitric Oxide Synthase in ...
This process is essential for staphylococcal nasal colonisation and resistance to the membrane-targeting antibiotic daptomycin.Missing: prevalence | Show results with:prevalence
[94]
The Evolution of Nitric Oxide Function: From Reactivity in the ...
Jun 22, 2022 · In an evolutionary context, it is reasonable to think that, in higher eukaryotes, mNOS evolved from simpler single-domain bacterial homologs, ...