How Biology Handles Nitrite

Generation of Nitric Oxide by a Nitrite Reductase Activity of Xanthine Oxidase: A Potential Pathway for Nitric Oxide Formation in the Absence of Nitric Oxide Synthase Activity

Zhang, Z., Naughton, D., Winyard, P. G., Benjamin, N., Blake, D. R., & Symons, M. C. R. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9226 · Cited by 246

Reaction of nitric oxide with heme proteins and model compounds of hemoglobin

Sharma, V. S., Traylor, T. G., Gardiner, R., & Mizukami, H. (1987) · Biochemistry · doi:10.1021/bi00387a015 · Cited by 245

Determination of the mechanism of free radical generation in human aortic endothelial cells exposed to anoxia and reoxygenation.

Zweier, J. L., Broderick, R., Kuppusamy, P., Thompson-Gorman, S. L., & Lutty, G. A. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)51062-6 · Cited by 244

Ferredoxin-dependent chloroplast enzymes

Knaff, D. B., & Hirasawa, M. (1991) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(05)80277-4 · Cited by 244

What is the function of neuroglobin?

Burmester, T., & Hankeln, T. (2009) · Journal of Experimental Biology · doi:10.1242/jeb.000729 · Cited by 244

Reactive oxygen species, antioxidant systems and nitric oxide in peroxisomes

del Río, L. A., Corpas, F. J., Sandalio, L. M., et al. (2002) · Journal of Experimental Botany · doi:10.1093/jxb/53.372.1255 · Cited by 244

A structure-based catalytic mechanism for the xanthine oxidase family of molybdenum enzymes

Huber, R., Hof, P., Duarte, R. O., Moura, J. J., Moura, I., Liu, M. Y., LeGall, J., Hille, R., Archer, M., & Romão, M. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.17.8846 · Cited by 242

Formation and possible roles of nitric oxide in plant roots

Stöhr, C., & Stremlau, S. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/erj058 · Cited by 242

Nitric Oxide Production Mediated by Nitrate Reductase in the Green Alga Chlamydomonas reinhardtii: an Alternative NO Production Pathway in Photosynthetic Organisms

Sakihama, Y., Nakamura, S., & Yamasaki, H. (2002) · Plant and Cell Physiology · doi:10.1093/pcp/pcf034 · Cited by 242

Prebiotic ammonia from reduction of nitrite by iron (II) on the early Earth

Summers, D. P., & Chang, S. (1993) · Nature · doi:10.1038/365630a0 · Cited by 241

Photosynthetic nitrate assimilation in cyanobacteria

Flores, E., Frías, J. E., Rubio, L. M., & Antonia Herrero, B. (2005) · Photosynthesis Research · doi:10.1007/s11120-004-5830-9 · Cited by 241

Before and beyond ABA: upstream sensing and internal signals that determine ABA accumulation and response under abiotic stress

Verslues, P. E., & Zhu, J. (2005) · Biochemical Society Transactions · doi:10.1042/bst0330375 · Cited by 241

Nitric oxide as a modulator of apoptosis

Li, C., & Wogan, G. N. (2004) · Cancer Letters · doi:10.1016/j.canlet.2004.10.021 · Cited by 239

Antimicrobial effect of acidified nitrite on gut pathogens: importance of dietary nitrate in host defense

Dykhuizen, R. S., Frazer, R., Duncan, C., Smith, C. C., Golden, M., Benjamin, N., & Leifert, C. (1996) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.40.6.1422 · Cited by 239

The 2.8 Å structure of hydroxylamine oxidoreductase from a nitrifying chemoautotrophic bacterium, Nitrosomonas europaea

Igarashi, N., Moriyama, H., Fujiwara, T., Fukumori, Y., & Tanaka, N. (1997) · Nature Structural Biology · doi:10.1038/nsb0497-276 · Cited by 238

Xanthine oxidoreductase-catalyzed reactive species generation: A process in critical need of reevaluation

Cantu-Medellin, N., & Kelley, E. E. (2013) · Redox Biology · doi:10.1016/j.redox.2013.05.002 · Cited by 237

Tissue-Specific Localization of an Abscisic Acid Biosynthetic Enzyme, AAO3, in Arabidopsis

Koiwai, H., Nakaminami, K., Seo, M., Mitsuhashi, W., Toyomasu, T., & Koshiba, T. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.036970 · Cited by 236

Gastroprotective and blood pressure lowering effects of dietary nitrate are abolished by an antiseptic mouthwash

Petersson, J., Carlström, M., Schreiber, O., Phillipson, M., Christoffersson, G., Jägare, A., Roos, S., Jansson, E. Å., Persson, A. E. G., Lundberg, J. O., et al. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.01.011 · Cited by 235

Extensive tyrosine nitration in human myocardial inflammation

Kooy, N. W., Lewis, S. J., Royall, J. A., Ye, Y. Z., Kelly, D. R., & Beckman, J. S. (1997) · Critical Care Medicine · doi:10.1097/00003246-199705000-00017 · Cited by 235

Nitrite–dependent nitric oxide production pathway: implications for involvement of active nitrogen species in photoinhibition in vivo

Yamasaki, H. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0708 · Cited by 235

An S -nitrosothiol (SNO) synthase function of hemoglobin that utilizes nitrite as a substrate

Angelo, M., Singel, D. J., & Stamler, J. S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600942103 · Cited by 233

Nitric oxide inhibition of respiration involves both competitive (heme) and noncompetitive (copper) binding to cytochrome c oxidase

Mason, M. G., Nicholls, P., Wilson, M. T., & Cooper, C. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506562103 · Cited by 233

Nitrifier genomics and evolution of the nitrogen cycle

Klotz, M. G., & Stein, L. Y. (2007) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2007.00970.x · Cited by 232

Human Neuroglobin, a Hexacoordinate Hemoglobin That Reversibly Binds Oxygen

Trent, J. T., Watts, R. A., & Hargrove, M. S. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.c100300200 · Cited by 231

The Structure of Copper-nitrite Reductase from Achromobacter cycloclastes at Five pH Values, with NO-2 Bound and with Type II Copper Depleted

Adman, E. T., Godden, J., & Turley, S. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.46.27458 · Cited by 230

Nitrosation Reactions and the Chemistry of Nitric Oxide

(2004) · Elsevier eBooks · doi:10.1016/b978-0-444-51721-0.x5000-2 · Cited by 229

Substrate Control of Free Radical Generation from Xanthine Oxidase in the Postischemic Heart

Xia, Y., & Zweier, J. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.32.18797 · Cited by 229

AraPerox. A Database of Putative Arabidopsis Proteins from Plant Peroxisomes

Reumann, S., Ma, C., Lemke, S., & Babujee, L. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.043695 · Cited by 229

Nitrite as the major source of nitric oxide production by Arabidopsis thaliana in response to Pseudomonas syringae

Modolo, L. V., Augusto, O., Almeida, I. M. G., Magalhaes, J. R., & Salgado, I. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.078 · Cited by 229

Nitrogen assimilation and growth of wheat under elevated carbon dioxide

Bloom, A. J., Smart, D. R., Nguyen, D. T., & Searles, P. S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022627299 · Cited by 229

A novel two‐over‐two α‐helical sandwich fold is characteristic of the truncated hemoglobin family

Pesce, A., Couture, M., Dewilde, S., Guertin, M., Yamauchi, K., Ascenzi, P., Moens, L., & Bolognesi, M. (2000) · The EMBO Journal · doi:10.1093/emboj/19.11.2424 · Cited by 228

Lysosomal release of Cathepsin D precedes relocation of Cytochrome C and loss of mitochondrial transmembrane potential during apoptosis induced by oxidative stress

Roberg, K. B., Johansson, U., & Öllinger, K. M. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(99)00146-x · Cited by 227

Redox signaling in cardiovascular health and disease

Madamanchi, N. R., & Runge, M. S. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.04.001 · Cited by 227

Natural Senescence of Pea Leaves (An Activated Oxygen-Mediated Function for Peroxisomes)

Pastori, G. M., & del Río, L. A. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.113.2.411 · Cited by 227

Nitrite-Derived Nitric Oxide Protects the Rat Kidney against Ischemia/Reperfusion Injury In Vivo: Role for Xanthine Oxidoreductase

Tripatara, P., Patel, N. S. A., Webb, A., Rathod, K., Lecomte, F. M. J., Mazzon, E., Cuzzocrea, S., Yaqoob, M. M., Ahluwalia, A., & Thiemermann, C. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006050450 · Cited by 226

Catalytic generation of N2O3 by the concerted nitrite reductase and anhydrase activity of hemoglobin

Basu, S., Grubina, R., Huang, J., Conradie, J., Huang, Z., Jeffers, A., Jiang, A., He, X., Azarov, I., Seibert, R., et al. (2007) · Nature Chemical Biology · doi:10.1038/nchembio.2007.46 · Cited by 224

Oxygen sensors in context

Ward, J. P. T. (2007) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2007.10.010 · Cited by 224

Endogenous S -nitrosothiols protect against myocardial injury

Lima, B., Lam, G. K. W., Xie, L., Diesen, D. L., Villamizar, N. R., Nienaber, J. J., Messina, E., Bowles, D. E., Kontos, C. D., Hare, J. M., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901043106 · Cited by 223

Indications for the Occurrence of Nitric Oxide Synthases in Fungi and Plants and the Involvement in Photoconidiation of Neurospora crassa*

Ninnemann, H., & Maier, J. (1996) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1996.tb02477.x · Cited by 223

Nitric Oxide Induces Phytoalexin Accumulation in Potato Tuber Tissues

Noritake, T., Kawakita, K., & Noriyuki Doke, A. (1996) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a028908 · Cited by 223

Cytoglobin is a respiratory protein in connective tissue and neurons, which is up-regulated by hypoxia

Schmidt, M., Gerlach, F., Avivi, A., Laufs, T., Wystub, S., Simpson, J. C., Nevo, E., Saaler-Reinhardt, S., Reuss, S., Hankeln, T., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m310540200 · Cited by 222

Absorption spectra and reaction kinetics of NO2, N2O3, and N2O4 in aqueous solution

Treinin, A., & Hayon, E. (1970) · Journal of the American Chemical Society · doi:10.1021/ja00723a001 · Cited by 221

Plant Haemoglobins, Nitric Oxide and Hypoxic Stress

Dordas, C. A. (2003) · Annals of Botany · doi:10.1093/aob/mcf115 · Cited by 221

Erythrocytes Possess an Intrinsic Barrier to Nitric Oxide Consumption

Vaughn, M. W., Huang, K., Kuo, L., & Liao, J. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.4.2342 · Cited by 220

Mechanism of Reaction of Myeloperoxidase with Nitrite

Burner, U., Furtmüller, P. G., Kettle, A. J., Koppenol, W. H., & Obinger, C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m000181200 · Cited by 220

Architecture of NarGH Reveals a Structural Classification of Mo-bisMGD Enzymes

Jormakka, M., Richardson, D. J., Byrne, B., & Iwata, S. (2004) · Structure · doi:10.1016/j.str.2003.11.020 · Cited by 219

Studies on the Reaction Mechanism for Reductive Nitrosylation of Ferrihemoproteins in Buffer Solutions

Hoshino, M., Maeda, M., Konishi, R., Seki, H., & Ford, P. C. (1996) · Journal of the American Chemical Society · doi:10.1021/ja953311w · Cited by 219

Nitrite supplementation reverses vascular endothelial dysfunction and large elastic artery stiffness with aging: Sodium nitrite and vascular dysfunction with aging

Sindler, A. L., Fleenor, B. S., Calvert, J. W., Marshall, K. D., Zigler, M. L., Lefer, D. J., & Seals, D. R. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00679.x · Cited by 218

Tissue Processing of Nitrite in Hypoxia

Feelisch, M., Fernandez, B. O., Bryan, N. S., Garcia-Saura, M. F., Bauer, S., Whitlock, D. R., Ford, P. C., Janero, D. R., Rodriguez, J., & Ashrafian, H. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m806654200 · Cited by 218

Nitric oxide moves myoglobin centre stage

Brunori, M. (2001) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(01)01824-2 · Cited by 218

N2O binding at a [4Cu:2S] copper–sulphur cluster in nitrous oxide reductase

Pomowski, A., Zumft, W. G., Kroneck, P. M. H., & Einsle, O. (2011) · Nature · doi:10.1038/nature10332 · Cited by 217

Cultivation of a novel cold-adapted nitrite oxidizing betaproteobacterium from the Siberian Arctic

Alawi, M., Lipski, A., Sanders, T., Pfeiffer, E., & Spieck, E. (2007) · The ISME Journal · doi:10.1038/ismej.2007.34 · Cited by 217

Nitrate Assimilation by Bacteria

Lin, J. T., & Stewart, V. J. (1997) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/s0065-2911(08)60014-4 · Cited by 216

Nitric oxide is consumed, rather than conserved, by reaction with oxyhemoglobin under physiological conditions

Joshi, M. S., Ferguson, T. B., Han, T. H., Hyduke, D. R., Liao, J. C., Rassaf, T., Bryan, N., Feelisch, M., & Lancaster, J. R. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152149699 · Cited by 216

Drug-Metabolizing Ability of Molybdenum Hydroxylases

Kitamura, S., Sugihara, K., & Ohta, S. (2006) · Drug Metabolism and Pharmacokinetics · doi:10.2133/dmpk.21.83 · Cited by 216

Purification and characterization of chlorite dismutase: a novel oxygen-generating enzyme

van Ginkel, C. G., Rikken, G., Kroon, A. G. M., & Kengen, S. W. M. (1996) · Archives of Microbiology · doi:10.1007/s002030050390 · Cited by 216

Neuroglobin-overexpressing transgenic mice are resistant to cerebral and myocardial ischemia

Khan, A. A., Wang, Y., Sun, Y., Mao, X. O., Xie, L., Miles, E., Graboski, J., Chen, S., Ellerby, L., Jin, K., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607497103 · Cited by 215

The mechanism of conversion of rat liver xanthine dehydrogenase from an NAD+-dependent form (type D) to an O2-dependent form (type O)

Waud, W. R., & Rajagopalan, K. V. (1976) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(76)90088-6 · Cited by 214

Nitrite reductase activity of cytochrome c

Basu, S., Azarova, N. A., Font, M. D., King, S. B., Hogg, N., Gladwin, M. T., Shiva, S., & Kim-Shapiro, D. B. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m806934200 · Cited by 214

Binding of human xanthine oxidase to sulphated glycosaminoglycans on the endothelial-cell surface

Adachi, T., Fukushima, T., Usami, Y., & Hirano, K. (1993) · Biochemical Journal · doi:10.1042/bj2890523 · Cited by 213

Structure of Nitrite Bound to Copper-containing Nitrite Reductase from Alcaligenes faecalis

Murphy, M. E. P., Turley, S., & Adman, E. T. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.45.28455 · Cited by 213

The Conversion of Xanthine Dehydrogenase to Xanthine Oxidase and the Role of the Enzyme in Reperfusion Injury1

Nishino, T. (1994) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a124480 · Cited by 212

Cardiolipin Switch in Mitochondria: Shutting off the Reduction of Cytochrome c and Turning on the Peroxidase Activity

Basova, L. V., Kurnikov, I. V., Wang, L., Ritov, V. B., Belikova, N. A., Vlasova, I. I., Pacheco, A. A., Winnica, D. E., Peterson, J., Bayir, H., et al. (2007) · Biochemistry · doi:10.1021/bi061854k · Cited by 212

The history and use of nitrate and nitrite in the curing of meat

Binkerd, E. F., & Kolari, O. E. (1975) · Food and Cosmetics Toxicology · doi:10.1016/0015-6264(75)90157-1 · Cited by 212

Nitric oxide partitioning into mitochondrial membranes and the control of respiration at cytochrome c oxidase

Shiva, S., Brookes, P. S., Patel, R. P., Anderson, P. G., & Darley-Usmar, V. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.131128898 · Cited by 212

Anaerobic killing of mucoid Pseudomonas aeruginosa by acidified nitrite derivatives under cystic fibrosis airway conditions

Yoon, S. S. (2006) · Journal of Clinical Investigation · doi:10.1172/jci24684 · Cited by 212

Pathophysiology of nitric oxide and related species: free radical reactions and modification of biomolecules

Eiserich, J. P., Patel, R. P., & O’Donnell, V. B. (1998) · Molecular Aspects of Medicine · doi:10.1016/s0098-2997(99)00002-3 · Cited by 211

Prominent roles of the NorR and Fur regulators in the Escherichia coli transcriptional response to reactive nitrogen species

Mukhopadhyay, P., Zheng, M., Bedzyk, L. A., LaRossa, R. A., & Storz, G. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307741100 · Cited by 211

A cereal haemoglobin gene is expressed in seed and root tissues under anaerobic conditions

Taylor, E. R., Nie, X., MacGregor, A. W., & Hill, R. D. (1994) · Plant Molecular Biology · doi:10.1007/bf00014440 · Cited by 211

Nitric oxide evolution and perception

Neill, S. J., Bright, J., Desikan, R., Hancock, J. T., Harrison, J., & Wilson, I. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm218 · Cited by 211

Reversible light/dark modulation of spinach leaf nitrate reductase activity involves protein phosphorylation

Huber, J. L. A., Huber, S. C., Campbell, W. H., & Redinbaugh, M. G. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90544-7 · Cited by 210

Abscisic aldehyde oxidase in leaves of Arabidopsis thaliana

Seo, M., Koiwai, H., Akaba, S., Komano, T., Oritani, T., Kamiya, Y., & Koshiba, T. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00812.x · Cited by 210

Chemical nature of nitric oxide storage forms in rat vascular tissue

Rodriguez, J., Maloney, R. E., Rassaf, T., Bryan, N. S., & Feelisch, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0234600100 · Cited by 210

Hypoxic Modulation of Exogenous Nitrite-Induced Vasodilation in Humans

Maher, A. R., Milsom, A. B., Gunaruwan, P., Abozguia, K., Ahmed, I., Weaver, R. A., Thomas, P., Ashrafian, H., Born, G. V. R., James, P. E., et al. (2008) · Circulation · doi:10.1161/circulationaha.107.719591 · Cited by 210

A cooperative oxygen-binding hemoglobin from Mycobacterium tuberculosis

Couture, M., Yeh, S., Wittenberg, B. A., Wittenberg, J. B., Ouellet, Y. H., Rousseau, D. L., & Guertin, M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.20.11223 · Cited by 208

Crystal Structures of the Active and Alloxanthine-Inhibited Forms of Xanthine Dehydrogenase from Rhodobacter capsulatus

Truglio, J. J., Theis, K. W., Leimkühler, S., Rappa, R., Rajagopalan, K. V., & Kisker, C. (2002) · Structure · doi:10.1016/s0969-2126(01)00697-9 · Cited by 207

Purification and properties of the NAD+-dependent (type D) and O2-dependent (type O) forms of rat liver xanthine dehydrogenase

Waud, W. R., & Rajagopalan, K. V. (1976) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(76)90087-4 · Cited by 207

Inhibition of cytochrome c oxidase in turnover by nitric oxide: mechanism and implications for control of respiration

Torres, J., Darley-Usmar, V. M., & Wilson, M. T. (1995) · Biochemical Journal · doi:10.1042/bj3120169 · Cited by 206

Emission of NO from several higher plant species

Wildt, J., Kley, D., Rockel, A., Rockel, P., & Segschneider, H. ‐. (1997) · Journal of Geophysical Research Atmospheres · doi:10.1029/96jd02968 · Cited by 206

Siroheme: A New Prosthetic Group Participating in Six-Electron Reduction Reactions Catalyzed by Both Sulfite and Nitrite Reductases

Murphy, M. J., Siegel, L. M., Tove, S. R., & Kamin, H. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.3.612 · Cited by 206

Bacillus anthracis -derived nitric oxide is essential for pathogen virulence and survival in macrophages

Shatalin, K., Gusarov, I., Avetissova, E., Shatalina, Y., McQuade, L. E., Lippard, S. J., & Nudler, E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710950105 · Cited by 205

Electronic Structure of Heme-Nitrosyls and Its Significance for Nitric Oxide Reactivity, Sensing, Transport, and Toxicity in Biological Systems

Goodrich, L. E., Paulat, F., Praneeth, V. K. K., & Lehnert, N. (2010) · Inorganic Chemistry · doi:10.1021/ic902304a · Cited by 204

Electronic Structure of the Perturbed Blue Copper Site in Nitrite Reductase: Spectroscopic Properties, Bonding, and Implications for the Entatic/Rack State

LaCroix, L. B., Shadle, S. E., Wang, Y., Averill, B. A., Hedman, B., Hodgson, K. O., & Solomon, E. I. (1996) · Journal of the American Chemical Society · doi:10.1021/ja961217p · Cited by 204

Nitrate transport and compartmentation in cereal root cells

Miller, T., & Smith, S. J. (1996) · Journal of Experimental Botany · doi:10.1093/jxb/47.7.843 · Cited by 204

Mechanisms Underlying Erythrocyte and Endothelial Nitrite Reduction to Nitric Oxide in Hypoxia: Role for Xanthine Oxidoreductase and Endothelial Nitric Oxide Synthase

Webb, A. J., Milsom, A. B., Rathod, K. S., Chu, W. L., Qureshi, S., Lovell, M. J., Lecomte, F. M. J., Perrett, D., Raimondo, C., Khoshbin, E., et al. (2008) · Circulation Research · doi:10.1161/circresaha.108.175810 · Cited by 203

Routes to S -nitroso-hemoglobin formation with heme redox and preferential reactivity in the β subunits

Luchsinger, B. P., Rich, E. N., Gow, A. J., Williams, E. M., Stamler, J. S., & Singel, D. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0233287100 · Cited by 202

Cell biology of molybdenum in plants and humans

Mendel, R. R., & Kruse, T. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.02.007 · Cited by 202

Cytochrome c Nitrite Reductase from Wolinella succinogenes

Einsle, O., Stach, P., Messerschmidt, A., Simon, J., Kröger, A., Huber, R., & Kroneck, P. M. H. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m006188200 · Cited by 202

The plant Mo‐hydroxylases aldehyde oxidase and xanthine dehydrogenase have distinct reactive oxygen species signatures and are induced by drought and abscisic acid

Yesbergenova, Z., Yang, G., Oron, E., Soffer, D., Fluhr, R., & Sagi, M. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2005.02422.x · Cited by 200

A hemoglobin from plants homologous to truncated hemoglobins of microorganisms

Watts, R. A., Hunt, P. W., Hvitved, A. N., Hargrove, M. S., Peacock, W. J., & Dennis, E. S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191349198 · Cited by 200

First exploration of Nitrobacter diversity in soils by a PCR cloning-sequencing approach targeting functional gene nxrA

Poly, F., Wertz, S., Brothier, E., & Degrange, V. (2007) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2007.00404.x · Cited by 199

Moonlighting is mainstream: Paradigm adjustment required

Copley, S. D. (2012) · BioEssays · doi:10.1002/bies.201100191 · Cited by 199

The Conversion of Nitrite to Nitrogen Oxide(s) by the Constitutive NAD(P)H-Nitrate Reductase Enzyme from Soybean

Dean, J. V., & Harper, J. E. (1988) · PLANT PHYSIOLOGY · doi:10.1104/pp.88.2.389 · Cited by 198

Role of the anion nitrite in ischemia-reperfusion cytoprotection and therapeutics

DEZFULIAN, C., RAAT, N., SHIVA, S., & GLADWIN, M. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.05.001 · Cited by 198

Nitric oxide, cytochrome-c oxidase and myoglobin

Brunori, M. (2001) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)01698-4 · Cited by 197

NO signal at the crossroads: polyamine-induced nitric oxide synthesis in plants?

Yamasaki, H., & Cohen, M. F. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2006.09.009 · Cited by 197

Mechanism and importance of post-translational regulation of nitrate reductase

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Growth, physiological and anatomical responses of two wheat genotypes to waterlogging and nutrient supply

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