Literature DB >> 16668778

Oxidation and reduction of leghemoglobin in root nodules of leguminous plants.

M Becana1, R V Klucas.   

Abstract

Reactions involving changes that affect the function of leghemoglobin (Lb) are reviewed. The chemical nature of Lb and conditions inside nodules, such as slightly acid pH and the presence of metal ions, chelators, and toxic metabolites (nitrite, superoxide radical, peroxides), are conducive for oxidation of ferrous Lb (Lb(2+)) or its oxygenated form (LbO(2)) to nonfunctional ferric Lb (Lb(3+)) and ferryl Lb. Because Lb(3+) is nearly nonexistent in nodules and undergoes observable reduction in vivo, mechanisms must operate in nodules to maintain Lb in the Lb(2+) state. Redox reactions of Lb are mediated, for the most part, by activated oxygen species: (a) oxidation of LbO(2) to Lb(3+) involves superoxide; (b) excess peroxide oxidizes LbO(2) and Lb(3+) to ferryl Lb and may cause breakdown of heme, release of iron, and generation of hydroxyl radicals (protein radicals may be formed in this process); (c) enzymatic reduction of Lb(3+) requires active flavin and thiol groups and involves formation of peroxide; and (d) direct reduction of Lb(3+) by NADH is mediated by superoxide and peroxide. Transition metal ions and certain small molecules of nodules such as flavins may act as intermediate electron carriers between NADH and Lb(3+), increasing the rate of reaction, which then proceeds via superoxide or flavin radicals, respectively.

Entities:  

Year:  1992        PMID: 16668778      PMCID: PMC1080335          DOI: 10.1104/pp.98.4.1217

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  16 in total

1.  Measurement of the fractional oxygenation of leghemoglobin in intact detached pea nodules by reflectance spectroscopy.

Authors:  J D Monroe; T G Owens; T A Larue
Journal:  Plant Physiol       Date:  1989-10       Impact factor: 8.340

2.  The reaction of ferrous leghemoglobin with hydrogen peroxide to form leghemoglobin(IV).

Authors:  I Aviram; A Wittenberg; J B Wittenberg
Journal:  J Biol Chem       Date:  1978-08-25       Impact factor: 5.157

3.  Regulation of o(2) concentration in soybean nodules observed by in situ spectroscopic measurement of leghemoglobin oxygenation.

Authors:  B J King; S Hunt; G E Weagle; K B Walsh; R H Pottier; D T Canvin; D B Layzell
Journal:  Plant Physiol       Date:  1988-06       Impact factor: 8.340

4.  Nicotinate, nicotinamide, and the reactivity of leghemoglobin in soybean root nodules.

Authors:  R V Klucas; C A Appleby
Journal:  Plant Physiol       Date:  1991-02       Impact factor: 8.340

5.  Lipid peroxidation in peribacteroid membranes from French-bean nodules.

Authors:  A Puppo; G Herrada; J Rigaud
Journal:  Plant Physiol       Date:  1991-07       Impact factor: 8.340

6.  Enzymatic and nonenzymatic mechanisms for ferric leghemoglobin reduction in legume root nodules.

Authors:  M Becana; R V Klucas
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

7.  Oxidation of glycine by Phaseolus leghaemoglobin with associated catabolic reactions at the haem.

Authors:  P Lehtovaara
Journal:  Biochem J       Date:  1978-11-15       Impact factor: 3.857

8.  Bile-pigment formation from different leghaemoglobins. Methine-bridge specificity of coupled oxidation.

Authors:  P Lehtovaara; U Perttilä
Journal:  Biochem J       Date:  1978-11-15       Impact factor: 3.857

9.  Ferric leghemoglobin reductase from soybean root nodules.

Authors:  L L Saari; R V Klucas
Journal:  Arch Biochem Biophys       Date:  1984-05-15       Impact factor: 4.013

10.  Study of the pseudoperoxidatic activity of soybean leghemoglobin and sperm whale myoglobin.

Authors:  G Sievers; M Rönnberg
Journal:  Biochim Biophys Acta       Date:  1978-04-26
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  8 in total

1.  Leghemoglobin green derivatives with nitrated hemes evidence production of highly reactive nitrogen species during aging of legume nodules.

Authors:  Joaquín Navascués; Carmen Pérez-Rontomé; Marina Gay; Manuel Marcos; Fei Yang; F Ann Walker; Alain Desbois; Joaquín Abián; Manuel Becana
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-30       Impact factor: 11.205

2.  Oxyleghemoglobin scavenges nitrogen monoxide and peroxynitrite: a possible role in functioning nodules?

Authors:  Susanna Herold; Alain Puppo
Journal:  J Biol Inorg Chem       Date:  2005-11-03       Impact factor: 3.358

3.  Molecular cloning, functional characterization, and subcellular localization of soybean nodule dihydrolipoamide reductase.

Authors:  Jose F Moran; Zhaohui Sun; Gautam Sarath; Raúl Arredondo-Peter; Euan K James; Manuel Becana; Robert V Klucas
Journal:  Plant Physiol       Date:  2002-01       Impact factor: 8.340

4.  Leghemoglobin is nitrated in functional legume nodules in a tyrosine residue within the heme cavity by a nitrite/peroxide-dependent mechanism.

Authors:  Martha Sainz; Laura Calvo-Begueria; Carmen Pérez-Rontomé; Stefanie Wienkoop; Joaquín Abián; Christiana Staudinger; Silvina Bartesaghi; Rafael Radi; Manuel Becana
Journal:  Plant J       Date:  2015-03       Impact factor: 6.417

5.  Uracil DNA glycosylase (UDG) activities in Bradyrhizobium diazoefficiens: characterization of a new class of UDG with broad substrate specificity.

Authors:  Ullas Valiya Chembazhi; Vinod Vikas Patil; Shivjee Sah; Wayne Reeve; Ravi P Tiwari; Euijeon Woo; Umesh Varshney
Journal:  Nucleic Acids Res       Date:  2017-06-02       Impact factor: 16.971

6.  Characterization of the Heme Pocket Structure and Ligand Binding Kinetics of Non-symbiotic Hemoglobins from the Model Legume Lotus japonicus.

Authors:  Laura Calvo-Begueria; Bert Cuypers; Sabine Van Doorslaer; Stefania Abbruzzetti; Stefano Bruno; Herald Berghmans; Sylvia Dewilde; Javier Ramos; Cristiano Viappiani; Manuel Becana
Journal:  Front Plant Sci       Date:  2017-04-04       Impact factor: 5.753

7.  Expressed Soybean Leghemoglobin: Effect on Escherichia coli at Oxidative and Nitrosative Stress.

Authors:  Olga V Kosmachevskaya; Elvira I Nasybullina; Konstantin B Shumaev; Alexey F Topunov
Journal:  Molecules       Date:  2021-11-28       Impact factor: 4.411

8.  Hemoglobin LjGlb1-1 is involved in nodulation and regulates the level of nitric oxide in the Lotus japonicus-Mesorhizobium loti symbiosis.

Authors:  Mitsutaka Fukudome; Laura Calvo-Begueria; Tomohiro Kado; Ken-Ichi Osuki; Maria Carmen Rubio; Ei-Ichi Murakami; Maki Nagata; Ken-Ichi Kucho; Niels Sandal; Jens Stougaard; Manuel Becana; Toshiki Uchiumi
Journal:  J Exp Bot       Date:  2016-07-21       Impact factor: 6.992

  8 in total

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