scholarly journals Reconstitution of H2 oxidation activity from H2 uptake-negative mutants of Rhizobium japonicum bacteroids.

1982 ◽  
Vol 257 (4) ◽  
pp. 2092-2096
Author(s):  
R.J. Maier ◽  
S. Mutaftschiev
1982 ◽  
Vol 152 (1) ◽  
pp. 422-430
Author(s):  
M R O'Brian ◽  
R J Maier

Membranes from free-living Rhizobium japonicum were isolated to study electron transport components involved in H2 oxidation. The H2/O2 uptake rate ratio in membranes was approximately 2. The electron transport inhibitors antimycin A, cyanide, azide, hydroxylamine, and 2-n-heptyl-4-hydroxyquinoline-N-oxide (HQNO) inhibited H2 uptake and H2-dependent O2 uptake significantly. H2-reduced minus O2-oxidized absorption difference spectra revealed peaks at 551.5, 560, and 603 nm, indicating the involvement of cytochromes c, b, and a-a3, respectively. H2-dependent cytochrome reduction was completely inhibited in the presence of 0.15 mM HQNO. This inhibition was relieved by the addition of 0.1 mM menadione. Evidence is presented for the involvement of two b-type cytochromes in H2 oxidation. One b-type cytochrome was not reduced by ascorbate and had an absorption peak at 560 nm. The reduction of this cytochrome by H2 was not inhibited by cyanide. A second b-type cytochrome, cytochrome b', was not reduced by H2 in the presence of cyanide. This cytochrome had an absorption peak at 558 nm. Carbon monoxide difference spectra with H2 as reductant provided evidence for the involvement of cytochrome o as well as cytochrome a3 in H2 oxidation. H2 uptake activity in cell-free extracts was inhibited by UV light irradiation. Most of the activity of the UV-treated extracts was restored with the addition of ubiquinone. The restored activity was inhibited by cyanide. A branched electron transport pathway from H2 to O2 is proposed.


1980 ◽  
Vol 66 (6) ◽  
pp. 1061-1066 ◽  
Author(s):  
David W. Emerich ◽  
Tomas Ruiz-Argüeso ◽  
Sterling A. Russell ◽  
Harold J. Evans

2018 ◽  
Vol 125 ◽  
pp. 239-243 ◽  
Author(s):  
Mondher Khdhiri ◽  
Sarah Piché-Choquette ◽  
Julien Tremblay ◽  
Susannah G. Tringe ◽  
Philippe Constant

Author(s):  
Catherine A. Taylor ◽  
Bruce M. Jarnot

Peroxisome induction can be expressed as an increase in peroxisome area (proliferation) or as an increase in peroxisomal fatty acid oxidation (activity). This study compares proliferation and activity as endpoints for hepatic peroxisome induction by perfluorodecanoic acid (PFDA). Fluorocarboxylic acids such as PFDA represent a class of compounds possessing commercially important surfactant properties. A single 50 mg/Kg ip. dose of PFDA produces a characteristic “wasting syndrome” in male F-344 rats. Symptoms include hypophagia, weight loss, hepatomegaly, and delayed lethality. Hepatic studies reveal changes similar to those seen with the hypolipidemic agent clofibrate. These include mitochondrial disruption, endoplasmic reticulum and peroxisome proliferation, and increased peroxisomal acyl-CoA oxidase activity.Male Fisher-344 rats received a single ip. dose of 2, 20, or 50mg/Kg PFDA dissolved in 1:1 propylene glycol/water and were sacrificed 8 days post-dose. All control rats received an equal volume of vehicle ip. Animals were provided food and water ad libitum, except pair-fed controls which received the same restrictive food intake consumed by their weight-paired dosed partners (50mg/Kg PFDA group) to simulate the hypophagia associated with PFDA.


Agronomie ◽  
1982 ◽  
Vol 2 (3) ◽  
pp. 243-248 ◽  
Author(s):  
Jean-Claude CLEYET-MAREL ◽  
Yves CROZAT
Keyword(s):  

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