cinidon-ethyl has been researched along with Hypoxia* in 2 studies
2 other study(ies) available for cinidon-ethyl and Hypoxia
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Glycolysis and the tricarboxylic acid cycle are linked by alanine aminotransferase during hypoxia induced by waterlogging of Lotus japonicus.
The role of nitrogen metabolism in the survival of prolonged periods of waterlogging was investigated in highly flood-tolerant, nodulated Lotus japonicus plants. Alanine production revealed to be a critical hypoxic pathway. Alanine is the only amino acid whose biosynthesis is not inhibited by nitrogen deficiency resulting from RNA interference silencing of nodular leghemoglobin. The metabolic changes that were induced following waterlogging can be best explained by the activation of alanine metabolism in combination with the modular operation of a split tricarboxylic acid pathway. The sum result of this metabolic scenario is the accumulation of alanine and succinate and the production of extra ATP under hypoxia. The importance of alanine metabolism is discussed with respect to its ability to regulate the level of pyruvate, and this and all other changes are discussed in the context of current models concerning the regulation of plant metabolism. Topics: Adenosine Triphosphate; Alanine; Alanine Transaminase; Citric Acid Cycle; Fermentation; Gene Expression Regulation, Plant; Glycolysis; Hypoxia; Leghemoglobin; Lotus; Nitrogen; Nitrogen Fixation; Pyruvic Acid; RNA Interference; Succinic Acid; Water | 2010 |
Cloning and characterization of Lotus japonicus formate dehydrogenase: a possible correlation with hypoxia.
Formate dehydrogenases (FDHs, EC 1.2.1.2) comprise a group of enzymes found in both prokaryotes and eukaryotes that catalyse the oxidation of formate to CO(2). FDH1 from the model legume Lotus japonicus (LjFDH1) was cloned and expressed in E. coli BL21(DE3) as soluble active protein. The enzyme was purified using affinity chromatography on Cibacron blue 3GA-Sepharose. The enzymatic properties of the recombinant enzyme were investigated and the kinetic parameters (K(m), k(cat)) for a number of substrates were determined. Molecular modelling studies were also employed to create a model of LjFDH1, based on the known structure of the Pseudomonas sp. 101 enzyme. The molecular model was used to help interpret biochemical data concerning substrate specificity and catalytic mechanism of the enzyme. The temporal expression pattern of LjFDH1 gene was studied by real-time RT-PCR in various plant organs and during the development of nitrogen-fixing nodules. Furthermore, the spatial transcript accumulation during nodule development and in young seedpods was determined by in situ RNA-RNA hybridization. These results considered together indicate a possible role of formate oxidation by LjFDH1 in plant tissues characterized by relative hypoxia. Topics: Amino Acid Sequence; Base Sequence; Cloning, Molecular; DNA Primers; Formate Dehydrogenases; Hypoxia; In Situ Hybridization; Lotus; Molecular Sequence Data; Polymerase Chain Reaction; Sequence Homology, Amino Acid | 2009 |