[HTML][HTML] Molecular breeding and drought tolerance in chickpea

R Asati, MK Tripathi, S Tiwari, RK Yadav, N Tripathi - Life, 2022 - mdpi.com
Cicer arietinum L. is the third greatest widely planted imperative pulse crop worldwide, and it
belongs to the Leguminosae family. Drought is the utmost common abiotic factor on plants …

The roles of polyamines during the lifespan of plants: from development to stress

AF Tiburcio, T Altabella, M Bitrián, R Alcázar - Planta, 2014 - Springer
Compelling evidence indicates that free polyamines (PAs)(mainly putrescine, spermidine,
spermine, and its isomer thermospermine), some PA conjugates to hydroxycinnamic acids …

Genetic dissection of drought and heat tolerance in chickpea through genome-wide and candidate gene-based association map** approaches

M Thudi, HD Upadhyaya, A Rathore, PM Gaur… - Plos one, 2014 - journals.plos.org
To understand the genetic basis of tolerance to drought and heat stresses in chickpea, a
comprehensive association map** approach has been undertaken. Phenotypic data were …

Plant amine oxidases “on the move”: an update

R Angelini, A Cona, R Federico, P Fincato… - Plant Physiology and …, 2010 - Elsevier
Amine oxidases (AOs) catalyse the oxidative de-amination of polyamines, ubiquitous
polycationic compounds involved in important events of cell life. They include the copper …

Copper-containing amine oxidases contribute to terminal polyamine oxidation in peroxisomes and apoplast of Arabidopsis thaliana

J Planas-Portell, M Gallart, AF Tiburcio, T Altabella - BMC Plant Biology, 2013 - Springer
Abstract Background Polyamines (PAs) are oxidatively deaminated at their primary or
secondary amino-groups by copper-containing amine oxidases (CuAOs) or FAD-dependent …

Polyamine catabolism: target for antiproliferative therapies in animals and stress tolerance strategies in plants

P Tavladoraki, A Cona, R Federico, G Tempera… - Amino acids, 2012 - Springer
Metabolism of polyamines spermidine and spermine, and their diamine precursor,
putrescine, has been a target for antineoplastic therapy since these naturally occurring alkyl …

Aldehyde Dehydrogenases in Arabidopsis thaliana: Biochemical Requirements, Metabolic Pathways, and Functional Analysis

N Stiti, TD Missihoun, SO Kotchoni, HH Kirch… - Frontiers in plant …, 2011 - frontiersin.org
Aldehyde dehydrogenases (ALDHs) are a family of enzymes which catalyze the oxidation of
reactive aldehydes to their corresponding carboxylic acids. Here we summarize molecular …

Betaine aldehyde dehydrogenase genes from Arabidopsis with different sub-cellular localization affect stress responses

TD Missihoun, J Schmitz, R Klug, HH Kirch, D Bartels - Planta, 2011 - Springer
Arabidopsis thaliana belongs to those plants that do not naturally accumulate glycine
betaine (GB), although its genome contains two genes, ALDH10A8 and ALDH10A9 that …

Regulation and mechanism of enzyme metabolism in germinated hemp seeds by ultrasound combined with exogenous calcium chloride treatment

MQ Liu, BR Wang, YC Qiu, HF Zhao, SY Xu… - International Journal of …, 2024 - Elsevier
Abstract γ-aminobutyric acid (GABA) plays an important role in anti-anxiety by inhibiting
neurotransmitter in the central nervous system (CNS) of mammals, which is generated in the …

Integrative analysis of metabolite and transcript abundance during the short‐term response to saline and oxidative stress in the brown alga Ectocarpus siliculosus

SM Dittami, A Gravot, D Renault… - Plant, cell & …, 2011 - Wiley Online Library
The model brown alga Ectocarpus siliculosus undergoes extensive transcriptomic changes
in response to abiotic stress, many of them related to primary metabolism and particularly to …