Wheat In Presence Research Articles

Alteration of Genetic Make-up in Karnal Bunt Pathogen (Tilletia indica) of Wheat in Presence of Host Determinants

Alteration of genetic make-up of the isolates and monosporidial strains of Tilletia indica causing Karnal bunt (KB) disease in wheat was analyzed using DNA markers and SDS-PAGE. The generation of new variation with different growth characteristics is not a generalized feature and is not only dependant on the original genetic make up of the base isolate/monosporidial strains but also on interaction with host. Host determinant(s) plays a significant role in the generation of variability and the effect is much pronounced in monosporidial strains with narrow genetic base as compared to broad genetic base. The most plausible explanation of genetic variation in presence of host determinant(s) are the recombination of genetic material from two different mycelial/sporidia through sexual mating as well as through para-sexual means. The morphological and development dependent variability further suggests that the variation in T. indica strains predominantly derived through the genetic rearrangements.

Reducing the allelopathic effect of Parthenium hysterophorus L. on wheat (Triticum aestivum L.) by Pseudomonas putida

The present study evaluates the role of Pseudomonasputida NBRIC19 in alleviating biotic stress of Partheniumhysterophorus (Parthenium) in Triticumaestivum. Due to presence of Parthenium there was 43.76, 53.08 and 78.65% inhibition in root length, shoot length and dry weight of wheat respectively. This inhibition was recovered when P. putida NBRIC19 treatment resulted in 52.29, 28.73 and 76.31% increase in root length, shoot length and dry weight respectively as compared to control. P. putida NBRIC19 was able to form more biofilm under toxic environment of allelochemicals and enhanced expression of stress responsive genes in wheat. Inoculated wheat plants showed lower activity of catalase and ascorbate peroxidase under biotic stress of Parthenium indicating that inoculated plants felt less stress as compared to uninoculated plants. Microbial community structure in bacterized and nonbacterized wheat rhizosphere in presence and absence of Parthenium, was investigated using Biolog. There was significant increase in microbial diversity in P. putida NBRIC19 bacterized wheat rhizosphere. Functional microbial diversity revealed that P. putida NBRIC19 had shifted the microflora in such a manner that utilization of phytotoxic allelochemicals increased to lessen its toxic effect and finally it resulted in better growth of wheat in presence of Parthenium. Principal component analysis showed that microbial community function in nonbacterized wheat rhizosphere in presence (WPC) and absence (WC) of Parthenium is totally different from each other but due to P. putida NBRIC19 treatment there was close clustering of WPT and WT indicating a total shift in microbial community structure.

Cadmium uptake by durum wheat in presence of citrate

The aim of this study was to determine the mechanisms underlying the uptake of Cd by durum wheat (Triticum turgidum L. ssp. durum cv. “acalou”) in the presence of citrate under hydroponic conditions. Wheat seedlings were exposed for 3 h to simplified nutrient solutions initially containing 35 nM of free Cd with or without citrate. Uptake experiments with citrate alone were also performed. Solutions were radio labelled with 109Cd or citrate-14C. The depletion of Cd and citrate in the exposure solution was followed, and at the end of the exposure Cd and citrate were quantified in all compartments of the experimental system (root surface, inner roots and aerial parts). The apparent rates of internalization of Cd (r Cd) and citrate (r cit) were estimated from the ratio of the uptake flux to the contents adsorbed at the root surface. About two times more Cd was taken up in the presence of citrate. Assuming that citrate and Cd–citrate complexes were taken up at the same rate, a direct uptake of intact complexes could not account for the higher uptake of Cd in presence of citrate. In addition, Cd was internalized at the same rate in the absence or presence of citrate (r Cd = 3.62 h−1), whereas the internalization rate constants of Cd and citrate were different (r Cd ≈ 8 r cit). This strengthens the idea that a direct uptake of non-dissociated Cd–citrate complexes probably did not account for the higher Cd uptake in presence of citrate. A dissociation of Cd–citrate complexes within the diffusion layer or at the root surface and the subsequent additional supply of free Cd were more likely to explain the higher Cd uptake in presence of citrate.