a b s t r a c tGrain protein content (GPC) in wheat has been a major trait of interest for breeders since it has enormous end use potential. In the present study, marker-assisted backcrossing (MABC) was successfully used to improve GPC in wheat cultivar HUW468. The genotype Glu269 was used as the donor parent for introgression of the gene Gpc-B1 that confers high GPC. In a segregating population, SSR marker Xucw108, with its locus linked to Gpc-B1 was used for foreground selection to select plants carrying Gpc-B1. Background selection, involving 86 polymorphic SSR markers dispersed throughout the genome, was exercised to recover the genome of HUW468. For eliminating linkage drag, markers spanning a 10 cM region around the gene Gpc-B1 were employed to select lines with a donor segment of the minimum size carrying the gene of interest. Improved lines had significantly higher GPC and displayed 88.4-92.3 per cent of the recurrent parent genome (RPG). For grain yield, selected lines were at par with the recurrent parent HUW468, suggesting that there was no yield penalty. The whole exercise of transfer of Gpc-B1 and reconstitution of the genome of HUW468 was completed within a period of two and half years (five crop cycles) demonstrating practical utility of MABC for developing high GPC lines in the background of any elite and popular wheat cultivar with relatively higher speed and precision.(http://creativecommons.org/licenses/by-nc-nd/3.0/).
The ToxA–Tsn1 system is an example of an inverse gene-for-gene relationship. The gene ToxA encodes a host-selective toxin (HST) which functions as a necrotrophic effector and is often responsible for the virulence of the pathogen. The genomes of several fungal pathogens (e.g., Pyrenophora tritici-repentis, Parastagonospora nodorum, and Bipolaris sorokiniana) have been shown to carry the ToxA gene. Tsn1 is a sensitivity gene in the host, whose presence generally helps a ToxA-positive pathogen to cause spot blotch in wheat. Cultivars lacking Tsn1 are generally resistant to spot blotch; this resistance is attributed to a number of other known genes which impart resistance in the absence of Tsn1. In the present study, 110 isolates of B. sorokiniana strains, collected from the ME5A and ME4C megaenvironments of India, were screened for the presence of the ToxA gene; 77 (70%) were found to be ToxA positive. Similarly, 220 Indian wheat cultivars were screened for the presence of the Tsn1 gene; 81 (36.8%) were found to be Tsn1 positive. When 20 wheat cultivars (11 with Tsn1 and 9 with tsn1) were inoculated with ToxA-positive isolates, seedlings of only those carrying the Tsn1 allele (not tsn1) developed necrotic spots surrounded by a chlorotic halo. No such distinction between Tsn1 and tsn1 carriers was observed when adult plants were inoculated. This study suggests that the absence of Tsn1 facilitated resistance against spot blotch of wheat. Therefore, the selection of wheat genotypes for the absence of the Tsn1 allele can improve resistance to spot blotch.
Chikungunya fever is a major public health issue in India affecting millions of people and occurs due to Chikungunya. Chikungunya virus (CHIKV) is a single stranded RNA virus from the family of Togaviridae and genus alpha virus. It contain three structural proteins: glycosylated E1 and E2, embedded in the viral envelope, and a non-glycosylated nucleocapsid protein. Till date, researchers are working on inhibition of CHIKV but till now no cheap and effective medicine is available in the market. Therefore, the authors of this work thought of isoquinoline based noscapine to inhibit the nsP3 protease of CHIKV. The aim of the work is to understand the mechanism for the synthesis of noscapine theoretically using DFT. Further study the potential of all four isomers of noscapines {(13 (S,R), 14 (R,R), 15 (R,S) and 16 (S,S)} against nsP3 protease of CHIKV with the help of docking and MD simulation. The integrated e-pharmacophore binding affinity based virtual screening, docking and molecular dynamics simulation recognized four hits isomers as inhibition nsP3 protease of CHIKV. The docking energies of all the isomers of noscapine (13-16) with nsP3 protease CHIKV was found out to be more negative than baicalin (À8.06 kcal/mol) on selected sites. Amongst the isomers of noscapine, CMPD 13 possessed best binding affinity with four hydrogen bonding interactions. Further, ADME properties and blood-brain barrier permeability properties have been calculated. DFT studies of all the isomers of noscapine was investigated.
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