Publications by authors named "U N Ondar"

Functionalized adsorbents with poly-(4,9-dioxododecane-1,12-guanidine) (SiO-PDDG) and mercaptophenyl groups (MPhS) were used for the separation of Se(VI) and Se(IV) for the first time. Fixation of PDDG was characterized by capillary electrophoresis and TGA/DSC. The quantitative extraction of Se(VI) proceeded due to anion exchange at pH 3-7.

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A simple and highly efficient method for the determination of highly toxic arsenic species using non-covalently aminated silica is proposed. The polyamines including poly(hexamethyleneguanidine), poly(4,9-dioxadodecane-1,12-guanidine), hexadimethrine, and poly(diallyldimethylammonium) were tested as silica modifiers. The prepared adsorbents allow effective preconcentration of anionic species of arsenic from aqueous solutions.

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A new deletion allele of the APETALA1 (AP1) gene encoding a type II MADS-box protein with the key role in the initiation of flowering and development of perianth organs has been identified in A. thaliana. The deletion of seven amino acids in the conserved region of the K domain in the ap1-20 mutant considerably delayed flowering and led to a less pronounced abnormality in the corolla development compared to the ap1-3 and apl-6 alleles with low and medium expression, respectively.

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We have studied the morphology and vein branching of rosette leaves in Arabidopsis thaliana mutants as and sa, which proved to be alleles of the A. thaliana AS1 and AS2 genes, respectively. We have also analyzed the localization of bioactive auxin, as measured by the expression of the DR5::GUS transgene, as well as the expression patterns of BP, as measured by the expression of the BP::GUS transgene in leaves of the mutants.

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The nucleotide sequence was analyzed for the temperature-sensitive allele abruptus (abr), which distorts polar auxin transport (PAT) in the floral shoot. The mutation C-->T was found in the second exon and led to an amino acid substitution (glycin-->glutamic acid) in the conserved domain of protein kinase encoded by the ABRUPTUS/PINOID (ABR/PID) gene. RT--PCR revealed a 100-fold decrease in transcription of the LEAFY (LFY) gene in the abr mutant with high expressiveness of the mutant character; transcription of the fused LFY::GUS gene was also low in the mutant.

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