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Evaluation of terrestrial plants extracts for uranium sorption and characterization of potent phytoconstituents
Sorption capacity of four plants (Funaria hygrometrica, Musa acuminata, Brassica juncea and Helianthus annuus) extracts/fractions for uranium, a radionuclide was investigated by EDXRF and tracer studies. The maximum sorption capacity, i.e., 100% (complete sorption) was observed in case of Musa acuminata extract and fractions. Carbohydrate, proteins, phenolics and flavonoids contents in the active fraction (having maximum sorption capacity) were also determined. Further purification of the most active fraction provided three pure molecules, mannitol, sorbitol and oxo-linked potassium oxalate. The characterization of isolated molecules was achieved by using FTIR, NMR, GC-MS, MS-MS, and by single crystal-XRD analysis. Of three molecules, oxo-linked potassium oxalate was observed to have 100% sorption activity. Possible binding mechanism of active molecule with the uranyl cation has been purposed
Effect of organic manure and plant spacing on biomass and quality of Mentha piperita L. in Himalaya in India
Mentha piperita L. (peppermint) is one of the economically important aromatic–medicinal herbs in India. Cultivation
of M. piperita has so far not been attempted under sub-temperate agro-climatic conditions in the mid-hill of Himalaya.
A study on rationalization of level of farmyard manure (FYM) and plant spacing for M. piperita crop was conducted
during 2007 and 2008 at IHBT (CSIR), Palampur. The treatments consisted of four levels of FYM (0, 15, 30,
45 t/ha), three plant spacing (25 4.х 15, 40 4. х 15 and 50 4.х 15 cm2). Crop yield significantly increased with the level
of FYM and was significantly higher at 45 t/ha of FYM. The oil content in the crop ranged from 0.2% to 0.3%; however,
it was not affected by FYM application. Menthone content significantly increased with application of FYM and
was significantly higher at 45 t/ha of FYM, whereas content of menthyl acetate, neo-menthol and menthofuran significantly
decreased with application of FYM. The crop yield, oil content and composition of the oil were not affected
by variation in plant spacing. However, planting of M. piperita at 50 4.х 15 cm2 spacing and application of FYM at
45 t/ha was found to be favorable for biomass production and content of menthone
Development of stevioside Pluronic-F-68 copolymer based PLA-nanoparticles as an antidiabetic nanomedicine
Stevioside (FDA approved nontoxic natural non-caloric sweetener) has been reported to have very good
antidiabetic potential but its use as therapeutic drug is restricted in human due to its deprived intestinal
absorption and poor bioavailability. We have nano-bioconjugated this molecule on biodegradable
Pluronic-F-68 copolymer based PLA nanoparticles by nanoprecipitation method (spherical, size range
110–130 nm) to overcome deprived intestinal absorption and to enhance the bioavailability. The drug
loading calculated by the standard calibrated HPLC was 16.32
±
4% (w/w). The in vitro release study
showed the initial burst followed by the sustained release. The half release and complete release were
observed on 25
±
4 h and 200
±
10 h respectively. This newly formulated nanostevioside showed very
high potential to be used as antidiabetic nanomedicine for safe and effective use in vivo
Overexpression of CsANR Increased Flavan-3-ols and Decreased Anthocyanins in Transgenic Tobacco
plants and synthesized by a common biosynthetic
pathway. Anthocyanin reductase (ANR) represents branching-
point enzyme of this pathway converting anthocyanidins
to flavan-3-ols. Since tea contains highest amount of flavonoids,
a cDNA encoding anthocyanin reductase from tea
(CsANR) was overexpressed in transgenic tobacco to check
the influence on anthocyanin and flavan-3-ols. The transgenic
tobacco was confirmed by genomic PCR and expression
of transgene was analyzed through semiquantitative
PCR. Interestingly flowers of transgenic tobacco were light
pink/white in color instead of dark pink in wild tobacco,
documenting the decrease in anthocyanins content. Upon
measurement, flower anthocyanin content was found to be
lesser. While flavan-3-ols (epicatechin and epigallocatechin)
contents were increased in leaf tissue of transgenic lines. The
expressions of other endogenous flavonoid biosynthetic
pathway genes in different floral parts (sepal, petal, stamen,
and carpel) of CsANR overexpressing tobacco as well as wild
tobacco were analyzed. The transcript levels of PAL and CHI
genes were downregulated, while transcript levels of F3H,
FLS, CHS, ANR1, and ANR2 genes were upregulated in all
floral parts of CsANR transgenic plants compared to wild
tobacco. The expressions of DFR and ANS genes were also
spatially modulated in different floral parts due to overexpression
of CsANR. Thus, CsANR overexpression increased
flavan-3-ols and decreased anthocyanin content by modulating
the expressions of various flavonoid biosynthetic
pathway genes in flower of tobacco. These changes might be
responsible for the observed pollen tube in the pollens of
CsANR overexpressing transgenic tobacco when they were
still in the anther before pollination
Biocatalysts for multicomponent Biginelli reaction: bovine serum albumin triggered waste-free synthesis of 3,4-dihydropyrimidin-2-(1H)-ones
Bovine serum albumin (BSA) promoted simple
and efficient one-pot procedure was developed for the
direct synthesis of 3,4-dihydropyrimidin-2(1H)-ones
including potent mitotic kinesin Eg5 inhibitor monastrol
under mild reaction conditions. The catalyst recyclability
and gram scale synthesis have also been demonstrated to
enhance the practical utility of process
A method to overcome the waxy surface, cell wall thickening and polyphenol induced necrosis at wound sites - the major deterrents to Agrobacterium mediated transformation of bamboo, a woody monocot
The method is the first successful report of Agrobacterium
mediated genetic transformation of the commercially
important bamboo, Dendrocalamus hamiltonii. It
shows how the resistance provided by the somatic embryos
of this woody monocot can be overcome using a simple and
effective method. The method thus standardized can be also
used for the genetic transformation of other important
bamboos. Identification of the factors responsible for the
resistance of the somatic embryos to Agrobacterium infection
was an absolute requirement for devising a successful
method. Necrosis due to polyphenol oxidation, lack of differentiation
due to cell wall thickening at wound sites, waxy
surfaces of somatic embryos with anti-microbial properties
were found to prevent Agrobacterium attachment and infection.
Therefore, the somatic embryos were transformed with
fresh overnight grown Agrobacterium culture containing
500 mg/l polyvinylpyrrolidone (PVP) and 0.01 % Tween-
20 as surfactant followed by co-cultivation on Murashige
and Skoog (MS) medium containing the vir gene inducer
acetosyringone (100 μM) and 1 mg/l 6-Benzylaminopurine
BAP for 2 days. Persistent GUS expression and strong
positive signals in PCR, slot blot and Southern hybridization
confirmed successful genetic transformation
Synthesis and anti-angiogenic activity of benzothiazole, benzimidazole containing phthalimide derivatives
Benzothiazole and benzimidazole containing phthalimide derivatives (NK037, NK041, NK042, NK0139A
and NK0148) have been synthesized and their anti-angiogenic activity was evaluated using ex vivo egg
yolk angiogenesis model. A comparative study with pure thalidomide (NKTA) has also been performed to
describe the efficacy of these derivatives in blocking angiogenesis. NK037, NK041 and NK042 were
equally potent in blocking egg yolk angiogenesis and the anti-angiogenesis effect was higher than NKTA
suggesting the efficacy of these three derivatives in blocking angiogenesis when compare to control.
Other two derivatives NK0139A and NK0148 showed effect less than NKTA and stronger than control
in ex vivo angiogenesis
Zephgrabetaine: A New Betaine-type Amaryllidaceae Alkaloid from Zephyranthes grandiflora
Zephgrabetaine (1), a new betaine type Amaryllidaceae alkaloid, along with seven known alkaloids, lycorine, galanthine, lycoramine, hamayne,
haemanthamine, tortuosine, and ungeremine were isolated from the bulbs of Zephyranthes grandiflora and their structures elucidated by spectroscopic data
analysis. The isolated alkaloids were tested for in vitro cytotoxic activities against two cell lines, C-6 (rat glioma cells) and CHO-K1 (Chinese hamster ovary
cells). A dose dependent cytotoxic effect was exhibited by all the alkaloids on these two cancer cell lines with prominent activity of lycorine and
haemanthamine
Removal of Pb from Water by Adsorption on Apple Pomace: Equilibrium, Kinetics, and Thermodynamics Studies
The adsorption-influencing factors such as pH, dose, and time were optimized by batch adsorption study. A 0.8 g dose, 4.0 pH, and
80 min of contact time were optimized for maximum adsorption of Pb on AP. e adsorption isotherms (Langmuir and Freundlich)
were well fitted to the data obtained with values of max (16.39 mg/g; r2 = 0.985) and K (16.14 mg/g; r2 = 0.998), respectively. The
kinetics study showed that lead adsorption follows the pseudo-second-order kinetics with correlation coefficient (r2) of 0.999 for
all of the concentration range. FTIR spectra also showed that the major functional groups like polyphenols (–OH) and carbonyl
(–CO) were responsible for Pb binding on AP. The thermodynamic parameters as ΔG, ΔH (33.54 J/mol), and ΔS (1.08 J/mol/K)
were also studied and indicate that the reaction is feasible, endothermic, and spontaneous in nature
Synthesis and SAR investigation of natural phenylpropenederived methoxylated cinnamaldehydes and their novel Schiff bases as potent antimicrobial and antioxidant agents
A series of cinnamyl compounds were synthesized
from abundantly available methoxylated phenylpropenes
and evaluated for their antimicrobial activity by the
broth microdilution method against fourteen opportunistic
bacterial and fungal human pathogens. Structure–activity
relationship studies indicated that methylenedioxy cinnamaldehyde
exhibited promising broad-spectrum activity
against the tested microorganisms and hence was used as a
lead structure to synthesize novel Schiff bases/heterocyclic
compounds (23–33) under microwave irradiation. Out of
these, thiazole-based Schiff bases have shown promising
antibacterial activity against B. subtilis (26; MIC 0.12 mM),
M. luteus (27; MIC 0.20 mM), and S. aureus (27; MIC
0.20 mM). Also, the compounds 23–33 were investigated for
in vitro antioxidant activity using DPPH• assay where
compound 28 showed a maximum of 80.71 % inhibition