Production of nickel bio-ore from hyperaccumulator plant biomass: applications in phytomining

An important step in phytomining operations is the recovery of metal from harvested plant material. In this work, a laboratory-scale horizontal tube furnace was used to generate Ni-enriched bio-ore from the dried biomass of Ni hyperaccumulator plants. Prior to furnace treatment, hairy roots of Alyssum bertolonii were exposed to Ni in liquid medium to give biomass Ni concentrations of 1.9% to 7.7% dry weight; whole plants of Berkheya coddii were grown in Ni-containing soil to produce above-ground Ni levels of up to 0.49% dry weight. The concentration of Ca in the Ni-treated B. coddii biomass was about 15 times greater than in A. bertolonii. After furnace treatment at 1200 degrees C under air, Ni-bearing residues with crystalline morphology and containing up to 82% Ni were generated from A. bertolonii. The net weight loss in the furnace and the degree of concentration of Ni were significantly reduced when the furnace was purged with nitrogen, reflecting the importance of oxidative processes in Ni enrichment. Ni in the B. coddii biomass was concentrated by a factor of about 17 to yield a residue containing 8.6% Ni; this bio-ore Ni content is substantially higher than the 1% to 2% Ni typically found in mined ore. However, the B. coddii samples after furnace treatment also contained about 34% Ca, mainly in the form of hydroxyapatite Ca(5)(PO(4))(3)OH. Such high Ca levels may present significant challenges for further metallurgical processing. This work demonstrates the feasibility of furnace treatment for generating Ni-rich bio-ore from hyperaccumulator plants. The results also suggest that minimizing the uptake of Ca and/or reducing the Ca content of the biomass prior to furnace treatment would be a worthwhile strategy for improving the quality of Ni bio-ore produced in phytomining operations.     

Perch Associated Expression of Phenotypic Plasticity in Limb Development and Sprint Speed in Agamid Lizard Calotes versicolor: A Laboratory Study

New born hatchlings of Calotes versicolor were reared in terrarium having narrow or wide perches for a period of 4-month and their snout vent length(SVL), tail, fore and hindlimb lengths were measured at monthly intervals. Limb postures(closer to the body or spread away from the body) were also recorded. The sprint speed was recorded in two and four-month old lizards on a 1 m long race track providing 45° or 60° slope. In both the groups, SVL and tail lengths were comparable but the limb lengths and their growth rates were significantly greater in lizards of wider perch group. The lizards reared with narrow perches positioned their limbs closer to the body; while those reared on wider perches spread their limbs away from their body. Further, the latter exhibited significantly higher sprint speed regardless of the slope of the race track over those of narrow perch group. Sprint speeds of lizards in both groups were correlated with the limb sizes. The study showed that the lizards reared on narrow or wide perches exhibited divergent adaptive responses(phenotypic plasticity) by developing longer or shorter limbs and corresponding changes in their sprint speeds. These findings support the idea that availability of perch structure during early development evokes adaptive plasticity in the limb development and associated locomotory performance in arboreal lizards like C. versicolor.     

Association between presence of <Emphasis Type="Italic">Triticum timopheevii</Emphasis> introgression and D-genome retention in hexaploid/tetraploid wheat crosses

The 2G Triticum timopheevii introgression harbours genes for multiple disease resistance and quality traits in bread wheat. In order to transfer this segment from bread wheat into durum, the bread wheat line Sunguard, which carries this introgressed 2G segment was crossed with three tetraploid durum parents. A significant difference was observed in the segregation ratio of the 2G segment in the different crosses at the F₂ generation with two of the three populations indicating segregation distortion against the hexaploid 2G segment. In these populations, the presence of the 2G segment was strongly correlated with the presence of D-genome chromosomes. These results were confirmed in the F₄ generation of these populations. Six plants were identified in the F₄ generation, which had retained the introgressed 2G segment in a homozygous condition and did not have a complete D-genome set. Two of these lines only had two non-homologous D-genome chromosomes in the F₅ generation. Thus, the 2G segment and possibly other translocations can be transferred into durum wheat through hexaploid/tetraploid hybridisation.     

<Emphasis Type="Italic">In vitro</Emphasis> shoot regeneration and enhanced synthesis of plumbagin in root callus of <Emphasis Type="Italic">Plumbago zeylanica</Emphasis> L.—an important medicinal herb

Plumbago zeylanica L., an important medicinal herb, possesses plumbagin, a valuable secondary metabolite. Roots of this plant, collected from four locations in Himachal Pradesh, India, were screened for plumbagin content with high-performance liquid chromatography. The chemotype collected from Hamirpur yielded the highest content (26.47?±?0.63 mg g^?1 dry weight). Callus cultures were established from nodal explants of this chemotype on Murashige and Skoog (MS) medium augmented with α-naphthaleneacetic acid (NAA), indole-3-butyric acid (IBA), 2,4-dichlorophenoxyacetic acid, (2,4-D), 6-benzyladenine (BA), isopentenyl adenine (2iP), or thidiazuron, (TDZ). After 45 d, 98% of the cultures induced bright-green, compact callus on MS?+?5 μM TDZ. Upon subculturing, this callus differentiated an average of 4.08?±?1.16 shoots in 62.5% of the cultures. After elongation on basal MS medium, excised shoots were transferred to indole-3-acetic acid, NAA, or IBA supplemented MS medium. A maximum of 4.3?±?1.36 roots with an average length of 15.31?±?2.76 cm were recorded on 5 μM IBA. Rooted plantlets were successfully acclimatized in a greenhouse, and their genetic fidelity was evaluated using inter simple sequence repeats and start codon targeted molecular markers, which revealed 97% similarity. A significant increase in plumbagin content (6.5- and 3.4-fold) was achieved in root callus employing 100 mg L^?1 yeast extract (YE) and 25 μM salicylic acid (SA), respectively. This is the first report of large-scale propagation of P. zeylanica and an increase of plumbagin through in vitro root callus.     

CD39 overexpression does not attenuate renal fibrosis in the unilateral ureteric obstructive model of chronic kidney disease

Chronic kidney disease has multiple etiologies, but its single, hallmark lesion is renal fibrosis. CD39 is a key purinergic enzyme in the hydrolysis of ATP and increased CD39 activity on regulatory T cells (Treg) is protective in adriamycin-induced renal fibrosis. We examined the effect of overexpression of human CD39 on the development of renal fibrosis in the unilateral ureteric obstructive (UUO) model, a model widely used to study the molecular and cellular factors involved in renal fibrosis. Mice overexpressing human CD39 (CD39Tg) and their wild-type (WT) littermates were subjected to UUO; renal histology and messenger RNA (mRNA) levels of adenosine receptors and markers of renal fibrosis were examined up to 14 days after UUO. There were no differences between CD39Tg mice and WT mice in the development of renal fibrosis at days 3, 7, and 14 of UUO. Relative mRNA expression of the adenosine A_2A receptor and endothelin-1 were higher in CD39Tg than WT mice at day 7 post UUO, but there were no differences in markers of fibrosis. We conclude that human CD39 overexpression does not attenuate the development of renal fibrosis in the UUO model. The lack of protection by CD39 overexpression in the UUO model is multifactorial due to the different effects of adenosinergic receptors on the development of renal fibrosis.     

Purification, properties and synthesis of delta-aminolaevulinate dehydratase from Neurospora crassa.

Delta-aminolaevulinate dehydratase, the second and rate-limiting enzyme of the haem-biosynthetic pathway, was purified 300-fold from induced cultures of Neurospora crassa. The native enzyme has a mol.wt. of about 350000, whereas the salt-treated enzyme after incubation at 37 degrees C for 10 min has a mol.wt. of about 232000. The mol.wt. of the subunit is about 38000. Antibodies to the purified enzyme were raised in rabbits. By using radiolabelling and immunoprecipitation techniques it was shown that addition of iron and laevulinate to iron-deficient cultures brings about a significant increase in the synthesis of the enzyme, and protoporphyrin, the penultimate end product of the pathway, represses enzyme synthesis.     

Biochemical effects of the porphyrinogenic drug allylisopropylacetamide. A comparative study with phenobarbital

Successive administrations of allylisopropylacetamide, a potent porphyrinogenic drug, increase liver weight, microsomal protein and phospholipid contents. There is an increase in the rate of microsomal protein synthesis in vivo and in vitro. The drug decreases microsomal ribonuclease activity and increases NADPH-cytochrome c reductase activity. Phenobarbital, which has been reported to exhibit all these changes mentioned, is a weaker inducer of delta-aminolaevulinate synthetase and increases the rate of haem synthesis only after a considerable time-lag in fed female rats, when compared with the effects observed with allylisopropylacetamide. Again, phenobarbital does not share the property of allylisopropylacetamide in causing an initial decrease in cytochrome P-450 content. Haematin does not counteract most of the biochemical effects caused by allylisopropylacetamide, although it is quite effective in the case of phenobarbital. Haematin does not inhibit the uptake of [2-(14)C]allylisopropylacetamide by any of the liver subcellular fractions.