Community structure of pollinating insects and its driving factors in different habitats of Shivapuri‐Nagarjun National Park,Nepal

Insect pollinators are important means for a stable ecosystem. The habitat types play a crucial role in the community composition, abundance, diversity, and species richness of the pollinators. The present study in Shivapuri‐Nagarjun National Park explored the species richness and abundances of insect pollinators in four different habitats and different environmental variables in determining the community composition of the pollinators. Data were collected from 1,500 m to 2,700 m using color pan traps and hand sweeping methods. Non‐Metric Multidimensional Scaling (NMDS) and Redundancy Analysis (RDA) were conducted to show the association between insect pollinators and environmental variables. The results firmly demonstrated that species richness and abundances were higher (158) in Open trail compared to other habitats. The distribution of the pollinator species was more uniform in the Open trail followed by the Grassland. Similarly, a strong positive correlation between flower resources and pollinators'' abundance (R² = .63, P < .001) was found. In conclusion, the Open trail harbors rich insect pollinators in lower elevation. The community structure of the pollinators was strongly influenced by the presence of flowers in the trails.     

Design and synthesis of 1,3-biarylsulfanyl derivatives as new anti-breast cancer agents

A new series of 1,3-biarylsulfanyl derivatives (homodibenzyl core motif) have been designed and synthesized as new estrogen receptor ligands by chopping benzothiophene core of raloxifene to engender seco-raloxifene scaffold. All the synthesized compounds were screened for anti-proliferative, anti-osteoporotic, and anti-implantation activity. Compounds (35, 36) having basic amino anti-estrogenic side chain were exhibiting potential anti-proliferative activity in MCF-7, MDA-MB-231 and ishikawa cell lines. Some of the synthesized compounds having homodibenzyl motif (5, 8, 10) have shown moderate anti-osteoporotic activity.     

Tree legumes as feedstock for sustainable biofuel production: Opportunities and challenges

Concerns about future fossil fuel supplies and the environmental effects of their consumption have prompted the search for alternative sources of liquid fuels, specifically biofuels. However, it is important that the sources of such biofuel have minimal impact on global food supplies, land use, and commodity prices. Many legume trees can be grown on so-called marginal land with beneficial effects to the environment through their symbiotic interaction with “Rhizobia” and the associated process of root nodule development and biological nitrogen fixation. Once established legume trees can live for many years and some produce an annual yield of oil-rich seeds. For example, the tropical and sub-tropical legume tree Pongamia pinnata produces large seeds (∼1.5-2 g) that contain about 40% oil, the quality and composition of which is regarded as highly desirable for sustainable biofuel production. Here we consider the benefits of legume trees as future energy crops, particularly in relation to their impact on nitrogen inputs and the net energy balance for biofuel production, and also ways in which these as yet fully domesticated species may be further improved for optimal use as biofuel feedstock.     

Discovery of 6-ethyl-2,4-diaminopyrimidine-based small molecule renin inhibitors

Novel 2,4-diaminopyrimidine-based small molecule renin inhibitors are disclosed. Through high throughput screening, parallel synthesis, X-ray crystallography, and structure based drug design, we have developed the first non-chiral, non-peptidic, small molecular template to possess moderate potency against renin. The designed compounds consist of a novel 6-ethyl-5-(1,2,3,4-tetrahydroquinolin-7-yl)pyrimidine-2,4-diamine ring system that exhibit moderate potency (IC(50): 91-650 nM) against renin while remaining 'Rule-of-five' compliant.     

High Yield Expression of Recombinant Human Proteins with the Transient Transfection of HEK293 Cells in Suspension

The art of producing recombinant proteins with complex post-translational modifications represents a major challenge for studies of structure and function. The rapid establishment and high recovery from transiently-transfected mammalian cell lines addresses this barrier and is an effective means of expressing proteins that are naturally channeled through the ER and Golgi-mediated secretory pathway. Here is one protocol for protein expression using the human HEK293F and HEK293S cell lines transfected with a mammalian expression vector designed for high protein yields. The applicability of this system is demonstrated using three representative glycoproteins that expressed with yields between 95-120 mg of purified protein recovered per liter of culture. These proteins are the human FcγRIIIa and the rat α2-6 sialyltransferase, ST6GalI, both expressed with an N-terminal GFP fusion, as well as the unmodified human immunoglobulin G1 Fc. This robust system utilizes a serum-free medium that is adaptable for expression of isotopically enriched proteins and carbohydrates for structural studies using mass spectrometry and nuclear magnetic resonance spectroscopy. Furthermore, the composition of the N-glycan can be tuned by adding a small molecule to prevent certain glycan modifications in a manner that does not reduce yield.     

Breeding habitat and nest-site selection of Bearded Vulture Gypaetus barbatus in the Annapurna Himalaya Range of Nepal

Quantitative studies on nesting habitat selection are important to understand and predict the resource requirements for breeding habitat. In this study, we analysed nest-site (cliff) and territory selection patterns of the Bearded Vulture in the Annapurna Range of the Himalayas (Nepal). Our study area represents high-elevation mountain range systems, where information on nest selection is lacking, despite having the largest remaining populations of Bearded Vultures in the world. Our models indicated selection patterns at both nest and territory spatial scales that are consistent with previous studies at lower altitudes (Pyrenees, the Caucasus), such as a preference for landscape patches with greater food availability. However, our models also indicated selection patterns that are probably a response to the higher altitudes and sheer reliefs of the Annapurna massif, such as avoidance of the steepest slopes and selection of cliffs facing south and west for nest-sites. We did not detect an impact of human activities on the distribution of nests or territories. However, the Annapurna massif is experiencing development of infrastructures (e.g. road construction). Further research efforts will be needed to monitor human impacts on Bearded Vulture populations in the Annapurna Range, as this is a global stronghold for this species.     

Biochemical analysis and structure determination of Paucimonas lemoignei poly(3‐hydroxybutyrate) (PHB) depolymerase PhaZ7 muteins reveal the PHB binding site and details of substrate–enzyme interactions

Five amino acids (Y105, Y176, Y189, Y189, W207) that constitute the substrate binding site of PHB depolymerase PhaZ7 were identified. All residues are located at a single surface‐exposed location of PhaZ7. Exchange of these amino acids by less hydrophobic, hydrophilic or negatively charged residues reduced binding of PhaZ7 to PHB. Modifications of other residues at the PhaZ7 surface (F9, Y66, Y103, Y124, Y169, Y172, Y173, F198, Y203, Y204, F251, W252) had no effect on substrate binding. The PhaZ7 wild‐type protein, three muteins with single amino acid exchanges (Y105A, Y105E, Y190E), a PhaZ7 variant with deletion of residues 202–208, and PhaZ7 in which the active‐site serine had been replaced by alanine (S136A) were crystallized and their structures were determined at 1.6–2.0 Å resolution. The structures were almost identical but revealed flexibility of some regions. Structural analysis of PhaZ7 (S136A) with bound 3‐hydroxybutyrate tetramer showed that the substrate binds in a cleft that is composed of Y105, Y176, Y189 and Y190 and thus confirmed the data obtained by site‐directed mutagenesis. To the best of our knowledge this is the first example in which the substrate binding site of a PHB depolymerase is documented at a molecular and structural level.