Evaluation of Populus deltoides clones under nursery,field and agrisilviculture system in subhumid tropics of Central India

Populus deltoides Bartr., a native of North America, is generally grown in India above latitude 28 °N. One hundred and six clones were evaluated for four years at Raipur situated at 21°12N latitude and 81°36E longitude. These were grown on vertisol soil. Based on growth and survival performance in the nursery for two successive years, nineteen clones were selected for field evaluation. The best five clones (G3, G48, 65/27, D121 and S7C1) were planted in an agrisilviculture system at a spacing of 4 × 4 m with soybean grown as an intercrop. After 4 years these clones had an increment of DBH by 66.5 to 77.5% and of height by 42.2 to 78.6% within one year when compared to that observed at 3 years of age. In rank order of growth the best five clones were 65/27 > G3 > D121 > G48 > S7C1. Total biomass varied between 20.9 to 35.8 Mg ha^–1 in different clones. Among the tree components, stemwood accounted for 52–61% of the total biomass, followed by branches (20–25%), bark (9–13%) and leaves (7–10%). No significant variation between net primary productivity and photosynthetic efficiency was found in different clones. Soybean productivity decreased as the trees aged, reaching 40.5 to 58.1% in 4-year-old trees.     

Establishment of Prosopis cineraria (L.) druce in the hot deserts of India

Prosopis cineraria (L.) Druce, commonly known as Jandi, is a deep rooted, nitrogen fixing, multipurpose tree endemic to the hot deserts of India. These trees are the essential component of the agroforestry land use system in these parts of India. The shade-intolerant tree reproduces poorly in nature and is difficult to propagate vegetatively. Germination up to 86.6% was observed after 15 days in seeds soaked in water at room temperature for 72 h. In another treatment, pouring of boiling water twice (at 0 and 6 h) over seeds and germinating after 12 h produced germination rates of 92.6%. Field establishment of containerized transplants in polythene bags (22×10 cm; 150 gauge) gave 90.3% survival after 6 months and 75.4% survival after 24 months. Seedlings were irrigated once during transplanting with 15 1 water. Bare root transplants and manual direct seeding after 6 months had a survival of 30.8 and 45.0%, respectively. Increased levels of nutrients (N, P and K), moisture content and organic carbon were observed under plantations as compared to open areas.     

Viability retention of seeds of shisham (Dalbergia sissoo Roxb.) on the trees after maturity

In 1991 and 1992 studies on Dalbergia sissoo Roxb. showed the availability of ample amount of viable seed from November to May. Viability of seeds collected from December to March was more than 90 per cent. There was a slight but significant decrease in germination from March to may. Again germination per cent was slightly and significantly decreased from May to July. Thereafter, seed availability and viability were got drastically reduced. Sufficient viable seed of Dalbergia sissoo Roxb. can be collected at any time from November to July.     

A functional and biochemical analysis of bovine class II MHC antigens using monoclonal antibodies

Monoclonal antibodies (MAbs) reacting with bovine (2) ovine (3), murine (1) or human (1) Class II MHC antigens were examined for reactivity with bovine peripheral blood leucocytes (PBL) and lymph node cells (LNC) by immunofluorescence, immunoprecipitation and the capacity to inhibit mixed lymphocyte responses (MLR), lectin- and antigen-induced blastogenesis. The 6 MAbs identified comparable percentages of Class II positive lymphocytes in PBL (40.8 to 54.2%) and LNC (6 to 11.5%) regardless of BoLA-A phenotype. Immunohistological staining of Class II MAb was localized principally to the lymphoid follicles in lymph nodes and to isolated epithelial reticular cells in the thymus. The anti-Class II MAb immunoprecipitated alpha- and beta- chains of 26-29K and 32-34K, respectively. These MAb inhibited proliferative responses in the MLR by between 25 and 74%, and diminished blastogenesis induced by specific antigens (purified protein derivative + PPD and ovalbumin) and B-lymphocyte mitogens (PPD, lipopolysaccharide and dextran sulphate) by between 45 and 75%, regardless of BoLA-A phenotype. In contrast, proliferation in response to concanavalin A and phytohaemagglutinin were unaffected by the anti- Class II MAb. Similarly these MAb did not affect lysis by cytotoxic T-lymphocytes, the activity of which was depressed by anti-Class I MAbs and monospecific alloantisera.     

Monoclonal antibodies to sheep MHC class I and class II molecules: biochemical characterization of three class I gene products and four distinct subpopulations of class II molecules

The availability of a panel of monoclonal antibodies to sheep MHC class I and class II gene products has allowed for the first time an assessment of the relative complexity of the sheep MHC. By using four monoclonal antibodies to MHC class I, and seven monoclonal antibodies to MHC class II molecules together with one-dimensional SDS-PAGE, sequential immunoprecipitation and 2-dimensional gel analysis, three class I gene products and four distinct subsets of class II molecules have been identified. Sheep class I molecules showed heterogeneity on 2-dimensional gels and as in mouse and man, represented the products of at least three different non-allelic class I genes. Interestingly, the sheep beta 2 microglobulin molecule also displayed heterogeneity, consistent with either two primary gene products or allelic variation. Four sheep class II monoclonal antibodies identified distinct, non-overlapping subsets of sheep class II molecules of Mr 32-36 K (alpha chain) and 25-28 K (beta chain). These class II molecules were co-expressed on sheep B lymphocytes and represented the primary products of different sheep MHC class II genes. The class II molecules within three of these subsets displayed allelic polymorphism essentially restricted to their beta polypeptides, while the fourth subset of class II molecules showed allelic variation in both their alpha and beta polypeptides. The results of this study represent the first evidence for gene duplication and heterogeneity within the sheep MHC. The identification of three primary class I gene products and four distinct subsets of class II molecules suggests three class I loci and up to four distinct class II subregions within the sheep MHC. Potentially large numbers of allelic variants of these different gene products may be expressed in normal sheep.     

Purification and Characterization of a Novel Alginate Lyase from a Marine Streptomyces Species Isolated from Seaweed

Alginate, a natural polysaccharide derived from brown seaweed, is finding multiple applications in biomedicine via its transformation through chemical, physical, and, increasingly, enzymatic processes. In this study a novel alginate lyase, AlyDS44, was purified and characterized from a marine actinobacterium, Streptomyces luridiscabiei, which was isolated from decomposing seaweed. The purified enzyme had a specific activity of 108.6 U/mg, with a molecular weight of 28.6 kDa, and was composed of 260 amino acid residues. AlyDS44 is a bifunctional alginate lyase, active on both polyguluronate and polymannuronate, though it preferentially degrades polyguluronate. The optimal pH of this enzyme is 8.5 and the optimal temperature is 45 °C. It is a salt-tolerant alginate lyase with an optimal activity at 0.6 M NaCl. Metal ions Mn²⁺, Co²⁺, and Fe²⁺ increased the alginate degrading activity, but it was inhibited in the presence of Zn²⁺ and Cu²⁺. The highly conserved regions of its amino acid sequences indicated that AlyDS44 belongs to the polysaccharide lyase family 7. The main breakdown products of the enzyme on alginate were disaccharides, trisaccharides, and tetrasaccharides, which demonstrated that this enzyme acted as an endo-type alginate lyase. AlyDS44 is a novel enzyme, with the potential for efficient production of alginate oligosaccharides with low degrees of polymerization.     

Population structure,genetic diversity,and sexual state of the rice brown spot pathogen Bipolaris oryzae from three Asian countries

Bipolaris oryzae causes brown spot in rice (Oryza sativa) inflicting substantial grain yield losses worldwide. Knowledge of the population structure, genetic diversity and sexual recombination of the fungal pathogen can help to implement effective disease management strategies. In this study, B. oryzae isolates sampled from Iran, the Philippines and Japan were analysed with 12 simple‐sequence repeat (SSR) markers, newly developed from the genome sequence of the fungus. Among the 288 B. oryzae isolates genotyped, 278 unique haplotypes were identified. High genotype numbers (richness) with even distribution (evenness) were found within the collection sites. Both mating types, MAT1‐1 and MAT1‐2, were present in each collection area, and the sexual state was induced under controlled conditions with production of viable ascospores. However, the tests of linkage disequilibrium rejected of the hypothesis of random mating. Discriminant analysis of principal components (DAPC) revealed that the B. oryzae collection formed three clusters, each consisting of isolates from different collection sites. Analysis of molecular variance (amova ) showed that genetic variation among clusters was 18.7%, with the rest of the variation distributed within clusters (R_ST = 0.187, P < 0.001). Statistically significant pairwise genetic differentiation was found between the clusters. These results show that Asian B. oryzae isolates are genetically diverse, and, overall, distributed in three groups. These findings will be helpful in managing the disease and guide the use of representative isolates needed for selection of resistant rice varieties.