Registration of ‘Serenut 5R’ Groundnut

‘Serenut 5R’ (Reg. No. CV-129, PI 676092) is a new high-yielding, spanish-type groundnut (Arachis hypogaea L. subsp. fastigiata var. vulgaris) with two seeds per pod. Serenut 5R was released in 2010 by the National Semi-Arid Resources Research Institute, Soroti, Uganda. It was a selection from the ICRISAT advanced line ICGV-SM 93535. Serenut 5R originated from a cross made between ICGM 522 and ‘RG 1’. ICGV-SM 93535 was developed by using repeated bulk selections for groundnut rosette disease resistance, using the infector row technique at the ICRISAT-Malawi research station. Performance tests in replicated trials were performed in Uganda in 2008 and 2009. Trials were performed in two seasons each year and averaged over 10 rainfed locations in Uganda. Serenut 5R matures in 100 to 110 d, similar to the widely grown control cultivar Serenut 3R. Serenut 5R resulted in significantly higher pod yields (16%) than Serenut 3R, and the shellout percentage for Serenut 5R was 4.8% higher than Serenut 3R. Seed testa is red, and the seeds are slightly larger than those of Serenut 3R. The sound mature kernel count for Serenut 5R was 38.7 g 100−1 compared with 32.38 g 100−1 for Serenut 3R, an increase of 19.51%. The dormancy period for Serenut 5R was significantly less than Serenut 3R

Registration of ICG 12991 peanut germplasm line

ICG 12991 is a short duration (90–110 d to maturation), drought-tolerant, spanish-type peanut (Arachis hypogaea L. subsp. fastigiata Waldron var. vulgaris Harz.) germplasm line (Reg. no. GP-122, PI 639691) with a high level of field resistance to groundnut rosette disease (Naidu et al., 1999a; Subrahmanyam et al., 2000). Groundnut rosette disease results from a synergism of three agents: Groundnut rosette assistor virus (GRAV, a luteovirus), Groundnut rosette virus (GRV, an umbravirus), and a satellite RNA (sat RNA) of GRV. ICG 12991 was originally collected from a farmer’s field in south India in 1988. In 1994, ICRISAT introduced ICG 12991 into Malawi for evaluation during a germplasm screening program for resistance to groundnut rosette disease and early leaf spot disease (caused by Cercospora arachidicola S. Hori). Subsequently, ICG 12991 was released in Malawi as ‘Baka’ in 2001 and in Uganda as ‘Serenut 4T’ in 2002, following extensive testing and distribution by the national programs of each country. Resistance to groundnut rosette disease in ICG 12991 is due to aphid resistance, not due to resistance to the virus complex (Naidu et al., 1999b)

Recent advances and perspectives on starch nanocomposites for packaging applications

Starch nanocomposites are popular and abundant materials in packaging sectors. The aim of this work is to review some of the most popular starch nanocomposite systems that have been used nowadays. Due to a wide range of applicable reinforcements, nanocomposite systems are investigated based on nanofiller type such as nanoclays, polysaccharides and carbonaceous nanofillers. Furthermore, the structures of starch and material preparation methods for their nanocomposites are also mentioned in this review. It is clearly presented that mechanical, thermal and barrier properties of plasticised starch can be improved with well-dispersed nanofillers in starch nanocomposites

Influence of yeasts and of their constituents on nucleoside uptake in peritoneal murine macrophages

A marked reduction of [3H]-uridine uptake was observed when mouse peritoneal macrophages (pM phi) were exposed to heat-killed Candida albicans or Saccharomyces cerevisiae. By contrast, an increased nucleoside uptake was promoted by yeast products such as zymosan, laminarin, or yeast cell-wall extracts, which are mainly composed of beta-glucans and alpha-mannans. In a search for the active fungal component(s), the uptake process was shown to be differently affected by monosaccharides and polysaccharides. These findings support the view that a specific recognition of a pM phi membrane receptor is mediating the effect of the various substances

Nucleoside uptake in macrophages from various murine strains: a short-time and a two-step stimulation model

Kinetics of [3H]-uridine uptake by murine peritoneal macrophages (pM phi) is early altered after exposure to a variety of stimuli. Alterations caused by Candida albicans, lipopolysaccharide (LPS) and recombinant interferon-gamma (rIFN-gamma) were similar in SAVO, C57BL/6, C3H/HeN and C3H/HeJ mice, and were not correlated with an activation process as shown by the amount of tumor necrosis factor-alpha (TNF-alpha) being released. Short-time exposure to all stimuli resulted in an increased nucleoside uptake by SAVO pM phi, suggesting that the tumoricidal function of this cell either depends from the type of stimulus or the time when the specific interaction with the cell receptor is taking place. Experiments with priming and triggering signals confirmed the above findings, indicating that the increase or the decrease of nucleoside uptake into the cell depends essentially on the chemical nature of the priming stimulus. The triggering stimulus, on the other hand, is only able to amplify the primary response