Development of highly sprouting tolerant wheat germplasm with reduced germination at low temperature

The development of sprouting tolerant spring and winter wheat varieties that retain dormancy in cool, wet conditions is a long-term objective in Hokkaido, Japan. A highly tolerant spring dwarf line, “OS21-5”, derived from “Tordo” × “Zenkoji”, was used to develop transgressive spring, “OS38” and “OS74”; and winter, “OW77”, “OW104” and “OW93” wheats. More recently, winter lines with improved agronomic performance, though still deficient in quality and scab resistance, have been identified. In general, germination percentage of mature grain at 10 ^°C was closely related to the mean temperature experienced during the 5 days prior to maturity (dough–yellow ripening stage) and to the capacity to maintain a high amylograph paste viscosity. Dormancy at 10 ^°C appeared to be determined by a combination of genotype and variation in sensitivity to temperature during the later stages of ripening. Genotypes such as “OS38” and ‘OWl04’ were both highly tolerant to germination at 10 ^°C and insensitive to temperature during ripening. By comparison, most of the other cultivars showed a similar, intermediate sensitivity to ripening temperature, and dormancy decreased as ripening temperature increased. Dormancy of‘RL4137’ at maturity, and to a lesser extent ‘Gifukomugi’ and ‘KKI354’, was very sensitive to ripening temperature and useful levels of dormancy only developed under cool ripening temperatures, mean temperature < 18–20 ^°C.     

Plant cell walls as suppliers of potassium and sodium ions for induced resistance in pea (Pisum sativum L.) and cowpea (Vigna unguiculata L.)

When an elicitor is applied to plants to induce resistance, one of the first detectable events is the efflux of ions from the treated tissue. Here we are the first to demonstrate that an elicitor from Mycosphaerella pinodes evokes leakage of Na⁺ and K⁺ ions from isolated cell walls of pea and cowpea in vitro, as observed for epicotyl tissues. Pharmacological experiments showed that this elicitor-stimulated leakage was sensitive to vanadate and N-(3-methylphenyl)biphenyl-4-sulfonamide (NGXT-191), that inhibit a cell wall-associated ATPase (apyrase). Vanadate or NGXT-191 suppressed elicitor-induced superoxide generation and expression of defense genes in vivo. On the basis of these results, we assume that the leakage of these ions, probably associated with an ATP-dependent process(es) in the cell wall, is likely associated with induced defenses of pea and cowpea.     

Historical Profiles of Trace Element Concentrations in Mangrove Sediments from the Ba Lat Estuary,Red River,Vietnam

Historical profiles of trace element concentrations were reconstructed from two mangrove sediment cores collected within the Ba Lat Estuary (BLE), Red River, Vietnam. Chronologies of sediment cores were determined by the ²¹⁰Pb method, which showed that each respective sediment core from the south and north entrances of BLE provided a record of sediment accumulation spanning approximately 100 and 60 years. The profiles of Pb, Zn, Cu, Cr, V, Co, Sb, and Sn concentrations markedly increased from the years of the 1920s–1950s, and leveled out from 1950s–1980s, and then gradually decreased from 1980s to present. The profiles of Cd and Ag concentrations increased from 1920s–1940s, and then decreased from 1940s to present. The profile of Mo concentrations progressively increased from 1920s–1980s, then decreased to present. The Mn concentrations failed to show a clear trend in both sediment cores. Results from contamination factors, Pearson’s correlation, and hierarchical cluster analysis suggest that the trace elements were likely attributed to discharge of untreated effluents from industry, domestic sewage, as well as non-point sources. Pollution Load Index (PLI) revealed levels higher than other mangrove sediment studies, and the long-term variations in PLI matched significant socioeconomic shifts and population growth in Vietnam. Geoaccumulation Index showed that mangrove sediments were moderately polluted by Pb and Ag, and from unpolluted to moderately polluted by Zn, Cu, and Sb. The concentrations of Pb, Zn, Cu, Cr, and Cd exceeded the threshold effect levels and effect range low concentrations of sediment quality guidelines, implying that the sediments may be occasionally associated with adverse biological effects to benthic organisms.     

Optimization of the supplemental essential amino acids to a fish meal-free diet based on fermented soybean meal for rainbow trout <Emphasis Type="Italic">Oncorhynchus mykiss</Emphasis>

To minimize the supplemental essential amino acids (EAAs) to a fish meal-free diet for rainbow trout Oncorhynchus mykiss, four types of fish meal-free diets and a control fish meal-based diet were fed to triplicate groups of trout (initial BW, 16 g) for 10 weeks. Two fish meal-free diets based on a fermented and an unfermented soybean meal were unsupplemented with EAAs (diet FSBM and SBM), and two fish meal-free diets based on the fermented soybean meal were supplemented with a combination of lysine and methionine (diet F + ML) and all EAAs (diet F + All), the EAA contents of which were lower than those of the control diet (diet FM). Although physiological conditions such as the biliary bile acid status and morphological features of fish fed diet FSBM were improved and similar to those of fish fed diet FM, the growth performance was not significantly different (P > 0.05) from fish fed diet SBM. The growth performances and whole body protein contents of fish fed F + ML and F + All diets were similarly improved compared to fish fed diet FSBM. These findings indicate that supplementation of lysine and methionine to a fermented soybean meal-based fish meal-free diet is enough to maximize the amino acid utilization of the diet.     

Isolation and characterization of the rbcS genes from a sterile mutant of Ulva pertusa (Ulvales,Chlorophyta) and transient gene expression using the rbcS gene promoter

We isolated two different genomic DNAs (UprbcS1 and UprbcS2) encoding the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase and portions of the 5′- and 3′-flanking regions from sterile Ulva pertusa Kjellman. The UprbcS1 and UprbcS2 genes had three introns in the coding region. Each predicted UprbcS polypeptide was a 180-amino-acid (AA) residue including a 38-AA transit peptide, although the 104th AA residue was replaced. The nucleotide sequences of UprbcS cDNAs isolated from a cDNA library corresponded to that of the UprbcS1 gene, suggesting that the UprbcS1 gene was predominantly expressed in sterile U. pertusa compared to UprbcS2. Southern blot analysis showed that each UprbcS gene was a single-copy gene in the sterile U. pertusa genome. Northern hybridization indicated that the expression of UprbcS was induced and repressed by dark and light treatments, respectively. When sterile U. pertusa cells were transformed with an expression vector containing the UprbcS1 promoter and terminator sequences fused with the green fluorescent protein (GFP) gene, GFP fluorescence was observed in the cells transformed. These results suggest that the UprbcS1 gene promoter is light regulated and highly active in the sterile U. pertusa cells and is available for genetic transformation system in the alga.     

Purification and characterization of lipovitellin from Pacific saury Cololabis saira

ABSTRACT:   Lipovitellin (Lv), the major yolk protein derived from vitellogenin (Vg), was purified from vitellogenic ovaries of Pacific saury Cololabis saira using hydroxylapatite column chromatography followed by gel filtration. The apparent native mass of purified Lv was approximately 420 kDa, while the tertiary structure of Lv revealed by sodium dodecylsulfate–polyacrylamide gel electrophoresis was typical of teleost Lvs, consisting of a heavy chain (∼99 kDa) and a light chain (∼34 kDa). Western blot analysis using rabbit antiserum raised against Pacific saury Lv revealed a specific reaction with a polypeptide (∼194 kDa) that is present in serum from female Pacific saury but not in male serum, suggesting the approximately 194-kDa polypeptide to be the Vg monomer. This study describes the first step toward the development of specific immunoassays for Pacific saury Vg, which will be an effective tool for monitoring the reproductive development of this species.     

GnRH systems in masu salmon and barfin flounder

Multiple forms of the gonadotropin-releasing hormone (GnRH) exist in teleost fish. A salmonid fish, masu salmon Oncorhynchus masou has salmon GnRH (sGnRH) and chicken GnRH-II (cGnRH-II). sGnRH neurons were scattered from the olfactory nerve through the ventral telencephalon (VT) and the preoptic area (POA). sGnRH but not cGnRH-II was detected in the pituitary. sGnRH mRNA levels in the VT and the POA increased during gonadal maturation, suggesting that sGnRH neurons in these areas are involved in gonadal maturation. sGnRH neurons were first detected in a cluster near the olfactory epithelium 40 days after fertilization. sGnRH neurons were not detected in the brain by the olfactory epithelia lesion, suggesting that sGnRH neurons are derived from the olfactory epithelium. A pleuronectiform fish, barfin flounder Verasper moseri has sGnRH, cGnRH-II and seabream GnRH (sbGnRH). sGnRH and cGnRH-II-immunoreactive fibers were observed throughout the brain, but not in the pituitary. sbGnRH neurons were located in the POA and sent fibers to the pituitary, indicating that sbGnRH is involved in GTH secretion. Judging from the location of neuronal somata and their projections, it is indicated that three GnRH systems exist in the barfin flounder; the TN-, the MT- and the POA-GnRH system. However, in masu salmon, clear anatomical identification of the TN- and the POA-GnRH system is difficult, because the GnRH neurons located in the ventral forebrain are consecutive and the GnRH form produced in these neurons is the same (sGnRH). Thus, it is suggested in masu salmon that sGnRH neurons are derived from the olfactory epithelium, migrate into the brain and play different roles according to the location in the brain.