Successful long term culture of immature porcine sertoli cells in the reconstructed testicular cell cord

The ultimate goal of this study was to establish an in vitro system to produce sperms. To pursue this goal, immature porcine testicular cells were cultured in stereostructural form and cultured testicular cord was investigated morphologically. At 4 weeks of age, the seminiferous tubules of the porcine testes consisted of undifferentiated germ cells (gonocytes and undifferentiated spermatogonia) and immature Sertoli cells. The interstitial tissue was largely occupied by Leydig cells. The testes were enzymatically digested, and the dispersed cells were encapsulated with alginate either immediately or after freeze-thawing. The resulting testicular cell cords were cultured for up to 10 weeks. After 2 weeks of culture, Sertoli cells, which were identified by their inhibin-positive reaction in immunohistochemistry, and Leydig cells, which were identified by their morphological characteristics, were observed in the cords. Neither undifferentiated nor differentiated types of germ cells were detected. The number of cells in the cords progressively decreased during the culture period. In order to discover the fate of the Sertoli cells, the level of inhibin in the spent media was determined. Inhibin in the media was at a detectable level after 2 days of culture. The levels increased and peaked at 2 weeks. When frozen-thawed testicular cells were applied to the culture, the peak level was maintained for over 8 weeks, in contrast to the gradual decrease of inhibin level when fresh cells were cultured. These results indicate that the culture conditions can sustain the survival of Sertoli cells. Further improvement is required for proliferation and differentiation of germ cells.     

Synthesis of self-pillared zeolite nanosheets by repetitive branching

Hierarchical zeolites are a class of microporous catalysts and adsorbents that also contain mesopores, which allow for fast transport of bulky molecules and thereby enable improved performance in petrochemical and biomass processing. We used repetitive branching during one-step hydrothermal crystal growth to synthesize a new hierarchical zeolite made of orthogonally connected microporous nanosheets. The nanosheets are 2 nanometers thick and contain a network of 0.5-nanometer micropores. The house-of-cards arrangement of the nanosheets creates a permanent network of 2- to 7-nanometer mesopores, which, along with the high external surface area and reduced micropore diffusion length, account for higher reaction rates for bulky molecules relative to those of other mesoporous and conventional MFI zeolites.     

Methionine Requirement of Juvenile Japanese Flounder Paralichthys olivaceus

Abstract.— Growth studies were conducted to determine the dietary methionine requirement of juvenile Japanese flounder Paralichthys olivaceus . A basal diet was formulated to contain 50% crude protein from casein and gelatin, as intact protein sources, supplemented with crystalline L-amino acids (CAA), to correspond to the amino acid pattern found in the whole body protein of the juvenile Japanese flounder, except methionine. Test diets contained six graded levels of L-methionine 0.53, 0.83, 1.13, 1.43, 1.73, and 2.03% of diet (dry matter basis) or 1.06, 1.66, 2.26, 2.86, 3.46 and 4.06% of protein. To prevent leaching losses of water-soluble amino acids, CAA were pre-coated with carboxymethylcellulose (CMC), and diets were further bound with both CMC and κ-carrageenan after addition of the pre-coated CAA. Weighing about 2.80 g, each triplicate group of the juvenile flounder were fed test diets twice a day (5% of body weight) for 40 d. Survival rate, specific growth rate, feed conversion efficiency and apparent protein retention were significantly ( P < 0.05) affected by dietary methionine concentrations. The optimum dietary level of methionine in the presence of 0.06% of dietary cystine for Japanese flounder juvenile was estimated by using break point analysis. The values determined based on weight gain and feed efficiency were 1.49% of diet (or 2.98% of protein) and 1.44% of diet (or 2.88% of protein), respectively. These requirement values are close to the methionine level of flounder whole body protein.     

Optimum Dietary Level of L-ascorbic Acid for Japanese Eel, Anguilla japonica

A feeding experiment was conducted to determine the optimum dietary level of ascorbic acid (AsA) for Japanese eel juveniles using L-ascorbic acid Ca based on growth, AsA content in tissues, hematology, and bactericidal activity of serum with Escherichia coli . Test diets with six levels of AsA (3, 10, 27,126, 645, and 3,135-mg/kg diet) as Ca ascorbate were fed to juvenile Japanese eels (11.0 ± 0.2 g) once a day for 8 wk. High survival rates (> 80%) were observed among all dietary treatment groups. The specific growth rates of the fish fed diets containing 3 and 10-mg AsA/kg were significantly (P < 0.05) lower than those of other groups. Liver and brain AsA contents of the fish fed diets containing 3, 10, and 27-mg AsA/kg were significantly (P < 0.05) lower than those of the fish fed diets containing 645 and 3,135-mg AsA/kg. Hemoglobin content tended to be higher in the fish fed diets containing 645 and 3,135-mg AsA/kg than those of the fish fed other diets. Hematocrit value and total serum protein content of the fish fed diets containing 645 and 3135 mg AsA/kg were significantly (P < 0.05) higher than those of the other groups. The fish fed diets containing more than 27-mg AsAlkg showed a higher bactericidal activity of serum than the fish fed the diets containing 3-mg and 10-mg AsA/kg. The optimum dietary level of AsA for the Japanese eel juveniles growth was estimated to be more than 27-mg AsA/kg. Furthermore, the inclusion of 645-mg AsA/kg or more also increased the hematocrit, hemoglobin, total serum protein value, and liver and brain vitamin C concentrations.     

Biochemical properties of the cell wall in the Arabidopsis mutant bor1‐1 in relation to boron nutrition

We examined concentrations of boron (B) and dimerization of rhamnogalacturonan II (RG‐II), a B‐binding polysaccharide, in the cell wall of a low‐B sensitive mutant of Arabidopsis thaliana, bor1‐1, to investigate possible effects of the bor1‐1 mutation on the biochemical form of pectins in the cell wall. In the bor1‐1 mutant, B concentrations in the cell wall from shoots were lower than those in the wild type at low B supply, whereas they were similar at sufficient B supply. The amount of B present as borate ester of the RG‐II dimer (dRG‐II‐B) in the bor1‐1 mutant was lower than that in the wild type at low B supply. In the wild type, about 90 % of RG‐II was present as dRG‐II‐B, both, at low and sufficient B supply. In the bor1‐1 mutant, about 60 % of RG‐II was in its monomeric form (mRG‐II) at low B supply, whereas more than 85 % of it was present as dRG‐II‐B at sufficient B supply. However, similar as the wild type, mRG‐II derived from the bor1‐1 mutant was able to form dRG‐II‐B in vitro in the presence of borate and lead. Sugar composition of cell wall fractions was similar in both genotypes. These results suggest that the polysaccharide composition in the cell wall was not strongly affected by the bor1‐1 mutation. The observed difference in dimerization of RG‐II at low B supply is most likely due to a reduced B concentration in the shoots of the bor1‐1 mutant.     

Introduction of Yeast Metallothionein Gene (CUP1) into Plant and Evaluation of Heavy Metal Tolerance of Transgenic Plant at the Callus Stage

For phytoremediation, it is necessary to use plants with a large biomass and ability to absorb and accumulate heavy metals. Attempts were made to produce heavy metal-tolerant plants by introducing a metallothionein gene, CUP 1, into plants with a large biomass. In the present study, we evaluated the heavy metal tolerance of sunflower plants at the callus stage in terms of 2,3,5-triphenyl-tetrazolium chloride (TTC)-reducing activity, measured the mRNA expression level of the introduced gene, and selected tolerant clones. The transgenic calli of several strains showed a high TTC-reducing activity even after treatment with Cd 200 μM for 10 d. In the transgenic calli of a few strains, which showed a low TTC-reducing activity, the amount of metallothionein was lower than that in the other transgenic strains. Conversely, some transgenic calli with a high TTC-reducing activity expressed a much higher amount of mRNA of the introduced gene.     

Intrinsic Biodegradation of Heavy Oil from Nakhodka and the Effect of Exogenous Fertilization at a Coastal Area of the Sea of Japan

We performed a field experiment in thebiodegradation of heavy oil spilled from the Russian tankerNakhodka on a beach in the Sea of Japan. We collectedoil-contaminated cobbles and treated half with nitrogen andphosphorus slow-release fertilizers to stimulate microbialdegradation of the oil; the other half acted as unfertilizedcontrols. The cobbles were placed in porous acrylic vessels andsubmerged. We monitored changes in the oils, macronutrients,microbial community structure and amount of chlorophyll a. There were no significant differences in these criteriabetween the fertilized and unfertilized vessels, apart from anincrease in chlorophyll a in the fertilized vessels.However, there was a major intrinsic degradation of semi-volatile oil compounds in the unfertilized vessels; this occurred at a rate similar to that in the fertilized vessels, despite the low concentration of macronutrients in the seawater at the site.     

Induction of short-term pseudopregnancy in gilts by the administration of estradiol benzoate or estradiol dipropionate to achieve ovulatory synchronization for embryo collection

A study was conducted to investigate whether ovulation in gilts could be synchronized for embryo collection by the administration of estradiol benzoate (EB) or estradiol dipropionate (EDP) to induce pseudopregnancy, followed by the treatment with prostaglandin F_2α (PGF_2α) on 10 days after. Ten gilts each received a total of 20 mg of EB or EDP on Day 10 or EB on Day 10 and 14 to induce pseudopregnancy (Day 0 = onset of estrus). Donors received PGF_2α 10 or 15 days (as a control) after the first administration of estrogens and subsequently eCG and hCG, and were then inseminated artificially. The embryos were collected 7 days after the administration of hCG, and assessed for embryo yield and their developmental stages. All protocols resulted in good embryo yield (9.8–13.2 embryos in average), and the embryos showed average ability to develop to the expanded blastocyst stage (3.29–4.03 as developmental scores) without any significant differences among the protocols. These results suggest that the administration of PGF_2α 10 days after the treatment of gilts with EB or EDP would allow synchronization of ovulation and embryo collection, as well as shortening the period from estrus detection to embryo collection, thus improving embryo collection efficiency.     

Excess polyspermy reduces the ability of porcine oocytes to promote male pronuclear formation after in vitro fertilization

Male pronucleus (MPN) formation is a very important physiological event during fertilization, which affects in vitro production of transferrable embryos. The aim of this study was to find out the correlation between the number of penetrated sperm and the occurrence of failure of MPN formation in porcine oocytes. In vitro matured porcine oocytes were fertilized in vitro with frozen epididymal sperm. Two different frozen sperm lots were tested in this study, which were different in terms of polyspermy rates. The numbers and the status of penetrated sperm in oocytes were evaluated 10 h after insemination. Under high polyspermy condition, the polyspermy rate was 83.5% with an average mean of 3.5 sperms per penetrated oocyte, whereas the percentage of polyspermy was 65.5% with an average mean of 2.4 sperms per penetrated oocyte under moderate polyspermic condition. Correlation analysis revealed a negative correlation between the number of penetrated sperm and their MPN formation percentage both in the sperm lot of high polyspermy (R = −0.560, p < 0.05) and in the sperm lot of moderate polyspermy (R = −0.405, p < 0.05) which suggests that penetration of excessive spermatozoa disables the oocyte cytoplasm to promote MPN formation.     

Distribution of photoperiod-insensitive alleles Ppd-B1a and Ppd-D1a and their effect on heading time in Japanese wheat cultivars

The genotypes of photoperiod response genes Ppd-B1 and Ppd-D1 in Japanese wheat cultivars were determined by a PCR-based method, and heading times were compared among genotypes. Most of the Japanese wheat cultivars, except those from the Hokkaido region, carried the photoperiod-insensitive allele Ppd-D1a, and heading was accelerated 10.3 days compared with the Ppd-D1b genotype. Early cultivars with Ppd-D1a may have been selected to avoid damage from preharvest rain. In the Hokkaido region, Ppd-D1a frequency was lower and heading date was late regardless of Ppd-D1 genotype, suggesting another genetic mechanism for late heading in Hokkaido cultivars. In this study, only 11 cultivars proved to carry Ppd-B1a, and all of them carried another photoperiod-insensitive allele, Ppd-D1a. The Ppd-B1a/Ppd-D1a genotype headed 6.7 days earlier than the Ppd-B1b/Ppd-D1a genotype, indicating a significant effect of Ppd-B1a in the genetic background with Ppd-D1a. Early-maturity breeding in Japan is believed to be accelerated by the introduction of the Ppd-B1a allele into medium-heading cultivars carrying Ppd-D1a. Pedigree analysis showed that Ppd-B1a in three extra-early commercial cultivars was inherited from ‘Shiroboro 21’ by early-heading Chugoku lines bred at the Chugoku Agriculture Experimental Station.