A highly CO₂-tolerant diatom, Thalassiosira weissflogii H1, enriched from coastal sea, and its fatty acid composition     

Yuzaburo Ishida  Norihiro Hiragushi  Hirotaka Kitaguchi  Atsushi Mitsutani  Satoshi Nagai and  Minoru Yoshimura 《Fisheries Science》2000,66(4):655-659

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Colchine-induced aneuploids from cell culture of sugarcane     

C. Nagai  B. S. Ahloowalia  D. Jheinz  T. L. Tew 《Euphytica》1986,35(3):1029-1038

Summary Sugarcane (Saccharum spp.) clones are amenable to gross chromosome manipulation due to their high polyploid nature (2n=100–120). This study was conducted to analyze the effects on plant morphology of altering chomosome number via callus culture. Callus cultures from clone H69-9092 were established, and plants were regenerated following colchicine treatment of cultured cells. Cytological analysis showed that variant somaclones were aneuploids with a wide range in chromosome numbers (2n=66–196). Some 22 visually distinct somaclones were planted in 1.35 m² plots with five replications to compare morphological and quality characteristics with H69-9092 at 8 months of growth. Extreme morphological variation was observed between somaclones, but coefficients of variation for quality factors-fibers %, refractometer solids %, pol %, and juice purity-and stomatal length were smaller than those for morphological traits associated with stalk volume and leaf area. Significant negative correlations were found between chromosome number and most morphological traits, e.g., stalk length (r=-0.58), number (r=-0.69), diameter (r=-0.54) and volume (r=-0.65); internode length (r=-0.57); and leaf area (r=-0.48). A positive correlation was found between chromosome number and stomatal length (r=-0.66). No significant correlations were found between chromosome number and quality factors. Aneuploids with higher than parental chromosome number had reduced growth. However, depression in growth was generally not observed in somaclones lower in chromosome number than the parent.Published with the approval of the Director as Paper No. 598 in the Journal Series of the Experiment Station, Hawaiian Sugar Planters' Association.  相似文献   

Insights into the reaction mechanism of the coagulation of soy protein isolates induced by subtilisin carlsberg     

Nagai K  Inouye K 《Journal of agricultural and food chemistry》2004,52(15):4921-4927

The reaction mechanism of the coagulation of soy protein isolates (SPIs) induced by subtilisin Carlsberg was investigated. Formation of the coagula was monitored by measuring the turbidity (OD660) of the SPI solution, which decreased at the initial stage (phase 1 or digestion phase) of the reaction, and then increased (phase 2 or coagulation phase) and finally reached the plateau level. The velocity of the coagulation increased with increasing enzyme concentration. The coagulation was inhibited dramatically by adding a serine protease inhibitor (phenylmethanesulfonyl fluoride, PMSF) when the turbidity reached the minimum value. This indicates that the SPI digests participating in the coagulation are produced mainly in phase 2; in other words, production of the coagulating fragments and their coagulation occur simultaneously in phase 2. Structural changes of SPI during proteolysis were measured by observing fluorescence changes of aromatic amino acids of SPI and an externally added hydrophobic probe. It was suggested that the hydrophilic surface areas of SPIs might be cleaved preferentially in phase 1, and that the hydrophobic inner areas might be cleaved in phase 2 with extensive decomposition of the 3-D structure of SPI proteins. The fragments formed in phase 2 are considered to coagulate through hydrophobic interactions.  相似文献   

Coagulation of soy protein isolates induced by subtilisin Carlsberg     

Inouye K  Nagai K  Takita T 《Journal of agricultural and food chemistry》2002,50(5):1237-1242

The coagulation of soy protein isolates (SPI) induced by subtilisin Carlsberg was studied. The proteins were digested to fragments of 16 kDa or less in the early stage of the reaction, followed by coagulation. The time-course of the coagulation measured by turbidity was separated into three phases. The turbidity decreased from the initial level observed at time zero to the minimum level (OD1) at time T1 (15-20 min) in the first phase. Then, it increased drastically to reach the maximum (OD2) at time T2 (60-70 min) in the second phase, which was followed by a slight decrease in the third phase. The coagulation was terminated at T2, where 30-35% of the weight of the SPI proteins was in coagula. Proteins in the coagula were degraded slowly in the prolonged incubation, and the protein content in the coagula was finally 15-20% of the weight. The time-course of the turbidity agreed well with that of the weight of the precipitates formed, indicating that the turbidity reflects the progress of the coagulation. The turbidity change (OD1 to OD2) from the start to the end of the coagulation increased proportionally to the SPI concentration (4.9-11 mg/mL), although the time (T1 to T2) needed for the coagulation was independent of the concentration. The growth of the coagula is promoted by increasing the SPI concentration and is rate-limiting in the coagulation.  相似文献   

Polymorphisms of the group-specific component (Gc) in three species of tamarins (Saguinus oedipus, S. labiatus, S. mystax)     

S Tsuchida  A Nagai  S Ikemoto 《Nippon juigaku zasshi. The Japanese journal of veterinary science》1990,52(3):649-651

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Functional targeting of DNA damage to a nuclear pore-associated SUMO-dependent ubiquitin ligase     

Nagai S  Dubrana K  Tsai-Pflugfelder M  Davidson MB  Roberts TM  Brown GW  Varela E  Hediger F  Gasser SM  Krogan NJ 《Science (New York, N.Y.)》2008,322(5901):597-602

Recent findings suggest important roles for nuclear organization in gene expression. In contrast, little is known about how nuclear organization contributes to genome stability. Epistasis analysis (E-MAP) using DNA repair factors in yeast indicated a functional relationship between a nuclear pore subcomplex and Slx5/Slx8, a small ubiquitin-like modifier (SUMO)-dependent ubiquitin ligase, which we show physically interact. Real-time imaging and chromatin immunoprecipitation confirmed stable recruitment of damaged DNA to nuclear pores. Relocation required the Nup84 complex and Mec1/Tel1 kinases. Spontaneous gene conversion can be enhanced in a Slx8- and Nup84-dependent manner by tethering donor sites at the nuclear periphery. This suggests that strand breaks are shunted to nuclear pores for a repair pathway controlled by a conserved SUMO-dependent E3 ligase.  相似文献   

Vitrification of fully grown and growing porcine oocytes using germinal vesicle transfer     

Nakagawa S  Maedomari N  Kikuchi K  Nagai T  Miyano T  Fulka J  Manabe N 《The Journal of reproduction and development》2011,57(3):335-341

The survival rate of vitrified germinal vesicle (GV) stage porcine oocytes is very low, and it is not known if the vitrification damages the nucleus, cytoplasm or both. We have evaluated the eventual GV or cytoplasmic damage in fully grown (FG) and growing vitrified oocytes. Fifty-five percent of nonvitrified FG cumulus-denuded oocytes reached the metaphase II (MII) stage in culture. When growing oocytes from preantral (PA) and early antral (EA) follicles were matured in vitro, almost all oocytes were arrested at the GV stage (GV stage: PA 88.9 and EA 79.5%, respectively). When fresh GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes and matured in vitro, some of them reached the MII stage (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). The maturation rate of vitrified FG oocytes was only 6.1% but increased dramatically when vitrified GVs from FG, PA and EA oocytes were transferred into fresh enucleated FG oocytes (MII stage: VitFG/FG 43.9%, VitPA/FG 7.1% and VitEA/FG 26.3%, respectively). These results were not significantly different from those for the nonvitrified groups (MII stage: FG/FG 57.5%, PA/FG 9.3% and EA/FG 35.3%, respectively). We activated the reconstructed oocytes that received fresh or vitrified GVs (FG/FG, EA/FG, VitFG/FG and VitEA/FG) and examined their embryonic development. Cleaved embryos (nonvitrified groups 13.0-61.8%, vitrified groups 33.3-40.0%) and blastocysts (nonvitrified groups 0.0-18.2%, vitrified groups 0.0-2.9%) were obtained after activation. These results demonstrate that vitrified porcine GVs maintain maturational and developmental competence and that vitrification predominantly damages the cytoplasm.  相似文献   

Effects of Chemical Activation Treatment on Development of Swamp Buffalo (Bubalus bubalis) Oocytes Matured In Vitro and Fertilized by Intracytoplasmic Sperm Injection     

YY Liang  DN Ye  C Laowtammathron  T Phermthai  T Nagai  T Somfai  R Parnpai 《Reproduction in domestic animals》2011,46(1):e67-e73

The objective of this study was to optimize the activation protocol for buffalo oocytes after intracytoplasmic sperm injection (ICSI). The release of the second polar body (PB) at 3, 6 and 9 h after ICSI of in‐vitro matured oocytes activated either with 5 μm ionomycin (Io) or with 7% ethanol (EtOH) was preliminary examined. The highest rate of second PB extrusion occurred at 3 h of activation, and the second PB extrusion in EtOH group was significantly higher than that in Io group. Oocytes that extruded the second PB were selected and cultured either with 1.9 mm 6‐dimethylaminopurine (6‐DMAP) for 3 h or with 10 μg/ml cycloheximide (CHX) for 5 h. Significantly higher rate of oocytes formed 2 pronuclei in EtOH combined with CHX (EtOH + CHX) (62%) group compared to those of Io + CHX (42%) and EtOH + 6‐DMAP (48%) groups (p < 0.01) whereas Io + 6‐DMAP group showed intermediate value (58%). Significantly higher blastocyst formation rates were obtained in Io + 6‐DMAP (29%) and EtOH + CHX (24%) groups than in Io + CHX (6%) and EtOH + 6‐DMAP (17%) groups. Our results indicate that buffalo ICSI oocytes are effectively activated by combination treatment of Io with 6‐DMAP and EtOH with CHX resulting in the highest cleavage and blastocyst formation rates.  相似文献   

Reactivity and prevalence of neutralizing antibodies against Japanese strains of bovine viral diarrhea virus subgenotypes     

Fujiko MinamiMakoto Nagai  Mika ItoTatsuhiko Matsuda  Hikaru TakaiYoshiko Jinkawa  Takeshi ShimanoMichiko Hayashi  Yoshihisa SekiYoshihiro Sakoda  Katsuaki SugiuraHiroomi Akashi 《Comparative immunology, microbiology and infectious diseases》2011,34(1):35-39

Bovine viral diarrhea virus (BVDV) field isolates show genetic and antigenic diversity. At least 14 subgenotypes of BVDV-1 and 4 of BVDV-2 have been identified in Artiodactyla worldwide. Of these, 6 subgenotypes of BVDV-1 and 1 of BVDV-2 have been isolated in Japan. Previously, we reported that each subgenotype virus expresses different antigenic characteristics. Here we investigated the reactivity of neutralizing antibodies against representative strains of Japanese BVDV subgenotypes using sera from 266 beef cattle to estimate the prevalence of this epidemic virus among cattle in Japan. Antibody titers at concentrations at least 4-fold higher than antibodies against other subgenotype viruses were considered subgenotype specific. Subgenotype-specific antibodies were detected from 117 (80.7%) of 145 sera samples (69.7% against BVDV-1a, 1.4% against BVDV-1b, 8.3% against BVDV-1c, and 1.4% against BVDV-2a). The results suggest that neutralization tests are useful in estimating currently epidemic subgenotypes of BVDV in the field.  相似文献   

Strain analysis of lumber containing a knot during tensile failure   总被引：1，自引：0，他引：1  

Hiroaki Nagai  Koji Murata  Takato Nakano 《Journal of Wood Science》2011,57(2):114-118

We analyzed the strain distribution of lumber containing a knot under a tensile load. The local tensile strain near the knot was measured using the digital image correlation method. Fracture often initiated near the knot where the fiber orientation changed in a three-dimensional manner. The fiber direction in this zone was different from that in the clear part, coinciding with the thickness direction and not with the longitudinal direction of the specimen. Our results disagree with those of previous models that assumed the longitudinal direction of lumber as the direction of crack propagation. Strain analysis showed that a nonlinear region existed around the knot just before ultimate fracture occurred. The results indicated that nonlinear characterization is necessary to determine the failure mechanism of lumber containing a knot, despite the brittleness fracture at the macroscopic scale.  相似文献