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211.
Konomi Sakamoto Wataru Honto Masaharu Iguchi Nobuhiro Ogawa Kazuhiro Ura Yasuaki Takagi 《Fisheries Science》2009,75(1):91-98
This study examines the following in the Japanese mitten crab: (1) the structure of the exoskeleton with special reference
to its calcification; (2) the progression of post-molt cuticle formation and calcification. In the crab, the structure and
calcification state of the exoskeleton at the molt and during the inter-molt stage were similar to those of other crustaceans.
During the inter-molt, the exoskeleton consisted of four cuticle layers; the outermost epicuticle, the exocuticle, the endocuticle
and the innermost membrane layer. Intense calcification was observed in the exo- and endocuticle. At the molt, the synthesis
of the epi- and exocuticle was already complete, and the addition of the endocuticle began after the molt. Calcification of
the exocuticle initiated soon after the molt, but there was a delay between endocuticle matrix synthesis and calcification.
Histology showed that the process of calcification was similar to that in other crustaceans. However, calcium concentrations
within the exoskeleton continued to increase and never reached the levels of the inter-molt stage at the end of the experiment.
This suggests that the Japanese mitten crab is relatively slow to calcify compared to other crustaceans. 相似文献
212.
Xiao Hui Li Jun Jie Bai Xing Ye Yin Chang Hu Sheng Jie Li Ling Yun Yu 《Fisheries Science》2009,75(2):351-358
213.
Gene expression pattern of digestive and antioxidant enzymes during the larval development of reared Atlantic bluefin tuna (ABFT), Thunnus thynnus L.
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214.
The relative efficacies of three natural estrogens viz., estrone (E1), estradiol-17β (E2) and estriol (E3) to induce synthesis of vitellogenin (Vg) and choriogenin (Chg) were assessed in primary hepatocyte cultures of the Indian
freshwater spotted snakehead, Channa punctata. Hepatocytes were isolated from the spotted snakehead liver by a non-enzymatic protocol. Optimum culture conditions were
standardized for ensuring their viability and functioning. Isolated hepatocytes were cultured for 48 h for monolayer formation
and then exposed to various concentrations (0.001–10 μM) of the three estrogens. Competitive homologous ELISAs, developed
and validated for spotted snakehead Vg and Chg were employed to determine the amounts of these two proteins secreted into
the culture medium after 48 h of incubation. The results reveal that although all the three estrogens were effective in inducing
the production of Vg and Chg in a dose-dependent manner, there were differences in their relative potencies. Of three estrogens,
E1 was the least potent and could induce synthesis of Vg and Chg only at a minimum concentration of 0.5 μM; whereas significant
levels of both the proteins were quantified in culture medium by exposing the hepatocytes to E2 or E3 even at a concentration of 0.001 μM. All three estrogens were effective in inducing synthesis of Vg and Chg in vivo also.
These results suggest the possibility of employing the above in vitro experimental design to monitor the presence of estrogens/estrogen-like
chemicals in natural waters, which could interfere with the estrogen receptor system of fish. This study further points to
the possibility of using Chg, in addition to Vg, as a parameter for screening various chemicals for their estrogenic activity. 相似文献
215.
Izquierdo MS Robaina L Juárez-Carrillo E Oliva V Hernández-Cruz CM Afonso JM 《Fish physiology and biochemistry》2008,34(2):117-127
The Δ6 and Δ5 desaturases and elongases show only very limited activity in marine fish, and little is known of the possibility
of enhancing Δ6 desaturase gene expression in these fish. The use of plant oils in marine fish diets is limited by their lack
of n−3 highly unsaturated fatty acids (HUFA) despite an abundant content of the 18C fatty acid precursor linoleic and α-linolenic
acids. The objective of the present study was to determine the ability of larval gilthead seabream to utilize vegetable oils
and assess the nutritional regulation of Δ6 desaturase gene expression. Seventeen-day-old gilthead seabream larvae were fed
during a 17-day period with one of four different microdiets formulated with either sardine fish oil (FO), soybean, rapeseed
or linseed oils, respectively, or a fifth diet containing defatted squid meal and linseed oil. Good larval survival and growth,
both in terms of total length and body weight, were obtained by feeding the larvae either rapeseed, soybean or linseed oils.
The presence of vegetable oils in the diet increased the levels of 20:2n−9 and 20:2n−6, 18:2n−9, 18:3n−6, 20:3n−6 and 20:4n−6, in larvae fed rapeseed and soybean oils in comparison to those fed FO. In addition, a sixfold increase in the relative
expression of Δ6 desaturase-like gene was found in larvae fed rapeseed and soybean oils, denoting the nutritional regulation
of desaturase activity through its gene expression in this fish species. However, feeding linseed oil did not increase the
expression of the Δ6 desaturase gene to such a high extent. 相似文献
216.
ABSTRACT: Hermatypic (reef-building) corals harbor dinoflagellate endo-symbionts Symbiodinium spp. In studying gene expression in such symbiotic corals, problems arise regarding how to distinguish the coral and symbiont mRNA, and how to estimate their fractions in the mRNA population of the holobiont (symbiotic complex of the coral and Symbiodinium cells). In this study, these issues were addressed using juveniles of hermatypic coral Acropora tenuis in symbiosis with Symbiodinium cells of strain PL-TS-1. First, the guanine-cytosine (GC) contents were determined in expressed sequence tags (EST) from PL-TS-1 cells cultured in vitro and symbiont-free larvae of A. tenuis , and their average GC contents were found to be significantly different. The average GC content of the EST from the holobiont was much closer to that of A. tenuis larvae, suggesting that the majority (>90%) of mRNA isolated from the holobiont originated in the host. In protein-coding sequences, little overlap was observed between the GC-content distributions of PL-TS-1 cells and A. tenuis larvae. All of the coding sequences ( n = 59) found in the A. tenuis EST had GC contents below 0.5, whereas the GC content exceeded 0.5 in the majority (43/44) of coding sequences from the nuclear genome of PL-TS-1 cells. 相似文献
217.
T. T. Chen L. B. Agellon C. M. Lin H. J. Tsai Peijun Zhang L. I. González-Villasénor D. A. Powers 《Fish physiology and biochemistry》1989,7(1-6):381-385
The primary structures of two rainbow trout growth hormone mRNAs (GH1 and GH2) have been deduced by direct sequencing of their
respective cDNA clones and portions of the mRNA. Both GH1 and GH2 mRNA contain open reading frames comprised of 630 nucleotides
and encode 210 amino acid residues of which 11 are variant. The translated regions of both mRNA are flanked by a short but
rather conserved 5′-end, and a relatively long but highly diverged 3′-end. The differences at translated and 3′-untranslated
regions suggest that the GH1 and GH2 mRNA originate from different loci. The GH1 and GH2 mRNA are likely transcribed from
two distinct loci which were duplicated during tetraploidization of salmonid genome between 50 to 100 million years ago.
The GH2 gene has been isolated and sequenced from a rainbow trout genomic library. This gene spans a region of approximately
4 kilobases. The trout GH gene is comprised of 6 exons and 5 introns, in contrast to 5 exons and 4 introns in mammals. The
additional intron in the trout gene interrupts the translated regions that are analogous to the last exon of the mammalian
counterpart. The alleged internally repeating sequences in mammalian GH, prolactin (Pr1) and placental lactogen (PL) are not
observed in the predicted polypeptide sequence of trout GH. In addition, direct repeats that flank exons I, III and V of mammalian
GH, Pr1 and PL genes are absent in trout gene. These findings indicate that the rainbow trout GH gene structure does not support
the current hypothesis that internally repeated regions in GH, Pr1 and PL arose from a small primordial gene. 相似文献
218.
Microsatellites have become the preferred molecular markers for strain selection and genetic breeding in fish. In this study
a total of 105 microsatellites were isolated and identified in gibel carp (Carassius auratus gibelio) by microsatellite sequence searches in GenBank and other databases and by screening and sequencing of positive clones from
the genomic library enriched for AG and GATA repeats. Moreover, nineteen microsatellites were randomly selected to design
locus-specific primer pairs, and these were successfully used to identify and discriminate different cultured strains of gibel
carp including strains A, D, L, and F. Three different types of microsatellite pattern were distinguished by the number and
length of fragments amplified from the 19 primer pairs, and some microsatellite primer pairs were found to produce different
microsatellite patterns among strains and strain-specific fragments. In addition, some duplicated alleles were also detected
in two microsatellite patterns. Therefore, the current study provides direct molecular markers to discriminate among different
cultured strains for selective breeding and aquaculture practice of gibel carp. 相似文献
219.
Erzsbet Jns Mria Rgyanszki Jnos Olh Lszl Boross 《Aquaculture (Amsterdam, Netherlands)》1983,30(1-4):145-154
The authors studied the pH, temperature dependence, heat inactivation and the reactive groups of the active centers of proteolytic enzymes extracted from the alimentary canal of silver carp, common carp and sheatfish. In these three fish species activation energy values of enzymes, active in a pH range near neutral (7.5) were nearly identical, i.e.: silver carp: 14 kcal/mol; common carp: 15.4 kcal/mol; sheatfish: 15.7 kcal/mol. Differences were found in heat stability. At 55°C time values for 50% activity loss were 3.8: 1.3 and 14.6 min in the case of silver carp, common carp and sheatfish, respectively. Activities of enzymes, active in a pH range near neutral were inhibited by 82–94% by 10−3M PMSF, and by 2–5% by 10−3M EDTA. Proteolytic enzymes of the three fish species proved not to be homogeneous, but the largest part consisted of seryl-proteinases. 相似文献
220.
Interannual variations in abundance, timing of outmigration from rivers, growth rate and condition of juvenile chum salmon
(Oncorhynchus keta) were studied in the Nemuro Strait (eastern Hokkaido, Japan) during 1999–2002 to establish a possible relationship to zooplankton
abundance. The otolith microstructure of juveniles was examined each year in late June to determine their time and size at
sea entry (i.e., outmigration), and to estimate the early marine growth rates. Salmon outmigration peaked in mid- or late
May, which coincided, in three of the four study years, with the peak release of juveniles into rivers within the study area.
Abundance, growth rate and condition of fish were higher in 2001, when—compared to other years—smaller fish experienced higher
growth rates, coinciding with greater zooplankton abundance for that year. Our results suggest that high zooplankton abundance
positively influenced juvenile chum salmon growth and the condition of the fish during their early marine life despite their
small size at sea entry. 相似文献