Changes in meat texture of three varieties of squid in the early stage of cold storage

ABSTRACT: The present study examined the changes in texture and protein components during cold storage of different squid varieties. Raw oval squid, Japanese common squid and arrow squid were sliced fresh and the muscles were stored at 4°C for 0, 4, 8, 12, 18, 24, 48 and 120 h. The rheological measurements, protein components and amounts of collagen were examined. The adhesiveness of each squid increased significantly in the early stage of cold storage. In all varieties, penetration decreased at 4 h, which is considered to be rigor mortis, then increased. The amounts of total collagen, 20°C water-soluble collagen and 70°C water-soluble collagen did not change significantly in each variety during cold storage. Sodium dodecylsulfate–polyacrylamide gel electrophoresis (SDS-PAGE) pattern showed that the 580 kDa component gradually disappeared up to 48 h. The correlations between the amounts of 580 kDa component and adhesiveness or firmness were high. Models of fit based on chemical kinetics accurately expressed the behavior of adhesiveness, firmness and penetration showing that 63.2% of adhesiveness changes occurred in 13–19 h and that 63.2% of firmness changes occurred in 18–24 h.     

Expression of pancreatic enzyme genes during the early larval stage of Japanese eel Anguilla japonica

ABSTRACT: To reveal the ontogeny of pancreatic exocrine function in the early larval stage of eel, cDNAs encoding major pancreatic enzymes, trypsinogen, amylase and lipase were identified from the Japanese eel Anguilla japonica and their expression pattern in larvae was analyzed. The cloned eel trypsinogen precursor consisted of 224 amino acids and showed 82.2% identity to trypsinogen-2 of winter flounder Pleuronectes americanus . The eel amylase precursor consisted of 512 amino acids and showed 77% identity to winter flounder amylase. Eel pancreatic lipase was composed of 470 amino acids and had 58.3% of identity to human pancreatic lipase. In the eel larvae, mRNA expression of trypsinogen and amylase was first detected at 6 days post-hatching (d.p.h.), and the expression level increased between 7 and 8 d.p.h. In contrast, mRNA expression of lipase was first detected at 8 d.p.h. Eel larvae start to feed actively at 8 d.p.h. Thus, it was indicated that eel pancreas starts to synthesize digestive enzymes at 6 d.p.h. and acquires full function by the onset of exogenous feeding at 8 d.p.h.     

Biosynthesis of estradiol-17β in the ovarian follicles of the red seabream Pagrus major during vitellogenesis

ABSTRACT: The red seabream Pagrus major is a useful experimental fish for studying the endocrine control of oogenesis in teleosts. This study investigated the steroidogenic pathway for estradiol-17β (E2) biosynthesis in the ovarian follicles of red seabream. Intact follicles were isolated during vitellogenesis and incubated in vitro with different radiolabeled steroid precursors. When 17-hydroxyprogesterone (17-P), dehydroepiandrosterone (DHEA), or androstenedione (AD) were used as precursors, both testosterone (T) and estrone (E1) were synthesized by follicles, leading to estradiol-17β (E2) production. Serum steroid levels measured by enzyme-linked immunosorbent assay showed that T, E1, and E2 were present in the circulation at levels ranging from 1 ng/mL to 2 ng/mL throughout the day during the spawning season. In vitro conversion of E1 into E2, however, was 15.8-fold greater than T conversion into E2, suggesting that E2 is synthesized mainly via E1 rather than T. The results showed that E2 was synthesized from pregnenolone via 17-hydroxypregnenolone, DHEA, AD, and E1. Thus, the study demonstrated the complete steroidogenic E2 synthesis pathway in the ovarian follicles of red seabream, and revealed that E1 is the major precursor of E2.     

Role of prostaglandin in the control of ovulation in the Japaneseeel Anguilla japonica

ABSTRACT:   The in vitro effects of 17,20β-dihydroxy-4-pregnen-3-one(DHP) and prostaglandins (PGE₁, PGE₂, PGF_1α,PGF_2α) on ovulation in the Japanese eel Anguillajaponica were examined. Oocytes with follicle layers at themigratory nucleus stage (approximately 850–900 µmdiameter) were removed using a polyethylene cannula from artificiallymatured fish. At concentrations of 10 and 100 ng/mL,DHP was found to induce both germinal vesicle breakdown and ovulation.The prostaglandins, except for PGE₁, effectively inducedovulation of previously matured oocytes by DHP treatment in vitro .Prostaglandin F_2α was the most effective. Asignificant increase in ovulation rate was observed even at a concentrationof 0.01 µg/mL PGF_2α.Indomethacin blocked the in vitro ovulation induced by DHPand addition of PGF_2α reversed indomethacin-blockedovulation. Actinomycin D and cycloheximide blocked DHP-induced ovulationand PGF_2α reversed the effects of both inhibitors. Theseresults indicate that DHP induces ovulation through endogenous prostaglandinsynthesis in the follicle layers of the Japanese eel.     

Evaluation of the suppression ability of rice (Oryza sativa) on Monochoria vaginalis by measuring photosynthetic photon flux density below rice canopy

Field experiments involving eight cultivars were conducted in 1998 and 16 cultivars in 1999 to study the ability of rice (Oryza sativa L.) to suppress Monochoria vaginalis (Burm. f ) Kunth through light competition. Dry weights of M. vaginalis shoots in early season culture exceeded those in normal season culture of any rice cultivars. The relative photosynthetic photon flux density (R‐PPFD), which was calculated as the ratio of the photosynthetic photon flux density (PPFD) below the rice canopy to that measured above the rice canopy, varied according to rice cultivar. A strong linear correlation was observed between the mean R‐PPFD at 29–35 days after transplanting (DAT) (r² = 0.80; p < 0.01 in 1998; r² = 0.63, p < 0.001; and r² = 0.93, p < 0.001 in 1999), or 36–42 DAT (r² = 0.66, p < 0.05 in 1998; r² = 0.72, p < 0.001; and r² = 0.97, p < 0.001 in 1999), and the dry weight of M. vaginalis shoots at approximately 60 DAT. Data from the three experiments could be pooled into one regression line because intercepts and regression coefficients were not significantly different. The r² values of the combined regression were highest when R‐PPFD was expressed as the mean of measurements taken during 14 days (from 29 to 42 DAT; r² = 0.81, p < 0.001). The shortest period for measuring mean R‐PPFD in order to obtain a meaningful relationship with M. vaginalis shoot dry weight was 7 days (from 29 to 35 DAT; r² = 0.78, p < 0.001). For that same period, relationships between M. vaginalis shoot dry weight at 60 DAT and rice tiller number or leaf area index (LAI) at ground level were weak. However, there were negative relationships between M. vaginalis shoot dry weights at 60 DAT and rice LAI measured 20 cm above the ground, plant heights or rice shoot dry weight, but these coefficients of determination were smaller than those calculated by R‐PPFD for the same period. Thus, the ability of rice to suppress M. vaginalis can be evaluated more accurately by measuring mean R‐PPFD below the rice canopy for 7 days (from 29 to 35 DAT) than by measuring rice LAI, plant height and shoot dry weight.