• 한국식품위생안전성학회지
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• 제16권3호
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• pp.232-240
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• 2001

시장에서 수집한 갈변병에 감염된 느타리버섯으로부터 125 균주를 분리하였고 그 중 45 균주는 병원성 균주로 조사되었다. WLFO 6 strains, WLFO 6 strains으로 나타났고, WLRO의 몇 균주는 병원성 검정 실험에서 약한 병원성을 나타내기도 했다. WLFO 6균주는 모두 느타리버섯의 갈변병 주원인균으로 알려진 P. tolaasii로 미생물 신속 동성을 (MIDI, gas chromatograph-microbial identification system)에 의해 동정되었고 WLRO는 P. gingeri, P. fluorescens biotype A and type C. 로 동정되었다. 그 외의 선발된 Pseudomonas spp.는 P. gingeri, P. agarici, P. fluorescens biotype B, P. chloroaphis, non-pathogenic P. tolaasii, P. putida biotype A, B 등으로 동정이 되었다. 분리된 병원성 세균의 세포배양 여과액으로 버섯에서의 갈변과 조직 함몰을 실험하였다. 병원성 검정에서 약한 병원성을 보인 분리균들은 갈변 또는 조직함몰이 나타나지 않았으나 강한 병원성을 나타냈던 균들은 두 현상이 모두 나타났다. P. tolaasii에 의해서 생성되는 세포외독소인 tolaasin의 활성을 조사하기 위하여 600 nm에서 용혈 활성을 측정하였다. P. tolaasii로 동정된 6 균주는 0.8∼0.9, 약한 병원성의 WLROs는 0.9∼1.0 그리고 Pseudomonas spp.는 10∼1.2로 나타났다. 공초점 현미경 기술을 이용하여 신선한 버섯에서의 조직을 optical sectioning image와 vertical sectioning image로 관찰하였고 또한 P. toiaasii에 의하여 오염된 조직부위의 영상을 회득하였다.

• 한국발생생물학회지:발생과생식
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• 제25권1호
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• pp.67-72
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• 2021

This study investigated the IGF-1 signal in specific tissues using Pacific oysters artificially matured via water temperature elevation. Pacific oysters were subjected to water temperature elevation from March to June, and 20 were randomly sampled each month. The condition index (CI) and tissue weight rate (TWR) were examined by measuring shell length, shell height, shell width, and soft tissue weight. The IGF-1 signal in tissues (adductor muscle, digestive glands, gills, labial palps, mantle edges, and gonads) was analyzed by sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. From April to June, the TWR of females and males increased from 19.1±2.9 to 21.0±3.6 and 18.2±2.0 to 19.2±2.5, respectively, while the CI remained the same. The IGF-1 signal in each tissue differed. IGF-1 was expressed in the adductor muscle, while tyrosine was expressed in all tissues. The phosphor (p)-ERK and p-AKT activities were high in the adductor muscle, mantle edge, and gonads. IGF-1 signaling affected the growth and maturity of the Pacific oysters examined.

• 한국수산과학회지
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• 제42권3호
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• pp.232-237
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• 2009

Norovirus surrogate (feline calicivirus) was inactivated by treatment at 50,000 psi for 60 sec by 6.8-$log_{10}TCID_{50}mL^{-1}$. Tissue obtained from oyster (digestive gland, gill and mantle) was qualitatively destroyed and distorted by treatment at pressure greater than 5,000 psi for 60 sec. High pressure treatment induced progressive changes in the color of the oyster adductor muscle. High pressure treatment effectively reduced norovirus surrogate but induced conformational changes in the tissue and color of oyster flesh.

• 분석과학
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• 제18권6호
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• pp.520-528
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• 2005

Two biological Certified Reference Materials (CRMs), KRISS 108-04-001 (oyster tissue) and 108-05-001 (water dropwort stem), were prepared by Korea Research Institute of Standards and Science (KRISS)during FY '01. The certified values of these materials had been determined by Isotope Dilution Mass Spectrometry (IDMS) for six elements (Cd, Cr, Cu, Fe, Pb and Zn). Additional analytical works are now progressing to certify the concentrations of a number of the environmental and nutrimental elements in these CRMs. The certified values in a CRM are usually determined by using a single primary method with confirmation by other method(s) or using two independent critically-evaluated methods. Instrumental Neutron Activation Analysis (INAA) plays an important role in the determination of certified values as it can eliminate the possibility of common error sources resulting from sample dissolution. In this study INAA procedure was used in determination of 23 elements in these two biological CRMs to acquire the concentration information and the results were compared with KRISS certified values.

• 한국패류학회지
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• 제27권1호
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• pp.35-42
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• 2011

In order to understand effect of polycyclic aromatic hydrocarbon (PAH) on shell repair of the Pacific oyster, Crassostrea gigas, shell regeneration experiments were carried out using oysters drilled a hole on the right valve. The change of pH and hemocytic characteristics in both extrapallial fluid and hemolymph were observed during the shell repair. The thickness of mantle tissue was apparently decreased, while necrosis in epithelium and periostracal gland was increased in response to PAH exposure. Our finding suggested that PAH could adversely influence on shell repair.

• 한국수산과학회지
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• 제39권1호
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• pp.9-15
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• 2006

As a part of the investigation for utilizing pearl oyster by-products, a rapid salt-fermented pearl oyster using commercial enzyme was prepared and also examined on the characteristics. The salt-fermented pearl oyster prepared by optimal condition, which was prepared by mixing of minced pearl oyster, 15% salt, and 1% $Protamex^\circledR$ and fermented for 4 weeks, was superior in hydrolysis degree (28.7%) and ACE inhibitory activity (92.6%) to salt-fermented pearl oyster prepared by other conditions, such as the use of whole tissue, different enzymes $(Alcalase^\circledR,\;Neutrase^\circledR\;and\;Flavourzyme^\circledR)$, different salt concentrations (20 and 25%), and different fermentation periods (2, 6 and 8 weeks). There were, however, some shortcomings with this product. It showed a dark green color and an unfavorable bitter taste. These shortcomings were improved by the addition of seasoning paste. The calcium and phosphorus contents of the seasoned salt-fermented pearl oyster were 64.2 mg/100 g and 71.6 mg/100 g, respectively, and the calcium content based on phosphorus was a good ratio for absorbing calcium. The total amino acid content of the seasoned and salt-fermented pearl oyster was 7,054 mg/100 g and the major amino acids ware aspartic acid (555.1 mg/100 g), glutamic acid (1,131.2 mg/100 g), alanine (658.2 mg/100 g), and lysine (695.5 mg/100 g). The seasoned salt-fermented pearl oyster, along with angiotensin I converting enzyme (ACE) inhibitory activity (98.3%), also showed a recognizable level (87.5%) of anti-oxidative activity.

• 한국수산과학회지
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• 제35권4호
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• pp.327-335
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• 2002

Effects of available food on growth of commercially cultured Pacific oysters, Crassostrea gigas in Goseong Bay on the south coast were studied using a numerical model. levels of total protein, carbohydrate and lipid in particulate organic matter in the water column as well as chlorophyll a concentration were determined for estimating total available food for oyster growth. Environmental parameters including water temperature, salinity and total suspended solid were also monitored for the model. Oyster growth was also monitored by means of measuring shell length and tissue wet weight increase on a monthly basis. Simulation results from the numerical model indicated that chlorophyll a is not a good representative of available food for the oysters in Goseong Bay. In contrast, available food in the water column measured by filtration of the organic particles and analyzed in terms of total lipids, carbohydrates and protein was well matched with simulated oyster growth in the Bay which is similar to observed growth. The model also suggested that oysters have relatively low retention efficiency of $50\%$ or less. This result indicates that oysters in the bay utilize only a part of food particle available in the water column, as reported in other studies.

• 한국수산과학회지
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• 제10권1호
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• pp.11-15
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• 1977

Brownish discoloration develops very rapidly in the storage of dried oyster. This undesirable browning is mainly caused by the series of reactions of sugar-amino condensation, enzymatic oxidation of tyrosine and/or the oxidative rancidity of lipids in the tissue of oyster. Sulfites are commonly used as inhibitors for Maillard type browning reactions in agricultural products. The inhibitory effect of sulfite treatment on canned oysters was also confirmed in some investigations. The results suggested that sulfites not only work on blocking tile amadori rearrangement but also on the reduction of free tyrosine which retards the progress of enzymatic oxidation of tyrosine tyrosinase. In this paper, the effect of sodium sulfite treatment on the reduction of reducing sugar and free tyrosine as a function i)f browning inhibition in oyster was tested and other treatment with glucose-oxidase and yeast were also applied. In preparation of samples, fresh oysters were soaked in sodium sulfite solution by various concentration for different treating times, washed in running water to remove the sulfite residue, and finally dried in the shade. In the result, the treatment of sodium sulfite was certainly effective on the reduction of both free tyrosine and reducing sugars in fresh oyster. The best results were obtained by the treatment of 0.5M sodium sulfite solution for 60 minutes each for soaking and washing. Treatment with, glucose-oxidase and yeast solutions, however, did appear somewhat effective but it required so much time for a certain effect that it seemed not practically applicable.

• 한국해양바이오학회지
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• 제2권4호
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• pp.263-266
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• 2007

Vibrio vulnificusis a causative agent of serious diseases in humans resulting from the contact of wound with seawater or consumption of raw seafood. Several studies aimed at detecting V. vulnificus have targeted vvh as a representative virulence toxin gene belonging to the bacterium. In this study, we targeted the rpoS gene, a general stress regulator, to detect V. vulnificus. PCR specificity was identified by amplification of 8 V. vulnificus templates and by the loss of a PCR product with 36 non-V. vulnificus strains. The PCR assay had the 273-bp fragment and the sensitivity of 10 pg DNA from V. vulnificus. SYBR Green I-based real-time PCR assay targeting the rpoS gene showed a melting temperature of approximately $84^{\circ}C$ for V. vulnificus strains. The minimum level of detection by real-time PCR was 2 pg of purified genomic DNA, or $10^3$ V. vulnificus cells from pure cultured broth and $10^3$ cells in 1g of oyster tissue homogenates. These data indicate that real-time PCR is a sensitive, species-specific, and rapid method for detecting this bacterium using the rpoS gene in pure cultures and in infected oyster tissues.

• 한국식품영양과학회지
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• 제33권8호
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• pp.1390-1397
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• 2004

우리나라 전통수산발효식품 중의 하나인 굴 젓갈을 소재로 하여 장기간 상온저장이 가능하며, 생굴의 풍미를 지닌 기름담금 염장발효 굴 제품을 가공하기 위한 최적 염장발효 조건과 염장발효 중의 성분변화에 대하여 살펴보았다. 염장발효 중 식염의 침투는 염장 초기에 완료되었으며, 아미노질소량은 저온숙성 20일째까지 계속 증가하다가 이후 일정한 함량을 유지하였고, 굴 자숙농축액을 첨가한 시료가 아미노질소의 함량이 가장 많았다. 염장발효 굴의 경도는 숙성 10일째까지 증가하다가 그 이후는 육 조직의 일부가 가수분해됨에 따라 점차 육질이 연화되어 감소하는 경향을 보였다. 염장직후의 생균수는 무염배지 및 2.5% 가염배지에서 각각 1.0∼1.1${\times}$$10^2$CFU/g, 6.7${\times}$$10^2$CFU/g이었고, 저온숙성 중 무염배지에서는 생균수가 전반적으로 변화를 보이지 않았으나, 2.5% 가염배지에서는 숙성 15일째까지 생균수가 뚜렷이 증가하다가 이후 감소하는 경향을 보였다. 염장발효 굴은 맛과 냄새 및 종합적 기호도 면에서 저온숙성 15∼20일째에 가장 좋았으며, 굴 자숙농축액을 첨가하여 염장발효시킨 시료가 특히 맛과 향기 면에서 우수하였다. 이상의 결과를 종합하여 볼 때, 기름담금 염장발효 굴 제품을 가공하기 위한 최적 염장발효 조건은 탈각한 생굴을 3% 식염수로서 수세하여 물 빼기를 한 다음, 포화식염수와 굴 자숙농축액의 2:1 혼합용액에 대해 1% sodium erythorbate와 0.2% polyphosphate를 각각 첨가한 염장액으로 물간하여 5$\pm$1$^{\circ}C$에서 15일간 발효 숙성시키는 것이 가장 좋았다.