• 제목/요약/키워드: brine shrimp

검색결과 67건 처리시간 0.025초

A New Cyclitol Derivative from a Sponge Stelletta Species

  • Zhao, Qingchun;Liu, Yong-Hong;Hong, Jong-Ki;Lee, Chong-O.;Park, Jong-Hee;Lee, Dong-Seok;Jung, Jee-H.
    • Natural Product Sciences
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    • 제9권1호
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    • pp.18-21
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    • 2003
  • Guided by the brine shrimp lethality assay, a new (4) and three known cyclitol derivatives (1-3) were isolated from the marine sponge Stelletta sp. Norsarcotride A (4) showed significant cytotoxicity against a small panel of five human tumor cell lines.

해양생물 유래의 항종양성 물질의 탐색과 개발

  • 손병화;최홍대;정우진;조용진
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 1993년도 제2회 신약개발 연구발표회 초록집
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    • pp.48-48
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    • 1993
  • 항종양성 물질의 탐색과 개발을 지향한 해양생물유래의 생물활성물질의 화학적 연구의 일환으로서 해조류(12종류), 해면동물(3종류), 강장동물(2종류). 극피동물(4종류), 연체동물(10종류) 및 원색동물(2종류)의 각 용매분획을 대상으로 brine shrimp bioassay에 의한 세포독성을 검색한 결과, 극피동물의 별불가사리 초산에틸액스(LC$_{50}$: 283$\mu\textrm{g}$/ml) 및 해삼 클로르포름엑스(LC$_{50}$: 274$\mu\textrm{g}$/ml) , 연채동물의 보말고동 부타놀액스(LC$_{50}$: 263$\mu\textrm{g}$/ml) 및 따게비의 물엑스(LC$_{50}$: 360$\mu\textrm{g}$/ml)에서 가장 강력한 세포독성이 관찰되었다. 그리고 생물별로 살펴본 세포독성빈도는 극피동물이 가장 유망한 것으로 생각되었다.로 생각되었다.

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PAHs와 TBT에 대한 동물플랑크톤의 반응

  • 장풍국;장민철;이재도;장만;신경순
    • 한국환경생물학회:학술대회논문집
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    • 한국환경생물학회 2002년도 학술대회
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    • pp.154-162
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    • 2002
  • 인간이나 환경에 해로운 영향을 주는 지속성 유기오염물질의 독성을 동물플랑크톤 중 요각류를 대상으로 실험하였다. 실험에 사용된 요각류는 장목만에서 주로 가을에 많은 출현을 보인 Acartia erythraea와 늦가을부터 그 다음해 봄까지 우점하는 A. omorli였다. 지속성 유기오염물에 대한 요각류의 독성을 평가하기 위해 3가지의 실험을 실시하였다. 광양만에서 주로 나타나는 5가지 PAHs에 대한 A. omorli 48h-LC50을 구하였고, 온도에 따른 Benzo(a)pyrene과 TBT의 독성의 변화를 Brine shrimp(Artemia)를 이용해 실험하였으며, PAHs 중에서 독성이 강한 Benso(a)Pyrene에 노출된 먹이를 섭취한 Acartia erythraea와 A. omorli의 egg Production, hatching rate, fecal Pellet의 변화를 측정하였다. A. omorli의 48h-LC50으로 조사된 결과 Fluoranthene과 Benzo(a)pyrene의 독성이 강하게 나타난다. 온도실험에서는 동일한 유해물질을 가지고 실험을 하더라도 온도의 변화에 따라 급격한 독성의 차이가 나타날 수 있고, 유해물질간에도 온도에 따라서 나타나는 독성에 대한 특성이 다르게 나타났다. Benzo(a)Pyrene에 노출된 먹이는 요각류의 egg Production, hatching rate, fecal Pellet에 영향을 미치고 있으며, 특히 농도와 실험시간에 따른 부정적 영향들을 보였다.

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Antimicrobial activity and cytotoxicity of Eclipta prostrata

  • Rahman, Mohammad S.;Rashid, Mohammad A.
    • Advances in Traditional Medicine
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    • 제8권1호
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    • pp.47-52
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    • 2008
  • The plant Eclipta prostrata, a member of the Compositae family, has folkloric reputation of being used as a medicinal agent in Bangladesh. In the present investigation, attempt was taken to explore the antimicrobial potency and cytotoxicity of its extractives and purified compounds. The methanolic extract of the whole plant, its n-hexane, carbon tetrachloride, chloroform, aqueous soluble fractions and two purified compounds, eclalbasaponin I (1) and II (2), obtained from Eclipta prostrata were subjected to screening for inhibition of microbial growth by the disc diffusion method at 300 and 100 ${\mu}g$/disc for extracts and pure compounds, respectively. In this case, the carbon tetrachloride and chloroform soluble fractions of the methanolic extract appeared very potent in terms of both zone of inhibition and spectrum of activity. However, all the extractives were also subjected to brine shrimp lethality bioassay for preliminary cytotoxicity evaluation. Here, the carbon tetrachloride soluble fraction of methanolic extract revealed the strongest cytotoxicity having $LC_{50}$ of 1.318 ${\mu}g$/ml.

New Cytotoxic Sulfated Saponins from the Starfish Certonardoa semiregularis

  • Wang Wei Hong;Jang Hyo Jin;Hong Jong Ki;Lee Chong Ok;Bae Song Ja;Shin Sook;Jung Jee H.
    • Archives of Pharmacal Research
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    • 제28권3호
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    • pp.285-289
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    • 2005
  • Two new sulfated saponins designated as certonardosides P$_{2}$ and I$_{3}$ (1 and 2) were isolated from the brine shrimp active fraction of the MeOH extract of the starfish Certonardoa semiregularis. The structures were determined on the basis of spectral analysis. Compounds 1 and 2 were tested for cytotoxicity against five human tumor cell lines (A549, SK-OV-3, SK-MEL-2, XF498, and HCT15), and compound 1 displayed significant cytotoxicity against the SK-MEL-2 skin cancer cell.

Xylomaticin and Gonionenin, Cytotoxic Annonaceous Acetogenins from the Seeds of Annona cherimolia

  • Kim, Dal-Hwan;Fang, Zhe;Lee, Young-Eun;Woo, Mi-Hee
    • Natural Product Sciences
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    • 제13권4호
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    • pp.355-358
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    • 2007
  • Further bioactivity-directed fractionation of the ethanol extract of the seeds of Annona cherimolia has led to the isolation of two mono-tetrahydrofuran acetogenins, xylomaticin (1) and gonionenin (2). The structures of these compounds were characterized on the basis of chemical and spectroscopic data. Compounds 1 and 2 have a relative stereochemistry relationship of threo/trans/threo across the mono-tetrahydrofuran ring with its two flanking hydroxyls. Compounds 1 and 2 are known, but are first isolated from this plant. In brine shrimp lethality test (BST), 1 and 2 exhibited cytotoxic activity.

학공치의 난발생과 부화자어 (Eggs Development ana Larvae of the Horn Fish, Hemiramphus sajori TEMMINCK et SCHLEGEL)

  • 김용억;명정구;최상웅
    • 한국수산과학회지
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    • 제17권2호
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    • pp.125-131
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    • 1984
  • 1983년 4월 13일 경상남도 남해군 삼동면 지족리앞 창선해협에 설치된 죽방염정치어장에서 성숙한 학공치를 채집하여 현장에서 인공수정시켜, 실험실로 옮겨와 실내에서 난발생과정과 부화자어를 관찰한 결과를 요약하면 다음과 같다. 난은 구형이며 침성난으로 동물극부근에 $4{\sim}6$개, 식물극부근에 1개의 부속계가 있으며, 난경은 $1.80{\sim}2.00mm$이고, 많은 소유구를 가진다. 사육수온은 $13.5^{\circ}C{\sim}20.0^{\circ}C$ 범위에서 수정후 약376시간만에 첫 부화를 하였다. 부화직후의 자어는 전장이 $7.40{\sim}8.00mm$(평균, 7.68mm)이며 근절수는 $40+16{\sim}17=56{\sim}57$. 꼬리지느러미에 8개의 지느러미 원기가 생긴다. 부화후 3일째의 자어는 전장이 $8.95{\sim}9.40mm$이며 brine shrimp유생을 먹기 시작한다. 부화후 4일째의 전장 $9.00{\sim}9.65mm$의 자어는 난황을 완전히 흡수한다. 부화후 14일째의 전장 13.25mm의 자어는 아래턱이 조금 돌출되며 가슴지느러미에 4개, 등지느러미에 14개, 뒷지느러미에 13개의 지느러미줄기가 나타난다.

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Amino acids profiles of six dinoflagellate species belonging to diverse families: possible use as animal feeds in aquaculture

  • Lim, An Suk;Jeong, Hae Jin;Kim, So Jin;Ok, Jin Hee
    • ALGAE
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    • 제33권3호
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    • pp.279-290
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    • 2018
  • Microalgae have been utilized in diverse industries including aquaculture. Among the microalgae, dinoflagellates are known to have various bioactive compounds, and thus the interest in their application to industry has increased. In order to test their potential as food materials for aquaculture animals, the crude protein contents and compositions of amino acids of six dinoflagellates Heterocapsa rotundata (family Heterocapsaceae), Ansanella granifera (Suessiaceae), Alexandrium andersonii (Ostreopsidaceae), Takayama tasmanica (Brachidiniaceae), Takayama helix, and Gymnodinium smaydae (Gymnodiniaceae) belonging to diverse families were analyzed. The percentage of the amount of the crude protein relative to dry weight of T. tasmanica was the highest (65%) and that of A. andersonii was the lowest (26%). However, the highest percentage of total detected amino acids in crude protein was found in A. andersonii (98.2%). In all six dinoflagellates, glutamic acid was the most dominant amino acid in crude protein. However, the second main amino acid was aspartic acid for H. rotundata, A. granifera, T. helix, and G. smaydae, but were arginine and leucine for A. andersonii and T. tasmanica, respectively. Furthermore, T. tasmanica and T. helix did not have taurine and gamma-aminobutyric acid, whereas the other dinoflagellates possessed them. The percentages of essential amino acid contents of the dinoflagellates met the requirement levels for juvenile shrimps. In addition, the dinoflagellates were not toxic to the brine shrimp Artemia salina. Compared with the other microalgae reported so far, H. rotundata and A. andersonii can be used for arginine-rich diets, T. tasmanica for valine and leucine-rich diets, A. granifera for histidine-rich diets, T. helix for threonine-rich diets, and G. smaydae for lysine-rich diets. Therefore, based on their biochemical composition and toxicity to Artemia, the dinoflagellates could be used as essential amino acid sources for cultivating animals in the aquaculture industry.

Mycotoxins and Invertase Enzyme of the Mycoflora of Molasses in Upper Egypt

  • El-Said, A.H.M.
    • Mycobiology
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    • 제30권3호
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    • pp.170-174
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    • 2002
  • A total of twenty-nine species and one species variety belonging to 12 genera was isolated from 30 samples of molasses on 1% glucose(10 genera, 22 species and 1 variety) and 50% sucrose(7, 21 and 1) Czapek's agar at $25^{\circ}C$ media. Aspergillus, Mucor, Mycosphaerella and Penicillium were the most common genera on the two types of media. From the above genera, the most prevalent species were: Aspergillus flavus, A. fumigatus, A. niger, Mycosphaerella tassiana, Penicillium chrysogenum, P. oxalicum and P. purpurogenum. Also, some species were only isolated on 50% sucrose such as Eurotium amstelodami, E. chevalieri, E. repens, Humicola fuscoatra, Penicillium aurantiogriseum and P. puberulum. About 65 fungal isolates isolated from 50% sucrose agar were tested for their ability to produce invertase enzyme in liquid medium and 93.8% of the isolates could produce this enzyme. From the positive isolates, 32 showed high invertase activity, 21 had moderate activity and the remaining 8 isolates were of weak activity. Sixty isolates of Aspergillus, Emericella, Eurotium, Mycosphaerella and Penicillium from the preceding study were screened for the presence of their respective mycotoxins. Larva of brine shrimp(Artema sauna L.) were used for toxicity test of the fungal crude extracts. Three isolates out of 60 tested were toxic. Using thin-layer chromatographic technique, 5 different known mycotoxin were detected aflatoxins : B1, B2, G1, G2 and citrinin.

C-Flavonoidal Glycosides from Erythrina caffra Flowers

  • El-Masry, Sawsan;Hammoda, Hala M.;Radwan, Mohamed M.;Ross, Samir A.;Zaatout, Hala H.
    • Natural Product Sciences
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    • 제16권4호
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    • pp.217-222
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    • 2010
  • A phytochemical investigation of the ethanolic extract of Erythrina caffra flowers from an Egyptian origin yielded three C-flavonoidal glycosides; 5,7,4'-trihydroxyflavone-8-C-$\beta$-D-glucopyranoside (vitexin) (1), 5,7,4'-trihydroxyflavone-6-C-$\beta$-D-glucopyranosyl-(1 $\rightarrow$ 2)-$\beta$-D-glucopyranoside (isovitexin-2"-$\beta$-D-glucopyranoside) (2), 5, 7, 4'-trihydroxyflavone-6, 8-di-C-$\beta$-D-glucopyranoside (vicenin-2) (3) and one O-flavonoidal glycoside; kaempferol-3-O-$\beta$-D.glucopyranosyl) (1 $\rightarrow$ 2)-$\beta$-D-glucopyranoside (4). The structures of the isolated compounds (1 - 4) were elucidated using different spectral techniques (UV, 1D and 2D NMR and HRESIMS). This is the first report for the isolation of flavonoidal glycosides from Erythrina caffra. The antibacterial, antifungal, antimalarial, and antileishmanial activities of the isolates were evaluated. In addition, the cytotoxic activity of the ethanolic extract and the main fractions were tested using brine shrimp bioassay.