Dissertations / Theses on the topic 'Carp'
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Cheng, Zhang. "Use of food waste feeds for culturing low trophic level fish (grass carp, bighead carp and mud carp): persistent toxic substances." HKBU Institutional Repository, 2014. https://repository.hkbu.edu.hk/etd_oa/76.
Full textHung, Ching Yee. "Survival strategies of common carp, cyprinus carpio, during prolonged starvation and hypoxia /." access full-text access abstract and table of contents, 2005. http://libweb.cityu.edu.hk/cgi-bin/ezdb/thesis.pl?phd-bch-b19887346a.pdf.
Full text"Submitted to Department of Biology and Chemistry in partial fulfillment of the requirements for the degree of Doctor of Philosophy." Includes bibliographical references (leaves 233-269).
DeGrandchamp, Kelly Lynn. "Habitat selection and movement of bighead carp and silver carp in the lower Illinois River /." Available to subscribers only, 2006. http://proquest.umi.com/pqdweb?did=1240695561&sid=9&Fmt=2&clientId=1509&RQT=309&VName=PQD.
Full textMcLean, Victoria Lynne. "Carp Impacts on Diked Wetland Communities." The Ohio State University, 1996. http://rave.ohiolink.edu/etdc/view?acc_num=osu1392915387.
Full textCopeland, Donald Lee. "Production of Recombinant Carp Leptin and its Effects on Lipid Metabolism in the Common Carp (Cyprinus Carpio)." University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1342135953.
Full textLaure, Lydie. "Etude du complexe CARP-Titine-Calpaïne 3 : de la fonction vers la thérapeutique." Thesis, Evry-Val d'Essonne, 2008. http://www.theses.fr/2008EVRY0004/document.
Full textCalpain 3, a protease of the skeletal muscle is defective in Limb-Girdle Muscular Dystrophies type 2A (LGMD2A). During our study, we demonstrated that CARP (Cardiac Ankyrin Repeat Protein), is a calpain 3 substrate. Our hypothesis is that calpain 3 enhances CARP interaction with sarcomere thus preventing its passage and its nuclear activities. Our experiments showed that CARP acts on the function of several transcription factors amongst which some are involved in the regulation of muscle mass and that CARP regulates the expression of proteins involved in remodelling. Together, our results suggest that CARP could intervene in the remodelling of sarcomere. The loss of such a mechanism could participate in the pathophysiology of LGMD2A. On the other hand, we showed that the expression of CARP increases in all dystrophic models studied, suggesting that CARP is a key marker of these diseases. The control of its overexpression may constitute a therapeutic option for these diseases
Williams, Paul Edwin. "Evaluation of a Common Carp (Cyprinus carpio L.) Exclusion and Trapping Device for Use in Aquatic Plant Founder Colony Establishment." Thesis, University of North Texas, 2008. https://digital.library.unt.edu/ark:/67531/metadc6038/.
Full textJuell, Rosemary Alice. "The Physiological Stress Response of Bighead Carp Hypophthalmichthys Nobilis, and the Efficacy of Three Chemical Anaesthetics in Bighead Carp Fingerlings." Thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for biologi, 2013. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-23677.
Full textVilizzi, Lorenzo. "Age, growth and early life history of Carp (Cyprinus carpio L.) in the River Murray, South Australia /." Title page, table of contents and synopsis only, 1997. http://web4.library.adelaide.edu.au/theses/09PH/09phv711.pdf.
Full textAddendum and erratum pasted onto back fly leaf. Copy of author's previously published work inserted. Includes bibliographical references (p. 169-215).
Brown, Gerald Francis. "Novel aspects of grass carp GHR gene regulation." Thesis, Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B41897080.
Full textFisher, Kevin J. "Novel aspects of bighead carp sperm storage and larval/juvenile rearing to address control of invasive Asian carp in the USA." The Ohio State University, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1593608879176277.
Full textCalkins, Heather Ann. "Linking Silver Carp Habitat Selection to Phytoplankton Consumption in the Mississippi River." OpenSIUC, 2010. https://opensiuc.lib.siu.edu/theses/345.
Full textSalehi, Hassan. "A strategic analysis of carp culture development in Iran." Thesis, University of Stirling, 1999. http://hdl.handle.net/1893/2643.
Full textPetruv, Renata. "Spatial and chromatic organization of the H1 horizontal cell network in the fish retina : involvement of nitric oxide." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321762.
Full textHaamedi, Sakineh. "Biophysical studies of the vertebrate (fish) outer retina : light adaptive cellular and synaptic plasticity." Thesis, Imperial College London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.367953.
Full textSzynkowski, Brittany Christine. "An examination of Asian carp spawning in pool 26 of the Mississippi River." OpenSIUC, 2013. https://opensiuc.lib.siu.edu/theses/1344.
Full textNinh, Nguyen Huu. "Communal or separate rearing of families in selective breeding of common carp (Cyprinus carpio L.)." Thesis, University of Stirling, 2009. http://hdl.handle.net/1893/1638.
Full textXavier, João Antônio Amaral. "Crescimento de Carpa Capim Ctenopharyngodon idella alimentada com diferentes gramíneas." reponame:Repositório Institucional da FURG, 2008. http://repositorio.furg.br/handle/1/2680.
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A carpa capim Ctenopharyngodon idella é uma das espécies de maior importância na aqüicultura mundial. Por ser herbívora, pode ser produzida com abaixo custo, uma vez que se alimenta de vegetação aquática, de gramíneasterrestres ou de outros vegetais. O objetivo deste trabalho foi verificar a possível utilização de gramíneas nativas da região Sul do Rio Grande do Sul, Brasil na alimentação da carpa capim. O experimento foi conduzido alimentando alevinos de carpa capim com peso inicial de 2,69 ± 0,47 g, com 4 gramíneas: Pennissetum purpureum, Cynodon dactylum, Paspalum urvillei e Spartina alterniflora. Foram utilizadas 12 caixas de polietileno com volume útil de 200 litros, com fluxo constante de água (600% ao dia). Foram colocados dez alevinos em cada caixa, os quais foram alimentados diariamente com as respectivas gramíneas acrescidas, a cada dois dias, de ração comercial (1% da biomassa). O experimento teve duração de 45 dias, realizando-se biometria quinzenalmente. Os resultados de Ganho de Peso (GP) e Taxa de Crescimento Especifica (TCE) mostraram que as carpas alimentadas com C.dactylum e P.urvillei obtiveram um maior GP (respectivamente 1,45 e 1,32g) e uma melhor TCE (respectivamente 0,95 e 0,88%), quando comparadas com carpas alimentadas com P. purpurem e S. alterniflora. Cynodon dactylum e P.urvillei são, portanto, gramíneas indicadas para alimentação da carpa capim.
The grass carp Ctenopharyngodon idella is one of the species of great importance in the world-wide aquaculture. As herbivore it can be produced by low cost, as soon as it is fed with aquatic vegetation, with grasses or other vegetables. The objective of this work was to analyze the possible use of natives grasses from south of Rio Grande do Sul, Brazil as food of the grass carp. The experiment was accomplished feeding grass carp fingerlings with initial weight of 2.69 ± 0.47 g, with 4 grasses type: Pennissetum purpureum,Cynodon dactylum, Paspalum urvillei and Spartina alterniflora. They were used 12 boxes of polyethylene with useful volume of 200 liters, with constant water flow (600 % by day). Ten fingerlings were placed in each box, which were fed daily with the respective grass, being added, each two days, commercial ration (1 % of the biomass). The experiment had duration of 45 days, happening biometry fortnightly. The results of Weight Gain (WG) and Specific Growth Rate (SGR) showed that the carps fed with C. dactylum and P. urvillei had a bigger WG (respectively 1.45 and 1.32g) and a better SGR (respectively 0,95 and 0,88%), when compared with carps fed with P. purpureum and S. alterniflora. Cynodon dactylum and P. urvillei are, so, grass indicated as food of the grass carp.
Silva, Roberto de Souza Gomes da. "Obtenção de gelatina utilizando cabeças de carpa comum (Cyprinus carpio): avaliação das etapas de pré-tratamento e extração." reponame:Repositório Institucional da FURG, 2010. http://repositorio.furg.br/handle/1/2574.
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A carpa comum (Cyprinus carpio) é conhecida por ser geradora de quantidade considerável de rejeitos mal aproveitados por indústrias pesqueiras. Estes rejeitos são constituídos por vísceras, peles, ossos e cabeças. Diversos fatores têm contribuído para a utilização de cabeças de carpa provenientes da industrialização, dentre estes a quantidade de cabeças desperdiçadas, que pode atingir 22% do volume da matériaprima, e é uma fonte de nutrientes de baixo custo e rica em colágeno. A maioria das gelatinas comerciais é derivada de mamíferos, sendo peles e ossos de bovinos e suínos as principais matérias-primas do produto. A gelatina é de uma proteína pura, digestível, que se obtém a partir da hidrólise à quente do colágeno, e por este motivo, o pescado torna-se uma potencial fonte de matéria-prima. A aplicação da gelatina é diversificada, podendo ser utilizada na indústria cosmética, farmacêutica,fotográfica e alimentícia. O presente estudo foi dividido em dois objetivos. Primeiramente foram avaliados os efeitos da concentração alcalina, tempo de pré-tratamento e prétratamentos com ou sem troca de solução alcalina do material para a obtenção de gelatina das peles das cabeças de carpa. Foi utilizado um planejamento fatorial 23 completo, e os fatores de estudo foram concentração de NaOH (3-4 M), tempo de prétratamento(45-105 min), e troca de solução de NaOH no pré-tratamento, tendo como respostas rendimento em gelatina, força do gel e ponto de fusão. Na segunda etapa, os ossos remanescentes deste processo foram utilizados para o estudo da influência da granulometria (1-2 mm) nas respostas consideradas das gelatinas extraídas da fração óssea, através da comparação das médias pela aplicação do teste de Tukey, com intervalo de 95% de confiança. Foram realizadas quatro extrações com pH e temperaturas de cada extração de 5,3-60°C, 4,4-70°C, 3,8-80°C e 3,6-85°C. Para as gelatinas extraídas das peles, o maior rendimento (2,27%) foi obtido com solução de NaOH 3 M, 45 min e sem troca de solução no pré-tratamento. Os maiores valores de força do gel (298,7 g) e ponto de fusão (29°C) foram obtidos a concentração de solução NaOH 3 M, 45 min e sem troca de solução alcalina. Para as gelatinas extraídas dos ossos, o maior rendimento (4,86%) foi obtido na granulometria de 1 mm. Os maiores valores de força do gel (128,2 e 131,5 g) não apresentaram diferença significativa (p≤0,05) e foram encontrados na primeira extração das granulometrias de 1 e 2 mm, respectivamente. Na fração óssea a 2 mm, se obteve o maior ponto de fusão, sendo 28,5°C na a primeira extração. O rendimento total da gelatina obtida a partir das cabeças de carpa foi de 7,13%.
Common carp (Cyprinus carpio) is known to produce large amount of byproduct does not made use for fisheries industries. These byproduct can be viscera, skin, bone and head, all riches in collagen. Several factors have been contributing to the use of the carp head coming from industrialization, among which the amount of carp head wasted, with which it can reach around 22% of the volume of the raw material, and it is a source of low costs nutrients. Most of commercial gelatin is derived from mammalian, being skins and bones of bovine and porcine the main raw material of this foodstuff. Gelatin is a pure and digestible protein, which is obtained from hydrolysis of the collagen, and for this reason, the fish become a potential source from raw material. Its application is branched out, being able to used in the cosmetic, pharmaceutical, photographic and food industries. The present study was divided into two parts. At first, it was valued the effect of alkaline concentration, pre-treatment time of the raw material, and treatment with and without change of alkaline solution, in the process of extraction of skin/muscles fraction gelatin of carp head coming from manufacturing processing of this fish. It was used 23 complete experimental design. Pre-treatment time (45-105 min), concentration of alkaline solution (3-4 M) and pre-treatment with change of alkaline solution were chosen as independent variable. Gelatin yield, gel strength and melting point were the response variable. At the second part, was valued of the influence of the bones granulometry (1-2 mm), remaining of the skin extraction of common carp head, in the gelatin yield, gel strength and melting point through the average results comparison by the Tukey test, where differences were considered significant at p≤0.05. It was used four extraction with pH and temperature of each extraction 5.3-60°C, 4.4-70°C, 3.8-80°C and 3.6-85°C. To the skin gelatin the higher gelatin yield (2.27%) was obtained with NaOH solution 3 M, 45 min and pre-treatment without change of alkaline solution. The higher gel strength (298.7 g) was achieved using NaOH solution 3 M, 105 min and pre-treatment without change of the alkaline solution. As for the melting point, the higher value (29.1°C) was obtained with NaOH solution 4 M, 45 min, and pre-treatment with change of NaOH solution. To the bones extraction, the higher gelatin yield was reached with size 1 mm (4.86%). The higher gel strength (128.2 and 131.5 g) were not significantly difference, and they were found in the first extraction with bones size 1 and 2 mm, respectively. Using 2 mm of granulometry, it was possible to obtain the higher melting point values, being 28.5°C to the first extraction.
Gilmore, Joseph M., Jared J. Sweetser, and Keith B. Klemm. "Analysis of aircraft carrier excess material offloaded to carp facilities." Monterey, California. Naval Postgraduate School, 2011. http://hdl.handle.net/10945/10768.
Full textThe Consumable Asset Reutilization Program (CARP) is an organization established under Naval Supply Systems Command to provide a specific warehousing service for excess material generated by commands operating under the Navy Working Capital Fund. This warehousing service would receive excess consumable material that had possible future demand, and hold that material until demand on that item was realized. Annually, CARP processes approximately 70,000 excess offload transactions from aircraft carriers, amphibious assault ships, and naval air stations. Of the three, aircraft carriers are the largest customer of this service. This MBA project employs exploratory research to empirically analyze material that is offloaded from aircraft carriers to CARP, and to identify drivers of the high volume of excess consumable material that is generated on-board aircraft carrier inventories. This project proposes policy-level changes to both the allowancing and offload processes for aircraft carriers, and, through statistical modeling and analysis, estimates the outcomes of these changes on inventories and costs.
Fung, Sai-kit, and 馮世傑. "Functional studies of pituitary activin/follistatin system in grass carp." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hdl.handle.net/10722/192776.
Full textHu, Guangfu, and 呼光富. "Novel pituitary actions of TAC3 gene products in grass carp." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/208050.
Full textZou, Jun. "Cloning and expression of grass carp (Ctenopharyngodon idella) growth hormone." Thesis, University of Aberdeen, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.245196.
Full textAlam, Mohammad Ashraful. "Effects of Environmental Factors on Bighead Carp (Hypophthalmichthys nobilis) Juveniles." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1515042773505047.
Full textEl-Feki, Mostafa A. E. "Studies of the host-parasite interaction between carp and saprolegnia." Thesis, Aston University, 1987. http://publications.aston.ac.uk/14524/.
Full textEid, Abd E. M. S. "The assessment of protein quality of carp (Cyprinus carpio) diets." Thesis, Aston University, 1987. http://publications.aston.ac.uk/14526/.
Full text周楚穎 and Chor-wing Vivian Ng. "Characterization and sequencing of sex hormone-binding globulin in common carp (cyprinus carpio)." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2000. http://hub.hku.hk/bib/B31224982.
Full textWilliams, Paul Edwin Hudak Paul F. "Evaluation of a common carp (Cyprinus carpio L.) exclusion and trapping device for use in aquatic plant founder colony establishment." [Denton, Tex.] : University of North Texas, 2008. http://digital.library.unt.edu/permalink/meta-dc-6038.
Full textMo, Wing Yin. "Food wastes as feeds incorporated with Chinese herbs and prebiotic fibers on growth and non-specific immunity of grass carp, bighead, mud carp and Nile tilapia." HKBU Institutional Repository, 2014. https://repository.hkbu.edu.hk/etd_oa/91.
Full textMacCarthy, Eugene. "Pentraxins and the acute phase response in common carp Cyprinus carpio." Thesis, Keele University, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.436139.
Full textRimbawan. "Digestibility and availability of amino acids from carp (Cyprinus carpio) muscle." Thesis, University of Nottingham, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306701.
Full textBarnard, Philip. "Gustatory and olfactory feeding responces in Japanese koi carp (Cyprinus carpio)." Thesis, Stellenbosch : University of Stellenbosch, 2006. http://hdl.handle.net/10019.1/1787.
Full textChemo-attraction and –stimulation facilitate the initial location (olfactory response) and final consumption (gustatory response) of food in the feeding process of fish. Chemo-attractants or chemo-stimulants is therefore generally included in feeds for especially slow-feeding species to help reduce water fouling and to promote feed efficiency and growth rate through improved feed intake. Considering this, a study was performed to evaluate the attraction and stimulation potential of selected cereals and free amino acids in diets for Japanese koi carp (Cyprinus carpio). Results are presented on the comparative evaluation of five cereals (maize, sorghum, wheat, rye and triticale), raw and cooked forms of maize and concentrations of betaine and selected free amino acids (alanine, arginine, lysine and methionine), as well as their additive effect.
Huang, Yun-Cheih, and 黃韻潔. "Studies on Distribution of the 43 kDa Zn-Binding Protein in Common Carp, Grass Carp, Silver Carp and Tilapia by Using Immunoassay." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/14620432929980057945.
Full text國立臺灣海洋大學
食品科學系
94
Abstract Common carp always has high concentration of zinc in its digestive tract tissue which mainly comes from a 43 kDa zinc-binding protein. Detergent (lubrol) was used to extract this 43 kDa zinc-binding protein from living organism. Lubrol only could extract 5% of the zinc-binding protein from nuclei/cell debris fraction of digestive tract tissue of common carp. Adding 4 M guanidine hydrochloride to the lubrol increased the extraction ratio to 85%. Zn2+-IMAC and SDS-PAGE analysis indicated that the major protein in the guanidine/lubrol extract was the 43 kDa zinc-binding protein. In immunoassay, the guanidine/lubrol extracts reacted with the antibody against 43 kDa zinc-binding protein dose dependently. A standard calibration curve of the guanidine hydrochloride/lubrol extract against the immuno-response was obtained. The standard calibration curve was used to examine whether the 43 kDa zinc-binding protein exist in the guanidine hydrochloride/lubrol extract of other fishes. It was found that the 43 kDa Zinc-binding protein both exist in common carp’s kidney and spleen. The 43 kDa zinc-binding protein also existed in the digestive tract tissue and spleen of grass carp and silver carp which are the same families of Cyprinidae. However, the protein does not exist in the muscle of common carp, grass carp and silver carp. In tilapia, the species and genus are far from common carp, in all tissue tilapia no immuno-response against the antibody of 43 kDa zinc-binding protein was found. Existence of the 43 kDa zinc-binding protein in animal tissue seems to be related to organisms’ species and genus.
Chang, Mau-Sun, and 張茂山. "Studies on Carp JAK1 Kinase." Thesis, 1997. http://ndltd.ncl.edu.tw/handle/26496254488977163962.
Full text國立臺灣大學
動物學研究所
85
Using the PCR strategy, we cloned the carp JAK1 kinase that encoded 1,156 amino acid residues. The overall amino acid sequence identity between carp JAK1 and murine JAK1, JAK2, JAK3 and human TYK2 is 57 %, 35.5 %, 31.3% and 42.4 %, respectively. In addition, carp JAK1 shows higher sequence homology to mammalian JAK1 in both the kinase-like (JH2) and kinase (JHI) domains (approximately 70 % identity). Therefore, carp JAK1 is a homologue of mammalian JAK1. In order to investigate the possible function of JH2 domain, full-length and various truncated forms of carp JAK1 were produced in the baculovirus system. Our results demonstrate that c-JH1 and c-JH2 associate with each other and c-JH2 can be tyrosine-phosphorylated by c-JAK1 and by c-JH(1+2).The JAK1 gene was also isolated from a carp genomic library and characterized. This gene is divided into 24 exons spanning at least 31 kb of genomic DNA. Exon I contains the 5''-untranslated region, and exon 2 contains the putative translation initiation site. The 2.5 kb DNA region upstream of the transcription initiation site contains numerous potential binding sites for transcription factors including NF-IL6, HNF-5, AP1, GHF-5, and E2A. When this DNA fragment was placed upstream of the chloramphenicol acetyltransferase (CAT) reporter gene and transfected into a carp CF cell line, it could drive the synthesis of CAT enzyme 16 times more efficiently than the promoterless pCAT- Basic. Deletion analysis defined a positive regulatory region between -1023 and - 528. A smaller region (-181 to +59) without any typical TATA-box sequences, G+C-rich sequences, or other binding sequences for known transcription factors still had promoter activity. Constructs without this region did not have detectable promoter activity. This suggests that this region of DNA may play an important role in the expression of carp JAK1 gene. There are two AP1 binding motifs located in the promoter region of JAK1 gene, 1449 and 1221 bp upstream to the transcription start site. In order to investigate whether carp AP1 may regulate the expression of carp JAK1 gene, we cloned the carp c-fos and junB cDNA. The carp c-fos encoded 347 amino acid residues and carp junB encoded 308 amino acid residues. The amino acid sequence identity of carp and human c-fos is 55.2% , and that of carp and human junB is 59.6%. However, the basic region and leucine zipper region of carp/ human c-fos and carp/ human junB showed higher amino acid sequence identity, up to 80% amino acid identity. The carp c-fos and junB was constructed with transfection vector pREP4 and named as RSV-c-fos and RSV-junB, respectively. The pJP1-CAT was cotransfected with RSV-c-fos and RSV-junB into CF cells. Cell extracts were prepared and assayed for the CAT activity at various transfecting time intervals after transfection. The data showed that the CAT activity of cotransfection of pJPI-CAT with both RSV-c-fos and RSV-junB could increase 5-10 times greater than that of pJPI-CAT alone. In addition, cotransfection of both RSV-c-fos and RSV-junB with pJPI-CAT drives more CAT activity than that of either RSV-c-fos or RSV-junB with pJPI-CAT. However, the mechanism how carp API regulates the promoter activity of carp JAK1 gene is still not clear. Further investigations will be needed to shed light on this question.
ZHANG, WANG-LONG, and 張王隆. "Annual survey of carp estrogen and the effect of gonadotropin on the steroid production by carp ovary." Thesis, 1986. http://ndltd.ncl.edu.tw/handle/18655243037013838325.
Full textCAI, YUAN-ZHANG, and 蔡元彰. "Sequencing of the cDNA encoding carp cholesterol side-chain cleavage enzyme (P450 SCC) of carp head kidney." Thesis, 1988. http://ndltd.ncl.edu.tw/handle/38334321939959246976.
Full textJIANG, YUN-JIN, and 江運金. "Studies on crystallins of carp and bullfrog." Thesis, 1988. http://ndltd.ncl.edu.tw/handle/10199446072003478274.
Full text賴意繡. "Toxicological Study of Grass Carp Bile Juice." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/94085010697130767171.
Full text國立海洋大學
水產食品科學研究所
83
Some Chinese people believe that eating the animal gallbladders, such as the bile of grass carp (Ctenopharyngodon idellus), common carp (Cyprinus carpio), snake and chicken, may improve their visual acuity. However, poisonig cases have been occasionally occurred when people ingested animal biles, especially grass carp bile. Among those cases, the major symptom of victims was acute renal failure. Impairments of liver, gastrointestinal tract and central nervous system were also noted. But the major toxic material is not clear so far. On the other hand, the toxicity of snake and chicken bile juices is also not clear. So the experiments were aimed to investigate the toxicity of grass carp, snake and chicken bile juices in male rats (Long-Evans, 150-200g), and to elcidate the responsible toxic components of grass carp in its bile juice. Experiment I-A: Rats were separately administered with saline (0.6ml), 0.3ml grass carp bile juice and 0.3ml saline solution, grass carp bile juice (0.6ml), snake bile juice (0.6ml) and chicken bile juice (0.6ml) by gastric intubation. At 6 and 24 hr after administration, the plasma of rats were examined for physiological functions of liver and kidney. The activities of aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), blood urea nitrogen (BUN) and creatinine were the highest in the plasma of rats treated with grass carp bile juice, and were clearly observed to increase with increasing bile dose. But the toxicity of snake bile juice and chicken bile juice is weak. Experiment I-B: The rats were administered with saline (0.6ml), garss carp bile juice (0.03ml and 0.3ml), snake bile juice and chicken bile juice (0.03ml, 0.3ml and 0.6ml) for 3-day periodically. On 1st, 10th, 19th and 28th day, the plasma of rats were examined for physiological functions of liver and kidney. Among nine groups, the values of AST, ALT, BUN and reatinine in the plasma of rats treated with 0.6ml grass carp bile juice were the highest. THe grass carp bile juice is the most toxic than snake and chicken bile juices. The rats administered with grass carp bile juice could induce the acute renal failure and the impairment of liver, but the rats administered with the snake and chicken bile juices induced the impairment of liver only. Experiment II: Attempts were made to purify and identify the 5α-cyprinolfrom grass carp bile juice. The toxicity of bile salts was also discussed. By IR, 1H-, 13C-NMR and MS spectrometry analyses, a compound with molecular formula of C27H48O5 and molecular weight of 452 was obtained from grass carp bile juice and identified as 5α-cyprinol. Then, the rats were separately administered with saline (0.6ml), gras carp bile juice (97.44mg/0.6ml), sodium cholate (100mg/0.6ml) and sodium chenodeoxycholate (100mg/0.6ml). After 6 hr, the plasma of rats were examined for physiological functions. The activities of AST and ALT in plasma of rats theated with grass carp bile juice, sodium cholate and sodium chenodeoxycholate were siginificantly higher than that of saline group. The subacute toxicity of bile salts was also discussed. The rats were administered with saline (0.6ml), sodium cholate (100mg/0.6ml) and sodium chenodeoxycholate (100mg/0.6ml) for 3-day periodically. On 1st, 10th, 19th and 28th day, the plasma of rats were examined for physiological functions of liver and kidney. The values of AST, ALT, BUN and creatinine in the plasma of rats treated with sodium cholate and sodium chenodeoxycholate were significantly higher than that of saline group. Moreover, the rats were separately administered with saline (0.6ml), grass carp bile juice (97.44mg/0.6ml) and 5α-cyprinol(97.44mg/0.6ml). After 6 hr, the plasma of rats were examined. The values of BUN and creatinine in the plasma of rats treated with grass carp bile juice and 5α-cyprinol were siginificantly higher than that of saline group. In conclusion, the toxins of grass carp bile juice included 5α-cyprinoland bile salts such as (sodium cholate and sodium chenodeoxycholate). In the way of acute toxicity of grass carp bile juice the function of liver is mainly effected by bile salts and the function of kidney is mainly effected by 5a-cyprinol.
Xu, Jia Zhang, and 徐佳璋. "Molecular cloning and expression of carp ZP2." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/63765102101385504335.
Full text國立臺灣大學
生化科學研究所
83
In this study, the nucleotide sequences of carp ZP2 cDNA were determined and their amino acid sequences were deduced. The deduced carp ZP2 contains 12 to 25 glutamine-rich tandem repeats of 12-13 residues in the N-terminal region followed by a sequence homologousto winter flounder and mammalian ZP2 in the C-terminal region. Northern blot analysis showed that ZP2 mRNA is only present in the ovary but not present in other tissues including liver、testis、head-kidney、kidney and brain. By Western blot analysis, ZP2 was only detected in the vitellogenic oocytes but not in the previtellogenic oocytes, nor in the plasma of estradiol-treated carp. All these results suggest that carp ZP2 is synthesized in the ovary. In addition, the carp ZP2 was found to play roles in the cross-linking of egg membrane components during egg maturation, ovulation and cortical reaction.
"Proteolytic activation of grass carp alcohol dehydrogenase." 1997. http://library.cuhk.edu.hk/record=b5889172.
Full textThesis (M.Phil.)--Chinese University of Hong Kong, 1997.
Includes bibliographical references (leaves 119-142).
ACKNOWLEDGMENTS --- p.I
ABSTRACT --- p.II
ABBREVIATIONS --- p.IV
TABLE OF CONTENTS --- p.V
Chapter CHAPTER 1 --- INTRODUCTION --- p.1
Chapter CHAPTER 2 --- PURIFICATION OF ADH-I & ADH-C --- p.25
Chapter CHAPTER 3 --- "PURIFICATION & IDENTIFICATION OF ""ADH-ACTIVATING"" PROTEASE" --- p.60
Chapter CHAPTER 4 --- ACTIVATION OF ADH-I BY COMMERCIAL PROTEASE & BY ACETIMIDYLATION --- p.90
Chapter CHAPTER 5 --- CONCLUSION --- p.114
REFERENCES --- p.118
Wei, Liang-Tai, and 魏良泰. "Cloning and Characterization of Carp Intersex Gene." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/30826044067672384493.
Full text國立臺灣大學
分子與細胞生物學研究所
94
Abstract The sex-determination of Drosophila melanogaster has been known clearly in previous studies. There is a gene called intersex (ix), which functions together with doublesex (dsx) at the bottom of the hierarchy in the sex deternination females. Drosophila ix is expressed in both sex, but only functions in female somatic cell. It has no effect on male. There is no recognizable DNA-binding domain on the amino acid sequence of ix for binding to DNA, but it contains a region like transcriptional activation domains to interact with other proteins, and ix might play a similar role as the C-terminal of DSXM when acts together with DSXF. Mediator complex was found in yeast, it is a protein complex composed over 20 subunits, and plays an essential role in the regulation of transcription. Brower et al. (2002) and Wang et al. (2004) also have cloned a navel gene of mammalian Mediator complex subunit, which is the homolog of Drosophila ix. Northern blot analysis demonstrated that ix is expressed in various tissues, and the protein is localized mainly to nucleus, supporting its function as a transcriptional regulator. Our laboratory also found a gene like Drosophila intersex in the testis of Cyprinus carpio (cIX). According to the significant function played by Drosophila ix in sex-determination, we are interested in the function of this gene in carp. To study the functions of cIX further, I cloned the full-length cDNA of cIX. The recombinant protein is produced and purified to serve as the antigen to induce antibody. The results of PCR and western blot analysis demonstrated that cIX is broadly existing in various tissue of carp, when the tissue specificity is not distinct. I also found that cIX has two mainly form, and the alignment of the homologs of other species indicates that IX proteins are conserved in C-terminal, and shows variation in N-terminal. The meaning of these information needs further study.
Lee, Kuan-Cheng, and 李冠徵. "Function and Regulation of Carp c-Mos." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/79085360317402725979.
Full text國立臺灣大學
分子與細胞生物學研究所
93
Abstract In most vertebrate animals, the development of the immature oocyte into a fertilizable gamete, a process known as oocyte maturation, involves an arrest in the meiotic cell cycle while awaiting fertilization. Mos, a serine/threonine kinase, is specifically expressed during meiotic maturation of vertebrate oocytes. After germinal vesicle breakdown (GVBD), Mos is involved in the regulation of meiotic spindle assembly and chromatin organization. The activation of this kinase is also essential for the maintenance of metaphase Ⅱ arrest. Ran GTPase, which belongs to the Ras superfamily of small GTPase, and the protein that regulate its GTP binding and hydrolysis has a well-defined role in nuclear transport. Recent studies indicate that Ran has a central role in spindle assembly and nuclear envelope reformation. It seems that Ran system and Mos pathway coordinate in some events in M phase. To understand the inter-relationship of them, I ectopically express Carp Mos gene in COS-1 cell and investigate Mos-interacting proteins. Heat Shock Protein-Hsp70 and Hsp90 are detected in Mos co-immunoprecipitation complex with or without kinase activity, but Ran dose not exist in the complex.
YIN, CHONG-JUN, and 尹重君. "Differential gene expression during oogenesis of carp." Thesis, 1991. http://ndltd.ncl.edu.tw/handle/01032794196286473805.
Full textJormay, Lim, and 林若梅. "Molecular Structure of Carp Visual Pigment Genes." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/21392460658395687634.
Full text國立臺灣大學
漁業學系
84
To investigate the molecular structures of the visual pigment genes and the initial biochemical reactions involved in the visual signal transduction relevant to fish physiology, the sequence of the visual pigment gene has to be determined. A putative cDNA encoding carp type I rhodopsin (Tsai et al., 1994) and a partial cDNA encoding type II rhodopsin (Chong, 1994) had been cloned from a retinal cDNA library. In the present work, the completely sequenced and analyzed. The deduced amino acid sequence of type II rhodopsin reveals that there are only five amino acid residues differences between type I and type II, i.e., (i) the 19th residue in type I is Val, instead of the Ile in type II (Val-19-Ile), (ii) Ile-54- Val, (iii) Ile-108-Val, (iv) Val-169-Glu, and (v) His-315-Asn. Besides, there are 4 polyadenylation signals in type II instead of 1 in type I, and the 3' untranslated region of type II is 99 bases longer. Furthermore, a genomic library of the common carp was constructed and the genomic DNA of type II rhodopsin was isolated. The genomic DNA was sequenced and the primer extension assay was performed to determine the transcription start site. The results reveal that (1) the gene is not interrupted by any intron, (2) the initiation of the transcripts of rhodopsin II is similar to that of other vertebrates, and (3) there are conserved regions and retina- specific nuclear protein binding sites found in the upstream region. The Southern analysis of genomic DNA and the reverse transcriptase-polymerase chain reaction imply that the two types of rhodopsins are from different individuals of the same population. On the other hand, a clone (3aV1) which resembles the retinal epithelium-specific protein gene was screened from the genomic library using the partial cDNA of green opsin as a probe. The results indicate that a fragment of the deletion clones of 3aV1 is 66% identical to the human satellite
Lin, Ruo Mei, and 林若梅. "Molecular structure of carp visual pigment genes." Thesis, 1996. http://ndltd.ncl.edu.tw/handle/80970835878206794217.
Full textHUANG, QUAN-ZHEN, and 黃銓珍. "Struoture and expression of carp gonadotropin genes." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/30531558615901278450.
Full textShiu, Jhe-Ruei, and 許哲睿. "Zinc-transferrin stimulates the proliferation of erythroid cell in the head kidney of grass carp, bighead carp, and tilapia." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/05800616921307132490.
Full text國立臺灣海洋大學
食品科學系
101
The common carp release zinc that stored in the fibroblast of digestive tract tissue when under stress. Free zinc combines with the transferrin in blood, and the zinc-transferrin complex is transported to head kidney by blood vessels. Zinc-transferrin complex interacts with the transferrin receptor on head kidney cells and were internalized to the cell, which stimulates the proliferation of erythroid cell to against stress in common carp. To understand whether zinc stimulates the proliferation of erythroid cell in the common carp head kidney is universal or not, grass carp and bighead carp which also are Cyprinidae, and tilapia which is classified to be Cichlidae, were used to study the effects of zinc on the proliferation of the erythroid cells in their head kidney. The grass carp, bighead carp, and tilapia head kidney cells were suspension-cultured with 4 different medium: medium only, medium + 10 % grass carp serum / bighead carp serum / tilapia serum, medium + 0.3 mM ZnCl2, medium + 10 % grass carp serum / bighead carp serum / tilapia serum + 0.3 mM ZnCl2 for 0, 1, 2, 4 days. The cell levels in total cell, and fractions 1 and 2 cell after Percoll separation were measured. The results show grass carp head kidney fraction 1 cell concentration that cultured with serum and ZnCl2 proliferated 6.22 times higher than the start after 4 days. Similar to grass carp, bighead carp head kidney fraction 1 cell level that cultured with serum and ZnCl2 were 3.02 times higher than the start after 4 days. But tilapia head kidney fraction 1 cells cultured with tilapia serum, regardless with or without ZnCl2, both proliferated to 2.89 and 2.82 times after 4 days. The results showed that adding ZnCl2 is no useful to tilapia head kidney fraction 1 cell growth. The grass carp, bighead carp, and tilapia head kidney cells were suspension-cultured with serum and ZnCl2 for 4 days, and then extracted with lubrol solution. The detergent extraction was subjected to Zn2+-IMAC (Immobilized metal ion affinity chromatography). The results show after 4 days, the Zn-binding proteins in head kidney of grass carp, bighead carp, and tilapia all increased 2-3 times higher than day 0. SDS-PAGE and nano-LC-MS/MS analysis indicated that all the Zn-binding protein were transferrin variants. These results indicated that the common carp, grass carp, bighead carp, and tilapia head kidney cells all have the same mechanism. In vitro, zinc combines with transferrin, and then the zinc-transferrin interacts with the transferrin receptor on head kidney cell. The zinc-transferrin complex is transported into the cell by endocytosis. In this case, zinc is the mitogen, and stimulates the proliferation of erythroid cells. After 4 days culture, zinc-transferrin induced common carp and grass carp head kidney cells proliferated 4.7 and 6.2 times, which were higher than bighead carp being proliferated only 3.6 times. The effect of zinc on tilapia head kidney cell growth is the least, only 2.8 times. However, in vivo, there are no enough zinc concentration in the grass carp and bighead carp head kidney cells, stimulation of the cell by zinc are limited. On the contrary , because the common carp has high zinc concentration in their digestive tracts, they can endure high stress. Common carp serum were used to replace grass carp / bighead carp serum in culturing grass carp / bighead carp head kidney cells. The results show that the fraction 1 cells also proliferation 5.28 and 3.97 times higher after 4 days. The results indicate that common carp serum has similar growth effect as their own serum. However, when common carp serum was used to replace tilapia serum, the tilapia head kidney fraction 1 cells only increased 1.9 times, which is lower than its own serum. The possible reason is Cyprinidae fish and tilapia transferrins have been diverged through evolution, so the common carp serum lost the ability to stimulates tilapia head kidney cell proliferation. In addition, the human-transferrin could not stimulate the proliferation of grass carp, bighead carp, and tilapia head kidney cells. This might be their homology between human-transferrin and grass carp, bighead carp and tilapia transferrins are too low to act on their head kidney cells. When the stressed grass carp and tilapia head kidney cells were cultured with serum and ZnCl2 for 4 days, the head kidney fraction 1 cells did not proliferate. The head kidney cell composition of the resting and stressed grass carp, and tilapia were compared. It was found that the fraction 1 cell concentrations of stressed fishs are higher than that of resting fishs. These results indicated that stressed grass carp and tilapia head kidney cells could not proliferate new erythroid cells when cultured with serum and ZnCl2 in vitro.
Li, Shwu-Huey, and 李淑慧. "Comparative Biochemical Study on Zinc and Zinc Binding Substances in Tissues of Common Carp, Crucian Carp, Goldfish and Other Fishes." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/49103783291820136668.
Full text國立海洋大學
食品科學系
87
Abstract Common carp (Cyprinus carpio) has extraordinarily high zinc concentrations (300-500 g/g fresh tissue) in its digestive tract tissue, the fish also has high zinc concentration (usually>100 g/g fresh tissue) in kidney, hepatopancreas and spleen. Zinc concentration of other aquatic organisms were in the level of 20 to 100 g/g fresh tissue. In order to understand whether the phenomenon also exist in its related species, e.g., crucian carp and goldfish, biochemical properties of zinc and zinc binding substances in the tissues of common carp, crucian carp and goldfish of Cyprinae of Cyprinidae, grass carp of Leuciscinae and silver carp of Hypophthalmichthyinae of the same family, and other fishes were examined. It was found that in Cyprinidae fishes, zinc concentrations of the digestive tract tissue of common carp, crucian carp and goldfish were about 20 times higher than those of other fishes; and kidney, spleen and hepatopancreas were about 2 times higher than those of other fishes. Zinc in subcellular fractions of tissues of common carp, crucian carp and goldfish mainly existed in the nuclei/cell debris fraction. Metallothionein-like substance were found in the cytosol of hepatopancreas of Cyprinidae fishes (crucian carp, goldfish, grass carp and silver carp), but the amount in common carp was very little. High correlation between the zinc concentrations of nuclei/cell debris fraction and total tissue of common carp, crucian carp and goldfish tissue was found. Besides, grass carp, silver carp and tilapia tissues also have the some kind of relationship. In result, zinc concentrations in the whole tissue and nuclei/cell debris fraction are related. The Debris Fraction of fish tissues was prepared by washing nuclei/cell debris fraction with 0.05 M Tris-HCl buffer pH 8.0. High correlation between the concentration of EDTA extractable-Zn and total tissue of common carp tissue, crucian carp and goldfish digestive tract tissues was found. The concentration of Total-SH and Free-SH in the Debris Fraction of digestive tract tissues of common carp, crucian carp and goldfish were measured. High correlation between the concentration of EDTA extractable-Zn and Bound-SH in the Debris Fraction of digestive tract tissues of common carp tissue, crucian carp and goldfish was found (r=0.94); this kind of correlation, however, was not found in grass carp, silver carp and tilapia. In digestive tract tissues of spotted chub mackerel, mackerel scad, kurma prawn and giant tiger prawn, high concentration of Total-SH was found, but there is little Bound-SH. The EDTA extractable-Zn are also very low, it is likely not correlation between Bound-SH and EDTA extractable-Zn concentration. Based on the experiments, high concentration of Zn in the digestive tract tissue seems to be a characteristics of Cyprinae fish, and the Zn might be bound in membrane protein of Debris Fraction. The Lubrol Extract of digestive tract tissues of common carp, crucian carp and goldfish were separated by IMAC. The IMAC-adsorbed proteins of digestive tract tissue of common carp, crucian carp and goldfish were compared on SDS-PAGE. It was found that crucian carp and goldfish also have ZnSBMP (zinc specific binding membrane proteins) same as common carp. Same three bands of ZnSBMP were also found in other tissues of common carp, but the concentration and composition percentage were different. In Marine fish, spotted chub mackerel, mackerel scad and scad also exist some of the bands of ZnSBMP.
Vilizzi, Lorenzo. "Age, growth and early life history of Carp (Cyprinus carpio L.) in the River Murray, South Australia / Lorenzo Vilizzi." Thesis, 1997. http://hdl.handle.net/2440/19083.
Full textBibliography: p. 169-215.
xiv, 215 p. : ill. (some col.) ; 30 cm.
Determines a reliable method of age determination, evaluates models of growth in wild populations, assesses growth patterns, describes the onset of the juvenile period, monitors the early life history of a wild population and reviews the literature on carp ecology.
Thesis (Ph.D.)--University of Adelaide, Dept. of Zoology, 1998?
Li, Zhao Chang, and 李肇昌. "Molecular cloning and expression of carp ovarian cystatin." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/23833939218947045001.
Full text國立臺灣大學
生化科學研究所
83
Three clones containing the inserts of 0.55、0.6 and 1.3 kb respectively, were isolated from a carp ovarian cDNA library. Nucleotide sequence analysis revealed that they are all homologous to the members of cystatin family of other vertebrates although they differ from each other. The open reading frames of all these cDNAs encode a protein of 129 amino acids which include a putative signal peptide of 18-20 amino acid residues. In addition, they also contain four invariable cysteine residues and three highly conserved regions found in cystatin family. The above data suggest that all the three cDNAs encode a polypeptide which belongs to the cystatin family of cysteine proteinase inhibitor. In this paper, the three cDNAs were also used as probes to detect the mRNAs expressed in carp tissues. In addition, they were constructed to an expression vector and expresse in E.coli. The expressed proteins were used as antigens to induce antibodies in rabbits, with which the distribution of these proteins in carp tissues or body fluids were investigated.The results indicate that both cystatin mRNAs and proteins are tissue-specifically expressed only in the ovary. The physiologicalroles of these proteins in carp remain to be investigated.