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김윤강,백장렬,장기범,김준수,김신아,문다예,김병현,김영화,박준철,최지환,송민호 충남대학교 농업과학연구소 2017 Korean Journal of Agricultural Science Vol.44 No.4
Soybean, one of most widely used swine feed component in the world, contains non-starch polysaccharides (NSP). The digestive system of weaned pigs is not yet fully developed, and thus weaned pigs cannot easily digest diets based on corn and soybean meal. Dietary exogenous enzymes supplementation has been intensively investigated to assist digestion of anti-nutritional factors, such as NSP. This experiment was conducted to investigate the effects of dietary enzyme cocktail on growth performance, intestinal morphology, and nutrient digestibility of weaned pigs. A total 36 weaned pigs (5.92 ± 0.48 kg BW; 28 d old) were randomly allotted to 2 dietary treatments (3 pigs/pen, 6 replicates/treatment) in a randomized complete block design. The dietary treatments were a typical diet based on corn and soybean meal (CON) and CON with 0.05% enzyme cocktail (Cocktail; mixture of xylanase, α-amylase, protease, β-glucanase, and pectinase). Pigs were fed their respective diets for 6 wk. Growth performance, morphology of ileum, apparent ileal digestibility (AID) and apparent total tract digestibility (ATTD) of dry matter, crude protein, and energy of weaned pigs were measured. No significant differences (p > 0.05) were observed for growth performance for the duration of the experimental period, and morphology of ileum, and nutrient digestibility between CON and Cocktail treatment groups. Therefore, the results from the current study indicated that enzyme cocktail supplementation in diets had no influence on growth performance, intestinal morphology, and nutrient digestibility of weaned pigs.
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Agrobacterium tumefaciens에 의한 강낭콩 키틴가수분해효소 유전자의 고려인삼으로의 도입
이행순,권석윤,백경희,김석원,이광웅,유장렬 한국식물생명공학회 1995 식물생명공학회지 Vol.22 No.2
본 연구는 이미 확립되어 있는 고려인삼의 체세포배발생을 통한 식물체 재분화와 Agrobacterium을 매개로 한 형질전환 시스템을 이용하여 항곰팡이성 인삼을 개발하고자 염기성인 강낭콩 키틴가수분해효소 유전자를 인삼으로 도입하였다. CaMV 35S promoter-강낭콩 키틴가수분해효소 유전자와 선발표지로서의 neomycin phosphotransferase II (NPT II) 유전자를 가진 pChi/748 binary 벡터를 pGA748로부터 제조하여 이를 도입한 A. tumefacience LBA4404와 인삼 접합배의 자엽절편을 1 mg/L 24-D, 0.1 mg/L kinetin이 첨가된 MS 액체배지에서 48시간 동안 공동배양한 후 동일배지에 100 mg/L kanamycine 500 mg/L carbenicillin을 첨가한 고체 배지에 옮겨 배양하였다. 배양 한달 후부터 절편의 절단면 부근으로부터 캘러스가 유도되기 시작하였으며 이어서 수많은 체세포배가 형성되었다. 이들 체세포배를 BA와 GA3가 각각 1 mg/L 첨가된 배지로 옮겨서 5주 경과되었을 때 식물체로 전환되었다. 재분화된 개체 중 선발된 8개의 식물체로부터 PCR과 이 산물의 Southern분석 결과 6개의 재분화 개체에서 강낭콩 키틴가수분해효소 유전자가 도입되었음을 확인하였다. We have previously established a system for plant regeneration through somatic embryogenesis and Agrobacterium-mediated transformation of Korean ginseng. In this study to produce a fungus-resistant plant, we introduced a bean chitinase gene into ginseng using the transformation system. A binary vector pChi/748 was constructed by introducing the bean basic chitinase gene into EcoRI site of pGA748 which carries the CaMV 35S promoter governing the introduced gene and neomycin phosphotransferase II(NPT-II)gene as a positive selection marker. Cotyledonary explants were cocultured with A. tumefaciens strain LBA4404 harboring the binary vertor pChi/748 for 48 h, and transferred to MS medium supplemented with l mg/L2,4-D,0.1mg/L kinetin, 100 mg/L kanamycin, and 500mg/L carbenicillin. Kanamycin-resistant calli were formed on the cut surface of cotyledonary explants after one month of culture, and subsequently they gave rise to somatic embryos. Upon transfer onto medium containing 1 mg/L each of BA and GA$_3$, most of them converted to plantlets after 5 weeks of culture. The genomic DNA of eight kanamycin-resistant regenerants was subjected to polymerase chain reaction (PCR) using two specific 21-mer oligonucleotides derived from the chitinase gene. PCR-Southern blot analysis confirmed that the chitinase gene was incorporated into six out of the eight regenerants..
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