• 제목/요약/키워드: medium development

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Trophoblastic Vesicle과 Estradiol-$17\beta$의 첨가가 가토배의 발달에 미치는 영향 (Effects of Trophoblastic Vesicle and Estradiol-$17\beta$ on the Development in Vitro of Rabbit Embryos)

  • 오하식;박충생
    • 한국가축번식학회지
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    • 제10권1호
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    • pp.76-82
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    • 1986
  • This experiment was conducted to determine the effects of trophoblastic vesicles (TV) and estradiol-17$\beta$ on the development in vitro of rabbit embryos. Thirty matured female rabbits were treated with PMSG followed by HCG injection and mating. Embryos were recovered with D-PBS (Dulbecco's Phosphate Buffered Saline) after superovulation, and normally developed to two-to four-cell embryos were used in the subsequent in vitro culture. Basal medium was Medium-199 su, pp.emented with 1.5% bovine serum albumin. Embryo on Day 5 after mating (Day 0) was cut into two or three pieces to remove the embryonic disc. Each piece of tissue was cultured for 24 hours at 37$^{\circ}C$ in 0.5 mlMedium-199 in 5% CO2. During culture, peices of trophoblastic tissue changed into spherical vesicles which were used for co-culture. These spheres were called trophoblstic vesicles. Two-to four-cell embryos were cultured for 4 days in Medium-199 in the absence or presence of trophoblastic vesicle, and two-to four-cell embryos cultured with varing concentration (0, 0.1, 1, 10ng/ml) of estradiol-17$\beta$ for 4 dyas. Culture vessels used were watch glass for coculture with trophoblastic vesicles and micortube for estradiol-17$\beta$ infusion. Compared with the Medium-199 alone as basal culture medium, more blastocysts (46.7% vs 15.1%; P<0.01) and morulae (84.4% vs 56.6%; P<0.05) were developed in the co-culture with trophoblastic vesicles. Estradiol-17$\beta$ infused in culture medium was not effective for embryo development to blastocysts (78.3% in control, 50.0% in 0.1ng/ml, 61.5% in 1ng/ml and 64.4% in 10ng/ml) and also to morulae (91.3% in control, 84.2% in 0.1ng/ml, 92.3% in 1ng/ml and 91.1% in 10ng/ml). Compared with the watch glass culture mehotd, more (P<0.01) blastocysts were developed in microtube culture (78.3% vs 56.6%) and more (P<0.01) morulae in microtube culture (91.3% vs 56.6%).

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Development of a Selective Medium for Surveillance of Fusarium Head Blight Disease

  • Hosung Jeon;Jung Wook Yang;Donghwan Shin;Donggyu Min;Byung Joo Kim;Kyunghun Min;Hokyoung Son
    • The Plant Pathology Journal
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    • 제40권2호
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    • pp.106-114
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    • 2024
  • Fusarium head blight (FHB), predominantly caused by Fusarium graminearum and F. asiaticum, is a significant fungal disease impacting small-grain cereals. The absence of highly resistant cultivars underscores the need for vigilant FHB surveillance to mitigate its detrimental effects. In 2023, a notable FHB outbreak occurred in the southern region of Korea. We assessed FHB disease severity by quantifying infected spikelets and grains. Isolating fungal pathogens from infected samples often encounters interference from various microorganisms. We developed a cost-effective, selective medium, named BGT (Burkholderia glumae Toxoflavin) medium, utilizing B. glumae, which is primarily known for causing bacterial panicle blight in rice. This medium exhibited selective growth properties, predominantly supporting Fusarium spp., while substantially inhibiting the growth of other fungi. Using the BGT medium, we isolated F. graminearum and F. asiaticum from infected wheat and barley samples across Korea. To further streamline the process, we used a direct PCR approach to amplify the translation elongation factor 1-α (TEF-1α) region without a separate genomic DNA extraction step. Phylogenetic analysis of the TEF-1α region revealed that the majority of the isolates were identified as F. asiaticum. Our results demonstrate that BGT medium is an effective tool for FHB diagnosis and Fusarium strain isolation.

New Cymbidium Variety "Yellow Evening", with Brownish Yellow Flower Color on Red Spot Lip and Medium Plant

  • Kim, Mi-Seon;Cho, Hae-Ryong;Rhee, Hye-Kyung;Lim, Jin-Hee;Lee, Young-Ran;Shin, Hak-Ki
    • 한국육종학회지
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    • 제41권3호
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    • pp.358-362
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    • 2009
  • A New Cymbidium variety "Yellow Evening" was developed from a cross between "Oji" and "Valley Flower Cherry Life" followed by seedling and line selections at the National Institute of Horticultural and Herbal Science (NIHHS), Rural Development Administration (RDA) in 2004. After investigation of the characteristics and selection for 9 years (1996-2004), it has been selected specifically pot orchid flower. "Yellow Evening" has medium plant height and semi-erect peduncle. It has medium flowering habit and brownish yellow flowers (RHS, Y11B: petal and sepal) with grayed purple GP183A) spot on lip, when fully opened. Each peduncle has 15.3 flowers with diameter of about 7.4 cm. It has adequate peduncle height, with some curved and spreading petal and sepals. Under optical culture conditions, it started to bloom early-winter (November).

테프그라스 조직배양을 통한 캘러스 형성 및 식물체 재분화 효율 (Callus Induction and Plant Regeneration Efficiency According to Tissue Culture Conditions in Teff grass (Eragrostis))

  • 이기원;문진용;박형수;최기준;김기용;지희정;황태영;이상훈
    • 한국축산시설환경학회지
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    • 제19권1호
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    • pp.55-62
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    • 2013
  • Teff grass is a warm season C4 annual grass that is used for dry hay, silage and haylage. We have developed a high-frequency plant regeneration system for teff grass via callus culture using mature seeds. It was revealed that mature seeds cultured on MS medium supplemented with 2 mg/l 2,4-D, 0.5 g/L proline, 0.5 g/L casamino acid and 3 g/L Gelrite under light condition produced the highest percentage of callus formation (91.9%). Addition of cytokinins (BA) at 0.0~0.5 mg/L to media containing 2 mg/l 2,4-D enhanced callus growth. The most suitable medium for plant regeneration from dehydrated calli was MS agar medium supplemented with 0.1 mg/l NAA, 1 mg/l BA, 0.5 g/L proline, 0.5 g/L casamino acid 3 g/L Gelrite which induced the highest percentage of calli forming shoots (47.0%). The shoots were rooted at the highest rate (100%) when transferred onto 1/2 MS medium and acclimated in greenhouse conditions.

로드셀을 장치한 버섯 병재배용 배지의 수분조절 방법 (Adjusting moisture contents of the substrates on the mushroom bottle cultivation by the device Load cell)

  • 정종천;이찬중;문지원;권재건;김혁주
    • 한국버섯학회지
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    • 제13권3호
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    • pp.233-236
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    • 2015
  • 본 보고는 버섯 병재배용 배지혼합기를 사용하여 배지를 조제할 때 매일 배지의 수분함량을 일정하게 유지하고자 로드셀을 장치하여 활용하는 방법을 고안한 결과이다. 배지혼합기의 하부에 로드셀을 장치하고 병당 입병량과 입병수로 계산한 무게에 도달했을 때 물 주입이 자동적으로 끝나도록 하는 장치를 개발하였다. 또한 배지재료별 수분함량을 측정하고 프로그램(Cheong et al., 2015)을 활용하여 배지 조제시 목표로 하는 수분함량에 도달하는 배지의 총 무게를 산출하였다. 이 방법은 로드셀의 표시부에 목표 수분함량에 따른 배지의 총 무게를 입력한 후, 물공급을 시작하여 혼합배지가 입력해 둔 무게에 도달하면 물 공급이 중단된다. 또한 물 공급을 자동화하여 반복되는 배지 조제 작업에서 사용자의 수고를 경감시켜 편의성을 향상시킬 수 있다. 그리고 버섯 종류별 배지 조성별로 혼합 배지의 알맞은 수분 함량의 정확도를 향상시킬 수 있고, 균 배양 기간, 버섯 발생 및 생육 기간이 균일하게 유지되어 배지를 안정적으로 생산할 수 있다. 따라서, 연중 버섯 품질 및 수량 안정으로 버섯 농가의 경영 안정을 도모할 수 있다.

3-Hyroxyflavone in Maturation Medium Supports In Vitro Development of Fertilized Bovine Follicular Oocytes

  • Kim, Se-Woong;Park, Jong-Im;Jung, Yeon-Gil;Roh, Sangho
    • Reproductive and Developmental Biology
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    • 제38권4호
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    • pp.143-146
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    • 2014
  • Antioxidants, as reactive oxygen species scavengers, are one of the beneficial additives in serum-free defined culture medium. In this study, three separate experiments were performed to determine the effects of 3-hyroxyflavone added to the culture medium on the developmental competence of follicular bovine oocytes during in vitro maturation (IVM) and/or in vitro culture (IVC). The rate of blastocyst developed from oocytes cultured in IVM medium with 3-hyroxyflavone was significantly higher than that from control oocytes (39.0% vs. 26.3%, p<0.001), respectively. However, oocytes cultured in the medium with addition of 3-hyroxyflavone only at IVC period did not show significance in the blastocyst development when compared with control. When 3-hyroxyflavone was added to both IVM and IVC media, the rate of blastocyst formation was even significantly lower (21.1%) than control (26.5%; p<0.05). The present findings suggested that antioxidative activity of 3-hydroxyflavone added to only IVM medium beneficially affected the developmental competence of follicular bovine.

'녹색 꽃잎 도라지'의 기관분화에 미치는 배지조성 및 생장조절제의 영향 (Medium Composition and Growth Regulator on Organogenesis Platycodon grandiflorum (Jacq.) A. DC. with Yellow Green Petals)

  • 권수정;조갑연;김학현
    • 한국자원식물학회지
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    • 제27권1호
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    • pp.43-50
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    • 2014
  • 본 연구는 '녹색 꽃잎 도라지'의 기내배양 시 배지구성물질의 적정농도 구명에 의한 대량번식을 목적으로 실시하였다. '녹색 꽃잎 도라지'의 절을 배양재료로 배양조건은 MS배지의 여러가지 구성물질의 농도를 달리한 결과, 1/4MS 배지에서 가장 양호한 부정근의 형성을 보였으나 생장은 1/2MS배지에서 좋았다. Sucrose첨가는 농도가 높을수록 신초와 부정근의 형성 및 생장이 좋았다. 활성탄은 무첨가구에서 가장 많은 부정근의 형성과 양호한 생장을 보였다. 배지의 pH는 4.8로 조절된 배지에서 가장 많은 부정근을 형성하였으며, pH가 높아질수록 그 형성은 낮아지는 경향을 보였고, 부정근과 신초의 생장 또한 pH 4.8에서 가장 왕성하였다. Agar 농도별 실험에서 부정근의 형성과 생장은 그 농도가 낮아질수록 양호한 경향을 보여 가장 낮은 첨가구인 0.4% 농도구에서 가장 많은 부정근의 형성과 왕성한 생장을 보였다. 생장조절제를 혼용 첨가한 경우 신초의 형성은 BA와 IAA의 혼용구가 kinetin과 IAA 또는 NAA 혼용구에 비해 효과적이었으며, BA 0.1 mg/L와 IAA 0.5 mg/L 혼용구에서 절편체당 3.9개로 가장 많은 신초가 형성되었다.

Development of Serum Free Medium and Optimization of Porcine Rotavirus Vaccine Production

  • Ko, Yun-Mi;Kim, Myoung-Hwa;Kim, Min-Young;Jeong, Yeon-Ho
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2005년도 생물공학의 동향(XVI)
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    • pp.207-209
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    • 2005
  • Serum is a potential source of bacterial, mycoplasmal and viral contamination, and it has a possibility of the introduction of serum proteins, prion and pyrogens into the final vaccine product. For porcine Rotavirus vaccine production, it is necessary to develop serum free medium which do not cause those problems. A new serum free medium was developed for porcine Rotavirus vaccine based on DMEM, and the performance of developed serum free medium was evaluated in terms of Vero cell growth and Rotavirus vaccine production. The cell density, gown in serum free medium developed, was similar with that in serum supplemented medium. Also, it was higher than that in other commercially available serum free medium. The productivity of Rotavirus vaccine using serum free medium developed and optimum production strategies will be also discussed.

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Effects of IGF-I and EGF Supplemented to PZM3 Culture Medium on the Development of Porcine Embryos In vitro

  • Kim, J.Y.;Park, M.C.;Kim, S.B.;Park, H.D.;Lee, J.H.;Kim, Jae-Myeoung
    • Asian-Australasian Journal of Animal Sciences
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    • 제22권8호
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    • pp.1117-1123
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    • 2009
  • This study investigated the effects of IGF-I and EGF on the development of blastocysts or hatched blastocysts during the in vitro culture of embryos from immature porcine oocytes. After the in vitro maturation and fertilization of cumulus-oocyte complexes (COCs) and their culture in vitro in PZM3 medium, we examined the embryo development rate for 168 h. When different concentrations of IGF-I (0, 1, 10, 20 ng/ml) were supplemented to fertilized porcine embryos in vitro, there were no significant differences in cleavage rate, blastocyst development rate or blastocyst hatching rate among the treated groups. On the other hand, when different concentrations of EGF (0, 1, 10, 20 ng/ml) were supplemented to the in vitro culture medium, blastocyst development rate was highest in the group in which EGF was not supplemented and, specifically, it was higher than in the 20 ng/ml treatment group (p<0.05). When 10 ng/ml IGF-I and 1 ng/ml EGF were supplemented separately or simultaneously, there were no significant differences among the treated groups in blastocyst hatching rate and the number of cells in each condition. This study demonstrated that the addition of IGF-I and EGF into PZM3 medium did not enhance development of the blastocyst stage and total cell number in blastocysts.

소 체외수정란의 초기발생에 있어서 수정후 발생배지로 옮기는 시기와 난관상피세포의 영향 (Effects of Co-Culture with Oviductal Cells, Time of Transfer into Culture Medium after Insemination on Early Development of In Vitro Fertilized Bovine Oocytes)

  • 김정익;박춘근;오세훈
    • 한국가축번식학회지
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    • 제17권2호
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    • pp.121-125
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    • 1993
  • Early development of bovine oocytes fertilized in vitro in the medium with caffeine and heparin was examined in different culture systems. When the oocytes were transferred into culture medium 8 h after insemination, 12%(7/60) of penetrated oocytes cleaved to 4-cell stage 24 h after insemination. The proportions of oocytes cleaved to 80to 16-cell stage 48 h after insemination had also a to be higher in oocytes transferred into culture medium 8 h (29%) than 16 h(10%) or 24 h(4%) after insemination. 52% of the 4-cell embryos developed to morula and blastocyst stages when they were co-cultured with oviductal epithelia, whereas only 5% of embryos cultured without the epithelial cells(P<0.001). In another experiment, embryos were co-cultured with ampulla, isthmus or utero-tubal junction of oviducts. There are no significant differences in the proportions of embryos developed to morula and blastocyst stage.

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